Incidental Mutation 'IGL02627:Wfdc16'
List |< first << previous [record 29 of 29]
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Wfdc16
Ensembl Gene ENSMUSG00000070530
Gene NameWAP four-disulfide core domain 16
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.052) question?
Stock #IGL02627
Quality Score
Chromosomal Location164634707-164638796 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 164638463 bp
Amino Acid Change Glutamic Acid to Aspartic acid at position 37 (E37D)
Ref Sequence ENSEMBL: ENSMUSP00000104960 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109336]
Predicted Effect possibly damaging
Transcript: ENSMUST00000109336
AA Change: E37D

PolyPhen 2 Score 0.455 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000104960
Gene: ENSMUSG00000070530
AA Change: E37D

transmembrane domain 10 28 N/A INTRINSIC
WAP 51 91 3.41e-1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000121070
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700001O22Rik T A 2: 30,795,765 K353M probably damaging Het
2610301B20Rik G A 4: 10,898,039 C207Y probably damaging Het
Arhgap32 T C 9: 32,246,006 Y100H probably damaging Het
Cdc45 C T 16: 18,798,729 M200I probably benign Het
Ckap5 A T 2: 91,576,021 N752I probably damaging Het
Dgkz T A 2: 91,938,710 probably benign Het
Egfr T A 11: 16,869,346 V292E probably damaging Het
Gnb3 T C 6: 124,834,715 T329A probably damaging Het
Igkv3-2 A T 6: 70,698,826 T40S probably damaging Het
Kcnq2 T C 2: 181,082,327 probably benign Het
Mbip T C 12: 56,335,805 Q292R probably benign Het
Mgat5b T C 11: 116,983,616 Y625H probably damaging Het
Ms4a4d A T 19: 11,548,623 E40D probably damaging Het
Naip1 T C 13: 100,425,648 E1003G possibly damaging Het
Ncf2 G A 1: 152,811,008 probably benign Het
Nfkbiz A G 16: 55,816,351 V529A probably damaging Het
Osr2 A G 15: 35,300,454 N52S possibly damaging Het
Prag1 A G 8: 36,139,439 D778G possibly damaging Het
Rsl1d1 G T 16: 11,194,551 A337E possibly damaging Het
Sall3 A T 18: 80,972,361 L784Q possibly damaging Het
Spen A G 4: 141,473,015 I2744T probably damaging Het
Tfip11 A C 5: 112,329,813 S145R possibly damaging Het
Tonsl T C 15: 76,634,095 D559G probably damaging Het
Trmt5 A T 12: 73,281,455 S325T probably damaging Het
Ubr1 A T 2: 120,940,991 V472D probably damaging Het
Vmn1r30 T A 6: 58,435,761 T29S probably benign Het
Vps29 T C 5: 122,362,845 S158P probably benign Het
Wdr82 T C 9: 106,176,687 V79A possibly damaging Het
Other mutations in Wfdc16
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01080:Wfdc16 APN 2 164638486 missense probably damaging 0.97
IGL03267:Wfdc16 APN 2 164638542 missense possibly damaging 0.46
R0541:Wfdc16 UTSW 2 164635853 missense possibly damaging 0.73
R1171:Wfdc16 UTSW 2 164638483 missense possibly damaging 0.66
R1579:Wfdc16 UTSW 2 164635923 missense possibly damaging 0.46
R1598:Wfdc16 UTSW 2 164635430 missense probably benign 0.00
R7584:Wfdc16 UTSW 2 164638627 splice site probably null
R7780:Wfdc16 UTSW 2 164635865 missense probably benign 0.04
Posted On2015-04-16