RARA - retinoic acid receptor alpha Gene

Also Known as RAR; NR1B1; RARalpha

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5914

About RARA

Cytogenetic location: 17q21.2 Genomic coordinates (GRCh38): 17:40,309,180-40,357,643 (from NCBI)

This gene has 10 transcripts (splice variants), 331 orthologues, 18 paralogues and is associated with 80 phenotypes. Ubiquitous expression in lung (RPKM 10.4), spleen (RPKM 8.4) and 25 other tissues.

Summary

This gene represents a nuclear retinoic acid receptor. The encoded protein, retinoic acid receptor alpha, regulates transcription in a ligand-dependent manner. This gene has been implicated in regulation of development, differentiation, Apoptosis, granulopoeisis, and transcription of clock genes. Translocations between this locus and several Other loci have been associated with acute promyelocytic leukemia. Alternatively spliced transcript variants have been found for this locus.[provided by RefSeq, Sep 2010]

RARA Products (13)

mRNA Protein Name
NM_001024809.4 NP_001019980.1 retinoic acid receptor alpha isoform 2
XM_011525095.2 XP_011523397.1 retinoic acid receptor alpha isoform X1
NM_001033603.1
XM_005257553.2 XP_005257610.1 retinoic acid receptor alpha isoform X1
XM_047436507.1 XP_047292463.1 retinoic acid receptor alpha isoform X1
NM_001145302.3 NP_001138774.1 retinoic acid receptor alpha isoform 4
NM_001145301.3 NP_001138773.1 retinoic acid receptor alpha isoform 1
XM_047436508.1 XP_047292464.1 retinoic acid receptor alpha isoform X1
XM_047436506.1 XP_047292462.1 retinoic acid receptor alpha isoform X1
XM_011525096.2 XP_011523398.1 retinoic acid receptor alpha isoform X2
XM_005257554.2 XP_005257611.1 retinoic acid receptor alpha isoform X1
XM_005257552.6 XP_005257609.1 retinoic acid receptor alpha isoform X3
NM_000964.4 NP_000955.1 retinoic acid receptor alpha isoform 1
Molecular Function GO Annotation Evidence Références Source
enables DNA-binding transcription factor activity IDA
IDA: Inferred from direct assay
18922886 GOA
enables DNA-binding transcription repressor activity IMP
IMP: Inferred from mutant phenotype
28122350 GOA
enables RNA polymerase II cis-regulatory region sequence-specific DNA binding IDA
IDA: Inferred from direct assay
20080953 GOA
enables RNA polymerase II cis-regulatory region sequence-specific DNA binding IMP
IMP: Inferred from mutant phenotype
28122350 GOA
enables RNA polymerase II transcription regulatory region sequence-specific DNA binding IDA
IDA: Inferred from direct assay
19917671 GOA
enables alpha-actinin binding IPI
IPI: Inferred from physical interaction
22351778 GOA
enables chromatin DNA binding IDA
IDA: Inferred from direct assay
19917671 GOA
enables chromatin binding IDA
IDA: Inferred from direct assay
20080953 GOA
enables enzyme binding IPI
IPI: Inferred from physical interaction
9628876 GOA
enables nuclear receptor activity IDA
IDA: Inferred from direct assay
2825025 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9653119 GOA
enables protein domain specific binding IPI
IPI: Inferred from physical interaction
20413580 GOA
enables protein kinase A binding IDA
IDA: Inferred from direct assay
20215566 GOA
enables protein kinase B binding IPI
IPI: Inferred from physical interaction
16417524 GOA
enables retinoic acid binding IDA
IDA: Inferred from direct assay
2825025 GOA
enables retinoic acid-responsive element binding IDA
IDA: Inferred from direct assay
19917671 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 GOA
enables signaling receptor binding IDA
IDA: Inferred from direct assay
19628791 GOA
enables transcription coactivator binding IPI
IPI: Inferred from physical interaction
17641689 GOA
Biological Process GO Annotation Evidence Références Source
involved in apoptotic cell clearance IMP
IMP: Inferred from mutant phenotype
19628791 GOA
involved in cellular response to estrogen stimulus IDA
IDA: Inferred from direct assay
20080953 GOA
involved in cellular response to retinoic acid IMP
IMP: Inferred from mutant phenotype
28122350 GOA
involved in mRNA transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
1310351 GOA
involved in negative regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
20080953 GOA
involved in negative regulation of granulocyte differentiation IDA
IDA: Inferred from direct assay
19917671 GOA
involved in negative regulation of miRNA transcription IMP
IMP: Inferred from mutant phenotype
28122350 GOA
involved in negative regulation of tumor necrosis factor production IDA
IDA: Inferred from direct assay
18416830 GOA
involved in negative regulation of type II interferon production IDA
IDA: Inferred from direct assay
18416830 GOA
involved in positive regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
18845237 GOA
involved in positive regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
19628791 GOA
involved in positive regulation of T-helper 2 cell differentiation IDA
IDA: Inferred from direct assay
18416830 GOA
involved in positive regulation of binding IMP
IMP: Inferred from mutant phenotype
20080953 GOA
involved in positive regulation of cell cycle IMP
IMP: Inferred from mutant phenotype
20080953 GOA
involved in positive regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
20080953 GOA
involved in positive regulation of interleukin-13 production IDA
IDA: Inferred from direct assay
18416830 GOA
involved in positive regulation of interleukin-4 production IDA
IDA: Inferred from direct assay
18416830 GOA
involved in positive regulation of interleukin-5 production IDA
IDA: Inferred from direct assay
18416830 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
9430642 GOA
involved in positive regulation of transcription by RNA polymerase II IMP
IMP: Inferred from mutant phenotype
20080953 GOA
involved in protein phosphorylation IMP
IMP: Inferred from mutant phenotype
16456540 GOA
involved in response to retinoic acid IMP
IMP: Inferred from mutant phenotype
17538076 GOA
involved in retinoic acid receptor signaling pathway IDA
IDA: Inferred from direct assay
2825025 GOA
involved in retinoic acid receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
17538076 GOA
Cellular Component GO Annotation Evidence Références Source
part of RNA polymerase II transcription regulator complex IDA
IDA: Inferred from direct assay
1310351 GOA
located in chromatin IDA
IDA: Inferred from direct assay
2825025 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
19850744 GOA
located in nucleus IDA
IDA: Inferred from direct assay
18845237 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
2825025 GOA
part of protein-containing complex IDA
IDA: Inferred from direct assay
19917671 GOA
part of transcription regulator complex IPI
IPI: Inferred from physical interaction
9430642 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

