Incidental Mutation 'R9044:2610008E11Rik'
ID 687934
Institutional Source Beutler Lab
Gene Symbol 2610008E11Rik
Ensembl Gene ENSMUSG00000060301
Gene Name RIKEN cDNA 2610008E11 gene
Synonyms
MMRRC Submission 068871-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # R9044 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 78900208-78933434 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 78902314 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 667 (Y667*)
Ref Sequence ENSEMBL: ENSMUSP00000044020 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039271] [ENSMUST00000218854] [ENSMUST00000220220]
AlphaFold G3X964
Predicted Effect probably null
Transcript: ENSMUST00000039271
AA Change: Y667*
SMART Domains Protein: ENSMUSP00000044020
Gene: ENSMUSG00000060301
AA Change: Y667*

DomainStartEndE-ValueType
KRAB 10 70 6.95e-32 SMART
ZnF_C2H2 215 237 1.61e2 SMART
ZnF_C2H2 243 266 4.24e-4 SMART
ZnF_C2H2 272 295 1.03e-2 SMART
ZnF_C2H2 301 324 1.76e-1 SMART
ZnF_C2H2 330 352 1.45e-2 SMART
ZnF_C2H2 358 380 1.58e-3 SMART
ZnF_C2H2 386 408 2.75e-3 SMART
ZnF_C2H2 414 437 4.61e-5 SMART
ZnF_C2H2 443 465 1.1e-2 SMART
ZnF_C2H2 471 493 5.81e-2 SMART
ZnF_C2H2 499 521 4.79e-3 SMART
ZnF_C2H2 527 549 3.58e-2 SMART
ZnF_C2H2 555 577 3.44e-4 SMART
ZnF_C2H2 583 605 6.78e-3 SMART
ZnF_C2H2 611 633 3.95e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000218854
Predicted Effect probably benign
Transcript: ENSMUST00000220220
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.1%
Validation Efficiency 95% (62/65)
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acacb A G 5: 114,373,578 (GRCm39) H1869R probably benign Het
Adgrb1 A G 15: 74,441,748 (GRCm39) T950A possibly damaging Het
Alms1 T A 6: 85,673,735 (GRCm39) L3110Q probably damaging Het
Ambra1 A T 2: 91,740,434 (GRCm39) probably benign Het
Brpf3 A T 17: 29,025,871 (GRCm39) N315Y possibly damaging Het
Clxn A G 16: 14,738,261 (GRCm39) D142G probably damaging Het
Cpne7 C T 8: 123,856,951 (GRCm39) P402L probably damaging Het
Cyba T A 8: 123,151,630 (GRCm39) D189V probably benign Het
Dexi A G 16: 10,321,385 (GRCm39) probably benign Het
Dnah2 C T 11: 69,420,247 (GRCm39) V156I probably benign Het
Drc7 T C 8: 95,797,077 (GRCm39) V420A probably damaging Het
Eef2k T A 7: 120,479,584 (GRCm39) V167E probably damaging Het
Eid2 T C 7: 27,968,038 (GRCm39) I220T possibly damaging Het
Fggy A C 4: 95,732,334 (GRCm39) T442P probably benign Het
Foxi3 T G 6: 70,933,683 (GRCm39) S57A probably benign Het
Foxi3 T A 6: 70,934,186 (GRCm39) probably null Het
Galntl5 C T 5: 25,415,326 (GRCm39) P286S possibly damaging Het
Gm5592 A G 7: 40,938,274 (GRCm39) K519E probably benign Het
Gse1 T A 8: 120,957,269 (GRCm39) S587T unknown Het
Kcns1 G T 2: 164,009,996 (GRCm39) F254L probably damaging Het
Kif15 A G 9: 122,840,781 (GRCm39) T23A probably benign Het
Kif16b T C 2: 142,541,577 (GRCm39) Q1241R possibly damaging Het
Lck A T 4: 129,450,098 (GRCm39) L205Q probably damaging Het
Map9 C T 3: 82,287,525 (GRCm39) A420V possibly damaging Het
Mdm2 A T 10: 117,530,960 (GRCm39) D170E Het
Mllt6 T A 11: 97,554,485 (GRCm39) C30S probably damaging Het
Muc5b T G 7: 141,411,795 (GRCm39) D1580E unknown Het
Oaf C T 9: 43,135,308 (GRCm39) A157T probably damaging Het
Or13a19 A G 7: 139,902,485 (GRCm39) probably benign Het
Or2ab1 T A 11: 58,489,126 (GRCm39) N295K possibly damaging Het
Or2n1d A T 17: 38,646,320 (GRCm39) T91S possibly damaging Het
Osbp2 T C 11: 3,667,128 (GRCm39) I8V probably damaging Het
Pcdh9 T C 14: 94,124,247 (GRCm39) Y641C probably damaging Het
Phf10 A T 17: 15,166,584 (GRCm39) C429S probably damaging Het
Plekha6 C G 1: 133,201,687 (GRCm39) P367A probably benign Het
Plekha6 C A 1: 133,201,688 (GRCm39) P367Q possibly damaging Het
Plod2 T A 9: 92,489,273 (GRCm39) I756K probably damaging Het
Plxnb2 C A 15: 89,044,566 (GRCm39) probably benign Het
Pop1 T A 15: 34,530,554 (GRCm39) M1014K possibly damaging Het
Prrt4 T C 6: 29,171,540 (GRCm39) D304G probably benign Het
Rcan2 C A 17: 44,147,245 (GRCm39) L28I probably benign Het
Rffl C T 11: 82,701,020 (GRCm39) V269I probably benign Het
Rhox3c C T X: 36,651,303 (GRCm39) probably benign Het
