基因ID | taxid | GeneDate LocusTag | Symbol Synonyms | Symbolfna Fullnamefna | dbXrefs | chromosome maplocation | description | genetype fnastatus | Otherdesignations | Featuretype |
7936 | 9606 | 20220707 | NELFE D6S45|NELF-E|RD|RDBP|RDP | NELFE negative elongation factor complex member E | MIM:154040|HGNC:HGNC:13974|Ensembl:ENSG00000204356|AllianceGenome:HGNC:13974 | 6 6p21.33 | negative elongation factor complex member E | protein-coding O | negative elongation factor E|RD RNA-binding protein|RNA-binding protein RD|major histocompatibility complex gene RD|negative elongation factor polypeptide E|nuclear protein | |
7937 | 9606 | 20190816 | RWS | MIM:179450 | 6 6p21.3 | Ragweed sensitivity | unknown | |||
7938 | 9606 | 20190816 | CP20 LCP20 | MIM:153380 | 6 6p21.3-p21.2 | lymphocyte cytosol polypeptide, 20 kD | protein-coding | lymphocyte cytosolic protein, molecular weight 20kD | ||
7939 | 9606 | 20190816 | LAP | MIM:150270 | 6 6p21.3-p21.2 | Laryngeal adductor paralysis | unknown | |||
7940 | 9606 | 20220513 | LST1 B144|D6S49E|LST-1 | LST1 leukocyte specific transcript 1 | MIM:109170|HGNC:HGNC:14189|Ensembl:ENSG00000204482|AllianceGenome:HGNC:14189 | 6 6p21.33 | leukocyte specific transcript 1 | protein-coding O | leukocyte-specific transcript 1 protein|lymphocyte antigen 117 | |
7941 | 9606 | 20220718 | PLA2G7 LDL-PLA2|LP-PLA2|PAFAD|PAFAH | PLA2G7 phospholipase A2 group VII | MIM:601690|HGNC:HGNC:9040|Ensembl:ENSG00000146070|AllianceGenome:HGNC:9040 | 6 6p12.3 | phospholipase A2 group VII | protein-coding O | platelet-activating factor acetylhydrolase|1-alkyl-2-acetylglycerophosphocholine esterase|2-acetyl-1-alkylglycerophosphocholine esterase|LDL-PLA(2)|LDL-associated phospholipase A2|PAF 2-acylhydrolase|PAF acetylhydrolase|gVIIA-PLA2|group-VIIA phospholipase A2|lipoprotein-associated phospholipase A2|phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) | |
7942 | 9606 | 20220707 | TFEB ALPHATFEB|BHLHE35|TCFEB | TFEB transcription factor EB | MIM:600744|HGNC:HGNC:11753|Ensembl:ENSG00000112561|AllianceGenome:HGNC:11753 | 6 6p21.1 | transcription factor EB | protein-coding O | transcription factor EB|T-cell transcription factor EB|class E basic helix-loop-helix protein 35 | |
7945 | 9606 | 20170408 | PUJO | MIM:143400 | pelviureteric junction obstruction | unknown | ||||
7948 | 9606 | 20191002 | PBCRA1 CRAPB|PBCRA | MIM:600790 | 6 6q | progressive bifocal chorioretinal atrophy 1 | unknown | |||
7952 | 9606 | 20200625 | TNDM DMTN|TNDM1 | 6 | diabetes mellitus, transient neonatal | unknown | ||||
7954 | 9606 | 20220417 | HBFQTL2 FCP|HPFH | MIM:142470 | 6 6q22.3-q23.1 | hereditary persistence of fetal hemoglobin, heterocellular | unknown | |||
7955 | 9606 | 20220513 | RNF217-AS1 STL | RNF217-AS1 RNF217 antisense RNA 1 (head to head) | MIM:602532|HGNC:HGNC:50866|Ensembl:ENSG00000236548|AllianceGenome:HGNC:50866 | 6 6q22.31 | RNF217 antisense RNA 1 (head to head) | ncRNA O | six-twelve leukemia | |
7956 | 9606 | 20190816 | NTT | MIM:602154 | 6 6q23-q24 | Noncoding transcript in T cells | ncRNA | |||
7957 | 9606 | 20220513 | EPM2A EPM2|MELF | EPM2A EPM2A glucan phosphatase, laforin | MIM:607566|HGNC:HGNC:3413|Ensembl:ENSG00000112425|AllianceGenome:HGNC:3413 | 6 6q24.3 | EPM2A glucan phosphatase, laforin | protein-coding O | laforin|EPM2A, laforin glucan phosphatase|LAFPTPase|epilepsy, progressive myoclonus type 2, Lafora disease (laforin)|epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)|glucan phosphatase|glycogen phosphatase|lafora PTPase | |
