Incidental Mutation 'R8461:1700067P10Rik'
ID 655301
Institutional Source Beutler Lab
Gene Symbol 1700067P10Rik
Ensembl Gene ENSMUSG00000021545
Gene Name RIKEN cDNA 1700067P10 gene
Synonyms
MMRRC Submission 067837-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.055) question?
Stock # R8461 (G1)
Quality Score 225.009
Status Not validated
Chromosome 17
Chromosomal Location 48400162-48401440 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to T at 48400849 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Stop codon at position 45 (E45*)
Ref Sequence ENSEMBL: ENSMUSP00000022028 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022028]
AlphaFold G3X8U2
Predicted Effect probably null
Transcript: ENSMUST00000022028
AA Change: E45*
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921539E11Rik T C 4: 103,112,712 (GRCm39) D132G probably benign Het
Abca16 T C 7: 120,035,918 (GRCm39) F334L possibly damaging Het
Ache T C 5: 137,288,582 (GRCm39) F96S probably damaging Het
Actg1 T C 11: 120,239,010 (GRCm39) T27A unknown Het
Ankrd27 T C 7: 35,326,911 (GRCm39) L752P probably damaging Het
Atp1a1 T A 3: 101,496,405 (GRCm39) T417S probably benign Het
Atp6v0a1 T G 11: 100,935,400 (GRCm39) L653R possibly damaging Het
Aurkb T C 11: 68,941,727 (GRCm39) V293A probably damaging Het
C2cd5 A T 6: 142,980,802 (GRCm39) D654E probably damaging Het
Cacna1s T C 1: 136,001,440 (GRCm39) V297A possibly damaging Het
Catsperg2 T C 7: 29,404,744 (GRCm39) D773G possibly damaging Het
Ccdc187 A G 2: 26,183,814 (GRCm39) L62P probably damaging Het
Cdh2 A G 18: 16,783,522 (GRCm39) V69A probably benign Het
D430041D05Rik A G 2: 103,998,280 (GRCm39) V1156A possibly damaging Het
Defb37 G A 8: 19,036,386 (GRCm39) H45Y unknown Het
Dgke T C 11: 88,939,819 (GRCm39) M367V possibly damaging Het
Dnah1 T C 14: 31,027,915 (GRCm39) K640R probably benign Het
Gm5478 A T 15: 101,554,652 (GRCm39) L148Q probably damaging Het
Hhla1 A T 15: 65,795,723 (GRCm39) S494R probably benign Het
Kcne4 G A 1: 78,795,433 (GRCm39) S27N probably benign Het
Klhdc7b A T 15: 89,271,824 (GRCm39) H244L probably damaging Het
Lrrc40 T C 3: 157,764,371 (GRCm39) S429P possibly damaging Het
Map3k21 A T 8: 126,671,361 (GRCm39) D883V probably benign Het
Med4 T C 14: 73,755,468 (GRCm39) S259P unknown Het
Mrm3 T C 11: 76,135,158 (GRCm39) I123T probably damaging Het
Mrpl1 T A 5: 96,361,646 (GRCm39) V11D probably damaging Het
Myl1 G A 1: 66,983,994 (GRCm39) P24L unknown Het
Necap2 T C 4: 140,797,531 (GRCm39) K168R probably damaging Het
Nnt A G 13: 119,505,038 (GRCm39) S559P unknown Het
Nox4 T C 7: 86,966,479 (GRCm39) F197L probably damaging Het
Nup93 T C 8: 95,007,963 (GRCm39) probably null Het
Nxph2 T C 2: 23,211,529 (GRCm39) V10A unknown Het
Or1e16 T A 11: 73,285,982 (GRCm39) I289F probably damaging Het
Or8c11 T A 9: 38,289,777 (GRCm39) V194D probably damaging Het
Or8k38 G A 2: 86,487,890 (GRCm39) T304I probably benign Het
P2ry2 G T 7: 100,647,895 (GRCm39) R137S possibly damaging Het
Plxnb3 T C X: 72,803,103 (GRCm39) Y324H probably damaging Het
Pmpca G C 2: 26,285,046 (GRCm39) E424Q possibly damaging Het
Ppme1 T C 7: 100,021,012 (GRCm39) S7G probably benign Het
Rabep1 T A 11: 70,775,681 (GRCm39) M85K possibly damaging Het
Ranbp2 T C 10: 58,312,216 (GRCm39) Y979H probably damaging Het
Rapgef5 T C 12: 117,677,844 (GRCm39) S360P probably benign Het
Rbm33 T A 5: 28,592,970 (GRCm39) H623Q probably damaging Het
Rev1 G T 1: 38,122,868 (GRCm39) T450K possibly damaging Het
Sec23ip T A 7: 128,373,926 (GRCm39) L716Q probably benign Het
Sp2 T C 11: 96,846,739 (GRCm39) T535A possibly damaging Het
Syne1 A G 10: 5,011,463 (GRCm39) S61P probably benign Het
Tcf4 T C 18: 69,598,501 (GRCm39) V72A probably benign Het
Tmem131 G A 1: 36,833,902 (GRCm39) S1726F probably damaging Het
Trim13 T C 14: 61,842,921 (GRCm39) Y313H probably benign Het
Ttn A G 2: 76,611,437 (GRCm39) V17365A possibly damaging Het
Uap1l1 G A 2: 25,255,422 (GRCm39) A69V probably benign Het
Upp2 A G 2: 58,670,068 (GRCm39) D258G probably benign Het
Vmn1r44 A T 6: 89,870,701 (GRCm39) H149L possibly damaging Het
Zbtb49 T C 5: 38,358,453 (GRCm39) D600G probably benign Het
Zfp869 G T 8: 70,160,305 (GRCm39) H89Q probably benign Het
Other mutations in 1700067P10Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00546:1700067P10Rik APN 17 48,401,096 (GRCm39) missense possibly damaging 0.90
IGL02792:1700067P10Rik APN 17 48,401,107 (GRCm39) missense probably benign 0.11
R0445:1700067P10Rik UTSW 17 48,400,542 (GRCm39) critical splice acceptor site probably null
R1025:1700067P10Rik UTSW 17 48,401,030 (GRCm39) missense probably damaging 1.00
R1494:1700067P10Rik UTSW 17 48,400,991 (GRCm39) missense probably benign
R2133:1700067P10Rik UTSW 17 48,400,972 (GRCm39) missense possibly damaging 0.94
R6059:1700067P10Rik UTSW 17 48,400,847 (GRCm39) missense probably benign
R8460:1700067P10Rik UTSW 17 48,400,849 (GRCm39) nonsense probably null
R8558:1700067P10Rik UTSW 17 48,400,849 (GRCm39) nonsense probably null
R8672:1700067P10Rik UTSW 17 48,400,849 (GRCm39) nonsense probably null
R8673:1700067P10Rik UTSW 17 48,400,849 (GRCm39) nonsense probably null
R8675:1700067P10Rik UTSW 17 48,400,849 (GRCm39) nonsense probably null
R8872:1700067P10Rik UTSW 17 48,401,164 (GRCm39) missense possibly damaging 0.62
Predicted Primers PCR Primer
(F):5'- GAAGTCAGGTTGGAATGTCCC -3'
(R):5'- GATAACAGCTGGGACTTGCC -3'

Sequencing Primer
(F):5'- AAGTCAGGTTGGAATGTCCCATTTTG -3'
(R):5'- TCAGCTTTTTCCTTCGGAGAG -3'
Posted On 2020-10-20