Incidental Mutation 'IGL00763:Lypd8l'
ID 28457
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Lypd8l
Ensembl Gene ENSMUSG00000037145
Gene Name LY6/PLAUR domain containing 8 like
Synonyms 2210407C18Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # IGL00763
Quality Score
Status
Chromosome 11
Chromosomal Location 58499030-58504318 bp(-) (GRCm39)
Type of Mutation utr 5 prime
DNA Base Change (assembly) T to G at 58503707 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000104449 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000048801] [ENSMUST00000108821]
AlphaFold Q6YI28
Predicted Effect probably benign
Transcript: ENSMUST00000048801
SMART Domains Protein: ENSMUSP00000039283
Gene: ENSMUSG00000037145

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
low complexity region 209 220 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000108821
SMART Domains Protein: ENSMUSP00000104449
Gene: ENSMUSG00000037145

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
low complexity region 209 220 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126695
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Bmp3 A C 5: 99,020,238 (GRCm39) R220S possibly damaging Het
Bms1 A G 6: 118,395,363 (GRCm39) probably benign Het
Ccdc138 T A 10: 58,411,537 (GRCm39) F635Y probably damaging Het
Ccdc81 T C 7: 89,518,823 (GRCm39) probably benign Het
Cntnap5a T C 1: 116,045,407 (GRCm39) I341T possibly damaging Het
Cog5 C T 12: 31,715,531 (GRCm39) probably benign Het
Dcaf4 G A 12: 83,586,107 (GRCm39) R358H probably damaging Het
Ddx10 A C 9: 53,071,326 (GRCm39) probably benign Het
Fgf15 T A 7: 144,453,629 (GRCm39) F201I probably damaging Het
Galp A G 7: 6,211,499 (GRCm39) Y40C probably damaging Het
Ints6 A G 14: 62,938,314 (GRCm39) probably benign Het
Iqcb1 A T 16: 36,676,649 (GRCm39) probably benign Het
Kif19a G A 11: 114,657,994 (GRCm39) V18I probably benign Het
Morc1 A C 16: 48,432,689 (GRCm39) Q719P probably damaging Het
Pla2g4a T C 1: 149,727,076 (GRCm39) D568G probably damaging Het
Plscr4 A G 9: 92,366,998 (GRCm39) E204G probably null Het
Rasgrf1 A G 9: 89,853,073 (GRCm39) T403A probably benign Het
Sec16b A G 1: 157,356,827 (GRCm39) T12A probably benign Het
Slc12a7 A T 13: 73,942,201 (GRCm39) N359I possibly damaging Het
Slc14a2 G T 18: 78,235,453 (GRCm39) D241E probably damaging Het
Slc23a2 G T 2: 131,943,420 (GRCm39) A27E probably benign Het
Slc38a8 T C 8: 120,220,958 (GRCm39) I200M probably benign Het
Thrap3 C T 4: 126,059,371 (GRCm39) G892S probably benign Het
Tmc6 A G 11: 117,669,872 (GRCm39) L20P probably damaging Het
Tnfsfm13 T C 11: 69,575,536 (GRCm39) D256G probably benign Het
Tonsl C T 15: 76,518,068 (GRCm39) A605T probably damaging Het
Usp28 A G 9: 48,939,463 (GRCm39) T240A probably benign Het
Zap70 A T 1: 36,818,333 (GRCm39) D340V possibly damaging Het
Zfp512b A T 2: 181,231,944 (GRCm39) F100I probably damaging Het
Other mutations in Lypd8l
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02341:Lypd8l APN 11 58,503,656 (GRCm39) missense possibly damaging 0.70
IGL02609:Lypd8l APN 11 58,503,442 (GRCm39) missense probably damaging 1.00
R0466:Lypd8l UTSW 11 58,503,331 (GRCm39) splice site probably benign
R0598:Lypd8l UTSW 11 58,499,230 (GRCm39) missense probably benign 0.27
R0612:Lypd8l UTSW 11 58,502,799 (GRCm39) splice site probably null
R2352:Lypd8l UTSW 11 58,503,676 (GRCm39) missense probably damaging 1.00
R2352:Lypd8l UTSW 11 58,502,934 (GRCm39) nonsense probably null
R2439:Lypd8l UTSW 11 58,501,603 (GRCm39) missense probably damaging 1.00
R2910:Lypd8l UTSW 11 58,499,252 (GRCm39) nonsense probably null
R2911:Lypd8l UTSW 11 58,499,252 (GRCm39) nonsense probably null
R2991:Lypd8l UTSW 11 58,501,516 (GRCm39) missense possibly damaging 0.81
R3609:Lypd8l UTSW 11 58,503,384 (GRCm39) missense possibly damaging 0.95
R4863:Lypd8l UTSW 11 58,503,338 (GRCm39) critical splice donor site probably null
R4925:Lypd8l UTSW 11 58,501,513 (GRCm39) missense probably damaging 0.96
R6954:Lypd8l UTSW 11 58,499,314 (GRCm39) missense probably benign 0.01
R7725:Lypd8l UTSW 11 58,499,325 (GRCm39) missense probably benign 0.21
R9148:Lypd8l UTSW 11 58,499,338 (GRCm39) missense probably benign 0.08
Z1186:Lypd8l UTSW 11 58,503,397 (GRCm39) missense probably benign 0.00
Z1186:Lypd8l UTSW 11 58,503,387 (GRCm39) missense probably benign 0.14
Z1186:Lypd8l UTSW 11 58,499,335 (GRCm39) missense probably benign 0.00
Z1187:Lypd8l UTSW 11 58,503,397 (GRCm39) missense probably benign 0.00
Z1187:Lypd8l UTSW 11 58,503,387 (GRCm39) missense probably benign 0.14
Z1187:Lypd8l UTSW 11 58,499,335 (GRCm39) missense probably benign 0.00
Z1188:Lypd8l UTSW 11 58,503,397 (GRCm39) missense probably benign 0.00
Z1188:Lypd8l UTSW 11 58,503,387 (GRCm39) missense probably benign 0.14
Z1188:Lypd8l UTSW 11 58,499,335 (GRCm39) missense probably benign 0.00
Z1189:Lypd8l UTSW 11 58,503,397 (GRCm39) missense probably benign 0.00
Z1189:Lypd8l UTSW 11 58,503,387 (GRCm39) missense probably benign 0.14
Z1189:Lypd8l UTSW 11 58,499,335 (GRCm39) missense probably benign 0.00
Z1190:Lypd8l UTSW 11 58,503,397 (GRCm39) missense probably benign 0.00
Z1190:Lypd8l UTSW 11 58,503,387 (GRCm39) missense probably benign 0.14
Z1190:Lypd8l UTSW 11 58,499,335 (GRCm39) missense probably benign 0.00
Z1191:Lypd8l UTSW 11 58,503,397 (GRCm39) missense probably benign 0.00
Z1191:Lypd8l UTSW 11 58,503,387 (GRCm39) missense probably benign 0.14
Z1191:Lypd8l UTSW 11 58,499,335 (GRCm39) missense probably benign 0.00
Z1192:Lypd8l UTSW 11 58,503,397 (GRCm39) missense probably benign 0.00
Z1192:Lypd8l UTSW 11 58,503,387 (GRCm39) missense probably benign 0.14
Z1192:Lypd8l UTSW 11 58,499,335 (GRCm39) missense probably benign 0.00
Posted On 2013-04-17