TERF1 - telomeric repeat binding factor 1 Gene

Also Known as TRF; PIN2; TRF1; TRBF1; t-TRF1; hTRF1-AS

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7013

About TERF1

Cytogenetic location: 8q21.11 Genomic coordinates (GRCh38): 8:73,008,864-73,048,123 (from NCBI)

This gene has 16 transcripts (splice variants), 197 orthologues and 1 paralogue. Ubiquitous expression in brain (RPKM 11.2), ovary (RPKM 9.8) and 25 other tissues.

Summary

This gene encodes a telomere specific protein which is a component of the telomere nucleoprotein complex. This protein is present at telomeres throughout the cell cycle and functions as an inhibitor of Telomerase, acting in cis to limit the elongation of individual chromosome ends. The protein structure contains a C-terminal Myb motif, a dimerization domain near its N-terminus and an acidic N-terminus. Multiple transcripts of this gene are alternatively spliced products. [provided by RefSeq, Aug 2022]

TERF1 Products (14)

mRNA Protein Name
NM_001410928.1 NP_001397857.1 telomeric repeat-binding factor 1 isoform 3
NM_001413364.1 NP_001400293.1 telomeric repeat-binding factor 1 isoform 4
NM_001413365.1 NP_001400294.1 telomeric repeat-binding factor 1 isoform 5
NM_001413366.1 NP_001400295.1 telomeric repeat-binding factor 1 isoform 6
NM_001413367.1 NP_001400296.1 telomeric repeat-binding factor 1 isoform 7
NM_001413368.1 NP_001400297.1 telomeric repeat-binding factor 1 isoform 8
NM_001413369.1 NP_001400298.1 telomeric repeat-binding factor 1 isoform 9
NM_001413370.1 NP_001400299.1 telomeric repeat-binding factor 1 isoform 10
NM_001413371.1 NP_001400300.1 telomeric repeat-binding factor 1 isoform 11
NM_001413372.1 NP_001400301.1 telomeric repeat-binding factor 1 isoform 12
NM_001413373.1 NP_001400302.1 telomeric repeat-binding factor 1 isoform 13
NM_001413374.1 NP_001400303.1 telomeric repeat-binding factor 1 isoform 14
NM_003218.4 NP_003209.2 telomeric repeat-binding factor 1 isoform 2
NM_017489.3 NP_059523.2 telomeric repeat-binding factor 1 isoform 1
Molecular Function GO Annotation Evidence References Source
enables DNA binding, bending IDA
IDA: Inferred from direct assay
9130722 GOA
enables G-rich strand telomeric DNA binding IDA
IDA: Inferred from direct assay
17694070 GOA
enables ankyrin repeat binding IPI
IPI: Inferred from physical interaction
11854288 GOA
enables double-stranded telomeric DNA binding IDA
IDA: Inferred from direct assay
1406665 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
9391075 GOA
enables microtubule binding IDA
IDA: Inferred from direct assay
11943150 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9391075 GOA
enables protein homodimerization activity IPI
IPI: Inferred from physical interaction
9130722 GOA
contributes to telomerase activity IDA
IDA: Inferred from direct assay
23685356 GOA
enables telomeric DNA binding IDA
IDA: Inferred from direct assay
9034193 GOA
Biological Process GO Annotation Evidence References Source
involved in negative regulation of DNA replication IDA
IDA: Inferred from direct assay
11327863 GOA
involved in negative regulation of establishment of RNA localization to telomere IMP
IMP: Inferred from mutant phenotype
26586433 GOA
involved in negative regulation of establishment of protein localization to telomere IMP
IMP: Inferred from mutant phenotype
25589350 GOA
involved in negative regulation of exonuclease activity IDA
IDA: Inferred from direct assay
15200954 GOA
involved in negative regulation of telomere maintenance via telomerase IGI
IGI: Inferred from genetic interaction
11971978 GOA
involved in negative regulation of telomeric D-loop disassembly IDA
IDA: Inferred from direct assay
15200954 GOA
involved in positive regulation of shelterin complex assembly IMP
IMP: Inferred from mutant phenotype
24270157 GOA
involved in telomere capping IDA
IDA: Inferred from direct assay
21852327 GOA
involved in telomere maintenance IMP
IMP: Inferred from mutant phenotype
24415760 GOA
involved in telomere maintenance via telomerase IDA
IDA: Inferred from direct assay
23685356 GOA
involved in telomere maintenance via telomerase IMP
IMP: Inferred from mutant phenotype
9034193 GOA
involved in telomeric D-loop disassembly IGI
IGI: Inferred from genetic interaction
22039056 GOA
Cellular Component GO Annotation Evidence References Source
located in chromosome, telomeric region IDA
IDA: Inferred from direct assay
9034193 GOA
part of nuclear telomere cap complex IDA
IDA: Inferred from direct assay
16880378 GOA
located in nucleolus IDA
IDA: Inferred from direct assay
11701125 GOA
located in nucleus IDA
IDA: Inferred from direct assay
1406665 GOA
part of shelterin complex IDA
IDA: Inferred from direct assay
15383534 GOA
part of shelterin complex IPI
IPI: Inferred from physical interaction
15383534 GOA
colocalizes with spindle IDA
IDA: Inferred from direct assay
11943150 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

