OPN1MW3
protein-coding gene in the species Homo sapiens
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OPN1MW3
Summary
OPN1MW3 is a gene[1]. OPN1MW3 is known by 4 alternative names across languages and contexts.[2]
Key Facts
- OPN1MW3's instance of is recorded as gene[3].
- OPN1MW3 is a type of protein-coding gene[4].
- OPN1MW3's HomoloGene ID is recorded as 88332[5].
- OPN1MW3's genomic start is recorded as 154257538[6].
- OPN1MW3's genomic start is recorded as 153448107[7].
- OPN1MW3's genomic start is recorded as 153485225[8].
- OPN1MW3's genomic end is recorded as 154271805[9].
- OPN1MW3's genomic end is recorded as 153461633[10].
- OPN1MW3's genomic end is recorded as 153498755[11].
- OPN1MW3's encodes is recorded as Opsin 1, medium wave sensitive 3[12].
- OPN1MW3's encodes is recorded as Medium-wave-sensitive opsin 3[13].
- OPN1MW3's encodes is recorded as Medium-wave-sensitive opsin 2[14].
- OPN1MW3's found in taxon is recorded as Homo sapiens[15].
- OPN1MW3's chromosome is recorded as human X chromosome[16].
- OPN1MW3's strand orientation is recorded as forward strand[17].
- OPN1MW3's exact match is recorded as http://identifiers.org/ncbigene/101060233[18].
- OPN1MW3's cytogenetic location is recorded as Xq28[19].
- OPN1MW3's expressed in is recorded as blood[20].
Why It Matters
OPN1MW3 is known by 4 alternative names across languages and contexts.[2]