UBAP1
Sign in to saveAlso known as NAG20, UAP, UBAP, UBAP-1, ubiquitin associated protein 1, SPG80
Ubiquitin-associated protein 1 is a protein that in humans is encoded by the UBAP1 gene.
Gene data
UBAP1- Name
- ubiquitin associated protein 1
- Type
- protein-coding
- Position
- 34,179,005–34,252,523 (+)
- Aliases
- NAG20, SPG80, UAP, UBAP, UBAP-1
- Ensembl
- ENSG00000165006
- RefSeq RNA
- NM_001171201.1, NM_001171202.1, NM_001171203.3, NM_001171204.3, NM_016525.5
- RefSeq protein
- NP_001164672.1, NP_001164673.1, NP_001164674.1, NP_001164675.1, NP_057609.2
This gene is a member of the UBA domain family, whose members include proteins having connections to ubiquitin and the ubiquitination pathway. The ubiquitin associated domain is thought to be a non-covalent ubiquitin binding domain consisting of a compact three helix bundle. This particular protein originates from a gene locus in a refined region on chromosome 9 undergoing loss of heterozygosity in nasopharyngeal carcinoma (NPC). Taking into account its cytogenetic location, this UBA domain family member is being studies as a putative target for mutation in nasopharyngeal carcinomas. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
ubiquitin associated protein 1
- Symbol
- UBAP1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 9:34,179,005-34,252,523
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
~1 min read
Encyclopedic overview
2 sectionsContents
- References
- Further reading
Ubiquitin-associated protein 1 is a protein that in humans is encoded by the UBAP1 gene.
This gene is a member of the ubiquitin-associated domain (UBA) family, whose members include proteins having connections to ubiquitin and the ubiquitination pathway. The ubiquitin associated domain is thought to be a non-covalent ubiquitin-binding domain consisting of a compact three-helix bundle. This particular protein originates from a gene locus in a refined region on chromosome 9 undergoing loss of heterozygosity in nasopharyngeal carcinoma (NPC). Taking into account its cytogenetic location, this UBA domain family member is being studies as a putative target for mutation in nasopharyngeal carcinomas. Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
Excerpted from Wikipedia’s “UBAP1” article, available under the CC BY-SA 4.0 licence.