基因库

基因ID	taxid	GeneDate LocusTag	Symbol Synonyms	Symbolfna Fullnamefna	dbXrefs	chromosome maplocation	description	genetype fnastatus	Otherdesignations	Featuretype
100188830	9606	20190816	AD12		MIM:611073	8 8p12-q22	Alzheimer disease 12	unknown
100188832	9606	20190816	AUTS1		MIM:209850	7 7q22	Autism, susceptibility to, 1	unknown
100188834	9606	20200822	HPC10		MIM:611100	8 8q24	Prostate cancer, hereditary, 10	unknown
100188835	9606	20190816	CINN		MIM:611109	4 4q32.3	Cinnamon odor, pleasantness of	unknown
100188836	9606	20190816	CHDS8		MIM:611139	9 9p21	Coronary heart disease, susceptibility to, 8	unknown
100188837	9606	20170408	AD13		MIM:611152	1 1q21	Alzheimer disease-13	unknown
100188838	9606	20190816	AD15		MIM:611155	3 3q22-q24	Alzheimer disease-15	unknown
100188839	9606	20190816	RLS5		MIM:611242	20 20p13	Restless legs syndrome, susceptibility to, 5	unknown
100188840	9606	20190816	ASRT6		MIM:611403	17 17q21	Asthma-related traits, susceptibility to, 6	unknown
100188841	9606	20200822	CRCS2		MIM:611469	8 8q24	Colorectal cancer, susceptibility to, 2	unknown
100188842	9606	20211220	ATFB5		MIM:611494	4 4q25	Atrial fibrillation, familial, 5	unknown
100188843	9606	20190816	MAFD5		MIM:611535	2 2q22-q24	Major affective disorder 5	unknown
100188844	9606	20190816	MAFD6 BPAD		MIM:611536	6 6q23-q24	Major affective disorder 6	unknown
100188845	9606	20170408	CODA		MIM:611543		Cavitary optic disc anomalies	unknown
100188846	9606	20190816	CELIAC6 AIS5		MIM:611598	4 4q27	Celiac disease, susceptibility to, 6	unknown
100188847	9606	20220513	MIR1225 MIRN1225	MIR1225 microRNA 1225	MIM:611621\|HGNC:HGNC:33931\|Ensembl:ENSG00000221656\|miRBase:MI0006311\|AllianceGenome:HGNC:33931	16 16p13.3	microRNA 1225	ncRNA O	hsa-mir-1225
100188848	9606	20190816	FMTLE ETL3		MIM:611630	4 4q13.2-q21.3	Epilepsy, familial mesial temporal lobe	unknown
100188849	9606	20190816	FEB9		MIM:611634	3 3p24.2-p23	Febrile convulsions, familial, 9	unknown
100188850	9606	20190816	HSCR9		MIM:611644	4 4q31.3-q32.3	Hirschsprung disease, susceptibility to, 9	unknown
100188851	9606	20190816	MGR12		MIM:611706	10 10q22-q23	Migraine, with or without aura, susceptibility to, 12	unknown
100188852	9606	20170408	SHEP8		MIM:611724		Skin/hair/eye pigmentation 8, freckling	unknown
100188853	9606	20190816	BMND7		MIM:611738	20 20p12.3	bone mineral density quantiative trait locus 7	unknown
100188854	9606	20190816	BMND8		MIM:611739	11 11p12	bone mineral density quantiative trait locus 8	unknown
100188855	9606	20190816	MNDEC		MIM:611863	4 4p16-p15	Microtia with nasolacrimal duct imperforation and eye coloboma	unknown
100188856	9606	20210607	DEL22Q11.2 C22DDELS\|C22DELq11.2		MIM:611867	22 22q11.2	Chromosome 22q11.2 deletion syndrome, distal	unknown
100188857	9606	20190816	AAA3		MIM:611891	9 9p21	Aneurysm, familial abdominal 3	unknown
100188858	9606	20190816	ANIB6		MIM:611892	9 9p21	Aneurysm, intracranial berry, 6	unknown
100188859	9606	20190816	EA7		MIM:611907	19 19q13	Episodic ataxia, type 7	unknown
100188860	9606	20190816	CPROTQ		MIM:611920	10 10q23-q24	C-reactive protein QTL	unknown
100188861	9606	20190816	EIG5		MIM:611934	10 10p11.22	Epilepsy, idiopathic generalized, susceptibility to, 5	unknown
100188862	9606	20190816	DUP3Q29 MICRODUP3Q29		MIM:611936	3 3q29	chromosome 3q29 microduplication syndrome	unknown
100188863	9606	20190816	ENDO1		MIM:131200	10 10q26	Endometriosis, susceptibility to, 1	unknown
100188864	9606	20190816	IH HHP		MIM:235000	11 11p15	Hemihypertrophy	unknown
100188865	9606	20190816	LMPH1B		MIM:611944	6 6q16.2-q22.1	Lymphedema, hereditary, IB	unknown
100188867	9606	20200822	HPC14		MIM:611958	11 11q13	Prostate cancer, hereditary, 14	unknown
100188868	9606	20190816	HPC15		MIM:611959	19 19q13.4	Prostate cancer, hereditary, 15	unknown
100188869	9606	20220102	DEL15Q13.3 EIG7\|MICRODEL15Q13.3\|SCZD13		MIM:612001	15 15q13.3	Chromosome 15q13.3 microdeletion syndrome	unknown
100188870	9606	20190816	CELIAC8		MIM:612006	2 2q11-q12	Celiac disease, susceptibility to, 8	unknown
100188871	9606	20190816	CELIAC9		MIM:612007	3 3p21	Celiac disease, susceptibility to, 9	unknown
100188872	9606	20190816	CELIAC10		MIM:612008	3 3q25-q26	Celiac disease, susceptibility to, 10	unknown
100188873	9606	20190816	CELIAC11		MIM:612009	3 3q28	Celiac disease, susceptibility to, 11	unknown
100188874	9606	20190816	CELIAC12		MIM:612010	6 6q25.3	Celiac disease, susceptibility to, 12	unknown
100188875	9606	20190816	CELIAC13		MIM:612011	12 12q24	Celiac disease, susceptibility to, 13	unknown
100188876	9606	20190816	IHPS3		MIM:612017	11 11q14-q22	Pyloric stenosis, infantile hypertrophic, 3	unknown
100188877	9606	20190816	CHDS9		MIM:612030	8 8p22	Coronary heart disease, suscpetibility to, 9	unknown
100188880	9606	20190816	HPRHP		MIM:612089	13 13q13.1	Hypophosphatemic rickets and hyperparathyroidism	unknown
100188881	9606	20190816	MFT2 TEM		MIM:612099	9 9p21	Trichoepithelioma, multiple familial, 2	unknown
100188882	9606	20190816	BMND9		MIM:612110	13 13q14	Bone mineral density QTL 9	unknown
100188883	9606	20190816	BMND10		MIM:612113	8 8q24	Bone mineral density QTL 10	unknown
100188884	9606	20190816	BMND11		MIM:612114	6 6q25	Bone mineral density QTL 11	unknown

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