Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Ensembl |
HGNC | UniGene | Nucleotide | OMIM | UCSC |
Home Page |
FLASH GENE |
Symbol | HEPACAM2 | contributors: mct/npt/pgu - updated : 13-01-2017 |
HGNC name | HEPACAM family member 2 |
HGNC id | 27364 |
|
DNA |
TYPE | functioning gene |
STRUCTURE | 43.71 kb 10 Exon(s) |
MAPPING | cloned | Y | linked | N | status |
RNA |
TRANSCRIPTS | type | messenger |
---|
EXPRESSION |
Type | restricted |
expressed in | (based on citations) | ||||||||||||||||||||||||||||||||||||||||
organ(s) |
|
cell lineage
cell lines
| fluid/secretion
| |
at STAGE |
PROTEIN |
PHYSICAL PROPERTIES
STRUCTURE
| |
motifs/domains
| |
| |
|
HOMOLOGY |
Homologene |
FAMILY |
CATEGORY | DNA associated |
SUBCELLULAR LOCALIZATION | intracellular |
intracellular,cytoplasm,organelle,Golgi | |
intracellular,cytoplasm,cytoskeleton,microtubule,centrosome | |
intracellular,cytoplasm,cytoskeleton,microtubule,mitotic spindle | |
text | |
|
basic FUNCTION |
CELLULAR PROCESS |
PHYSIOLOGICAL PROCESS |
PATHWAY |
metabolism |
signaling |
a component |
INTERACTION |
DNA |
RNA |
small molecule |
protein |
cell & other |
REGULATION |
inhibited by | by RNA interference induced abnormalities in mitosis and nuclear morphology, similar to myelodysplasia |
ASSOCIATED DISORDERS |
corresponding disease(s) |
Other morbid association(s) |
|
Susceptibility |
Variant & Polymorphism
| |
Candidate gene | for both mental retardation and microcephaly in del7q21 with myoclonus dystonia plus syndrome. | |
Marker
Therapy target
|
| |
ANIMAL & CELL MODELS |