YY1 - YY1 transcription factor Gene

Also Known as DELTA; NF-E1; UCRBP; GADEVS; INO80S; YIN-YANG-1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7528

About YY1

Cytogenetic location: 14q32.2 Genomic coordinates (GRCh38): 14:100,239,144-100,282,788 (from NCBI)

This gene has 9 transcripts (splice variants), 223 orthologues, 2 paralogues and is associated with 4 phenotypes. Ubiquitous expression in thyroid (RPKM 24.9), bone marrow (RPKM 20.9) and 25 other tissues.

Summary

YY1 is a ubiquitously distributed transcription factor belonging to the GLI-Kruppel class of zinc finger proteins. The protein is involved in repressing and activating a diverse number of promoters. YY1 may direct histone deacetylases and histone acetyltransferases to a promoter in order to activate or repress the promoter, thus implicating histone modification in the function of YY1. [provided by RefSeq, Jul 2008]

YY1 Products (1)

mRNA Protein Name
NM_003403.5 NP_003394.1 transcriptional repressor protein YY1
Molecular Function GO Annotation Evidence Verweise Source
enables DNA binding IDA
IDA: Inferred from direct assay
21729784 GOA
enables DNA-binding transcription activator activity, RNA polymerase II-specific IDA
IDA: Inferred from direct assay
30241939 GOA
enables DNA-binding transcription factor activity, RNA polymerase II-specific IDA
IDA: Inferred from direct assay
15329343 GOA
enables DNA-binding transcription factor binding IPI
IPI: Inferred from physical interaction
15674325 GOA
enables DNA-binding transcription repressor activity, RNA polymerase II-specific IDA
IDA: Inferred from direct assay
1655281 GOA
enables RNA binding IDA
IDA: Inferred from direct assay
21729784 GOA
enables RNA polymerase II cis-regulatory region sequence-specific DNA binding IDA
IDA: Inferred from direct assay
30241939 GOA
enables SMAD binding IMP
IMP: Inferred from mutant phenotype
15329343 GOA
enables cis-regulatory region sequence-specific DNA binding IDA
IDA: Inferred from direct assay
16260628 GOA
enables cis-regulatory region sequence-specific DNA binding IMP
IMP: Inferred from mutant phenotype
15329343 GOA
enables four-way junction DNA binding IDA
IDA: Inferred from direct assay
18026119 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
7853498 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 GOA
enables transcription cis-regulatory region binding IDA
IDA: Inferred from direct assay
9857059 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in DNA damage response IMP
IMP: Inferred from mutant phenotype
18026119 GOA
involved in cellular response to UV IMP
IMP: Inferred from mutant phenotype
18026119 GOA
involved in chromatin remodeling IDA
IDA: Inferred from direct assay
21303910 GOA
involved in double-strand break repair via homologous recombination IMP
IMP: Inferred from mutant phenotype
18026119 GOA
involved in negative regulation of gene expression IMP
IMP: Inferred from mutant phenotype
22065573 GOA
involved in negative regulation of interferon-beta production IDA
IDA: Inferred from direct assay
16260628 GOA
acts upstream of or within negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
9857059 GOA
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
1655281 GOA
involved in positive regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
27641337 GOA
involved in regulation of DNA replication IMP
IMP: Inferred from mutant phenotype
25016522 GOA
involved in regulation of DNA strand elongation IMP
IMP: Inferred from mutant phenotype
25016522 GOA
involved in regulation of cell cycle IMP
IMP: Inferred from mutant phenotype
26340092 GOA
involved in regulation of chromosome organization IMP
IMP: Inferred from mutant phenotype
26340092 GOA
involved in regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
15329343 GOA
involved in response to UV-C IMP
IMP: Inferred from mutant phenotype
18026119 GOA
Cellular Component GO Annotation Evidence Verweise Source
part of Ino80 complex IDA
IDA: Inferred from direct assay
18026119 GOA
located in nucleus IDA
IDA: Inferred from direct assay
10791971 GOA
located in nucleus IMP
IMP: Inferred from mutant phenotype
22065573 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

