Incidental Mutation 'IGL03393:1700113H08Rik'
ID 421157
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700113H08Rik
Ensembl Gene ENSMUSG00000047129
Gene Name RIKEN cDNA 1700113H08 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # IGL03393
Quality Score
Status
Chromosome 10
Chromosomal Location 86893909-87066451 bp(+) (GRCm39)
Type of Mutation utr 5 prime
DNA Base Change (assembly) A to G at 86909902 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000140447 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000169849] [ENSMUST00000189456]
AlphaFold E9Q9Q5
Predicted Effect probably benign
Transcript: ENSMUST00000169849
SMART Domains Protein: ENSMUSP00000130852
Gene: ENSMUSG00000047129

DomainStartEndE-ValueType
Pfam:DUF4607 71 325 2.1e-113 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000189456
SMART Domains Protein: ENSMUSP00000140447
Gene: ENSMUSG00000047129

DomainStartEndE-ValueType
Pfam:DUF4607 45 206 6.2e-38 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts5 G T 16: 85,665,083 (GRCm39) S627Y probably damaging Het
Allc G A 12: 28,610,010 (GRCm39) R196C probably damaging Het
Ccdc65 A C 15: 98,618,568 (GRCm39) E241A probably benign Het
Dclk3 T C 9: 111,317,741 (GRCm39) probably benign Het
Fzd4 T C 7: 89,056,505 (GRCm39) V184A probably benign Het
Gfap T A 11: 102,784,083 (GRCm39) probably null Het
Gpr149 A G 3: 62,511,366 (GRCm39) V211A probably benign Het
Gprc6a A G 10: 51,491,355 (GRCm39) I623T probably damaging Het
Gucy2c T C 6: 136,696,665 (GRCm39) T687A probably benign Het
Kcnc4 T G 3: 107,355,243 (GRCm39) M402L possibly damaging Het
Ktn1 T C 14: 47,928,391 (GRCm39) L584S probably damaging Het
Mrgprb2 C T 7: 48,202,650 (GRCm39) S25N probably benign Het
Muc5b T A 7: 141,417,875 (GRCm39) V3607E probably benign Het
Or4c58 C A 2: 89,674,913 (GRCm39) V135L probably benign Het
Or6c3b T C 10: 129,527,147 (GRCm39) I254M probably damaging Het
Otx2 A G 14: 48,898,781 (GRCm39) I75T probably damaging Het
Pabpc4l T C 3: 46,400,972 (GRCm39) D224G probably damaging Het
Peg3 A T 7: 6,710,648 (GRCm39) C1525S probably damaging Het
Polq A T 16: 36,865,156 (GRCm39) L669F probably damaging Het
Prss40 A C 1: 34,597,182 (GRCm39) V122G probably damaging Het
Rims2 A G 15: 39,326,009 (GRCm39) probably null Het
Rrp12 A T 19: 41,860,232 (GRCm39) M997K possibly damaging Het
Sbno2 G A 10: 79,902,735 (GRCm39) R414W probably damaging Het
Scn1a T C 2: 66,148,362 (GRCm39) D41G probably benign Het
Serpinb1c A T 13: 33,066,044 (GRCm39) D300E probably damaging Het
Timeless G A 10: 128,087,924 (GRCm39) D1165N probably damaging Het
Tnpo1 T G 13: 99,024,981 (GRCm39) K66N probably damaging Het
Trappc11 A T 8: 47,963,912 (GRCm39) N629K possibly damaging Het
Ubr4 T A 4: 139,179,989 (GRCm39) L255M probably damaging Het
Vmn1r10 T A 6: 57,091,042 (GRCm39) Y211* probably null Het
Vmn2r76 T G 7: 85,879,034 (GRCm39) N422T probably benign Het
Xylt1 C A 7: 117,192,940 (GRCm39) N415K probably damaging Het
Zfp786 A T 6: 47,798,458 (GRCm39) V160E possibly damaging Het
Other mutations in 1700113H08Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01688:1700113H08Rik APN 10 87,000,985 (GRCm39) missense probably damaging 1.00
IGL01764:1700113H08Rik APN 10 86,909,910 (GRCm39) start codon destroyed probably benign 0.02
IGL02173:1700113H08Rik APN 10 87,061,754 (GRCm39) missense possibly damaging 0.63
IGL02756:1700113H08Rik APN 10 87,000,970 (GRCm39) missense probably damaging 0.99
IGL03202:1700113H08Rik APN 10 86,909,911 (GRCm39) start codon destroyed probably null 0.35
R0255:1700113H08Rik UTSW 10 87,061,907 (GRCm39) missense probably damaging 1.00
R0409:1700113H08Rik UTSW 10 87,061,816 (GRCm39) missense probably damaging 0.98
R0744:1700113H08Rik UTSW 10 87,000,931 (GRCm39) missense probably damaging 1.00
R0833:1700113H08Rik UTSW 10 87,000,931 (GRCm39) missense probably damaging 1.00
R1163:1700113H08Rik UTSW 10 86,957,284 (GRCm39) missense probably damaging 0.99
R2128:1700113H08Rik UTSW 10 87,066,066 (GRCm39) missense possibly damaging 0.94
R2129:1700113H08Rik UTSW 10 87,066,066 (GRCm39) missense possibly damaging 0.94
R4108:1700113H08Rik UTSW 10 87,061,796 (GRCm39) missense probably damaging 1.00
R5541:1700113H08Rik UTSW 10 87,061,808 (GRCm39) missense probably benign 0.00
R6345:1700113H08Rik UTSW 10 87,061,913 (GRCm39) missense probably benign 0.43
R6372:1700113H08Rik UTSW 10 87,066,088 (GRCm39) missense possibly damaging 0.92
R6710:1700113H08Rik UTSW 10 87,061,923 (GRCm39) missense probably benign 0.00
R6971:1700113H08Rik UTSW 10 87,000,903 (GRCm39) missense possibly damaging 0.91
R7055:1700113H08Rik UTSW 10 87,062,083 (GRCm39) missense probably damaging 0.99
R7713:1700113H08Rik UTSW 10 87,066,173 (GRCm39) missense possibly damaging 0.80
R7808:1700113H08Rik UTSW 10 86,957,297 (GRCm39) missense probably benign 0.33
R7838:1700113H08Rik UTSW 10 87,042,061 (GRCm39) splice site probably null
R8293:1700113H08Rik UTSW 10 87,061,864 (GRCm39) missense possibly damaging 0.92
R9041:1700113H08Rik UTSW 10 87,062,054 (GRCm39) missense probably benign 0.03
R9351:1700113H08Rik UTSW 10 87,066,068 (GRCm39) missense probably benign 0.27
Posted On 2016-08-02