TERF1 Protein Structure

TRF

TRF: Telomere repeat binding factor (TRF) (77 - 268)

Myb_DNA-binding

Myb_DNA-binding: Myb-like DNA-binding domain (380 - 427)

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

telomeric repeat-binding factor 1

  • NIMA-interacting protein 2

TERF1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TERF1 P54274 MAPRE1 Homo sapiens Q15691
Y2H
11701125
Intra
TERF1 P54274 MAPRE1 Homo sapiens Q15691 11943150
Intra
TERF1 P54274 ACAT2 Homo sapiens Q9BWD1 21044950
Intra
TERF1 P54274 FES Homo sapiens P07332 21044950
Intra
TERF1 P54274 TNKS Homo sapiens O95271
IF
20696165
Intra
TERF1 P54274 TNKS Homo sapiens O95271 33961781
Intra
TERF1 P54274 TNKS Homo sapiens O95271 26496610
Intra
TERF1 P54274 CUSTOS Homo sapiens Q96C57 21044950
Intra
TERF1 P54274 STAG1 Homo sapiens Q8WVM7 17962804
Intra
TERF1 P54274 TERB1 Homo sapiens Q8NA31 29083416
Intra
TERF1 P54274 TERB1 Homo sapiens Q8NA31 29083416
Intra
TERF1 P54274 PRDX6 Homo sapiens P30041 21044950
Cross
TERF1 P54274 P0C6X7-PRO_0000037315 Human SARS coronavirus P0C6X7-PRO_0000037315 22046132
Cross
TERF1 P54274 P0C6X7-PRO_0000037315 Human SARS coronavirus P0C6X7-PRO_0000037315 22046132
Intra
TERF1 P54274 CEP85 Homo sapiens Q6P2H3 21044950
Intra
TERF1 P54274 DDX39A Homo sapiens O00148 21044950
Intra
TERF1 P54274 PRDX1 Homo sapiens Q06830 21044950
Intra
TERF1 P54274 NAP1L1 Homo sapiens P55209 21044950
Intra
TERF1 P54274 DNAJB1 Homo sapiens P25685 21044950
Intra
TERF1 P54274 HGD Homo sapiens Q93099 21044950
Intra
TERF1 P54274 NUB1 Homo sapiens Q9Y5A7 27214791
Intra
TERF1 P54274 NUB1 Homo sapiens Q9Y5A7
Y2H
27214791
Intra
TERF1 P54274 NUB1 Homo sapiens Q9Y5A7 27214791
Intra
TERF1 P54274 NUB1 Homo sapiens Q9Y5A7 27214791
Intra
TERF1 P54274 TNPO2 Homo sapiens O14787 21044950
Intra
TERF1 P54274 TNKS2 Homo sapiens Q9H2K2 33961781
Intra
TERF1 P54274 BLM Homo sapiens P54132 15229185
Intra
TERF1 P54274 SOAT1 Homo sapiens P35610 21044950
Intra
TERF1 P54274 MDH1 Homo sapiens P40925 21044950
