Incidental Mutation 'IGL01468:Gm10153'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10153
Ensembl Gene ENSMUSG00000066101
Gene Namepredicted gene 10153
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01468
Quality Score
Chromosomal Location142189427-142190389 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 142190041 bp
Amino Acid Change Serine to Glycine at position 117 (S117G)
Ref Sequence ENSEMBL: ENSMUSP00000147568 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084415] [ENSMUST00000210290]
Predicted Effect unknown
Transcript: ENSMUST00000084415
AA Change: S97G
SMART Domains Protein: ENSMUSP00000081452
Gene: ENSMUSG00000066101
AA Change: S97G

low complexity region 2 140 N/A INTRINSIC
low complexity region 144 153 N/A INTRINSIC
low complexity region 158 174 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000210290
AA Change: S117G
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca7 G A 10: 80,003,877 V781I probably benign Het
Aldh5a1 G T 13: 24,911,553 probably benign Het
Arhgap12 T C 18: 6,057,576 T435A probably benign Het
Atrnl1 G A 19: 57,699,712 V870I probably benign Het
Cerkl A T 2: 79,343,215 probably null Het
Cntnap2 T A 6: 47,271,371 L13* probably null Het
Cr2 G A 1: 195,168,535 P208S probably damaging Het
Dapk1 A G 13: 60,760,798 D1075G probably benign Het
Dhx57 T A 17: 80,255,610 K863* probably null Het
Dnaaf5 C A 5: 139,151,480 probably null Het
Fbxw7 T A 3: 84,972,499 I336K probably benign Het
Ftcd A G 10: 76,584,587 D385G probably benign Het
Gzmb T C 14: 56,260,315 Y156C probably benign Het
Herc3 T A 6: 58,854,895 D83E probably benign Het
Kif2b A G 11: 91,576,365 V364A probably damaging Het
Mknk2 A G 10: 80,667,664 probably benign Het
Olfr1352 A T 10: 78,983,862 Q24L probably damaging Het
Pgm2 A T 4: 99,962,170 N197I possibly damaging Het
Prss39 C T 1: 34,499,400 probably benign Het
Shroom3 T C 5: 92,940,342 V236A probably damaging Het
Slc17a8 C T 10: 89,592,021 probably null Het
Slc24a3 A G 2: 145,613,580 Y463C probably benign Het
Slc4a7 A G 14: 14,737,480 E149G probably damaging Het
Synj1 G A 16: 91,010,172 probably benign Het
Tas2r138 T A 6: 40,612,476 M279L probably benign Het
Terb1 A G 8: 104,482,167 probably benign Het
Tiparp G T 3: 65,552,609 G442* probably null Het
Trmt5 C T 12: 73,281,104 V442I probably benign Het
Tsc2 T C 17: 24,621,097 I383V possibly damaging Het
Uchl4 A G 9: 64,235,716 T160A possibly damaging Het
Vmn2r3 A T 3: 64,274,961 M439K possibly damaging Het
Vmn2r4 A T 3: 64,406,395 N388K probably damaging Het
Vmn2r52 A T 7: 10,158,941 L757Q probably damaging Het
Zfp518a T C 19: 40,916,031 V1468A probably benign Het
Zxdc A T 6: 90,373,779 E404V probably damaging Het
Other mutations in Gm10153
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1224:Gm10153 UTSW 7 142190335 missense unknown
R1490:Gm10153 UTSW 7 142190142 missense unknown
R7571:Gm10153 UTSW 7 142189664 nonsense probably null
R7576:Gm10153 UTSW 7 142190122 missense unknown
Posted On2015-04-16