ID: 10367 | mitochondrial calcium uptake 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (72367340..72626079, complement) | CALC, CBARA1, EFHA3, MPXPS, ara CALC | 605084 |
ID: 10864 | solute carrier family 22 member 7 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (43295714..43305538) | NLT, OAT2, hOAT11 | 604995 |
ID: 8858 | protein Z, vitamin K dependent plasma glycoprotein [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113158648..113172386) | PZ | 176895 |
ID: 64577 | aldehyde dehydrogenase 8 family member A1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (134917393..134950101, complement) | ALDH12, DJ352A20.2 | 606467 |
ID: 123876 | acyl-CoA synthetase medium chain family member 2A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20451521..20487669) | A-923A4.1, ACSM2 | 614358 |
ID: 5345 | serpin family F member 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (1742871..1755265) | A2AP, AAP, ALPHA-2-PI, API, PLI, alpha2AP | 613168 |
ID: 1579 | cytochrome P450 family 4 subfamily A member 11 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (46929188..46941476, complement) | CP4Y, CYP4A2, CYP4AII, CYPIVA11 | 601310 |
ID: 348158 | acyl-CoA synthetase medium chain family member 2B [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20536226..20576367, complement) | ACSM2, HXMA, HYST1046 | 614359 |
ID: 10841 | formimidoyltransferase cyclodeaminase [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46136262..46155579, complement) | LCHC1 | 606806 |
ID: 1757 | sarcosine dehydrogenase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133659418..133739955, complement) | BPR-2, DMGDHL1, SAR, SARD, SDH | 604455 |
ID: 5091 | pyruvate carboxylase [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66848420..66958383, complement) | PCB | 608786 |
ID: 1582 | cytochrome P450 family 8 subfamily B member 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (42872192..42875879, complement) | CP8B, CYP12, CYPVIIIB1 | 602172 |
ID: 9970 | nuclear receptor subfamily 1 group I member 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (161229669..161238203, complement) | CAR, CAR1, MB67 | 603881 |
ID: 727 | complement C5 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (120952335..121074865, complement) | C5Da, C5b, CPAMD4, ECLZB, C5 | 120900 |
ID: 64816 | cytochrome P450 family 3 subfamily A member 43 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (99828013..99866093) | | 606534 |
ID: 3242 | 4-hydroxyphenylpyruvate dioxygenase [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (121839527..121888611, complement) | 4-HPPD, 4HPPD, GLOD3, HPPD, HPPDASE, PPD | 609695 |
ID: 199920 | FYN binding protein 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (56718789..56826914, complement) | ARAP, C1orf168 | 618478 |
ID: 10246 | solute carrier family 17 member 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (25912754..25930691, complement) | NPT3 | 611049 |
ID: 114571 | solute carrier family 22 member 9 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (63369785..63410294) | HOAT4, OAT4, OAT7, UST3H, ust3 | 607579 |
ID: 58510 | proline dehydrogenase 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (35799988..35812845, complement) | HSPOX1, HYPDH | 616377 |