YY1 Protein Structure

zf-C2H2_4

zf-C2H2_4: C2H2-type zinc finger (297 - 320)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (340 - 365)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (369 - 395)

  • 0
  • 100
  • 200
  • 300
  • 414 a.a.
Protein Preferred Names Protein Names

transcriptional repressor protein YY1

  • INO80 complex subunit S

YY1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
YY1 P25490 KRTAP10-8 Homo sapiens P60410 32296183
Intra
YY1 P25490 KRTAP10-8 Homo sapiens P60410 32296183
Intra
YY1 P25490 KRTAP10-8 Homo sapiens P60410 32296183
Intra
YY1 P25490 KRTAP10-9 Homo sapiens P60411 32296183
Intra
YY1 P25490 KRTAP10-5 Homo sapiens P60370 32296183
Intra
YY1 P25490 KRTAP4-2 Homo sapiens Q9BYR5 32296183
Intra
YY1 P25490 KRTAP12-2 Homo sapiens P59991 32296183
Intra
YY1 P25490 KRTAP5-6 Homo sapiens Q6L8G9 32296183
Intra
YY1 P25490 KRTAP9-3 Homo sapiens Q9BYQ3 32296183
Intra
YY1 P25490 KRTAP9-3 Homo sapiens Q9BYQ3 32296183
Intra
YY1 P25490 KRTAP9-3 Homo sapiens Q9BYQ3 32296183
Intra
YY1 P25490 DMWD Homo sapiens G5E9A7 32814053
Intra
YY1 P25490 DMWD Homo sapiens G5E9A7 32814053
Intra
YY1 P25490 DMWD Homo sapiens G5E9A7 32814053
Intra
YY1 P25490 KRTAP1-5 Homo sapiens Q9BYS1 32296183
Intra
YY1 P25490 KRTAP1-5 Homo sapiens Q9BYS1 32296183
Intra
YY1 P25490 KRTAP1-5 Homo sapiens Q9BYS1 32296183
Intra
YY1 P25490 KRTAP1-3 Homo sapiens Q8IUG1 32296183
Intra
YY1 P25490 KRTAP1-3 Homo sapiens Q8IUG1 32296183
Intra
YY1 P25490 KRTAP12-3 Homo sapiens P60328 32296183
Intra
YY1 P25490 VWC2 Homo sapiens Q2TAL6 32296183
Intra
YY1 P25490 VWC2 Homo sapiens Q2TAL6 32296183
Intra
YY1 P25490 VWC2 Homo sapiens Q2TAL6 32296183
Intra
YY1 P25490 KRTAP9-8 Homo sapiens Q9BYQ0 32296183
Intra
YY1 P25490 KRTAP9-8 Homo sapiens Q9BYQ0 32296183
Intra
YY1 P25490 KRTAP9-8 Homo sapiens Q9BYQ0 32296183
Intra
YY1 P25490 KRTAP17-1 Homo sapiens Q9BYP8 32296183
Intra
YY1 P25490 KRTAP17-1 Homo sapiens Q9BYP8 32296183
Intra
YY1 P25490 KRTAP17-1 Homo sapiens Q9BYP8 32296183
Intra
YY1 P25490 KRTAP4-5 Homo sapiens Q9BYR2 32296183
Intra
YY1 P25490 LHX3 Homo sapiens Q9UBR4-2 32296183
Intra
YY1 P25490 LHX3 Homo sapiens Q9UBR4-2 32296183
Intra
YY1 P25490 LHX3 Homo sapiens Q9UBR4-2 32296183
Intra
YY1 P25490 YY1AP1 Homo sapiens Q9H869-2
Y2H
14744866
Intra
YY1 P25490 YY1AP1 Homo sapiens Q9H869-2 14744866
Intra
YY1 P25490 YY1AP1 Homo sapiens Q9H869-2 14744866
Intra
YY1 P25490 ESM1 Homo sapiens Q9NQ30 32296183
Intra
YY1 P25490 ESM1 Homo sapiens Q9NQ30 32296183
