|Institutional Source||Beutler Lab|
|Gene Name||unc-5 netrin receptor B|
|Synonyms||Unc5h2, D10Bwg0792e, 6330415E02Rik|
|Is this an essential gene?||Essential (E-score: 1.000)|
|Stock #||R4116 (G1)|
|Chromosomal Location||60762593-60831581 bp(-) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||G to T at 60774700 bp|
|Amino Acid Change||Threonine to Lysine at position 446 (T446K)|
|Ref Sequence||ENSEMBL: ENSMUSP00000077080 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000077925] [ENSMUST00000218637]|
|Predicted Effect||probably damaging
AA Change: T446K
PolyPhen 2 Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)
AA Change: T446K
|Predicted Effect||noncoding transcript
|Predicted Effect||possibly damaging
AA Change: T435K
PolyPhen 2 Score 0.956 (Sensitivity: 0.79; Specificity: 0.95)
|Coding Region Coverage||
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the netrin family of receptors. This particular protein mediates the repulsive effect of netrin-1 and is a vascular netrin receptor. This encoded protein is also in a group of proteins called dependence receptors (DpRs) which are involved in pro- and anti-apoptotic processes. Many DpRs are involved in embryogenesis and in cancer progression. Two alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2011]
PHENOTYPE: Mice homozygous for a severely hypomorphic allele exhibit background sensitive lethality during organogenesis. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Unc5b||
(F):5'- AGAAATCGCCTGGGTACGTG -3'
(R):5'- CCAATCTGGCCACTAGTTTCCTATAG -3'
(F):5'- GGAGGACACCCAGCAGG -3'
(R):5'- TATAGCAGTTGAGCCTTCCGCAG -3'