Incidental Mutation 'IGL03217:Gm9755'
ID413512
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9755
Ensembl Gene ENSMUSG00000030735
Gene Namepredicted pseudogene 9755
Synonyms
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.875) question?
Stock #IGL03217
Quality Score
Status
Chromosome8
Chromosomal Location67514000-67515606 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to C at 67514383 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000032981
SMART Domains Protein: ENSMUSP00000091180
Gene: ENSMUSG00000030735

DomainStartEndE-ValueType
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: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aaas A G 15: 102,349,995 I29T probably damaging Het
Adam2 G A 14: 66,034,813 P640L possibly damaging Het
Ccl4 T C 11: 83,662,678 S6P unknown Het
Cd300lf T A 11: 115,124,291 T151S possibly damaging Het
Elk4 A G 1: 132,018,040 T219A probably benign Het
Eml1 G T 12: 108,534,942 E680D probably benign Het
Hmcn1 A T 1: 150,743,667 I1232N possibly damaging Het
Maml2 T C 9: 13,619,999 S170P probably damaging Het
Mettl16 T A 11: 74,817,703 M536K probably damaging Het
Nelfcd G A 2: 174,426,832 A559T possibly damaging Het
Nxf2 T C X: 134,955,532 I287V probably benign Het
Nyap2 A G 1: 81,087,322 D17G probably damaging Het
Pde6b T C 5: 108,419,566 C270R probably damaging Het
Ptchd1 T C X: 155,573,959 D750G probably damaging Het
Rrn3 G A 16: 13,809,011 E490K possibly damaging Het
Slc27a2 G A 2: 126,586,252 G519D possibly damaging Het
Sox5 A G 6: 143,907,497 S352P probably damaging Het
Spg20 G T 3: 55,128,491 probably benign Het
Sult1e1 T C 5: 87,590,088 T45A possibly damaging Het
Tat G A 8: 109,995,186 V242I probably benign Het
Zfp442 A G 2: 150,409,794 probably benign Het
Other mutations in Gm9755
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01655:Gm9755 APN 8 67515233 exon noncoding transcript
IGL03229:Gm9755 APN 8 67514672 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