Intra
YY1 P25490 ESM1 Homo sapiens Q9NQ30 32296183
Intra
YY1 P25490 KRTAP2-4 Homo sapiens Q9BYR9 32296183
Intra
YY1 P25490 ZNF85 Homo sapiens Q49A12 32296183
Intra
YY1 P25490 ZNF85 Homo sapiens Q49A12 32296183
Intra
YY1 P25490 ZNF85 Homo sapiens Q49A12 32296183
Intra
YY1 P25490 XAGE1A Homo sapiens Q9HD64 32296183
Intra
YY1 P25490 XAGE1A Homo sapiens Q9HD64 32296183
Intra
YY1 P25490 XAGE1A Homo sapiens Q9HD64 32296183
Intra
YY1 P25490 SF3A2 Homo sapiens Q15428 32296183
Intra
YY1 P25490 SF3A2 Homo sapiens Q15428 32296183
Intra
YY1 P25490 SF3A2 Homo sapiens Q15428 32296183
Intra
YY1 P25490 GMCL1 Homo sapiens Q96IK5 32296183
Intra
YY1 P25490 GMCL1 Homo sapiens Q96IK5 32296183
Intra
YY1 P25490 GMCL1 Homo sapiens Q96IK5 32296183
Intra
YY1 P25490 GRN Homo sapiens P28799-2 32814053
Intra
YY1 P25490 GRN Homo sapiens P28799-2 32814053
Intra
YY1 P25490 GRN Homo sapiens P28799-2 32814053
Intra
YY1 P25490 LHX4 Homo sapiens Q969G2 32296183
Intra
YY1 P25490 LHX4 Homo sapiens Q969G2 32296183
Intra
YY1 P25490 LHX4 Homo sapiens Q969G2 32296183
Intra
YY1 P25490 TGFBR2 Homo sapiens P37173 32814053
Intra
YY1 P25490 TGFBR2 Homo sapiens P37173 32814053
Intra
YY1 P25490 TGFBR2 Homo sapiens P37173 32814053
Intra
YY1 P25490 SERPINH1 Homo sapiens P50454 32814053
Intra
YY1 P25490 SERPINH1 Homo sapiens P50454 32814053
Intra
YY1 P25490 SERPINH1 Homo sapiens P50454 32814053
Intra
YY1 P25490 PRKDC Homo sapiens P78527 18026119
Intra
YY1 P25490 PRKDC Homo sapiens P78527 18026119
Intra
YY1 P25490 RUVBL2 Homo sapiens Q9Y230 35271311
Intra
YY1 P25490 RUVBL2 Homo sapiens Q9Y230 18026119
Intra
YY1 P25490 RUVBL2 Homo sapiens Q9Y230
TAP
27705803
Intra
YY1 P25490 RUVBL2 Homo sapiens Q9Y230 18026119
Intra
YY1 P25490 RUVBL2 Homo sapiens Q9Y230 35140242
Intra
YY1 P25490 RUVBL1 Homo sapiens Q9Y265 18026119
Intra
YY1 P25490 RUVBL1 Homo sapiens Q9Y265
TAP
27705803
Intra
YY1 P25490 RUVBL1 Homo sapiens Q9Y265 18026119
Intra
YY1 P25490 RUVBL1 Homo sapiens Q9Y265 35271311
Intra
YY1 P25490 ACTL6A Homo sapiens O96019
TAP
27705803
Intra
YY1 P25490 ACTL6A Homo sapiens O96019 18026119
Intra
YY1 P25490 ACTL6A Homo sapiens O96019 35271311
Intra
YY1 P25490 ACTL6A Homo sapiens O96019 18026119
Intra
YY1 P25490 ACTL6A Homo sapiens O96019 35140242
Intra
YY1 P25490 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
YY1 P25490 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
YY1 P25490 MED20 Homo sapiens Q9H944 32296183
Intra
YY1 P25490 MED20 Homo sapiens Q9H944 32296183
