Incidental Mutation 'IGL00978:0610009L18Rik'
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ID306639
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 0610009L18Rik
Ensembl Gene ENSMUSG00000043644
Gene NameRIKEN cDNA 0610009L18 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL00978
Quality Score
Status
Chromosome11
Chromosomal Location120348678-120351190 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 120350947 bp
ZygosityHeterozygous
Amino Acid Change (L125P)
Predicted Effect noncoding transcript
AA Change: L125P
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alpk2 A T 18: 65,291,534 Het
Angptl8 T C 9: 21,837,053 Het
AU040320 T A 4: 126,828,839 D383E probably benign Het
Cep97 C T 16: 55,924,960 silent Het
Clcn4 A T 7: 7,287,673 L709H probably damaging Het
Col5a2 T C 1: 45,376,739 N1416S probably benign Het
Erbb2 C T 11: 98,435,630 P1027S probably damaging Het
Eya1 A G 1: 14,270,701 Het
Gfm2 T C 13: 97,162,977 I402T probably benign Het
Gmeb2 A T 2: 181,259,043 V187E probably benign Het
Hectd1 T C 12: 51,791,390 H662R possibly damaging Het
Ifne T C 4: 88,880,031 Q50R probably benign Het
Kidins220 A G 12: 25,057,474 D1672G probably damaging Het
Klhl32 T A 4: 24,682,245 D146V probably damaging Het
Krt36 T C 11: 100,102,948 I355V probably damaging Het
Lrrcc1 T A 3: 14,536,128 S73R possibly damaging Het
Ltbp3 A T 19: 5,754,019 H853L probably benign Het
Map3k5 G A 10: 20,141,567 R1377Q probably damaging Het
Mcm8 A G 2: 132,821,406 N176S probably benign Het
Mylk3 A T 8: 85,355,526 L344* probably null Het
Nras T C 3: 103,058,916 noncoding transcript Het
Olfr135 A T 17: 38,208,982 I246F probably damaging Het
Olfr670 A T 7: 104,960,716 N5K probably damaging Het
Os9 A T 10: 127,120,509 Y67N probably damaging Het
Pitpnm1 A G 19: 4,101,228 D15G possibly damaging Het
Reg3a A T 6: 78,382,301 R95* probably null Het
Rnf17 C T 14: 56,512,271 P1425S probably damaging Het
Smad2 T C 18: 76,299,775 Het
Ttll5 C T 12: 85,933,482 Q947* probably null Het
Uri1 A T 7: 37,996,731 noncoding transcript Het
Vmn2r102 G T 17: 19,678,923 probably null Het
Vmn2r70 T G 7: 85,563,799 M467L probably benign Het
Zfp318 T A 17: 46,413,726 D2218E possibly damaging Het
Zfp692 T C 11: 58,314,029 I405T possibly damaging Het
Zfp692 A G 11: 58,309,998 H235R possibly damaging Het
Posted OnApr 16, 2015