Incidental Mutation 'IGL00226:1810062G17Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1810062G17Rik
Ensembl Gene ENSMUSG00000027713
Gene NameRIKEN cDNA 1810062G17 gene
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.114) question?
Stock #IGL00226
Quality Score
Chromosomal Location36475937-36482299 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) C to A at 36479541 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000143650 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000029266] [ENSMUST00000029268] [ENSMUST00000199478]
Predicted Effect probably benign
Transcript: ENSMUST00000029266
SMART Domains Protein: ENSMUSP00000029266
Gene: ENSMUSG00000027712

ANX 30 82 1.65e-24 SMART
ANX 102 154 4.52e-22 SMART
ANX 186 238 3.54e-15 SMART
ANX 261 313 4.52e-22 SMART
Predicted Effect unknown
Transcript: ENSMUST00000029268
AA Change: H55N
SMART Domains Protein: ENSMUSP00000029268
Gene: ENSMUSG00000027713
AA Change: H55N

low complexity region 97 108 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184519
Predicted Effect probably benign
Transcript: ENSMUST00000199478
SMART Domains Protein: ENSMUSP00000143650
Gene: ENSMUSG00000027712

ANX 30 90 4.8e-5 SMART
ANX 91 137 4.9e-9 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5430419D17Rik T A 7: 131,238,094 probably null Het
Ankib1 G A 5: 3,727,573 S439L probably benign Het
Cpd G T 11: 76,797,789 H886N probably benign Het
Dhrs7 A G 12: 72,659,350 C94R probably damaging Het
Dmxl2 T A 9: 54,415,993 H1369L probably damaging Het
Dnah5 A G 15: 28,272,342 N1068S probably benign Het
Dopey1 T A 9: 86,551,679 D2329E possibly damaging Het
Eif1ad A G 19: 5,368,184 probably benign Het
Fam149a T C 8: 45,339,343 R693G probably damaging Het
Fbxw18 T A 9: 109,693,343 T153S probably benign Het
Glg1 A T 8: 111,159,849 C1104S probably damaging Het
Jak3 T C 8: 71,681,697 probably benign Het
Kctd6 C T 14: 8,222,856 R233C possibly damaging Het
Kpna3 A G 14: 61,374,288 V300A possibly damaging Het
Msh5 A T 17: 35,029,881 Y725* probably null Het
Myh2 T C 11: 67,185,233 S749P possibly damaging Het
Olfr1215 A G 2: 89,001,339 probably benign Het
Olfr199 A T 16: 59,216,496 M39K probably damaging Het
Olfr27 T A 9: 39,144,757 I219N possibly damaging Het
Olfr697 T A 7: 106,741,701 T78S probably benign Het
Pdcd1 A G 1: 94,040,135 probably benign Het
Pde5a T A 3: 122,794,357 F391I probably damaging Het
Ptpn12 A C 5: 20,998,668 S371A probably damaging Het
Sec16b A G 1: 157,538,330 Y254C probably damaging Het
Slc2a10 G A 2: 165,514,780 C120Y probably damaging Het
Spink5 G A 18: 43,987,871 probably benign Het
Svil A G 18: 5,099,045 Q1250R probably benign Het
Tph1 G T 7: 46,656,870 N222K probably benign Het
Vmn2r83 A T 10: 79,478,971 D351V probably damaging Het
Zfp54 A G 17: 21,433,559 D105G possibly damaging Het
Zfp623 T C 15: 75,948,203 I336T probably damaging Het
Other mutations in 1810062G17Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2010:1810062G17Rik UTSW 3 36481806 missense unknown
R2495:1810062G17Rik UTSW 3 36481960 missense unknown
R5045:1810062G17Rik UTSW 3 36476178 unclassified probably benign
R5905:1810062G17Rik UTSW 3 36479569 critical splice donor site probably null
R6028:1810062G17Rik UTSW 3 36479569 critical splice donor site probably null
R7120:1810062G17Rik UTSW 3 36481867 missense unknown
R7126:1810062G17Rik UTSW 3 36481839 missense unknown
Posted On2015-04-16