Incidental Mutation 'IGL02624:Gm5070'
ID300995
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5070
Ensembl Gene ENSMUSG00000096177
Gene Namepredicted gene 5070
Synonyms
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.255) question?
Stock #IGL02624
Quality Score
Status
Chromosome3
Chromosomal Location95410346-95411207 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to G at 95410908 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000177599
SMART Domains Protein: ENSMUSP00000136183
Gene: ENSMUSG00000096177

DomainStartEndE-ValueType
low complexity region 2 37 N/A INTRINSIC
Pfam:Ribosomal_S5 86 150 8.1e-33 PFAM
Pfam:Ribosomal_S5_C 169 240 6.6e-30 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000198054
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A930004D18Rik A G 2: 18,027,193 V38A unknown Het
Armc8 T C 9: 99,527,069 probably benign Het
Brk1 T G 6: 113,604,844 I22M possibly damaging Het
Cd3g A G 9: 44,974,161 probably null Het
Cep192 T C 18: 67,880,795 V2422A probably benign Het
Ces2g T C 8: 104,964,748 V172A probably damaging Het
Clcn2 G T 16: 20,703,348 S830R probably damaging Het
Cyp26b1 T C 6: 84,584,339 S114G probably benign Het
Dnali1 T C 4: 125,058,998 Q244R probably benign Het
Entpd1 A T 19: 40,726,058 K204* probably null Het
Gpsm2 G T 3: 108,682,033 D596E probably benign Het
Hectd1 C T 12: 51,762,450 A1743T possibly damaging Het
Kcnq5 T G 1: 21,402,430 L845F probably benign Het
Lmx1a G T 1: 167,844,623 probably benign Het
Lrp1 A T 10: 127,572,422 I1795N probably damaging Het
Lsp1 C T 7: 142,490,551 probably benign Het
Mcm6 C T 1: 128,349,448 A213T possibly damaging Het
Mylk G T 16: 34,929,896 V1202L probably benign Het
Myo5b T C 18: 74,714,939 Y1083H probably damaging Het
Ncoa5 T A 2: 165,013,061 D47V probably damaging Het
Npat C T 9: 53,566,810 T954I probably damaging Het
Olfr1367 A G 13: 21,347,512 T195A probably benign Het
Olfr491 A T 7: 108,316,923 T10S probably benign Het
Pfkm T C 15: 98,126,395 I428T probably benign Het
Rai1 T C 11: 60,188,743 F1211S probably damaging Het
Reln T C 5: 22,103,357 E338G probably benign Het
Tbx18 T C 9: 87,727,406 Y192C probably damaging Het
Tex21 T A 12: 76,214,624 D250V probably damaging Het
Tpo A G 12: 30,100,414 V489A probably benign Het
Tspo T C 15: 83,571,415 M1T probably null Het
Wdr38 A T 2: 38,998,412 N7I probably damaging Het
Wnk2 C T 13: 49,102,802 G281D probably damaging Het
Zfhx2 T C 14: 55,066,628 T1300A probably benign Het
Other mutations in Gm5070
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02210:Gm5070 APN 3 95410625 unclassified noncoding transcript
IGL02492:Gm5070 APN 3 95411043 unclassified noncoding transcript
R1822:Gm5070 UTSW 3 95411044 unclassified noncoding transcript
R5807:Gm5070 UTSW 3 95410654 unclassified noncoding transcript
Posted On2015-04-16