Incidental Mutation 'R1577:Lypd6'
ID 171199
Institutional Source Beutler Lab
Gene Symbol Lypd6
Ensembl Gene ENSMUSG00000050447
Gene Name LY6/PLAUR domain containing 6
Synonyms E130115E03Rik
MMRRC Submission 039615-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.723) question?
Stock # R1577 (G1)
Quality Score 225
Status Not validated
Chromosome 2
Chromosomal Location 49956441-50083581 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 50080710 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 133 (R133*)
Ref Sequence ENSEMBL: ENSMUSP00000131002 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053208] [ENSMUST00000112712] [ENSMUST00000128451] [ENSMUST00000169232]
AlphaFold Q8BPP5
Predicted Effect probably null
Transcript: ENSMUST00000053208
AA Change: R133*
SMART Domains Protein: ENSMUSP00000061578
Gene: ENSMUSG00000050447
AA Change: R133*

DomainStartEndE-ValueType
signal peptide 1 25 N/A INTRINSIC
LU 47 141 1.04e-1 SMART
Predicted Effect probably null
Transcript: ENSMUST00000112712
AA Change: R133*
SMART Domains Protein: ENSMUSP00000108332
Gene: ENSMUSG00000050447
AA Change: R133*

DomainStartEndE-ValueType
signal peptide 1 25 N/A INTRINSIC
LU 47 141 1.04e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000128451
SMART Domains Protein: ENSMUSP00000116803
Gene: ENSMUSG00000050447

DomainStartEndE-ValueType
signal peptide 1 25 N/A INTRINSIC
Blast:LU 47 123 4e-51 BLAST
Predicted Effect probably null
Transcript: ENSMUST00000169232
AA Change: R133*
SMART Domains Protein: ENSMUSP00000131002
Gene: ENSMUSG00000050447
AA Change: R133*

