Incidental Mutation 'IGL00562:AU016765'
ID332614
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol AU016765
Ensembl Gene ENSMUSG00000073377
Gene Nameexpressed sequence AU016765
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.218) question?
Stock #IGL00562
Quality Score
Status
Chromosome17
Chromosomal Location64514081-64555660 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) C to A at 64519882 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model
Predicted Effect noncoding transcript
Transcript: ENSMUST00000097295
Predicted Effect noncoding transcript
Transcript: ENSMUST00000168379
Predicted Effect noncoding transcript
Transcript: ENSMUST00000168920
Predicted Effect noncoding transcript
Transcript: ENSMUST00000169472
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1500035N22Rik T C 5: 24,997,621 probably benign Het
Chaf1b T C 16: 93,900,191 probably benign Het
Clstn2 A G 9: 97,582,452 probably benign Het
Crip1 T A 12: 113,153,612 probably null Het
Cubn A G 2: 13,294,230 S3211P probably benign Het
Dlx6 C T 6: 6,865,143 R172W probably damaging Het
Fktn A T 4: 53,747,007 probably null Het
Focad T A 4: 88,348,809 M1019K unknown Het
Fuca2 A T 10: 13,505,907 D188V probably damaging Het
Kcna3 A G 3: 107,036,730 D103G probably damaging Het
Mrpl19 A G 6: 81,965,872 V19A probably benign Het
Ndufb3 T A 1: 58,595,799 H103Q possibly damaging Het
Pkd1l3 T C 8: 109,656,147 V1675A possibly damaging Het
Ptger4 A T 15: 5,243,133 S2T probably benign Het
Saxo1 C T 4: 86,445,572 E225K probably damaging Het
Sftpb G T 6: 72,309,862 A228S probably benign Het
Slc22a29 T A 19: 8,161,629 T490S probably benign Het
Slc29a1 T C 17: 45,589,992 N50S probably damaging Het
Smc6 T A 12: 11,301,531 S854T probably benign Het
Smim23 T C 11: 32,821,893 T58A probably benign Het
Tas2r134 T C 2: 51,628,088 I193T possibly damaging Het
Thsd7a G T 6: 12,379,659 probably null Het
Trav13n-4 T G 14: 53,363,966 V64G possibly damaging Het
Trmt10a G A 3: 138,147,416 E13K probably damaging Het
Txndc11 T C 16: 11,104,632 S239G probably damaging Het
Vmn2r96 T A 17: 18,583,815 N442K probably benign Het
Vps13a C T 19: 16,734,714 probably null Het
Other mutations in AU016765
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00563:AU016765 APN 17 64519882 exon noncoding transcript
R1718:AU016765 UTSW 17 64555438 exon noncoding transcript
R1936:AU016765 UTSW 17 64519878 exon noncoding transcript
R1940:AU016765 UTSW 17 64519878 exon noncoding transcript
R2140:AU016765 UTSW 17 64520000 exon noncoding transcript
R4665:AU016765 UTSW 17 64519921 exon noncoding transcript
Posted On2015-08-05