Incidental Mutation 'IGL02132:4930432E11Rik'
ID 281026
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 # IGL02132
Quality Score
Status
Chromosome 7
Chromosomal Location 29255998-29276204 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to T at 29262704 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: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921513I03Rik G A 10: 120,614,635 (GRCm39) probably benign Het
Adcy10 T C 1: 165,400,112 (GRCm39) V1507A probably damaging Het
Ap3b2 T A 7: 81,110,746 (GRCm39) M1010L unknown Het
Bmp10 T C 6: 87,411,130 (GRCm39) S308P probably benign Het
Cnih3 C A 1: 181,282,274 (GRCm39) Y169* probably null Het
Cpsf4l A G 11: 113,590,685 (GRCm39) S222P possibly damaging Het
Cyp2d10 G A 15: 82,288,808 (GRCm39) probably benign Het
Dcstamp A T 15: 39,617,928 (GRCm39) E112D probably damaging Het
Fras1 C T 5: 96,929,496 (GRCm39) Q3967* probably null Het
Gcm1 C A 9: 77,972,121 (GRCm39) P354H possibly damaging Het
Gen1 A G 12: 11,291,867 (GRCm39) S706P probably benign Het
Glb1l3 G T 9: 26,736,466 (GRCm39) T532N probably benign Het
Gm5069 T A 1: 180,154,872 (GRCm39) probably benign Het
Gzmc A C 14: 56,471,422 (GRCm39) F40V probably benign Het
Itgb2 G T 10: 77,385,895 (GRCm39) C286F probably damaging Het
Jak3 A G 8: 72,131,124 (GRCm39) Y48C probably damaging Het
Lrp2 G A 2: 69,367,960 (GRCm39) S184L probably benign Het
Myo1f T A 17: 33,798,945 (GRCm39) N203K probably benign Het
Nrxn2 G A 19: 6,522,306 (GRCm39) G182R probably damaging Het
Or4k15c T C 14: 50,321,943 (GRCm39) N65S probably damaging Het
Or4p8 A G 2: 88,727,503 (GRCm39) V146A probably benign Het
Or5g23 A C 2: 85,438,664 (GRCm39) L197V probably benign Het
Otog C T 7: 45,954,903 (GRCm39) S2692L probably damaging Het
Pde9a C T 17: 31,672,444 (GRCm39) T34I probably benign Het
Phip T C 9: 82,763,394 (GRCm39) T1295A possibly damaging Het
Pik3cb A G 9: 98,953,430 (GRCm39) V451A probably benign Het
Psd2 T G 18: 36,137,809 (GRCm39) probably benign Het
Pycr2 T C 1: 180,733,762 (GRCm39) I118T probably damaging Het
Rnf17 T G 14: 56,658,623 (GRCm39) M104R probably benign Het
Rp1l1 T C 14: 64,266,259 (GRCm39) V615A probably benign Het
Sel1l3 T A 5: 53,327,747 (GRCm39) R511W possibly damaging Het
Sis T C 3: 72,854,804 (GRCm39) N478D probably benign Het
Trps1 T A 15: 50,685,674 (GRCm39) S584C probably damaging Het
Vmn2r124 T C 17: 18,284,491 (GRCm39) probably benign Het
Vmn2r9 G A 5: 108,991,502 (GRCm39) L620F probably damaging Het
Zc3h13 T C 14: 75,567,787 (GRCm39) S1027P probably benign Het
Zfp644 A T 5: 106,783,760 (GRCm39) I929K 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
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
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