Incidental Mutation 'IGL00226:1810062G17Rik'
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ID306788
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1810062G17Rik
Ensembl Gene ENSMUSG00000027713
Gene NameRIKEN cDNA 1810062G17 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.087) question?
Stock #IGL00226
Quality Score
Status
Chromosome3
Chromosomal Location36475937-36482299 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) C to A at 36479541 bp
ZygosityHeterozygous
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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
Posted On2015-04-16