Incidental Mutation 'R0094:4930432E11Rik'
ID 17033
Institutional Source Beutler Lab
Gene Symbol 4930432E11Rik
Ensembl Gene ENSMUSG00000046958
Gene Name RIKEN cDNA 4930432E11 gene
Synonyms
MMRRC Submission 038380-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # R0094 (G1)
Quality Score
Status Validated
Chromosome 7
Chromosomal Location 29255998-29276204 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 29260236 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
  • 1x: 84.5%
  • 3x: 75.9%
  • 10x: 43.5%
  • 20x: 12.9%
Validation Efficiency 86% (51/59)
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700006A11Rik T C 3: 124,203,427 (GRCm39) probably benign Het
4931429L15Rik T A 9: 46,218,184 (GRCm39) T185S possibly damaging Het
Ahnak T A 19: 8,991,257 (GRCm39) D4180E probably benign Het
Amotl1 A G 9: 14,486,683 (GRCm39) S441P probably benign Het
Ankrd12 A T 17: 66,277,171 (GRCm39) D2034E probably damaging Het
B3gnt2 T C 11: 22,786,655 (GRCm39) R178G probably damaging Het
Colgalt1 T C 8: 72,075,802 (GRCm39) V483A probably damaging Het
Ctsj A C 13: 61,151,519 (GRCm39) probably null Het
Dap3 T A 3: 88,834,335 (GRCm39) M294L probably benign Het
Ddias T C 7: 92,509,108 (GRCm39) N269S possibly damaging Het
Dsg2 A T 18: 20,724,910 (GRCm39) T439S probably benign Het
Eif2b1 A G 5: 124,709,829 (GRCm39) F250L probably benign Het
Emc1 T A 4: 139,087,796 (GRCm39) F100Y probably damaging Het
Hfm1 T A 5: 107,065,344 (GRCm39) M112L probably benign Het
Lipg T C 18: 75,078,917 (GRCm39) Y445C probably benign Het
Lrp1b T C 2: 41,172,042 (GRCm39) probably benign Het
Ltbp2 A G 12: 84,846,200 (GRCm39) Y897H probably damaging Het
Mfap5 G A 6: 122,502,951 (GRCm39) V54I probably damaging Het
Mvd C T 8: 123,166,442 (GRCm39) R65H probably benign Het
Mybpc2 A G 7: 44,166,328 (GRCm39) Y221H probably damaging Het
Nbeal1 T A 1: 60,344,468 (GRCm39) I2323N possibly damaging Het
Or14c40 A G 7: 86,313,502 (GRCm39) S211G probably benign Het
Otol1 G A 3: 69,926,016 (GRCm39) A64T probably benign Het
Pcdh8 G T 14: 80,005,588 (GRCm39) D933E probably damaging Het
Pkd1 A G 17: 24,800,250 (GRCm39) T3004A possibly damaging Het
Pkhd1 T A 1: 20,279,470 (GRCm39) R2949S probably damaging Het
Ptpro T C 6: 137,363,350 (GRCm39) Y495H probably benign Het
Rad54b T C 4: 11,599,681 (GRCm39) V72A possibly damaging Het
Ranbp3 A G 17: 57,016,338 (GRCm39) probably benign Het
Rpa2 T C 4: 132,497,893 (GRCm39) S52P probably damaging Het
Serping1 T G 2: 84,603,620 (GRCm39) R140S probably benign Het
Slc34a2 T C 5: 53,221,310 (GRCm39) F252S probably benign Het
Spata45 A G 1: 190,772,059 (GRCm39) probably benign Het
Sptan1 T C 2: 29,896,635 (GRCm39) S1174P probably benign Het
Ss18l2 T C 9: 121,541,699 (GRCm39) L64P probably benign Het
Tmem81 A G 1: 132,435,787 (GRCm39) I198V probably benign Het
Trappc9 A T 15: 72,894,929 (GRCm38) probably benign Het
Ubr3 C T 2: 69,781,706 (GRCm39) T628I probably damaging Het
Zzef1 C T 11: 72,708,791 (GRCm39) T130I 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
IGL02484:4930432E11Rik APN 7 29,262,777 (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
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 2013-01-20