Incidental Mutation 'IGL02229:0610040J01Rik'
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ID285435
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 0610040J01Rik
Ensembl Gene ENSMUSG00000060512
Gene NameRIKEN cDNA 0610040J01 gene
Synonyms
Accession Numbers
Stock #IGL02229
Quality Score
Status
Chromosome5
Chromosomal Location63812495-63899619 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 63898353 bp
ZygosityHeterozygous
Amino Acid Change Aspartic acid to Glycine (D-G)
Predicted Effect possibly damaging

PolyPhen 2 Score 0.510 (Sensitivity: 0.00; Specificity: 0.00)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrg1 G T 8: 95,003,511 D⇒Y probably damaging Het
Ago4 T A 4: 126,511,532 N⇒I probably benign Het
Aoc1 C T 6: 48,905,909 Q⇒* probably null Het
Atl1 G A 12: 69,926,025 V⇒I probably benign Het
Cdh2 T C 18: 16,624,753 I⇒V probably benign Het
Cic C A 7: 25,290,950 Q⇒K probably benign Het
Cmya5 C T 13: 93,092,686 E⇒K probably benign Het
Csgalnact1 C A 8: 68,401,492 G219V probably damaging Het
Cspp1 T C 1: 10,083,556 S⇒P possibly damaging Het
D130043K22Rik T C 13: 24,875,924 Y⇒H probably damaging Het
Dck A G 5: 88,774,105 Y⇒C probably damaging Het
Eea1 A T 10: 96,018,184 E⇒V probably damaging Het
Gabra3 A G X: 72,501,077 Het
Gucy2f A G X: 142,179,988 S⇒P probably benign Het
Hbb-bh1 T A 7: 103,842,825 I⇒F possibly damaging Het
Hook1 T C 4: 96,001,251 S⇒P probably damaging Het
Hoxd12 G A 2: 74,675,934 R⇒H probably damaging Het
Iglc2 C T 16: 19,198,733 A⇒T probably benign Het
Il1r1 A G 1: 40,313,358 K⇒E probably damaging Het
Kcns3 A T 12: 11,092,092 M⇒K probably damaging Het
Krt7 C A 15: 101,427,616 A⇒D probably benign Het
Ltk C T 2: 119,758,573 R⇒H probably damaging Het
Macf1 G T 4: 123,509,826 D582E probably damaging Het
Mbnl3 A T X: 51,139,341 Y⇒N probably damaging Het
Mpp1 T C X: 75,121,428 Het
Myo18b A G 5: 112,878,110 S25P unknown Het
Olfr26 T A 9: 38,855,416 M⇒K probably damaging Het
Pacs2 A G 12: 113,056,800 Het
Rab3gap2 A G 1: 185,259,383 K⇒E possibly damaging Het
Sva T A 6: 42,042,222 C⇒S possibly damaging Het
Taf3 T C 2: 9,952,834 N⇒S probably damaging Het
Tbc1d5 A T 17: 50,852,600 M⇒K probably damaging Het
Tmem242 A T 17: 5,411,407 S⇒T probably benign Het
Ttn A T 2: 76,871,169 Het
Whsc1l1 A G 8: 25,710,748 N⇒S probably damaging Het
Other mutations in 0610040J01Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01621:0610040J01Rik APN 5 63898383 missense possibly damaging 0.60
IGL02389:0610040J01Rik APN 5 63896483 missense probably benign 0.20
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
R3161:0610040J01Rik UTSW 5 63896490 splice 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
R6115:0610040J01Rik UTSW 5 63897974 missense probably damaging 1.00
Posted OnApr 16, 2015