Incidental Mutation 'IGL00324:Gm17027'
ID332254
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm17027
Ensembl Gene ENSMUSG00000093926
Gene Namepredicted gene 17027
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL00324
Quality Score
Status
Chromosome14
Chromosomal Location42157290-42162622 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 42159310 bp
ZygosityHeterozygous
Amino Acid Change Asparagine to Lysine at position 196 (N196K)
Gene Model predicted gene model for transcript(s):
Predicted Effect unknown
Transcript: ENSMUST00000171202
AA Change: N196K
SMART Domains Protein: ENSMUSP00000128369
Gene: ENSMUSG00000093926
AA Change: N196K

DomainStartEndE-ValueType
Pfam:Takusan 57 137 9.1e-27 PFAM
coiled coil region 161 186 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcd3 T C 3: 121,776,993 probably benign Het
Cdk12 T A 11: 98,245,388 L1156Q unknown Het
Ctsl T C 13: 64,368,168 Y66C probably damaging Het
Esd C T 14: 74,736,027 H21Y probably damaging Het
Fcrlb A C 1: 170,908,824 Y128D possibly damaging Het
Gm4553 T C 7: 142,165,227 S155G unknown Het
Hpcal1 A G 12: 17,791,145 S175G probably benign Het
Itgam A T 7: 128,085,661 D401V probably damaging Het
Kank1 A G 19: 25,411,758 T932A probably benign Het
Lmod1 A G 1: 135,364,478 K357R probably benign Het
Muc4 A G 16: 32,778,812 I3271V probably benign Het
Nlrc5 A G 8: 94,521,479 K1692E probably damaging Het
Ocln A G 13: 100,535,013 W279R probably damaging Het
Olfr1181 T C 2: 88,423,786 I80V probably benign Het
Pcsk1 A G 13: 75,132,087 K677R probably benign Het
Pitrm1 T A 13: 6,568,666 L586Q probably damaging Het
Plppr3 G A 10: 79,866,669 S217L probably damaging Het
Pnldc1 A T 17: 12,905,758 probably benign Het
Pramef12 A G 4: 144,394,740 L238P possibly damaging Het
Pramef8 T A 4: 143,416,667 M1K probably null Het
Sema6b C T 17: 56,130,048 D204N probably damaging Het
Slc12a5 A G 2: 164,997,121 N1063S probably damaging Het
Tg T C 15: 66,693,424 V1205A probably benign Het
Tmem260 T C 14: 48,486,879 F205L probably benign Het
Trappc11 A T 8: 47,503,302 probably benign Het
Tsen34 A G 7: 3,700,531 *296W probably null Het
Ubr2 A G 17: 46,986,060 probably benign Het
Vmn2r23 T A 6: 123,729,725 W505R possibly damaging Het
Wbp11 A G 6: 136,821,670 probably benign Het
Znfx1 A T 2: 167,036,729 M1909K possibly damaging Het
Other mutations in Gm17027
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6649:Gm17027 UTSW 14 42159279 missense unknown
Posted On2015-08-05