Incidental Mutation 'R6579:Gm3045'
ID 523948
Institutional Source Beutler Lab
Gene Symbol Gm3045
Ensembl Gene ENSMUSG00000110477
Gene Name predicted gene 3045
Synonyms
MMRRC Submission 044703-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.129) question?
Stock # R6579 (G1)
Quality Score 221.009
Status Validated
Chromosome 13
Chromosomal Location 56574407-56581566 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 56578103 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Leucine at position 180 (S180L)
Ref Sequence ENSEMBL: ENSMUSP00000148690 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000212844]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000212844
AA Change: S180L

PolyPhen 2 Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)
Meta Mutation Damage Score 0.6329 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.6%
  • 20x: 92.4%
Validation Efficiency 100% (36/36)
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017B05Rik A T 9: 57,161,507 (GRCm39) V80D possibly damaging Het
6330409D20Rik T C 2: 32,630,663 (GRCm39) probably benign Het
Adam15 C T 3: 89,252,936 (GRCm39) V261M probably damaging Het
Adam29 G T 8: 56,325,779 (GRCm39) T225K probably damaging Het
Ankrd52 A G 10: 128,223,011 (GRCm39) T654A probably damaging Het
AU021092 T A 16: 5,040,020 (GRCm39) I35F probably damaging Het
Cdk20 G T 13: 64,584,348 (GRCm39) Q114H probably benign Het
Col22a1 A C 15: 71,753,502 (GRCm39) S133A probably benign Het
Cyp3a44 A T 5: 145,727,516 (GRCm39) F271Y probably damaging Het
Dchs1 A T 7: 105,412,120 (GRCm39) V1332E probably benign Het
Dhrs7l A T 12: 72,668,658 (GRCm39) D117E probably benign Het
Dnai7 A T 6: 145,124,744 (GRCm39) M527K probably benign Het
Dnajc5 A G 2: 181,189,209 (GRCm39) N62D possibly damaging Het
Hycc1 A T 5: 24,171,381 (GRCm39) V347D possibly damaging Het
Igkv14-130 T A 6: 67,768,421 (GRCm39) Y93* probably null Het
Myo1c C T 11: 75,562,461 (GRCm39) P918S probably benign Het
Nell2 A T 15: 95,282,957 (GRCm39) Y362N possibly damaging Het
Or5an1c C T 19: 12,218,726 (GRCm39) V100I probably benign Het
Peli1 A T 11: 21,097,059 (GRCm39) T150S probably benign Het
Pkhd1 T C 1: 20,271,047 (GRCm39) T3169A probably benign Het
Polr2m T A 9: 71,393,002 (GRCm39) E26V probably damaging Het
Rhbdf2 A G 11: 116,495,289 (GRCm39) V238A probably benign Het
Rims1 G T 1: 22,496,166 (GRCm39) P820H probably damaging Het
Rnf213 A G 11: 119,327,106 (GRCm39) T1698A probably damaging Het
Scgn C T 13: 24,143,717 (GRCm39) A216T probably damaging Het
Serpina11 T A 12: 103,951,007 (GRCm39) D238V probably damaging Het
Setd2 A T 9: 110,378,846 (GRCm39) E887V possibly damaging Het
Tiam2 CGGG CGGGG 17: 3,464,897 (GRCm39) probably null Het
Trak1 C A 9: 121,272,704 (GRCm39) N197K probably benign Het
Trpm2 C T 10: 77,773,660 (GRCm39) R585Q probably benign Het
Uchl5 T A 1: 143,674,130 (GRCm39) Y211N probably damaging Het
Usf3 T A 16: 44,039,197 (GRCm39) S1226T possibly damaging Het
Utrn T C 10: 12,623,750 (GRCm39) T163A probably benign Het
Ywhaz T C 15: 36,791,166 (GRCm39) Y19C probably damaging Het
Zcchc14 T C 8: 122,331,206 (GRCm39) probably benign Het
Other mutations in Gm3045
AlleleSourceChrCoordTypePredicted EffectPPH Score
R8398:Gm3045 UTSW 13 56,577,280 (GRCm39) missense possibly damaging 0.94
R9347:Gm3045 UTSW 13 56,578,160 (GRCm39) missense unknown
R9667:Gm3045 UTSW 13 56,577,253 (GRCm39) missense possibly damaging 0.73
Predicted Primers PCR Primer
(F):5'- CCAAAGGTTCCCCACTTGAC -3'
(R):5'- GAGGCACTGGAGTATGACTC -3'

Sequencing Primer
(F):5'- ACTTGACAGAACTTGGCCTAGGTC -3'
(R):5'- GAGTATGACTCCCCAGAAGTCC -3'
Posted On 2018-06-22