SCX - scleraxis bHLH transcription factor Gene

Also Known as SCXA; SCXB; bHLHa48

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 642658

About SCX

Cytogenetic location: 8q24.3 Genomic coordinates (GRCh38): 8:144,266,453-144,268,481 (from NCBI)

This gene has 1 transcript (splice variant), 222 orthologues and 13 paralogues. Ubiquitous expression in appendix (RPKM 1.6), prostate (RPKM 1.6) and 25 other tissues.

Summary

Enables DNA-binding transcription activator activity, RNA polymerase II-specific and bHLH transcription factor binding activity. Contributes to E-box binding activity. Involved in positive regulation of transcription by RNA polymerase II. Located in nucleus. Part of transcription regulator complex. [provided by Alliance of Genome Resources, Apr 2022]

SCX Products (1)

mRNA Protein Name
NM_001080514.3 NP_001073983.1 basic helix-loop-helix transcription factor scleraxis
Molecular Function GO Annotation Evidence Verweise Source
enables DNA-binding transcription activator activity, RNA polymerase II-specific IDA
IDA: Inferred from direct assay
10775504 GOA
contributes to E-box binding IDA
IDA: Inferred from direct assay
10775504 GOA
enables bHLH transcription factor binding IPI
IPI: Inferred from physical interaction
10775504 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
10775504 GOA
Cellular Component GO Annotation Evidence Verweise Source
located in nucleus IDA
IDA: Inferred from direct assay
10775504 GOA
part of transcription regulator complex IDA
IDA: Inferred from direct assay
10775504 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
Protein Preferred Names Protein Names

basic helix-loop-helix transcription factor scleraxis

  • class A basic helix-loop-helix protein 41

SCX Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
SCX Q7RTU7 TCF4 Homo sapiens P15884-3 32296183
Intra
SCX Q7RTU7 TCF4 Homo sapiens P15884-3 32296183
Intra
SCX Q7RTU7 MYF5 Homo sapiens P13349 32296183
Intra
SCX Q7RTU7 MYF5 Homo sapiens P13349 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Calcific Tendinitis
  • Calcific Tendinitis Nos

Anomalous Left Coronary Artery From The Pulmonary Artery
  • Bland White Garland Syndrome

  • Alcapa

  • Bland-White-Garland Syndrome

  • White-Garland Syndrome

Acromesomelic Dysplasia 2a
  • Chondrodysplasia, Grebe Type

  • Acromesomelic Dysplasia, Grebe Type

  • Grebe Chondrodysplasia

  • Amdg

  • Grebe Syndrome

  • AMD2A

  • Grebe Dysplasia

  • Achondrogenesis, Brazilian

  • Achondrogenesis, Type Ii, Formerly

  • Acromesomelic Dysplasia-2a

  • Achondrogenesis Type Ii

  • Brazilian Achondrogenesis

  • Acromesomelic Chondrodysplasia, Grebe Type

Tendinitis
  • Tendinopathy

Cleft Soft Palate
  • Cleft Velum

  • Cleft Velum Palatinum

  • Soft Cleft Palate

  • Soft Palate Perforation

Fibrodysplasia Ossificans Progressiva
  • Myositis Ossificans Progressiva

  • Progressive Myositis Ossificans

  • FOP

  • Progressive Ossifying Myositis

  • Myositis Ossificans

  • Stone Man Syndrome

  • Man Of Stone

  • Myositis Ossificans Progressive

  • Diffuse Progressive Ossifying Polymyositis

  • Fibrodysplasia Ossificans Congenita

  • Myositis Ossificans Progressiva, Site Unspecified

  • Münchmeyer Disease

  • Fop - [Fibrodysplasia Ossificans Progressiva]

  • Progressive Myositis Ossificans Calcification

Lacrimoauriculodentodigital Syndrome
  • Ladd Syndrome

  • Levy-Hollister Syndrome

  • Lacrimo-Auriculo-Dento-Digital Syndrome

  • LADD

  • Lacrimoauriculodento-Digital Syndrome

  • Levy Hollister Syndrome

  • Lard Syndrome

  • Lacrimoauriculoradiodental Syndrome

  • LADDS

  • Congenital Duodenal Obstruction Due To Malrotation Of Intestine

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
Rattus norvegicus SCX RGD RGD:1588254
Bos taurus SCX VGNC VGNC:58408
Mus musculus SCX MGD MGI:102934
Macaca mulatta SCX VGNC VGNC:84112
Others SCX NCBI