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GeneQ18040143· pop 5· linked from 3 articles

Also 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
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].

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
View on Ensembl →

via Ensembl · EMBL-EBI

~1 min read

Encyclopedic overview

2 sections
Contents
  • 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.

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