OPN1MW2
protein-coding gene in the species Homo sapiens
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OPN1MW2
Summary
OPN1MW2 is a gene[1].
Key Facts
- OPN1MW2's instance of is recorded as gene[2].
- OPN1MW2 is a type of protein-coding gene[3].
- OPN1MW2's HomoloGene ID is recorded as 88332[4].
- OPN1MW2's genomic start is recorded as 154219756[5].
- OPN1MW2's genomic start is recorded as 153448107[6].
- OPN1MW2's genomic start is recorded as 153485225[7].
- OPN1MW2's genomic end is recorded as 154233286[8].
- OPN1MW2's genomic end is recorded as 153461633[9].
- OPN1MW2's genomic end is recorded as 153498755[10].
- OPN1MW2's encodes is recorded as Opsin 1, medium wave sensitive 3[11].
- OPN1MW2's encodes is recorded as Medium-wave-sensitive opsin 1[12].
- OPN1MW2's encodes is recorded as Medium-wave-sensitive opsin 2[13].
- OPN1MW2's encodes is recorded as Medium-wave-sensitive opsin 3[14].
- OPN1MW2's found in taxon is recorded as Homo sapiens[15].
- OPN1MW2's chromosome is recorded as human X chromosome[16].
- OPN1MW2's strand orientation is recorded as forward strand[17].
- OPN1MW2's exact match is recorded as http://identifiers.org/ncbigene/728458[18].
- OPN1MW2's cytogenetic location is recorded as Xq28[19].
- OPN1MW2's expressed in is recorded as gonad[20].
- OPN1MW2's expressed in is recorded as appendix[21].
- OPN1MW2's expressed in is recorded as skin of leg[22].