Incidental Mutation 'IGL02485:Gm17175'
ID 295409
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm17175
Ensembl Gene ENSMUSG00000091142
Gene Name predicted gene 17175
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # IGL02485
Quality Score
Status
Chromosome 14
Chromosomal Location 51806349-51811520 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) T to C at 51807068 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000127078 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096170] [ENSMUST00000162998] [ENSMUST00000172117]
AlphaFold E9Q528
Predicted Effect probably benign
Transcript: ENSMUST00000096170
SMART Domains Protein: ENSMUSP00000093884
Gene: ENSMUSG00000079244

DomainStartEndE-ValueType
Pfam:Takusan 56 144 1.3e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000162998
SMART Domains Protein: ENSMUSP00000125409
Gene: ENSMUSG00000068399

DomainStartEndE-ValueType
Pfam:Takusan 35 115 2.2e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000172117
SMART Domains Protein: ENSMUSP00000127078
Gene: ENSMUSG00000091142

DomainStartEndE-ValueType
Pfam:Takusan 23 103 3.3e-26 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agl A G 3: 116,572,729 (GRCm39) S841P probably benign Het
Cd59b A C 2: 103,911,449 (GRCm39) probably benign Het
Dop1b T C 16: 93,567,710 (GRCm39) L1379P probably damaging Het
Ercc2 G A 7: 19,127,970 (GRCm39) A433T possibly damaging Het
Gm5150 A T 3: 16,044,916 (GRCm39) I103N probably damaging Het
Igf1 A G 10: 87,700,608 (GRCm39) M11V probably benign Het
Incenp T C 19: 9,870,732 (GRCm39) N299S unknown Het
Maneal A T 4: 124,750,563 (GRCm39) S398T probably damaging Het
Map1a A G 2: 121,129,769 (GRCm39) N195S probably damaging Het
Mars2 T C 1: 55,276,750 (GRCm39) F118L possibly damaging Het
Mast4 A G 13: 102,872,004 (GRCm39) S2263P probably benign Het
Mrgprb1 C A 7: 48,097,465 (GRCm39) R149L possibly damaging Het
Myo1d T C 11: 80,557,407 (GRCm39) D511G probably damaging Het
Ntan1 T C 16: 13,652,540 (GRCm39) probably benign Het
Nxf2 A G X: 133,857,216 (GRCm39) F158L probably damaging Het
Odr4 A G 1: 150,239,240 (GRCm39) probably null Het
Or10g3b T A 14: 52,587,501 (GRCm39) M1L possibly damaging Het
Potefam1 A T 2: 111,058,670 (GRCm39) V94E probably damaging Het
Trpm1 C T 7: 63,918,862 (GRCm39) A734V possibly damaging Het
Upf2 G A 2: 6,032,102 (GRCm39) E883K unknown Het
Ush1c T C 7: 45,878,674 (GRCm39) I83V probably damaging Het
Vmn2r60 C A 7: 41,844,890 (GRCm39) T751N possibly damaging Het
Zfp146 A G 7: 29,862,015 (GRCm39) I9T probably benign Het
Zfp592 G A 7: 80,687,718 (GRCm39) probably benign Het
Zswim8 C T 14: 20,761,955 (GRCm39) L243F probably damaging Het
Other mutations in Gm17175
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00966:Gm17175 APN 14 51,810,526 (GRCm39) missense possibly damaging 0.77
IGL01347:Gm17175 APN 14 51,808,307 (GRCm39) missense probably damaging 0.99
IGL01553:Gm17175 APN 14 51,808,279 (GRCm39) missense probably benign 0.00
IGL02436:Gm17175 APN 14 51,807,108 (GRCm39) utr 3 prime probably benign
IGL03171:Gm17175 APN 14 51,809,065 (GRCm39) missense probably damaging 1.00
R4120:Gm17175 UTSW 14 51,810,534 (GRCm39) missense probably damaging 0.97
R4614:Gm17175 UTSW 14 51,809,042 (GRCm39) missense probably benign 0.28
R6496:Gm17175 UTSW 14 51,810,534 (GRCm39) missense probably benign 0.05
R6817:Gm17175 UTSW 14 51,810,478 (GRCm39) missense possibly damaging 0.91
R7000:Gm17175 UTSW 14 51,811,418 (GRCm39) start codon destroyed probably null
R7814:Gm17175 UTSW 14 51,811,492 (GRCm39) start gained probably benign
R8074:Gm17175 UTSW 14 51,809,080 (GRCm39) missense probably damaging 0.97
R8423:Gm17175 UTSW 14 51,809,070 (GRCm39) missense possibly damaging 0.80
R9608:Gm17175 UTSW 14 51,809,099 (GRCm39) missense probably damaging 0.99
Posted On 2015-04-16