ID: 79948 | phospholipid phosphatase related 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (812488..823797, complement) | LPPR3, LPR3, PRG-2, PRG2 | 610391 |
ID: 375607 | N-acetyltransferase 16 (putative) [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101170496..101180293, complement) | C7orf52 | 615783 |
ID: 6656 | SRY-box transcription factor 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (112067149..112071706) | | 602148 |
ID: 27164 | spalt like transcription factor 3 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78979818..78998969) | ZNF796 | 605079 |
ID: 5459 | POU class 4 homeobox 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (146338839..146341728) | BRN3C, DFNA15, DFNA42, DFNA52 | 602460 |
ID: 222183 | serine/arginine repetitive matrix 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76201896..76287287) | | |
ID: 94030 | leucine rich repeat containing 4B [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50516892..50568435, complement) | HSM, LRIG4, NGL-3 | |
ID: 3208 | hippocalcin [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (32885996..32894646) | BDR2, DYT2 | 142622 |
ID: 2902 | glutamate ionotropic receptor NMDA type subunit 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (137139154..137168756) | DEE101, GluN1, MRD8, NDHMSD, NDHMSR, NMD-R1, NMDA1, NMDAR1, NR1 | 138249 |
ID: 440073 | IQ motif and Sec7 domain ArfGEF 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (66767..178455) | | 612118 |
ID: 4761 | neuronal differentiation 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39603768..39607920, complement) | DEE72, EIEE72, NDRF, bHLHa1 | 601725 |
ID: 2290 | forkhead box G1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (28766787..28770277) | BF1, BF2, FHKL3, FKH2, FKHL1, FKHL2, FKHL3, FKHL4A, FOXG1B, FOXG1C, HBF-1, HBF-2, HBF-3, HBF-G2, HBF2, HFK1, HFK2, HFK3, KHL2, QIN, FOXG1 | 164874 |
ID: 1113 | chromogranin A [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92922664..92935285) | CGA, PHE5, PHES | 118910 |
ID: 146330 | F-box and leucine rich repeat protein 16 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (692500..705801, complement) | C16orf22, Fbl16, c380A1.1 | 609082 |
ID: 60482 | solute carrier family 5 member 7 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (107986524..108013994) | CHT, CHT1, CMS20, DHMNVP, HMN7A, HMND7, hCHT1 | 608761 |
ID: 140679 | solute carrier family 32 member 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38724486..38729372) | DEE114, GEFSP12, VGAT, VIAAT, VIAAT GEFSP12 | 616440 |
ID: 56896 | dihydropyrimidinase like 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26847995..26950351) | CRAM, CRMP-5, CRMP5, CV2, RTSC4, Ulip6 | 608383 |
ID: 220107 | deleted in lymphocytic leukemia 7 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50711026..50843939, complement) | | 618634 |
ID: 4062 | lymphocyte antigen 6 family member H [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143157916..143160654, complement) | NMLY6 | 603625 |
ID: 22986 | sortilin related VPS10 domain containing receptor 3 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (104641290..105265242) | SORCS | 606285 |