Incidental Mutation 'IGL02389:0610040J01Rik'
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ID291689
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 0610040J01Rik
Ensembl Gene ENSMUSG00000060512
Gene NameRIKEN cDNA 0610040J01 gene
Synonyms
Accession Numbers
Stock #IGL02389
Quality Score
Status
Chromosome5
Chromosomal Location63812495-63899619 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 63896483 bp
ZygosityHeterozygous
Amino Acid Change Serine to Asparagine (S-N)
Predicted Effect probably benign

PolyPhen 2 Score 0.200 (Sensitivity: 0.00; Specificity: 0.00)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aqp9 T C 9: 71,122,906 I⇒V probably benign Het
BC100530 C A 16: 36,367,486 V⇒F possibly damaging Het
Cntn2 T C 1: 132,525,321 E⇒G probably damaging Het
Csgalnact1 C A 8: 68,401,492 G⇒V probably damaging Het
Dennd3 A G 15: 73,567,056 D⇒G probably damaging Het
Dock2 T C 11: 34,698,740 Het
Dscam T A 16: 96,640,897 I⇒F probably benign Het
Egflam A T 15: 7,250,078 N⇒K probably benign Het
Fam216a T C 5: 122,367,511 T⇒A probably damaging Het
Fbxo40 T C 16: 36,969,774 M⇒V probably benign Het
Fbxw8 C T 5: 118,128,955 V⇒M probably damaging Het
Fcgbp C T 7: 28,075,171 R⇒C probably damaging Het
Gnpnat1 A G 14: 45,380,931 Het
Gria2 T C 3: 80,709,422 T⇒A unknown Het
H2-T3 A G 17: 36,186,608 M⇒T probably benign Het
Jakmip1 C T 5: 37,100,843 Q⇒* probably null Het
Krtap21-1 C T 16: 89,403,424 G⇒D unknown Het
Myo7a C T 7: 98,106,991 Het
Nlrp9c T A 7: 26,394,207 Q⇒L probably benign Het
Olfr1442 A T 19: 12,674,535 D⇒V probably benign Het
Olfr298 A G 7: 86,489,128 L⇒P possibly damaging Het
Olfr767 A C 10: 129,079,230 I⇒M possibly damaging Het
Olfr790 T A 10: 129,501,070 M⇒K probably benign Het
Pdzd8 A G 19: 59,301,393 I⇒T probably benign Het
Pign A T 1: 105,646,781 L⇒* probably null Het
Pik3r4 T G 9: 105,650,331 I⇒M probably benign Het
Pkhd1 T A 1: 20,117,720 I⇒F probably damaging Het
Prmt3 C T 7: 49,848,758 Q⇒* probably null Het
Prrc2c A G 1: 162,692,870 F⇒L unknown Het
Ptger3 C T 3: 157,567,171 R⇒C probably damaging Het
Rfx2 T C 17: 56,808,325 Het
Sh3bp4 T C 1: 89,145,148 F⇒L probably damaging Het
Slc18a2 G T 19: 59,263,301 Het
Slc26a8 T A 17: 28,638,650 I⇒F probably benign Het
Slc5a4b A T 10: 76,072,465 Y⇒* probably null Het
Slitrk1 A G 14: 108,912,322 I⇒T probably benign Het
Stxbp5l C T 16: 37,208,205 A⇒T probably benign Het
Tnks2 T A 19: 36,884,103 S⇒R probably benign Het
Trim30c A G 7: 104,382,174 F⇒S probably benign Het
Tyro3 C T 2: 119,804,864 Het
Vmn1r34 A T 6: 66,637,058 L⇒Q unknown Het
Zfp148 T A 16: 33,495,446 C⇒S probably damaging Het
Zzef1 T A 11: 72,899,538 V⇒D probably damaging Het
Zzef1 C T 11: 72,891,217 P⇒S probably benign Het
Other mutations in 0610040J01Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01621:0610040J01Rik APN 5 63898383 missense possibly damaging 0.60
IGL02229:0610040J01Rik APN 5 63898353 missense possibly damaging 0.51
IGL02411:0610040J01Rik APN 5 63898116 missense probably benign 0.00
R0243:0610040J01Rik UTSW 5 63898463 missense probably benign 0.09
R0411:0610040J01Rik UTSW 5 63896491 splice donor site probably benign
R1978:0610040J01Rik UTSW 5 63898537 nonsense probably null
R2072:0610040J01Rik UTSW 5 63898737 missense possibly damaging 0.79
R2202:0610040J01Rik UTSW 5 63898668 missense possibly damaging 0.89
R3160:0610040J01Rik UTSW 5 63896490 splice donor site probably benign
R3161:0610040J01Rik UTSW 5 63896490 splice donor site probably benign
R3162:0610040J01Rik UTSW 5 63896490 splice site probably benign
R4428:0610040J01Rik UTSW 5 63898839 missense unknown
R4429:0610040J01Rik UTSW 5 63898839 missense unknown
R4430:0610040J01Rik UTSW 5 63898839 missense unknown
R4431:0610040J01Rik UTSW 5 63898839 missense unknown
R4464:0610040J01Rik UTSW 5 63898839 missense unknown
R4465:0610040J01Rik UTSW 5 63898839 missense unknown
R4467:0610040J01Rik UTSW 5 63898839 missense unknown
R4491:0610040J01Rik UTSW 5 63898469 missense probably damaging 1.00
R5161:0610040J01Rik UTSW 5 63898001 nonsense probably null
Posted OnApr 16, 2015