Incidental Mutation 'R4538:3110018I06Rik'
ID 333421
Institutional Source Beutler Lab
Gene Symbol 3110018I06Rik
Ensembl Gene ENSMUSG00000060375
Gene Name RIKEN cDNA 3110018I06 gene
Synonyms
MMRRC Submission 041775-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.100) question?
Stock # R4538 (G1)
Quality Score 225
Status Validated
Chromosome 12
Chromosomal Location 107454891-107455895 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 107455096 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Methionine at position 61 (V61M)
Ref Sequence ENSEMBL: ENSMUSP00000080894 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000082269]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000082269
AA Change: V61M
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222644
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223301
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.5%
Validation Efficiency 97% (36/37)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc9 A G 6: 142,560,138 (GRCm39) probably null Het
Adcy10 A T 1: 165,340,696 (GRCm39) M234L probably benign Het
B4galt3 T C 1: 171,100,280 (GRCm39) F150S probably damaging Het
Bag4 C T 8: 26,259,516 (GRCm39) A228T probably benign Het
Chd4 A T 6: 125,097,649 (GRCm39) D1377V probably damaging Het
Cope T A 8: 70,759,157 (GRCm39) I16N probably damaging Het
Cpd A T 11: 76,681,825 (GRCm39) N1140K probably benign Het
Cyp7b1 A T 3: 18,151,745 (GRCm39) I156N possibly damaging Het
Depdc5 T C 5: 33,141,290 (GRCm39) Y1397H probably damaging Het
Dnajc13 CT C 9: 104,064,004 (GRCm39) probably benign Het
Ebf1 T A 11: 44,798,822 (GRCm39) D289E probably benign Het
Egflam T C 15: 7,281,918 (GRCm39) Y406C probably damaging Het
Hfm1 T C 5: 107,022,756 (GRCm39) T949A possibly damaging Het
Ifih1 A G 2: 62,447,756 (GRCm39) V316A probably damaging Het
Kif1a C T 1: 93,004,769 (GRCm39) V142M probably damaging Het
Kng2 C A 16: 22,806,813 (GRCm39) R462L probably benign Het
Lrrn1 T A 6: 107,545,598 (GRCm39) N465K probably benign Het
Mdn1 T A 4: 32,722,334 (GRCm39) L2372Q probably damaging Het
Men1 T C 19: 6,386,784 (GRCm39) F159L possibly damaging Het
Mul1 T C 4: 138,165,706 (GRCm39) probably benign Het
Or2l13b A T 16: 19,349,381 (GRCm39) C96* probably null Het
Pramel6 T G 2: 87,338,903 (GRCm39) H34Q probably benign Het
Ripk4 A T 16: 97,544,352 (GRCm39) L702* probably null Het
Slc5a4a C T 10: 76,013,929 (GRCm39) R379* probably null Het
Slc9a3 T C 13: 74,309,851 (GRCm39) V513A possibly damaging Het
Strada A C 11: 106,058,651 (GRCm39) M245R probably damaging Het
Sycp1 A T 3: 102,748,278 (GRCm39) I838K probably benign Het
Tns2 C T 15: 102,017,369 (GRCm39) R281C probably damaging Het
Trbv17 A C 6: 41,140,286 (GRCm39) N47T probably benign Het
Washc3 T A 10: 88,051,871 (GRCm39) S87T probably benign Het
Other mutations in 3110018I06Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0944:3110018I06Rik UTSW 12 107,455,268 (GRCm39) missense unknown
R7661:3110018I06Rik UTSW 12 107,455,215 (GRCm39) missense unknown
Z1176:3110018I06Rik UTSW 12 107,455,114 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TGAGTCAGCACAAGAGTCTATC -3'
(R):5'- ATACATCCTGGAAACCAAGGG -3'

Sequencing Primer
(F):5'- GAGTCAGCACAAGAGTCTATCTTAGC -3'
(R):5'- GTGAAATGTGAACTTAAGGGTGTC -3'
Posted On 2015-08-18