DNM3
Sign in to saveAlso known as Dyna III, dynamin 3
Dynamin-3 is a protein that in humans is encoded by the DNM3 gene. The protein encoded by this gene is a member of the dynamin family which possess mechanochemical properties involved in actin-membrane processes, predominantly in membrane budding. DNM3 is upregulated in Sézary's syndrome.
In the Vinony graph
Vinony's link graph records 349 inbound references to DNM3, and connects out to COPII, AP-type membrane coat adaptor complex and PubMed.
It is catalogued under the topic Genes on human chromosome 1.
Vinony links it to 6 Wikipedia language editions.
Gene data
DNM3- Name
- dynamin 3
- Type
- protein-coding
- Position
- 171,817,887–172,418,466 (+)
- Aliases
- Dyna III
- Ensembl
- ENSG00000197959
- RefSeq RNA
- NM_001136127.3, NM_001278252.2, NM_001350204.2, NM_001350205.2, NM_001350206.2
- RefSeq protein
- NP_001129599.1, NP_001265181.1, NP_001337133.1, NP_001337134.1, NP_001337135.1
This gene encodes a member of a family of guanosine triphosphate (GTP)-binding proteins that associate with microtubules and are involved in vesicular transport. The encoded protein functions in the development of megakaryocytes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
dynamin 3
- Symbol
- DNM3
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 1:171,817,887-172,418,466
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 22906
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/26052
- genomic end
- 172387606
- genomic start
- 171817887
- chromosome
- human chromosome 1
- cytogenetic location
- 1q24.3
- expressed in
- orbitofrontal cortex
Sources (4)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- References
- Further reading
- External links
Dynamin-3 is a protein that in humans is encoded by the DNM3 gene. The protein encoded by this gene is a member of the dynamin family which possess mechanochemical properties involved in actin-membrane processes, predominantly in membrane budding. DNM3 is upregulated in Sézary's syndrome.
==References==
Excerpted from Wikipedia’s “DNM3” article, available under the CC BY-SA 4.0 licence.