2. Gene
  3. SUPT20H - SPT20 homolog, SAGA complex component Gene

SUPT20H - SPT20 homolog, SAGA complex component Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as C13; FP757; P38IP; SPT20; FAM48A; C13orf19

Gene ID: 55578 | Gene type: protein coding

About SUPT20H

Cytogenetic location: 13q13.3 Genomic coordinates (GRCh38): 13:37,009,312-37,059,688 (from NCBI)

This gene has 23 transcripts (splice variants), 212 orthologues and 2 paralogues. Broad expression in testis (RPKM 29.4), endometrium (RPKM 11.5) and 25 other tissues.

Summary

Predicted to enable transcription coregulator activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within positive regulation of gluconeogenesis and positive regulation of transcription by RNA polymerase II. Part of SAGA-type complex. [provided by Alliance of Genome Resources, Apr 2022]

SUPT20H Products(5)

mRNA Protein Name
NM_001014286.3 NP_001014308.2 transcription factor SPT20 homolog isoform a
NM_001278480.2 NP_001265409.1 transcription factor SPT20 homolog isoform c
NM_001278481.2 NP_001265410.1 transcription factor SPT20 homolog isoform b
NM_001278482.2 NP_001265411.1 transcription factor SPT20 homolog isoform b
NM_017569.4 NP_060039.1 transcription factor SPT20 homolog isoform b

SUPT20H Protein Structure

Spt20

Spt20: Spt20 family (62 - 221)

  • 0
  • 200
  • 400
  • 600
  • 779 a.a.
Protein Preferred Names Protein Names

transcription factor SPT20 homolog

family with sequence similarity 48, member A

Related Diseases

Diseases Alias
Rheumatoid Arthritis

RA

Arthritis, Rheumatoid

Rheumatoid Arthritis, Susceptibility To

Arthritis Or Polyarthritis, Rheumatic

Atrophic Arthritis

Rheumatism Arthritis

Rheumatoid Polyarthritis
Spinocerebellar Ataxia, X-Linked 3

Scax3

X-Linked Spinocerebellar Ataxia 3

X-Linked Ataxia-Deafness Syndrome

X-Linked Spinocerebellar Ataxia Type 3

Ataxia-Deafness Syndrome, X-Linked

Spinocerebellar Ataxia X-Linked Type 3

Ataxia-Deafness Syndrome X-Linked

X-Linked Ataxia-Hearing Loss Syndrome

Spinocerebellar Ataxia, X-Linked, 3
Spinocerebellar Ataxia, X-Linked 4

Scax4

X-Linked Spinocerebellar Ataxia 4

X-Linked Ataxia-Dementia Syndrome

X-Linked Spinocerebellar Ataxia Type 4

Ataxia-Dementia Syndrome, X-Linked

Spinocerebellar Ataxia X-Linked Type 4

Ataxia-Dementia Syndrome X-Linked

Spinocerebellar Ataxia, X-Linked, 4
Macular Degeneration, Age-Related, 8

Age Related Macular Degeneration 8

ARMD8

Macular Degeneration, Age-Related, Type 8
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

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS14035 SUPT20H Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus SUPT20H VGNC VGNC:102339
Macaca mulatta SUPT20H VGNC VGNC:78182
Bos taurus SUPT20H VGNC VGNC:53835
Canis familiaris SUPT20H VGNC VGNC:59097
Mus musculus SUPT20H MGD MGI:1929651
Rattus norvegicus SUPT20H RGD RGD:1307812