Incidental Mutation 'IGL03260:4933406P04Rik'
ID414792
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4933406P04Rik
Ensembl Gene ENSMUSG00000069713
Gene NameRIKEN cDNA 4933406P04 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL03260
Quality Score
Status
Chromosome10
Chromosomal Location20310506-20312294 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to G at 20311325 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000140428 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043881] [ENSMUST00000092678] [ENSMUST00000185800] [ENSMUST00000186100] [ENSMUST00000190156]
Predicted Effect probably benign
Transcript: ENSMUST00000043881
SMART Domains Protein: ENSMUSP00000043583
Gene: ENSMUSG00000037608

DomainStartEndE-ValueType
low complexity region 3 94 N/A INTRINSIC
Pfam:THRAP3_BCLAF1 108 766 1.6e-181 PFAM
low complexity region 793 824 N/A INTRINSIC
low complexity region 861 874 N/A INTRINSIC
low complexity region 898 919 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000092678
SMART Domains Protein: ENSMUSP00000090349
Gene: ENSMUSG00000037608

DomainStartEndE-ValueType
low complexity region 3 94 N/A INTRINSIC
Pfam:THRAP3_BCLAF1 108 789 5.4e-191 PFAM
low complexity region 812 825 N/A INTRINSIC
low complexity region 849 870 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000092680
Predicted Effect probably benign
Transcript: ENSMUST00000185800
SMART Domains Protein: ENSMUSP00000140623
Gene: ENSMUSG00000037608

DomainStartEndE-ValueType
low complexity region 3 92 N/A INTRINSIC
Pfam:THRAP3_BCLAF1 106 787 7.2e-191 PFAM
low complexity region 791 822 N/A INTRINSIC
low complexity region 859 872 N/A INTRINSIC
low complexity region 896 917 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000186100
SMART Domains Protein: ENSMUSP00000140101
Gene: ENSMUSG00000037608

DomainStartEndE-ValueType
low complexity region 3 94 N/A INTRINSIC
Pfam:THRAP3_BCLAF1 108 742 6.4e-177 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000187338
Predicted Effect probably benign
Transcript: ENSMUST00000190156
SMART Domains Protein: ENSMUSP00000140428
Gene: ENSMUSG00000037608

DomainStartEndE-ValueType
low complexity region 3 92 N/A INTRINSIC
Pfam:THRAP3_BCLAF1 106 740 4.2e-180 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215262
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216560
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 A G 1: 71,284,099 L1608P probably damaging Het
Akr1b8 G T 6: 34,363,459 probably benign Het
Appbp2 A G 11: 85,216,457 V69A probably benign Het
Ces1e T C 8: 93,223,917 N79D probably benign Het
Cldn34b3 A G X: 76,266,873 T16A probably damaging Het
Frmd4b A T 6: 97,396,224 F103Y probably damaging Het
Ifi47 T C 11: 49,096,105 F233S probably damaging Het
Igkv8-30 A T 6: 70,117,355 M24K probably damaging Het
Krt72 C T 15: 101,778,273 A413T probably damaging Het
Lingo4 A G 3: 94,401,943 T63A probably benign Het
Naa35 T G 13: 59,627,885 S125A probably benign Het
Olfr5 A T 7: 6,480,659 C166S probably damaging Het
Olfr809 T C 10: 129,776,652 V261A probably damaging Het
Padi1 T C 4: 140,828,194 H240R probably benign Het
Ppp1r12a A G 10: 108,261,245 T240A probably benign Het
Ppp2ca A G 11: 52,113,148 N44S probably damaging Het
Prg4 T A 1: 150,455,627 probably benign Het
Rab33a A G X: 48,519,668 E23G probably benign Het
Scarb2 G T 5: 92,446,437 A422E probably damaging Het
Scn4b A T 9: 45,147,689 N86I probably damaging Het
Serpina1d G A 12: 103,763,849 T358I probably damaging Het
Slc12a3 T A 8: 94,333,242 I172N probably damaging Het
Slc18a1 T C 8: 69,075,114 E15G probably benign Het
Snx7 A G 3: 117,782,293 probably benign Het
Srpx T A X: 10,055,748 K216* probably null Het
Ugt2a3 G A 5: 87,336,580 P195L probably damaging Het
Unc13c A G 9: 73,931,344 S742P probably benign Het
Vmn2r104 C T 17: 20,042,821 C126Y probably benign Het
Vmn2r63 A T 7: 42,929,192 N92K probably damaging Het
Other mutations in 4933406P04Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00163:4933406P04Rik APN 10 20311224 unclassified probably benign
R0605:4933406P04Rik UTSW 10 20311227 unclassified probably benign
R1544:4933406P04Rik UTSW 10 20311359 unclassified probably benign
R1616:4933406P04Rik UTSW 10 20311341 unclassified probably benign
R1800:4933406P04Rik UTSW 10 20311147 unclassified probably benign
Posted On2016-08-02