Incidental Mutation 'IGL02001:Vdac3-ps1'
ID183034
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vdac3-ps1
Ensembl Gene ENSMUSG00000075053
Gene Namevoltage-dependent anion channel 3, pseudogene 1
SynonymsENSMUSG00000075053
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.506) question?
Stock #IGL02001
Quality Score
Status
Chromosome13
Chromosomal Location18030324-18031629 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) A to G at 18031388 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000099736
SMART Domains Protein: ENSMUSP00000137236
Gene: ENSMUSG00000075053

DomainStartEndE-ValueType
Pfam:Porin_3 3 276 4.8e-85 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930444G20Rik A T 10: 22,067,277 M268K probably benign Het
A530064D06Rik T C 17: 48,166,674 N25S possibly damaging Het
Als2 A T 1: 59,180,188 probably benign Het
Asah2 T A 19: 32,043,539 K255* probably null Het
Bclaf1 A G 10: 20,323,016 probably benign Het
Bpifb2 T C 2: 153,891,275 probably benign Het
Cacna2d2 G A 9: 107,522,116 V669I probably benign Het
Cep89 T A 7: 35,403,007 probably benign Het
Chl1 T G 6: 103,642,056 L29R possibly damaging Het
Defb2 T C 8: 21,843,337 Y43H probably damaging Het
Disc1 A G 8: 125,251,042 Y799C probably damaging Het
Egf G T 3: 129,716,768 A34E probably damaging Het
Fat2 A T 11: 55,312,245 M1K probably null Het
Gprin1 T C 13: 54,739,192 E423G probably damaging Het
Kcnh6 T C 11: 106,027,549 probably benign Het
Kcnt1 A G 2: 25,908,152 E925G probably damaging Het
Kctd16 A T 18: 40,258,680 K107I possibly damaging Het
Lrig1 T C 6: 94,607,324 K913R probably benign Het
March7 A G 2: 60,234,891 T504A possibly damaging Het
Mrpl11 C T 19: 4,963,652 R154* probably null Het
Nlrp4a T C 7: 26,449,969 F334L probably benign Het
Olfr30 C T 11: 58,455,509 V147M probably benign Het
Olfr545 T A 7: 102,494,539 T79S probably benign Het
Parp6 A G 9: 59,649,961 T610A possibly damaging Het
Pcdhb15 T G 18: 37,474,038 L108V probably benign Het
Pomgnt1 G T 4: 116,152,908 E156* probably null Het
Psma2 T G 13: 14,623,607 F105V possibly damaging Het
Rapgef4 A G 2: 72,225,052 probably benign Het
Sclt1 A T 3: 41,681,721 S282T possibly damaging Het
Serpina3f A G 12: 104,219,466 Y310C probably damaging Het
Sh3pxd2a T C 19: 47,273,447 K331R probably damaging Het
Tectb T C 19: 55,189,595 F183L possibly damaging Het
Tgfbr1 A G 4: 47,403,388 H327R probably damaging Het
Try10 T A 6: 41,356,589 D89E probably benign Het
Ttn G A 2: 76,756,784 S21623L probably damaging Het
Ttn A G 2: 76,781,938 L15489P probably damaging Het
Vmn2r69 T A 7: 85,407,226 Q568L probably benign Het
Wdr36 T A 18: 32,852,888 D548E probably damaging Het
Zfand4 T A 6: 116,273,652 H14Q probably benign Het
Other mutations in Vdac3-ps1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01133:Vdac3-ps1 APN 13 18031449 exon noncoding transcript
IGL01530:Vdac3-ps1 APN 13 18031506 exon noncoding transcript
IGL02028:Vdac3-ps1 APN 13 18030884 exon noncoding transcript
IGL02275:Vdac3-ps1 APN 13 18030794 exon noncoding transcript
IGL02965:Vdac3-ps1 APN 13 18030846 exon noncoding transcript
R1292:Vdac3-ps1 UTSW 13 18031295 exon noncoding transcript
R4582:Vdac3-ps1 UTSW 13 18031592 exon noncoding transcript
R5941:Vdac3-ps1 UTSW 13 18031202 exon noncoding transcript
Posted On2014-05-07