Incidental Mutation 'IGL02484:4930432E11Rik'
ID 295342
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930432E11Rik
Ensembl Gene ENSMUSG00000046958
Gene Name RIKEN cDNA 4930432E11 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # IGL02484
Quality Score
Status
Chromosome 7
Chromosomal Location 29255998-29276204 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to C at 29262777 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000053635
SMART Domains Protein: ENSMUSP00000049518
Gene: ENSMUSG00000046958

DomainStartEndE-ValueType
Blast:WD40 43 79 3e-11 BLAST
WD40 131 172 1.97e2 SMART
WD40 175 214 2.24e-2 SMART
Blast:WD40 257 296 4e-15 BLAST
WD40 393 437 1.32e2 SMART
WD40 494 533 2.15e-4 SMART
low complexity region 598 617 N/A INTRINSIC
low complexity region 1082 1094 N/A INTRINSIC
low complexity region 1107 1148 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000063585
SMART Domains Protein: ENSMUSP00000063695
Gene: ENSMUSG00000051976

DomainStartEndE-ValueType
low complexity region 15 28 N/A INTRINSIC
internal_repeat_1 35 67 3.29e-5 PROSPERO
internal_repeat_1 73 102 3.29e-5 PROSPERO
low complexity region 122 135 N/A INTRINSIC
coiled coil region 161 182 N/A INTRINSIC
low complexity region 216 233 N/A INTRINSIC
low complexity region 239 249 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185541
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Araf A G X: 20,720,148 (GRCm39) probably benign Het
Arrb2 T A 11: 70,330,300 (GRCm39) V308E probably damaging Het
Asap3 A G 4: 135,956,768 (GRCm39) probably benign Het
Astn2 G A 4: 65,910,516 (GRCm39) probably benign Het
Cactin T A 10: 81,158,808 (GRCm39) I258N probably benign Het
Calhm6 T C 10: 34,002,400 (GRCm39) T228A probably benign Het
Catsperg1 T C 7: 28,910,345 (GRCm39) probably benign Het
Ccna1 C T 3: 54,955,915 (GRCm39) D146N probably benign Het
Chrna3 T C 9: 54,922,821 (GRCm39) Y329C probably damaging Het
Ctps2 G A X: 161,693,005 (GRCm39) G56D probably damaging Het
Cyp4b1 T C 4: 115,504,754 (GRCm39) D44G probably benign Het
D3Ertd751e A G 3: 41,708,155 (GRCm39) probably null Het
Daxx T C 17: 34,131,216 (GRCm39) V381A probably damaging Het
Dhx37 T A 5: 125,496,401 (GRCm39) I714F possibly damaging Het
Dnah7b T C 1: 46,234,478 (GRCm39) V1470A probably damaging Het
Efl1 T C 7: 82,332,247 (GRCm39) I297T probably damaging Het
Fnd3c2 A T X: 105,289,092 (GRCm39) H442Q probably damaging Het
Glp2r A C 11: 67,630,992 (GRCm39) V126G possibly damaging Het
Gm5699 G T 1: 31,037,843 (GRCm39) noncoding transcript Het
Gpt2 A G 8: 86,242,862 (GRCm39) D298G probably damaging Het
Gse1 G T 8: 121,302,001 (GRCm39) probably benign Het
Hand1 T C 11: 57,722,420 (GRCm39) T65A probably benign Het
Ints8 G A 4: 11,208,834 (GRCm39) Q955* probably null Het
Lrguk C T 6: 34,069,726 (GRCm39) P534S probably damaging Het
Lrp6 A G 6: 134,518,886 (GRCm39) F60L probably benign Het
Mamld1 T C X: 70,162,258 (GRCm39) I423T possibly damaging Het
Mrpl22 G A 11: 58,063,888 (GRCm39) S36N possibly damaging Het
Mug2 A G 6: 122,049,712 (GRCm39) E915G probably damaging Het
Oosp2 T C 19: 11,628,847 (GRCm39) T85A probably benign Het
Or5b94 T C 19: 12,652,223 (GRCm39) F218S possibly damaging Het
