CTBP2 - C-terminal binding protein 2 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 1488

About CTBP2

Cytogenetic location: 10q26.13 Genomic coordinates (GRCh38): 10:124,984,317-125,162,463 (from NCBI)

This gene has 14 transcripts (splice variants), 200 orthologues and 3 paralogues. Ubiquitous expression in thyroid (RPKM 13.6), endometrium (RPKM 9.4) and 24 other tissues.

Summary

This gene produces alternative transcripts encoding two distinct proteins. One protein is a transcriptional repressor, while the Other isoform is a major component of specialized synapses known as synaptic ribbons. Both proteins contain a NAD+ binding domain similar to NAD+-dependent 2-hydroxyacid dehydrogenases. A portion of the 3' untranslated region was used to map this gene to chromosome 21q21.3; however, it was noted that similar loci elsewhere in the genome are likely. Blast analysis shows that this gene is present on chromosome 10. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Feb 2014]

CTBP2 Products (9)

mRNA Protein Name
NM_001083914.3 NP_001077383.1 C-terminal-binding protein 2 isoform 1
NM_001290214.3 NP_001277143.1 C-terminal-binding protein 2 isoform 1
NM_001290215.3 NP_001277144.1 C-terminal-binding protein 2 isoform 1
NM_001321012.2 NP_001307941.1 C-terminal-binding protein 2 isoform 1
NM_001321013.2 NP_001307942.1 C-terminal-binding protein 2 isoform 1
NM_001321014.2 NP_001307943.1 C-terminal-binding protein 2 isoform 1
NM_001329.4 NP_001320.1 C-terminal-binding protein 2 isoform 1
NM_001363508.2 NP_001350437.1 C-terminal-binding protein 2 isoform 3
NM_022802.3 NP_073713.2 C-terminal-binding protein 2 isoform 2
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables protein kinase binding IPI
IPI: Inferred from physical interaction
23393140 GOA
enables protein-containing complex binding IPI
IPI: Inferred from physical interaction
23393140 GOA
enables transcription corepressor binding IPI
IPI: Inferred from physical interaction
29628311 GOA
Biological Process GO Annotation Evidence References Source
acts upstream of or within positive regulation of retinoic acid receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
23775127 GOA
acts upstream of or within positive regulation of transcription by RNA polymerase II IMP
IMP: Inferred from mutant phenotype
23775127 GOA
Cellular Component GO Annotation Evidence References Source
located in nucleus IDA
IDA: Inferred from direct assay
16702210 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

CTBP2 Protein Structure

2-Hacid_dh

2-Hacid_dh: D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain (44 - 358)

2-Hacid_dh_C

2-Hacid_dh_C: D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain (140 - 323)

