基因ID | taxid | GeneDate LocusTag | Symbol Synonyms | Symbolfna Fullnamefna | dbXrefs | chromosome maplocation | description | genetype fnastatus | Otherdesignations | Featuretype |
100188771 | 9606 | 20190816 | AGA2 | MIM:300710 | X Xq11-q12 | Alopecia, androgenetic, 2 | unknown | |||
100188772 | 9606 | 20190816 | IHPS4 | MIM:300711 | X Xq23 | Pyloric stenosis, infantile hypertrophic, 4 | unknown | |||
100188773 | 9606 | 20190816 | CFSS | MIM:300712 | X Xq26-q27 | craniofacioskeletal syndrome | unknown | |||
100188774 | 9606 | 20190816 | DFCTRPS | MIM:300719 | X | Deafness, cataract, retinitis pigmentosa, and sperm abnormalities | unknown | |||
100188775 | 9606 | 20210116 | LOAS | MIM:308905 | Leber optic atrophy, susceptibility to | unknown | ||||
100188776 | 9606 | 20190816 | HEY | MIM:425500 | Y Yq | hairy ears, Y-linked | unknown | |||
100188782 | 9606 | 20190816 | NIDDM4 | MIM:608036 | 5 5q34-q35.2 | Diabetes mellitus, noninsulin-dependent | unknown | |||
100188784 | 9606 | 20190816 | AFA1 MPB | MIM:109200 | 3 3q26 | Alopecia, androgenetic | unknown | |||
100188785 | 9606 | 20170408 | ITC1 | 8 | hypertrichosis universalis congenita, Ambras type | unknown | ||||
100188787 | 9606 | 20200619 | WM1 | MIM:153600 | Macroglobulinemia, Waldenstrom, susceptibility to, 1 | unknown | ||||
100188788 | 9606 | 20190816 | DEL3Q29 MICRODEL3Q29 | MIM:609425 | 3 3q29 | Chromosome 3q29 microdeletion syndrome | unknown | |||
100188789 | 9606 | 20190816 | HPC6 | MIM:609558 | 22 22q12.3 | Prostate cancer, susceptibility to | unknown | |||
100188790 | 9606 | 20190816 | MGR8 | MIM:609570 | 5 5q21 | Migraine, susceptibility to, 8 | unknown | |||
100188791 | 9606 | 20190816 | CLLS1 | MIM:609630 | 11 11p11 | Leukemia, chronic lymphocytic, susceptibility to, 1 | unknown | |||
100188792 | 9606 | 20190816 | MAFD3 BPEO | MIM:609633 | 21 21q22.13 | Major affective disorder 3, early onset | unknown | |||
100188793 | 9606 | 20190816 | BSZQTL | MIM:609656 | 17 17q23 | Bone size QTL | unknown | |||
100188794 | 9606 | 20190816 | BSZQTL2 | MIM:609657 | 5 5q | Bone size QTL | unknown | |||
100188795 | 9606 | 20190816 | AD11 | MIM:609790 | 9 9p22.1 | Alzheimer disease-11 | unknown | |||
100188796 | 9606 | 20170408 | GEFSP4 | MIM:609800 | 2 2p24 | Epilepsy, generalized, with febrile seizures plus, type 4 | unknown | |||
100188797 | 9606 | 20190816 | BMND6 | MIM:609876 | 21 21q22.13-qter | Bone mineral density QTL 6 | unknown | |||
100188798 | 9606 | 20190816 | SLEB5 | MIM:609903 | 13 13q32 | Systemic lupus erythematosus, susceptibility to, 5 | unknown | |||
100188800 | 9606 | 20190816 | ASPG4 | MIM:609954 | 3 3p24-p21 | Asperger syndrome, susceptibility to, 4 | unknown | |||
100188801 | 9606 | 20170408 | ASRT3 | MIM:609958 | 2 2p16 | Asthma-related traits, susceptibility to, 3 | unknown | |||
100188802 | 9606 | 20190816 | ODS1 | MIM:610064 | 17 | Opioid dependence, susceptibility to, 1 | unknown | |||
100188803 | 9606 | 20190816 | SLEB7 | MIM:610065 | 20 20p12 | Systemic lupus erythematosus, susceptibility to, 7 | unknown | |||
