Incidental Mutation 'IGL02411:0610040J01Rik'
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ID292316
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 0610040J01Rik
Ensembl Gene ENSMUSG00000060512
Gene NameRIKEN cDNA 0610040J01 gene
Synonyms
Accession Numbers
Stock #IGL02411
Quality Score
Status
Chromosome5
Chromosomal Location63812495-63899619 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 63898116 bp
ZygosityHeterozygous
Amino Acid Change Glutamic Acid to Glycine (E-G)
Predicted Effect probably benign
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc8 G A 7: 46,107,007 R⇒C probably damaging Het
Adcy3 A T 12: 4,209,407 N⇒Y probably damaging Het
AI661453 T G 17: 47,467,338 L⇒R probably damaging Het
Arhgef10 A T 8: 14,954,819 Y⇒F probably benign Het
Atrx G T X: 105,830,981 S⇒R probably damaging Het
Clca1 T C 3: 145,028,002 T⇒A possibly damaging Het
Clec1b A G 6: 129,401,841 Y⇒C probably damaging Het
Cobll1 A G 2: 65,097,740 S⇒P probably benign Het
Crb1 C A 1: 139,248,475 C⇒F probably damaging Het
Crim1 C T 17: 78,335,334 R⇒* probably null Het
Cyp3a25 A T 5: 146,001,447 Het
Dntt T A 19: 41,052,985 Het
Gjb1 T C X: 101,385,005 C⇒R probably damaging Het
Glp1r T A 17: 30,924,511 C⇒S probably damaging Het
Gm5414 A T 15: 101,627,834 Y⇒N probably benign Het
Gm9631 G A 11: 121,943,652 Q⇒* probably null Het
Gm9796 G T 11: 95,697,930 A405D noncoding transcript Het
Gm9956 T C 10: 56,745,292 F17L unknown Het
Il1rap A T 16: 26,710,616 D⇒V probably damaging Het
Impa1 T C 3: 10,322,958 K⇒E possibly damaging Het
Iqub G A 6: 24,449,811 A⇒V possibly damaging Het
Jade3 T C X: 20,512,824 V⇒A probably damaging Het
Kif3a C A 11: 53,570,698 P⇒T possibly damaging Het
Kndc1 G T 7: 139,921,913 Het
Lyst G A 13: 13,660,956 C1741Y probably benign Het
Maged2 G T X: 150,809,759 D⇒E possibly damaging Het
Magi2 T C 5: 19,678,709 S⇒P probably damaging Het
Nxph3 A T 11: 95,510,830 *⇒R unknown Het
Oog2 A T 4: 144,195,048 H⇒L possibly damaging Het
Pcbd2 T G 13: 55,732,951 W⇒G probably benign Het
Pcdhb14 T G 18: 37,449,770 L⇒R probably damaging Het
Plch1 G T 3: 63,697,756 R⇒S probably damaging Het
Poln G T 5: 34,113,322 S⇒* probably null Het
Ppp2r1a T C 17: 20,951,334 Het
Rsu1 T G 2: 13,077,497 Het
Serpina10 A T 12: 103,616,943 M⇒K possibly damaging Het
Sox30 A T 11: 45,981,124 K⇒* probably null Het
Thbs1 T C 2: 118,114,970 V⇒A probably benign Het
Tie1 C A 4: 118,486,563 E⇒* probably null Het
Tm2d1 G T 4: 98,380,674 P⇒Q probably damaging Het
Tpp1 G T 7: 105,749,619 P⇒Q probably damaging Het
Trim13 A G 14: 61,605,149 E⇒G probably damaging 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
IGL02389:0610040J01Rik APN 5 63896483 missense probably benign 0.20
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