Incidental Mutation 'IGL01762:9030612E09Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 9030612E09Rik
Ensembl Gene ENSMUSG00000045008
Gene NameRIKEN cDNA 9030612E09 gene
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.060) question?
Stock #IGL01762
Quality Score
Chromosomal Location43174704-43176562 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 43174851 bp
Amino Acid Change Leucine to Stop codon at position 47 (L47*)
Ref Sequence ENSEMBL: ENSMUSP00000049699 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040275] [ENSMUST00000053792]
Predicted Effect probably benign
Transcript: ENSMUST00000040275
SMART Domains Protein: ENSMUSP00000040072
Gene: ENSMUSG00000038248

low complexity region 125 139 N/A INTRINSIC
internal_repeat_1 149 201 2.34e-5 PROSPERO
Pfam:SOBP 224 543 1.5e-88 PFAM
low complexity region 565 583 N/A INTRINSIC
low complexity region 590 603 N/A INTRINSIC
low complexity region 625 639 N/A INTRINSIC
low complexity region 695 714 N/A INTRINSIC
low complexity region 725 747 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000053792
AA Change: L47*
SMART Domains Protein: ENSMUSP00000049699
Gene: ENSMUSG00000045008
AA Change: L47*

low complexity region 10 25 N/A INTRINSIC
low complexity region 45 58 N/A INTRINSIC
low complexity region 59 72 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000189221
Predicted Effect noncoding transcript
Transcript: ENSMUST00000189987
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A T 11: 9,315,423 T3033S probably benign Het
Atp1a2 C A 1: 172,284,913 V503L possibly damaging Het
BC030867 T C 11: 102,255,596 C233R probably benign Het
Cacna1e T A 1: 154,471,373 D770V possibly damaging Het
Camkk1 A G 11: 73,030,801 probably null Het
Cd34 T A 1: 194,939,033 M23K probably benign Het
Cndp1 T A 18: 84,622,286 I265F probably damaging Het
Cux2 A G 5: 121,873,145 I574T probably damaging Het
Fam129a T C 1: 151,636,491 V48A probably damaging Het
Fhdc1 G A 3: 84,444,735 A1061V possibly damaging Het
Galk1 A G 11: 116,010,008 Y236H probably damaging Het
Gbp11 T C 5: 105,327,607 I292V probably benign Het
Gprc5c A G 11: 114,864,024 I176V probably benign Het
Myh6 T C 14: 54,962,081 K258E probably benign Het
Nlrp9c T A 7: 26,385,425 D243V probably damaging Het
Nobox T G 6: 43,303,993 K516Q probably damaging Het
Nudcd3 A G 11: 6,150,560 S195P probably damaging Het
Pde10a T C 17: 8,942,918 I477T possibly damaging Het
Pgbd5 C T 8: 124,370,610 A394T probably damaging Het
Piezo1 G A 8: 122,487,929 R1553* probably null Het
Prkd1 T C 12: 50,387,230 I577V probably benign Het
Prss34 T C 17: 25,299,812 I256T probably benign Het
Ptprg A G 14: 12,037,386 T189A probably benign Het
Ptprr C T 10: 116,236,733 T200I probably damaging Het
Samd8 C T 14: 21,780,100 P198L probably damaging Het
Sema3c T C 5: 17,694,851 L447P possibly damaging Het
Slc22a23 A T 13: 34,204,001 F371I possibly damaging Het
Slc2a2 A G 3: 28,717,472 R184G probably damaging Het
Slitrk6 T A 14: 110,751,624 D217V probably damaging Het
Tlr2 A G 3: 83,836,994 V594A probably benign Het
Vmn2r109 A G 17: 20,554,392 F234L probably benign Het
Vmn2r12 A C 5: 109,086,564 L594R probably damaging Het
Vmn2r124 A G 17: 18,063,172 Q376R possibly damaging Het
Vmn2r7 T C 3: 64,691,435 D567G probably benign Het
Other mutations in 9030612E09Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02342:9030612E09Rik APN 10 43175001 missense probably damaging 0.99
IGL02671:9030612E09Rik APN 10 43174891 missense probably benign
R0801:9030612E09Rik UTSW 10 43174991 missense possibly damaging 0.66
R2411:9030612E09Rik UTSW 10 43174800 missense possibly damaging 0.66
R6548:9030612E09Rik UTSW 10 43174773 missense probably damaging 0.97
Posted On2014-02-04