Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01408:Wfdc12'

79876

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Wfdc12

Ensembl Gene

ENSMUSG00000042845

Gene Name

WAP four-disulfide core domain 12

Synonyms

Swam2, WAP2

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01408

Quality Score

Status

Chromosome

Chromosomal Location

164031151-164032528 bp(-) (GRCm39)

Type of Mutation

makesense

DNA Base Change (assembly)

A to G at 164031581 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Stop codon to Arginine at position 86 (*86R)

Ref Sequence

ENSEMBL: ENSMUSP00000050836 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000051272]

AlphaFold

Q9JHY3

Predicted Effect

probably null
Transcript: ENSMUST00000051272
AA Change: *86R

SMART Domains

Protein: ENSMUSP00000050836
Gene: ENSMUSG00000042845
AA Change: *86R

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
WAP	29	72	4.11e-1	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: 42 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9530068E07Rik	A	G	11: 52,294,193 (GRCm39)	R145G	probably damaging	Het
Akr1c21	T	A	13: 4,627,431 (GRCm39)	M175K	probably benign	Het
Apol7a	C	T	15: 77,273,530 (GRCm39)	A311T	probably damaging	Het
Atxn10	G	T	15: 85,260,896 (GRCm39)	E214*	probably null	Het
Bmp2k	C	T	5: 97,234,823 (GRCm39)	Q749*	probably null	Het
Ccdc141	G	A	2: 76,876,023 (GRCm39)	A669V	probably benign	Het
Cndp2	A	C	18: 84,689,036 (GRCm39)	C249G	probably benign	Het
Cnr1	A	G	4: 33,944,802 (GRCm39)	I397V	possibly damaging	Het
Col19a1	T	C	1: 24,345,331 (GRCm39)		probably benign	Het
Dbn1	T	C	13: 55,630,117 (GRCm39)		probably benign	Het
Dmgdh	C	T	13: 93,845,803 (GRCm39)	P486S	probably damaging	Het
Dpys	A	G	15: 39,656,702 (GRCm39)	V455A	possibly damaging	Het
Farp2	A	G	1: 93,546,702 (GRCm39)	N907S	probably benign	Het
Fndc3c1	C	T	X: 105,476,378 (GRCm39)	E894K	probably benign	Het
Gm6685	A	T	11: 28,289,473 (GRCm39)	N114K	probably damaging	Het
Golga3	A	T	5: 110,365,675 (GRCm39)		probably null	Het
Grin2c	A	G	11: 115,151,708 (GRCm39)	L84P	probably damaging	Het
Gucy2c	A	G	6: 136,675,009 (GRCm39)	F1001L	probably benign	Het
Hcn4	A	G	9: 58,767,169 (GRCm39)	H910R	unknown	Het
Kdm4b	T	C	17: 56,660,518 (GRCm39)		probably benign	Het
Lrrfip2	A	G	9: 111,043,284 (GRCm39)	T497A	probably benign	Het
Man2c1	A	G	9: 57,048,884 (GRCm39)	Y924C	probably damaging	Het
Nkain2	T	A	10: 32,278,237 (GRCm39)	T63S	probably damaging	Het
Nlrp1a	T	A	11: 71,013,742 (GRCm39)	T503S	probably benign	Het
Or52n3	T	C	7: 104,530,037 (GRCm39)	V41A	probably benign	Het
Or52n4	T	A	7: 104,294,136 (GRCm39)	I146F	possibly damaging	Het
Pitrm1	T	A	13: 6,623,078 (GRCm39)	C780S	probably damaging	Het
Plekha5	C	T	6: 140,516,042 (GRCm39)		probably benign	Het
Rapgef4	C	T	2: 72,005,185 (GRCm39)	R193*	probably null	Het
Rbm20	A	G	19: 53,840,044 (GRCm39)	E1011G	possibly damaging	Het
Rfx3	A	T	19: 27,746,050 (GRCm39)	D685E	probably benign	Het
Ror1	T	C	4: 100,190,984 (GRCm39)	S114P	probably damaging	Het
Slc17a6	A	G	7: 51,318,863 (GRCm39)	K502E	probably benign	Het
Spink2	A	T	5: 77,359,174 (GRCm39)		probably benign	Het
Sptb	A	T	12: 76,659,921 (GRCm39)	I993N	possibly damaging	Het
Stxbp4	A	G	11: 90,512,475 (GRCm39)		probably benign	Het
Tes	A	T	6: 17,099,878 (GRCm39)	Y291F	probably damaging	Het
Tmtc4	G	T	14: 123,163,366 (GRCm39)		probably benign	Het
Trpa1	T	C	1: 14,959,637 (GRCm39)	E683G	probably benign	Het
Vmn2r73	T	C	7: 85,521,455 (GRCm39)	D171G	probably benign	Het
Wbp11	A	G	6: 136,791,612 (GRCm39)		probably benign	Het
Zfp281	T	C	1: 136,553,853 (GRCm39)	V277A	probably damaging	Het

Other mutations in Wfdc12

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00500:Wfdc12	APN	2	164,032,170 (GRCm39)	missense	probably damaging	1.00
IGL00537:Wfdc12	APN	2	164,032,387 (GRCm39)	missense	probably null	1.00
R2357:Wfdc12	UTSW	2	164,032,170 (GRCm39)	missense	probably damaging	1.00
R9166:Wfdc12	UTSW	2	164,032,193 (GRCm39)	nonsense	probably null

Posted On

2013-11-05