RD3
protein-coding gene in the species Homo sapiens
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RD3
Summary
RD3 is a gene[1].
Key Facts
- RD3's instance of is recorded as gene[2].
- RD3 is a type of protein-coding gene[3].
- RD3's HomoloGene ID is recorded as 11373[4].
- RD3's genomic start is recorded as 211476522[5].
- RD3's genomic start is recorded as 211649864[6].
- RD3's genomic end is recorded as 211666259[7].
- RD3's genomic end is recorded as 211492162[8].
- RD3's ortholog is recorded as Rd3[9].
- RD3's ortholog is recorded as Rd3[10].
- RD3's ortholog is recorded as rd3[11].
- RD3's encodes is recorded as Retinal degeneration 3, GUCY2D regulator[12].
- RD3's found in taxon is recorded as Homo sapiens[13].
- RD3's chromosome is recorded as human chromosome 1[14].
- RD3's genetic association is recorded as Leber congenital amaurosis 12[15].
- RD3's strand orientation is recorded as reverse strand[16].
- RD3's exact match is recorded as http://identifiers.org/ncbigene/343035[17].
- RD3's cytogenetic location is recorded as 1q32.3[18].
- RD3's expressed in is recorded as gonad[19].
- RD3's expressed in is recorded as buccal mucosa cell[20].
- RD3's expressed in is recorded as right lung[21].
- RD3's expressed in is recorded as retinal pigment epithelium[22].
- RD3's expressed in is recorded as body of stomach[23].
- RD3's expressed in is recorded as pituitary gland[24].
- RD3's expressed in is recorded as ectocervix[25].
- RD3's expressed in is recorded as smooth muscle tissue[26].