ID: 9749 | phosphatase and actin regulator 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (143536878..143831185) | C6orf56 | 608724 |
ID: 56928 | signal peptide peptidase like 2B [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2328684..2355095) | IMP-4, IMP4, PSH4, PSL1 | 608239 |
ID: 51690 | LSM7 homolog, U6 small nuclear RNA and mRNA degradation associated [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2321521..2328586, complement) | YNL147W | 607287 |
ID: 84498 | family with sequence similarity 120 member B [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170290703..170407067) | CCPG, KIAA1838, PGCC1, SAN1, dJ894D12.1 | 612266 |
ID: 6326 | sodium voltage-gated channel alpha subunit 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165239414..165392304) | BFIC3, BFIS3, BFNIS, DEE11, EA9, EIEE11, HBA, HBSCI, HBSCII, NAC2, Na(v)1.2, Nav1.21, SCN2A2, SCN2A | 182390 |
ID: 552891 | DNAJC25-GNG10 readthrough [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111631334..111670226) | | |
ID: 548645 | DnaJ heat shock protein family (Hsp40) member C25 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111631334..111654345) | bA16L21.2.1 | |
ID: 8731 | RNA guanine-7 methyltransferase [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (13726673..13764556) | CMT1, CMT1c, MET, Met, N7-MTase, RG7MT1, cm1p, hCMT1, hMet | 603514 |
ID: 65005 | mitochondrial ribosomal protein L9 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151759647..151763496, complement) | L9mt, bL9m | 611824 |
ID: 1392 | corticotropin releasing hormone [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (66176376..66178464, complement) | CRF1, CRH | 122560 |
ID: 114984 | FLYWCH family member 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2883195..2899382) | | |
ID: 84306 | programmed cell death 2 like [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34404399..34426168) | | 615661 |
ID: 55638 | syntabulin [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (109573978..109691600, complement) | GOLSYN, OCSYN, SNPHL | 611568 |
ID: 284131 | endonuclease V [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80415167..80438086) | | 619821 |
ID: 2948 | glutathione S-transferase mu 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (109656099..109667727) | GSTM4-4, GTM4 | 138333 |
ID: 9024 | BR serine/threonine kinase 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (1389934..1462689) | C11orf7, PEN11B, SAD-A, SAD1, SADA, STK29 | 609236 |
ID: 10142 | A-kinase anchoring protein 9 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (91940862..92110673) | AKAP-9, AKAP350, AKAP450, CG-NAP, HYPERION, LQT11, MU-RMS-40.16A, PPP1R45, PRKA9, YOTIAO | 604001 |
ID: 30850 | cerebellar degeneration related protein 2 like [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (74987632..75005800) | HUMPPA | |
ID: 8209 | glutamine amidotransferase class 1 domain containing 3 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44133683..44145711) | C21orf33, ES1A, GT335, HES1, KNPH, KNPI, GATD3 | 601659 |
ID: 8925 | HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (63608618..63833948, complement) | MDFPMR, p532, p619 | 605109 |