CA2, carbonic anhydrase 2, 760

N. diseases: 210; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs118203933
rs118203933
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0345407
Disease:
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3
0.810 GeneticVariation BEFREE Kinetic analysis of a mutant (His107-->Tyr) responsible for human carbonic anhydrase II deficiency syndrome. 8444854 1993
dbSNP: rs118203933
rs118203933
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0345407
Disease:
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3
0.810 GeneticVariation UNIPROT
dbSNP: rs118203933
rs118203933
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0345407
Disease:
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3
T 0.810 CausalMutation CLINVAR
dbSNP: rs10504813
rs10504813
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs779869368
rs779869368
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0345407
Disease:
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3
T 0.700 GeneticVariation CLINVAR Carbonic anhydrase II deficiency: single-base deletion in exon 7 is the predominant mutation in Caribbean Hispanic patients. 8128957 1994
dbSNP: rs573750741
rs573750741
Entrez Id: 760;100996348
Gene Symbol: CA2;CA3-AS1
CA2;CA3-AS1
CUI: C0345407
Disease:
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3
A 0.700 CausalMutation CLINVAR A splice junction mutation in intron 2 of the carbonic anhydrase II gene of osteopetrosis patients from Arabic countries. 1301935 1992
dbSNP: rs118203931
rs118203931
Entrez Id: 760;100996348
Gene Symbol: CA2;CA3-AS1
CA2;CA3-AS1
CUI: C4017251
Disease:
CARBONIC ANHYDRASE II VARIANT
G 0.700 CausalMutation CLINVAR
dbSNP: rs118203932
rs118203932
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C4017251
Disease:
CARBONIC ANHYDRASE II VARIANT
A 0.700 CausalMutation CLINVAR
dbSNP: rs118203934
rs118203934
Entrez Id: 760;100996348
Gene Symbol: CA2;CA3-AS1
CA2;CA3-AS1
CUI: C0345407
Disease:
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3
G 0.700 CausalMutation CLINVAR
dbSNP: rs1304160279
rs1304160279
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0345407
Disease:
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3
0.700 GeneticVariation UNIPROT
dbSNP: rs1554709677
rs1554709677
Entrez Id: 760;100996348
Gene Symbol: CA2;CA3-AS1
CA2;CA3-AS1
CUI: C0345407
Disease:
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3
A 0.700 CausalMutation CLINVAR
dbSNP: rs201928238
rs201928238
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C1275685
Disease:
Avellino corneal dystrophy
0.020 GeneticVariation BEFREE The R124H mutation of the keratoepithelin gene (TGFBI) causes Avellino corneal dystrophy whereas the N544S mutation of this same gene gives rise to lattice corneal dystrophy. 19461933 2009
dbSNP: rs201928238
rs201928238
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C1275685
Disease:
Avellino corneal dystrophy
0.020 GeneticVariation BEFREE An unusual clinical phenotype of Avellino corneal dystrophy associated with an Arg124His beta iG-H3 mutation in an African-American woman. 15059726 2004
dbSNP: rs201928238
rs201928238
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0010036
Disease:
Corneal dystrophy
0.010 GeneticVariation BEFREE The clinical manifestations of the two cases with both R124H and N544S mutations appeared to be a summation of Avellino and lattice corneal dystrophies. 19461933 2009
dbSNP: rs201928238
rs201928238
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0155127
Disease:
Familial Amyloid Polyneuropathy, Type V
0.010 GeneticVariation BEFREE The R124H mutation of the keratoepithelin gene (TGFBI) causes Avellino corneal dystrophy whereas the N544S mutation of this same gene gives rise to lattice corneal dystrophy. 19461933 2009
dbSNP: rs118203933
rs118203933
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0005944
Disease:
Metabolic Bone Disorder
0.010 GeneticVariation BEFREE One mutation associated with MBD entails the H107Y substitution where H107 is a highly conserved residue in the carbonic anhydrase protein family. 18189416 2008
dbSNP: rs118203933
rs118203933
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0085584
