Incidental Mutation 'IGL01772:1810065E05Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1810065E05Rik
Ensembl Gene ENSMUSG00000013653
Gene NameRIKEN cDNA 1810065E05 gene
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.091) question?
Stock #IGL01772
Quality Score
Chromosomal Location58421111-58426024 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 58422884 bp
Amino Acid Change Proline to Serine at position 113 (P113S)
Ref Sequence ENSEMBL: ENSMUSP00000013797 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000013797]
Predicted Effect probably benign
Transcript: ENSMUST00000013797
AA Change: P113S

PolyPhen 2 Score 0.299 (Sensitivity: 0.91; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000013797
Gene: ENSMUSG00000013653
AA Change: P113S

signal peptide 1 26 N/A INTRINSIC
low complexity region 222 235 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ano2 T C 6: 126,036,858 Y881H probably damaging Het
Coro2b G T 9: 62,425,808 P131T probably damaging Het
Glra3 A G 8: 56,089,055 I278V probably benign Het
Grin2d T C 7: 45,858,466 D392G probably benign Het
Ifrd2 A G 9: 107,592,132 S360G probably benign Het
Kdelr3 A T 15: 79,522,920 probably benign Het
Mtdh T A 15: 34,139,881 S345R probably damaging Het
Ncor1 G A 11: 62,349,347 probably benign Het
Nf1 T A 11: 79,390,249 V110D probably damaging Het
Nlk T A 11: 78,589,375 H256L probably damaging Het
Olfr618 T A 7: 103,597,913 I199N probably benign Het
Olfr692 A T 7: 105,368,434 D36V probably benign Het
Olfr894 A T 9: 38,219,609 Y262F probably damaging Het
Pgr T C 9: 8,946,636 probably benign Het
Ptprn A G 1: 75,252,270 Y834H probably damaging Het
Rbfox3 G T 11: 118,496,971 A241E probably damaging Het
Skiv2l2 A G 13: 112,891,325 F667S probably benign Het
Tarbp1 G A 8: 126,447,231 probably benign Het
Ttn A T 2: 76,767,711 D19619E probably damaging Het
Unc13d C A 11: 116,076,532 E45D possibly damaging Het
Vil1 A G 1: 74,415,119 I14V probably benign Het
Other mutations in 1810065E05Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0060:1810065E05Rik UTSW 11 58422182 splice site probably benign
R0060:1810065E05Rik UTSW 11 58422182 splice site probably benign
R2141:1810065E05Rik UTSW 11 58423926 missense probably damaging 1.00
R2156:1810065E05Rik UTSW 11 58422308 critical splice donor site probably null
R4925:1810065E05Rik UTSW 11 58425714 nonsense probably null
R5010:1810065E05Rik UTSW 11 58422804 missense possibly damaging 0.77
R5716:1810065E05Rik UTSW 11 58421768 missense possibly damaging 0.77
R6026:1810065E05Rik UTSW 11 58425755 missense probably benign 0.06
R7110:1810065E05Rik UTSW 11 58425745 missense possibly damaging 0.80
R7282:1810065E05Rik UTSW 11 58425756 missense probably damaging 0.98
Posted On2014-02-04