Incidental Mutation 'IGL01552:Gm10197'
ID 90610
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10197
Ensembl Gene ENSMUSG00000067085
Gene Name predicted gene 10197
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.240) question?
Stock # IGL01552
Quality Score
Status
Chromosome 19
Chromosomal Location 53359997-53360197 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 53360122 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 26 (V26I)
Ref Sequence ENSEMBL: ENSMUSP00000084100 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000003870] [ENSMUST00000025998] [ENSMUST00000086887] [ENSMUST00000111737]
AlphaFold F6QEY5
Predicted Effect silent
Transcript: ENSMUST00000003870
SMART Domains Protein: ENSMUSP00000003870
Gene: ENSMUSG00000025025

DomainStartEndE-ValueType
low complexity region 16 45 N/A INTRINSIC
HLH 140 192 4.4e-11 SMART
low complexity region 230 252 N/A INTRINSIC
Predicted Effect silent
Transcript: ENSMUST00000025998
SMART Domains Protein: ENSMUSP00000025998
Gene: ENSMUSG00000025025

DomainStartEndE-ValueType
low complexity region 11 27 N/A INTRINSIC
HLH 73 125 4.4e-11 SMART
low complexity region 163 185 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000086887
AA Change: V26I

PolyPhen 2 Score 0.455 (Sensitivity: 0.89; Specificity: 0.90)
Predicted Effect silent
Transcript: ENSMUST00000111737
SMART Domains Protein: ENSMUSP00000107366
Gene: ENSMUSG00000025025

DomainStartEndE-ValueType
HLH 37 89 4.4e-11 SMART
low complexity region 127 149 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arl8a T C 1: 135,080,606 (GRCm39) probably null Het
Bivm A G 1: 44,165,933 (GRCm39) N128D probably benign Het
Cfhr4 A G 1: 139,667,040 (GRCm39) Y412H probably damaging Het
Chil3 C A 3: 106,056,164 (GRCm39) G330V probably damaging Het
Dscaml1 A G 9: 45,359,206 (GRCm39) H155R probably damaging Het
Elapor1 A G 3: 108,388,628 (GRCm39) W252R possibly damaging Het
Etl4 T A 2: 20,783,000 (GRCm39) V687D probably damaging Het
Fbxw10 A T 11: 62,748,510 (GRCm39) probably null Het
Gfpt2 G T 11: 49,695,832 (GRCm39) E21* probably null Het
Golim4 T C 3: 75,863,502 (GRCm39) E35G probably damaging Het
Igdcc4 A G 9: 65,029,784 (GRCm39) probably benign Het
Ino80d A G 1: 63,097,136 (GRCm39) probably benign Het
Ipo13 A G 4: 117,758,161 (GRCm39) M734T probably benign Het
Klk1b27 C T 7: 43,704,039 (GRCm39) L61F probably damaging Het
Lamtor5 T C 3: 107,186,324 (GRCm39) V31A probably benign Het
Lrp1 A T 10: 127,424,379 (GRCm39) L769* probably null Het
Nipsnap1 A T 11: 4,839,124 (GRCm39) S135C probably damaging Het
Or4k35 C A 2: 111,100,257 (GRCm39) G152C probably damaging Het
Pparg A T 6: 115,467,083 (GRCm39) H452L probably benign Het
Rab34 C T 11: 78,082,264 (GRCm39) A202V probably damaging Het
Ryr3 T A 2: 112,656,228 (GRCm39) T1923S possibly damaging Het
Sall4 A G 2: 168,598,043 (GRCm39) S266P probably damaging Het
Sh2d4b T C 14: 40,582,605 (GRCm39) Q195R probably benign Het
Sik2 C A 9: 50,828,822 (GRCm39) probably benign Het
Slc25a36 A G 9: 96,961,286 (GRCm39) V111A probably benign Het
Slco1a8 T C 6: 141,933,432 (GRCm39) K451R possibly damaging Het
Sptbn5 A T 2: 119,884,903 (GRCm39) probably benign Het
Tac2 G A 10: 127,561,970 (GRCm39) E25K possibly damaging Het
Tnc A G 4: 63,888,645 (GRCm39) V1807A probably damaging Het
Top3b T C 16: 16,705,687 (GRCm39) probably benign Het
Zfp827 A G 8: 79,802,820 (GRCm39) E464G probably damaging Het
Other mutations in Gm10197
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4092:Gm10197 UTSW 19 53,360,196 (GRCm39) utr 3 prime probably benign
Posted On 2013-12-09