1. Gene
  2. YWHAB - tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta Gene

YWHAB - tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta Gene

Homo sapiens

Also known as HS1; GW128; YWHAA; KCIP-1; HEL-S-1

Gene ID: 7529 | Gene type: protein coding

About YWHAB

Cytogenetic location: 20q13.12 Genomic coordinates (GRCh38): 20:44,885,705-44,908,532 (from NCBI)

This gene has 8 transcripts (splice variants), 269 orthologues and 6 paralogues. Ubiquitous expression in brain (RPKM 158.2), lymph node (RPKM 85.8) and 24 other tissues.

Summary

This gene encodes a protein belonging to the 14-3-3 family of proteins, members of which mediate signal transduction by binding to phosphoserine-containing proteins. This highly conserved protein family is found in both Plants and mammals. The encoded protein has been shown to interact with RAF1 and CDC25 phosphatases, suggesting that it may play a role in linking mitogenic signaling and the cell cycle machinery. Two transcript variants, which encode the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008]

YWHAB Products(2)

mRNA Protein Name
NM_003404.5 NP_003395.1 2014/3/3 protein beta/alpha
NM_139323.4 NP_647539.1 2014/3/3 protein beta/alpha
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables enzyme binding IPI
IPI: Inferred from physical interaction
17255105 GOA
enables histone deacetylase binding IPI
IPI: Inferred from physical interaction
10869435 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
17085597 GOA
enables phosphoprotein binding IPI
IPI: Inferred from physical interaction
10869435 GOA
enables phosphoserine residue binding IPI
IPI: Inferred from physical interaction
10869435 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
7644510 GOA
enables protein domain specific binding IPI
IPI: Inferred from physical interaction
11984006 GOA
enables protein kinase inhibitor activity IDA
IDA: Inferred from direct assay
11555644 GOA
Biological Process GO Annotation Evidence Reference Source
involved in cytoplasmic sequestering of protein IDA
IDA: Inferred from direct assay
10869435 GOA
involved in negative regulation of G protein-coupled receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
21224381 GOA
involved in positive regulation of catalytic activity IDA
IDA: Inferred from direct assay
17255105 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cytoplasm IDA
IDA: Inferred from direct assay
10869435 GOA
located in cytosol IDA
IDA: Inferred from direct assay
31906564 GOA
located in nucleus IDA
IDA: Inferred from direct assay
31906564 GOA
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
12963375 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

YWHAB Protein Structure

14-3-3

14-3-3: 14-3-3 protein (6 - 237)

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

14-3-3 protein beta/alpha

14-3-3 alpha

Recombinant YWHAB Proteins

Cat. No. Product Name Accession Purity
HY-P74439 14-3-3 beta Protein, Human (GST) P31946 (M1-N246) ≥95%
HY-P74440 14-3-3 beta Protein, Human P31946 (M1-N246) ≥95%
HY-P700304 14-3-3 beta Protein, Human (His) P31946 (M1-N246) ≥95%

Related Diseases

Diseases Alias
Chlamydia

Chlamydial Infection

Chlamydia Trachomatis Infectious Disease

Chlamydial Disease

Chlamydia Infections

Eosinophilic Meningitis

Eosinophilic Meningoencephalitis Due To Angiostrongylus Cantonensis

Hyperinsulinemic Hypoglycemia, Familial, 5

Hyperinsulinism Due To Insr Deficiency

HHF5

Familial Hyperinsulinemic Hypoglycemia 5

Hyperinsulinemic Hypoglycemia Due To Insr Deficiency

Hyperinsulinemic Hypoglycemia Due To Insulin Receptor Deficiency

Congenital Hyperinsulinism

Persistent Hyperinsulinemic Hypoglycemia Of Infancy

Phhi

Hyperinsulinemic Hypoglycemia Familial 5

Chronic Meningitis
Lymphogranuloma Venereum

Climatic Or Tropical Bubo

Durand-Nicolas-Favre Disease

Lymphogranuloma Inguinale

Poradenitis Inguinale

Strumous Bubo

Lgv

Granuloma Inguinale

Donovanosis

Pudendal Ulcer

Granuloma Inguinale Tropicum

Granuloma Pudendi Tropicum

Chromosome 17p13.3, Centromeric, Duplication Syndrome

Chromosome 17p13.3 Duplication Syndrome

17p13.3 Duplication Syndrome

17p13.3 Microduplication Syndrome

Trisomy 17p13.3

Chromosome 17p13.3 Centromeric Duplication Syndrome

Dup(17)(P13.3)

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
Canis familiaris YWHAB VGNC VGNC:48508
Rattus norvegicus YWHAB RGD RGD:61998
Mus musculus YWHAB MGD MGI:1891917
Felis catus YWHAB VGNC VGNC:67154
Macaca mulatta YWHAB VGNC VGNC:78819
Bos taurus YWHAB VGNC VGNC:37044
Macaca fascicularis YWHAB NCBI NCBI:101926442
Others YWHAB NCBI