Incidental Mutation 'IGL01654:Gm3327'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm3327
Ensembl Gene ENSMUSG00000090594
Gene Namepredicted gene 3327
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.246) question?
Stock #IGL01654
Quality Score
Chromosomal Location44123851-44129043 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 44124860 bp
Amino Acid Change Glutamic Acid to Glycine at position 72 (E72G)
Gene Model predicted gene model for transcript(s):
Predicted Effect unknown
Transcript: ENSMUST00000168906
AA Change: E72G
SMART Domains Protein: ENSMUSP00000130980
Gene: ENSMUSG00000090594
AA Change: E72G

Pfam:Takusan 57 137 4.3e-27 PFAM
coiled coil region 164 186 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000226712
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700034J05Rik T A 6: 146,953,340 E68V probably damaging Het
Abcb1a T C 5: 8,715,065 probably null Het
Abcg2 T A 6: 58,683,321 probably null Het
Adgrf5 T C 17: 43,451,170 I1252T possibly damaging Het
Apol10b A T 15: 77,588,796 D19E probably benign Het
Bbs9 T A 9: 22,490,942 probably null Het
Bod1l T C 5: 41,818,176 T1932A probably damaging Het
C2cd5 A G 6: 143,081,407 V124A probably benign Het
Cd151 T A 7: 141,470,362 I170N probably benign Het
Ckap5 C T 2: 91,577,609 H827Y probably benign Het
Clk3 C T 9: 57,751,763 V572M probably damaging Het
Ddrgk1 T C 2: 130,654,709 D245G probably damaging Het
Enpp5 A G 17: 44,081,175 D165G possibly damaging Het
Epha6 A C 16: 59,839,303 N817K probably benign Het
Fbxw14 T C 9: 109,286,580 probably benign Het
Fes C T 7: 80,386,810 probably null Het
Gemin4 A T 11: 76,213,398 L179H probably damaging Het
Gm4847 C T 1: 166,638,348 R224Q probably damaging Het
Lonp2 T C 8: 86,714,086 V357A probably damaging Het
Mc2r A G 18: 68,408,072 I50T probably benign Het
Mmp19 C T 10: 128,798,520 A310V probably damaging Het
Naip6 C T 13: 100,299,345 R890Q probably benign Het
Npdc1 T C 2: 25,407,637 S101P possibly damaging Het
Phldb1 T C 9: 44,718,357 probably null Het
Pkd2l1 T C 19: 44,154,223 N460S probably damaging Het
Pnpo A G 11: 96,943,729 probably null Het
Prkcq A T 2: 11,283,843 T536S probably damaging Het
Rft1 T A 14: 30,676,880 V269E probably damaging Het
Skint4 A T 4: 112,120,057 I215F probably damaging Het
Slc12a5 G A 2: 164,973,755 D41N possibly damaging Het
Srp68 T C 11: 116,247,812 probably benign Het
Wdr17 T C 8: 54,662,879 T623A probably damaging Het
Zfand2a A G 5: 139,482,068 probably benign Het
Zfp644 T C 5: 106,635,930 Y917C probably damaging Het
Zmym6 C T 4: 127,123,726 S1008L probably damaging Het
Other mutations in Gm3327
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2496:Gm3327 UTSW 14 44126263 missense unknown
R5098:Gm3327 UTSW 14 44124835 missense unknown
R7054:Gm3327 UTSW 14 44126275 missense
R7384:Gm3327 UTSW 14 44124877 missense
Z1177:Gm3327 UTSW 14 44124800 missense
Posted On2014-01-21