WAS
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human X chromosome[14]
- Cytogenetic location
- Xp11.23[19]
- Encodes
- WASP actin nucleation promoting factor, Wiskott-Aldrich syndrome (Eczema-thrombocytopenia), isoform CRA_a[11][12]
- Expressed in
- granulocyte, mononuclear cell, monocyte, blood, appendix, spleen, mucosa of ileum, bone marrow cell, lymph node, trabecular bone[20][21][22][23][24][25][26][27][28][29]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- Wiskott-Aldrich syndrome, severe congenital neutropenia, X linked thrombocytopenia[15][16][17]
- HomoloGene ID
- 30970[3]
- Strand orientation
- forward strand[18]
🏷️ Also known as
en IMD2
en SCNX
en THC
en THC1
en WAS
en WASp
en WASPA
en WASP actin nucleation promoting factor
en Wiskott-Aldrich syndrome
id Protein Wiskott–Aldrich syndrome
ru белок синдрома Вискотта — Олдрича
🔖 Identifiers · 10
- Image (Wikimedia Commons)
- PBB Protein WAS image.jpg ↗
- Ensembl gene ID
- ENSG00000015285
- Ensembl transcript ID
- ENST00000490627, ENST00000376701, ENST00000450772, ENST00000465982, ENST00000470107, ENST00000474174, ENST00000483750
- Entrez Gene ID
- 7454
- Exact match
- identifiers.org
- HGNC ID
- 12731
- HGNC gene symbol
- WAS
- OMIM ID
- 300392
- RefSeq RNA ID
- XM_011543977, NM_000377, XM_017029786, XM_047442432, XM_047442433, XM_047442434
- UMLS CUI
- C1421478
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Summary
WAS is a gene[1].