HEXA
protein-coding gene in the species Homo sapiens
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HEXA
Summary
HEXA is a gene[1]. HEXA ranks in the top 1% of gene entities by monthly Wikipedia readership (69 views/month).[2]
Key Facts
- HEXA's instance of is recorded as gene[3].
- HEXA is a type of protein-coding gene[4].
- HEXA's Commons category is recorded as HEXA[5].
- HEXA's HomoloGene ID is recorded as 20146[6].
- HEXA's genomic start is recorded as 72635775[7].
- HEXA's genomic start is recorded as 72340924[8].
- HEXA's genomic end is recorded as 72668817[9].
- HEXA's genomic end is recorded as 72376420[10].
- HEXA's ortholog is recorded as Hexa[11].
- HEXA's ortholog is recorded as Hexa[12].
- HEXA's ortholog is recorded as hexa[13].
- HEXA's encodes is recorded as Hexosaminidase subunit alpha[14].
- HEXA's found in taxon is recorded as Homo sapiens[15].
- HEXA's chromosome is recorded as human chromosome 15[16].
- HEXA's genetic association is recorded as Tay-Sachs disease[17].
- HEXA's strand orientation is recorded as reverse strand[18].
- HEXA's exact match is recorded as http://identifiers.org/ncbigene/3073[19].
- HEXA's cytogenetic location is recorded as 15q23[20].
- HEXA's expressed in is recorded as beta cell[21].
- HEXA's expressed in is recorded as gallbladder[22].
Why It Matters
HEXA ranks in the top 1% of gene entities by monthly Wikipedia readership (69 views/month).[2]