Gene Map - Chromosome: 22 - OMIM

OMIM Gene/Loci: 308 - 317 of 421 on Chromosome 22 (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)
22:40,824,535
22q13.2 		ST13, P48, HOP Suppression of tumorigenicity 13 606796 St13
22:40,857,148
22q13.2 		XPNPEP3, APP3, NPHPL1 X-prolyl aminopeptidase 3 613553 Nephronophthisis-like nephropathy 1 613159 AR 3 Xpnpep3
22:40,859,549
22q13.2 		DNAJB7, DJ5, HSC3 DNAJ/HSP40 homolog, subfamily B, member 7 611336 Dnajb7
22:40,951,378
22q13.2 		RBX1, ROC1 RING-box 1 603814 Rbx1, Rbx1-ps
22:41,092,592
22q13.2 		EP300, RSTS2, MKHK2 E1A-binding protein, 300kD 602700 Colorectal cancer, somatic 114500 3 Ep300
Menke-Hennekam syndrome 2 618333 AD 3
Rubinstein-Taybi syndrome 2 613684 AD 3
22:41,205,312
22q13.2 		L3MBTL2, L3MBT L3MBTL histone methyl-lysine-binding protein 2 611865 L3mbtl2
22:41,229,513
22q13.2 		CHADL Chondroadherin-like 616236 Chadl
22:41,244,779
22q13.2 		RANGAP1 GTPase-activating protein, RAN, 1 602362 Rangap1
22:41,301,525
22q13.2 		ZC3H7B, ROXAN1, KIAA1031 Zinc finger CCCH domain-containing protein 7B 618206 Zc3h7b
22:41,367,455
22q13.2 		TEF Thyrotroph embryonic factor 188595 Tef

pter  |  « Towards pter  |  Towards qter »  |  qter
OMIM Gene/Loci: 308 - 317 of 421 on Chromosome 22 (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)
22:40,824,535-40,856,639
22q13.2 		ST13, P48, HOP Suppression of tumorigenicity 13 606796 St13
22:40,857,148-40,932,815
22q13.2 		XPNPEP3, APP3, NPHPL1 X-prolyl aminopeptidase 3 613553 Nephronophthisis-like nephropathy 1 613159 Autosomal recessive 3 Xpnpep3
22:40,859,549-40,862,113
22q13.2 		DNAJB7, DJ5, HSC3 DNAJ/HSP40 homolog, subfamily B, member 7 611336 Dnajb7
22:40,951,378-40,973,309
22q13.2 		RBX1, ROC1 RING-box 1 603814 Rbx1, Rbx1-ps
22:41,092,592-41,180,077
22q13.2 		EP300, RSTS2, MKHK2 E1A-binding protein, 300kD 602700 Colorectal cancer, somatic 114500 3 Ep300
Menke-Hennekam syndrome 2 618333 Autosomal dominant 3
Rubinstein-Taybi syndrome 2 613684 Autosomal dominant 3
22:41,205,312-41,231,271
22q13.2 		L3MBTL2, L3MBT L3MBTL histone methyl-lysine-binding protein 2 611865 L3mbtl2
22:41,229,513-41,240,931
22q13.2 		CHADL Chondroadherin-like 616236 Chadl
22:41,244,779-41,302,369
22q13.2 		RANGAP1 GTPase-activating protein, RAN, 1 602362 Rangap1
22:41,301,525-41,360,147
22q13.2 		ZC3H7B, ROXAN1, KIAA1031 Zinc finger CCCH domain-containing protein 7B 618206 Zc3h7b
22:41,367,455-41,399,326
22q13.2 		TEF Thyrotroph embryonic factor 188595 Tef


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 25, 2024
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