Incidental Mutation 'R4224:9330182O14Rik'
ID 319977
Institutional Source Beutler Lab
Gene Symbol 9330182O14Rik
Ensembl Gene ENSMUSG00000094112
Gene Name RIKEN cDNA 9330182O14 gene
Synonyms
MMRRC Submission 041044-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # R4224 (G1)
Quality Score 225
Status Validated
Chromosome 15
Chromosomal Location 39997761-40013406 bp(+) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to C at 40005672 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000154680 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000179120] [ENSMUST00000228780]
AlphaFold J3QNB2
Predicted Effect probably null
Transcript: ENSMUST00000179120
Predicted Effect probably null
Transcript: ENSMUST00000228780
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 96.0%
Validation Efficiency 95% (42/44)
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abl2 A G 1: 156,461,417 (GRCm39) T440A probably damaging Het
Acat2 T C 17: 13,181,772 (GRCm39) probably benign Het
Acsbg1 C T 9: 54,523,325 (GRCm39) R434H possibly damaging Het
Aif1l A T 2: 31,852,251 (GRCm39) S40C probably damaging Het
Atosa T A 9: 74,916,008 (GRCm39) N209K probably damaging Het
Atp6v1a C A 16: 43,922,174 (GRCm39) A355S probably damaging Het
Corin T C 5: 72,500,451 (GRCm39) E391G probably damaging Het
Dnah11 T G 12: 118,094,627 (GRCm39) S814R probably benign Het
Fer1l4 A C 2: 155,862,309 (GRCm39) V1788G probably benign Het
Gm7964 T G 7: 83,406,030 (GRCm39) N281K probably damaging Het
Grin1 T C 2: 25,187,332 (GRCm39) probably benign Het
Ica1 T C 6: 8,659,960 (GRCm39) K112R probably benign Het
Itpr3 T C 17: 27,326,232 (GRCm39) V1334A probably damaging Het
Khdc3 C G 9: 73,010,153 (GRCm39) H70D possibly damaging Het
Lama3 T C 18: 12,583,460 (GRCm39) C683R probably damaging Het
Mettl21a G T 1: 64,647,115 (GRCm39) Y147* probably null Het
Mr1 A T 1: 155,006,465 (GRCm39) I294N possibly damaging Het
Or52z12 A G 7: 103,233,966 (GRCm39) T246A probably damaging Het
Or7e170 T A 9: 19,794,896 (GRCm39) Y235F probably benign Het
Pals1 A G 12: 78,876,492 (GRCm39) K479E probably damaging Het
Pcdhgb7 T A 18: 37,886,856 (GRCm39) D675E probably benign Het
Polr1has T C 17: 37,269,617 (GRCm39) probably benign Het
Ptbp1 T C 10: 79,695,047 (GRCm39) I125T probably benign Het
Rnf213 C T 11: 119,327,649 (GRCm39) R1879* probably null Het
Slc8a1 A G 17: 81,956,781 (GRCm39) F86L probably damaging Het
Spdya G A 17: 71,869,519 (GRCm39) V105I probably benign Het
Sspo G T 6: 48,428,091 (GRCm39) V313L possibly damaging Het
Stard9 A G 2: 120,495,472 (GRCm39) T116A possibly damaging Het
Tnnt1 T C 7: 4,513,006 (GRCm39) H92R probably damaging Het
Trim37 T A 11: 87,107,289 (GRCm39) C907S probably damaging Het
Trim43b T A 9: 88,972,692 (GRCm39) Q154L probably benign Het
Tssk3 T C 4: 129,384,392 (GRCm39) D3G probably benign Het
Ubash3a T C 17: 31,456,902 (GRCm39) Y521H probably damaging Het
Vmn1r73 T C 7: 11,490,506 (GRCm39) I108T probably damaging Het
Vmn2r14 A G 5: 109,364,149 (GRCm39) M589T probably benign Het
Vmn2r60 A T 7: 41,765,952 (GRCm39) T20S probably benign Het
Vps13b A G 15: 35,876,565 (GRCm39) T2799A probably damaging Het
Zcchc18 A T X: 135,895,415 (GRCm39) N10I probably damaging Het
Other mutations in 9330182O14Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R5426:9330182O14Rik UTSW 15 40,011,933 (GRCm39) missense unknown
R5426:9330182O14Rik UTSW 15 40,011,932 (GRCm39) missense unknown
R7124:9330182O14Rik UTSW 15 40,008,303 (GRCm39) missense unknown
R7569:9330182O14Rik UTSW 15 40,008,344 (GRCm39) missense unknown
R9169:9330182O14Rik UTSW 15 40,005,632 (GRCm39) nonsense probably null
R9697:9330182O14Rik UTSW 15 40,005,500 (GRCm39) start gained probably benign
Predicted Primers PCR Primer
(F):5'- GTCTGCCAGTACTTTCCAGC -3'
(R):5'- CAGTTGGCAGGATGTATGGC -3'

Sequencing Primer
(F):5'- AGTACTTTCCAGCCCAGGC -3'
(R):5'- CAGGGGAGGGGTTCTGACTC -3'
Posted On 2015-06-12