Incidental Mutation 'IGL00157:D830013O20Rik'
ID 306553
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol D830013O20Rik
Ensembl Gene ENSMUSG00000056359
Gene Name RIKEN cDNA D830013O20 gene
Synonyms LOC380765
Accession Numbers
Essential gene? Probably non essential (E-score: 0.210) question?
Stock # IGL00157
Quality Score
Status
Chromosome 12
Chromosomal Location 73410849-73456337 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 73411021 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: ENSMUST00000070425
Predicted Effect noncoding transcript
Transcript: ENSMUST00000221180
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222671
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acp4 A G 7: 43,902,875 (GRCm39) V331A possibly damaging Het
Casr C A 16: 36,316,172 (GRCm39) V633F probably damaging Het
Cblb T G 16: 52,003,670 (GRCm39) V716G probably benign Het
Cbln2 C T 18: 86,734,509 (GRCm39) Q156* probably null Het
Cnn1 G T 9: 22,010,693 (GRCm39) L14F possibly damaging Het
Drd1 A G 13: 54,207,897 (GRCm39) S99P probably damaging Het
Fat1 T C 8: 45,404,707 (GRCm39) V486A possibly damaging Het
Galnt7 T C 8: 57,993,073 (GRCm39) N416S probably damaging Het
Gm10735 T C 13: 113,178,018 (GRCm39) probably benign Het
H2-T5 A T 17: 36,476,246 (GRCm39) probably null Het
Jag2 T C 12: 112,876,338 (GRCm39) T790A probably benign Het
Klhdc1 T A 12: 69,288,782 (GRCm39) Y31N possibly damaging Het
Lama1 A T 17: 68,122,923 (GRCm39) M2769L probably benign Het
Mms19 A G 19: 41,933,896 (GRCm39) probably null Het
Msrb2 C A 2: 19,399,152 (GRCm39) P172T probably damaging Het
Or8g35 A G 9: 39,381,539 (GRCm39) V161A probably benign Het
Or8k41 T C 2: 86,313,562 (GRCm39) S175G probably benign Het
Pcdhb9 T A 18: 37,536,332 (GRCm39) D775E possibly damaging Het
Pkhd1 T C 1: 20,637,098 (GRCm39) probably null Het
Preb A T 5: 31,113,308 (GRCm39) D375E probably damaging Het
Prkdc T C 16: 15,515,090 (GRCm39) I1010T probably damaging Het
Rbp2 A G 9: 98,380,950 (GRCm39) probably null Het
Septin9 A G 11: 117,243,010 (GRCm39) T66A probably damaging Het
Serpinb9b A T 13: 33,219,608 (GRCm39) E178D probably benign Het
Shld2 A G 14: 33,990,582 (GRCm39) V108A probably benign Het
Tg A G 15: 66,719,015 (GRCm39) Y258C probably damaging Het
Tmprss7 T C 16: 45,483,731 (GRCm39) R548G probably benign Het
Uba7 G A 9: 107,856,310 (GRCm39) A536T probably benign Het
Vmn2r114 G A 17: 23,510,639 (GRCm39) P614S probably damaging Het
Xpc A G 6: 91,469,246 (GRCm39) probably benign Het
Yrdc T C 4: 124,747,754 (GRCm39) S86P probably damaging Het
Zbed6 G T 1: 133,585,114 (GRCm39) A741D probably damaging Het
Other mutations in D830013O20Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01472:D830013O20Rik APN 12 73,411,090 (GRCm39) unclassified noncoding transcript
R0164:D830013O20Rik UTSW 12 73,411,105 (GRCm39) unclassified noncoding transcript
R0164:D830013O20Rik UTSW 12 73,411,105 (GRCm39) unclassified noncoding transcript
R0195:D830013O20Rik UTSW 12 73,411,095 (GRCm39) unclassified noncoding transcript
R2012:D830013O20Rik UTSW 12 73,418,162 (GRCm39) exon noncoding transcript
Posted On 2015-04-16