Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Orphanet | Ensembl |
HGNC | UniGene | Nucleotide | OMIM | UCSC |
Home Page |
FLASH GENE |
Symbol | SPTBN2 | contributors: mct/npt - updated : 21-05-2019 |
HGNC name | spectrin, beta, non-erythrocytic 2 |
HGNC id | 11276 |
|
RNA |
TRANSCRIPTS | type | messenger |
---|
|
EXPRESSION |
Type | widely |
tissue |
|
cells |
|
cell lineage
cell lines
| fluid/secretion
| |
at STAGE |
PROTEIN |
PHYSICAL PROPERTIES
STRUCTURE
| |
motifs/domains
| |
| |
| |
|
HOMOLOGY |
interspecies | homolog to murine Spnb3 |
Homologene |
FAMILY |
CATEGORY | structural protein |
SUBCELLULAR LOCALIZATION | extracellular |
intracellular | |
intracellular,cytoplasm,cytosolic | |
intracellular,cytoplasm,cytoskeleton |
basic FUNCTION | |
| |
| |
| |
| |
| |
|
CELLULAR PROCESS |
PHYSIOLOGICAL PROCESS |
PATHWAY |
metabolism |
signaling |
a component |
INTERACTION |
DNA |
RNA |
small molecule |
protein |
cell & other |
REGULATION |
Other | SPTBN2 and downstream molecules are regulated in multiple forms of cardiovascular disease via Ca(2+)- and calpain-dependent proteolysis |
ASSOCIATED DISORDERS |
corresponding disease(s) | SCA5 , SCAR14 |
Other morbid association(s) |
|
Susceptibility |
|
Variant & Polymorphism other | DNA methylation of one CpG site in SPTBN2 is associated with attention deficits in children |
Candidate gene
Marker
| Therapy target
|
| |
ANIMAL & CELL MODELS |