Incidental Mutation 'IGL03381:A330017A19Rik'
ID 420711
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol A330017A19Rik
Ensembl Gene ENSMUSG00000073388
Gene Name RIKEN cDNA A330017A19 gene
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL03381
Quality Score
Status
Chromosome 17
Chromosomal Location 47200142-47201331 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 47200812 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000048696 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040434]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000040434
SMART Domains Protein: ENSMUSP00000048696
Gene: ENSMUSG00000036430

DomainStartEndE-ValueType
low complexity region 26 47 N/A INTRINSIC
PDB:2L3L|A 48 132 3e-10 PDB
low complexity region 133 143 N/A INTRINSIC
low complexity region 153 165 N/A INTRINSIC
CARP 206 243 1.62e-6 SMART
CARP 244 278 1.99e-6 SMART
Predicted Effect unknown
Transcript: ENSMUST00000086675
AA Change: E107G
SMART Domains Protein: ENSMUSP00000083879
Gene: ENSMUSG00000073388
AA Change: E107G

DomainStartEndE-ValueType
transmembrane domain 21 43 N/A INTRINSIC
low complexity region 57 71 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 T C 7: 120,127,041 (GRCm39) F1243S probably benign Het
Adgrv1 A G 13: 81,666,086 (GRCm39) V1990A probably damaging Het
Arhgdib G A 6: 136,909,314 (GRCm39) T69I probably benign Het
Atf2 G A 2: 73,659,012 (GRCm39) A214V probably benign Het
Ccr2 G A 9: 123,906,409 (GRCm39) V230I probably benign Het
Cnksr1 T C 4: 133,959,482 (GRCm39) E384G probably damaging Het
Epha5 T A 5: 84,479,191 (GRCm39) D271V probably damaging Het
Fut2 C T 7: 45,300,193 (GRCm39) G193E possibly damaging Het
Gpr15 A G 16: 58,538,339 (GRCm39) F250S probably damaging Het
Gzmf A T 14: 56,444,450 (GRCm39) V41E probably benign Het
H2-T10 C T 17: 36,430,246 (GRCm39) D232N probably benign Het
H2-T10 T A 17: 36,430,249 (GRCm39) K231* probably null Het
Hsd3b6 A G 3: 98,715,128 (GRCm39) V88A possibly damaging Het
Kit C T 5: 75,767,788 (GRCm39) T57M probably benign Het
Klhl22 A G 16: 17,610,591 (GRCm39) D614G possibly damaging Het
Matr3 T A 18: 35,712,078 (GRCm39) probably benign Het
Mff A G 1: 82,719,661 (GRCm39) Y213C probably damaging Het
Mrnip A G 11: 50,090,417 (GRCm39) T194A probably benign Het
Msh6 T C 17: 88,292,537 (GRCm39) F431L probably damaging Het
Mttp G A 3: 137,810,704 (GRCm39) R637C probably damaging Het
Nlrc3 A G 16: 3,782,179 (GRCm39) V410A probably benign Het
Or4c120 A G 2: 89,001,523 (GRCm39) I11T possibly damaging Het
Or52a5b T C 7: 103,417,044 (GRCm39) I187V probably benign Het
Or5b108 T A 19: 13,168,769 (GRCm39) V246D probably damaging Het
Pramel21 T C 4: 143,343,625 (GRCm39) probably benign Het
Psip1 T C 4: 83,404,022 (GRCm39) T2A probably benign Het
Rbm33 T C 5: 28,599,390 (GRCm39) F921L unknown Het
Rhbdl2 T C 4: 123,716,610 (GRCm39) V189A possibly damaging Het
Rpap2 C T 5: 107,768,067 (GRCm39) P302S probably benign Het
Sec23ip T A 7: 128,352,029 (GRCm39) V32D probably damaging Het
Sh3yl1 T C 12: 30,976,836 (GRCm39) I47T possibly damaging Het
Spmip4 T C 6: 50,566,116 (GRCm39) S120G probably damaging Het
Tenm2 A C 11: 35,959,238 (GRCm39) S1104A probably benign Het
Ufd1 A G 16: 18,644,507 (GRCm39) D190G probably damaging Het
Ugt1a7c T C 1: 88,023,512 (GRCm39) F224L probably benign Het
Utp20 G T 10: 88,657,867 (GRCm39) F64L probably damaging Het
Vmn1r198 A G 13: 22,539,006 (GRCm39) Y164C probably benign Het
Wdcp T A 12: 4,901,926 (GRCm39) V594D probably damaging Het
Xirp2 A C 2: 67,344,570 (GRCm39) E2270D probably benign Het
Other mutations in A330017A19Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R5752:A330017A19Rik UTSW 17 47,200,966 (GRCm39) unclassified probably benign
R8211:A330017A19Rik UTSW 17 47,201,309 (GRCm39) unclassified probably benign
Posted On 2016-08-02