ID: 8482 | semaphorin 7A (JohnMiltonHagen blood group) [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (74409289..74433958, complement) | CD108, CDw108, H-SEMA-K1, H-Sema-L, JMH, PFIC11, SEMAK1, SEMAL | 607961 |
ID: 1289 | collagen type V alpha 1 chain [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (134641803..134844843) | EDSC, EDSCL1, FMDMF | 120215 |
ID: 30850 | cerebellar degeneration related protein 2 like [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (74987632..75005800) | HUMPPA | |
ID: 253827 | methionine sulfoxide reductase B3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (65278683..65466907) | DFNB74 | 613719 |
ID: 6415 | selenoprotein W [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47778703..47784682) | SEPW1, selW | 603235 |
ID: 9414 | tight junction protein 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (69121264..69255208) | C9DUPq21.11, DFNA51, DUP9q21.11, FHCA1, PFIC4, X104, ZO2 | 607709 |
ID: 56652 | twinkle mtDNA helicase [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (100987543..100994403) | ATXN8, C10orf2, IOSCA, MTDPS7, PEO, PEO1, PEOA3, PRLTS5, SANDO, SCA8, TWINL | 606075 |
ID: 25915 | NADH:ubiquinone oxidoreductase complex assembly factor 3 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49020452..49023495) | 2P1, C3orf60, E3-3, MC1DN18 | 612911 |
ID: 8451 | cullin 4A [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113208193..113267108) | | 603137 |
ID: 93129 | ORAI calcium release-activated calcium modulator 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30949068..30954938) | TMEM142C | 610930 |
ID: 84545 | mitochondrial ribosomal protein L43 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (100977820..100987497, complement) | L43mt, MRP-L43, bMRP36a, mL43 | 611848 |
ID: 10712 | endosomal transmembrane epsin interactor 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155247205..155255483, complement) | C1orf2, COTE1, FAM189B | 619447 |
ID: 226 | aldolase, fructose-bisphosphate A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30064279..30070420) | ALDA, GSD12, HEL-S-87p | 103850 |
ID: 56204 | atos homolog A [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (52581321..52709815, complement) | FAM214A, KIAA1370 | 620168 |
ID: 56262 | leucine rich repeat containing 8 VRAC subunit A [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128882133..128918039) | AGM5, HsLRRC8A, LRRC8, SWELL1 | 608360 |
ID: 55795 | PCI domain containing 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113165002..113208669, complement) | F10 | 613713 |
ID: 3363 | 5-hydroxytryptamine receptor 7 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (90740823..90858039, complement) | 5-HT7 | 182137 |
ID: 63922 | chromosome transmission fidelity factor 18 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (788620..798074) | C16orf41, C321D2.2, C321D2.3, C321D2.4, CHL12, Ctf18, RUVBL | 613201 |
ID: 10901 | dehydrogenase/reductase 4 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (23953770..23969279) | CR, NRDR, PHCR, PSCD, SCAD-SRL, SDR-SRL, SDR25C1, SDR25C2 | 611596 |
ID: 389 | ras homolog family member C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (112701131..112707408, complement) | ARH9, ARHC, H9, RHOH9 | 165380 |