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OMIM Gene/Loci: 908 - 915 of 915 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:155,997,696 Xq28	IL9R	Interleukin-9 receptor	300007					in PAR2 pseudoautosomal region	Il9r
X:1 Chr.X	CCCSX	Cerebral-cerebellar-coloboma syndrome, X-linked	300864	Cerebral-cerebellar-coloboma syndrome, X-linked	300864	XLR	2
X:1 Chr.X	CVMRF	Cubitus valgus with impaired intellectual development and unusual facies	300471	Cubitus valgus with impaired intellectual development and unusual facies	300471	XLR	2
X:1 Chr.X	DFCTRPS	Deafness, cataract, retinitis pigmentosa, and sperm abnormalities	300719	Deafness, cataract, retinitis pigmentosa, and sperm abnormalities	300719	XLR	2
X:1 Chr.X	MCOPCB1	Microphthalmia, isolated, with coloboma 1	300345	Microphthalmia with coloboma 1	300345		2
X:1 Chr.X	MRXS32	Intellectual developmental disorder, X-linked, syndromic 32	300886	Intellectual developmental disorder, X-linked, syndromic 32	300886	XLR	2
X:1 Chr.X	OFD8	Orofaciodigital syndrome VIII	300484	Orofaciodigital syndrome VIII	300484	XLR	2
X:1 Chr.X	XLID95, MRX95	Intellectual developmental disorder, X-linked 95	300716	Intellectual developmental disorder, X-linked 95	300716	XLD	2

pter | « Towards pter | Towards qter » | qter

OMIM Gene/Loci: 908 - 915 of 915 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:155,997,696-156,013,020 Xq28	IL9R	Interleukin-9 receptor	300007					in PAR2 pseudoautosomal region	Il9r
X:1-156,040,895 Chr.X	CCCSX	Cerebral-cerebellar-coloboma syndrome, X-linked	300864	Cerebral-cerebellar-coloboma syndrome, X-linked	300864	X-linked recessive	2
X:1-156,040,895 Chr.X	CVMRF	Cubitus valgus with impaired intellectual development and unusual facies	300471	Cubitus valgus with impaired intellectual development and unusual facies	300471	X-linked recessive	2
X:1-156,040,895 Chr.X	DFCTRPS	Deafness, cataract, retinitis pigmentosa, and sperm abnormalities	300719	Deafness, cataract, retinitis pigmentosa, and sperm abnormalities	300719	X-linked recessive	2
X:1-156,040,895 Chr.X	MCOPCB1	Microphthalmia, isolated, with coloboma 1	300345	Microphthalmia with coloboma 1	300345		2
X:1-156,040,895 Chr.X	MRXS32	Intellectual developmental disorder, X-linked, syndromic 32	300886	Intellectual developmental disorder, X-linked, syndromic 32	300886	X-linked recessive	2
X:1-156,040,895 Chr.X	OFD8	Orofaciodigital syndrome VIII	300484	Orofaciodigital syndrome VIII	300484	X-linked recessive	2
X:1-156,040,895 Chr.X	XLID95, MRX95	Intellectual developmental disorder, X-linked 95	300716	Intellectual developmental disorder, X-linked 95	300716	X-linked dominant	2

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^® 1966-2025 Johns Hopkins University.
Printed: Aug. 6, 2025

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