RARA Protein Structure

zf-C4

zf-C4: Zinc finger, C4 type (two domains) (87 - 155)

Hormone_recep

Hormone_recep: Ligand-binding domain of nuclear hormone receptor (220 - 394)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 462 a.a.
Protein Preferred Names Protein Names

retinoic acid receptor alpha

  • PML-DDX5-RARA fusion

  • PML-DDX5-RARA fusion protein

  • RAR-alpha

  • nuclear receptor subfamily 1 group B member 1

  • nucleophosmin-retinoic acid receptor alpha fusion protein NPM-RAR long form

  • retinoic acid receptor, alpha polypeptide

RARA Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Références
Intra
RARA P10276 ACTN4 Homo sapiens O43707-1 22351778
Intra
RARA P10276 ACTN4 Homo sapiens O43707-1 22351778
Intra
RARA P10276 SIRT1 Homo sapiens Q96EB6 19934264
Intra
RARA P10276 BBS4 Homo sapiens Q96RK4 32296183
Intra
RARA P10276 BBS4 Homo sapiens Q96RK4 32296183
Intra
RARA P10276 BBS4 Homo sapiens Q96RK4 32296183
Intra
RARA P10276 NR2C1 Homo sapiens P13056-2 32296183
Intra
RARA P10276 NCOR1 Homo sapiens O75376 20543827
Intra
RARA P10276 NCOR1 Homo sapiens O75376 25303530
Intra
RARA P10276 NCOR1 Homo sapiens O75376 20543827
Intra
RARA P10276 NCOR1 Homo sapiens O75376
Y2H
16606617
Intra
RARA P10276 MCRS1 Homo sapiens Q96EZ8 32296183
Intra
RARA P10276 PRKDC Homo sapiens P78527 25303530
Intra
RARA P10276 GNAQ Homo sapiens P50148 22056876
Intra
RARA P10276 GNAQ Homo sapiens P50148 22056876
Intra
RARA P10276 GNAQ Homo sapiens P50148
PLA
22056876
Intra
RARA P10276 MED1 Homo sapiens Q15648 9653119
Intra
RARA P10276 MED1 Homo sapiens Q15648 25303530
Intra
RARA P10276 MED25 Homo sapiens Q71SY5 17641689
Intra
RARA P10276 MED25 Homo sapiens Q71SY5
Y2H
17641689
Intra
RARA P10276 NCOA1 Homo sapiens Q15788 16456540
Intra
RARA P10276 NCOA1 Homo sapiens Q15788
Y2H
16606617
Intra
RARA P10276 NCOA1 Homo sapiens Q15788 20543827
Intra
RARA P10276 NCOA1 Homo sapiens Q15788 20543827
Intra
RARA P10276 EZH2 Homo sapiens Q15910 17560333
Cross
RARA P10276 Asxl1 Mus musculus P59598 16606617
Cross
RARA P10276 Asxl1 Mus musculus P59598 16606617
Cross
RARA P10276 Asxl1 Mus musculus P59598 16606617
Intra
RARA P10276 PHF8 Homo sapiens Q9UPP1-2 23518351
Intra
RARA P10276 RXRG Homo sapiens P48443 32296183
Intra
RARA P10276 RXRG Homo sapiens P48443 25416956
Intra
RARA P10276 RXRG Homo sapiens P48443
Y2H
21516116
Intra
RARA P10276 RXRG Homo sapiens P48443 32296183
Intra
RARA P10276 RXRG Homo sapiens P48443 25416956