Intra
YY1 P25490 MED20 Homo sapiens Q9H944 32296183
Intra
YY1 P25490 SPRED1 Homo sapiens Q7Z699 32814053
Intra
YY1 P25490 SPRED1 Homo sapiens Q7Z699 32814053
Intra
YY1 P25490 SPRED1 Homo sapiens Q7Z699 32814053
Intra
YY1 P25490 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
YY1 P25490 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
YY1 P25490 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
YY1 P25490 ALOXE3 Homo sapiens Q9BYJ1 32296183
Intra
YY1 P25490 ALOXE3 Homo sapiens Q9BYJ1 32296183
Intra
YY1 P25490 ALOXE3 Homo sapiens Q9BYJ1 32296183
Intra
YY1 P25490 FHL2 Homo sapiens Q14192 32296183
Intra
YY1 P25490 WFS1 Homo sapiens O76024 32814053
Intra
YY1 P25490 WFS1 Homo sapiens O76024 32814053
Intra
YY1 P25490 WFS1 Homo sapiens O76024 32814053
Intra
YY1 P25490 MDFI Homo sapiens Q99750 32296183
Intra
YY1 P25490 MDFI Homo sapiens Q99750 32296183
Intra
YY1 P25490 MDFI Homo sapiens Q99750 32296183
Intra
YY1 P25490 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
YY1 P25490 CEP76 Homo sapiens Q8TAP6 32296183
Intra
YY1 P25490 CEP76 Homo sapiens Q8TAP6 32296183
Intra
YY1 P25490 CEP76 Homo sapiens Q8TAP6 32296183
Intra
YY1 P25490 ARRB1 Homo sapiens P49407 19879840
Cross
YY1 P25490 E1A Human adenovirus B Q8JSK4 7853498
Intra
YY1 P25490 RAD23A Homo sapiens P54725 32814053
Intra
YY1 P25490 RAD23A Homo sapiens P54725 32814053
Intra
YY1 P25490 RAD23A Homo sapiens P54725 32814053
Intra
YY1 P25490 GRN Homo sapiens P28799 32814053
Intra
YY1 P25490 GRN Homo sapiens P28799 32814053
Intra
YY1 P25490 GRN Homo sapiens P28799 32814053
Intra
YY1 P25490 INO80 Homo sapiens Q9ULG1 35140242
Intra
YY1 P25490 INO80 Homo sapiens Q9ULG1 35271311
Intra
YY1 P25490 INO80 Homo sapiens Q9ULG1 35140242
Intra
YY1 P25490 INO80 Homo sapiens Q9ULG1 18026119
Intra
YY1 P25490 INO80 Homo sapiens Q9ULG1
TAP
24981860
Intra
YY1 P25490 INO80 Homo sapiens Q9ULG1
TAP
27705803
Intra
YY1 P25490 INO80 Homo sapiens Q9ULG1 18026119
Intra
YY1 P25490 CBX5 Homo sapiens P45973 32814053
Intra
YY1 P25490 CBX5 Homo sapiens P45973 32814053
Intra
YY1 P25490 CBX5 Homo sapiens P45973 32814053
Cross
YY1 P25490 Rybp Mus musculus Q8CCI5 10369680
Intra
YY1 P25490 YY1AP1 Homo sapiens Q9H869 14744866
Intra
YY1 P25490 YY1AP1 Homo sapiens Q9H869 14744866
Cross
YY1 P25490 e1a_ade12 Human adenovirus A P03259 7853498
Cross
YY1 P25490 e1a_ade12 Human adenovirus A P03259
Y2H
7853498
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant YY1 Proteins

