AP1S2

Summary

AP1S2 is a gene^[1].

Key Facts

• AP1S2's instance of is recorded as gene^[2].
• AP1S2 is a type of protein-coding gene^[3].
• AP1S2's HomoloGene ID is recorded as 2908^[4].
• AP1S2's genomic start is recorded as 15825806^[5].
• AP1S2's genomic start is recorded as 15843929^[6].
• AP1S2's genomic end is recorded as 15873054^[7].
• AP1S2's genomic end is recorded as 15854931^[8].
• AP1S2's ortholog is recorded as Ap1s2^[9].
• AP1S2's ortholog is recorded as APS1^[10].
• AP1S2's ortholog is recorded as Ap1s2^[11].
• AP1S2's ortholog is recorded as ap1s2^[12].
• AP1S2's ortholog is recorded as aps-1^[13].
• AP1S2's ortholog is recorded as AP-1sigma^[14].
• AP1S2's encodes is recorded as Adaptor related protein complex 1 subunit sigma 2^[15].
• AP1S2's encodes is recorded as Adaptor-related protein complex 1, sigma 2 subunit, isoform CRA_e^[16].
• AP1S2's found in taxon is recorded as Homo sapiens^[17].
• AP1S2's chromosome is recorded as human X chromosome^[18].
• AP1S2's genetic association is recorded as X-linked intellectual disability^[19].
• AP1S2's strand orientation is recorded as reverse strand^[20].
• AP1S2's exact match is recorded as http://identifiers.org/ncbigene/8905^[21].
• AP1S2's cytogenetic location is recorded as Xp22.2^[22].
• AP1S2's expressed in is recorded as corpus epididymis^[23].
• AP1S2's expressed in is recorded as tail of epididymis^[24].
• AP1S2's expressed in is recorded as monocyte^[25].
• AP1S2's expressed in is recorded as retinal pigment epithelium^[26].