Incidental Mutation 'IGL01762:9030612E09Rik'
ID153278
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 9030612E09Rik
Ensembl Gene ENSMUSG00000045008
Gene NameRIKEN cDNA 9030612E09 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.060) question?
Stock #IGL01762
Quality Score
Status
Chromosome10
Chromosomal Location43174704-43176562 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 43174851 bp
ZygosityHeterozygous
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

DomainStartEndE-ValueType
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*

DomainStartEndE-ValueType
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