Intra
RARA P10276 RXRG Homo sapiens P48443 16189514
Intra
RARA P10276 RXRG Homo sapiens P48443 20211142
Intra
RARA P10276 RXRG Homo sapiens P48443 32296183
Intra
RARA P10276 RXRG Homo sapiens P48443 25303530
Intra
RARA P10276 RXRG Homo sapiens P48443 31515488
Intra
RARA P10276 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
RARA P10276 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
RARA P10276 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
RARA P10276 NRIP1 Homo sapiens P48552
Y2H
17641689
Intra
RARA P10276 NRIP1 Homo sapiens P48552 25416956
Intra
RARA P10276 RXRB Homo sapiens P28702 32296183
Intra
RARA P10276 RXRB Homo sapiens P28702 16189514
Intra
RARA P10276 RXRB Homo sapiens P28702 20211142
Intra
RARA P10276 RXRB Homo sapiens P28702
Y2H
29892012
Intra
RARA P10276 RXRB Homo sapiens P28702 25303530
Intra
RARA P10276 RXRB Homo sapiens P28702 29892012
Intra
RARA P10276 RXRB Homo sapiens P28702 32296183
Intra
RARA P10276 RXRB Homo sapiens P28702 32296183
Intra
RARA P10276 CCNDBP1 Homo sapiens O95273 32296183
Intra
RARA P10276 CCNDBP1 Homo sapiens O95273 32296183
Intra
RARA P10276 TEKT4 Homo sapiens Q8WW24 31515488
Intra
RARA P10276 TEKT4 Homo sapiens Q8WW24 25416956
Intra
RARA P10276 ALX1 Homo sapiens Q15699 32296183
Intra
RARA P10276 ALX1 Homo sapiens Q15699 32296183
Intra
RARA P10276 ALX1 Homo sapiens Q15699 32296183
Intra
RARA P10276 PPARG Homo sapiens P37231 32296183
Intra
RARA P10276 PPARG Homo sapiens P37231 32296183
Intra
RARA P10276 PPARG Homo sapiens P37231 32296183
Intra
RARA P10276 RXRA Homo sapiens P19793 19345331
Intra
RARA P10276 RXRA Homo sapiens P19793
GMS
21478865
Intra
RARA P10276 RXRA Homo sapiens P19793 21478865
Intra
RARA P10276 RXRA Homo sapiens P19793 21478865
Intra
RARA P10276 RXRA Homo sapiens P19793 21478865
Intra
RARA P10276 RXRA Homo sapiens P19793 21478865
Intra
RARA P10276 RXRA Homo sapiens P19793 25303530
Intra
RARA P10276 RXRA Homo sapiens P19793 16769902
Intra
RARA P10276 SUMO1 Homo sapiens P63165 24819975
Intra
RARA P10276 SUMO1 Homo sapiens P63165 24819975
Intra
RARA P10276 NCOR2 Homo sapiens Q9Y618 25303530
Intra
RARA P10276 NCOR2 Homo sapiens Q9Y618
Y2H
20543827
Intra
RARA P10276 NCOR2 Homo sapiens Q9Y618 20543827
Intra
RARA P10276 NCOA3 Homo sapiens Q9Y6Q9 16456540
Intra
RARA P10276 NCOA3 Homo sapiens Q9Y6Q9 25303530
Intra
RARA P10276 ZNF423 Homo sapiens Q2M1K9 19345331
Cross: Cross-species interaction Intra: Intraspecies interaction

