Incidental Mutation 'R1282:Gm12789'
ID 151050
Institutional Source Beutler Lab
Gene Symbol Gm12789
Ensembl Gene ENSMUSG00000078625
Gene Name predicted gene 12789
Synonyms
MMRRC Submission 039348-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.110) question?
Stock # R1282 (G1)
Quality Score 225
Status Not validated
Chromosome 4
Chromosomal Location 101844037-101847428 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 101845487 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tryptophan to Arginine at position 59 (W59R)
Ref Sequence ENSEMBL: ENSMUSP00000102528 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000106914] [ENSMUST00000106915]
AlphaFold B1AUV7
Predicted Effect probably damaging
Transcript: ENSMUST00000106914
AA Change: W59R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000106915
AA Change: W59R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000151553
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.4%
  • 20x: 93.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acmsd T C 1: 127,666,297 (GRCm39) Y23H probably damaging Het
Alkbh2 C T 5: 114,262,287 (GRCm39) E148K probably damaging Het
Atp2a2 G T 5: 122,629,817 (GRCm39) T84K probably benign Het
Cfap65 T A 1: 74,964,263 (GRCm39) T562S probably benign Het
Cyp2b10 G A 7: 25,625,505 (GRCm39) C436Y probably damaging Het
Dnajc7 T C 11: 100,475,467 (GRCm39) D381G probably damaging Het
Dnase1l3 T C 14: 7,983,117 (GRCm38) D129G probably benign Het
Espl1 A G 15: 102,223,826 (GRCm39) T1126A probably benign Het
Exoc3 T C 13: 74,330,411 (GRCm39) N506S probably benign Het
Fastkd3 C A 13: 68,732,676 (GRCm39) N332K possibly damaging Het
Fbxw15 G A 9: 109,387,314 (GRCm39) S227F probably damaging Het
Foxp4 G A 17: 48,186,568 (GRCm39) P404S unknown Het
Gjb3 G A 4: 127,220,224 (GRCm39) R103W probably damaging Het
Greb1l T A 18: 10,547,289 (GRCm39) N1502K probably benign Het
H2-K2 A C 17: 34,218,421 (GRCm39) I165S probably damaging Het
Ipo9 A G 1: 135,330,030 (GRCm39) I470T possibly damaging Het
Kcnu1 A T 8: 26,395,985 (GRCm39) I657F probably benign Het
Lrp1b A T 2: 40,750,773 (GRCm39) N2930K probably damaging Het
Or56a5 T A 7: 104,792,859 (GRCm39) I220F probably benign Het
Prag1 T C 8: 36,567,068 (GRCm39) V73A probably damaging Het
Prrc2b T C 2: 32,113,456 (GRCm39) I1963T probably damaging Het
Rep15 C T 6: 146,934,727 (GRCm39) R189* probably null Het
Resf1 C T 6: 149,230,670 (GRCm39) Q1239* probably null Het
Rtp3 T C 9: 110,815,988 (GRCm39) K188E probably benign Het
Scd2 T C 19: 44,283,620 (GRCm39) L101P probably damaging Het
Scn7a A T 2: 66,531,193 (GRCm39) H561Q probably damaging Het
Sfr1 T C 19: 47,721,407 (GRCm39) S118P probably damaging Het
Slf1 C T 13: 77,191,959 (GRCm39) M958I probably damaging Het
Snrk G T 9: 121,989,586 (GRCm39) R310L possibly damaging Het
Snx11 T C 11: 96,663,987 (GRCm39) Y35C probably damaging Het
Supt6 T C 11: 78,119,594 (GRCm39) T404A possibly damaging Het
Svep1 C A 4: 58,100,032 (GRCm39) L1337F possibly damaging Het
Traf3ip2 C T 10: 39,502,401 (GRCm39) T183M probably damaging Het
Vmn2r28 A T 7: 5,484,301 (GRCm39) M633K probably damaging Het
Vmn2r67 A G 7: 84,785,932 (GRCm39) V691A probably benign Het
Other mutations in Gm12789
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0267:Gm12789 UTSW 4 101,845,319 (GRCm39) missense probably benign 0.03
R1551:Gm12789 UTSW 4 101,846,131 (GRCm39) missense probably benign 0.08
R2039:Gm12789 UTSW 4 101,846,183 (GRCm39) splice site probably benign
R4090:Gm12789 UTSW 4 101,845,526 (GRCm39) missense possibly damaging 0.78
R4168:Gm12789 UTSW 4 101,847,159 (GRCm39) missense possibly damaging 0.50
R4585:Gm12789 UTSW 4 101,847,159 (GRCm39) missense possibly damaging 0.50
R4817:Gm12789 UTSW 4 101,846,079 (GRCm39) missense probably damaging 0.99
R4866:Gm12789 UTSW 4 101,846,182 (GRCm39) splice site probably benign
R4900:Gm12789 UTSW 4 101,846,182 (GRCm39) splice site probably benign
R5429:Gm12789 UTSW 4 101,847,158 (GRCm39) missense possibly damaging 0.50
R9723:Gm12789 UTSW 4 101,846,083 (GRCm39) missense possibly damaging 0.61
Predicted Primers PCR Primer
(F):5'- GCTAAATGCTCCACCAGGTTCCTTC -3'
(R):5'- TCTGAGCTGTCCTGACCTATGACTG -3'

Sequencing Primer
(F):5'- CTGAATATCTATCAGGATGAGCACC -3'
(R):5'- GCATGTCGATGACATCATTAGCC -3'
Posted On 2014-01-29