|Institutional Source||Beutler Lab|
|Gene Name||pleckstrin homology domain interacting protein|
|Synonyms||Wdr11, 2810004D21Rik, 4632404O06Rik, Ndrp|
|Is this an essential gene?||Essential (E-score: 1.000)|
|Stock #||R1658 (G1)|
|Chromosomal Location||82866159-82975516 bp(-) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||A to G at 82871498 bp|
|Amino Acid Change||Valine to Alanine at position 1731 (V1731A)|
|Ref Sequence||ENSEMBL: ENSMUSP00000034787 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000034787]|
|Predicted Effect||probably benign
AA Change: V1731A
PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
AA Change: V1731A
|Predicted Effect||noncoding transcript
|Coding Region Coverage||
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that binds to the insulin receptor substrate 1 protein and regulates glucose transporter translocation in skeletal muscle cells. The encoded protein may also regulate growth and survival of pancreatic beta cells. Elevated copy number of this gene may be associated with melanoma severity and the encoded protein may promote melanoma metastasis in human patients. [provided by RefSeq, Oct 2016]
PHENOTYPE: Mice homozygous for a gene trapped allele exhibit postnatal and premature lethality associated with reduced body size, small myocardial cells and hepatocytes, hypoglycemia, increased insulin sensitivity, and reduced cell growth. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Phip||
(F):5'- CAAGGAGGTGTCCTCGAACAACAG -3'
(R):5'- ACACCAGCAGTGGTGAAGTGAC -3'
(F):5'- AGCTGTCTCTGTTCTTCCTCC -3'
(R):5'- TGTGCAAAGCAGGAAAACTC -3'