RARA Anticorps

Cat. No. Nom du produit Application Reactivity
HY-P80308 Retinoic Acid Receptor alpha Antibody (YA096) WB, FC Human

Related Diseases

Diseases Alias
Intracranial Hypertension, Idiopathic
  • Pseudotumor Cerebri

  • Benign Intracranial Hypertension

  • Idiopathic Intracranial Hypertension

  • Iih

  • Benign Intracran. Hypt.

Leukemia
  • Leukemias

  • Leukaemia, Unspecified, Without Mention Of Remission

  • Aleukemic Leukaemia

  • Chronic Leukaemia

  • Subacute Leukaemia

  • Leukaemia Disorder

  • Leukaemia Nos

Hematologic Cancer
  • Hematologic Neoplasm

  • Hematologic Malignancies

  • Hematologic Neoplasms

  • Blood Cancer

  • Hematologic Malignancy

  • Hematological Tumors

  • Hematopoietic And Lymphoid System Tumor

  • Hematopoietic Cancer

  • Hematopoietic Neoplasm

  • Hematopoietic Tumors

  • Malignant Hematopoietic Neoplasm

  • Liquid Tumor

  • Hematopoietic Neoplasms

Wilms Tumor 1
  • Nephroblastoma

  • Wilms Tumor

  • WT1

  • Wilms' Tumor

  • Bilateral Wilms Tumor

  • Wilms Tumor, Type 1

  • Wilms Tumor, Somatic

  • Adult Nephroblastoma

  • Wt1 Disorder

  • Renal Embryonic Tumor

  • Adult Kidney Wilms Tumor

  • Childhood Kidney Wilms Tumor

  • Nonanaplastic Kidney Wilms Tumor

Rhabdomyosarcoma
Cleft Lip
  • Cheiloschisis

  • Labium Leporinum

  • Cleft Lip, Unilateral, Complete

  • Complete Unilateral Cleft Lip

  • Hare Lip

  • Congenital Fissure Of Lip

  • Isolated Cleft Lip

  • Cleft Lip Without Cleft Palate

  • Cleft Lip Without Cleft Palate, Unilateral

  • Isolated Cleft Lip, Unilateral

  • Cleft Lip Without Cleft Palate, Bilateral

  • Isolated Cleft Lip, Bilateral

Langerhans Cell Histiocytosis
  • Histiocytosis X

  • Lch

  • Langerhans Cell Granulomatosis

  • Langerhans-Cell Histiocytosis

  • Letterer-Siwe Disease

  • Hashimoto-Pritzger Disease

  • Histiocytosis, Langerhans-Cell

  • Langerhan'S Cell Histiocytosis

  • Letterer-Siwe Disease Involving Intra-Abdominal Lymph Nodes

  • Letterer-Siwe Disease Involving Intrapelvic Lymph Nodes

  • Letterer-Siwe Disease Involving Intrathoracic Lymph Nodes

  • Letterer-Siwe Disease Involving Lymph Nodes Of Axilla And Upper Limb

  • Letterer-Siwe Disease Involving Lymph Nodes Of Head, Face And Neck

  • Letterer-Siwe Disease Involving Lymph Nodes Of Head, Face, And Neck

  • Letterer-Siwe Disease Involving Lymph Nodes Of Inguinal Region And Lower Limb

  • Letterer-Siwe Disease Involving Lymph Nodes Of Multiple Sites

  • Letterer-Siwe Disease Involving Spleen

  • Letterer-Siwe Disease Of Intra-Abdominal Lymph Nodes

  • Letterer-Siwe Disease Of Intrapelvic Lymph Nodes

  • Letterer-Siwe Disease Of Intrathoracic Lymph Nodes

  • Letterer-Siwe Disease Of Lymph Nodes Of Axilla And Upper Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Axilla And/Or Upper Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Head, Face And Neck

