Incidental Mutation 'IGL01654:Gm3327'
ID102905
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm3327
Ensembl Gene ENSMUSG00000090594
Gene Namepredicted gene 3327
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.246) question?
Stock #IGL01654
Quality Score
Status
Chromosome14
Chromosomal Location44123851-44129043 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 44124860 bp
ZygosityHeterozygous
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

DomainStartEndE-ValueType
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