SPTA1 Chromosome 1

Spectrin alpha, erythrocytic 1
348 variants 348 Health Risk

Upload your DNA to see your personal genotypes for variants in SPTA1.

What This Gene Does
This gene encodes a member of a family of molecular scaffold proteins that link the plasma membrane to the actin cytoskeleton and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation. It forms a component of the erythrocyte plasma membrane. Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis-2, pyropoikilocytosis, and spherocytosis, type 3. [provided by RefSeq, Aug 2017]
Gene Info
Gene Group
"EF-hand domain containing|Spectrins"
Locus Type
gene with protein product
Location
1q23.1
Ensembl
ENSG00000163554
Associated Conditions (25)
Hereditary spherocytosis type 3
Pyropoikilocytosis
hereditary
Elliptocytosis 2
SPTA1-related disorder
Lung cancer
Acute myeloid leukemia
Familial hemolytic anemia
Hemolytic anemia
Intellectual developmental disorder
X-linked 111
Malignant lymphoma
large B-cell
diffuse
Inborn genetic diseases
Thymoma
See cases
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome
Spherocytosis
Abnormality of blood and blood-forming tissues
+5 more conditions
Key Variants
All Variants (348)
RSID Category Clinical Significance Conditions
RS2525331949 Health Risk Likely pathogenic
RS2525391483 Health Risk Likely pathogenic Spherocytosis, Spherocytosis
RS2525400290 Health Risk Likely pathogenic
RS2526152872 Health Risk Likely pathogenic
RS2526152917 Health Risk Likely pathogenic
RS2526183559 Health Risk Likely pathogenic
RS2526221510 Health Risk Likely pathogenic Pyropoikilocytosis, hereditary, Hereditary spherocytosis type 3
RS2526289187 Health Risk Likely pathogenic Pyropoikilocytosis, hereditary, Hereditary spherocytosis type 3
RS2526289582 Health Risk Likely pathogenic
RS2526378544 Health Risk Likely pathogenic
RS2526419037 Health Risk Likely pathogenic
RS373407146 Health Risk Likely pathogenic
RS531944041 Health Risk Likely pathogenic
RS749880846 Health Risk Likely pathogenic
RS752114200 Health Risk Likely pathogenic Pyropoikilocytosis, hereditary, Pyropoikilocytosis
RS753042073 Health Risk Likely pathogenic
RS758378706 Health Risk Likely pathogenic SPTA1-related disorder, SPTA1-related disorder
RS767854151 Health Risk Likely pathogenic
RS773168610 Health Risk Likely pathogenic Abnormality of blood and blood-forming tissues, Abnormality of blood and blood-forming tissues
RS774632615 Health Risk Likely pathogenic Anemia, SPTA1-related disorder, Anemia
RS936665671 Health Risk Likely pathogenic SPTA1-related disorder, SPTA1-related disorder
RS1172797322 Health Risk Pathogenic
RS121918637 Health Risk Pathogenic Pyropoikilocytosis, hereditary, Elliptocytosis 2
RS1236696892 Health Risk Pathogenic
RS1354777824 Health Risk Pathogenic
RS1383401833 Health Risk Pathogenic
RS1394141324 Health Risk Pathogenic Pyropoikilocytosis, hereditary, Elliptocytosis 2
RS1553231217 Health Risk Pathogenic Familial hemolytic anemia, Familial hemolytic anemia
RS1553234309 Health Risk Pathogenic Hereditary spherocytosis type 3, Hereditary spherocytosis type 3
RS1557961718 Health Risk Pathogenic Pyropoikilocytosis, hereditary, Pyropoikilocytosis
RS1650918653 Health Risk Pathogenic
RS1651716612 Health Risk Pathogenic Elliptocytosis 2, Elliptocytosis 2
RS1652094925 Health Risk Pathogenic SPTA1-related disorder, SPTA1-related disorder
RS1652531375 Health Risk Pathogenic
RS1652590413 Health Risk Pathogenic Elliptocytosis 2, Elliptocytosis 2
RS1652848700 Health Risk Pathogenic
RS1652849551 Health Risk Pathogenic
RS1653612721 Health Risk Pathogenic
RS1654812809 Health Risk Pathogenic
RS201844450 Health Risk Pathogenic Hereditary spherocytosis type 3, Elliptocytosis 2, Pyropoikilocytosis
RS2101857591 Health Risk Pathogenic Hereditary spherocytosis type 3, Hereditary spherocytosis type 3
RS2101908951 Health Risk Pathogenic
RS2101916656 Health Risk Pathogenic
RS2525027053 Health Risk Pathogenic Hereditary spherocytosis type 3, Hereditary spherocytosis type 3
RS2525133855 Health Risk Pathogenic
RS2525134307 Health Risk Pathogenic
RS2525200720 Health Risk Pathogenic SPTA1-related disorder, SPTA1-related disorder
RS2525241090 Health Risk Pathogenic
RS2525252642 Health Risk Pathogenic
RS2525311821 Health Risk Pathogenic
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