Intra
TERF1 P54274 SUPT5H Homo sapiens O00267 21044950
Intra
TERF1 P54274 AMPH Homo sapiens P49418 21044950
Intra
TERF1 P54274 PAK4 Homo sapiens O96013 21044950
Intra
TERF1 P54274 RNF10 Homo sapiens Q8N5U6 21044950
Intra
TERF1 P54274 TINF2 Homo sapiens Q9BSI4 25416956
Intra
TERF1 P54274 TINF2 Homo sapiens Q9BSI4 21044950
Intra
TERF1 P54274 TINF2 Homo sapiens Q9BSI4
Y2H
11701125
Intra
TERF1 P54274 TINF2 Homo sapiens Q9BSI4 16169070
Intra
TERF1 P54274 TINF2 Homo sapiens Q9BSI4 21044950
Intra
TERF1 P54274 TINF2 Homo sapiens Q9BSI4 17589526
Intra
TERF1 P54274 TINF2 Homo sapiens Q9BSI4 16880378
Intra
TERF1 P54274 TINF2 Homo sapiens Q9BSI4 33961781
Intra
TERF1 P54274 DDX19B Homo sapiens Q9UMR2 21044950
Intra
TERF1 P54274 WFS1 Homo sapiens O76024 21044950
Intra
TERF1 P54274 LRSAM1 Homo sapiens Q6UWE0 21044950
Intra
TERF1 P54274 WARS1 Homo sapiens P23381 21044950
Intra
TERF1 P54274 PINX1 Homo sapiens Q96BK5 11701125
Intra
TERF1 P54274 PINX1 Homo sapiens Q96BK5
Y2H
11701125
Intra
TERF1 P54274 PINX1 Homo sapiens Q96BK5
Y2H
27214791
Intra
TERF1 P54274 PINX1 Homo sapiens Q96BK5 21044950
Intra
TERF1 P54274 RECQL4 Homo sapiens O94761 21044950
Intra
TERF1 P54274 PPM1G Homo sapiens O15355 21044950
Intra
TERF1 P54274 ACY1 Homo sapiens Q03154 21044950
Intra
TERF1 P54274 PACSIN2 Homo sapiens Q9UNF0 21044950
Intra
TERF1 P54274 DNPH1 Homo sapiens O43598 21044950
Intra
TERF1 P54274 TRMT1 Homo sapiens Q9NXH9 21044950
Intra
TERF1 P54274 HCLS1 Homo sapiens P14317 21044950
Intra
TERF1 P54274 CRYBB1 Homo sapiens P53674 21044950
Intra
TERF1 P54274 SYK Homo sapiens P43405 21044950
Intra
TERF1 P54274 KLHDC4 Homo sapiens Q8TBB5 21044950
Intra
TERF1 P54274 AMPD2 Homo sapiens Q01433 21044950
Intra
TERF1 P54274 FBXO4 Homo sapiens Q9UKT5-1 16275645
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant TERF1 Proteins

Cat. No. Product Name Accession Purity
HY-P74493 TRF1 Protein, Human (sf9, His) P54274-2/NP_003209 (M1-D419) ≥ 90%, as determined by reducing SDS-PAGE.

