TCF23 - transcription factor 23 Gene

Also Known as OUT; TCF-23; bHLHa24

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 150921

About TCF23

Cytogenetic location: 2p23.3 Genomic coordinates (GRCh38): 2:27,149,004-27,156,974 (from NCBI)

This gene has 2 transcripts (splice variants), 180 orthologues and 13 paralogues. Biased expression in endometrium (RPKM 12.5), ovary (RPKM 9.5) and 2 other tissues.

Summary

The gene encodes a member of the basic helix-loop-helix transcription factor family. Studies of the orthologous gene in mouse have shown the encoded protein does not bind DNA but may negatively regulate Other basic helix-loop-helix factors via the formation of a functionally inactive heterodimeric complex. [provided by RefSeq, May 2010]

TCF23 Products (1)

mRNA Protein Name
NM_175769.3 NP_786951.1 transcription factor 23
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
Biological Process GO Annotation Evidence References Source
acts upstream of or within decidualization IMP
IMP: Inferred from mutant phenotype
24571987 GOA
acts upstream of or within positive regulation of gene expression IMP
IMP: Inferred from mutant phenotype
24571987 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

TCF23 Protein Structure

HLH

HLH: Helix-loop-helix DNA-binding domain (82 - 128)

  • 0
  • 100
  • 200
  • 214 a.a.
Protein Preferred Names Protein Names

transcription factor 23

  • class A basic helix-loop-helix protein 24

TCF23 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TCF23 Q7RTU1 TCF12 Homo sapiens Q99081-3 32296183
Intra
TCF23 Q7RTU1 TCF12 Homo sapiens Q99081-3 32296183
Intra
TCF23 Q7RTU1 TCF12 Homo sapiens Q99081-3 32296183
Intra
TCF23 Q7RTU1 TCF4 Homo sapiens P15884-3 32296183
Intra
TCF23 Q7RTU1 TCF4 Homo sapiens P15884-3 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Retinal Arteries, Tortuosity Of
  • Retinal Arterial Tortuosity

  • Retinal Hemorrhage With Vascular Tortuosity

  • RATOR

  • Tortuosity Of Retinal Arteries

  • Retinal Arteriolar Tortuosity

  • Familial Isolated Retinal Arterial Tortuosity

  • Tortuosity, Arteries, Retinal

Ras-Associated Autoimmune Leukoproliferative Disorder
  • RALD

  • Autoimmune Lymphoproliferative Syndrome Type 4

  • Alps4

  • Autoimmune Lymphoproliferative Syndrome, Type Iv

  • Ras-Associated Autoimmune Leukoproliferative Disease

  • Ras-Associated Autoimmune Lymphoproliferative Syndrome Type Iv, Somatic

  • Alps Type 4

  • Alps Type Iv

  • Autoimmune Lymphoproliferative Syndrome Type Iv

  • Autoimmune Lymphoproliferative Syndrome 4

Fanconi Anemia, Complementation Group E
  • Fanconi Anemia Complementation Group E

  • FANCE

  • Face

  • Faces Syndrome

Western Equine Encephalitis
  • Western Equine Encephalomyelitis

  • Wee

  • Encephalomyelitis, Western Equine

  • Western Equine Encephalitis Virus Infection

  • Wee - [Western Equine Encephalitis]

  • Western Equine Encephalitis Virus

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
Bos taurus TCF23 VGNC VGNC:35691
Felis catus TCF23 VGNC VGNC:81235
Macaca mulatta TCF23 VGNC VGNC:79156
Rattus norvegicus TCF23 RGD RGD:1586500
Canis familiaris TCF23 VGNC VGNC:47194
Mus musculus TCF23 MGD MGI:1934960
Others TCF23 NCBI