Incidental Mutation 'IGL02456:0610009O20Rik'
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ID294156
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 0610009O20Rik
Ensembl Gene ENSMUSG00000024442
Gene NameRIKEN cDNA 0610009O20 gene
Synonyms
Accession Numbers
Stock #IGL02456
Quality Score
Status
Chromosome18
Chromosomal Location38250249-38262629 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 38261124 bp
ZygosityHeterozygous
Amino Acid Change Leucine to Glutamine (L-Q)
Predicted Effect probably damaging

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 0.00)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921511C20Rik T A X: 127,394,961 Y⇒* probably null Het
Apc C A 18: 34,313,882 S⇒* probably null Het
Atp8b5 A G 4: 43,365,578 T⇒A probably benign Het
Bcl2a1c T A 9: 114,330,390 F⇒I probably damaging Het
Brip1 G T 11: 86,065,099 L⇒I probably damaging Het
Cbx4 T A 11: 119,082,112 K⇒* probably null Het
Ccdc36 G T 9: 108,406,621 T⇒K probably benign Het
Ces1a C T 8: 93,039,498 V⇒I possibly damaging Het
Ces5a C T 8: 93,528,644 Het
Cfhr1 A C 1: 139,556,393 N⇒K probably benign Het
Clcn3 T C 8: 60,941,357 D⇒G possibly damaging Het
Cntnap1 T G 11: 101,178,129 I⇒S probably benign Het
Cntnap3 A T 13: 64,799,058 Het
Cntnap5c T A 17: 58,407,744 Het
Ddx23 A T 15: 98,647,549 V⇒E probably damaging Het
Gcm2 T C 13: 41,103,001 Y⇒C probably damaging Het
Gm9964 A G 11: 79,296,370 F⇒L unknown Het
Grn T A 11: 102,436,104 D⇒E probably benign Het
Kdm5c G A X: 152,246,318 D⇒N probably damaging Het
Ly75 C T 2: 60,293,781 M⇒I probably benign Het
Map1a C A 2: 121,298,653 P⇒T probably damaging Het
Mpp2 C A 11: 102,059,373 A⇒S possibly damaging Het
Mtr T C 13: 12,199,094 I⇒M possibly damaging Het
Npas3 A T 12: 54,048,767 I⇒F unknown Het
Nup85 T C 11: 115,581,865 Het
Olfr118 T A 17: 37,672,449 M⇒K probably damaging Het
Olfr325 T A 11: 58,581,198 L⇒H probably damaging Het
Olfr517 A G 7: 108,869,050 Y⇒H probably damaging Het
Olfr630 T A 7: 103,755,493 I⇒F possibly damaging Het
Olfr683 T C 7: 105,143,759 N⇒S possibly damaging Het
Pdia4 A T 6: 47,803,495 D⇒E probably damaging Het
Phf2 C A 13: 48,828,846 G⇒C probably damaging Het
Polr2h T A 16: 20,720,602 L⇒H probably damaging Het
Rbm47 G A 5: 66,027,021 R⇒C probably damaging Het
Sfmbt1 T C 14: 30,785,880 S⇒P possibly damaging Het
Slc5a12 T C 2: 110,616,834 Het
Tacc2 T C 7: 130,626,261 S⇒P probably damaging Het
Tbc1d16 T G 11: 119,210,546 H⇒P probably damaging Het
Tbck A G 3: 132,734,714 Het
Tmtc4 A T 14: 122,925,962 Het
Ttc13 T C 8: 124,690,361 Het
Ttc17 T C 2: 94,362,785 Het
Vmn1r121 T A 7: 21,098,513 M⇒L unknown Het
Vps13c T C 9: 67,952,976 S⇒P possibly damaging Het
Zan A C 5: 137,446,844 S⇒A unknown Het
Zfp39 G T 11: 58,902,800 Y⇒* probably null Het
Zfp407 T C 18: 84,558,641 N⇒S unknown Het
Zhx2 C A 15: 57,823,639 D⇒E probably benign Het
Other mutations in 0610009O20Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02216:0610009O20Rik APN 18 38252860 missense probably damaging 1.00
R0134:0610009O20Rik UTSW 18 38261264 missense probably benign 0.37
R0225:0610009O20Rik UTSW 18 38261264 missense probably benign 0.37
R0511:0610009O20Rik UTSW 18 38254071 critical splice donor site probably null
R0560:0610009O20Rik UTSW 18 38254498 missense probably damaging 1.00
R1899:0610009O20Rik UTSW 18 38258342 missense probably benign 0.08
R3005:0610009O20Rik UTSW 18 38259959 missense possibly damaging 0.92
R3552:0610009O20Rik UTSW 18 38258365 splice site probably benign
R4418:0610009O20Rik UTSW 18 38261287 unclassified probably null
X0067:0610009O20Rik UTSW 18 38258023 splice acceptor site probably benign
Posted OnApr 16, 2015