Incidental Mutation 'R5647:1700010L04Rik'
ID 441217
Institutional Source Beutler Lab
Gene Symbol 1700010L04Rik
Ensembl Gene ENSMUSG00000030636
Gene Name RIKEN cDNA 1700010L04 gene
Synonyms
MMRRC Submission 043295-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # R5647 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 82500807-82509057 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 82505606 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: ENSMUST00000032872
Predicted Effect noncoding transcript
Transcript: ENSMUST00000178848
Predicted Effect noncoding transcript
Transcript: ENSMUST00000179662
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209046
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.0%
  • 20x: 94.7%
Validation Efficiency 95% (55/58)
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9330159F19Rik A T 10: 29,101,250 (GRCm39) D541V probably damaging Het
Abcc5 T C 16: 20,218,597 (GRCm39) I262V probably damaging Het
Acvr1c T A 2: 58,185,976 (GRCm39) D169V probably damaging Het
Aldh16a1 A G 7: 44,803,889 (GRCm39) V6A probably benign Het
Brd10 A G 19: 29,731,210 (GRCm39) S601P possibly damaging Het
Cd36 A C 5: 18,019,763 (GRCm39) S113A probably damaging Het
Cdt1 G T 8: 123,296,947 (GRCm39) R247L possibly damaging Het
Ces4a G A 8: 105,872,712 (GRCm39) V322M probably benign Het
Cngb3 A T 4: 19,364,266 (GRCm39) T157S possibly damaging Het
Cpped1 T C 16: 11,646,010 (GRCm39) probably benign Het
Ctr9 G T 7: 110,654,751 (GRCm39) R1094L unknown Het
Cyld A T 8: 89,461,554 (GRCm39) I664L probably benign Het
Dvl2 C T 11: 69,900,275 (GRCm39) P690S possibly damaging Het
Fbxo7 A C 10: 85,864,974 (GRCm39) E94D probably damaging Het
Fstl5 A C 3: 76,496,399 (GRCm39) K387N probably damaging Het
Gm9845 A C 3: 39,412,520 (GRCm39) noncoding transcript Het
Hk1 T C 10: 62,111,523 (GRCm39) D746G probably damaging Het
Lmbr1 A G 5: 29,468,391 (GRCm39) probably null Het
Lrp2 C T 2: 69,350,258 (GRCm39) A705T probably null Het
Lrrc37 T C 11: 103,508,300 (GRCm39) probably benign Het
Mybpc3 A G 2: 90,952,067 (GRCm39) probably null Het
Myo15b T A 11: 115,762,337 (GRCm39) L1219Q probably damaging Het
Naa35 G A 13: 59,770,680 (GRCm39) probably benign Het
Or4g16 G T 2: 111,137,392 (GRCm39) A281S possibly damaging Het
Or5b111 A T 19: 13,291,553 (GRCm39) I32N probably damaging Het
Or5b113 T C 19: 13,342,541 (GRCm39) V183A probably damaging Het
Pcdhb18 G A 18: 37,623,537 (GRCm39) R289Q probably benign Het
Pcnt T C 10: 76,221,675 (GRCm39) T1984A probably benign Het
Plcg1 T C 2: 160,593,588 (GRCm39) L251P probably benign Het
Plin1 T A 7: 79,371,320 (GRCm39) D468V probably benign Het
Pmp2 A G 3: 10,248,845 (GRCm39) V12A probably benign Het
Rnf19a T A 15: 36,266,109 (GRCm39) probably benign Het
Rnf214 G A 9: 45,779,344 (GRCm39) Q469* probably null Het
Rrp1b T G 17: 32,274,985 (GRCm39) probably benign Het
Rtl1 C T 12: 109,561,113 (GRCm39) R242Q unknown Het
Sema3e A T 5: 14,275,567 (GRCm39) E224V probably damaging Het
Sphkap A G 1: 83,385,720 (GRCm39) S5P probably damaging Het
Stab1 A C 14: 30,879,397 (GRCm39) Y694* probably null Het
Stambpl1 T C 19: 34,211,686 (GRCm39) L249P probably benign Het
Thap4 A T 1: 93,642,665 (GRCm39) H515Q probably damaging Het
Ticam1 TCACACA TCACA 17: 56,577,629 (GRCm39) probably null Het
Uaca A G 9: 60,779,380 (GRCm39) R1256G probably benign Het
Usp17lb T A 7: 104,489,881 (GRCm39) N348Y possibly damaging Het
Vmn1r42 A G 6: 89,822,314 (GRCm39) I85T probably benign Het
Vps9d1 A T 8: 123,975,598 (GRCm39) L149Q probably damaging Het
Zdhhc17 A T 10: 110,809,694 (GRCm39) I153N probably damaging Het
Zfp207 G A 11: 80,283,959 (GRCm39) S293N possibly damaging Het
Zfp346 A G 13: 55,270,170 (GRCm39) D198G probably damaging Het
Zfp953 A T 13: 67,491,536 (GRCm39) C139S possibly damaging Het
Other mutations in 1700010L04Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R5524:1700010L04Rik UTSW 7 82,503,150 (GRCm39) intron noncoding transcript
Predicted Primers PCR Primer
(F):5'- TCCCTAAGTGAGCCCAAAGC -3'
(R):5'- TCCTACATAACCCCAGGTGTAC -3'

Sequencing Primer
(F):5'- GAGACCACCAAGAGTTCTAAATTC -3'
(R):5'- TGTTACAACTTGTTCTCAAATTAAGC -3'
Posted On 2016-11-08