Incidental Mutation 'IGL01121:Lypd5'
ID51594
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Lypd5
Ensembl Gene ENSMUSG00000030484
Gene NameLy6/Plaur domain containing 5
Synonyms
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL01121
Quality Score
Status
Chromosome7
Chromosomal Location24349196-24355109 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 24351551 bp
ZygosityHeterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 29 (Y29F)
Ref Sequence ENSEMBL: ENSMUSP00000032683 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032683]
Predicted Effect probably benign
Transcript: ENSMUST00000032683
AA Change: Y29F

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000032683
Gene: ENSMUSG00000030484
AA Change: Y29F

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
Blast:LU 24 119 7e-38 BLAST
LU 132 225 1.19e-1 SMART
low complexity region 230 248 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700046A07Rik G A 18: 62,755,148 noncoding transcript Het
4930432E11Rik A T 7: 29,574,001 noncoding transcript Het
Alg3 T C 16: 20,610,647 E31G probably damaging Het
Arhgap29 A G 3: 122,009,863 E764G probably damaging Het
Atp5j2 C A 5: 145,184,568 V68L probably benign Het
Birc6 T A 17: 74,631,038 I2645K probably benign Het
Capn11 A G 17: 45,639,132 S369P probably benign Het
Car4 A T 11: 84,964,346 probably null Het
Ccdc185 C T 1: 182,748,657 V156I probably benign Het
Cpsf2 G T 12: 101,988,706 E245D probably damaging Het
Dnah11 T C 12: 118,050,695 D2019G probably benign Het
Dscc1 A G 15: 55,082,325 probably benign Het
Dzip3 T C 16: 48,944,881 D490G probably benign Het
E2f8 G A 7: 48,867,821 Q745* probably null Het
Fat3 T A 9: 15,998,401 T2102S probably benign Het
Fgf7 C T 2: 126,088,232 probably benign Het
Fstl4 T C 11: 52,814,637 F47L probably benign Het
Gm15097 A T X: 149,804,328 R129S possibly damaging Het
Gm4297 C T X: 24,552,615 D200N probably benign Het
Itgb5 G T 16: 33,919,989 D490Y probably benign Het
Kansl1 A G 11: 104,335,596 S912P probably benign Het
Kcnq3 A T 15: 66,005,977 probably benign Het
Kctd6 A G 14: 8,222,656 H166R possibly damaging Het
Kel T C 6: 41,702,409 D140G probably benign Het
Lrif1 C A 3: 106,735,664 S177* probably null Het
Lrp1 A T 10: 127,583,853 C962* probably null Het
Mmrn1 A G 6: 60,975,944 D403G possibly damaging Het
Nhsl1 T G 10: 18,511,710 V244G probably damaging Het
Olfr781 T C 10: 129,332,935 I18T probably benign Het
Ptprd A T 4: 75,954,201 probably benign Het
Rcan2 A T 17: 44,017,884 I69L probably damaging Het
Rprd2 A G 3: 95,776,550 L373P probably damaging Het
Slc10a4 T C 5: 73,007,586 C174R probably damaging Het
Tas2r134 C T 2: 51,627,989 T160I probably damaging Het
Tbc1d19 T A 5: 53,897,062 L464* probably null Het
Tmem45a2 C T 16: 57,040,790 D225N possibly damaging Het
Unc79 G A 12: 103,165,631 C2139Y probably damaging Het
Vmn2r101 G T 17: 19,589,674 G241C probably damaging Het
Vmn2r91 T C 17: 18,136,504 V811A possibly damaging Het
Wdr11 T C 7: 129,628,022 Y844H probably benign Het
Wdr70 T C 15: 7,873,174 K656E possibly damaging Het
Zfp579 C A 7: 4,993,247 C555F possibly damaging Het
Other mutations in Lypd5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01066:Lypd5 APN 7 24353485 missense probably benign 0.10
IGL01689:Lypd5 APN 7 24352629 splice site probably benign
IGL02584:Lypd5 APN 7 24353568 missense possibly damaging 0.59
IGL02888:Lypd5 APN 7 24352619 missense probably damaging 0.98
R5167:Lypd5 UTSW 7 24352464 missense possibly damaging 0.79
R5982:Lypd5 UTSW 7 24353037 missense probably damaging 1.00
R6746:Lypd5 UTSW 7 24353106 splice site probably null
R7951:Lypd5 UTSW 7 24351635 missense probably damaging 0.96
X0057:Lypd5 UTSW 7 24349221 utr 5 prime probably benign
Z1177:Lypd5 UTSW 7 24352613 missense probably damaging 1.00
Posted On2013-06-21