ID: 83693 | hydroxysteroid dehydrogenase like 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (84122141..84145177, complement) | SDR12C3 | 619067 |
ID: 1861 | torsin family 1 member A [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (129812942..129824136, complement) | AMC5, DQ2, DYT1 | 605204 |
ID: 23078 | von Willebrand factor A domain containing 8 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41566835..41961109, complement) | KIAA0564, P7BP2, RP97 | 617509 |
ID: 10607 | transducin beta like 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1972053..1982929) | SAZD, UTP13 | 605915 |
ID: 9815 | GIT ArfGAP 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109929804..110000164, complement) | CAT-2, CAT2, PKL | 608564 |
ID: 123872 | dynein axonemal assembly factor 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (84145308..84177920) | CILD13, DAU1, LRRC50, ODA7, swt | 613190 |
ID: 1186 | chloride voltage-gated channel 7 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1444935..1475028, complement) | CLC-7, CLC7, HOD, OPTA2, OPTB4, PPP1R63 | 602727 |
ID: 5338 | phospholipase D2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (4807152..4823430) | PLD1C | 602384 |
ID: 7782 | solute carrier family 30 member 4 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (45479606..45522755, complement) | ZNT4, znT-4 | 602095 |
ID: 55795 | PCI domain containing 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113165002..113208669, complement) | F10 | 613713 |
ID: 23312 | Dmx like 2 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (51447791..51622771, complement) | DEE81, DFNA71, EIEE81, PEPNS, RC3 | 612186 |
ID: 26233 | F-box and leucine rich repeat protein 6 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144355431..144358472, complement) | FBL6, FBL6A, PP14630 | 609076 |
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: 51479 | ankyrin repeat and FYVE domain containing 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (4163821..4263979, complement) | ANKHZN, BTBD23, ZFYVE14 | 607927 |
ID: 84622 | zinc finger protein 594 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (5174083..5191868, complement) | | |
ID: 348180 | cytosolic thiouridylase subunit 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88706503..88715396) | C16orf84, MFRG, NCS2, UPF0432 | 617057 |
ID: 9094 | unc-119 lipid binding chaperone [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28546707..28552628, complement) | CORD24, HRG4, IMD13, POC7, POC7A | 604011 |
ID: 50628 | gem nuclear organelle associated protein 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (744421..754410, complement) | HC56, HCAP1, HHRF-1, NEDMCR, p97 | 606969 |
ID: 79581 | solute carrier family 52 member 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144358552..144361272) | BVVLS2, D15Ertd747e, GPCR41, GPR172A, HuPAR-1, PAR1, RFT3, RFVT2, hRFT3 | 607882 |
ID: 138639 | protein tyrosine phosphatase domain containing 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94030813..94109856) | PTP9Q22 | |