ID: 23349 | PHD finger protein 24 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (34665607..34982544) | GINIP | 619928 |
ID: 161436 | EMAP like 5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88612431..88792953, complement) | EMAP-2, EMAP-5, FAP16 | 618119 |
ID: 284716 | ribosomal modification protein rimK like family member A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (42380792..42424232) | FAM80A, NAAGS, NAAGS-II, NAAGS2 | 618949 |
ID: 147495 | APC down-regulated 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (10454635..10489949) | B7323, DRAPC1, FP7019, HHS, HTS, HYPT1 | 607479 |
ID: 3069 | high density lipoprotein binding protein [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241227291..241315672, complement) | HBP, PRO2900, VGL | 142695 |
ID: 30837 | suppressor of cytokine signaling 7 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38351844..38405593) | NAP4, NCKAP4 | 608788 |
ID: 80148 | solute carrier family 66 member 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79902420..79951653, complement) | PQLC1 | |
ID: 123096 | solute carrier family 25 member 29 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100278567..100306444, complement) | C14orf69, CACL, ORNT3 | 615064 |
ID: 23277 | clustered mitochondria homolog [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (2689387..2712020, complement) | CLU1 | 616184 |
ID: 117247 | solute carrier family 16 member 10 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (111087503..111231194) | MCT10, PRO0813, TAT1 | 607550 |
ID: 158405 | KIAA1958 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (112486827..112669397) | | 617390 |
ID: 9026 | huntingtin interacting protein 1 related [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (122834748..122862961) | HIP12, HIP3, ILWEQ | 605613 |
ID: 4782 | nuclear factor I C [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3359630..3469217) | CTF, CTF5, NF-I, NFI | 600729 |
ID: 9722 | nitric oxide synthase 1 adaptor protein [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (162069691..162370475) | 6330408P19Rik, CAPON, NPHS22 | 605551 |
ID: 783 | calcium voltage-gated channel auxiliary subunit beta 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (18140424..18543557) | CAB2, CACNLB2, CAVB2, MYSB | 600003 |
ID: 6576 | solute carrier family 25 member 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19175581..19178736, complement) | CIC, CMS23, CTP, D2L2AD, SEA, SLC20A3 | 190315 |
ID: 9144 | synaptogyrin 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78168545..78172964) | | 603926 |
ID: 114991 | zinc finger protein 618 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (113876309..114056593) | FP13169, NEDD10 | 617077 |
ID: 6573 | solute carrier family 19 member 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45502517..45563025, complement) | CHMD, FOLT, IFC-1, IFC1, IMD114, MEGAF, REFC, RFC, RFC1, RFT-1, hRFC, hSLC19A1 | 600424 |
ID: 79632 | family with sequence similarity 184 member A [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (118959763..119149128, complement) | C6orf60 | |