TERF1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P83494 TERF1 Antibody (YA3239) WB, ICC/IF Human, Mouse

Related Diseases

Diseases Alias
Townes-Brocks Syndrome
  • Townes Syndrome

  • Renal-Ear-Anal-Radial Syndrome

  • Anus, Imperforate, With Hand, Foot And Ear Anomalies

  • Imperforate Anus-Hand, Foot And Ear Anomalies Syndrome

  • Rear Syndrome

  • Sensorineural Deafness With Imperforate Anus And Hypoplastic Thumbs

  • Tbs

  • Deafness, Sensorineural, With Imperforate Anus And Hypoplastic Thumbs

  • Imperforate Anus With Hand, Foot And Ear Anomalies

  • Anal-Ear-Renal-Radial Malformation Syndrome

  • Deafness-Imperforate Anus-Hypoplastic Thumbs Syndrome

  • Imperforate Anus-Hand And Foot Anomalies Syndrome

  • Sensorineural Deafness-Imperforate Anus-Hypoplastic Thumbs Syndrome

  • Sensorineural Hearing Loss With Imperforate Anus And Hypoplastic Thumbs

Cherubism
  • CRBM

  • Familial Benign Giant-Cell Tumor Of The Jaw

  • Familial Fibrous Dysplasia Of Jaw

  • Familial Multilocular Cystic Disease Of The Jaws

Dyskeratosis Congenita
  • Dyskeratosis Congenita Autosomal Dominant

  • Dc

  • Dkc

  • Zinsser-Engman-Cole Syndrome

  • Dyskeratosis Congenita, Autosomal Dominant

  • Autosomal Dominant Dyskeratosis Congenita

  • Dkca

  • Dyskeratosis Congenita Scoggins Type

  • Zinsser-Cole-Engman Syndrome

  • X-Linked Dyskeratosis Congenita

  • Hoyeraal-Hreidarsson Syndrome

Dyskeratosis Congenita, Autosomal Dominant 3
  • DKCA3

  • Autosomal Dominant Dyskeratosis Congenita 3

  • Dyskeratosis Congenita, Autosomal Dominant, 3

  • Dyskeratosis Congenita, Autosomal Dominant, Type 3

Werner Syndrome
  • Werner'S Syndrome

  • WRN

  • Adult Progeria

  • Ws

  • Adult Premature Ageing Syndrome

  • Adult Premature Aging Syndrome

  • Werners Syndrome

Arthrogryposis, Renal Dysfunction, And Cholestasis 1
  • Arc Syndrome

  • ARCS1

  • Arthrogryposis Renal Dysfunction Cholestasis Syndrome

  • Arthrogryposis-Renal Dysfunction-Cholestasis Syndrome

  • Arcs

  • Arthrogryposis, Renal Dysfunction And Cholestasis Syndrome

  • Arthrogryposis, Renal Dysfunction, And Cholestasis

  • Arthrogryposis-Renal Dysfunction-Cholestasis

  • Arthrogryposis - Renal Dysfunction - Cholestasis

  • Arthrogryposis Multiplex Congenita, Renal Dysfunction, And Cholestasis

  • Arthrogryposis, Renal Dysfunction And Cholestasis Syndrome 1

  • Arthrogryposis Renal Dysfunction And Cholestasis 1

  • Arthrogryposis With Renal Dysfunction And Cholestasis Syndrome

  • Arthrogryposis, Renal Dysfunction, Cholestasis, Type 1

  • Kidney Failure

  • Renal Insufficiency

Revesz Syndrome
  • Exudative Retinopathy With Bone Marrow Failure

  • DKCA5

  • Dyskeratosis Congenita, Autosomal Dominant 5

  • Dyskeratosis Congenita With Bilateral Exudative Retinopathy

