SPTAN1 Chromosome 9

Spectrin alpha, non-erythrocytic 1
288 variants 288 Health Risk

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What This Gene Does
Spectrins are a family of filamentous cytoskeletal proteins that function as essential scaffold proteins that stabilize the plasma membrane and organize intracellular organelles. Spectrins are composed of alpha and beta dimers that associate to form tetramers linked in a head-to-head arrangement. This gene encodes an alpha spectrin that is specifically expressed in nonerythrocytic cells. The encoded protein has been implicated in other cellular functions including DNA repair and cell cycle regulation. Mutations in this gene are the cause of early infantile epileptic encephalopathy-5. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Sep 2010]
Gene Info
Gene Group
"EF-hand domain containing|Spectrins"
Locus Type
gene with protein product
Location
9q34.11
Ensembl
ENSG00000197694
Associated Conditions (39)
Early-infantile DEE
Developmental and epileptic encephalopathy
5
Inborn genetic diseases
Neuronopathy
distal hereditary motor
autosomal dominant 11
Spastic paraplegia 91
autosomal dominant
with or without cerebellar ataxia
Developmental delay with or without epilepsy
SPTAN1-related disorder
Clear cell carcinoma of kidney
Colon adenocarcinoma
Gastric cancer
Thymoma
Melanoma
Familial cancer of breast
Bilateral tonic-clonic seizure
Neuromuscular disease
+19 more conditions
Key Variants
RS1003067844
Conflicting classifications of pathogenicity
Early-infantile DEE, Early-infantile DEE
Health Risk
RS1057520841
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 5, Early-infantile DEE
Health Risk
RS1057521149
Conflicting classifications of pathogenicity
Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
Health Risk
RS1057523269
Conflicting classifications of pathogenicity
Early-infantile DEE, Early-infantile DEE, Early-infantile DEE
Health Risk
RS1176851202
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 5, Early-infantile DEE
Health Risk
RS11792065
Conflicting classifications of pathogenicity
Early-infantile DEE, Early-infantile DEE
Health Risk
RS1232614751
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 5, Early-infantile DEE
Health Risk
RS1265382491
Conflicting classifications of pathogenicity
Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
Health Risk
RS1276832919
Conflicting classifications of pathogenicity
Early-infantile DEE, Early-infantile DEE
Health Risk
RS1317904463
Conflicting classifications of pathogenicity
Neuronopathy, distal hereditary motor, autosomal dominant 11
Health Risk
RS1334812460
Conflicting classifications of pathogenicity
Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
Health Risk
RS1336849921
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 5, Inborn genetic diseases
Health Risk
All Variants (288)
RSID Category Clinical Significance Conditions
RS769320860 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS770046688 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS770189298 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS771286283 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS771825373 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS771862017 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS771886198 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS772281075 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS772780483 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Inborn genetic diseases
RS773023641 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS773288631 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Inborn genetic diseases
RS773663318 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS774283264 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS775190610 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Inborn genetic diseases
RS775634580 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS776648566 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS777182182 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS777407223 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS778121117 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS778489951 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Inborn genetic diseases
RS778709187 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS779759134 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS779993051 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Inborn genetic diseases
RS780622472 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Inborn genetic diseases
RS780696613 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Inborn genetic diseases
RS781124530 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS781453058 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS794727356 Health Risk Conflicting classifications of pathogenicity Landau-Kleffner syndrome, Developmental and epileptic encephalopathy, 5
RS794727389 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Developmental delay with or without epilepsy
RS796053298 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS796053300 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS796053301 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS796053304 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS796053305 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS796053306 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS796053315 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS796053320 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS796053322 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Inborn genetic diseases
RS796053323 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Developmental and epileptic encephalopathy
RS796053329 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Developmental and epileptic encephalopathy
RS797046004 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS904041405 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Inborn genetic diseases, Early-infantile DEE
RS942861981 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS968327265 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 5, Early-infantile DEE
RS971082831 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS1193718145 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1305659962 Health Risk Likely pathogenic
RS1554746442 Health Risk Likely pathogenic
RS1554767335 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 5, Developmental and epileptic encephalopathy
RS1554769022 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 5, Developmental and epileptic encephalopathy
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