ASNS
protein-coding gene in the species Homo sapiens
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ASNS
Summary
ASNS is a gene[1].
Key Facts
- ASNS's instance of is recorded as gene[2].
- ASNS is a type of protein-coding gene[3].
- ASNS's HomoloGene ID is recorded as 69113[4].
- ASNS's genomic start is recorded as 97481430[5].
- ASNS's genomic start is recorded as 97851677[6].
- ASNS's genomic end is recorded as 97872542[7].
- ASNS's genomic end is recorded as 97501854[8].
- ASNS's ortholog is recorded as Asns[9].
- ASNS's ortholog is recorded as Asns[10].
- ASNS's ortholog is recorded as asns[11].
- ASNS's ortholog is recorded as asns-1[12].
- ASNS's encodes is recorded as Asparagine synthetase (glutamine-hydrolyzing)[13].
- ASNS's found in taxon is recorded as Homo sapiens[14].
- ASNS's chromosome is recorded as human chromosome 7[15].
- ASNS's genetic association is recorded as congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome[16].
- ASNS's strand orientation is recorded as reverse strand[17].
- ASNS's exact match is recorded as http://identifiers.org/ncbigene/440[18].
- ASNS's cytogenetic location is recorded as 7q21.3[19].
- ASNS's expressed in is recorded as cerebellar hemisphere[20].
- ASNS's expressed in is recorded as right hemisphere of cerebellum[21].
- ASNS's expressed in is recorded as superior frontal gyrus[22].
- ASNS's expressed in is recorded as Brodmann area 9[23].
- ASNS's expressed in is recorded as primary visual cortex[24].
- ASNS's expressed in is recorded as islet of Langerhans[25].
- ASNS's expressed in is recorded as right frontal lobe[26].