ID: 768206 | photoreceptor disc component [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76527586..76553580) | RP36 | 610598 |
ID: 441295 | olfactory receptor family 2 subfamily A member 9 pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (144299521..144300505) | FKSG35, HSDJ0798C17, OR2A19, OR2A22P, OR2A9 | |
ID: 401428 | olfactory receptor family 2 subfamily A member 20 pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (144250674..144251603, complement) | OR2A20 | |
ID: 401427 | olfactory receptor family 2 subfamily A member 7 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (144257663..144264792, complement) | HSDJ0798C17, OR2A21 | |
ID: 285440 | cytochrome P450 family 4 subfamily V member 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186191567..186213463) | BCD, CYP4AH1 | 608614 |
ID: 114902 | C1q and TNF related 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (119338942..119346705, complement) | CTRP5, MFRP | 608752 |
ID: 90362 | family with sequence similarity 110 member B [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (57994523..58148784) | C8orf72 | 611394 |
ID: 89885 | fetal and adult testis expressed 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (151716035..151723194) | CT43, FATE | 300450 |
ID: 84935 | mesenteric estrogen dependent adipogenesis [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (30906271..30925572) | AWMS3, C13orf33, MEDA-4, MEDA4, hAWMS3 | |
ID: 84858 | zinc finger protein 503 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (75279725..75401916, complement) | NOLZ-1, NOLZ1, Nlz2 | 613902 |
ID: 83888 | fibroblast growth factor binding protein 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (15960245..15963175, complement) | HBP17RP, KSP37 | 607713 |
ID: 83552 | membrane frizzled-related protein [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (119338942..119346705, complement) | CTRP5, MCOP5, NNO2, RD6 | 606227 |
ID: 80207 | outer mitochondrial membrane lipid metabolism regulator OPA3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45527427..45584802, complement) | MGA3 | 606580 |
ID: 80025 | pantothenate kinase 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3888781..3929887) | C20orf48, HARP, HSS, NBIA1, PKAN | 606157 |
ID: 80008 | transmembrane protein 156 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (38966744..39032409, complement) | | |
ID: 79788 | zinc finger protein 665 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (53162424..53193358, complement) | ZFP160L | |
ID: 79738 | Bardet-Biedl syndrome 10 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (76344474..76348415, complement) | C12orf58 | 610148 |
ID: 64218 | semaphorin 4A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156147373..156177744) | CORD10, RP35, SEMAB, SEMB | 607292 |
ID: 57030 | solute carrier family 17 member 7 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49429401..49441527, complement) | BNPI, VGLUT1 | 605208 |
ID: 57001 | succinate dehydrogenase complex assembly factor 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (97117698..97181763) | ACN9, DC11, LYRM10, Sdh7 | 615773 |