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OMIM Gene/Loci: 581 - 590 of 683 on Chromosome 10 (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)
10:114,431,110 10q25.3	LIMAB1	LIM actin-binding protein-1	602330						Ablim1
10:114,821,780 10q25.3	FHIP2A, FAM160B1, KIAA1600	FHF complex subunit hook-interacting protein 2A	617312						Fhip2a
10:114,938,195 10q25.3	TRUB1, PUS4	TRUB pseudouridine synthase, E. coli, homolog of, 1	610726						Trub1
10:115,093,365 10q25.3	ATRNL1, KIAA0534, ALP	Attractin-like 1	612869						Atrnl1
10:116,056,925 10q25.3	GFRA1, GDNFRA, GDNFR, RHDA4	GDNF family receptor, alpha-1	601496	Renal hypodysplasia/aplasia 4	619887	AR	3		Gfra1
10:116,545,931 10q25.3	PNLIP, PNLIPD	Pancreatic lipase	246600	?Pancreatic lipase deficiency	614338	AR	3	mutation identified in 1 family	Pnlip
10:116,590,959 10q25.3	PNLIPRP1, PLRP1	Pancreatic lipase-related protein 1	604422						Pnliprp1
10:116,620,953 10q25.3	PNLIPRP2, PLRP2	Pancreatic lipase-related protein 2	604423						Pnliprp2
10:116,671,192 10q25.3	HSPA12A, KIAA0417	Heat-shock 70kD protein 12A	610701						Hspa12a
10:116,849,499 10q25.3	ENO4, ENOS	Enolase 4	131375						Eno4

pter | « Towards pter | Towards qter » | qter

OMIM Gene/Loci: 581 - 590 of 683 on Chromosome 10 (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)
10:114,431,110-114,801,373 10q25.3	LIMAB1	LIM actin-binding protein-1	602330						Ablim1
10:114,821,780-114,899,832 10q25.3	FHIP2A, FAM160B1, KIAA1600	FHF complex subunit hook-interacting protein 2A	617312						Fhip2a
10:114,938,195-114,977,676 10q25.3	TRUB1, PUS4	TRUB pseudouridine synthase, E. coli, homolog of, 1	610726						Trub1
10:115,093,365-115,948,999 10q25.3	ATRNL1, KIAA0534, ALP	Attractin-like 1	612869						Atrnl1
10:116,056,925-116,274,705 10q25.3	GFRA1, GDNFRA, GDNFR, RHDA4	GDNF family receptor, alpha-1	601496	Renal hypodysplasia/aplasia 4	619887	Autosomal recessive	3		Gfra1
10:116,545,931-116,567,855 10q25.3	PNLIP, PNLIPD	Pancreatic lipase	246600	?Pancreatic lipase deficiency	614338	Autosomal recessive	3	mutation identified in 1 family	Pnlip
10:116,590,959-116,609,175 10q25.3	PNLIPRP1, PLRP1	Pancreatic lipase-related protein 1	604422						Pnliprp1
10:116,620,953-116,645,143 10q25.3	PNLIPRP2, PLRP2	Pancreatic lipase-related protein 2	604423						Pnliprp2
10:116,671,192-116,850,747 10q25.3	HSPA12A, KIAA0417	Heat-shock 70kD protein 12A	610701						Hspa12a
10:116,849,499-116,912,375 10q25.3	ENO4, ENOS	Enolase 4	131375						Eno4

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.
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Printed: Nov. 25, 2024