  • Letterer-Siwe Disease Of Lymph Nodes Of Head, Face And/Or Neck

  • Letterer-Siwe Disease Of Lymph Nodes Of Inguinal Region Amd/Or Lower Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Inguinal Region And Lower Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Inguinal Region And/Or Lower Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Multiple Sites

  • Letterer-Siwe Disease Of Spleen

  • Familial Letterer-Siwe Disease

  • Langerhans-Cell Histiocytosis Nos

Squamous Cell Carcinoma, Head And Neck
  • Squamous Cell Carcinoma Of The Head And Neck

  • HNSCC

  • Head And Neck Squamous Cell Carcinoma

  • Head And Neck Cancer

  • Squamous Cell Carcinoma Of Lip

  • Squamous Cell Carcinoma, Head And Neck, Somatic

  • Carcinoma Of The Head And Neck

  • Squamous Cell Carcinomas Of Head And Neck

  • Scchn

  • Squamous Cell Carcinoma Of The Hypopharynx

  • Squamous Cell Carcinoma Of The Oropharynx

  • Squamous Cell Carcinoma Of Salivary Glands

  • Squamous Cell Carcinoma Of The Nasal Cavity And Paranasal Sinuses

  • Squamous Cell Carcinoma Of The Nasal Cavity And Sinuses

  • Squamous Cell Carcinoma Of The Oral Cavity

  • Squamous Cell Carcinoma Of The Lip

  • Carcinoma, Squamous Cell Of Head And Neck

  • Lip Squamous Cell Carcinoma

  • Cancer, Head/Neck

  • Carcinoma, Squamous Cell, Head And Neck

  • Salivary Gland Squamous Cell Carcinoma

  • Cancer Of Head And Neck

  • Squamous Cell Carcinoma Of Oropharynx Nos

Myeloid Leukemia
  • Myeloid Leukaemia

  • Leukaemia Myelogenous

  • Leukemia Myelogenous

  • Myeloid Granulocytic Leukaemia

  • Myeloid Granulocytic Leukemia

  • Non-Lymphocytic Leukemia

  • Leukemia, Myeloid

  • Granulocytic Leukaemia

  • Myelogenous Leukaemia

  • Myeloid Leukaemia, Unspecified, Without Mention Of Remission

Leukemia, Acute Myeloid
  • Acute Myeloid Leukemia

  • Leukemia, Acute Myelogenous

  • Acute Myelogenous Leukemia

  • AML

  • Leukemia, Acute Myeloid, Susceptibility To

  • Acute Myeloblastic Leukemia

  • Leukemia, Acute Myeloid, Reduced Survival In, Somatic

  • Acute Myeloid Leukaemia

  • Leukemia, Myelocytic, Acute

  • Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

  • Secondary Aml

  • Acute Myelocytic Leukemia

  • Leukemia, Myeloid, Acute

  • Acute Myeloid Leukemia, Somatic

  • Leukemia, Acute Myeloid, Somatic

  • Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

  • Acute Myeloblastic Leukaemia

  • Acute Myelogenous Leukaemia

  • Aml - Acute Myeloid Leukemia

  • Acute Myeloid Leukemia With Cebpa Somatic Mutations

  • Aml With Cebpa Somatic Mutations

  • Inherited Acute Myeloid Leukemia

  • Familial Aml

  • Inherited Aml

  • Pure Familial Aml

  • Pure Familial Acute Myeloid Leukemia

  • Secondary Acute Myeloid Leukemia

  • Therapy-Related Aml And Myelodysplastic Syndrome

  • Acute Myeloid Leukemia, Secondary

  • Acute Non-Lymphoblastic Leukemia

  • Acute Non-Lymphocytic Leukemia

  • Acute Biphenotypic Leukemia

