Incidental Mutation 'IGL00971:Gm8979'
ID306623
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm8979
Ensembl Gene ENSMUSG00000095649
Gene Namepredicted gene 8979
SynonymsGm21884
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.200) question?
Stock #IGL00971
Quality Score
Status
Chromosome7
Chromosomal Location106076751-106084046 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) G to A at 106081801 bp
ZygosityHeterozygous
Amino Acid Change
Predicted Effect noncoding transcript
Transcript: ENSMUST00000176647
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183386
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930596D02Rik C T 14: 35,810,213 C135Y possibly damaging Het
Afdn T A 17: 13,852,313 probably benign Het
Akap10 A G 11: 61,904,796 V347A possibly damaging Het
Ankrd11 A G 8: 122,895,353 S587P probably damaging Het
Ces1g T C 8: 93,303,032 Y524C probably damaging Het
Cubn T C 2: 13,278,408 N3573S possibly damaging Het
Cyp1a1 G T 9: 57,700,707 C206F probably damaging Het
Fam166b A G 4: 43,428,377 L51P probably damaging Het
Fbxo30 T C 10: 11,290,298 Y255H probably benign Het
Ggnbp2 T C 11: 84,840,404 I295V possibly damaging Het
Gpatch8 A G 11: 102,479,917 Y932H unknown Het
Heatr6 C T 11: 83,759,309 P197L probably damaging Het
Helb T C 10: 120,094,263 D737G possibly damaging Het
Helz A T 11: 107,663,653 I1226F possibly damaging Het
Ipo11 A T 13: 106,856,769 I749N probably damaging Het
Ipo13 T C 4: 117,914,367 E2G possibly damaging Het
Jam3 A C 9: 27,101,892 D127E probably damaging Het
Kif16b G T 2: 142,711,744 Q1045K probably benign Het
Kin T C 2: 10,090,348 W121R possibly damaging Het
Man1b1 T G 2: 25,343,325 S237A possibly damaging Het
Mmel1 C T 4: 154,887,832 probably benign Het
Morn4 T C 19: 42,076,120 N143S possibly damaging Het
Nlrp4b A G 7: 10,714,955 T362A possibly damaging Het
Ntpcr C T 8: 125,747,762 T153M probably damaging Het
Olfr62 T A 4: 118,666,278 F254I probably damaging Het
Pdzd2 A G 15: 12,374,718 L1777P probably benign Het
Postn A G 3: 54,369,276 N192S possibly damaging Het
Prkar1a A T 11: 109,661,051 Y122F probably benign Het
Serpinb7 A G 1: 107,428,246 probably benign Het
Setd3 A T 12: 108,160,237 I121N probably damaging Het
Slamf7 T A 1: 171,639,242 I132L probably benign Het
Syt4 T C 18: 31,447,174 probably benign Het
Tesc G A 5: 118,056,439 probably null Het
Tsc1 C A 2: 28,670,940 S270* probably null Het
Wap C A 11: 6,636,808 C97F probably damaging Het
Zfp451 A G 1: 33,783,153 S155P probably benign Het
Zfp469 A G 8: 122,269,733 probably benign Het
Zfp51 C T 17: 21,463,582 T153M probably benign Het
Zfp579 A G 7: 4,993,391 I507T probably damaging Het
Other mutations in Gm8979
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01125:Gm8979 APN 7 106082814 missense unknown 0.00
IGL01392:Gm8979 APN 7 106083755 missense probably benign 0.01
R1184:Gm8979 UTSW 7 106083952 missense probably benign 0.03
R1411:Gm8979 UTSW 7 106083479 missense probably benign 0.39
R2198:Gm8979 UTSW 7 106083551 missense probably benign 0.00
R2311:Gm8979 UTSW 7 106083590 missense probably damaging 0.99
R2380:Gm8979 UTSW 7 106082167 missense possibly damaging 0.86
R3825:Gm8979 UTSW 7 106083573 missense possibly damaging 0.92
R4397:Gm8979 UTSW 7 106082923 exon noncoding transcript
R4693:Gm8979 UTSW 7 106082378 exon noncoding transcript
R4787:Gm8979 UTSW 7 106081834 exon noncoding transcript
R4840:Gm8979 UTSW 7 106081420 exon noncoding transcript
R4972:Gm8979 UTSW 7 106083314 exon noncoding transcript
R5221:Gm8979 UTSW 7 106083974 exon noncoding transcript
R5296:Gm8979 UTSW 7 106081848 exon noncoding transcript
Posted On2015-04-16