Incidental Mutation 'IGL01431:Gm17093'
ID 84132
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm17093
Ensembl Gene ENSMUSG00000091429
Gene Name predicted gene 17093
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.195) question?
Stock # IGL01431
Quality Score
Status
Chromosome 14
Chromosomal Location 44755733-44760901 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 44759122 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000170427
SMART Domains Protein: ENSMUSP00000132075
Gene: ENSMUSG00000091429

DomainStartEndE-ValueType
Pfam:Takusan 57 137 2.6e-27 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000227180
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts7 A G 9: 90,089,838 (GRCm39) I897T possibly damaging Het
Aqp2 G A 15: 99,477,301 (GRCm39) V90M possibly damaging Het
Atf6 T C 1: 170,680,571 (GRCm39) probably benign Het
Cdh3 T C 8: 107,274,301 (GRCm39) Y607H probably damaging Het
Cer1 T A 4: 82,801,068 (GRCm39) E198D probably benign Het
Dscam A G 16: 96,453,278 (GRCm39) probably null Het
Ecel1 C T 1: 87,079,226 (GRCm39) R484H probably damaging Het
Entpd7 C A 19: 43,718,278 (GRCm39) H575Q probably benign Het
F11r T C 1: 171,290,477 (GRCm39) V279A probably damaging Het
Got1 T A 19: 43,491,488 (GRCm39) K321* probably null Het
Gpn1 T C 5: 31,664,882 (GRCm39) V302A probably benign Het
Hivep1 G T 13: 42,311,493 (GRCm39) K1244N probably damaging Het
Idh3b T C 2: 130,123,817 (GRCm39) T116A possibly damaging Het
Itgb4 C A 11: 115,897,283 (GRCm39) probably benign Het
Mybl1 G T 1: 9,742,872 (GRCm39) L579I probably damaging Het
Myh14 T A 7: 44,263,782 (GRCm39) T1694S probably null Het
Mylk3 T C 8: 86,063,030 (GRCm39) D537G probably damaging Het
Myo1d A C 11: 80,565,665 (GRCm39) F387V probably damaging Het
Nek9 T C 12: 85,361,361 (GRCm39) Y448C probably benign Het
Or8k40 A T 2: 86,584,508 (GRCm39) H191Q probably benign Het
Paxbp1 T C 16: 90,832,804 (GRCm39) probably benign Het
Potefam1 A T 2: 111,055,740 (GRCm39) probably benign Het
Retreg2 T A 1: 75,121,749 (GRCm39) probably null Het
Ripply3 G A 16: 94,129,402 (GRCm39) C16Y possibly damaging Het
Robo3 G A 9: 37,330,407 (GRCm39) probably benign Het
Rrm1 C A 7: 102,106,759 (GRCm39) probably benign Het
Rsad2 T A 12: 26,498,666 (GRCm39) R269S probably benign Het
Sbp A T 17: 24,164,322 (GRCm39) probably benign Het
Schip1 A T 3: 68,525,110 (GRCm39) Q162L probably damaging Het
Senp1 T C 15: 97,980,144 (GRCm39) Y67C probably damaging Het
Slc25a25 C T 2: 32,309,103 (GRCm39) R233K probably damaging Het
Smoc1 C A 12: 81,199,525 (GRCm39) S220* probably null Het
Stab1 C A 14: 30,870,952 (GRCm39) R1299I probably benign Het
Stk17b A G 1: 53,805,074 (GRCm39) probably benign Het
Tmc7 T G 7: 118,151,985 (GRCm39) D312A probably damaging Het
Vmn1r79 T C 7: 11,910,327 (GRCm39) S70P possibly damaging Het
Zfc3h1 C A 10: 115,259,128 (GRCm39) T1591K possibly damaging Het
Other mutations in Gm17093
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01401:Gm17093 APN 14 44,758,984 (GRCm39) missense unknown
IGL01911:Gm17093 APN 14 44,758,277 (GRCm39) splice site probably benign
IGL02324:Gm17093 APN 14 44,755,807 (GRCm39) missense unknown
IGL02418:Gm17093 APN 14 44,758,185 (GRCm39) missense unknown
IGL03072:Gm17093 APN 14 44,758,129 (GRCm39) splice site probably benign
R3419:Gm17093 UTSW 14 44,759,047 (GRCm39) missense unknown
R4838:Gm17093 UTSW 14 44,755,805 (GRCm39) missense unknown
R4994:Gm17093 UTSW 14 44,756,779 (GRCm39) missense probably damaging 1.00
R5819:Gm17093 UTSW 14 44,758,986 (GRCm39) missense unknown
R8167:Gm17093 UTSW 14 44,758,139 (GRCm39) missense
R8962:Gm17093 UTSW 14 44,758,149 (GRCm39) missense
R9757:Gm17093 UTSW 14 44,758,990 (GRCm39) missense
Posted On 2013-11-11