Gene Map - Chromosome: X - OMIM

OMIM Gene/Loci: 603 - 612 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:119,646,738
Xq24 		MIR766 Micro RNA 766 301062 located in intron of SEPT6
X:119,786,504
Xq24 		RPL39 Ribosomal protein L39 300899
X:119,805,311
Xq24 		UPF3B, RENT3B, MRXS14 UPF3B regulator of nonsense-mediated mRNA decay 300298 Intellectual developmental disorder, X-linked syndromic 14 300676 XLR 3
X:119,870,475
Xq24 		RNF113A, ZNF183, TTD5 RING finger protein 113A 300951 Trichothiodystrophy 5, nonphotosensitive 300953 XL 3
X:119,871,832
Xq24 		NDUFA1, MWFE, MC1DN12 NADH-ubiquinone oxidoreductase subunit A1 300078 Mitochondrial complex I deficiency, nuclear type 12 301020 XLR 3
X:119,895,893
Xq24 		AKAP14, AKAP28 A-kinase anchor protein 14 300462
X:119,920,672
Xq24 		NKAP, MRXSHD NFKB-activating protein 300766 Intellectual developmental disorder, X-linked syndromic, Hackman-Di Donato type 301039 XLR 3
X:120,010,717
Xq24 		RHOXF1P1 RHOX homeobox family member 1, pseudogene 1 300973
X:120,109,051
Xq24 		RHOXF1, OTEX, PEPP1 RHOX homeobox family, member 1 300446
X:120,158,613
Xq24 		RHOXF2, PEPP2 RHOX homeobox family, member 2 300447

pter  |  « Towards pter  |  Towards qter »  |  qter
OMIM Gene/Loci: 603 - 612 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:119,646,738-119,646,848
Xq24 		MIR766 Micro RNA 766 301062 located in intron of SEPT6
X:119,786,504-119,791,630
Xq24 		RPL39 Ribosomal protein L39 300899
X:119,805,311-119,852,963
Xq24 		UPF3B, RENT3B, MRXS14 UPF3B regulator of nonsense-mediated mRNA decay 300298 Intellectual developmental disorder, X-linked syndromic 14 300676 X-linked recessive 3
X:119,870,475-119,871,733
Xq24 		RNF113A, ZNF183, TTD5 RING finger protein 113A 300951 Trichothiodystrophy 5, nonphotosensitive 300953 X-linked 3
X:119,871,832-119,876,662
Xq24 		NDUFA1, MWFE, MC1DN12 NADH-ubiquinone oxidoreductase subunit A1 300078 Mitochondrial complex I deficiency, nuclear type 12 301020 X-linked recessive 3
X:119,895,893-119,920,716
Xq24 		AKAP14, AKAP28 A-kinase anchor protein 14 300462
X:119,920,672-119,943,751
Xq24 		NKAP, MRXSHD NFKB-activating protein 300766 Intellectual developmental disorder, X-linked syndromic, Hackman-Di Donato type 301039 X-linked recessive 3
X:120,010,717-120,015,551
Xq24 		RHOXF1P1 RHOX homeobox family member 1, pseudogene 1 300973
X:120,109,051-120,120,438
Xq24 		RHOXF1, OTEX, PEPP1 RHOX homeobox family, member 1 300446
X:120,158,613-120,165,630
Xq24 		RHOXF2, PEPP2 RHOX homeobox family, member 2 300447


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 3, 2024
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