HMX1
protein-coding gene in the species Homo sapiens
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HMX1
Summary
HMX1 is a gene[1].
Key Facts
- HMX1's instance of is recorded as gene[2].
- HMX1 is a type of protein-coding gene[3].
- HMX1's HomoloGene ID is recorded as 49241[4].
- HMX1's genomic start is recorded as 8846076[5].
- HMX1's genomic start is recorded as 8847802[6].
- HMX1's genomic end is recorded as 8873543[7].
- HMX1's genomic end is recorded as 8871839[8].
- HMX1's ortholog is recorded as Hmx1[9].
- HMX1's ortholog is recorded as Hmx1[10].
- HMX1's encodes is recorded as H6 family homeobox 1[11].
- HMX1's found in taxon is recorded as Homo sapiens[12].
- HMX1's chromosome is recorded as human chromosome 4[13].
- HMX1's genetic association is recorded as oculoauricular syndrome[14].
- HMX1's strand orientation is recorded as reverse strand[15].
- HMX1's exact match is recorded as http://identifiers.org/ncbigene/3166[16].
- HMX1's cytogenetic location is recorded as 4p16.1[17].
- HMX1's expressed in is recorded as testicle[18].
- HMX1's expressed in is recorded as gonad[19].
- HMX1's expressed in is recorded as amygdala[20].
- HMX1's expressed in is recorded as putamen[21].
- HMX1's expressed in is recorded as hypothalamus[22].
- HMX1's expressed in is recorded as substantia nigra[23].
- HMX1's expressed in is recorded as hippocampus proper[24].
- HMX1's expressed in is recorded as caudate nucleus[25].
- HMX1's expressed in is recorded as anterior cingulate cortex[26].