Art. -Nr. Produktname Accession Reinheit
HY-P71136 YY1 Protein, Human (His) P25490 (V221-G321) ≥ 95%, as determined by reducing SDS-PAGE.

YY1 Antibodies

Art. -Nr. Produktname Anwendung Reactivity
HY-P82701 YY1 Antibody (YA2446) WB, IHC-P, ICC/IF, FC Human, Mouse, Rat
HY-P82701A YY1 Antibody (YA2446)(PBS only) WB, IP Human, Mouse, Rat

Related Diseases

Diseases Alias
Gabriele-De Vries Syndrome
  • GADEVS

  • Gabriele De Vries Syndrome

  • Yy1 Intellectual Disability Syndrome

  • Yy1 Haploinsufficiency Syndrome

Insulinoma
  • Islet Cell Adenoma

  • Insulin-Producing Tumor Of Islet Cells

  • Adenoma Islet Cell

  • Islet Cell Tumor

  • Experimental Organism Islet Cell Adenoma Neoplasm

Pregnancy Loss, Recurrent 1
  • Pregnancy Loss, Recurrent, Susceptibility To, 1

  • Rpl

  • RPRGL1

  • Rprgl

  • Recurrent Miscarriage

  • Recurrent Spontaneous Abortion

  • Abortion, Spontaneous, Recurrent

  • Fetal Loss, Recurrent

  • Fetal Loss, Recurrent, Susceptibility To

  • Miscarriage, Recurrent

  • Embryonic Loss, Recurrent

  • Stillbirth, Recurrent

  • Pregnancy Loss, Recurrent, 1

  • Recurrent Embryonic Loss

  • Recurrent Fetal Loss

  • Recurrent Stillbirth

  • Spontaneous Recurrent Abortion

  • Miscarriage Recurrent

  • Pregnancy Loss, Recurrent, Susceptibility To, Type 1

  • Abortion, Habitual

Grange Syndrome
  • Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly

  • Grange Occlusive Arterial Syndrome

  • GRNG

  • Progressive Arterial Occlusive Disease-Hypertension-Heart Defects-Bone Fragility-Brachysyndactyly Syndrome

Fibromuscular Dysplasia
Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease
  • PKD3

