ID: 254042 | methionyl aminopeptidase type 1D, mitochondrial [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171999953..172082430) | MAP 1D, MAP1D, MetAP 1D, Metap1l | 610267 |
ID: 55646 | Ly1 antibody reactive [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (4267701..4290154, complement) | ZC2HC2, ZLYAR | 617684 |
ID: 10527 | importin 7 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (9384652..9448127) | Imp7, RANBP7 | 605586 |
ID: 9025 | ring finger protein 8 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (37353983..37394734) | hRNF8 | 611685 |
ID: 285203 | EGF domain specific O-linked N-acetylglucosamine transferase [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (68975225..69013684, complement) | AER61, AOS4, C3orf641, EOGT | 614789 |
ID: 5921 | RAS p21 protein activator 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (87267883..87391916) | CM-AVM, CMAVM, CMAVM1, GAP, PKWS, RASA, RASGAP, p120, p120GAP, p120RASGAP | 139150 |
ID: 51193 | zinc finger protein 639 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (179322876..179338583) | ANC-2H01, ANC_2H01, ZASC1 | 619214 |
ID: 10920 | COP9 signalosome subunit 8 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (237085889..237100474) | COP9, CSN8, SGN8 | 616011 |
ID: 81502 | histocompatibility minor 13 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (31514442..31569543) | H13, IMP1, IMPAS, IMPAS-1, MSTP086, PSENL3, PSL3, SPP, SPPL1 | 607106 |
ID: 57514 | Rho GTPase activating protein 31 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (119294383..119420714) | AOS, AOS1, CDGAP | 610911 |
ID: 10180 | RNA binding motif protein 6 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49940150..50077249) | 3G2, DEF-3, DEF3, HLC-11, NY-LU-12, g16 | 606886 |
ID: 55186 | solute carrier family 25 member 36 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (140941836..140980995) | HHF8, PNC2 | 616149 |
ID: 81890 | queuine tRNA-ribosyltransferase catalytic subunit 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10701439..10713365) | FP3235, TGT, TGUT | 609615 |
ID: 80854 | SET domain containing 7, histone lysine methyltransferase [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (139492974..139556219, complement) | KMT7, SET7, SET7/9, SET9 | 606594 |
ID: 7220 | transient receptor potential cation channel subfamily C member 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (142724034..142807888) | HTRP-1, TRP1 | 602343 |
ID: 78987 | cysteine rich with EGF like domains 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (9933834..9945406) | AVSD2, CIRRIN, JELANS | 607170 |
ID: 1678 | translocase of inner mitochondrial membrane 8A [Homo sapiens (human)] | Chromosome X, NC_000023.11 (101345661..101348742, complement) | DDP, DDP1, DFN1, MTS, TIM8 | 300356 |
ID: 51566 | armadillo repeat containing X-linked 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (101623151..101627843) | ALEX3, GASP6, dJ545K15.2 | 300364 |
ID: 27300 | zinc finger protein 544 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (58228914..58277455) | | |
ID: 2547 | X-ray repair cross complementing 6 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41621295..41664041) | CTC75, CTCBF, G22P1, KU70, ML8, TLAA | 152690 |