  • Retinopathy-Anemia-Central Nervous System Anomalies Syndrome

  • Revesz-Debuse Syndrome

  • Dyskeratosis Congenita, Autosomal Dominant, 5

  • Revesz Debuse Syndrome

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

Ataxia-Telangiectasia
  • Ataxia Telangiectasia

  • Louis-Bar Syndrome

  • AT

  • At1

  • Ataxia-Telangiectasia Syndrome

  • Ataxia - Telangiectasia Variant

  • Boder-Sedgwick Syndrome

  • Louis Bar Syndrome

  • Cerebello-Oculocutaneous Telangiectasia

  • Immunodeficiency With Ataxia Telangiectasia

  • A-T

  • Ataxia Telangiectasia Syndrome

  • Atm

  • Telangiectasia, Cerebello-Oculocutaneous

  • Ataxia-Telangiectasia Variant

Anaplastic Astrocytoma
  • Grade Iii Astrocytoma

  • Astrocytoma, Anaplastic

  • Grade Iii Astrocytic Tumor

Melanoma, Cutaneous Malignant 1
  • Familial Melanoma

  • Melanoma, Cutaneous Malignant, Susceptibility To, 1

  • Melanoma, Malignant

  • CMM1

  • Melanoma, Cutaneous Malignant

  • Cmm

  • Familial Atypical Mole-Malignant Melanoma Syndrome

  • Fammm

  • Melanoma, Familial

  • Mlm

  • Dysplastic Nevus Syndrome, Hereditary

  • Dns

  • B-K Mole Syndrome

  • Melanoma, Cutaneous Malignant, 1

  • Malignant Melanoma, Cutaneous

  • Melanoma, Cutaneous, Malignant, Susceptibility To, Type 1

  • Dysplastic Nevus Syndrome

  • Cutaneous Melanoma

  • Familial Atypical Mole Melanoma Syndrome

  • Hereditary Melanoma

Coats Disease
  • Exudative Retinopathy

  • Retinal Telangiectasis

  • Coats' Disease

  • Leber Miliary Aneurysm

  • Coats' Syndrome

  • Congenital Retinal Telangiectasia

Gastric Cancer
  • Stomach Cancer

  • Gastric Carcinoma

  • Stomach Carcinoma

  • Gastric Cancer, Somatic

  • Gastric Neoplasm

  • Carcinoma Of Stomach

  • Stomach Neoplasms

  • Malignant Neoplasm Of Stomach

  • Gastric Cancer Risk After H. Pylori Infection

  • Cancer Of The Stomach

  • Adult Stomach Cancer

  • Adult Stomach Carcinoma

  • GASC

  • Gastric Cancer Intestinal

  • Gastric Cancers

  • Gastric Carcinomas

  • Cancer, Gastric

  • Stomach Neoplasm

  • Malignant Neoplasm Of Body Of Stomach

  • Malignant Tumor Of Lesser Curve Of Stomach

  • Gastrocarcinoma Of Unspecified Site

  • Leather Bottle Stomach

  • Carcinoma Of Fundus Of Stomach

  • Cancer Of Fundus Of Stomach

  • Primary Malignant Neoplasm Of Body Of Stomach

  • Cancer Of Body Of Stomach

  • Primary Malignant Neoplasm Of Pyloric Antrum

  • Pyloric Antrum Cancer

  • Malignant Tumour Of Stomach

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

Aplastic Anemia
  • Aplastic Anemia, Susceptibility To

  • Anemia Aplastic

  • Idiopathic Aplastic Anemia

  • Secondary Aplastic Anemia

  • Idiopathic Bone Marrow Failure

  • Aplastic Anemia Idiopathic

  • AA

  • Anemia, Aplastic

  • Aplastic Anemia, Idiopathic

  • Erythroid Aplasia

  • Aa - [Aplastic Anaemia]

