LAT2
Sign in to saveAlso known as LAB, NTAL, WBSCR15, WBSCR5, WSCR5, HSPC046, linker for activation of T-cells family member 2, linker for activation of T cells family member 2
Linker for activation of T-cells family member 2 is a protein that in humans is encoded by the LAT2 gene.
In the Vinony graph
Vinony's link graph records 4 inbound references to LAT2, and connects out to PubMed, human chromosome 7 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 7.
Vinony links it to 6 Wikipedia language editions.
Gene data
LAT2- Name
- linker for activation of T cells family member 2
- Type
- protein-coding
- Position
- 74,199,652–74,242,501 (+)
- Aliases
- HSPC046, LAB, NTAL, WBSCR15, WBSCR5, WSCR5
- Ensembl
- ENSG00000086730
- RefSeq RNA
- NM_014146.4, NM_032463.3, NM_032464.3, XM_011516558.2, XM_047420801.1
- RefSeq protein
- NP_054865.2, NP_115852.1, NP_115853.2, XP_011514860.1, XP_047276757.1
This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
linker for activation of T cells family member 2
- Symbol
- LAT2
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 7:74,199,652-74,242,501
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 11297
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/7462
- chromosome
- human chromosome 7
- genomic start
- 73613982
- genomic end
- 73644161
- cytogenetic location
- 7q11.23
- expressed in
- superficial temporal artery
Sources (4)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- References
- Further reading
Linker for activation of T-cells family member 2 is a protein that in humans is encoded by the LAT2 gene.
This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein.
Excerpted from Wikipedia’s “LAT2” article, available under the CC BY-SA 4.0 licence.