100188804 | 9606 | 20190816 | SLEB8 | MIM:610066 | 20 20q13 | Systemic lupus erythematosus, susceptibility to, 8 | unknown | |||
100188805 | 9606 | 20190816 | STBMS1 | MIM:185100 | 7 7p22.1 | Strabismus, susceptibility to, 1 | unknown | |||
100188806 | 9606 | 20190816 | HDLCQ4 | MIM:610239 | 4 4q32.3 | High density lipoprotein cholesterol level QTL 4 | unknown | |||
100188807 | 9606 | 20190816 | HYT5 | MIM:610261 | 20 20q11-q13 | Hypertension, essential, susceptibility to, 5 | unknown | |||
100188808 | 9606 | 20190816 | HYT6 | MIM:610262 | 5 5p13-q12 | Hypertension, essential, susceptibility to, 6 | unknown | |||
100188809 | 9606 | 20190816 | HPC7 | MIM:610321 | 15 15q12 | Prostate cancer, hereditary, 7 | unknown | |||
100188810 | 9606 | 20170408 | ANIB5 | MIM:610402 | Aneurysm, intracranial berry, 5 | unknown | ||||
100188811 | 9606 | 20190816 | WM2 | MIM:610430 | 4 4q | Macroglobulinemia, Waldenstrom, susceptibility to, 2 | unknown | |||
100188812 | 9606 | 20190816 | RLS3 | MIM:610438 | 9 9p24-p22 | Restless legs syndrome 3 | unknown | |||
100188813 | 9606 | 20190816 | RLS4 | MIM:610439 | 2 2q33 | Restless legs syndrome 4 | unknown | |||
100188814 | 9606 | 20190816 | DEL16P13.3 RSTSS | MIM:610543 | 16 16p13.3 | Chromosome 16p13.3 deletion syndrome | unknown | |||
100188815 | 9606 | 20190816 | BSZQTL3 | MIM:610649 | 8 8q24 | Bone size quantitative trait locus 3 | unknown | |||
100188816 | 9606 | 20190816 | AUTS7 | MIM:610676 | 17 17q21 | Autism, susceptibility to, 7 | unknown | |||
100188817 | 9606 | 20170408 | CLQTL2 | MIM:610760 | 2 2p24-p22 | Cholesterol level QTL 2 | unknown | |||
100188818 | 9606 | 20190816 | HDLCQ5 | MIM:610761 | 3 3q24-q26 | High density lipoprotein cholesterol level QTL 5 | unknown | |||
100188819 | 9606 | 20170402 | HDLCQ6 | MIM:610762 | High density lipoprotein cholesterol level QTL 6 | unknown | ||||
100188820 | 9606 | 20170408 | AUTS11 | MIM:610836 | 1 1q24.2 | Autism, susceptibility to, 11 | unknown | |||
100188821 | 9606 | 20190816 | OS4 GOA1 | MIM:610839 | 2 2q33.3 | Osteoarthritis, generalized, without dysplasia, susceptibility to | unknown | |||
100188822 | 9606 | 20190816 | MENAQ1 | MIM:610873 | 22 22q13 | Menarche, age at, QTL | unknown | |||
100188823 | 9606 | 20170408 | ASRT4 | MIM:610906 | 1 1p31 | Asthma-related traits, susceptibility to, 4 | unknown | |||
100188825 | 9606 | 20190816 | HYT7 | MIM:610948 | 3 3p14.1-q12.3 | Hypertension, essential, susceptibility to, 7 | unknown | |||
100188826 | 9606 | 20190816 | HPC9 | MIM:610997 | 17 17q21-q22 | Prostate cancer, hereditary, 9 | unknown | |||
100188827 | 9606 | 20190816 | SQTL1 | MIM:611003 | 10 10q22 | Smoking as a quantitative trait locus 1 | unknown | |||
100188828 | 9606 | 20190816 | SQTL2 | MIM:611004 | 22 22q12 | Smoking as a quantitative trait locus 2 | unknown | |||
100188829 | 9606 | 20190816 | MTBS2 | MIM:611046 | 8 8q12-q13 | Mycobacterium tuberculosis, susceptibility to, 2 | unknown |
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