Incidental Mutation 'IGL01772:1810065E05Rik'
ID153685
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1810065E05Rik
Ensembl Gene ENSMUSG00000013653
Gene NameRIKEN cDNA 1810065E05 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.091) question?
Stock #IGL01772
Quality Score
Status
Chromosome11
Chromosomal Location58421111-58426024 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 58422884 bp
ZygosityHeterozygous
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

DomainStartEndE-ValueType
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