Incidental Mutation 'IGL01764:Gm10639'
ID153651
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10639
Ensembl Gene ENSMUSG00000074179
Gene Namepredicted gene 10639
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.093) question?
Stock #IGL01764
Quality Score
Status
Chromosome9
Chromosomal Location78289923-78305525 bp(+) (GRCm38)
Type of Mutationsplice site (4 bp from exon)
DNA Base Change (assembly) A to T at 78304507 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000113635 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000119823] [ENSMUST00000121273]
Predicted Effect probably null
Transcript: ENSMUST00000119823
SMART Domains Protein: ENSMUSP00000113211
Gene: ENSMUSG00000074179

DomainStartEndE-ValueType
Pfam:GST_N 5 77 3.7e-22 PFAM
Pfam:GST_C 99 192 5.9e-21 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000121273
SMART Domains Protein: ENSMUSP00000113635
Gene: ENSMUSG00000074179

DomainStartEndE-ValueType
Pfam:GST_N 5 77 7.8e-20 PFAM
Pfam:GST_C 99 192 1.5e-18 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126625
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700113H08Rik A T 10: 87,074,046 M1L probably benign Het
BC025920 T A 10: 81,609,150 Y36N probably damaging Het
BC030867 T C 11: 102,255,596 C233R probably benign Het
Cdk11b G A 4: 155,628,803 R112H possibly damaging Het
Ctu2 G A 8: 122,479,422 probably benign Het
Ddx56 A C 11: 6,265,692 V219G probably null Het
Dnah14 T C 1: 181,744,777 V2891A probably benign Het
Fbn2 G T 18: 58,045,351 N1938K probably damaging Het
Fbxw20 A G 9: 109,223,359 M302T possibly damaging Het
Fhdc1 G A 3: 84,444,735 A1061V possibly damaging Het
Gpat2 T C 2: 127,427,536 I36T probably benign Het
Hmcn2 A G 2: 31,405,630 E2617G possibly damaging Het
Krba1 C T 6: 48,415,836 R895W probably benign Het
Large2 G T 2: 92,367,186 probably benign Het
Lrp1b C T 2: 40,697,442 V165M unknown Het
Mapk1 T A 16: 16,983,733 M36K possibly damaging Het
Nf1 A G 11: 79,384,187 T25A probably benign Het
Nrxn3 G A 12: 90,204,750 V1316I possibly damaging Het
Pik3r4 G A 9: 105,685,122 probably benign Het
Plekhh1 G T 12: 79,054,905 A250S probably benign Het
Polr3g G A 13: 81,682,119 T145M possibly damaging Het
Prss32 A G 17: 23,856,111 D145G probably damaging Het
Rab11fip3 T C 17: 26,068,693 K162R probably benign Het
Spag7 A G 11: 70,664,107 probably benign Het
Spata2l T A 8: 123,234,175 Q125L probably benign Het
Tlr9 G T 9: 106,225,805 C765F probably damaging Het
Trip11 A T 12: 101,884,631 I773N probably damaging Het
Vcan T G 13: 89,725,388 T116P probably damaging Het
Vmn2r22 C T 6: 123,650,420 probably null Het
Yme1l1 T C 2: 23,162,544 I70T probably benign Het
Zfp938 T A 10: 82,227,790 probably benign Het
Other mutations in Gm10639
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0117:Gm10639 UTSW 9 78304418 missense probably damaging 1.00
R0480:Gm10639 UTSW 9 78302817 missense probably benign 0.08
R0645:Gm10639 UTSW 9 78299021 missense possibly damaging 0.93
R2509:Gm10639 UTSW 9 78294807 start codon destroyed probably null 1.00
R2510:Gm10639 UTSW 9 78294807 start codon destroyed probably null 1.00
R2519:Gm10639 UTSW 9 78304439 missense probably damaging 0.98
R4797:Gm10639 UTSW 9 78304397 missense probably benign 0.01
R6174:Gm10639 UTSW 9 78304455 nonsense probably null
Posted On2014-02-04