1. Gene
  2. SIAH2 - siah E3 ubiquitin protein ligase 2 Gene

SIAH2 - siah E3 ubiquitin protein ligase 2 Gene

Homo sapiens

Also known as hSiah2

Gene ID: 6478 | Gene type: protein coding

About SIAH2

Cytogenetic location: 3q25.1 Genomic coordinates (GRCh38): 3:150,741,125-150,763,169 (from NCBI)

This gene has 3 transcripts (splice variants), 198 orthologues and 3 paralogues. Ubiquitous expression in adrenal (RPKM 42.6), placenta (RPKM 22.5) and 24 other tissues.

Summary

This gene encodes a protein that is a member of the seven in absentia homolog (SIAH) family. The protein is an E3 Ligase and is involved in ubiquitination and proteasome-mediated degradation of specific proteins. The activity of this ubiquitin Ligase has been implicated in regulating cellular response to hypoxia. [provided by RefSeq, Jul 2008]

SIAH2 Products(1)

mRNA Protein Name
NM_005067.7 NP_005058.3 E3 ubiquitin-protein ligase SIAH2
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
21586138 GOA
Biological Process GO Annotation Evidence Reference Source
involved in canonical Wnt signaling pathway IMP
IMP: Inferred from mutant phenotype
28546513 GOA
involved in negative regulation of apoptotic process IMP
IMP: Inferred from mutant phenotype
21586138 GOA
acts upstream of or within negative regulation of canonical Wnt signaling pathway IGI
IGI: Inferred from genetic interaction
12952940 GOA
involved in negative regulation of cysteine-type endopeptidase activity involved in apoptotic process IMP
IMP: Inferred from mutant phenotype
21586138 GOA
involved in negative regulation of extrinsic apoptotic signaling pathway IMP
IMP: Inferred from mutant phenotype
21586138 GOA
involved in regulation of circadian rhythm IMP
IMP: Inferred from mutant phenotype
26392558 GOA
involved in ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
26392558 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cytosol IDA
IDA: Inferred from direct assay
21586138 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

SIAH2 Protein Structure

Sina

Sina: Seven in absentia protein family (122 - 318)

  • 0
  • 100
  • 200
  • 300
  • 324 a.a.
Protein Preferred Names Protein Names

E3 ubiquitin-protein ligase SIAH2

RING-type E3 ubiquitin transferase SIAH2

SIAH2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
SIAH2 O43255 OPRM1 Homo sapiens P35372
Y2H
23840749
Intra
SIAH2 O43255 SH3RF1 Homo sapiens Q7Z6J0
Anti Tag CoIP
25438054
Intra
SIAH2 O43255 SH3RF1 Homo sapiens Q7Z6J0
Y2H
21586138
Intra
SIAH2 O43255 LATS2 Homo sapiens Q9NRM7
Pull Down
25438054
Intra
SIAH2 O43255 LATS2 Homo sapiens Q9NRM7
Anti Tag CoIP
25438054
Intra
SIAH2 O43255 LATS1 Homo sapiens O95835
Anti Tag CoIP
25438054
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Dyskeratosis Congenita, Autosomal Dominant 3

DKCA3

Autosomal Dominant Dyskeratosis Congenita 3

Dyskeratosis Congenita, Autosomal Dominant, 3

Dyskeratosis Congenita, Autosomal Dominant, Type 3

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 SIAH2 VGNC VGNC:102843
Macaca mulatta SIAH2 VGNC VGNC:77215
Bos taurus SIAH2 VGNC VGNC:34614
Mus musculus SIAH2 MGD MGI:108062
Rattus norvegicus SIAH2 RGD RGD:620778