Or5p68 C T 7: 107,945,813 (GRCm39) R125Q probably damaging Het
Pde4c T A 8: 71,200,701 (GRCm39) probably benign Het
Pdxdc1 T C 16: 13,693,945 (GRCm39) E159G possibly damaging Het
Poln T C 5: 34,286,721 (GRCm39) E149G probably damaging Het
Pou5f2 T G 13: 78,174,024 (GRCm39) L322R probably damaging Het
Ppm1k A T 6: 57,501,997 (GRCm39) S55R possibly damaging Het
Ptges2 T A 2: 32,287,719 (GRCm39) I149N probably damaging Het
Pus7l A G 15: 94,427,369 (GRCm39) V471A possibly damaging Het
Raet1e A T 10: 22,056,666 (GRCm39) M81L probably benign Het
Sipa1l3 A G 7: 29,098,956 (GRCm39) S438P probably damaging Het
Skint5 T A 4: 113,799,750 (GRCm39) K126* probably null Het
Stfa2 T C 16: 36,225,569 (GRCm39) T37A probably damaging Het
Ttll12 A G 15: 83,465,897 (GRCm39) I433T possibly damaging Het
Vmn2r32 C T 7: 7,467,116 (GRCm39) G804D probably damaging Het
Zc3h14 A G 12: 98,740,560 (GRCm39) T84A probably benign Het
Other mutations in 4930432E11Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01121:4930432E11Rik APN 7 29,273,426 (GRCm39) unclassified noncoding transcript
IGL01955:4930432E11Rik APN 7 29,273,420 (GRCm39) unclassified noncoding transcript
IGL01971:4930432E11Rik APN 7 29,273,987 (GRCm39) unclassified noncoding transcript
IGL02132:4930432E11Rik APN 7 29,262,704 (GRCm39) unclassified noncoding transcript
P0016:4930432E11Rik UTSW 7 29,262,537 (GRCm39) unclassified noncoding transcript
R0051:4930432E11Rik UTSW 7 29,278,526 (GRCm39) exon noncoding transcript
R0060:4930432E11Rik UTSW 7 29,273,595 (GRCm39) unclassified noncoding transcript
R0094:4930432E11Rik UTSW 7 29,260,236 (GRCm39) exon noncoding transcript
R0268:4930432E11Rik UTSW 7 29,274,027 (GRCm39) unclassified noncoding transcript
R0423:4930432E11Rik UTSW 7 29,261,825 (GRCm39) exon noncoding transcript
R0478:4930432E11Rik UTSW 7 29,262,014 (GRCm39) exon noncoding transcript
R0646:4930432E11Rik UTSW 7 29,260,710 (GRCm39) exon noncoding transcript
R1208:4930432E11Rik UTSW 7 29,260,708 (GRCm39) exon noncoding transcript
R1778:4930432E11Rik UTSW 7 29,260,131 (GRCm39) exon noncoding transcript
R1779:4930432E11Rik UTSW 7 29,278,591 (GRCm39) exon noncoding transcript
R1918:4930432E11Rik UTSW 7 29,273,514 (GRCm39) unclassified noncoding transcript
R2360:4930432E11Rik UTSW 7 29,274,214 (GRCm39) unclassified noncoding transcript
R3736:4930432E11Rik UTSW 7 29,273,996 (GRCm39) unclassified noncoding transcript
R3780:4930432E11Rik UTSW 7 29,260,263 (GRCm39) exon noncoding transcript
R4427:4930432E11Rik UTSW 7 29,278,678 (GRCm39) exon noncoding transcript
R4835:4930432E11Rik UTSW 7 29,274,326 (GRCm39) unclassified noncoding transcript
R4929:4930432E11Rik UTSW 7 29,273,467 (GRCm39) unclassified noncoding transcript
R5042:4930432E11Rik UTSW 7 29,273,927 (GRCm39) unclassified noncoding transcript
R5129:4930432E11Rik UTSW 7 29,260,786 (GRCm39) exon noncoding transcript
R5371:4930432E11Rik UTSW 7 29,261,918 (GRCm39) exon noncoding transcript
R5381:4930432E11Rik UTSW 7 29,262,393 (GRCm39) unclassified noncoding transcript
R5586:4930432E11Rik UTSW 7 29,277,153 (GRCm39) unclassified noncoding transcript
R5874:4930432E11Rik UTSW 7 29,280,610 (GRCm39) exon noncoding transcript
Posted On 2015-04-16