7959 | 9606 | 20190815 | FEA | MIM:137010 | F9 embryonic antigen | other | ||||
7960 | 9606 | 20190815 | MRBC | MIM:158050 | Monkey RBC receptor | other | ||||
7962 | 9606 | 20190816 | PBCA | MIM:600089 | 6 6p21.3 | Pancreatic beta cell, agenesis of | unknown | |||
7963 | 9606 | 20190815 | TS546 | MIM:187330 | Temperature sensitivity complementation, cell cycle specific | unknown | ||||
7965 | 9606 | 20220703 | AIMP2 HLD17|JTV-1|JTV1|P38 | AIMP2 aminoacyl tRNA synthetase complex interacting multifunctional protein 2 | MIM:600859|HGNC:HGNC:20609|Ensembl:ENSG00000106305|AllianceGenome:HGNC:20609 | 7 7p22.1 | aminoacyl tRNA synthetase complex interacting multifunctional protein 2 | protein-coding O | aminoacyl tRNA synthase complex-interacting multifunctional protein 2|ARS-interacting multi-functional protein 2|multisynthase complex auxiliary component p38|multisynthetase complex auxiliary component p38|protein JTV-1 | |
7971 | 9606 | 20170402 | GHS | MIM:141400 | Goldenhar syndrome | unknown | ||||
7974 | 9606 | 20190816 | HRX | MIM:145290 | 7 7q | Hyperreflexia | unknown | |||
7975 | 9606 | 20220522 | MAFK NFE2U|P18 | MAFK MAF bZIP transcription factor K | MIM:600197|HGNC:HGNC:6782|Ensembl:ENSG00000198517|AllianceGenome:HGNC:6782 | 7 7p22.3 | MAF bZIP transcription factor K | protein-coding O | transcription factor MafK|basic-leucine zipper transcription factor MafK|erythroid transcription factor NF-E2 p18 subunit|nuclear factor erythroid-2, ubiquitous (p18)|v-maf avian musculoaponeurotic fibrosarcoma oncogene family, protein K|v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog K|v-maf musculoaponeurotic fibrosarcoma oncogene homolog K | |
7976 | 9606 | 20220522 | FZD3 Fz-3 | FZD3 frizzled class receptor 3 | MIM:606143|HGNC:HGNC:4041|Ensembl:ENSG00000104290|AllianceGenome:HGNC:4041 | 8 8p21.1 | frizzled class receptor 3 | protein-coding O | frizzled-3|frizzled 3, seven transmembrane spanning receptor|frizzled family receptor 3|frizzled homolog 3 | |
7977 | 9606 | 20170408 | MHS3 | MIM:154276 | 7 7q21-q22 | Malignant hyperthermia susceptibility 3 | unknown | |||
7978 | 9606 | 20220623 | MTERF1 MTERF | MTERF1 mitochondrial transcription termination factor 1 | MIM:602318|HGNC:HGNC:21463|Ensembl:ENSG00000127989|AllianceGenome:HGNC:21463 | 7 7q21.2 | mitochondrial transcription termination factor 1 | protein-coding O | transcription termination factor 1, mitochondrial|transcription termination factor, mitochondrial | |
7979 | 9606 | 20220513 | SEM1 C7orf76|DSS1|ECD|PSMD15|SHFD1|SHFM1|SHSF1|Shfdg1 | SEM1 SEM1 26S proteasome subunit | MIM:601285|HGNC:HGNC:10845|Ensembl:ENSG00000127922|AllianceGenome:HGNC:10845 | 7 7q21.3 | SEM1 26S proteasome subunit | protein-coding O | 26S proteasome complex subunit SEM1|26S proteasome complex subunit DSS1|SEM1 26S proteasome complex subunit|deleted in split hand/split foot protein 1|deleted in split-hand/split-foot 1|split hand/foot deleted protein 1|split hand/foot malformation (ectrodactyly) type 1|split hand/foot malformation type 1 protein | |
7980 | 9606 | 20220703 | TFPI2 PP5|REF1|TFPI-2 | TFPI2 tissue factor pathway inhibitor 2 | MIM:600033|HGNC:HGNC:11761|Ensembl:ENSG00000105825|AllianceGenome:HGNC:11761 | 7 7q21.3 | tissue factor pathway inhibitor 2 | protein-coding O | tissue factor pathway inhibitor 2|placental protein 5|retinal pigment epithelium cell factor 1 | |
