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
Is this an essential gene? Possibly non essential (E-score: 0.331) question?
Stock # IGL01431
Quality Score
Status
Chromosome 14
Chromosomal Location 44518276-44523444 bp(+) (GRCm38)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 44521665 bp (GRCm38)
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
4930430A15Rik A T 2: 111,225,395 probably benign Het
Adamts7 A G 9: 90,207,785 I897T possibly damaging Het
Aqp2 G A 15: 99,579,420 V90M possibly damaging Het
Atf6 T C 1: 170,853,002 probably benign Het
Cdh3 T C 8: 106,547,669 Y607H probably damaging Het
Cer1 T A 4: 82,882,831 E198D probably benign Het
Dscam A G 16: 96,652,078 probably null Het
Ecel1 C T 1: 87,151,504 R484H probably damaging Het
Entpd7 C A 19: 43,729,839 H575Q probably benign Het
F11r T C 1: 171,462,909 V279A probably damaging Het
Got1 T A 19: 43,503,049 K321* probably null Het
Gpn1 T C 5: 31,507,538 V302A probably benign Het
Hivep1 G T 13: 42,158,017 K1244N probably damaging Het
Idh3b T C 2: 130,281,897 T116A possibly damaging Het
Itgb4 C A 11: 116,006,457 probably benign Het
Mybl1 G T 1: 9,672,647 L579I probably damaging Het
Myh14 T A 7: 44,614,358 T1694S probably null Het
Mylk3 T C 8: 85,336,401 D537G probably damaging Het
Myo1d A C 11: 80,674,839 F387V probably damaging Het
Nek9 T C 12: 85,314,587 Y448C probably benign Het
Olfr1090 A T 2: 86,754,164 H191Q probably benign Het
Paxbp1 T C 16: 91,035,916 probably benign Het
Retreg2 T A 1: 75,145,105 probably null Het
Ripply3 G A 16: 94,328,543 C16Y possibly damaging Het
Robo3 G A 9: 37,419,111 probably benign Het
Rrm1 C A 7: 102,457,552 probably benign Het
Rsad2 T A 12: 26,448,667 R269S probably benign Het
Sbp A T 17: 23,945,348 probably benign Het
Schip1 A T 3: 68,617,777 Q162L probably damaging Het
Senp1 T C 15: 98,082,263 Y67C probably damaging Het
Slc25a25 C T 2: 32,419,091 R233K probably damaging Het
Smoc1 C A 12: 81,152,751 S220* probably null Het
Stab1 C A 14: 31,148,995 R1299I probably benign Het
Stk17b A G 1: 53,765,915 probably benign Het
Tmc7 T G 7: 118,552,762 D312A probably damaging Het
Vmn1r79 T C 7: 12,176,400 S70P possibly damaging Het
Zfc3h1 C A 10: 115,423,223 T1591K possibly damaging Het
Other mutations in Gm17093
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01401:Gm17093 APN 14 44521527 missense unknown
IGL01911:Gm17093 APN 14 44520820 splice site probably benign
IGL02324:Gm17093 APN 14 44518350 missense unknown
IGL02418:Gm17093 APN 14 44520728 missense unknown
IGL03072:Gm17093 APN 14 44520672 splice site probably benign
R3419:Gm17093 UTSW 14 44521590 missense unknown
R4838:Gm17093 UTSW 14 44518348 missense unknown
R4994:Gm17093 UTSW 14 44519322 missense probably damaging 1.00
R5819:Gm17093 UTSW 14 44521529 missense unknown
R8167:Gm17093 UTSW 14 44520682 missense
R8962:Gm17093 UTSW 14 44520692 missense
Posted On 2013-11-11