Incidental Mutation 'IGL01911:Gm17093'
ID179823
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm17093
Ensembl Gene ENSMUSG00000091429
Gene Namepredicted gene 17093
Synonyms
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.310) question?
Stock #IGL01911
Quality Score
Status
Chromosome14
Chromosomal Location44518276-44523444 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to C at 44520820 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
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: 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