Incidental Mutation 'R1152:4921517D22Rik'
ID 101621
Institutional Source Beutler Lab
Gene Symbol 4921517D22Rik
Ensembl Gene ENSMUSG00000049902
Gene Name RIKEN cDNA 4921517D22 gene
Synonyms
MMRRC Submission 039225-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.066) question?
Stock # R1152 (G1)
Quality Score 217
Status Not validated
Chromosome 13
Chromosomal Location 59835216-59841917 bp(-) (GRCm39)
Type of Mutation frame shift
DNA Base Change (assembly) GCC to GC at 59839412 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000153380 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000061597] [ENSMUST00000225373]
AlphaFold Q8CET0
Predicted Effect probably null
Transcript: ENSMUST00000061597
Predicted Effect probably null
Transcript: ENSMUST00000225373
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225788
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.2%
  • 10x: 95.9%
  • 20x: 91.5%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 8 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap28 C A 17: 68,164,459 (GRCm39) Q554H probably damaging Het
Brd2 ATCTTCTTC ATCTTC 17: 34,332,981 (GRCm39) probably benign Het
Col1a2 G A 6: 4,518,822 (GRCm39) probably benign Het
F5 G C 1: 164,026,486 (GRCm39) R1686P probably damaging Het
Ntrk1 C T 3: 87,685,900 (GRCm39) E741K probably benign Het
Prps1 T G X: 139,369,656 (GRCm39) S160A probably benign Het
Spopfm1 A G 3: 94,173,102 (GRCm39) M37V probably benign Het
Triobp G A 15: 78,850,679 (GRCm39) A278T probably benign Het
Other mutations in 4921517D22Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00827:4921517D22Rik APN 13 59,837,290 (GRCm39) missense probably benign 0.00
IGL01516:4921517D22Rik APN 13 59,838,548 (GRCm39) missense probably benign 0.00
PIT4677001:4921517D22Rik UTSW 13 59,838,305 (GRCm39) missense probably benign 0.12
R0395:4921517D22Rik UTSW 13 59,837,470 (GRCm39) missense possibly damaging 0.94
R0579:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R0664:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R0757:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R0758:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R0777:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R0779:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R0814:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R0870:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R0872:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R0873:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1062:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1064:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1149:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1149:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1151:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1207:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1207:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1285:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1339:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1358:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1359:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1360:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1361:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R1679:4921517D22Rik UTSW 13 59,839,412 (GRCm39) frame shift probably null
R4703:4921517D22Rik UTSW 13 59,837,342 (GRCm39) missense possibly damaging 0.94
R4785:4921517D22Rik UTSW 13 59,839,406 (GRCm39) missense probably benign
R4823:4921517D22Rik UTSW 13 59,838,718 (GRCm39) missense probably damaging 0.99
R5054:4921517D22Rik UTSW 13 59,837,315 (GRCm39) missense probably damaging 0.97
R6144:4921517D22Rik UTSW 13 59,837,347 (GRCm39) missense probably damaging 0.99
R6977:4921517D22Rik UTSW 13 59,839,394 (GRCm39) missense possibly damaging 0.66
R7009:4921517D22Rik UTSW 13 59,838,624 (GRCm39) missense possibly damaging 0.89
R7791:4921517D22Rik UTSW 13 59,838,508 (GRCm39) missense probably benign
R8319:4921517D22Rik UTSW 13 59,838,486 (GRCm39) missense probably benign
R8422:4921517D22Rik UTSW 13 59,839,443 (GRCm39) start codon destroyed probably null 0.01
R8520:4921517D22Rik UTSW 13 59,838,423 (GRCm39) missense possibly damaging 0.90
Predicted Primers
Posted On 2014-01-15