Incidental Mutation 'IGL01911:Gm17093'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm17093
Ensembl Gene ENSMUSG00000091429
Gene Namepredicted gene 17093
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.310) question?
Stock #IGL01911
Quality Score
Chromosomal Location44518276-44523444 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to C at 44520820 bp
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect probably benign
Transcript: ENSMUST00000170427
SMART Domains Protein: ENSMUSP00000132075
Gene: ENSMUSG00000091429

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: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A830010M20Rik A G 5: 107,508,580 H903R probably damaging Het
Aox3 T C 1: 58,152,560 F424L probably benign Het
Arhgap11a T C 2: 113,840,732 T301A probably damaging Het
Atp9a C A 2: 168,653,561 R575L probably damaging Het
Brca2 G A 5: 150,567,613 D3088N probably damaging Het
Brd3 G A 2: 27,459,800 T247I probably damaging Het
Cacna1i A G 15: 80,391,732 N1908S probably benign Het
Ccdc40 A T 11: 119,231,971 probably null Het
Cdyl T C 13: 35,863,243 V389A probably damaging Het
Col28a1 A G 6: 8,014,963 F814S probably damaging Het
Cstf3 T C 2: 104,646,631 F149S probably damaging Het
Dglucy T C 12: 100,838,525 Y122H probably damaging Het
Dram1 T C 10: 88,325,341 D222G probably damaging Het
Ets2 G A 16: 95,711,758 R96H probably damaging Het
Gm11563 T A 11: 99,658,701 R76* probably null Het
Gm21738 G A 14: 19,416,979 S144L probably benign Het
Gpi1 A T 7: 34,220,922 V136D probably damaging Het
Hfm1 G A 5: 106,911,544 T204M possibly damaging Het
Itgae T C 11: 73,116,137 I403T probably damaging Het
Krt75 A T 15: 101,568,102 D409E probably damaging Het
Limk2 T G 11: 3,355,340 T76P probably benign Het
Mtus2 A T 5: 148,078,220 M608L probably benign Het
Obscn C A 11: 59,008,595 E979* probably null Het
Olfr598 T G 7: 103,329,273 F262L probably benign Het
P2rx7 C T 5: 122,658,768 A166V probably damaging Het
Pomgnt2 T C 9: 121,982,788 E309G probably benign Het
Pqlc2 A G 4: 139,301,073 V186A probably benign Het
Sbno2 A T 10: 80,069,624 Y199* probably null Het
Setd2 C A 9: 110,617,431 probably null Het
Vmn2r84 T A 10: 130,386,408 I648F probably damaging Het
Vrtn C T 12: 84,650,206 R577W probably benign Het
Znhit6 A G 3: 145,578,098 probably benign Het
Other mutations in Gm17093
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01401:Gm17093 APN 14 44521527 missense unknown
IGL01431:Gm17093 APN 14 44521665 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
Posted On2014-05-07