Gene Map Search - 11q13

Search: '11q13 '

Did you mean: '( chromosome:11 AND chromosome_location_start:[* TO 77400000] AND chromosome_location_end:[600001 TO *] )' ?

Results: 260 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:	11:31,000,001 11p13-q14.1	MRT23	Intellectual developmental disorder, autosomal recessive 23	614344	Intellectual developmental disorder, autosomal recessive 23	614344	AR	2	between rs604518 and rs10899421
2:	11:55,800,001 11q12.1-q13.5	FNL2	Fibronectin-like-2	135610
3:	11:55,800,001 11q12-q13.1	PURAQTL1	Polyunsaturated fatty acids plasma level QTL1	612795	[Polyunsaturated fatty acids plasma level QTL1]	612795		2	associated with rs174537
4:	11:63,574,462 11q12.3-q13.1	PLAAT3, PLA2G16, HRASLS3, HRSL3, HREV107, FPLD9	Phospholipase A and acyltransferase 3	613867	Lipodystrophy, familial partial, type 9	620683	AR	3		Plaat3
5:	11:63,600,001 11q13-q22	ESA4	Esterase-A4	133220
6:	11:63,600,001 11q13	HMNR3	Neuronopathy, distal hereditary motor, autosomal recessive 3	607088	Neuronopathy, distal hereditary motor, autosomal recessive 3	607088	AR	2	no mutations found in IGHMBP2
7:	11:63,600,001 11q13	HPC14	Prostate cancer, hereditary, 14	611958	{Prostate cancer, hereditary, 14}	611958		2	associated with rs7931342
8:	11:63,600,001 11q13	IDDM4	Insulin-dependent diabetes mellitus-4	600319	{Diabetes mellitus, insulin-dependent, 4}	600319		2
9:	11:63,600,001 11q13	OTDD, DEL11q13, C11DELq13	Otodental dysplasia (chromosome 11q13 deletion syndrome)	166750	Otodental dysplasia chromosome deletion syndrome	166750	AD	4	between rs9666584 and rs41408348
10:	11:63,600,001 11q13	PGA3	Pepsinogen A3	169710

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Results: 260 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)
11:31,000,001-85,900,000 11p13-q14.1	MRT23	Intellectual developmental disorder, autosomal recessive 23	614344	Intellectual developmental disorder, autosomal recessive 23	614344	Autosomal recessive	2	between rs604518 and rs10899421
11:55,800,001-77,400,000 11q12.1-q13.5	FNL2	Fibronectin-like-2	135610
11:55,800,001-66,100,000 11q12-q13.1	PURAQTL1	Polyunsaturated fatty acids plasma level QTL1	612795	[Polyunsaturated fatty acids plasma level QTL1]	612795		2	associated with rs174537
11:63,574,462-63,616,927 11q12.3-q13.1	PLAAT3, PLA2G16, HRASLS3, HRSL3, HREV107, FPLD9	Phospholipase A and acyltransferase 3	613867	Lipodystrophy, familial partial, type 9	620683	Autosomal recessive	3		Plaat3
11:63,600,001-110,600,000 11q13-q22	ESA4	Esterase-A4	133220
11:63,600,001-77,400,000 11q13	HMNR3	Neuronopathy, distal hereditary motor, autosomal recessive 3	607088	Neuronopathy, distal hereditary motor, autosomal recessive 3	607088	Autosomal recessive	2	no mutations found in IGHMBP2
11:63,600,001-77,400,000 11q13	HPC14	Prostate cancer, hereditary, 14	611958	{Prostate cancer, hereditary, 14}	611958		2	associated with rs7931342
11:63,600,001-77,400,000 11q13	IDDM4	Insulin-dependent diabetes mellitus-4	600319	{Diabetes mellitus, insulin-dependent, 4}	600319		2
11:63,600,001-77,400,000 11q13	OTDD, DEL11q13, C11DELq13	Otodental dysplasia (chromosome 11q13 deletion syndrome)	166750	Otodental dysplasia chromosome deletion syndrome	166750	Autosomal dominant	4	between rs9666584 and rs41408348
11:63,600,001-77,400,000 11q13	PGA3	Pepsinogen A3	169710

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