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

C-terminal-binding protein 2

  • ribeye

CTBP2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CTBP2 P56545 CTBP1 Homo sapiens Q13363-2 25416956
Intra
CTBP2 P56545 CTBP1 Homo sapiens Q13363-2 27107012
Intra
CTBP2 P56545 NOL4 Homo sapiens O94818-2 25416956
Intra
CTBP2 P56545 ZNF750 Homo sapiens Q32MQ0 25416956
Intra
CTBP2 P56545 ZNF750 Homo sapiens Q32MQ0 25416956
Intra
CTBP2 P56545 ZNF750 Homo sapiens Q32MQ0 25416956
Intra
CTBP2 P56545 HIC1 Homo sapiens Q14526 19486893
Intra
CTBP2 P56545 ZNF516 Homo sapiens Q92618 35271311
Intra
CTBP2 P56545 FUNDC1 Homo sapiens Q8IVP5 25416956
Intra
CTBP2 P56545 FUNDC1 Homo sapiens Q8IVP5 25416956
Intra
CTBP2 P56545 PLCB1 Homo sapiens Q9NQ66 25416956
Intra
CTBP2 P56545 PLCB1 Homo sapiens Q9NQ66 25416956
Intra
CTBP2 P56545 IKZF2 Homo sapiens Q9UKS7 25416956
Intra
CTBP2 P56545 IKZF2 Homo sapiens Q9UKS7 25416956
Intra
CTBP2 P56545 PROX1 Homo sapiens Q92786 21988832
Cross
CTBP2 P56545 Zbp1 Mus musculus A2APF7 21903422
Intra
CTBP2 P56545 NOL4L Homo sapiens Q96MY1 25416956
Intra
CTBP2 P56545 NOL4L Homo sapiens Q96MY1 35271311
Intra
CTBP2 P56545 TGIF1 Homo sapiens Q15583 16189514
Intra
CTBP2 P56545 TGIF1 Homo sapiens Q15583 25416956
Intra
CTBP2 P56545 TGIF1 Homo sapiens Q15583
Y2H
21516116
Intra
CTBP2 P56545 PPP1R15A Homo sapiens O75807 21988832
Intra
CTBP2 P56545 PPP1R15A Homo sapiens O75807
Y2H
21988832
Intra
CTBP2 P56545 FHL3 Homo sapiens Q13643 27107012
Intra
CTBP2 P56545 CCNH Homo sapiens P51946 21988832
Intra
CTBP2 P56545 CCNH Homo sapiens P51946 21988832
Intra
CTBP2 P56545 IKZF1 Homo sapiens Q13422 25416956
Intra
CTBP2 P56545 IKZF1 Homo sapiens Q13422
Y2H
21516116
Intra
CTBP2 P56545 LCOR Homo sapiens Q96JN0 31515488
Intra
CTBP2 P56545 LCOR Homo sapiens Q96JN0 25416956
Intra
CTBP2 P56545 LCOR Homo sapiens Q96JN0 35271311
Intra
CTBP2 P56545 LCOR Homo sapiens Q96JN0 25416956
Intra
CTBP2 P56545 RAI2 Homo sapiens Q9Y5P3 25416956
Intra
CTBP2 P56545 RAI2 Homo sapiens Q9Y5P3 25416956
Intra
CTBP2 P56545 RAI2 Homo sapiens Q9Y5P3 16189514
Intra
CTBP2 P56545 CTBP1 Homo sapiens Q13363 35271311
Intra
CTBP2 P56545 CTBP1 Homo sapiens Q13363
Y2H
21988832
Intra
CTBP2 P56545 CTBP1 Homo sapiens Q13363 31515488
Intra
CTBP2 P56545 CTBP1 Homo sapiens Q13363 36414381
Intra
CTBP2 P56545 BCL3 Homo sapiens P20749
Y2H
21988832
Intra
CTBP2 P56545 FOXP2 Homo sapiens O15409 25416956
Intra
CTBP2 P56545 FOXP2 Homo sapiens O15409 25416956
Intra
CTBP2 P56545 FOXP2 Homo sapiens O15409 21653829
Cross: Cross-species interaction Intra: Intraspecies interaction

CTBP2 Antibodies

Cat. No. Product Name Application Reactivity
HY-P83090 CTBP2 Antibody (YA2835) WB, IHC-F, IHC-P, ICC/IF Human, Mouse, Rat
HY-P83090A CTBP2 Antibody (YA2835)(PBS only) WB, IHC-F, IHC-P, ICC/IF Human, Mouse, Rat

