WAS
protein-coding gene in the species Homo sapiens
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WAS
Summary
WAS is a gene[1].
Key Facts
- WAS's instance of is recorded as gene[2].
- WAS is a type of protein-coding gene[3].
- WAS's Commons category is recorded as Wiskott-Aldrich syndrome protein[4].
- WAS's HomoloGene ID is recorded as 30970[5].
- WAS's genomic start is recorded as 48676596[6].
- WAS's genomic start is recorded as 48534985[7].
- WAS's genomic end is recorded as 48691427[8].
- WAS's genomic end is recorded as 48549818[9].
- WAS's ortholog is recorded as Was[10].
- WAS's ortholog is recorded as Was[11].
- WAS's ortholog is recorded as wasa[12].
- WAS's ortholog is recorded as wasb[13].
- WAS's encodes is recorded as WASP actin nucleation promoting factor[14].
- WAS's encodes is recorded as Wiskott-Aldrich syndrome (Eczema-thrombocytopenia), isoform CRA_a[15].
- WAS's found in taxon is recorded as Homo sapiens[16].
- WAS's chromosome is recorded as human X chromosome[17].
- WAS's genetic association is recorded as Wiskott-Aldrich syndrome[18].
- WAS's genetic association is recorded as severe congenital neutropenia[19].
- WAS's genetic association is recorded as X linked thrombocytopenia[20].
- WAS's strand orientation is recorded as forward strand[21].
- WAS's exact match is recorded as http://identifiers.org/ncbigene/7454[22].
- WAS's cytogenetic location is recorded as Xp11.23[23].
- WAS's expressed in is recorded as granulocyte[24].
- WAS's expressed in is recorded as mononuclear cell[25].
- WAS's expressed in is recorded as monocyte[26].