ID: 23250 | ATPase phospholipid transporting 11A [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (112690038..112887168) | ATPIH, ATPIS, AUNA2, DFNA84, HLD24 | 605868 |
ID: 284439 | solute carrier family 25 member 42 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (19063994..19113030) | MECREN | 610823 |
ID: 283450 | HECT domain E3 ubiquitin protein ligase 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (112160195..112382431, complement) | C12ord51, C12orf51, HEEL, NEDSSCC, POTAGE | 620209 |
ID: 115704 | ecotropic viral integration site 5 like [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (7830218..7864976) | | |
ID: 23196 | family with sequence similarity 120 member A [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93451685..93566112) | C9orf10, HBVPTPAP, OSSA | 612265 |
ID: 4350 | N-methylpurine DNA glycosylase [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (77007..85846) | AAG, ADPG, APNG, CRA36.1, MDG, Mid1, PIG11, PIG16, anpg | 156565 |
ID: 3705 | inositol-tetrakisphosphate 1-kinase [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92936914..93115925, complement) | ITRPK1 | 601838 |
ID: 23164 | myosin phosphatase Rho interacting protein [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (17042457..17192643) | M-RIP, MRIP, RHOIP3, RIP3, p116Rip | 612935 |
ID: 7763 | zinc finger AN1-type containing 5 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (72351413..72365208, complement) | ZA20D2A, ZNF216, ZFAND5 | 604761 |
ID: 10565 | ARF guanine nucleotide exchange factor 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (67173511..67343781, complement) | ARFGEP1, BIG1, DEDISB, P200 | 604141 |
ID: 112398 | egl-9 family hypoxia inducible factor 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40799191..40808434) | EIT-6, EIT6, HIF-PH1, HIFPH1, HPH-1, HPH-3, PHD1 | 606424 |
ID: 5887 | RAD23 homolog B, nucleotide excision repair protein [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (107283279..107332194) | HHR23B, HR23B, P58 | 600062 |
ID: 347902 | adhesion molecule with Ig like domain 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (47075707..47079959, complement) | ALI1, AMIGO-2, DEGA | 615690 |
ID: 1984 | eukaryotic translation initiation factor 5A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7306999..7312463) | EIF-5A1, FABAS, eIF-4D, eIF5AI, EIF5A | 600187 |
ID: 22870 | protein phosphatase 6 regulatory subunit 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (55228218..55259017, complement) | KIAA1115, PP6R1, SAP190, SAPS1 | 610875 |
ID: 84991 | RNA binding motif protein 17 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (6089034..6117447) | SPF45 | 606935 |
ID: 5527 | protein phosphatase 2 regulatory subunit B'gamma [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (101760573..101927992) | B56G, B56gamma, PR61G | 601645 |
ID: 339287 | MSL complex subunit 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (40121971..40136917) | MSL-1 | 614801 |
ID: 10452 | translocase of outer mitochondrial membrane 40 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (44891254..44903689) | C19orf1, D19S1177E, PER-EC1, PEREC1, TOM40 | 608061 |
ID: 170394 | PWWP domain containing 2B [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (132397200..132417859) | PWWP2, bA432J24.1, pp8607 | |