Incidental Mutation 'IGL01897:Wfdc15a'
ID 179434
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Wfdc15a
Ensembl Gene ENSMUSG00000051769
Gene Name WAP four-disulfide core domain 15A
Synonyms 1700049M11Rik, Wfdcl1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # IGL01897
Quality Score
Status
Chromosome 2
Chromosomal Location 164040783-164042050 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 164041896 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Lysine at position 21 (Q21K)
Ref Sequence ENSEMBL: ENSMUSP00000070718 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063251]
AlphaFold Q8BH89
Predicted Effect probably benign
Transcript: ENSMUST00000063251
AA Change: Q21K

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000070718
Gene: ENSMUSG00000051769
AA Change: Q21K

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
WAP 32 76 3.34e-6 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135739
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143202
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr3 A G 1: 125,346,025 (GRCm39) Y21H possibly damaging Het
Adamts15 A T 9: 30,813,448 (GRCm39) S906T probably damaging Het
Brat1 A G 5: 140,703,670 (GRCm39) D641G probably benign Het
Ccdc42 G A 11: 68,485,101 (GRCm39) R205H probably benign Het
Cdadc1 T C 14: 59,829,986 (GRCm39) probably null Het
Cfi T C 3: 129,652,034 (GRCm39) V235A probably damaging Het
Ctps1 T A 4: 120,424,476 (GRCm39) D46V probably damaging Het
Cyb5d1 A T 11: 69,284,587 (GRCm39) D188E probably benign Het
Cyp19a1 G T 9: 54,075,813 (GRCm39) T414N probably benign Het
Cyp2c40 A T 19: 39,792,217 (GRCm39) C242* probably null Het
Eif3b A T 5: 140,411,202 (GRCm39) T218S possibly damaging Het
Fasn A T 11: 120,698,765 (GRCm39) L2475Q probably damaging Het
Gm10717 C T 9: 3,025,616 (GRCm39) S67L probably benign Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Heyl A T 4: 123,140,400 (GRCm39) I320F probably damaging Het
Itpr3 T A 17: 27,330,236 (GRCm39) V1618E probably damaging Het
Kif7 A T 7: 79,350,800 (GRCm39) I1007N probably damaging Het
Lat2 A G 5: 134,635,481 (GRCm39) probably benign Het
Lipm A T 19: 34,098,708 (GRCm39) D394V probably damaging Het
Lmbrd1 T A 1: 24,782,977 (GRCm39) I307K possibly damaging Het
Mief1 T C 15: 80,132,709 (GRCm39) probably benign Het
Mta2 C T 19: 8,925,130 (GRCm39) Q333* probably null Het
Neb T A 2: 52,170,587 (GRCm39) E1695V possibly damaging Het
Npc1l1 A T 11: 6,177,879 (GRCm39) N510K probably benign Het
Or5af1 T C 11: 58,722,465 (GRCm39) F162L probably damaging Het
P2rx3 A C 2: 84,853,825 (GRCm39) probably benign Het
Pdgfc A G 3: 81,111,639 (GRCm39) E198G possibly damaging Het
Pkdcc T A 17: 83,527,548 (GRCm39) I242N probably damaging Het
Pkn3 C T 2: 29,972,824 (GRCm39) probably benign Het
Rcan2 T G 17: 44,147,325 (GRCm39) D54E probably damaging Het
Tmeff2 T A 1: 51,171,369 (GRCm39) Y202N probably damaging Het
Unc13c A G 9: 73,453,309 (GRCm39) L1827P probably damaging Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Zfp951 C A 5: 104,963,149 (GRCm39) S139I probably benign Het
Other mutations in Wfdc15a
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4930:Wfdc15a UTSW 2 164,041,725 (GRCm39) missense probably benign 0.16
R6089:Wfdc15a UTSW 2 164,041,586 (GRCm39) nonsense probably null
R8415:Wfdc15a UTSW 2 164,041,671 (GRCm39) missense probably damaging 1.00
R9330:Wfdc15a UTSW 2 164,041,632 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07