Incidental Mutation 'R6982:4931417E11Rik'
ID542726
Institutional Source Beutler Lab
Gene Symbol 4931417E11Rik
Ensembl Gene ENSMUSG00000056197
Gene NameRIKEN cDNA 4931417E11 gene
Synonyms
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.093) question?
Stock #R6982 (G1)
Quality Score225.009
Status Validated
Chromosome6
Chromosomal Location73468573-73469667 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) A to T at 73469544 bp
ZygosityHeterozygous
Amino Acid Change Tyrosine to Stop codon at position 7 (Y7*)
Ref Sequence ENSEMBL: ENSMUSP00000068770 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000070163]
Predicted Effect probably null
Transcript: ENSMUST00000070163
AA Change: Y7*
SMART Domains Protein: ENSMUSP00000068770
Gene: ENSMUSG00000056197
AA Change: Y7*

DomainStartEndE-ValueType
Pfam:DUF766 3 294 3.1e-113 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.2%
  • 20x: 96.7%
Validation Efficiency 98% (55/56)
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts16 T A 13: 70,768,520 probably null Het
Adamtsl3 C A 7: 82,515,063 P362H probably damaging Het
Ambra1 G A 2: 91,917,473 V1065I probably damaging Het
Ankrd66 T C 17: 43,539,035 T79A probably damaging Het
Ano2 G A 6: 125,992,893 R724H probably benign Het
Bmp8a A G 4: 123,325,141 L158P probably damaging Het
C1ra G A 6: 124,517,725 E316K probably benign Het
Cilp T C 9: 65,279,805 Y1061H probably damaging Het
Clybl G A 14: 122,401,947 G308R probably damaging Het
Cntnap5c C T 17: 58,092,252 P367S possibly damaging Het
Col20a1 T C 2: 180,996,706 V371A probably benign Het
Col24a1 G T 3: 145,315,046 G393* probably null Het
Dnah12 A G 14: 26,799,076 probably null Het
Dnah8 T A 17: 30,767,925 S3183T probably benign Het
Dph2 A T 4: 117,889,796 I435N probably benign Het
Fam3c G T 6: 22,322,301 A107D probably damaging Het
Fezf2 G T 14: 12,343,645 Q367K probably damaging Het
Gbp2 A G 3: 142,630,085 D182G probably damaging Het
Gpr162 T A 6: 124,860,956 I244F probably damaging Het
Jakmip1 A T 5: 37,124,941 N159I probably damaging Het
Kdm4a A T 4: 118,153,439 probably null Het
Klf5 A G 14: 99,313,235 H416R probably damaging Het
Lrrc63 A G 14: 75,084,771 V631A probably benign Het
Man1a T C 10: 54,074,723 E101G possibly damaging Het
Msantd4 T A 9: 4,384,061 N127K possibly damaging Het
Myo3b A T 2: 70,426,065 E1248D probably benign Het
Ncapd2 A T 6: 125,176,736 I672N probably damaging Het
Nfic T C 10: 81,420,800 probably null Het
Nr1h3 A G 2: 91,190,759 S228P probably damaging Het
Olfr951 T C 9: 39,394,322 I174T probably damaging Het
Pccb A T 9: 101,023,296 probably null Het
Pcmtd1 T G 1: 7,147,682 V118G probably damaging Het
Pkhd1l1 A T 15: 44,566,268 N3294I probably damaging Het
Plscr4 A G 9: 92,482,743 T74A probably benign Het
Rasa2 A T 9: 96,560,750 I540N probably damaging Het
Serpina3j C A 12: 104,317,297 T218K probably benign Het
Slc16a4 A G 3: 107,299,273 D173G probably benign Het
Slc19a2 T C 1: 164,256,859 L106P possibly damaging Het
Slc22a19 C T 19: 7,682,969 V359M probably benign Het
Slc22a7 T A 17: 46,434,637 M323L probably benign Het
Spata21 A T 4: 141,096,873 N149I possibly damaging Het
Spink5 T C 18: 44,010,042 probably null Het
Spink5 G A 18: 43,977,725 G121D probably damaging Het
Ssbp4 T C 8: 70,608,165 S6G possibly damaging Het
Sytl2 T C 7: 90,396,564 S641P probably damaging Het
Tcf3 A T 10: 80,417,550 F215I probably damaging Het
Tmem150c C A 5: 100,092,821 D61Y probably benign Het
Ttc7 T A 17: 87,307,009 F201I probably damaging Het
Tyw3 T C 3: 154,580,230 I208V probably benign Het
Vmn1r202 T C 13: 22,501,747 T167A probably benign Het
Vmn1r83 A T 7: 12,321,836 L98Q probably damaging Het
Vmn2r95 T C 17: 18,452,061 Y687H probably damaging Het
Wdr59 A T 8: 111,460,813 F783L probably benign Het
Zfhx4 A G 3: 5,403,830 Y3016C probably damaging Het
Zfp518b T C 5: 38,672,905 T586A probably benign Het
Other mutations in 4931417E11Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01566:4931417E11Rik APN 6 73468690 missense probably damaging 1.00
IGL01768:4931417E11Rik APN 6 73468916 missense possibly damaging 0.83
IGL02903:4931417E11Rik APN 6 73469120 missense probably damaging 1.00
R0084:4931417E11Rik UTSW 6 73468935 nonsense probably null
R0123:4931417E11Rik UTSW 6 73469419 missense possibly damaging 0.49
R0225:4931417E11Rik UTSW 6 73469419 missense possibly damaging 0.49
R1478:4931417E11Rik UTSW 6 73469056 missense probably damaging 1.00
R1640:4931417E11Rik UTSW 6 73468886 missense probably benign 0.13
R4616:4931417E11Rik UTSW 6 73469269 missense probably benign 0.02
R5451:4931417E11Rik UTSW 6 73468867 missense probably benign 0.00
R5875:4931417E11Rik UTSW 6 73469045 missense possibly damaging 0.50
R5911:4931417E11Rik UTSW 6 73468691 missense probably damaging 0.99
R6784:4931417E11Rik UTSW 6 73468935 nonsense probably null
R7990:4931417E11Rik UTSW 6 73469545 missense probably damaging 1.00
R8365:4931417E11Rik UTSW 6 73469346 missense probably benign 0.02
R8381:4931417E11Rik UTSW 6 73468912 missense probably damaging 1.00
X0024:4931417E11Rik UTSW 6 73469050 missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- ATAGCGCAGAGACTTGCTGG -3'
(R):5'- GTCAGGACCAAGCACTTGAAC -3'

Sequencing Primer
(F):5'- TTGCTGGAAAAACACACCTCTGG -3'
(R):5'- GCACTTGAACCCAAAAGAAGAATG -3'
Posted On2018-11-28