Incidental Mutation 'IGL01690:4931429P17Rik'
ID 104090
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4931429P17Rik
Ensembl Gene ENSMUSG00000047324
Gene Name RIKEN cDNA 4931429P17 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.100) question?
Stock # IGL01690
Quality Score
Status
Chromosome 13
Chromosomal Location 48113806-48172084 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 48114446 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000061899
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agap2 T C 10: 126,918,827 (GRCm39) probably benign Het
Bicra G A 7: 15,721,678 (GRCm39) T613I probably benign Het
Cd163 T C 6: 124,284,277 (GRCm39) S150P possibly damaging Het
Cfap107 G A 4: 144,165,098 (GRCm39) T26M probably damaging Het
F830045P16Rik T G 2: 129,314,614 (GRCm39) Q221P probably damaging Het
Fam135b T A 15: 71,328,784 (GRCm39) M1172L probably benign Het
Fbxo2 G T 4: 148,249,581 (GRCm39) probably null Het
Frem1 C T 4: 82,877,533 (GRCm39) probably benign Het
Galnt17 C T 5: 131,114,734 (GRCm39) probably null Het
Gipc2 A G 3: 151,833,771 (GRCm39) I170T probably damaging Het
Gm2399 C T 13: 12,717,417 (GRCm39) noncoding transcript Het
Hdac10 T A 15: 89,010,194 (GRCm39) M283L probably benign Het
Icam5 A G 9: 20,946,095 (GRCm39) E309G possibly damaging Het
Ift70a1 A G 2: 75,810,277 (GRCm39) V602A probably benign Het
Igkv3-5 T A 6: 70,640,865 (GRCm39) S115R probably benign Het
Impg2 A G 16: 56,025,568 (GRCm39) R67G probably damaging Het
Kansl1l T C 1: 66,840,232 (GRCm39) Y356C probably damaging Het
Ly75 T C 2: 60,168,655 (GRCm39) D751G probably damaging Het
Lyst A G 13: 13,917,831 (GRCm39) D3297G probably damaging Het
Mall A G 2: 127,571,699 (GRCm39) F30L probably benign Het
Map1b C T 13: 99,571,512 (GRCm39) G403D probably damaging Het
Mmp11 T C 10: 75,762,730 (GRCm39) Y241C probably damaging Het
Niban1 C A 1: 151,579,555 (GRCm39) R425S probably damaging Het
Or4a72 A G 2: 89,405,557 (GRCm39) V171A probably benign Het
Pcnt C T 10: 76,228,609 (GRCm39) A1519T probably damaging Het
Pcsk2 A G 2: 143,529,490 (GRCm39) M96V probably benign Het
Piwil4 T C 9: 14,614,391 (GRCm39) D124G probably damaging Het
Plb1 A T 5: 32,471,041 (GRCm39) I538F probably damaging Het
Polq A G 16: 36,883,200 (GRCm39) D1788G probably damaging Het
Pus7 A G 5: 23,980,962 (GRCm39) S134P probably damaging Het
Sec61a2 G A 2: 5,891,363 (GRCm39) S56L possibly damaging Het
Sel1l G T 12: 91,810,033 (GRCm39) D26E probably benign Het
Slc25a48 G A 13: 56,612,758 (GRCm39) probably benign Het
Tas2r126 T C 6: 42,412,241 (GRCm39) F258S probably benign Het
Tnfrsf13b G A 11: 61,032,146 (GRCm39) V59I possibly damaging Het
Usp6nl G A 2: 6,445,879 (GRCm39) V619M probably benign Het
Vmn1r67 A G 7: 10,180,767 (GRCm39) I10M possibly damaging Het
Vmn2r71 A G 7: 85,264,782 (GRCm39) D38G probably damaging Het
Other mutations in 4931429P17Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02075:4931429P17Rik APN 13 48,114,224 (GRCm39) exon noncoding transcript
R0323:4931429P17Rik UTSW 13 48,114,493 (GRCm39) splice site noncoding transcript
R1630:4931429P17Rik UTSW 13 48,114,201 (GRCm39) exon noncoding transcript
R1707:4931429P17Rik UTSW 13 48,114,481 (GRCm39) exon noncoding transcript
Posted On 2014-01-21