ROM1
Sign in to saveAlso known as ROM, ROSP1, RP7, TSPAN23, retinal outer segment membrane protein 1
Rod outer segment membrane protein 1 is a protein that in humans is encoded by the ROM1 gene.
In the Vinony graph
Vinony's link graph records 71 inbound references to ROM1, and connects out to PubMed, human chromosome 11 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 11.
Vinony links it to 7 Wikipedia language editions.
Gene data
ROM1- Name
- retinal outer segment membrane protein 1
- Type
- protein-coding
- Position
- 62,611,722–62,615,116 (+)
- Aliases
- ROM, ROSP1, RP7, TSPAN23
- Ensembl
- ENSG00000149489
- RefSeq RNA
- NM_000327.4
- RefSeq protein
- NP_000318.2
This gene is a member of a photoreceptor-specific gene family and encodes an integral membrane protein found in the photoreceptor disk rim of the eye. This protein can form homodimers or can heterodimerize with another photoreceptor, retinal degeneration slow (RDS). It is essential for disk morphogenesis, and may also function as an adhesion molecule involved in the stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. Certain defects in this gene have been associated with the degenerative eye disease retinitis pigmentosa. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
via MyGene.info
Gene · Ensembl
retinal outer segment membrane protein 1
- Symbol
- ROM1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 11:62,611,722-62,615,116
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 276
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/6094
- genomic end
- 62615116
- genomic start
- 62379194
- chromosome
- human chromosome 11
- cytogenetic location
- 11q12.3
Sources (4)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- References
- Further reading
Rod outer segment membrane protein 1 is a protein that in humans is encoded by the ROM1 gene.
This gene is a member of a photoreceptor-specific gene family and encodes an integral membrane protein found in the photoreceptor disk rim of the eye. This protein can form homodimers or can heterodimerize with another photoreceptor protein, peripherin-2 (PRPH2; retinal degeneration, slow; RDS). It is essential for disk morphogenesis, and may also function as an adhesion molecule involved in the stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. Certain defects in this gene have been associated with the degenerative eye disease retinitis pigmentosa.
Excerpted from Wikipedia’s “ROM1” article, available under the CC BY-SA 4.0 licence.