H-Inv cluster ID |
HIX0025091 |
Genomic location
|
Chromosome |
6
|
Location |
6p21.1
|
Position |
42664333-
42690370
|
Strand |
-
|
Representative H-Inv ID |
HIT000196049
|
Representative H-Inv protein ID |
HIP000029577
|
Coding potential |
Protein coding;
|
Definition |
Peripherin-2; Retinal degeneration slow protein; Tetraspanin-22; Tspan-22; |
Similarity category
|
Category:
Identical to known human protein(Category I).
|
Identical to known human protein (P23942)
[Identity/coverage = 100.0%/100.0%] to
Homo sapiens (Human). protein.
|
Gene family / group |
NA
|
Gene symbol/name |
HGNC symbol |
PRPH2
|
HGNC aliases |
"retinal degeneration, slow (retinitis pigmentosa 7)", "retinal degeneration, slow"
|
HGNC name |
peripherin 2 (retinal degeneration, slow)
|
Database links |
RefSeq |
NA
|
Ensembl |
NA
|
Entrez Gene |
Entrez Gene ID:5961;
|
KEGG GENES |
KEGG GENES(5961);
|
GeneCard |
PRPH2;
*GeneCards is provided free to academic non-profit institutions.
|
etc |
Human-Gene diversity Of Life-style related Diseases;
|