  • Polycystic Kidney Disease, Adult, Type Iii

  • Apkd3

  • Polycystic Kidney Disease 3

  • Polycystic Kidney Disease, Type 3

  • Polycystic Kidney Disease 3 Without Polycystic Liver Disease

  • Polycystic Kidney Disease 3, Autosomal Dominant

Cervical Cancer
  • Cervical Cancer, Somatic

  • Neoplasm Of Uterine Cervix

  • Cervix Cancer

  • Uterine Cervical Neoplasm

  • Cervical Neoplasm

  • Cervix Uteri Cancer

  • Tumor Of The Cervix Uteri

  • CERCA

  • Uterine Cervical Cancer

  • Neoplasms Cervical

  • Uterine Cervical Neoplasms

  • Cervical Cancers

  • Cancer, Cervical, Somatic

  • Malignant Tumor Of Cervix

  • Cervix Carcinoma

Lung Cancer
  • Lung Carcinoma

  • Non-Small Cell Lung Carcinoma

  • Lung Cancer, Susceptibility To

  • Lung Cancer, Protection Against

  • Adenocarcinoma Of Lung, Somatic

  • Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer

  • Lung Neoplasm

  • Carcinoma Of Lung

  • Lung Non-Small Cell Carcinoma

  • Non-Small Cell Lung Cancer

  • Nsclc

  • Lung Neoplasms

  • Malignant Neoplasm Of Lung

  • Alveolar Cell Carcinoma

  • Nonsmall Cell Lung Cancer, Somatic

  • Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer, Susceptibility To

  • Lung Cancer, Somatic

  • Lung Cancer, Resistance To

  • Cancer Of Lung

  • Cancer Of Bronchus

  • Cancer Of The Lung

  • Lung Malignancies

  • Lung Malignant Tumors

  • Malignant Lung Tumor

  • Malignant Tumor Of Lung

  • Pulmonary Cancer

  • Pulmonary Carcinoma

  • Pulmonary Neoplasms

  • Respiratory Carcinoma

  • LNCR

  • Adenocarcinoma Of Lung

  • Neoplasm Of Lung

  • Cancer Lung

  • Carcinoma Non-Small Cell Lung

  • Carcinoma, Non-Small-Cell Lung

  • Lung Cancers

  • Lung Carcinomas

  • Cancer, Lung

  • Cancer, Lung, Non-Small Cell

  • Primary Malignant Neoplasm Of Lung

  • Bronchioloalveolar Adenocarcinoma

Developmental And Epileptic Encephalopathy 66
  • DEE66

  • Epileptic Encephalopathy, Early Infantile, 66

  • Eiee66

  • Developmental And Epileptic Encephalopathy, 66

  • Early Infantile Epileptic Encephalopathy 66

  • Encephalopathy, Epileptic, Early Infantile, Type 66

Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
  • ADLD

  • Adult-Onset Autosomal Dominant Demyelinating Leukodystrophy

  • Leukodystrophy, Adult-Onset, Autosomal Dominant

  • Adult-Onset Autosomal Dominant Leukodystrophy

  • Autosomal Dominant Leukodystrophy With Autonomic Disease

  • Autosomal Dominant Adult-Onset Demyelinating Leukodystrophy

  • Multiple Sclerosis-Like Disorder

  • Pelizaeus-Merzbacher Disease, Autosomal Dominant Or Late-Onset Type, Formerly

  • Autosomal-Dominant Or Late-Onset Type Pelizaeus-Merzbacher Disease

  • Pelizaeus-Merzbacher Disease, Autosomal Dominant Or Late-Onset Type

  • Adult-Onset Autosomal Dominant Leukodystrophy With Autonomic Symptoms

  • Lmnb1-Related Adult-Onset Autosomal Dominant Leukodystrophy

  • Leukodystrophy, Demyelinating, Autosomal Dominant, Adult-Onset

  • Pelizaeus-Merzbacher Disease Autosomal Dominant

  • Pelizaeus-Merzbacher Disease Late-Onset Type

  • Adult Onset Autosomal Dominant Leukodystrophy

Human Immunodeficiency Virus Type 1
  • Aids

  • Hiv/Aids

  • Aids, Delayed/Rapid Progression To

  • Hiv-1, Susceptibility To

  • Hiv-1 Viremia, Susceptibility To

  • Human Immunodeficiency Virus Type 1, Susceptibility To

  • Hiv-1

  • Aids, Slow Progression To

  • Rapid Progression To Aids From Hiv1 Infection

  • Hiv1 Infection, Resistance To

  • Hiv1 Infection

  • Hiv-1 Viremia

  • Aids, Resistance To

  • Aids, Rapid Progression To

  • Hiv/Aids, Susceptibility To

  • Hiv-1, Resistance To

  • Hiv1, Resistance To

  • Hiv1

  • Hiv-1 Disease, Delayed Progression Of

  • Hiv-1 Disease, Rapid Progression Of

  • Hiv Infection, Resistance To

  • Hiv Type 1, Susceptibility To

  • Hiv Type 1

  • Hiv-1 Infection

  • Human Immunodeficiency Virus I Infection

  • Acquired Immunodeficiency Syndrome

  • Hiv-Infection/Aids

Rett Syndrome
  • Atypical Rett Syndrome

  • RTT

  • Rett Disorder

  • Rts

  • Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use

  • Rett Syndrome, Preserved Speech Variant

