Incidental Mutation 'R5692:1700128F08Rik'
ID 443736
Institutional Source Beutler Lab
Gene Symbol 1700128F08Rik
Ensembl Gene ENSMUSG00000031998
Gene Name RIKEN cDNA 1700128F08 gene
Synonyms
MMRRC Submission 043179-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.872) question?
Stock # R5692 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 8221890-8241988 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) G to A at 8221991 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000034483
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213708
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy10 A G 1: 165,342,875 (GRCm39) N247S probably benign Het
Ago3 T C 4: 126,248,862 (GRCm39) probably null Het
Aldh16a1 A G 7: 44,797,223 (GRCm39) V168A probably damaging Het
Aqp7 G A 4: 41,035,510 (GRCm39) T115I probably benign Het
Arhgap26 T A 18: 39,254,945 (GRCm39) V274E probably damaging Het
Clec4d T C 6: 123,245,104 (GRCm39) probably null Het
Dennd4b T C 3: 90,185,090 (GRCm39) Y1166H probably damaging Het
Egln3 T C 12: 54,227,447 (GRCm39) probably null Het
Fetub C T 16: 22,751,081 (GRCm39) R143C probably damaging Het
Fhad1 T A 4: 141,690,768 (GRCm39) M434L probably benign Het
Gfm1 T G 3: 67,342,955 (GRCm39) M163R probably damaging Het
Isg15 A T 4: 156,284,279 (GRCm39) L83Q probably damaging Het
Ly9 GCCTTTGGGGGACAATTCC GCC 1: 171,432,755 (GRCm39) probably null Het
Med1 G T 11: 98,047,206 (GRCm39) probably benign Het
Mrc2 T A 11: 105,227,468 (GRCm39) V567D probably damaging Het
Nnmt G T 9: 48,514,780 (GRCm39) T79K probably benign Het
Opn1sw G A 6: 29,379,840 (GRCm39) probably benign Het
Optc G T 1: 133,828,714 (GRCm39) probably benign Het
Pcdh17 C T 14: 84,685,980 (GRCm39) P816S probably benign Het
Pcdhb15 T C 18: 37,607,502 (GRCm39) S245P probably benign Het
Pcdhb18 G A 18: 37,623,537 (GRCm39) R289Q probably benign Het
Sacs T C 14: 61,445,288 (GRCm39) F2445L probably benign Het
Sel1l T C 12: 91,778,652 (GRCm39) N721S probably benign Het
Slc35e2 C T 4: 155,694,483 (GRCm39) P10L probably benign Het
Slc7a11 C G 3: 50,326,780 (GRCm39) V494L probably benign Het
Sulf2 C A 2: 165,923,426 (GRCm39) A598S probably benign Het
Tph2 A T 10: 115,020,732 (GRCm39) D21E probably damaging Het
Trf T C 9: 103,103,324 (GRCm39) Y110C possibly damaging Het
Ttn C T 2: 76,628,202 (GRCm39) E14653K possibly damaging Het
Vmn2r18 A G 5: 151,485,724 (GRCm39) I590T possibly damaging Het
Zfp607b G T 7: 27,402,889 (GRCm39) K448N probably benign Het
Zfp689 T C 7: 127,048,071 (GRCm39) probably benign Het
Zfp709 C T 8: 72,643,999 (GRCm39) P476L probably damaging Het
Other mutations in 1700128F08Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0472:1700128F08Rik UTSW 9 8,222,123 (GRCm39) exon noncoding transcript
R1114:1700128F08Rik UTSW 9 8,222,179 (GRCm39) exon noncoding transcript
R4732:1700128F08Rik UTSW 9 8,222,174 (GRCm39) exon noncoding transcript
R4733:1700128F08Rik UTSW 9 8,222,174 (GRCm39) exon noncoding transcript
R4970:1700128F08Rik UTSW 9 8,222,066 (GRCm39) exon noncoding transcript
R5699:1700128F08Rik UTSW 9 8,225,320 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- TGTTCAGGCATAGCTGGAACC -3'
(R):5'- TGTCACCATACCGGGAGAAC -3'

Sequencing Primer
(F):5'- CATAGCTGGAACCTGGGTAC -3'
(R):5'- CATACCGGGAGAACTTCTCTTTGG -3'
Posted On 2016-11-09