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
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 Leucine to Proline (L-P)
Predicted Effect unknown
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 probably benign Het
AU040320 T A 4: 126,828,839 D383E probably benign Het
Cep97 C T 16: 55,924,960 probably benign Het
Clcn4-2 A T 7: 7,287,673 L709H possibly damaging Het
Col5a2 T C 1: 45,376,739 N⇒S possibly damaging 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
Gm6484 T C 9: 21,837,053 probably benign Het
Gmeb2 A T 2: 181,259,043 V187E probably benign Het
Hectd1 T C 12: 51,791,390 H663R possibly damaging Het
Ifne T C 4: 88,880,031 Q50R probably damaging Het
Kidins220 A G 12: 25,057,474 D1672G probably damaging Het
Klhl32 T A 4: 24,682,245 D146V possibly damaging Het
Krt36 T C 11: 100,102,948 I355V probably benign 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 Het
Olfr135 A T 17: 38,208,982 I246F possibly damaging Het
Olfr670 A T 7: 104,960,716 N5K probably damaging Het
Os9 A T 10: 127,120,509 Y67N possibly 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 probably benign Het
Ttll5 C T 12: 85,933,482 Q947* probably null Het
Uri1 A T 7: 37,996,731 probably benign 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 probably benign Het
Zfp692 T C 11: 58,314,029 I405T probably damaging Het
Zfp692 A G 11: 58,309,998 H235R probably benign Het
Posted OnApr 16, 2015