Incidental Mutation 'IGL00226:1810062G17Rik'
ID 306788
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1810062G17Rik
Ensembl Gene ENSMUSG00000027713
Gene Name RIKEN cDNA 1810062G17 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.185) question?
Stock # IGL00226
Quality Score
Status
Chromosome 3
Chromosomal Location 36530086-36536448 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to A at 36533690 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000143650 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000029266] [ENSMUST00000029268] [ENSMUST00000199478]
AlphaFold G3X8Y2
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
Ankib1 G A 5: 3,777,573 (GRCm39) S439L probably benign Het
Cdcp3 T A 7: 130,839,823 (GRCm39) probably null Het
Cpd G T 11: 76,688,615 (GRCm39) H886N probably benign Het
Dhrs7 A G 12: 72,706,124 (GRCm39) C94R probably damaging Het
Dmxl2 T A 9: 54,323,277 (GRCm39) H1369L probably damaging Het
Dnah5 A G 15: 28,272,488 (GRCm39) N1068S probably benign Het
Dop1a T A 9: 86,433,732 (GRCm39) D2329E possibly damaging Het
Eif1ad A G 19: 5,418,212 (GRCm39) probably benign Het
Fam149a T C 8: 45,792,380 (GRCm39) R693G probably damaging Het
Fbxw18 T A 9: 109,522,411 (GRCm39) T153S probably benign Het
Glg1 A T 8: 111,886,481 (GRCm39) C1104S probably damaging Het
Jak3 T C 8: 72,134,341 (GRCm39) probably benign Het
Kctd6 C T 14: 8,222,856 (GRCm38) R233C possibly damaging Het
Kpna3 A G 14: 61,611,737 (GRCm39) V300A possibly damaging Het
Msh5 A T 17: 35,248,857 (GRCm39) Y725* probably null Het
Myh2 T C 11: 67,076,059 (GRCm39) S749P possibly damaging Het
Or2ag15 T A 7: 106,340,908 (GRCm39) T78S probably benign Het
Or4c110 A G 2: 88,831,683 (GRCm39) probably benign Het
Or5ac17 A T 16: 59,036,859 (GRCm39) M39K probably damaging Het
Or8g19 T A 9: 39,056,053 (GRCm39) I219N possibly damaging Het
Pdcd1 A G 1: 93,967,860 (GRCm39) probably benign Het
Pde5a T A 3: 122,588,006 (GRCm39) F391I probably damaging Het
Ptpn12 A C 5: 21,203,666 (GRCm39) S371A probably damaging Het
Sec16b A G 1: 157,365,900 (GRCm39) Y254C probably damaging Het
Slc2a10 G A 2: 165,356,700 (GRCm39) C120Y probably damaging Het
Spink5 G A 18: 44,120,938 (GRCm39) probably benign Het
Svil A G 18: 5,099,045 (GRCm39) Q1250R probably benign Het
Tph1 G T 7: 46,306,294 (GRCm39) N222K probably benign Het
Vmn2r83 A T 10: 79,314,805 (GRCm39) D351V probably damaging Het
Zfp54 A G 17: 21,653,821 (GRCm39) D105G possibly damaging Het
Zfp623 T C 15: 75,820,052 (GRCm39) I336T probably damaging Het
Other mutations in 1810062G17Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2010:1810062G17Rik UTSW 3 36,535,955 (GRCm39) missense unknown
R2495:1810062G17Rik UTSW 3 36,536,109 (GRCm39) missense unknown
R5045:1810062G17Rik UTSW 3 36,530,327 (GRCm39) unclassified probably benign
R5905:1810062G17Rik UTSW 3 36,533,718 (GRCm39) critical splice donor site probably null
R6028:1810062G17Rik UTSW 3 36,533,718 (GRCm39) critical splice donor site probably null
R7120:1810062G17Rik UTSW 3 36,536,016 (GRCm39) missense unknown
R7126:1810062G17Rik UTSW 3 36,535,988 (GRCm39) missense unknown
R9304:1810062G17Rik UTSW 3 36,536,072 (GRCm39) missense unknown
R9709:1810062G17Rik UTSW 3 36,530,356 (GRCm39) missense unknown
Posted On 2015-04-16