Incidental Mutation 'IGL02424:Gm7732'
ID 292827
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7732
Ensembl Gene ENSMUSG00000096857
Gene Name predicted gene 7732
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.269) question?
Stock # IGL02424
Quality Score
Status
Chromosome 17
Chromosomal Location 21349613-21351139 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 21349709 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: ENSMUST00000170486
SMART Domains Protein: ENSMUSP00000126785
Gene: ENSMUSG00000096857

DomainStartEndE-ValueType
low complexity region 6 23 N/A INTRINSIC
S_TKc 28 276 8.33e-94 SMART
low complexity region 436 451 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930579F01Rik A G 3: 137,880,466 (GRCm39) probably benign Het
A930011G23Rik A G 5: 99,377,236 (GRCm39) S404P probably damaging Het
A930011G23Rik G A 5: 99,377,241 (GRCm39) P402L probably damaging Het
Abl1 G A 2: 31,691,144 (GRCm39) V888I probably benign Het
Adcy9 G T 16: 4,106,461 (GRCm39) N884K probably damaging Het
Alyref T C 11: 120,486,133 (GRCm39) N176D probably benign Het
Amtn T C 5: 88,529,456 (GRCm39) probably benign Het
Baz1b T C 5: 135,246,833 (GRCm39) Y761H probably damaging Het
Cckar T A 5: 53,863,770 (GRCm39) T64S possibly damaging Het
Csmd1 A G 8: 16,142,340 (GRCm39) F1521S probably benign Het
Cyp11b1 T C 15: 74,711,085 (GRCm39) T198A probably benign Het
Def8 G T 8: 124,186,387 (GRCm39) L399F possibly damaging Het
Epha7 A T 4: 28,948,790 (GRCm39) probably benign Het
Ets1 T A 9: 32,665,589 (GRCm39) Y181* probably null Het
Fas A T 19: 34,304,434 (GRCm39) M232L probably damaging Het
Fkbp10 T A 11: 100,306,782 (GRCm39) V37E probably damaging Het
Galnt3 A G 2: 65,926,132 (GRCm39) probably null Het
Gdap1 T C 1: 17,231,402 (GRCm39) V249A probably damaging Het
Gm5356 T A 8: 89,913,594 (GRCm39) noncoding transcript Het
Gpr3 G T 4: 132,938,405 (GRCm39) A89E probably damaging Het
Kat2a A G 11: 100,601,973 (GRCm39) probably null Het
Kit T G 5: 75,799,766 (GRCm39) D499E probably benign Het
Kmt2a C T 9: 44,735,932 (GRCm39) probably benign Het
Med12l T C 3: 59,000,143 (GRCm39) L666P probably benign Het
Mmp2 T G 8: 93,562,635 (GRCm39) C291G probably damaging Het
Neb A G 2: 52,154,203 (GRCm39) Y2303H probably damaging Het
Or14a259 C A 7: 86,012,688 (GRCm39) V286L probably benign Het
Or1d2 T A 11: 74,256,299 (GRCm39) M268K probably benign Het
Or1o2 T C 17: 37,543,263 (GRCm39) probably benign Het
Pde1b T A 15: 103,436,646 (GRCm39) probably benign Het
Prl7a2 A C 13: 27,851,953 (GRCm39) C9G probably null Het
Rabl6 A G 2: 25,477,469 (GRCm39) V327A probably benign Het
Robo2 T A 16: 73,770,189 (GRCm39) I516F possibly damaging Het
Ror2 C T 13: 53,264,764 (GRCm39) S764N probably damaging Het
Slc35a3 G A 3: 116,488,267 (GRCm39) T140I possibly damaging Het
Slc38a7 A G 8: 96,568,200 (GRCm39) V395A probably damaging Het
Stag3 T A 5: 138,280,247 (GRCm39) C37* probably null Het
Stag3 T C 5: 138,289,628 (GRCm39) L266P probably damaging Het
Strn A G 17: 78,991,780 (GRCm39) S180P probably damaging Het
Sulf1 A G 1: 12,867,064 (GRCm39) T83A probably benign Het
Vmn1r69 T C 7: 10,314,585 (GRCm39) I49V probably benign Het
Vrk2 G A 11: 26,426,564 (GRCm39) P387L probably benign Het
Xdh A T 17: 74,233,565 (GRCm39) M183K probably benign Het
Other mutations in Gm7732
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02549:Gm7732 APN 17 21,349,649 (GRCm39) exon noncoding transcript
R0718:Gm7732 UTSW 17 21,350,106 (GRCm39) exon noncoding transcript
R1612:Gm7732 UTSW 17 21,350,177 (GRCm39) exon noncoding transcript
Posted On 2015-04-16