Gene Map - Chromosome: 17 - OMIM

OMIM Gene/Loci: 486 - 495 of 1,069 on Chromosome 17 (All Entries)
pter  |  « Towards pter  |  Towards qter »  |  qter
Phenotype Only Entries All Entries

Location
(from NCBI, GRCh38) 		Gene/Locus Gene/Locus name Gene/Locus
MIM number 		Phenotype Phenotype
MIM number
Inheritance Pheno
map
key 		Comments Mouse
symbol
(from MGI)
17:39,728,510
17q12 		MIEN1, C17orf37, RDX12 Migration and invasion enhancer 1 611802 Mien1
17:39,737,938
17q12 		GRB7 Growth factor receptor-bound protein 7 601522 Grb7
17:39,757,715
17q12-q21.1 		IKZF3, ZNFN1A3, AIOLOS, IMD84 Ikaros family zinc finger 3 606221 ?Immunodeficiency 84 619437 AD 3 mutation identified in 1 IMD84 family Ikzf3
17:39,800,001
17q21 		ASRT6 Asthma-related traits, susceptibility to, 6 611403 {Asthma-related traits, susceptibility to, 6} 611403 2 strongly associated with rs7216389
17:39,800,001
17q21 		AUTS7 Autism, susceptibility to, 7 610676 {Autism susceptibility 7} 610676 2 max lod at D17S2180
17:39,800,001
17q21-q22 		MYP5 Myopia 5 608474 Myopia 5 608474 AD 2 between D17S787 and D17S1811
17:39,800,001
17q21-q22 		PTLAH, FPAH Patella aplasia or hypoplasia 168860 Patella aplasia or hypoplasia 168860 AD 2
17:39,868,202
17q21.1 		ZPBP2, ZPBPL Zona pellucida-binding protein 2 608499 Zpbp2
17:39,904,595
17q21.1 		GSDMB, GSDML Gasdermin B 611221
17:39,921,041
17q21.1 		ORMDL3 ORM1-like protein 3 610075 Ormdl3

pter  |  « Towards pter  |  Towards qter »  |  qter
OMIM Gene/Loci: 486 - 495 of 1,069 on Chromosome 17 (All Entries)

Location
(from NCBI, GRCh38) 		Gene/Locus Gene/Locus name Gene/Locus
MIM
number 		Phenotype Phenotype
MIM
number 		Inheritance Pheno
map
key 		Comments Mouse
symbol
(from MGI)
17:39,728,510-39,730,532
17q12 		MIEN1, C17orf37, RDX12 Migration and invasion enhancer 1 611802 Mien1
17:39,737,938-39,747,285
17q12 		GRB7 Growth factor receptor-bound protein 7 601522 Grb7
17:39,757,715-39,864,312
17q12-q21.1 		IKZF3, ZNFN1A3, AIOLOS, IMD84 Ikaros family zinc finger 3 606221 ?Immunodeficiency 84 619437 Autosomal dominant 3 mutation identified in 1 IMD84 family Ikzf3
17:39,800,001-52,100,000
17q21 		ASRT6 Asthma-related traits, susceptibility to, 6 611403 {Asthma-related traits, susceptibility to, 6} 611403 2 strongly associated with rs7216389
17:39,800,001-52,100,000
17q21 		AUTS7 Autism, susceptibility to, 7 610676 {Autism susceptibility 7} 610676 2 max lod at D17S2180
17:39,800,001-59,500,000
17q21-q22 		MYP5 Myopia 5 608474 Myopia 5 608474 Autosomal dominant 2 between D17S787 and D17S1811
17:39,800,001-59,500,000
17q21-q22 		PTLAH, FPAH Patella aplasia or hypoplasia 168860 Patella aplasia or hypoplasia 168860 Autosomal dominant 2
17:39,868,202-39,877,896
17q21.1 		ZPBP2, ZPBPL Zona pellucida-binding protein 2 608499 Zpbp2
17:39,904,595-39,918,635
17q21.1 		GSDMB, GSDML Gasdermin B 611221
17:39,921,041-39,927,601
17q21.1 		ORMDL3 ORM1-like protein 3 610075 Ormdl3


NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.
Printed: July 19, 2024
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