ID: 429 | achaete-scute family bHLH transcription factor 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (102957674..102960513) | ASH1, HASH1, MASH1, bHLHa46 | 100790 |
ID: 441430 | ankyrin repeat domain 20 family member A2, pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (40222102..40282358) | ANKRD20A2 | |
ID: 27133 | potassium voltage-gated channel subfamily H member 5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (62699464..63045458, complement) | DEE112, EAG2, H-EAG2, Kv10.2, hEAG2 | 605716 |
ID: 134829 | clavesin 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (122996235..123072925) | C6orf212, C6orf213, RLBP1L2, bA160A10.4 | 616945 |
ID: 3763 | potassium inwardly rectifying channel subfamily J member 6 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37607373..37916457, complement) | BIR1, GIRK-2, GIRK2, KATP-2, KATP2, KCNJ7, KIR3.2, KPLBS, hiGIRK2 | 600877 |
ID: 441631 | tetraspanin 11 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30926748..31016502) | VSSW1971 | |
ID: 2912 | glutamate metabotropic receptor 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (51707068..51718613) | GLUR2, GPRC1B, MGLUR2, mGlu2 | 604099 |
ID: 440073 | IQ motif and Sec7 domain ArfGEF 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (66767..178455) | | 612118 |
ID: 259236 | transmembrane inner ear [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (46693778..46710886) | DFNB6 | 607237 |
ID: 6861 | synaptotagmin 5 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (55171196..55180289, complement) | | 600782 |
ID: 27164 | spalt like transcription factor 3 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78979818..78998969) | ZNF796 | 605079 |
ID: 5458 | POU class 4 homeobox 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (146638893..146642474) | BRN3.2, BRN3B, Brn-3b | 113725 |
ID: 375607 | N-acetyltransferase 16 (putative) [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101170496..101180293, complement) | C7orf52 | 615783 |
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: 79948 | phospholipid phosphatase related 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (812488..823797, complement) | LPPR3, LPR3, PRG-2, PRG2 | 610391 |
ID: 11078 | TRIO and F-actin binding protein [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37697048..37776556) | DFNB28, HRIHFB2122, TAP68, TARA, dJ37E16.4 | 609761 |
ID: 128414 | sodium/potassium transporting ATPase interacting 4 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63240784..63254921, complement) | C20orf58, FAM77A, bA261N11.2 | 612873 |
ID: 56341 | protein arginine methyltransferase 8 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (3381349..3593973) | HRMT1L3, HRMT1L4 | 610086 |
ID: 64211 | LIM homeobox 5 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (113462033..113471871, complement) | | 605992 |
ID: 4744 | neurofilament heavy chain [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29480218..29491390) | CMT2CC, NFH | 162230 |