DLX5
protein-coding gene in the species Homo sapiens
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DLX5
Summary
DLX5 is a gene[1].
Key Facts
- DLX5's instance of is recorded as gene[2].
- DLX5 is a type of protein-coding gene[3].
- DLX5's HomoloGene ID is recorded as 3825[4].
- DLX5's genomic start is recorded as 96649704[5].
- DLX5's genomic start is recorded as 97020396[6].
- DLX5's genomic end is recorded as 96654409[7].
- DLX5's genomic end is recorded as 97024950[8].
- DLX5's ortholog is recorded as Dlx5[9].
- DLX5's ortholog is recorded as Dlx5[10].
- DLX5's ortholog is recorded as dlx5a[11].
- DLX5's encodes is recorded as Distal-less homeobox 5[12].
- DLX5's found in taxon is recorded as Homo sapiens[13].
- DLX5's chromosome is recorded as human chromosome 7[14].
- DLX5's genetic association is recorded as split hand-foot malformation 1 with sensorineural hearing loss[15].
- DLX5's strand orientation is recorded as reverse strand[16].
- DLX5's exact match is recorded as http://identifiers.org/ncbigene/1749[17].
- DLX5's cytogenetic location is recorded as 7q21.3[18].
- DLX5's expressed in is recorded as tibia[19].
- DLX5's expressed in is recorded as gonad[20].
- DLX5's expressed in is recorded as skin of leg[21].
- DLX5's expressed in is recorded as endometrium[22].
- DLX5's expressed in is recorded as skin of abdomen[23].
- DLX5's expressed in is recorded as testicle[24].
- DLX5's expressed in is recorded as Achilles tendon[25].
- DLX5's expressed in is recorded as placenta[26].