Gene Map - Chromosome: 6

OMIM Gene/Loci: 763 - 772 of 1,044 on Chromosome 6 (All Entries)

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| 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)
6:109,440,724 6q21	SMPD2, NSMASE1	Sphingomyelin phosphodiesterase 2	603498						Smpd2
6:109,444,062 6q21	MICAL1, NICAL, MICAL	Microtubule-associated monooxygenase, calponin and LIM domains-containing 1	607129						Mical1
6:109,462,594 6q21	ZBTB24, PATZ2, ZNF450, KIAA0441, ICF2	Zinc finger- and BTB domain-containing protein 24	614064	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	AR	3		Zbtb24
6:109,492,855 6q21	AK9, SPGF89	Adenylate kinase 9	615358	Spermatogenic failure 89	620705	AR	3		Ak9
6:109,691,296 6q21	FIG4, KIAA0274, SAC3, ALS11, YVS, BTOP	FIG4 phosphoinositide 5-phosphatase	609390	?Polymicrogyria, bilateral temporooccipital	612691	AR	3	mutation identified in 1 BTOP family	Fig4
				Amyotrophic lateral sclerosis 11	612577	AD	3
				Charcot-Marie-Tooth disease, type 4J	611228	AR	3
				Yunis-Varon syndrome	216340	AR	3
6:109,978,311 6q21	GPR6	G protein-coupled receptor-6	600553						Gpr6
6:110,099,819 6q21	WASF1, WAVE, WAVE1, SCAR1, NEDALVS	WAS protein family member 1	605035	Neurodevelopmental disorder with absent language and variable seizures	618707	AD	3		Wasf1
6:110,180,427 6q21	CDC40, PRP17, PCH15	Cell division cycle 40	605585	?Pontocerebellar hypoplasia, type 15	619302	AR	3	mutation identified in 1 PCH15 patient	Cdc40
6:110,388,321 6q21	DDO, DASOX	D-aspartate oxidase	124450						Ddo
6:110,424,687 6q21	SLC22A16, FLIPT2, CT2	Solute carrier family 22 (organic cation transporter), member 16	608276						Slc22a16

pter | « Towards pter | Towards qter » | qter

OMIM Gene/Loci: 763 - 772 of 1,044 on Chromosome 6 (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)
6:109,440,724-109,443,919 6q21	SMPD2, NSMASE1	Sphingomyelin phosphodiesterase 2	603498						Smpd2
6:109,444,062-109,465,968 6q21	MICAL1, NICAL, MICAL	Microtubule-associated monooxygenase, calponin and LIM domains-containing 1	607129						Mical1
6:109,462,594-109,483,219 6q21	ZBTB24, PATZ2, ZNF450, KIAA0441, ICF2	Zinc finger- and BTB domain-containing protein 24	614064	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	Autosomal recessive	3		Zbtb24
6:109,492,855-109,691,202 6q21	AK9, SPGF89	Adenylate kinase 9	615358	Spermatogenic failure 89	620705	Autosomal recessive	3		Ak9
6:109,691,296-109,825,426 6q21	FIG4, KIAA0274, SAC3, ALS11, YVS, BTOP	FIG4 phosphoinositide 5-phosphatase	609390	?Polymicrogyria, bilateral temporooccipital	612691	Autosomal recessive	3	mutation identified in 1 BTOP family	Fig4
				Amyotrophic lateral sclerosis 11	612577	Autosomal dominant	3
				Charcot-Marie-Tooth disease, type 4J	611228	Autosomal recessive	3
				Yunis-Varon syndrome	216340	Autosomal recessive	3
6:109,978,311-109,980,720 6q21	GPR6	G protein-coupled receptor-6	600553						Gpr6
6:110,099,819-110,179,670 6q21	WASF1, WAVE, WAVE1, SCAR1, NEDALVS	WAS protein family member 1	605035	Neurodevelopmental disorder with absent language and variable seizures	618707	Autosomal dominant	3		Wasf1
6:110,180,427-110,232,232 6q21	CDC40, PRP17, PCH15	Cell division cycle 40	605585	?Pontocerebellar hypoplasia, type 15	619302	Autosomal recessive	3	mutation identified in 1 PCH15 patient	Cdc40
6:110,388,321-110,415,575 6q21	DDO, DASOX	D-aspartate oxidase	124450						Ddo
6:110,424,687-110,476,613 6q21	SLC22A16, FLIPT2, CT2	Solute carrier family 22 (organic cation transporter), member 16	608276						Slc22a16

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Printed: July 16, 2024