Gene Map Search - 5p15

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Results: 69 entries.

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Genomic context table	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)
1:	5:1 5p	ASD1	Atrial septal defect 1	108800	Atrial septal defect 1	108800	AD	2	max lod at D5S406
2:	5:1 5p15.33	BCC3	Basal cell carcinoma, susceptibility to, 3	613059	{Basal cell carcinoma, susceptibility to, 3}	613059		2
3:	5:1 5p15.33	GLM8	Glioma susceptibility 8	613033	{Glioma susceptibility 8}	613033		2	associated with rs2736100
4:	5:1 5p15.33	LNCR3	Lung cancer susceptibility 3	612571	{Lung cancer susceptibility 3}	612571		2	associated with rs402710 and rs2736100
5:	5:1 5p	MHS6	Malignant hyperthermia susceptibility 6	601888	{Malignant hyperthermia susceptibility 6}	601888		2
6:	5:1 5p15.33-p15.2	MYP16	Myopia 16	612554	Myopia 16	612554		2	max lod at D5S2505
7:	5:1 5p15	TST2	Tuberculin skin test reactivity quantitative trait locus	613637	[Tuberculin skin test reactivity QTL]	613637		2	max lod at 16:2.70Mb
8:	5:92,168 5p15.33	PLEKHG4B	Pleckstrin homology domain- and RhoGEF domain-containing protein G4B	620665
9:	5:218,320 5p15.33	SDHA, SDH1, SDHF, CMD1GG, PPGL5, MC2DN1, NDAXOA	Succinate dehydrogenase complex, flavoprotein subunit A	600857	Cardiomyopathy, dilated, 1GG	613642	AR	3	copy on 3q29	Sdha
					Mitochondrial complex II deficiency, nuclear type 1	252011	AR	3
					Neurodegeneration with ataxia and late-onset optic atrophy	619259	AD	3
					Pheochromocytoma/paraganglioma syndrome 5	614165	AD	3
10:	5:271,646 5p15.33	PDCD6, ALG2	Programmed cell death 6	601057						Pdcd6

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Results: 69 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)
5:1-48,800,001 5p	ASD1	Atrial septal defect 1	108800	Atrial septal defect 1	108800	Autosomal dominant	2	max lod at D5S406
5:1-4,400,000 5p15.33	BCC3	Basal cell carcinoma, susceptibility to, 3	613059	{Basal cell carcinoma, susceptibility to, 3}	613059		2
5:1-4,400,000 5p15.33	GLM8	Glioma susceptibility 8	613033	{Glioma susceptibility 8}	613033		2	associated with rs2736100
5:1-4,400,000 5p15.33	LNCR3	Lung cancer susceptibility 3	612571	{Lung cancer susceptibility 3}	612571		2	associated with rs402710 and rs2736100
5:1-48,800,001 5p	MHS6	Malignant hyperthermia susceptibility 6	601888	{Malignant hyperthermia susceptibility 6}	601888		2
5:1-15,000,000 5p15.33-p15.2	MYP16	Myopia 16	612554	Myopia 16	612554		2	max lod at D5S2505
5:1-18,400,000 5p15	TST2	Tuberculin skin test reactivity quantitative trait locus	613637	[Tuberculin skin test reactivity QTL]	613637		2	max lod at 16:2.70Mb
5:92,168-189,966 5p15.33	PLEKHG4B	Pleckstrin homology domain- and RhoGEF domain-containing protein G4B	620665
5:218,320-268,746 5p15.33	SDHA, SDH1, SDHF, CMD1GG, PPGL5, MC2DN1, NDAXOA	Succinate dehydrogenase complex, flavoprotein subunit A	600857	Cardiomyopathy, dilated, 1GG	613642	Autosomal recessive	3	copy on 3q29	Sdha
				Mitochondrial complex II deficiency, nuclear type 1	252011	Autosomal recessive	3
				Neurodegeneration with ataxia and late-onset optic atrophy	619259	Autosomal dominant	3
				Pheochromocytoma/paraganglioma syndrome 5	614165	Autosomal dominant	3
5:271,646-314,974 5p15.33	PDCD6, ALG2	Programmed cell death 6	601057						Pdcd6

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