Incidental Mutation 'IGL01892:Wfdc15b'
ID 179272
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Wfdc15b
Ensembl Gene ENSMUSG00000018211
Gene Name WAP four-disulfide core domain 15B
Synonyms Wfdc15, 9230106L14Rik, Swam1
Accession Numbers
Essential gene? Not available question?
Stock # IGL01892
Quality Score
Status
Chromosome 2
Chromosomal Location 164056374-164063580 bp(-) (GRCm39)
Type of Mutation start codon destroyed
DNA Base Change (assembly) A to T at 164057388 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 1 (M1K)
Ref Sequence ENSEMBL: ENSMUSP00000132507 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000018355] [ENSMUST00000109376] [ENSMUST00000164567]
AlphaFold Q9JHY4
Predicted Effect probably null
Transcript: ENSMUST00000018355
AA Change: M1K

PolyPhen 2 Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000018355
Gene: ENSMUSG00000018211
AA Change: M1K

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
WAP 32 76 9.87e-4 SMART
Predicted Effect probably null
Transcript: ENSMUST00000109376
AA Change: M1K

PolyPhen 2 Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000105001
Gene: ENSMUSG00000018211
AA Change: M1K

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
WAP 32 76 9.87e-4 SMART
Predicted Effect probably null
Transcript: ENSMUST00000164567
AA Change: M1K

PolyPhen 2 Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000132507
Gene: ENSMUSG00000018211
AA Change: M1K

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
WAP 32 76 9.87e-4 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cplane1 A T 15: 8,271,749 (GRCm39) probably benign Het
Cyp2c68 T A 19: 39,722,788 (GRCm39) E253D probably benign Het
Gbp2b A G 3: 142,309,381 (GRCm39) D164G probably benign Het
Gm10717 C T 9: 3,025,616 (GRCm39) S67L probably benign Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
Lct G T 1: 128,235,342 (GRCm39) T555N probably damaging Het
Ncam2 T A 16: 81,386,587 (GRCm39) H655Q possibly damaging Het
Or52a24 A T 7: 103,381,687 (GRCm39) M185L possibly damaging Het
Or8b57 C A 9: 40,004,114 (GRCm39) L45F probably damaging Het
Pglyrp4 A G 3: 90,646,348 (GRCm39) N293S probably benign Het
Pofut2 C A 10: 77,101,717 (GRCm39) D251E probably benign Het
Prdm2 T C 4: 142,860,974 (GRCm39) E772G probably damaging Het
Prkd3 A T 17: 79,279,930 (GRCm39) D254E probably benign Het
Prr36 G A 8: 4,265,243 (GRCm39) P169L probably damaging Het
Pwp2 T C 10: 78,014,841 (GRCm39) Y381C probably damaging Het
Rasgrp1 G A 2: 117,124,323 (GRCm39) T293M probably damaging Het
Snd1 G A 6: 28,888,123 (GRCm39) probably null Het
Suclg2 A T 6: 95,556,169 (GRCm39) D237E probably damaging Het
Tenm3 T C 8: 48,729,431 (GRCm39) N1509S probably benign Het
Thbd A T 2: 148,248,988 (GRCm39) H293Q possibly damaging Het
Tie1 T A 4: 118,333,115 (GRCm39) Y871F probably benign Het
Vmn1r38 A T 6: 66,753,360 (GRCm39) V252D probably benign Het
Vmn1r60 C A 7: 5,547,309 (GRCm39) V264F probably benign Het
Vmn1r68 T C 7: 10,261,334 (GRCm39) T255A possibly damaging Het
Vmn2r49 A T 7: 9,718,690 (GRCm39) V458E probably benign Het
Vmn2r9 A T 5: 108,995,700 (GRCm39) V316D probably damaging Het
Other mutations in Wfdc15b
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4304:Wfdc15b UTSW 2 164,057,388 (GRCm39) start codon destroyed probably null 0.86
R7200:Wfdc15b UTSW 2 164,057,037 (GRCm39) missense probably benign
Posted On 2014-05-07