1. Gene
  2. SIN3B - SIN3 transcription regulator family member B Gene

SIN3B - SIN3 transcription regulator family member B Gene

Homo sapiens
Gene ID: 23309 | Gene type: protein coding

About SIN3B

Cytogenetic location: 19p13.11 Genomic coordinates (GRCh38): 19:16,829,398-16,880,349 (from NCBI)

This gene has 12 transcripts (splice variants), 206 orthologues, 1 paralogue and is associated with 2 phenotypes. Ubiquitous expression in testis (RPKM 19.2), endometrium (RPKM 17.1) and 25 other tissues.

Summary

Predicted to enable transcription corepressor activity. Predicted to be involved in histone deacetylation; negative regulation of transcription by RNA polymerase II; and striated muscle tissue development. Predicted to be located in nucleus. Predicted to be part of Sin3 complex. Predicted to be active in chromatin. [provided by Alliance of Genome Resources, Apr 2022]

SIN3B Products(3)

mRNA Protein Name
NM_001297595.2 NP_001284524.1 paired amphipathic helix protein Sin3b isoform 2
NM_001297597.2 NP_001284526.1 paired amphipathic helix protein Sin3b isoform 3
NM_015260.4 NP_056075.1 paired amphipathic helix protein Sin3b isoform 1

SIN3B Protein Structure

PAH

PAH: Paired amphipathic helix repeat (59 - 105)

PAH

PAH: Paired amphipathic helix repeat (180 - 236)

PAH

PAH: Paired amphipathic helix repeat (322 - 366)

Sin3_corepress

Sin3_corepress: Sin3 family co-repressor (393 - 444)

Sin3_corepress

Sin3_corepress: Sin3 family co-repressor (453 - 524)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1162 a.a.
Protein Preferred Names Protein Names

paired amphipathic helix protein Sin3b

SIN3 homolog B, transcriptional regulator

Related Diseases

Diseases Alias
Witteveen-Kolk Syndrome

WITKOS

Sin3a-Related Intellectual Disability Syndrome Due To A Point Mutation

Sin3a-Related Intellectual Disability Syndrome

Acute Promyelocytic Leukemia

Leukemia, Acute Promyelocytic

Acute Myeloblastic Leukemia Type 3

Aml M3

APL

Leukemia, Acute Promyelocytic, Somatic

Aml With T(15

17)(Q22

Q12)

(Pml/Raralpha) And Variants

Apml

Acute Myeloblastic Leukemia 3

Acute Myeloid Leukemia With T(15

17)(Q22

Q12)

(Pml/Raralpha) And Variants

Acute Myeloblastic Leukaemia Type 3

Acute Myeloid Leukaemia M3

Acute Myeloid Leukemia M3

Acute Promyelocytic Leukaemia

M3 Anll

Myeloid Leukemia, Acute, M3

Leukemia Promyelocytic Acute

Leukemia, Promyelocytic, Acute

Leukemia, Acute, Promyelocytic

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 SIN3B MGD MGI:107158
Bos taurus SIN3B VGNC VGNC:34625
Macaca mulatta SIN3B VGNC VGNC:77276
Rattus norvegicus SIN3B RGD RGD:1587989
Canis familiaris SIN3B VGNC VGNC:46178
Felis catus SIN3B VGNC VGNC:65151