ID: 9341 | vesicle associated membrane protein 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (7771296..7781432) | CEB | 603657 |
ID: 7873 | mesencephalic astrocyte derived neurotrophic factor [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (51385291..51389397) | ARMET, ARP, DDDS | 601916 |
ID: 54765 | tripartite motif containing 44 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (35662775..35818007) | AN3, DIPB, HSA249128, MC7 | 612298 |
ID: 23507 | leucine rich repeat containing 8 VRAC subunit B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (89524829..89597861) | TA-LRRP, TALRRP | 612888 |
ID: 26100 | WD repeat domain, phosphoinositide interacting 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (5190233..5233855) | ATG18B, Atg21, CGI-50, IDDSSA, WIPI-2 | 609225 |
ID: 4802 | nuclear transcription factor Y subunit gamma [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (40691704..40771603) | CBF-C, CBFC, H1TF2A, HAP5, HSM, NF-YC | 605344 |
ID: 51668 | intraflagellar transport 25 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (53911576..53946305, complement) | C1orf41, CFAP232, FAP232, HSPB11, HSPCO34, PP25 | 620841 |
ID: 57655 | GRAM domain containing 1A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34994727..35026469) | KIAA1533 | 620178 |
ID: 11315 | Parkinsonism associated deglycase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (7961711..7985505) | DJ-1, DJ1, GATD2, HEL-S-67p | 602533 |
ID: 4831 | NME/NM23 nucleoside diphosphate kinase 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (51165536..51171744) | NDKB, NDPK-B, NDPKB, NM23-H2, NM23B, PUF | 156491 |
ID: 4790 | nuclear factor kappa B subunit 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (102501359..102617302) | CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1, NF-kappaB, NF-kappabeta, NFKB-p105, NFKB-p50, NFkappaB | 164011 |
ID: 127829 | ADP ribosylation factor like GTPase 8A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (202133404..202144737, complement) | ARL10B, GIE2 | 616597 |
ID: 7461 | CAP-Gly domain containing linker protein 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74289407..74405935) | CLIP, CLIP-115, CYLN2, WBSCR3, WBSCR4, WSCR3, WSCR4 | 603432 |
ID: 5825 | ATP binding cassette subfamily D member 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (94385131..94518663) | ABC43, CBAS5, PMP70, PXMP1, ZWS2 | 170995 |
ID: 8455 | attractin [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3471018..3651118) | DPPT-L, MGCA | 603130 |
ID: 119559 | sideroflexin 4 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (119140767..119165714, complement) | BCRM1, COXPD18, SLC56A4 | 615564 |
ID: 9371 | kinesin family member 3B [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32277651..32335011) | FLA8, HH0048, KLP-11, OTSC12, RP89 | 603754 |
ID: 55167 | MSL complex subunit 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (136148917..136196335, complement) | MSL-2L1, RNF184, MSL2 | 614802 |
ID: 79703 | TOP6B like initiator of meiotic double strand breaks [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66744736..66843516) | C11orf80, HYDM4, TOPOVIBL | 616109 |
ID: 375190 | family with sequence similarity 228 member B [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (24076833..24169638) | | |