  • Acute Undifferentiated Leukemia

  • Acute Myeloblastic Leukaemia With Multilineage Dysplasia

  • Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

  • Acute Myeloid Leukaemia With Myelodysplasia-Related Features

Childhood Acute Myeloid Leukemia
  • Childhood Acute Myeloid Leukaemia

  • Paediatric Acute Myeloid Leukaemia

  • Pediatric Acute Myeloid Leukemia

Cleft Palate, Isolated
  • Cleft Palate

  • Isolated Cleft Palate

  • CPI

  • Cp

  • Palatoschisis

  • Cleft Palate Isolated

  • Uranostaphyloschisis

  • Congenital Fissure Of Palate

  • Cleft Of Secondary Palate

Basal Cell Carcinoma
  • Basal Cell Cancer

  • Basal Cell Neoplasm

  • Basal Cell Carcinoma Of Skin

  • Malignant Basal Cell Tumor

  • Basal Cell Tumor

  • Epithelioma Basal Cell

  • Malignant Basal Cell Neoplasm

  • Rodent Ulcer

  • Carcinoma Basal Cell

  • Neoplasms, Basal Cell

  • Basal Cell Carcinomas

  • Experimental Organism Basal Cell Carcinoma

  • Nodulo-Ulcerative Basal Cell Carcinoma

  • Basalioma

  • Basal Cell Epithelioma Of Skin

  • Bcc - [Basal Cell Carcinoma] Of Skin

  • Rodent Ulcer Of Skin

  • Rodent Ulcer Of Unspecified Site

  • Basal Cell Epithelioma Of Unspecified Site

Breast Cancer
  • Breast Carcinoma

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Male Breast Cancer

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Embryonal Carcinoma
  • Embryonal Neoplasm

  • Embryonal Cancer

  • Primary Extragonadal Embryonal Carcinoma

  • Embryo Neoplasm

  • Carcinoma Embryonal

  • Cancer Embryonal

  • Carcinoma, Embryonal

  • Extragonadal Embryonal Carcinoma

  • Cancer, Embryonal

Keratomalacia
  • Vitamin A Deficiency

  • Night Blindness

  • Retinol Deficiency

  • Xerotic Keratitis

  • VAD

  • Vitamin A

  • Hypovitaminosis A

  • Bitot Spots

  • Bitot Spots In The Young Child

  • Conjunctival Xerosis With Bitot'S Spots

  • Vitamin A Deficiency With Cornea Xerosis

  • Vitamin A Deficiency With Cornea Ulceration Or Xerosis

Ovarian Cancer
  • Ovarian Carcinoma

  • Ovarian Neoplasm

  • Malignant Tumour Of Ovary

  • Epithelial Ovarian Cancer

  • Neoplasm Of Ovary

  • Ovarian Neoplasms

  • Ovarian Cancers

  • Malignant Neoplasm Of Ovary

  • Primary Malignant Neoplasm Of Ovary

  • Ovarian Cancer, Somatic

  • Malignant Ovarian Tumor

  • Ovary Neoplasm

  • Primary Ovarian Cancer

  • Tumor Of The Ovary

  • Cancer Of The Ovary

  • Malignant Neoplasm Of The Ovary

  • Malignant Tumor Of The Ovary

  • Ovarian Malignant Tumor

  • OC

  • Ovarian Carcinomas

  • Cancer, Ovarian

  • Cancer Of Ovary

  • Ovary Cancer

  • Ca Ovary

Acute Promyelocytic Leukemia
  • Leukemia, Acute Promyelocytic

  • Acute Myeloblastic Leukemia Type 3

  • Aml M3

  • APL

  • Leukemia, Acute Promyelocytic, Somatic

  • Aml With T(15

  • 17)(Q22

  • Q12)

  • (Pml/Raralpha) And Variants

  • Apml

  • Acute Myeloblastic Leukemia 3

  • Acute Myeloid Leukemia With T(15

  • 17)(Q22

  • Q12)