  • Haematopoietic Aplasia

  • Aleukia Haemorrhagica

  • Anaemia Due To Decreased Red Cell Production

  • Aplasia Bone Marrow

  • Aplastic Bone Marrow

  • Hypoplastic Anaemia Nos

  • Myeloid Bone Marrow Aplasia

  • Pancytopenia

  • Panhaematopenia

  • Hypoproliferative Anaemia

  • Medullary Hypoplasia

  • Red Blood Cells Hypoplastic Anaemia

  • Panmyelophthisis

  • Panhemocytopenia

  • Refractive Hypoproliferative Anaemia

  • Toxic Anaemia

  • Toxic Aplastic Anaemia

  • Aplastic Anaemia Due To Toxic Cause

  • Idiopathic Aplastic Anaemia Nos

Meningioma, Familial
  • Meningioma

  • Familial Meningioma

  • Meningioma, Familial, Susceptibility To

  • Meningeal Neoplasm

  • Meningeal Neoplasms

  • Meningiomas

  • Meningioma, Nf2-Related, Somatic

  • Meningioma, Sis-Related

  • Meningothelial Cell Tumor

  • Neoplasm Of The Meninges

  • Primary Meningeal Tumor

  • Familial Multiple Meningioma

  • MNGMA

  • Meningioma, Benign, No Icd-O Subtype

  • Intracranial Meningioma

  • Meningothelial Cell Neoplasm

  • Supratentorial Meningioma

  • Primary Neoplasm Of Spinal Meninges

  • Benign Intracranial Meningioma

  • Benign Meningioma

  • Meningeal Tumours

  • Meningeal Sarcoma Of Unspecified Site

  • Meningothelial Sarcoma Of Unspecified Site

Interstitial Lung Disease 2
  • Idiopathic Pulmonary Fibrosis

  • Ipf

  • Fibrocystic Pulmonary Dysplasia

  • Pulmonary Fibrosis, Idiopathic

  • Pulmonary Fibrosis, Idiopathic, Susceptibility To

  • Cryptogenic Fibrosing Alveolitis

  • ILD2

  • Idiopathic Pulmonary Fibrosis, Familial

  • Fibrosing Alveolitis, Cryptogenic

  • Uip

  • Fibrosing Alveolitis

  • Interstitial Pneumonitis, Usual

  • Familial Idiopathic Pulmonary Fibrosis

  • Idiopathic Fibrosing Alveolitis, Chronic Form

  • Usual Interstitial Pneumonia

  • Fibrosing Alveolitis Cryptogenic

  • Hamman-Rich Disease

  • Idiopathic Pulmonary Fibrosis Familial

  • Interstitial Pneumonitis Usual

  • Fibrosis Idiopathic Pulmonary

  • Fibrosis, Pulmonary, Idiopathic

  • Hamman-Rich Syndrome

  • Chronic Idiopathic Pulmonary Fibrosis

  • Acute Interstitial Pneumonia

  • Interstitial Pulmonary Fibrosis

  • Ipf - [Idiopathic Pulmonary Fibrosis]

  • Idiopathic Lung Fibrosis

  • Fibrosing Lung Disease

  • Pulmonary Fibrosis Nos

  • Fibrosing Pneumonitis

Fanconi Anemia, Complementation Group A
  • Fanconi Anemia

  • Fanconi Pancytopenia

  • Fanconi Anemia Complementation Group A

  • FANCA

  • Fa

  • Fanconi Panmyelopathy

  • Fanconi'S Anemia

  • Fanconi Anaemia

  • Fanconi'S Anaemia

  • Fanconi Hypoplastic Anemia

  • Estren-Dameshek Variant Of Fanconi Anemia

  • Estren-Dameshek Variant Of Fanconi Pancytopenia

  • Fanconi Anemia Estren-Dameshek Variant

  • Fanconis Anemia

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 TERF1 MGD MGI:109634
Canis familiaris TERF1 VGNC VGNC:47254
Bos taurus TERF1 VGNC VGNC:35749
Rattus norvegicus TERF1 RGD RGD:1311574
Felis catus TERF1 VGNC VGNC:66083
Macaca mulatta TERF1 VGNC VGNC:78311
Others TERF1 NCBI