Incidental Mutation 'R0676:Gm10845'
ID 61658
Institutional Source Beutler Lab
Gene Symbol Gm10845
Ensembl Gene ENSMUSG00000095959
Gene Name predicted gene 10845
Synonyms
MMRRC Submission 038861-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # R0676 (G1)
Quality Score 123
Status Validated
Chromosome 14
Chromosomal Location 80097961-80106616 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to A at 80100644 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000179430]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000179430
SMART Domains Protein: ENSMUSP00000137634
Gene: ENSMUSG00000095959

DomainStartEndE-ValueType
low complexity region 31 36 N/A INTRINSIC
low complexity region 45 56 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180427
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228217
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.4%
  • 20x: 95.2%
Validation Efficiency 100% (52/52)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310003L06Rik A G 5: 88,112,516 (GRCm39) probably benign Het
Arhgef25 A G 10: 127,019,879 (GRCm39) probably null Het
B3galnt2 T C 13: 14,170,378 (GRCm39) S243P probably benign Het
Col11a2 A G 17: 34,276,249 (GRCm39) N799D probably damaging Het
Cpb1 T C 3: 20,320,697 (GRCm39) probably null Het
Crot A C 5: 9,043,622 (GRCm39) probably benign Het
Ctnna3 A C 10: 64,245,040 (GRCm39) H451P probably benign Het
Cts6 C T 13: 61,345,298 (GRCm39) probably benign Het
Dock2 T C 11: 34,586,063 (GRCm39) T540A probably damaging Het
Dysf C A 6: 84,090,318 (GRCm39) F956L probably benign Het
Gabrg3 A T 7: 56,374,169 (GRCm39) Y466N probably damaging Het
H2-M5 A G 17: 37,300,034 (GRCm39) F47L possibly damaging Het
H4c9 T C 13: 22,225,276 (GRCm39) probably null Het
Il1rl1 CTTGTTGTTGTTGTTGTTG CTTGTTGTTGTTGTTGTTGTTG 1: 40,481,734 (GRCm39) probably benign Het
Immt A G 6: 71,828,828 (GRCm39) S128G probably benign Het
Klb A T 5: 65,536,398 (GRCm39) D576V probably damaging Het
Lpin1 A T 12: 16,590,980 (GRCm39) N817K possibly damaging Het
Lrrk1 C T 7: 65,944,729 (GRCm39) R627H probably damaging Het
Luzp1 A G 4: 136,269,996 (GRCm39) K740E probably damaging Het
Mapk9 T C 11: 49,773,983 (GRCm39) *382Q probably null Het
Mn1 A G 5: 111,568,900 (GRCm39) S957G possibly damaging Het
Mrgprb8 A T 7: 48,038,412 (GRCm39) M28L probably benign Het
Myo1a A G 10: 127,555,749 (GRCm39) I913V probably benign Het
Nolc1 T A 19: 46,068,528 (GRCm39) probably benign Het
Pde4dip A C 3: 97,624,413 (GRCm39) probably benign Het
Rbpj C T 5: 53,803,390 (GRCm39) probably benign Het
Ric1 T C 19: 29,555,047 (GRCm39) I387T probably benign Het
Ruvbl1 A G 6: 88,450,182 (GRCm39) R58G probably damaging Het
Scarb1 C A 5: 125,374,278 (GRCm39) probably benign Het
Sh3tc1 A T 5: 35,876,458 (GRCm39) probably benign Het
Slc22a23 G A 13: 34,379,462 (GRCm39) T435I probably damaging Het
Slc22a26 A T 19: 7,773,509 (GRCm39) probably benign Het
Taf6l T C 19: 8,750,733 (GRCm39) I114V probably benign Het
Tbc1d8b A G X: 138,613,025 (GRCm39) S284G possibly damaging Het
Tmem131l C T 3: 83,842,122 (GRCm39) probably benign Het
Vmn2r115 C T 17: 23,565,238 (GRCm39) S375F probably benign Het
Other mutations in Gm10845
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0106:Gm10845 UTSW 14 80,100,644 (GRCm39) exon noncoding transcript
R0106:Gm10845 UTSW 14 80,100,644 (GRCm39) exon noncoding transcript
R1620:Gm10845 UTSW 14 80,100,669 (GRCm39) exon noncoding transcript
R3433:Gm10845 UTSW 14 80,100,851 (GRCm39) exon noncoding transcript
R4374:Gm10845 UTSW 14 80,100,563 (GRCm39) exon noncoding transcript
R5727:Gm10845 UTSW 14 80,100,770 (GRCm39) exon noncoding transcript
R5975:Gm10845 UTSW 14 80,100,614 (GRCm39) exon noncoding transcript
Predicted Primers
Posted On 2013-07-30