Incidental Mutation 'R1019:A830031A19Rik'
ID 96772
Institutional Source Beutler Lab
Gene Symbol A830031A19Rik
Ensembl Gene ENSMUSG00000055010
Gene Name RIKEN cDNA A830031A19 gene
Synonyms LOC268391
MMRRC Submission 039123-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.249) question?
Stock # R1019 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 23998955-24025054 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 23999438 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Cysteine at position 53 (R53C)
Ref Sequence ENSEMBL: ENSMUSP00000063283 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000068360]
AlphaFold Q8BNT5
Predicted Effect unknown
Transcript: ENSMUST00000068360
AA Change: R53C
SMART Domains Protein: ENSMUSP00000063283
Gene: ENSMUSG00000055010
AA Change: R53C

DomainStartEndE-ValueType
low complexity region 42 57 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
6430548M08Rik G C 8: 120,872,209 (GRCm39) E46Q probably damaging Het
9130401M01Rik A G 15: 57,885,823 (GRCm39) I353T possibly damaging Het
Abcc6 T C 7: 45,663,531 (GRCm39) R378G possibly damaging Het
Adam10 A G 9: 70,668,922 (GRCm39) N413D probably benign Het
Csmd2 T C 4: 128,415,807 (GRCm39) V2712A probably benign Het
Dnhd1 T C 7: 105,358,378 (GRCm39) F3289S probably damaging Het
Hectd1 A G 12: 51,795,440 (GRCm39) S2330P probably damaging Het
Ift74 C T 4: 94,524,072 (GRCm39) A196V probably benign Het
Kifc1 G A 17: 34,103,685 (GRCm39) R195C probably benign Het
Lipo2 A T 19: 33,708,257 (GRCm39) C252* probably null Het
Mrgpra1 C G 7: 46,984,833 (GRCm39) C282S probably benign Het
Nfatc2 A T 2: 168,346,799 (GRCm39) L765Q probably damaging Het
Or13a26 C T 7: 140,284,407 (GRCm39) P81L probably damaging Het
Or1l8 A G 2: 36,817,764 (GRCm39) F121L probably benign Het
Otof C A 5: 30,528,087 (GRCm39) V1924L probably damaging Het
Pdhb T C 14: 8,171,442 (GRCm38) Q62R probably benign Het
Plbd1 A G 6: 136,628,903 (GRCm39) V55A probably benign Het
Poteg T A 8: 27,937,852 (GRCm39) F3I possibly damaging Het
Rptor A G 11: 119,734,569 (GRCm39) D46G probably damaging Het
Slc18a1 C T 8: 69,527,685 (GRCm39) probably null Het
Slc37a1 A G 17: 31,534,568 (GRCm39) N80S probably benign Het
Slc6a18 T A 13: 73,825,998 (GRCm39) R17S probably damaging Het
Spata31d1a A G 13: 59,850,182 (GRCm39) S649P probably benign Het
Syngr3 G T 17: 24,906,534 (GRCm39) Q94K possibly damaging Het
Tgm2 C A 2: 157,966,074 (GRCm39) E527* probably null Het
Tnc T A 4: 63,880,319 (GRCm39) T1952S probably damaging Het
Ubqln3 C T 7: 103,790,593 (GRCm39) R499Q probably benign Het
Uck1 A G 2: 32,146,205 (GRCm39) V230A possibly damaging Het
Unc13d G A 11: 115,958,900 (GRCm39) R754C probably benign Het
Zfp708 C T 13: 67,222,162 (GRCm39) A73T probably benign Het
Other mutations in A830031A19Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03007:A830031A19Rik APN 11 23,999,248 (GRCm39) utr 3 prime probably benign
R5524:A830031A19Rik UTSW 11 24,008,776 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- GCGTTGGCTCAGATCCCCTTATTAG -3'
(R):5'- GAGAAGAGTTTTCCTGGACCCTGC -3'

Sequencing Primer
(F):5'- TCAGATCCCCTTATTAGAAGTACATC -3'
(R):5'- gttactgttactgttactgttcctg -3'
Posted On 2014-01-05