  • Rett Syndrome, Atypical

  • Rett'S Disorder

  • Rett Syndrome Variant

  • Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome

  • Cerebroatrophic Hyperammonemia

  • Rett Like Syndrome

  • Rett'S Syndrome

  • Atypical Rtt

  • Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use

  • Rett Syndrome Preserved Speech Variant

  • Rett Syndrome Zappella Variant

  • Rett Syndrome, Zappella Variant

Pancreatic Cancer
  • Pancreatic Carcinoma

  • Carcinoma Of Pancreas

  • Familial Pancreatic Carcinoma

  • Pancreatic Neoplasm

  • Pancreatic Carcinoma, Familial

  • Malignant Neoplasm Of Pancreas

  • Pancreatic Acinar Carcinoma

  • Pancreatic Tumor

  • Familial Pancreatic Cancer

  • Neoplasm Of The Pancreas

  • Cancer Of The Pancreas

  • Pancreatic Carcinoma, Somatic

  • Pancreatic Cancer, Somatic

  • Ca Body Of Pancreas

  • Ca Head Of Pancreas

  • Ca Tail Of Pancreas

  • Malignant Neoplasm Of Body Of Pancreas

  • Malignant Neoplasm Of Head Of Pancreas

  • Malignant Neoplasm Of Tail Of Pancreas

  • Pancreas Neoplasm

  • Exocrine Cancer

  • Exocrine Pancreas Carcinoma

  • Hereditary Pancreatic Cancer

  • Hereditary Pancreatic Carcinoma

  • PNCA

  • Pancreatic Cancer, Susceptibility To

  • Carcinoma Of Head Of Pancreas

  • Pancreatic Neoplasms

  • Pancreatic Tumors

  • Cancer, Pancreatic

  • Cancer Of Pancreas

  • Mixed Islet Cell With Exocrine Carcinoma Of Unspecified Site

Dystonia
  • Dystonic Disease

  • Dystonic Disorder

  • Dystonia Disorders

  • Neuroleptic Dyskinesia

Coffin-Siris Syndrome 1
  • Coffin-Siris Syndrome

  • Fifth Digit Syndrome

  • Css

  • CSS1

  • Mrd12

  • Mental Retardation, Autosomal Dominant 12

  • Hhid

  • Dwarfism-Onychodysplasia

  • Hypertrichosis, Hyperkeratosis, Mental Retardation, And Distinctive Facial Features

  • Autosomal Dominant Mental Retardation 12

  • Short Stature-Onychodysplasia.

  • Intellectual Disability With Absent Fifth Fingernail And Terminal Phalanx

  • Mental Retardation With Hypoplastic Fifth Fingernails And Toenails

  • Short Stature-Onychodysplasia

  • Coffin-Siris Syndrome, Type 1

  • Mental Retardation, Autosomal Dominant, Type 12

Prostate Cancer
  • Prostate Carcinoma

  • Prostate Cancer, Familial

  • Prostate Neoplasm

  • Prostate Cancer, Somatic

  • Prostate Cancer, Susceptibility To

  • Prostatic Cancer

  • Prostatic Neoplasms

  • Hereditary Prostate Cancer

  • Prostatic Neoplasm

  • Cancer Of Prostate

  • Carcinoma Of Prostate

  • Familial Prostate Cancer

  • Familial Prostate Carcinoma

  • Malignant Tumor Of Prostate

  • Malignant Neoplasm Of Prostate

  • Prostate Cancer, Familial, Susceptibility To

  • Malignant Tumor Of The Prostate

  • Ngp - New Growth Of Prostate

  • Tumor Of The Prostate

  • Prostate Cancer, Hereditary

  • Cancer Of The Prostate

  • Malignant Neoplasm Of The Prostate

  • Prostatic Carcinoma

  • PC

  • Prca

  • Cancer, Prostate

  • Malignant Prostatic Tumour

  • Malignant Tumour Of Prostate

  • Primary Prostate Cancer

  • Primary Malignant Neoplasm Of Prostate

  • Prostate Gland Cancer

Cystic Fibrosis
  • Mucoviscidosis

  • CF

  • Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

  • Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

  • Cystic Fibrosis Lung Disease, Modifier Of

  • Cystic Fibrosis Of Pancreas

  • Fibrocystic Disease Of Pancreas

  • Cf - [Cystic Fibrosis]

  • Cystic Fibrosis Nos

  • Fibrocystic Disease

  • Fibrocystic Disease Of The Pancreas

  • Mucoviscidosis Of Pancreas

  • Nonproliferative Fibrocystic Disease

  • Pancreatic Cystic Fibrosis

Lymphoma, Non-Hodgkin, Familial
  • Non-Hodgkin Lymphoma

  • Lymphoma, Non-Hodgkin

  • NHL

  • Lymphoma, Non-Hodgkin, Somatic

  • Lymphoma, Follicular, Somatic

  • Familial Non-Hodgkin Lymphoma

  • Lymphoma Non-Hodgkins

  • Follicular Lymphoma, Somatic

  • Lymphosarcoma

  • Non-Hodgkins Lymphoma

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
Mus musculus YY1 MGD MGI:99150
Macaca mulatta YY1 VGNC VGNC:99343
Rattus norvegicus YY1 RGD RGD:3982
Canis familiaris YY1 VGNC VGNC:51693
Bos taurus YY1 VGNC VGNC:55896
Others YY1 NCBI