RNF135
Sign in to saveAlso known as MMFD, REUL, Riplet, L13, ring finger protein 135
RING finger protein 135 is a protein that in humans is encoded by the RNF135 gene.
In the Vinony graph
Vinony's link graph records 4 inbound references to RNF135, and connects out to PubMed, human chromosome 17 and Ensembl genome database project.
It is catalogued under topics including Genes on human chromosome 17 and RING finger proteins.
Vinony links it to 5 Wikipedia language editions.
Gene data
RNF135- Name
- ring finger protein 135
- Type
- protein-coding
- Position
- 30,970,513–30,999,911 (+)
- Aliases
- L13, MMFD, REUL, Riplet
- Ensembl
- ENSG00000181481
- RefSeq RNA
- NM_001184992.2, NM_032322.4, NM_197939.2, XM_024451000.2, XM_024451001.2
- RefSeq protein
- NP_001171921.1, NP_115698.3, NP_922921.1, XP_024306768.1, XP_024306769.1
The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. This gene is located in a chromosomal region known to be frequently deleted in patients with neurofibromatosis. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
ring finger protein 135
- Symbol
- RNF135
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 17:30,970,513-30,999,911
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 12427
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/84282
- genomic end
- 29326929
- genomic start
- 30970984
- chromosome
- human chromosome 17
- cytogenetic location
- 17q11.2
- expressed in
- synovial joint
Sources (3)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- Interactions
- References
- Further reading
RING finger protein 135 is a protein that in humans is encoded by the RNF135 gene.
The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. This gene is located in a chromosomal region known to be frequently deleted in patients with neurofibromatosis. Alternatively spliced transcript variants encoding distinct isoforms have been reported.
Excerpted from Wikipedia’s “RNF135” article, available under the CC BY-SA 4.0 licence.