FHIT
protein-coding gene in the species Homo sapiens
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FHIT
Summary
FHIT is a gene[1]. FHIT ranks in the top 2% of gene entities by monthly Wikipedia readership (3 views/month).[2]
Key Facts
- FHIT's instance of is recorded as gene[3].
- FHIT is a type of protein-coding gene[4].
- FHIT's HomoloGene ID is recorded as 21661[5].
- FHIT's genomic start is recorded as 59735036[6].
- FHIT's genomic start is recorded as 59747277[7].
- FHIT's genomic end is recorded as 61251459[8].
- FHIT's genomic end is recorded as 61237133[9].
- FHIT's ortholog is recorded as Fhit[10].
- FHIT's ortholog is recorded as HNT2[11].
- FHIT's ortholog is recorded as Fhit[12].
- FHIT's ortholog is recorded as fhit[13].
- FHIT's encodes is recorded as Fragile histidine triad diadenosine triphosphatase[14].
- FHIT's found in taxon is recorded as Homo sapiens[15].
- FHIT's chromosome is recorded as human chromosome 3[16].
- FHIT's genetic association is recorded as myopia[17].
- FHIT's genetic association is recorded as cleft lip and cleft palate[18].
- FHIT's genetic association is recorded as Asperger syndrome[19].
- FHIT's genetic association is recorded as attention deficit hyperactivity disorder[20].
- FHIT's strand orientation is recorded as reverse strand[21].
- FHIT's exact match is recorded as http://identifiers.org/ncbigene/2272[22].
- FHIT's cytogenetic location is recorded as 3p14.2[23].
- FHIT's expressed in is recorded as right adrenal gland[24].
- FHIT's expressed in is recorded as right adrenal cortex[25].
- FHIT's expressed in is recorded as left adrenal cortex[26].
- FHIT's expressed in is recorded as apex of heart[27].
Why It Matters
FHIT ranks in the top 2% of gene entities by monthly Wikipedia readership (3 views/month).[2] FHIT is known by 5 alternative names across languages and contexts.[28]