Incidental Mutation 'R1189:9930022D16Rik'
ID 102433
Institutional Source Beutler Lab
Gene Symbol 9930022D16Rik
Ensembl Gene ENSMUSG00000045065
Gene Name RIKEN cDNA 9930022D16 gene
Synonyms
MMRRC Submission 039261-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.083) question?
Stock # R1189 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 109304743-109311231 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 109308934 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 100 (H100R)
Ref Sequence ENSEMBL: ENSMUSP00000062888 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055404]
AlphaFold Q8BG27
Predicted Effect unknown
Transcript: ENSMUST00000055404
AA Change: H100R
Coding Region Coverage
  • 1x: 98.6%
  • 3x: 97.2%
  • 10x: 92.5%
  • 20x: 81.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 19 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc2 T A 19: 43,807,852 (GRCm39) V831D probably damaging Het
Akap11 A T 14: 78,750,787 (GRCm39) S533R probably benign Het
Aldh1a2 G T 9: 71,171,105 (GRCm39) A198S possibly damaging Het
Cbarp C A 10: 79,967,630 (GRCm39) R537L possibly damaging Het
Crybg1 T A 10: 43,874,790 (GRCm39) S773C probably damaging Het
Cyp3a13 G T 5: 137,909,892 (GRCm39) probably null Het
Gatad1 T A 5: 3,693,701 (GRCm39) D156V probably damaging Het
Ift172 T A 5: 31,443,174 (GRCm39) probably null Het
Lrrtm2 C T 18: 35,346,545 (GRCm39) W252* probably null Het
Mitf T C 6: 97,983,086 (GRCm39) C270R possibly damaging Het
Muc6 T A 7: 141,232,122 (GRCm39) S1002C probably damaging Het
Or4k2 A G 14: 50,424,539 (GRCm39) I45T probably damaging Het
Or5b113 A T 19: 13,342,543 (GRCm39) M184L probably benign Het
Pcdhb8 C T 18: 37,489,620 (GRCm39) Q92* probably null Het
Plekhm1 A G 11: 103,277,888 (GRCm39) S403P probably benign Het
Ppara A G 15: 85,682,365 (GRCm39) I354V probably benign Het
Psmd2 T C 16: 20,480,644 (GRCm39) M761T probably benign Het
Xirp2 T A 2: 67,343,805 (GRCm39) N2015K probably damaging Het
Zbtb39 C G 10: 127,578,175 (GRCm39) Q250E probably benign Het
Other mutations in 9930022D16Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01019:9930022D16Rik APN 11 109,308,737 (GRCm39) splice site probably benign
R4608:9930022D16Rik UTSW 11 109,308,855 (GRCm39) missense unknown
R6586:9930022D16Rik UTSW 11 109,308,786 (GRCm39) missense unknown
R8163:9930022D16Rik UTSW 11 109,304,883 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- CGGGGTTTTACCACGATGCTGATAC -3'
(R):5'- GGCACAATTTGCTCTGCCATTTGAC -3'

Sequencing Primer
(F):5'- TTACCACGATGCTGATACTACGG -3'
(R):5'- CATTTGACACTATGCCTTTGGG -3'
Posted On 2014-01-15