OPHN1
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OPHN1
Summary
OPHN1 is a gene[1]. OPHN1 ranks in the top 2% of gene entities by monthly Wikipedia readership (9 views/month).[2]
Key Facts
- OPHN1's instance of is recorded as gene[3].
- OPHN1 is a type of protein-coding gene[4].
- OPHN1's HomoloGene ID is recorded as 1913[5].
- OPHN1's genomic start is recorded as 67262186[6].
- OPHN1's genomic start is recorded as 67949349[7].
- OPHN1's genomic end is recorded as 68433913[8].
- OPHN1's genomic end is recorded as 67653755[9].
- OPHN1's ortholog is recorded as Ophn1[10].
- OPHN1's ortholog is recorded as Ophn1[11].
- OPHN1's encodes is recorded as Oligophrenin 1[12].
- OPHN1's found in taxon is recorded as Homo sapiens[13].
- OPHN1's chromosome is recorded as human X chromosome[14].
- OPHN1's genetic association is recorded as X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance[15].
- OPHN1's strand orientation is recorded as reverse strand[16].
- OPHN1's exact match is recorded as http://identifiers.org/ncbigene/4983[17].
- OPHN1's cytogenetic location is recorded as Xq12[18].
- OPHN1's expressed in is recorded as corpus callosum[19].
- OPHN1's expressed in is recorded as Achilles tendon[20].
- OPHN1's expressed in is recorded as sural nerve[21].
- OPHN1's expressed in is recorded as ventricular zone[22].
- OPHN1's expressed in is recorded as ganglionic eminence[23].
- OPHN1's expressed in is recorded as amygdala[24].
- OPHN1's expressed in is recorded as nucleus accumbens[25].
- OPHN1's expressed in is recorded as caudate nucleus[26].
- OPHN1's expressed in is recorded as putamen[27].
Why It Matters
OPHN1 ranks in the top 2% of gene entities by monthly Wikipedia readership (9 views/month).[2]