Incidental Mutation 'IGL02940:Ppp1r36dn'
ID 364456
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ppp1r36dn
Ensembl Gene ENSMUSG00000073000
Gene Name Ppp1r36 downstream neighbor
Synonyms Gm10451
Accession Numbers
Essential gene? Probably non essential (E-score: 0.125) question?
Stock # IGL02940
Quality Score
Status
Chromosome 12
Chromosomal Location 76491271-76495472 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to C at 76497944 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000101281
Predicted Effect noncoding transcript
Transcript: ENSMUST00000219367
Predicted Effect noncoding transcript
Transcript: ENSMUST00000220043
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrg3 T A 8: 95,760,084 (GRCm39) V101D possibly damaging Het
Brca1 T C 11: 101,380,738 (GRCm39) D1765G probably benign Het
Cadps2 T C 6: 23,496,808 (GRCm39) K450R probably benign Het
Cc2d2a A T 5: 43,885,636 (GRCm39) probably null Het
Dbh A G 2: 27,058,321 (GRCm39) Y163C probably damaging Het
Drc7 T A 8: 95,800,925 (GRCm39) I649N probably damaging Het
Dst G A 1: 34,328,668 (GRCm39) A7097T probably benign Het
Fbxo46 A G 7: 18,869,537 (GRCm39) H52R probably benign Het
Gm9944 T C 4: 144,179,709 (GRCm39) probably benign Het
Lsm14a G T 7: 34,070,596 (GRCm39) S100* probably null Het
Mrc2 C T 11: 105,231,997 (GRCm39) R850C probably damaging Het
Musk A G 4: 58,373,364 (GRCm39) D763G probably damaging Het
Ncan C T 8: 70,562,735 (GRCm39) V508I probably benign Het
Or4k35 A T 2: 111,100,073 (GRCm39) L213Q probably damaging Het
Pgls C T 8: 72,046,741 (GRCm39) S18L probably damaging Het
Phf20l1 A G 15: 66,467,000 (GRCm39) T98A probably damaging Het
Prdm13 T A 4: 21,683,421 (GRCm39) K180* probably null Het
Rai1 T C 11: 60,077,844 (GRCm39) V636A probably benign Het
Setd5 T C 6: 113,091,899 (GRCm39) F240S possibly damaging Het
Slco1a5 A G 6: 142,187,731 (GRCm39) L536P probably damaging Het
Stk39 C T 2: 68,051,243 (GRCm39) probably null Het
Tenm2 T C 11: 35,932,471 (GRCm39) T1707A probably damaging Het
Tlr2 A T 3: 83,743,781 (GRCm39) D767E probably benign Het
Tlr7 C T X: 166,090,830 (GRCm39) V219I probably benign Het
Tmprss7 A G 16: 45,476,818 (GRCm39) S815P probably damaging Het
Trav12-1 T A 14: 53,776,017 (GRCm39) W57R probably damaging Het
Uxt T C X: 20,826,025 (GRCm39) E66G possibly damaging Het
Vmn2r45 A T 7: 8,475,369 (GRCm39) M553K probably damaging Het
Vmn2r67 A G 7: 84,785,951 (GRCm39) W685R probably benign Het
Vstm5 A C 9: 15,168,962 (GRCm39) D144A probably damaging Het
Zfp592 A G 7: 80,674,575 (GRCm39) H513R probably damaging Het
Zfp830 T A 11: 82,656,295 (GRCm39) probably benign Het
Zfp990 A G 4: 145,261,492 (GRCm39) probably null Het
Other mutations in Ppp1r36dn
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02691:Ppp1r36dn APN 12 76,498,073 (GRCm39) unclassified noncoding transcript
R0648:Ppp1r36dn UTSW 12 76,498,070 (GRCm39) unclassified noncoding transcript
Posted On 2015-12-18