PHLDA1
Sign in to saveAlso known as DT1P1B11, PHRIP, TDAG51, pleckstrin homology like domain family A member 1
Pleckstrin homology-like domain family A member 1 (PHLDA1) is a protein that in humans is encoded by the PHLDA1 gene.
In the Vinony graph
Vinony's link graph records 5 inbound references to PHLDA1, and connects out to PubMed, human chromosome 12 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 12.
Vinony links it to 5 Wikipedia language editions.
Gene data
PHLDA1- Name
- pleckstrin homology like domain family A member 1
- Type
- protein-coding
- Position
- 76,025,447–76,032,560 (−)
- Aliases
- DT1P1B11, PHRIP, TDAG51
- Ensembl
- ENSG00000139289
- RefSeq RNA
- NM_007350.3
- RefSeq protein
- NP_031376.3
This gene encodes an evolutionarily conserved proline-histidine rich nuclear protein. The encoded protein may play an important role in the anti-apoptotic effects of insulin-like growth factor-1. [provided by RefSeq, Jul 2008].
Gene Ontology
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
pleckstrin homology like domain family A member 1
- Symbol
- PHLDA1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 12:76,025,447-76,032,560
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 7203
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/22822
- genomic end
- 76031776
- genomic start
- 76419227
- chromosome
- human chromosome 12
- cytogenetic location
- 12q21.2
Sources (3)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- Interactions
- References
- Further reading
Pleckstrin homology-like domain family A member 1 (PHLDA1) is a protein that in humans is encoded by the PHLDA1 gene.
This gene encodes an evolutionarily conserved proline-histidine rich nuclear protein. The encoded protein may play an important role in the anti-apoptotic effects of insulin-like growth factor-1.
Excerpted from Wikipedia’s “PHLDA1” article, available under the CC BY-SA 4.0 licence.