Incidental Mutation 'IGL03336:Ypel4'
ID 417045
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ypel4
Ensembl Gene ENSMUSG00000034059
Gene Name yippee like 4
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.321) question?
Stock # IGL03336
Quality Score
Status
Chromosome 2
Chromosomal Location 84564402-84568999 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 84567871 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 98 (Y98C)
Ref Sequence ENSEMBL: ENSMUSP00000088231 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000090729] [ENSMUST00000111643] [ENSMUST00000181711]
AlphaFold Q65Z93
Predicted Effect noncoding transcript
Transcript: ENSMUST00000083550
Predicted Effect probably damaging
Transcript: ENSMUST00000090729
AA Change: Y98C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000088231
Gene: ENSMUSG00000034059
AA Change: Y98C

DomainStartEndE-ValueType
Pfam:Yippee-Mis18 27 122 2.9e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000111643
Predicted Effect noncoding transcript
Transcript: ENSMUST00000151399
Predicted Effect noncoding transcript
Transcript: ENSMUST00000151647
Predicted Effect probably benign
Transcript: ENSMUST00000181711
SMART Domains Protein: ENSMUSP00000137761
Gene: ENSMUSG00000097187

DomainStartEndE-ValueType
low complexity region 29 45 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933412E24Rik A G 15: 59,888,251 (GRCm39) V63A probably benign Het
Ankrd11 A G 8: 123,618,582 (GRCm39) S1757P probably benign Het
Atp8a1 G T 5: 67,887,150 (GRCm39) Y629* probably null Het
Cenpf T C 1: 189,384,844 (GRCm39) K2479E probably damaging Het
Clip1 G T 5: 123,791,633 (GRCm39) S179* probably null Het
Cmya5 A G 13: 93,230,013 (GRCm39) S1692P possibly damaging Het
Cyp17a1 T C 19: 46,659,474 (GRCm39) S119G probably benign Het
Fndc5 T C 4: 129,033,711 (GRCm39) F160L probably benign Het
Muc5b T C 7: 141,418,100 (GRCm39) V3682A probably damaging Het
Myh8 G T 11: 67,175,528 (GRCm39) D328Y probably damaging Het
Or10a5 T A 7: 106,635,542 (GRCm39) M60K probably damaging Het
Or4c121 T C 2: 89,024,241 (GRCm39) T46A probably benign Het
Or51f1 C T 7: 102,505,823 (GRCm39) C222Y probably benign Het
Or51k2 T C 7: 103,596,616 (GRCm39) L281P probably damaging Het
Or6c203 T C 10: 129,010,098 (GRCm39) E264G probably benign Het
Paxbp1 T C 16: 90,831,060 (GRCm39) I439V probably benign Het
Pcdhb3 T C 18: 37,436,014 (GRCm39) V660A possibly damaging Het
Pcyt2 T C 11: 120,506,758 (GRCm39) D32G probably damaging Het
Pdzph1 A T 17: 59,281,229 (GRCm39) V351D probably benign Het
Ribc2 C T 15: 85,017,114 (GRCm39) Q51* probably null Het
Scn2a A G 2: 65,519,088 (GRCm39) E438G probably damaging Het
Slc18a3 T C 14: 32,184,785 (GRCm39) probably benign Het
Slc5a1 G A 5: 33,304,287 (GRCm39) V296I probably benign Het
Slit3 A T 11: 35,560,928 (GRCm39) T958S probably damaging Het
Spag8 C T 4: 43,652,114 (GRCm39) probably benign Het
Susd3 A C 13: 49,392,258 (GRCm39) S144R probably benign Het
Synpo2 T C 3: 122,907,828 (GRCm39) E496G possibly damaging Het
Tbcel T C 9: 42,350,427 (GRCm39) T269A probably benign Het
Tmem156 A G 5: 65,233,107 (GRCm39) Y152H probably benign Het
Tmem247 A G 17: 87,225,857 (GRCm39) E99G probably damaging Het
Tuba3b A G 6: 145,565,450 (GRCm39) D306G possibly damaging Het
Vps13c T A 9: 67,858,924 (GRCm39) D2791E possibly damaging Het
Other mutations in Ypel4
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4303:Ypel4 UTSW 2 84,567,151 (GRCm39) utr 5 prime probably benign
R5006:Ypel4 UTSW 2 84,567,182 (GRCm39) missense probably benign 0.07
R6463:Ypel4 UTSW 2 84,567,087 (GRCm39) start gained probably benign
R9508:Ypel4 UTSW 2 84,567,304 (GRCm39) missense probably damaging 1.00
R9657:Ypel4 UTSW 2 84,568,068 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02