Incidental Mutation 'R0060:1810011H11Rik'
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ID16398
Institutional Source Beutler Lab
Gene Symbol 1810011H11Rik
Ensembl Gene ENSMUSG00000041707
Gene NameRIKEN cDNA 1810011H11 gene
Synonyms
MMRRC Submission 038353-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.036) question?
Stock #R0060 (G1)
Quality Score
Status Validated
Chromosome14
Chromosomal Location32785963-32817984 bp(+) (GRCm38)
Type of Mutationintron
DNA Base Change (assembly) C to A at 32806769 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000039191] [ENSMUST00000227060] [ENSMUST00000227871]
Predicted Effect probably benign
Transcript: ENSMUST00000039191
SMART Domains Protein: ENSMUSP00000132997
Gene: ENSMUSG00000041707

DomainStartEndE-ValueType
Pfam:DUF4514 16 75 3.6e-40 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000227060
Predicted Effect probably benign
Transcript: ENSMUST00000227871
Predicted Effect probably benign
Transcript: ENSMUST00000228481
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228955
Coding Region Coverage
  • 1x: 90.4%
  • 3x: 88.3%
  • 10x: 83.8%
  • 20x: 78.1%
Validation Efficiency 94% (74/79)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1810065E05Rik A C 11: 58,422,182 probably benign Het
4930432E11Rik A G 7: 29,574,170 noncoding transcript Het
A630091E08Rik A G 7: 98,543,668 noncoding transcript Het
Abca8a T C 11: 110,070,480 T539A probably damaging Het
Adam34 A T 8: 43,675,883 probably benign Het
Ankrd60 A T 2: 173,572,613 M1K probably null Het
Cald1 T C 6: 34,715,459 probably benign Het
Capn7 T C 14: 31,365,604 probably benign Het
Cd109 G A 9: 78,703,107 E1145K probably damaging Het
Celsr1 A T 15: 85,922,198 V2353D probably damaging Het
Cep135 A T 5: 76,621,350 I616F probably benign Het
Cep162 T A 9: 87,237,825 probably benign Het
Cep350 C T 1: 155,928,626 D904N probably damaging Het
Cep85 T C 4: 134,167,300 D65G probably damaging Het
Cfdp1 T C 8: 111,840,354 probably benign Het
Chl1 T A 6: 103,711,058 probably benign Het
Colec10 G A 15: 54,439,146 probably benign Het
Crxos A G 7: 15,898,523 T40A possibly damaging Het
Dnhd1 A G 7: 105,668,514 D472G probably damaging Het
Dpp6 C A 5: 27,598,819 N254K probably damaging Het
Eps8l3 T C 3: 107,879,541 L11S probably damaging Het
Flad1 G A 3: 89,402,245 R515* probably null Het
Fzd5 T C 1: 64,735,676 T309A probably benign Het
Gm19685 T C 17: 60,768,423 Het
Gsdme A G 6: 50,221,029 I317T possibly damaging Het
Hist1h2ba A T 13: 23,933,945 I71N possibly damaging Het
Incenp A G 19: 9,885,459 probably benign Het
Itgad T C 7: 128,202,986 S979P probably damaging Het
Kat2b T C 17: 53,654,543 V557A probably damaging Het
Lamc1 A T 1: 153,241,868 probably benign Het
Lgi4 G A 7: 31,063,571 G157D probably damaging Het
Mga T C 2: 119,960,961 probably null Het
Nubpl T C 12: 52,310,687 probably benign Het
Olfr1105 T C 2: 87,033,774 Y149C probably damaging Het
Olfr124 T C 17: 37,806,000 L285P probably damaging Het
Olfr898 C T 9: 38,349,512 S143F probably benign Het
Peak1 A T 9: 56,227,823 I78K probably damaging Het
Prune2 T A 19: 17,003,733 F85I probably damaging Het
Rbm11 G T 16: 75,598,779 D113Y probably damaging Het
Rif1 C T 2: 52,111,117 R1528C probably damaging Het
Sema4d A G 13: 51,705,257 probably benign Het
Slc30a4 T A 2: 122,685,184 T381S probably benign Het
Slf2 G T 19: 44,948,004 G696V probably damaging Het
Suv39h2 T C 2: 3,464,916 Y134C probably damaging Het
Tmem89 T A 9: 108,915,417 V126D probably damaging Het
Trf T C 9: 103,220,922 T46A probably benign Het
Trmt6 C T 2: 132,806,769 R415Q possibly damaging Het
Trp53bp1 T C 2: 121,204,525 K1625E probably damaging Het
Usp6nl T A 2: 6,440,890 D559E probably benign Het
Wdr75 A G 1: 45,816,617 D476G probably benign Het
Wrap53 A C 11: 69,563,430 L261V possibly damaging Het
Zcchc4 T A 5: 52,807,078 I292N possibly damaging Het
Other mutations in 1810011H11Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01930:1810011H11Rik APN 14 32816857 missense probably benign 0.12
IGL03225:1810011H11Rik APN 14 32805176 missense probably damaging 0.97
R0255:1810011H11Rik UTSW 14 32808363 missense possibly damaging 0.91
R1520:1810011H11Rik UTSW 14 32805126 intron probably benign
R4641:1810011H11Rik UTSW 14 32806882 missense probably damaging 0.99
R5218:1810011H11Rik UTSW 14 32816836 splice site probably null
R6111:1810011H11Rik UTSW 14 32806798 missense possibly damaging 0.93
R6793:1810011H11Rik UTSW 14 32806821 missense probably benign
Posted On2013-01-20