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
Is this an essential gene? Probably non essential (E-score: 0.210) question?
Stock # IGL00157
Quality Score
Status
Chromosome 12
Chromosomal Location 73364075-73371445 bp(-) (GRCm38)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 73364247 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
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: 44,253,451 V331A possibly damaging Het
Casr C A 16: 36,495,810 V633F probably damaging Het
Cblb T G 16: 52,183,307 V716G probably benign Het
Cbln2 C T 18: 86,716,384 Q156* probably null Het
Cnn1 G T 9: 22,099,397 L14F possibly damaging Het
Drd1 A G 13: 54,053,878 S99P probably damaging Het
Fam35a A G 14: 34,268,625 V108A probably benign Het
Fat1 T C 8: 44,951,670 V486A possibly damaging Het
Galnt7 T C 8: 57,540,039 N416S probably damaging Het
Gm10735 T C 13: 113,041,484 probably benign Het
Gm8909 A T 17: 36,165,354 probably null Het
Jag2 T C 12: 112,912,718 T790A probably benign Het
Klhdc1 T A 12: 69,242,008 Y31N possibly damaging Het
Lama1 A T 17: 67,815,928 M2769L probably benign Het
Mms19 A G 19: 41,945,457 probably null Het
Msrb2 C A 2: 19,394,341 P172T probably damaging Het
Olfr228 T C 2: 86,483,218 S175G probably benign Het
Olfr955 A G 9: 39,470,243 V161A probably benign Het
Pcdhb9 T A 18: 37,403,279 D775E possibly damaging Het
Pkhd1 T C 1: 20,566,874 probably null Het
Preb A T 5: 30,955,964 D375E probably damaging Het
Prkdc T C 16: 15,697,226 I1010T probably damaging Het
Rbp2 A G 9: 98,498,897 probably null Het
Sept9 A G 11: 117,352,184 T66A probably damaging Het
Serpinb9b A T 13: 33,035,625 E178D probably benign Het
Tg A G 15: 66,847,166 Y258C probably damaging Het
Tmprss7 T C 16: 45,663,368 R548G probably benign Het
Uba7 G A 9: 107,979,111 A536T probably benign Het
Vmn2r114 G A 17: 23,291,665 P614S probably damaging Het
Xpc A G 6: 91,492,264 probably benign Het
Yrdc T C 4: 124,853,961 S86P probably damaging Het
Zbed6 G T 1: 133,657,376 A741D probably damaging Het
Other mutations in D830013O20Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01472:D830013O20Rik APN 12 73364316 unclassified noncoding transcript
R0164:D830013O20Rik UTSW 12 73364331 unclassified noncoding transcript
R0164:D830013O20Rik UTSW 12 73364331 unclassified noncoding transcript
R0195:D830013O20Rik UTSW 12 73364321 unclassified noncoding transcript
R2012:D830013O20Rik UTSW 12 73371388 exon noncoding transcript
Posted On 2015-04-16