7982 | 9606 | 20220605 | ST7 ETS7q|FAM4A|FAM4A1|HELG|RAY1|SEN4|TSG7 | ST7 suppression of tumorigenicity 7 | MIM:600833|HGNC:HGNC:11351|Ensembl:ENSG00000004866|AllianceGenome:HGNC:11351 | 7 7q31.2 | suppression of tumorigenicity 7 | protein-coding O | suppressor of tumorigenicity 7 protein|family with sequence similarity 4, subfamily A, member 1|suppression of tumorigenicity 7 (breast) | |
7984 | 9606 | 20220522 | ARHGEF5 GEF5|P60|TIM|TIM1 | ARHGEF5 Rho guanine nucleotide exchange factor 5 | MIM:600888|HGNC:HGNC:13209|Ensembl:ENSG00000050327|AllianceGenome:HGNC:13209 | 7 7q35 | Rho guanine nucleotide exchange factor 5 | protein-coding O | rho guanine nucleotide exchange factor 5|Rho guanine nucleotide exchange factor (GEF) 5|ephexin-3|ephexin3|guanine nucleotide regulatory protein TIM|oncogene TIM|p60 TIM|transforming immortalized mammary oncogene | |
7986 | 9606 | 20191002 | GPDS1 PDS1 | MIM:600510 | 7 7q35-q36 | glaucoma-related pigment dispersion syndrome 1 | unknown | Pigment dispersion syndrome-1 | ||
7988 | 9606 | 20220623 | ZNF212 C2H2-150|ZNF182|ZNFC150 | ZNF212 zinc finger protein 212 | MIM:602386|HGNC:HGNC:13004|Ensembl:ENSG00000170260|AllianceGenome:HGNC:13004 | 7 7q36.1 | zinc finger protein 212 | protein-coding O | zinc finger protein 212|Zinc finger protein C2H2-150 | |
7991 | 9606 | 20220707 | TUSC3 D8S1992|M33|MRT22|MRT7|MagT2|N33|OST3A|SLC58A2 | TUSC3 tumor suppressor candidate 3 | MIM:601385|HGNC:HGNC:30242|Ensembl:ENSG00000104723|AllianceGenome:HGNC:30242 | 8 8p22 | tumor suppressor candidate 3 | protein-coding O | tumor suppressor candidate 3|dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit TUSC3|magnesium uptake/transporter TUSC3|oligosaccharyl transferase subunit TUSC3|oligosaccharyltransferase 3 homolog A|putative prostate cancer tumor suppressor | |
7993 | 9606 | 20220703 | UBXN8 D8S2298E|REP8|UBXD6 | UBXN8 UBX domain protein 8 | MIM:602155|HGNC:HGNC:30307|Ensembl:ENSG00000104691|AllianceGenome:HGNC:30307 | 8 8p12 | UBX domain protein 8 | protein-coding O | UBX domain-containing protein 8|Reproduction/chromosome 8|UBX domain-containing protein 6|rep-8 protein|reproduction 8 protein | |
7994 | 9606 | 20220707 | KAT6A ARTHS|MOZ|MRD32|MYST-3|MYST3|RUNXBP2|ZC2HC6A|ZNF220 | KAT6A lysine acetyltransferase 6A | MIM:601408|HGNC:HGNC:13013|Ensembl:ENSG00000083168|AllianceGenome:HGNC:13013 | 8 8p11.21 | lysine acetyltransferase 6A | protein-coding O | histone acetyltransferase KAT6A|K(lysine) acetyltransferase 6A|MOZ, YBF2/SAS3, SAS2 and TIP60 protein 3|MYST histone acetyltransferase (monocytic leukemia) 3|histone acetyltransferase MYST3|monocytic leukemia zinc finger protein|runt-related transcription factor binding protein 2|zinc finger protein 220 | |
8000 | 9606 | 20220513 | PSCA PRO232|lncPSCA | PSCA prostate stem cell antigen | MIM:602470|HGNC:HGNC:9500|Ensembl:ENSG00000167653|AllianceGenome:HGNC:9500 | 8 8q24.3 | prostate stem cell antigen | protein-coding O | ||
8001 | 9606 | 20220522 | GLRA3 | GLRA3 glycine receptor alpha 3 | MIM:600421|HGNC:HGNC:4328|Ensembl:ENSG00000145451|AllianceGenome:HGNC:4328 | 4 4q34.1 | glycine receptor alpha 3 | protein-coding O | glycine receptor subunit alpha-3|glycine receptor, alpha-3 polypeptide|ligand gated ion channel | |
8009 | 9606 | 20190816 | LALL | MIM:247640 | 9 9p22-p21 | Lymphomatous acute lymphoblastic leukemia | unknown | |||
8011 | 9606 | 20191002 | MROS MRS | MIM:155900 | 9 9p11 | Melkersson-Rosenthal syndrome | unknown | |||