DomainStartEndE-ValueType
signal peptide 1 25 N/A INTRINSIC
LU 47 141 1.04e-1 SMART
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 97.8%
  • 10x: 94.6%
  • 20x: 87.3%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Members of the LY6 protein family (see SLURP1; MIM 606119), such as LYPD6, have at least one 80-amino acid LU domain that contains 10 conserved cysteines with a defined disulfide-bonding pattern (Zhang et al., 2010 [PubMed 19653121]).[supplied by OMIM, Apr 2010]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrb3 T C 1: 25,133,264 (GRCm39) N404S possibly damaging Het
Cep85 T C 4: 133,879,599 (GRCm39) E383G probably damaging Het
Chst4 A T 8: 110,756,476 (GRCm39) H379Q probably benign Het
Clca3b A T 3: 144,529,280 (GRCm39) I798N probably damaging Het
Cldnd1 T G 16: 58,553,016 (GRCm39) L159R possibly damaging Het
Cntnap3 T C 13: 64,906,104 (GRCm39) E834G probably damaging Het
Col2a1 C T 15: 97,877,083 (GRCm39) R1065Q probably damaging Het
Dchs1 T C 7: 105,415,162 (GRCm39) D674G probably damaging Het
Dntt A G 19: 41,044,224 (GRCm39) Y463C probably damaging Het
Egfr A G 11: 16,819,241 (GRCm39) E257G probably benign Het
Eif4b C T 15: 101,998,336 (GRCm39) R339* probably null Het
Fat1 C T 8: 45,476,420 (GRCm39) T1822M probably benign Het
Fgd3 T C 13: 49,435,413 (GRCm39) N282D probably damaging Het
Fmo4 T C 1: 162,631,269 (GRCm39) M233V possibly damaging Het
Gabbr2 T A 4: 46,684,319 (GRCm39) M652L probably benign Het
Gal3st2c G A 1: 93,934,650 (GRCm39) V13M probably damaging Het
Gapvd1 C T 2: 34,599,240 (GRCm39) G686D probably damaging Het
Gdap1l1 T G 2: 163,280,524 (GRCm39) L20R probably damaging Het
Gm5800 A T 14: 51,952,016 (GRCm39) M82K probably benign Het
Grm6 T A 11: 50,753,972 (GRCm39) C759S probably damaging Het
Hs3st1 A T 5: 39,772,393 (GRCm39) D83E probably benign Het
Il12rb1 A G 8: 71,263,250 (GRCm39) D39G probably damaging Het
Ldhb C A 6: 142,438,324 (GRCm39) K244N possibly damaging Het
Med13l G A 5: 118,859,457 (GRCm39) G215S probably damaging Het
Ncoa1 T C 12: 4,345,196 (GRCm39) D606G probably damaging Het
Noc2l C T 4: 156,325,079 (GRCm39) T151M probably damaging Het
Or10q3 T C 19: 11,847,741 (GRCm39) T280A probably damaging Het
Or2ag2 T C 7: 106,485,217 (GRCm39) K269R probably benign Het
Or2at4 T C 7: 99,384,563 (GRCm39) L71P probably damaging Het
Or2t26 T A 11: 49,040,016 (GRCm39) C311S probably benign Het
Or5aq1b T C 2: 86,901,741 (GRCm39) T246A probably benign Het
Ppm1l G A 3: 69,460,403 (GRCm39) G327R probably damaging Het
Rapgef5 C T 12: 117,558,911 (GRCm39) A282V probably benign Het
Rnf139 T C 15: 58,771,367 (GRCm39) V464A probably damaging Het
Rprd2 C T 3: 95,672,047 (GRCm39) E1119K probably damaging Het
Sipa1l2 G A 8: 126,219,001 (GRCm39) T112I probably benign Het
Skint6 T C 4: 113,005,720 (GRCm39) T363A possibly damaging Het
Slc22a16 G T 10: 40,479,811 (GRCm39) E607* probably null Het
Slc24a2 T C 4: 86,909,648 (GRCm39) Y690C probably damaging Het
Slc25a23 T C 17: 57,354,306 (GRCm39) S115G probably benign Het
Slc4a3 T C 1: 75,527,535 (GRCm39) L168P probably damaging Het
Spats2 T A 15: 99,076,333 (GRCm39) I137N possibly damaging Het
Stard4 A T 18: 33,338,151 (GRCm39) V133D probably damaging Het
Syn3 A G 10: 86,284,728 (GRCm39) probably null Het
Tfpi A G 2: 84,263,447 (GRCm39) I305T probably damaging Het
Tmtc1 T A 6: 148,314,318 (GRCm39) probably null Het
Tpcn1 A C 5: 120,682,485 (GRCm39) W508G probably damaging Het
Ubr5 A T 15: 38,030,974 (GRCm39) N406K possibly damaging Het
Xrcc1 T A 7: 24,265,052 (GRCm39) L118* probably null Het
Zbtb5 T C 4: 44,995,129 (GRCm39) Y85C probably damaging Het
Zfand4 C A 6: 116,306,373 (GRCm39) Y735* probably null Het
Zfp180 G T 7: 23,805,333 (GRCm39) C584F probably damaging Het
Other mutations in Lypd6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01470:Lypd6 APN 2 50,078,795 (GRCm39) missense probably benign 0.16
IGL02476:Lypd6 APN 2 50,080,740 (GRCm39) missense possibly damaging 0.84
R0098:Lypd6 UTSW 2 50,080,792 (GRCm39) missense probably benign 0.01
R0098:Lypd6 UTSW 2 50,080,792 (GRCm39) missense probably benign 0.01
R0302:Lypd6 UTSW 2 50,055,679 (GRCm39) splice site probably benign
R0464:Lypd6 UTSW 2 50,080,690 (GRCm39) missense probably damaging 1.00
R1843:Lypd6 UTSW 2 50,078,774 (GRCm39) missense possibly damaging 0.94
R2849:Lypd6 UTSW 2 50,055,664 (GRCm39) missense probably damaging 1.00
R4663:Lypd6 UTSW 2 50,063,623 (GRCm39) nonsense probably null
R4716:Lypd6 UTSW 2 50,078,855 (GRCm39) critical splice donor site probably null
R5802:Lypd6 UTSW 2 50,063,613 (GRCm39) missense probably benign 0.25
R8171:Lypd6 UTSW 2 50,080,759 (GRCm39) missense possibly damaging 0.90
R8798:Lypd6 UTSW 2 50,078,774 (GRCm39) missense possibly damaging 0.94
R9653:Lypd6 UTSW 2 50,080,758 (GRCm39) missense probably benign 0.01
Z1177:Lypd6 UTSW 2 50,080,819 (GRCm39) frame shift probably null
Predicted Primers PCR Primer
(F):5'- TGAAACCTAGCAGCCACAGGTGAG -3'
(R):5'- TGTGTCACTACTGCCAAGCCAATG -3'

Sequencing Primer
(F):5'- TGAACGTCAGACGGCATTTC -3'
(R):5'- TACTGCCAAGCCAATGACTTC -3'
Posted On 2014-04-13