Incidental Mutation 'R3424:6030469F06Rik'
ID 267862
Institutional Source Beutler Lab
Gene Symbol 6030469F06Rik
Ensembl Gene ENSMUSG00000095953
Gene Name RIKEN cDNA 6030469F06 gene
Synonyms
MMRRC Submission 040642-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.106) question?
Stock # R3424 (G1)
Quality Score 225
Status Not validated
Chromosome 12
Chromosomal Location 31218861-31235921 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) G to T at 31234632 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: ENSMUST00000179160
Predicted Effect noncoding transcript
Transcript: ENSMUST00000218473
Predicted Effect noncoding transcript
Transcript: ENSMUST00000218642
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp8b3 T C 10: 80,372,181 (GRCm39) E16G probably benign Het
BC016579 T A 16: 45,449,846 (GRCm39) I191F probably damaging Het
Cdh23 T G 10: 60,212,660 (GRCm39) I1584L possibly damaging Het
Cep250 G A 2: 155,823,381 (GRCm39) D1011N probably benign Het
Coro2b A T 9: 62,336,590 (GRCm39) probably null Het
Csf3r A G 4: 125,937,549 (GRCm39) D811G probably damaging Het
Dst T G 1: 34,237,586 (GRCm39) probably benign Het
Gabrr1 T C 4: 33,158,058 (GRCm39) L227P probably damaging Het
Galnt10 T C 11: 57,536,539 (GRCm39) V52A probably benign Het
Golga4 A C 9: 118,363,715 (GRCm39) D229A probably benign Het
Heatr5b G A 17: 79,075,833 (GRCm39) T1495I possibly damaging Het
Hoxd4 A G 2: 74,557,657 (GRCm39) Y12C probably damaging Het
Hps1 A T 19: 42,748,952 (GRCm39) M522K possibly damaging Het
Lrrc8e A T 8: 4,284,611 (GRCm39) I279F probably damaging Het
Mettl24 C T 10: 40,559,637 (GRCm39) Q96* probably null Het
Muc2 A G 7: 141,279,595 (GRCm39) N193S probably damaging Het
Mysm1 A G 4: 94,853,558 (GRCm39) L347P probably benign Het
Or10g9 T A 9: 39,911,830 (GRCm39) E231V probably damaging Het
Oxtr G T 6: 112,454,191 (GRCm39) H24Q probably benign Het
Paxip1 A G 5: 27,980,671 (GRCm39) probably benign Het
Pclo C T 5: 14,730,432 (GRCm39) probably benign Het
Ros1 C A 10: 52,004,512 (GRCm39) probably null Het
Slc18b1 T G 10: 23,698,874 (GRCm39) M348R probably damaging Het
Slco4c1 A T 1: 96,768,976 (GRCm39) S295R probably benign Het
Tmeff2 A G 1: 51,018,776 (GRCm39) probably benign Het
Tspan31 T A 10: 126,904,371 (GRCm39) Q141L probably benign Het
Virma G T 4: 11,513,177 (GRCm39) E344* probably null Het
Zbtb17 G T 4: 141,192,299 (GRCm39) G415C probably damaging Het
Other mutations in 6030469F06Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01957:6030469F06Rik APN 12 31,235,042 (GRCm39) intron noncoding transcript
R0411:6030469F06Rik UTSW 12 31,234,730 (GRCm39) intron noncoding transcript
R1464:6030469F06Rik UTSW 12 31,234,914 (GRCm39) intron noncoding transcript
R1464:6030469F06Rik UTSW 12 31,234,914 (GRCm39) intron noncoding transcript
R4391:6030469F06Rik UTSW 12 31,234,622 (GRCm39) intron noncoding transcript
R5524:6030469F06Rik UTSW 12 31,234,862 (GRCm39) intron noncoding transcript
R8176:6030469F06Rik UTSW 12 31,235,135 (GRCm39) missense noncoding transcript
R8296:6030469F06Rik UTSW 12 31,235,058 (GRCm39) missense noncoding transcript
Predicted Primers PCR Primer
(F):5'- TCATGAGTGCACCCATCAAG -3'
(R):5'- AAGAGCTCCTGGGTGTTCTC -3'

Sequencing Primer
(F):5'- AGAGGGGCTCTCCTGTACCAC -3'
(R):5'- GAGCTCCTGGGTGTTCTCTTCTTC -3'
Posted On 2015-02-18