Disease:
Encephalopathies
0.010 GeneticVariation BEFREE Unfolding a folding disease: folding, misfolding and aggregation of the marble brain syndrome-associated mutant H107Y of human carbonic anhydrase II. 15327960 2004
dbSNP: rs118203933
rs118203933
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C1446648
Disease:
Non-specific brain syndrome
0.010 GeneticVariation BEFREE Unfolding a folding disease: folding, misfolding and aggregation of the marble brain syndrome-associated mutant H107Y of human carbonic anhydrase II. 15327960 2004
dbSNP: rs765669662
rs765669662
Entrez Id: 760;100996348
Gene Symbol: CA2;CA3-AS1
CA2;CA3-AS1
CUI: C1332977
Disease:
Childhood Leukemia
0.010 GeneticVariation BEFREE The allelic frequencies of G/A80 were nearly identical for the non-leukemia (42.2% CGC and 57.8% CAC) and leukemia (40.7% CGC and 59.3% CAC) genomic DNAs. 11705857 2001
dbSNP: rs765669662
rs765669662
Entrez Id: 760;100996348
Gene Symbol: CA2;CA3-AS1
CA2;CA3-AS1
CUI: C0023418
Disease:
leukemia
0.010 GeneticVariation BEFREE In genomic DNAs prepared from 105 leukemia (n = 54) and non-leukemia (n = 51) specimens, PCR amplifications and direct sequencing of exon 3 identified a high-frequency G to A single nucleotide polymorphism at position 80 that resulted in a change of arginine-27 to histidine-27. 11705857 2001
dbSNP: rs765669662
rs765669662
Entrez Id: 760;100996348
Gene Symbol: CA2;CA3-AS1
CA2;CA3-AS1
CUI: C0023418
Disease:
leukemia
0.010 GeneticVariation BEFREE The allelic frequencies of G/A80 were nearly identical for the non-leukemia (42.2% CGC and 57.8% CAC) and leukemia (40.7% CGC and 59.3% CAC) genomic DNAs. 11705857 2001
dbSNP: rs765669662
rs765669662
Entrez Id: 760;100996348
Gene Symbol: CA2;CA3-AS1
CA2;CA3-AS1
CUI: C1332977
Disease:
Childhood Leukemia
0.010 GeneticVariation BEFREE In genomic DNAs prepared from 105 leukemia (n = 54) and non-leukemia (n = 51) specimens, PCR amplifications and direct sequencing of exon 3 identified a high-frequency G to A single nucleotide polymorphism at position 80 that resulted in a change of arginine-27 to histidine-27. 11705857 2001
dbSNP: rs201928238
rs201928238
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0544848
Disease:
Dystrophy, granular
0.010 GeneticVariation BEFREE Arg124His mutation of the betaig-h3 gene was found in a pedigree with granular dystrophy. 9603385 1998
dbSNP: rs886063150
rs886063150
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0007102
Disease:
Malignant tumor of colon
0.010 GeneticVariation BEFREE Four distinct sequence alterations were identified: (a) in one gastric and one esophageal tumor, an A to C transversion occurred at nucleotide 5795 (CAC-->CCC), leading to a His-->Pro substitution at codon 179; (b) a second esophageal tumor had a C to T transition at nucleotide 8291 (ACC-->ATC), leading to a Thr-->Ile substitution at codon 277 of IGFBP-3; (c) one alteration comprised a G to C transversion in exon 1 at nucleotide 2132 (GGG-->GCG), leading to a Gly-->Ala substitution at codon 32 in two gastric cancers, seven esophageal cancers, and nine colon cancers; and (d) a C to G transversion located 17 nucleotides from the 3' splice site in intron 1 was observed in three colon cancers and four esophageal cancers. 9809981 1998
dbSNP: rs886063150
rs886063150
Entrez Id: 760
Gene Symbol: CA2
CA2
CUI: C0014859
Disease:
Esophageal Neoplasms
0.010 GeneticVariation BEFREE Four distinct sequence alterations were identified: (a) in one gastric and one esophageal tumor, an A to C transversion occurred at nucleotide 5795 (CAC-->CCC), leading to a His-->Pro substitution at codon 179; (b) a second esophageal tumor had a C to T transition at nucleotide 8291 (ACC-->ATC), leading to a Thr-->Ile substitution at codon 277 of IGFBP-3; (c) one alteration comprised a G to C transversion in exon 1 at nucleotide 2132 (GGG-->GCG), leading to a Gly-->Ala substitution at codon 32 in two gastric cancers, seven esophageal cancers, and nine colon cancers; and (d) a C to G transversion located 17 nucleotides from the 3' splice site in intron 1 was observed in three colon cancers and four esophageal cancers. 9809981 1998