  • (Pml/Raralpha) And Variants

  • Acute Myeloblastic Leukaemia Type 3

  • Acute Myeloid Leukaemia M3

  • Acute Myeloid Leukemia M3

  • Acute Promyelocytic Leukaemia

  • M3 Anll

  • Myeloid Leukemia, Acute, M3

  • Leukemia Promyelocytic Acute

  • Leukemia, Promyelocytic, Acute

  • Leukemia, Acute, Promyelocytic

Acute Leukemia
  • Stem Cell Leukaemia

  • Stem Cell Leukemia

  • Acute Leukemias

  • Acute Undifferentiated Leukemia

  • Undifferentiated Leukemia

  • Acute Leukaemia Of Unspecified Cell Type Without Mention Of Remission

  • Blast Cell Leukaemia

  • Blast Leukaemia

  • Blastic Leukaemia

  • Undifferentiated Leukaemia

Teratocarcinoma
  • Mixed Embryonal Carcinoma And Teratoma

Myelodysplastic Syndrome
  • Myelodysplastic Syndromes

  • Myelodysplasia

  • MDS

  • Myelodysplastic Syndrome Included

  • Myelodysplastic Syndrome, Susceptibility To, Included

  • Myelodysplastic Syndrome, Somatic

  • Myelodysplastic Syndrome, Susceptibility To

Juvenile Myelomonocytic Leukemia
  • Leukemia, Juvenile Myelomonocytic

  • JMML

  • Leukemia, Juvenile Myelomonocytic, Somatic

  • Juvenile Chronic Myelomonocytic Leukemia

  • Juvenile Chronic Myelogenous Leukemia

  • Leukemia, Myelomonocytic, Juvenile

  • Juvenile Myelomonocytic Leukaemia Without Mention Of Remission

Aleukemic Leukemia Cutis
Monocytic Leukemia
  • Monocytic Leukaemia

  • Schilling'S Leukaemia

  • Schilling'S Leukemia

  • M5b Acute Differentiated Monocytic Leukemia

Leukemia, Acute Monocytic
  • Acute Monocytic Leukemia

  • Acute Monoblastic Leukemia And Acute Monocytic Leukemia

  • Acute Monocytic Leukaemia

  • Acute Monocytic Leukaemia Without Mention Of Remission

  • Acute Monocytic Leukemia Without Mention Of Remission

  • Acute Monocytic Leukemia, Fab M5

  • Acute Monocytic Leukemia, Morphology

  • Leukemia, Monocytic, Acute

  • M5b Acute Differentiated Monocytic Leukemia

Smith-Magenis Syndrome
  • SMS

  • Chromosome 17p11.2 Deletion Syndrome

  • 17p11.2 Microdeletion Syndrome

  • 17p11.2 Monosomy

  • Chromosome 17p Deletion Syndrome

  • Del(17)

  • P11.2

  • 17p- Syndrome

  • Deletion 17p Syndrome

  • Partial Monosomy 17p

Leukemia, Chronic Myeloid
  • Chronic Myeloid Leukemia

  • Chronic Myelogenous Leukemia

  • CML

  • Chronic Granulocytic Leukemia

  • Leukemia, Philadelphia Chromosome-Positive, Resistant To Imatinib

  • Chronic Myeloid Leukaemia

  • Chronic Granulocytic Leukaemia

  • Chronic Myelogenous Leukaemia

  • Myeloid Leukemia, Chronic

  • Leukemia, Chronic Myelogenous

  • Leukemia, Chronic Myeloid, Philadelphia Chromosome Positive, Somatic

  • Cml - Chronic Myelogenous Leukemia

  • Cgl

  • Chronic Myelocytic Leukemia

  • Leukemia, Chronic Myeloid, Atypical

  • ACML

  • Atypical Chronic Myeloid Leukemia Bcr-Abl1 Negative

  • Myeloid Leukemia Chronic

  • Leukemia, Myeloid, Chronic

  • Leukemia, Myeloid, Chronic, Atypical, Bcr-Abl Negative

  • Cml- [Chronic Myeloid Leukaemia]

  • Cgl - [Chronic Granulocytic Leukaemia]

  • Chronic Myelocytic Leukaemia

Primary Cutaneous T-Cell Non-Hodgkin Lymphoma
  • Cutaneous T-Cell Lymphoma

  • Cutaneous T Cell Lymphoma

  • Lymphoma, T-Cell, Cutaneous

  • Ctcl

  • Lymphoma T-Cell Cutaneous

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus RARA VGNC VGNC:69240
Rattus norvegicus RARA RGD RGD:3534
Bos taurus RARA VGNC VGNC:33729
Macaca mulatta RARA VGNC VGNC:76662
Canis familiaris RARA VGNC VGNC:45351
Mus musculus RARA MGD MGI:97856
Others RARA NCBI