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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 2
4 OMIM references -
5 associated genes
No signs/symptoms info
Autosomal dominant distal renal tubular acidosis
Hereditary spherocytosis

SLC4A1 ANK1
EPB42
SLC4A1
SPTA1
SPTB


COMMON
GENES
SLC4A1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SLC4A1
SLC4A1
(0.83)
(0.63)
ANK1
EPB42



Citations in the biomedical literature:


Autosomal dominant distal renal tubular acidosis
SLC4A1
Hereditary spherocytosis
ANK1 EPB42 SPTA1 SPTB



Autosomal dominant distal renal tubular acidosis
Hereditary spherocytosis

Synonym(s):
- AD dRTA
- Renal tubular acidosis type 1a

Synonym(s):
- Minkowski-Chauffard disease

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease

Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
4 OMIM references -
2 MeSH references: C536356 / D013103

No signs/symptoms info available.