Incidental Mutation 'IGL03229:Gm9755'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9755
Ensembl Gene ENSMUSG00000030735
Gene Namepredicted pseudogene 9755
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.886) question?
Stock #IGL03229
Quality Score
Chromosomal Location67514000-67515606 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) C to A at 67514672 bp
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000032981
SMART Domains Protein: ENSMUSP00000091180
Gene: ENSMUSG00000030735

Pfam:GTP_EFTU 55 249 1.4e-55 PFAM
Pfam:GTP_EFTU_D2 272 341 4.8e-17 PFAM
Pfam:GTP_EFTU_D3 345 440 1.5e-25 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb4 T C 5: 8,940,936 I832T probably damaging Het
Adcyap1r1 T C 6: 55,478,123 S124P probably damaging Het
Coq4 A G 2: 29,788,485 D41G probably benign Het
Cpb1 A T 3: 20,249,837 Y354* probably null Het
Dip2b T C 15: 100,207,838 probably benign Het
Dmxl2 C T 9: 54,404,172 R1755H probably damaging Het
Dyrk4 G T 6: 126,886,642 probably benign Het
E2f7 T C 10: 110,754,346 V120A probably benign Het
Fsip2 A T 2: 82,978,076 I1580F possibly damaging Het
Gm7030 C T 17: 36,127,722 G259E probably damaging Het
Gprc6a T G 10: 51,616,603 N480T probably damaging Het
Hdlbp T C 1: 93,430,187 I331V probably benign Het
Heatr6 G T 11: 83,781,445 G1093V probably benign Het
Hist2h2ac C T 3: 96,220,637 A70T probably damaging Het
Kri1 T C 9: 21,282,070 E162G probably damaging Het
Nckipsd T C 9: 108,811,614 V116A probably benign Het
Nek10 A G 14: 14,986,686 H997R probably benign Het
Nov A G 15: 54,749,308 T238A probably benign Het
Nxph1 A G 6: 9,247,830 Y267C probably damaging Het
Olfr1090 A T 2: 86,754,016 C241S probably damaging Het
Olfr294 T C 7: 86,616,078 D189G probably benign Het
Ppip5k2 A T 1: 97,728,961 V829E probably damaging Het
Prkcz A C 4: 155,262,506 S573A probably benign Het
Prl2c1 T A 13: 27,856,629 probably benign Het
Rgs22 T A 15: 36,015,779 probably benign Het
Scn1a T A 2: 66,299,713 I1253F probably damaging Het
Tarm1 A G 7: 3,496,897 C146R probably damaging Het
Tor2a A T 2: 32,759,692 I189F probably damaging Het
Trappc9 A T 15: 73,058,456 L17Q probably damaging Het
Trim45 T A 3: 100,923,069 L53Q probably damaging Het
Ubr7 T C 12: 102,769,155 L291P probably damaging Het
Unc79 T C 12: 103,134,539 V1878A probably damaging Het
Wdr90 T C 17: 25,845,463 probably benign Het
Xpnpep1 T C 19: 53,025,380 H42R probably benign Het
Zfp750 G A 11: 121,512,952 H366Y possibly damaging Het
Zmynd11 A G 13: 9,689,565 C462R probably damaging Het
Other mutations in Gm9755
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01655:Gm9755 APN 8 67515233 exon noncoding transcript
IGL03217:Gm9755 APN 8 67514383 exon noncoding transcript
R1110:Gm9755 UTSW 8 67515058 exon noncoding transcript
R1630:Gm9755 UTSW 8 67514660 exon noncoding transcript
R4257:Gm9755 UTSW 8 67514477 exon noncoding transcript
R4743:Gm9755 UTSW 8 67514277 exon noncoding transcript
R5960:Gm9755 UTSW 8 67515188 exon noncoding transcript
Posted On2016-08-02