Related Diseases

Diseases Alias
46,Xy Sex Reversal 9
  • SRXY9

  • 46,Xy Sex Reversal, Zfpm2-Related

  • 46xy Sex Reversal 9

Developmental And Epileptic Encephalopathy 75
  • DEE75

  • Epileptic Encephalopathy, Early Infantile, 75

  • Eiee75

  • Developmental And Epileptic Encephalopathy, 75

  • Early Infantile Epileptic Encephalopathy 75

Hepatocellular Carcinoma
  • Liver Cancer

  • Primary Liver Cancer

  • HCC

  • Hepatoma

  • Malignant Neoplasm Of Liver

  • Liver Neoplasms

  • Cancer, Hepatocellular

  • Liver Cell Carcinoma

  • Lcc

  • Hepatoblastoma, Somatic

  • Hepatic Cancer

  • Primary Malignant Neoplasm Of Liver

  • Rare Tumor Of Liver And Intrahepatic Biliary Tract

  • Hepatocellular Carcinoma, Somatic

  • Hepatocellular Carcinoma, Childhood Type, Somatic

  • Hepatocellular Cancer, Somatic

  • Ca Liver - Primary

  • Hepatic Neoplasm

  • Malignant Hepato-Biliary Neoplasm

  • Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary

  • Malignant Neoplasm Of Liver, Primary

  • Malignant Tumor Of Liver

  • Neoplasm Of Liver

  • Non-Resectable Primary Hepatic Malignant Neoplasm

  • Resectable Malignant Neoplasm Of Liver

  • Resectable Malignant Neoplasm Of The Liver

  • Primary Liver Carcinoma

  • Primary Malignant Liver Neoplasm

  • Primary Cancer Of Liver

  • Primary Tumor Of The Liver

  • Rare Tumor Of Liver And Ibt

  • Hepatocellular Cancer

  • Neoplasm Of The Liver

  • Carcinoma, Hepatocellular

  • Hepatomas

  • Liver Neoplasm

  • Liver Carcinoma

  • Liver And Intrahepatic Biliary Tract Carcinoma

  • Malignant Hepatobiliary Neoplasm

  • Adult Primary Hepatocellular Carcinoma

  • Hepatoblastoma

  • Carcinoma Of Liver

  • Malignant Liver Tumour

  • Malignant Hepatic Tumour

Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Congenital Stationary Night Blindness
  • Night Blindness, Congenital Stationary

  • Congenital Essential Nyctalopia

  • Oguchi Disease

  • Blindness, Night, Stationary, Congenital

Sensorineural Hearing Loss
  • Sensory Hearing Loss

  • Sensorineural Deafness

  • Sensorineural Hearing Loss Disorder

  • Hearing Loss, Sensorineural

  • Central Hearing Loss

  • High Frequency Deafness

  • High Frequency Hearing Loss

  • High-Frequency Hearing Loss

  • Perceptive Deafness

  • Perceptive Hearing Loss

  • Perceptive Hearing Loss Or Deafness

  • Hearing Loss Sensorineural

  • Deafness Sensorineural

  • Hearing Loss High-Frequency

  • Hearing Loss, Central

  • Hearing Loss, High-Frequency

Leber Plus Disease
  • Leber Congenital Amaurosis

  • Lca

  • Leber'S Amaurosis

  • Leber'S Disease

  • Amaurosis Congenita Of Leber

  • Amaurosis Congenita Of Leber, Type 1

  • Lhon Plus Disease

  • Congenital Absence Of The Rods And Cones

  • Congenital Retinal Blindness

  • Crb

  • Congenital Amaurosis Of Retinal Origin

  • Leber'S Congenital Amaurosis

  • Leber Congenital Amaurosis 1

  • Leber'S Congenital Tapetoretinal Degeneration

  • Leber'S Congenital Tapetoretinal Dysplasia

  • Lca1

  • Leber Congenital Amaurosis Type 1

  • Retinal Blindness, Congenital

  • Amaurosis, Leber Congenital

  • Dysgenesis Neuroepithelialis Retinae

  • Hereditary Epithelial Dysplasia Of Retina

  • Hereditary Retinal Aplasia

  • Heredoretinopathia Congenitalis

  • Leber Abiotrophy

  • Leber Congenital Tapetoretinal Degeneration

  • Lebers Congenital Amaurosis

  • Optic Atrophy, Hereditary, Leber

Cone-Rod Dystrophy 2
  • Cone-Rod Dystrophy

  • CORD2

  • Cone-Rod Retinal Dystrophy

  • Rcrd2

  • Cone-Rod Retinal Dystrophy 2

  • Crd2

  • Cord

  • Crd

  • Retinal Cone-Rod Dystrophy

  • Cone-Rod Retinal Dystrophy-2

  • Retinal Cone-Rod Dystrophy 2

  • Tapetoretinal Degeneration

  • Cone-Rod Degeneration

  • Cone Rod Dystrophy

  • Dystrophy, Cone-Rod

  • Dystrophy, Cone-Rod, Type 2

  • Retinitis Pigmentosa

  • Retinitis Pigmentosa 2

  • Progressive Cone-Rod Dystrophy

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Fundus Dystrophy
  • Retinal Dystrophy

  • Retinal Dystrophies

  • Dystrophy, Retinal

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 CTBP2 VGNC VGNC:61243
Canis familiaris CTBP2 VGNC VGNC:39687
Mus musculus CTBP2 MGD MGI:1201686
Rattus norvegicus CTBP2 RGD RGD:68372
Macaca mulatta CTBP2 VGNC VGNC:103803
Bos taurus CTBP2 VGNC VGNC:55942
Others CTBP2 NCBI