8013 | 9606 | 20220522 | NR4A3 CHN|CSMF|MINOR|NOR1 | NR4A3 nuclear receptor subfamily 4 group A member 3 | MIM:600542|HGNC:HGNC:7982|Ensembl:ENSG00000119508|AllianceGenome:HGNC:7982 | 9 9q31.1 | nuclear receptor subfamily 4 group A member 3 | protein-coding O | nuclear receptor subfamily 4 group A member 3|chondrosarcoma, extraskeletal myxoid, fused to EWS|mitogen-induced nuclear orphan receptor|neuron-derived orphan receptor 1|nuclear hormone receptor NOR-1|translocated in extraskeletal chondrosarcoma | |
8019 | 9606 | 20220623 | BRD3 ORFX|RING3L | BRD3 bromodomain containing 3 | MIM:601541|HGNC:HGNC:1104|Ensembl:ENSG00000169925|AllianceGenome:HGNC:1104 | 9 9q34.2 | bromodomain containing 3 | protein-coding O | bromodomain-containing protein 3|RING3-like protein | |
8021 | 9606 | 20220703 | NUP214 CAIN|CAN|IIAE9 | NUP214 nucleoporin 214 | MIM:114350|HGNC:HGNC:8064|Ensembl:ENSG00000126883|AllianceGenome:HGNC:8064 | 9 9q34.13 | nucleoporin 214 | protein-coding O | nuclear pore complex protein Nup214|CAN protein, putative oncogene|nucleoporin 214kDa | |
8022 | 9606 | 20220623 | LHX3 CPHD3|LIM3|M2-LHX3 | LHX3 LIM homeobox 3 | MIM:600577|HGNC:HGNC:6595|Ensembl:ENSG00000107187|AllianceGenome:HGNC:6595 | 9 9q34.3 | LIM homeobox 3 | protein-coding O | LIM/homeobox protein Lhx3|LIM homeobox protein 3|LIM/homeodomain protein LHX3 | |
8023 | 9606 | 20190815 | H142T | MIM:187290 | Temperature sensitivity complementation, H142 | unknown | ||||
8024 | 9606 | 20170408 | RDPA | MIM:600964 | refsum disease, adult, with increased pipecolicacidemia | unknown | ||||
8026 | 9606 | 20190816 | DGS2 DGCR2 | MIM:601362 | 10 10p14-p13 | DiGeorge syndrome/velocardiofacial syndrome complex 2 | unknown | |||
8027 | 9606 | 20220703 | STAM STAM-1|STAM1 | STAM signal transducing adaptor molecule | MIM:601899|HGNC:HGNC:11357|Ensembl:ENSG00000136738|AllianceGenome:HGNC:11357 | 10 10p12.33 | signal transducing adaptor molecule | protein-coding O | signal transducing adapter molecule 1|HSE1 homolog|signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 | |
8028 | 9606 | 20220513 | MLLT10 AF10 | MLLT10 MLLT10 histone lysine methyltransferase DOT1L cofactor | MIM:602409|HGNC:HGNC:16063|Ensembl:ENSG00000078403|AllianceGenome:HGNC:16063 | 10 10p12.31 | MLLT10 histone lysine methyltransferase DOT1L cofactor | protein-coding O | protein AF-10|ALL1-fused gene from chromosome 10 protein|myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 10|myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10|type I AF10 protein|type III AF10 protein|type IV AF10 protein | |
8029 | 9606 | 20220707 | CUBN IFCR|IGS|IGS1|MGA1|gp280 | CUBN cubilin | MIM:602997|HGNC:HGNC:2548|Ensembl:ENSG00000107611|AllianceGenome:HGNC:2548 | 10 10p13 | cubilin | protein-coding O | cubilin|460 kDa receptor|cubilin (intrinsic factor-cobalamin receptor)|intestinal intrinsic factor receptor|intrinsic factor-vitamin B12 receptor | |
8030 | 9606 | 20220703 | CCDC6 D10S170|H4|PTC|TPC|TST1 | CCDC6 coiled-coil domain containing 6 | MIM:601985|HGNC:HGNC:18782|Ensembl:ENSG00000108091|AllianceGenome:HGNC:18782 | 10 10q21.2 | coiled-coil domain containing 6 | protein-coding O | coiled-coil domain-containing protein 6|papillary thyroid carcinoma-encoded protein | |
8031 | 9606 | 20220623 | NCOA4 ARA70|ELE1|PTC3|RFG | NCOA4 nuclear receptor coactivator 4 | MIM:601984|HGNC:HGNC:7671|Ensembl:ENSG00000266412|AllianceGenome:HGNC:7671 | 10 10q11.22 | nuclear receptor coactivator 4 | protein-coding O | nuclear receptor coactivator 4|70 kDa AR-activator|70 kDa androgen receptor coactivator|NCoA-4|RET-activating gene ELE1|androgen receptor-associated protein of 70 kDa|ret fused |
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