Ric1 C T 19: 29,577,294 (GRCm39) A1066V probably damaging Het
Rsf1 ATGGCG ATGGCGACGGTGGCG 7: 97,229,111 (GRCm39) probably benign Het
Ryr2 A T 13: 11,752,989 (GRCm39) Y1777* probably null Het
Scart2 G T 7: 139,828,010 (GRCm39) G73C probably damaging Het
Sh3tc1 T G 5: 35,854,834 (GRCm39) K1288Q possibly damaging Het
Slc10a5 A C 3: 10,399,792 (GRCm39) I289M probably damaging Het
Slc16a9 A G 10: 70,110,797 (GRCm39) T128A probably benign Het
Slc7a11 T C 3: 50,333,632 (GRCm39) H373R probably benign Het
Spesp1 A G 9: 62,180,623 (GRCm39) I95T probably benign Het
Sra1 C T 18: 36,800,946 (GRCm39) V131I probably benign Het
Stxbp5l A G 16: 37,024,930 (GRCm39) V556A possibly damaging Het
Sycp2 T C 2: 177,989,617 (GRCm39) E1414G probably damaging Het
Trac A T 14: 54,458,148 (GRCm39) K57* probably null Het
Trps1 T C 15: 50,686,003 (GRCm39) E724G probably benign Het
Tubgcp6 T G 15: 88,987,397 (GRCm39) D1192A possibly damaging Het
Usp48 G A 4: 137,340,996 (GRCm39) G332E probably benign Het
Vps18 T G 2: 119,128,034 (GRCm39) I952M probably damaging Het
Wdr36 T C 18: 32,970,499 (GRCm39) F20S probably damaging Het
Wdr62 C A 7: 29,962,062 (GRCm39) R450L probably benign Het
Xab2 T C 8: 3,668,641 (GRCm39) K76E probably benign Het
Zpr1 A G 9: 46,190,995 (GRCm39) D300G probably damaging Het
Other mutations in 2610008E11Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01551:2610008E11Rik APN 10 78,924,147 (GRCm39) missense possibly damaging 0.79
IGL01905:2610008E11Rik APN 10 78,903,582 (GRCm39) missense probably damaging 1.00
IGL02522:2610008E11Rik APN 10 78,903,633 (GRCm39) missense probably benign 0.27
IGL02999:2610008E11Rik APN 10 78,903,424 (GRCm39) missense possibly damaging 0.74
K7371:2610008E11Rik UTSW 10 78,903,767 (GRCm39) missense probably benign 0.01
R0557:2610008E11Rik UTSW 10 78,903,519 (GRCm39) missense probably damaging 0.99
R0761:2610008E11Rik UTSW 10 78,903,833 (GRCm39) missense probably benign 0.00
R1528:2610008E11Rik UTSW 10 78,903,530 (GRCm39) missense possibly damaging 0.72
R1801:2610008E11Rik UTSW 10 78,903,230 (GRCm39) missense probably damaging 1.00
R1923:2610008E11Rik UTSW 10 78,903,743 (GRCm39) missense probably damaging 0.98
R2444:2610008E11Rik UTSW 10 78,904,561 (GRCm39) missense possibly damaging 0.95
R4223:2610008E11Rik UTSW 10 78,930,286 (GRCm39) missense probably damaging 1.00
R4653:2610008E11Rik UTSW 10 78,903,264 (GRCm39) missense probably benign 0.42
R5127:2610008E11Rik UTSW 10 78,902,826 (GRCm39) missense probably damaging 1.00
R5784:2610008E11Rik UTSW 10 78,903,441 (GRCm39) missense possibly damaging 0.68
R6175:2610008E11Rik UTSW 10 78,902,448 (GRCm39) missense probably damaging 0.98
R6990:2610008E11Rik UTSW 10 78,902,925 (GRCm39) missense probably damaging 0.99
R7055:2610008E11Rik UTSW 10 78,903,681 (GRCm39) missense probably damaging 0.98
R7133:2610008E11Rik UTSW 10 78,902,474 (GRCm39) missense probably benign 0.33
R7133:2610008E11Rik UTSW 10 78,902,473 (GRCm39) missense probably benign 0.02
R7142:2610008E11Rik UTSW 10 78,903,446 (GRCm39) missense probably damaging 1.00
R7382:2610008E11Rik UTSW 10 78,903,103 (GRCm39) missense probably damaging 1.00
R7577:2610008E11Rik UTSW 10 78,902,325 (GRCm39) missense possibly damaging 0.95
R8103:2610008E11Rik UTSW 10 78,903,668 (GRCm39) missense probably benign
R8117:2610008E11Rik UTSW 10 78,930,289 (GRCm39) missense probably benign 0.07
R8296:2610008E11Rik UTSW 10 78,903,568 (GRCm39) missense probably benign 0.09
R8316:2610008E11Rik UTSW 10 78,903,573 (GRCm39) missense probably damaging 1.00
R8477:2610008E11Rik UTSW 10 78,924,174 (GRCm39) missense probably benign 0.00
R8790:2610008E11Rik UTSW 10 78,928,285 (GRCm39) missense possibly damaging 0.85
R9147:2610008E11Rik UTSW 10 78,903,406 (GRCm39) nonsense probably null
R9148:2610008E11Rik UTSW 10 78,903,406 (GRCm39) nonsense probably null
R9474:2610008E11Rik UTSW 10 78,903,565 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGTCACAGTACTTCACACCTG -3'
(R):5'- TCAGAGAACTCACACGCATG -3'

Sequencing Primer
(F):5'- GCATTTTGACAAGTGGCATCCAG -3'
(R):5'- CACGCATGAAAAACCTTATGAATG -3'
Posted On 2021-11-19