OMIM Entry Search - 120920 134370 138470 188040 217030 235400 612926

Search: '120920 134370 138470 188040 217030 235400 612926' (Search in: mim number)
Results: 1 - 7 of 7

1 :	# 612926. HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6	Gene Tests, Links Clinical Resources Clinical Trials Gene Tests Gene Reviews OrphaNet Genetic Alliance Genetics Home Reference Animal Models NCBI HomoloGene MGI Mouse Phenotype Cellular Pathways Reactome
	Cytogenetic location: 20p11.21 Matching terms: 612926

2 :	* 134370. COMPLEMENT FACTOR H; CFH	Gene Tests, Links Genome Ensembl NCBI Map Viewer UCSC Genome Browser DNA Ensembl NCBI RefSeq UCSC Genome Browser Protein UniProt HPRD Gene Info BioGPS Ensembl NCBI Gene GeneCards KEGG PharmGKB Clinical Resources Gene Tests Genetics Home Reference Variation Genetics Association DB GWAS Central HGVS MutaDATABASE Locus Specific DBs Animal Models NCBI HomoloGene MGI Mouse Phenotype KOMP IKMC MGI Mouse Gene ZFin OMIA Cellular Pathways KEGG Reactome
	FACTOR H-LIKE 1, INCLUDED Cytogenetic location: 1q31.3 , Genomic coordinates (GRCh37): 1:196,621,007 - 196,716,633 Matching terms: 134370

3 :	+ 138470. COMPLEMENT FACTOR B; CFB	Links Genome Ensembl NCBI Map Viewer UCSC Genome Browser DNA Ensembl NCBI RefSeq UCSC Genome Browser Protein UniProt HPRD Gene Info BioGPS Ensembl NCBI Gene GeneCards KEGG PharmGKB Clinical Resources Clinical Trials Genetic Alliance Variation Genetics Association DB GWAS Central HGVS MutaDATABASE Animal Models NCBI HomoloGene MGI Mouse Phenotype ZFin Cellular Pathways KEGG Reactome
	COMPLEMENT FACTOR B DEFICIENCY, INCLUDED Cytogenetic location: 6p21.33 , Genomic coordinates (GRCh37): 6:31,913,720 - 31,919,860 Matching terms: 138470

4 :	# 235400. HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1	Gene Tests, Links Clinical Resources Clinical Trials Gene Tests OrphaNet Genetic Alliance GARD Genetics Home Reference Animal Models NCBI HomoloGene MGI Mouse Phenotype OMIA Cellular Pathways Reactome Atypical hemolytic uremic syndrome with antibody anti-factor H Atypical hemolytic uremic syndrome Typical hemolytic uremic syndrome Atypical hemolytic uremic syndrome with H factor anomaly Hemolytic uremic syndrome Hemolytic uremic syndrome, atypical
	HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED Cytogenetic locations: 1q31.3 , 1q31.3 , 1q31.3 Matching terms: 235400

5 :	* 120920. CD46 ANTIGEN; CD46	Gene Tests, Links Genome Ensembl NCBI Map Viewer UCSC Genome Browser DNA Ensembl NCBI RefSeq UCSC Genome Browser Protein UniProt HPRD Gene Info BioGPS Ensembl NCBI Gene GeneCards KEGG PharmGKB Clinical Resources Gene Tests Variation Genetics Association DB GWAS Central HGVS MutaDATABASE Animal Models NCBI HomoloGene MGI Mouse Phenotype KOMP IKMC MGI Mouse Gene Cellular Pathways KEGG Reactome
	Cytogenetic location: 1q32.2 , Genomic coordinates (GRCh37): 1:207,925,382 - 207,968,860 Matching terms: 120920

6 :	* 217030. COMPLEMENT FACTOR I; CFI	Gene Tests, Links Genome Ensembl NCBI Map Viewer UCSC Genome Browser DNA Ensembl NCBI RefSeq UCSC Genome Browser Protein UniProt HPRD Gene Info BioGPS Ensembl NCBI Gene GeneCards KEGG PharmGKB Clinical Resources Gene Tests Genetics Home Reference Variation Genetics Association DB GWAS Central HGVS MutaDATABASE Locus Specific DBs Animal Models NCBI HomoloGene KOMP IKMC MGI Mouse Gene Cellular Pathways KEGG Reactome
	Cytogenetic location: 4q25 , Genomic coordinates (GRCh37): 4:110,661,847 - 110,723,334 Matching terms: 217030

7 :	* 188040. THROMBOMODULIN; THBD	Gene Tests, Links Genome Ensembl NCBI Map Viewer UCSC Genome Browser DNA Ensembl NCBI RefSeq UCSC Genome Browser Protein UniProt HPRD Gene Info BioGPS Ensembl NCBI Gene GeneCards KEGG PharmGKB Clinical Resources Gene Tests GARD Variation Genetics Association DB GWAS Central HGVS MutaDATABASE Animal Models NCBI HomoloGene MGI Mouse Phenotype KOMP IKMC MGI Mouse Gene Cellular Pathways KEGG Reactome
	Cytogenetic location: 20p11.21 , Genomic coordinates (GRCh37): 20:23,026,269 - 23,030,300 Matching terms: 188040

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