Incidental Mutation 'IGL01468:Gm10153'
ID278508
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10153
Ensembl Gene ENSMUSG00000066101
Gene Namepredicted gene 10153
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01468
Quality Score
Status
Chromosome7
Chromosomal Location142189427-142190389 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 142190041 bp
ZygosityHeterozygous
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

DomainStartEndE-ValueType
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