Gene Map - Chromosome: X - OMIM

OMIM Gene/Loci: 657 - 666 of 884 on Chromosome X (All Entries)
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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)
X:129,803,288
Xq26.1 		ZDHHC9, DHHC9, MRXSR Zinc finger DHHC domain-containing protein 9 300646 Intellectual developmental disorder, X-linked syndromic, Raymond type 300799 XL 3 Zdhhc9
X:129,906,164
Xq26.1 		UTP14A UTP14 small subunit processome component 300508 Utp14a, Utp14b
X:129,980,313
Xq26.1 		BCORL1, SHUVER BCL6 corepressor-like 1 300688 Shukla-Vernon syndrome 301029 XLR 3 Bcorl1
X:130,063,955
Xq26.1 		ELF4, MEF, AIFBL2 E74-like ETS transcription factor 4 300775 Autoinflammatory syndrome, familial, X-linked, Behcet-like 2 301074 XLR 3 Elf4
X:130,129,362
Xq26.1 		AIFM1, PDCD8, AIF, COXPD6, COWCK, CMTX4, DFNX5, SEMDHL Apoptosis-inducing factor, mitochondrion-associated, 1 300169 Combined oxidative phosphorylation deficiency 6 300816 XLR 3 Aifm1
Cowchock syndrome 310490 XLR 3
Deafness, X-linked 5 300614 XLR 3
Spondyloepimetaphyseal dysplasia, X-linked, with hypomyelinating leukodystrophy 300232 XLR 3
X:130,110,623
Xq26.1 		RAB33A Ras-associated protein RAB33A 300333 Rab33a
X:130,339,919
Xq26.1 		SLC25A14, BMCP1 Solute carrier family 25 (mitochondrial carrier), member 14 300242 Slc25a14
X:130,379,449
Xq26.1 		GPR119, GPCR2 G protein-coupled receptor 119 300513 Gpr119
X:130,622,325
Xq26.1 		ENOX2 ECTO-NOX disulfide-thiol exchanger 2 300282 Enox2
X:131,058,346
Xq26.1 		ARHGAP36 Rho GTPase-activating protein 36 300937 Arhgap36

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OMIM Gene/Loci: 657 - 666 of 884 on Chromosome X (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)
X:129,803,288-129,843,886
Xq26.1 		ZDHHC9, DHHC9, MRXSR Zinc finger DHHC domain-containing protein 9 300646 Intellectual developmental disorder, X-linked syndromic, Raymond type 300799 X-linked 3 Zdhhc9
X:129,906,164-129,929,752
Xq26.1 		UTP14A UTP14 small subunit processome component 300508 Utp14a, Utp14b
X:129,980,313-130,058,071
Xq26.1 		BCORL1, SHUVER BCL6 corepressor-like 1 300688 Shukla-Vernon syndrome 301029 X-linked recessive 3 Bcorl1
X:130,063,955-130,111,927
Xq26.1 		ELF4, MEF, AIFBL2 E74-like ETS transcription factor 4 300775 Autoinflammatory syndrome, familial, X-linked, Behcet-like 2 301074 X-linked recessive 3 Elf4
X:130,129,362-130,165,841
Xq26.1 		AIFM1, PDCD8, AIF, COXPD6, COWCK, CMTX4, DFNX5, SEMDHL Apoptosis-inducing factor, mitochondrion-associated, 1 300169 Combined oxidative phosphorylation deficiency 6 300816 X-linked recessive 3 Aifm1
Cowchock syndrome 310490 X-linked recessive 3
Deafness, X-linked 5 300614 X-linked recessive 3
Spondyloepimetaphyseal dysplasia, X-linked, with hypomyelinating leukodystrophy 300232 X-linked recessive 3
X:130,110,623-130,184,870
Xq26.1 		RAB33A Ras-associated protein RAB33A 300333 Rab33a
X:130,339,919-130,373,357
Xq26.1 		SLC25A14, BMCP1 Solute carrier family 25 (mitochondrial carrier), member 14 300242 Slc25a14
X:130,379,449-130,385,674
Xq26.1 		GPR119, GPCR2 G protein-coupled receptor 119 300513 Gpr119
X:130,622,325-130,903,209
Xq26.1 		ENOX2 ECTO-NOX disulfide-thiol exchanger 2 300282 Enox2
X:131,058,346-131,089,885
Xq26.1 		ARHGAP36 Rho GTPase-activating protein 36 300937 Arhgap36


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 16, 2024
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