ID: 11112 | 3-hydroxyisobutyrate dehydrogenase [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (27525442..27662883, complement) | NS5ATP1 | 608475 |
ID: 672 | BRCA1 DNA repair associated [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43044295..43170327, complement) | BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4, PPP1R53, PSCP, RNF53 | 113705 |
ID: 1312 | catechol-O-methyltransferase [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19941772..19969975) | HEL-S-98n | 116790 |
ID: 59272 | angiotensin converting enzyme 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (15518197..15607211, complement) | ACEH | 300335 |
ID: 6647 | superoxide dismutase 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31659693..31668931) | ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP, hSod1, homodimer | 147450 |
ID: 1994 | ELAV like RNA binding protein 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (7958573..8005641, complement) | ELAV1, HUR, Hua, MelG | 603466 |
ID: 6678 | secreted protein acidic and cysteine rich [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151661096..151686915, complement) | BM-40, OI17, ON, ONT | 182120 |
ID: 7037 | transferrin receptor [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196049284..196082090, complement) | CD71, IMD46, T9, TFR, TFR1, TR, TRFR, p90 | 190010 |
ID: 2876 | glutathione peroxidase 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49357176..49358353, complement) | GPXD, GSHPX1 | 138320 |
ID: 5727 | patched 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95442980..95516971, complement) | BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH | 601309 |
ID: 3939 | lactate dehydrogenase A [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (18394563..18408425) | GSD11, HEL-S-133P, LDHM, PIG19 | 150000 |
ID: 7531 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (1344275..1400222, complement) | 14-3-3E, HEL2, KCIP-1, MDCR, MDS | 605066 |
ID: 10971 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (9583967..9630997, complement) | 14-3-3, 1C5, HS1 | 609009 |
ID: 360 | aquaporin 3 (Gill blood group) [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (33441160..33447593, complement) | AQP-3, GIL | 600170 |
ID: 8451 | cullin 4A [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113208193..113267108) | | 603137 |
ID: 708 | complement C1q binding protein [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (5432777..5439155, complement) | COXPD33, GC1QBP, HABP1, SF2AP32, SF2p32, gC1Q-R, gC1qR, p32 | 601269 |
ID: 22926 | activating transcription factor 6 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (161766320..161964070) | ACHM7A, ATP6alpha, ATF6 | 605537 |
ID: 80332 | ADAM metallopeptidase domain 33 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3667975..3682010, complement) | C20orf153, DJ964F7.1 | 607114 |
ID: 5350 | phospholamban [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (118548296..118561716) | CMD1P, CMH18, PLB | 172405 |
ID: 3073 | hexosaminidase subunit alpha [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72340924..72376014, complement) | TSD | 606869 |