Genular: Defining Cellular Identity and Function

Details for: Phlda2

Gene ID: 22113

Symbol: Phlda2

Ensembl ID: ENSMUSG00000010760

Description: pleckstrin homology like domain, family A, member 2

Associated with

Animal organ morphogenesis
(GO:0009887)
Cytoplasm
(GO:0005737)
Membrane
(GO:0016020)
Phosphatidylinositol phosphate binding
(GO:1901981)
Placenta development
(GO:0001890)
Positive regulation of apoptotic process
(GO:0043065)
Regulation of cell migration
(GO:0030334)
Regulation of embryonic development
(GO:0045995)
Regulation of gene expression
(GO:0010468)
Regulation of glycogen metabolic process
(GO:0070873)
Regulation of growth hormone activity
(GO:1903547)
Regulation of spongiotrophoblast cell proliferation
(GO:0060721)

Other Information

Proteins

Pleckstrin homology-like domain family A member 2

Genular Protein ID: 2500992997

Symbol: PHLA2_MOUSE

Name: Pleckstrin homology-like domain family A member 2

UniProtKB Accession Codes:

O08969

Database IDs:

Citations:

PubMed ID: 9328465

Title: The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis.

PubMed ID: 9328465

DOI: 10.1093/hmg/6.12.2021

PubMed ID: 16141072

Title: The transcriptional landscape of the mammalian genome.

PubMed ID: 16141072

DOI: 10.1126/science.1112014

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 10594239

Title: A novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1: tissue-specific expression, chromosomal location, and parental imprinting.

PubMed ID: 10594239

DOI: 10.1007/s003359901182

PubMed ID: 12374806

Title: Phosphoinositide binding by the pleckstrin homology domains of Ipl and Tih1.

PubMed ID: 12374806

DOI: 10.1074/jbc.m206497200

PubMed ID: 12032310

Title: Placental overgrowth in mice lacking the imprinted gene Ipl.

PubMed ID: 12032310

DOI: 10.1073/pnas.122039999

PubMed ID: 15327781

Title: Placental growth retardation due to loss of imprinting of Phlda2.

PubMed ID: 15327781

DOI: 10.1016/j.mod.2004.05.017

Sequence Information:

Length: 144
Mass: 16727
Checksum: 9BD64B97BA22C1A9
Sequence:

MASKIVMSSK TVKTSDEILC EGELEKRSDS LFQVWKKKRC VLTADRLRLF SGKTSPAKEL 
FFHSILKVDC VEHTSKYVYF TIVTNYYKEI DFRCTVESCW NAAITMALID FQNRRALQDF 
PRYRYQRSES EMPSEPGEQS ALGP

The gene details are incomplete or unavailable at the moment.

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.

Details for: Phlda2

Associated with

Other Information

The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis. PubMed ID: 9328465

The transcriptional landscape of the mammalian genome. PubMed ID: 16141072

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). PubMed ID: 15489334

A novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1: tissue-specific expression, chromosomal location, and parental imprinting. PubMed ID: 10594239

Phosphoinositide binding by the pleckstrin homology domains of Ipl and Tih1. PubMed ID: 12374806

Placental overgrowth in mice lacking the imprinted gene Ipl. PubMed ID: 12032310

Placental growth retardation due to loss of imprinting of Phlda2. PubMed ID: 15327781