Mutagenetix > Incidental Mutation

Incidental Mutation 'R8348:Wscd2'

660426

Institutional Source

Beutler Lab

Gene Symbol

Wscd2

Ensembl Gene

ENSMUSG00000063430

Gene Name

WSC domain containing 2

Synonyms

4933413A10Rik, C530024P05Rik

MMRRC Submission

067732-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R8348 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

113638199-113727786 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 113710371 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Glutamine at position 298 (H298Q)

Ref Sequence

ENSEMBL: ENSMUSP00000092021 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000094452]

AlphaFold

D4PHA7

Predicted Effect

possibly damaging
Transcript: ENSMUST00000094452
AA Change: H298Q

PolyPhen 2 Score 0.891 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000092021
Gene: ENSMUSG00000063430
AA Change: H298Q

Domain	Start	End	E-Value	Type
transmembrane domain	21	43	N/A	INTRINSIC
low complexity region	44	61	N/A	INTRINSIC
WSC	133	225	6.11e-44	SMART
WSC	236	330	9.49e-41	SMART
Blast:WSC	389	409	2e-6	BLAST

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.4%

Validation Efficiency

100% (59/59)

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1600014C10Rik	A	G	7: 37,894,384 (GRCm39)	Y139C	possibly damaging	Het
A430033K04Rik	A	G	5: 138,634,514 (GRCm39)	D43G	probably damaging	Het
Actn3	C	A	19: 4,915,361 (GRCm39)	V464L	possibly damaging	Het
Adamts15	C	T	9: 30,813,846 (GRCm39)	R773Q	probably benign	Het
Angpt2	G	A	8: 18,791,135 (GRCm39)	R54*	probably null	Het
Arhgef28	G	T	13: 98,190,375 (GRCm39)	P195T	possibly damaging	Het
Axdnd1	A	T	1: 156,245,854 (GRCm39)	D107E	probably benign	Het
Cdh23	C	T	10: 60,167,507 (GRCm39)	V1828M	probably benign	Het
Cep95	A	G	11: 106,704,593 (GRCm39)	T440A	possibly damaging	Het
Ctdp1	G	A	18: 80,493,325 (GRCm39)	A390V	probably benign	Het
Desi2	T	A	1: 178,083,906 (GRCm39)		probably benign	Het
Dnah2	A	T	11: 69,320,273 (GRCm39)	M3932K	possibly damaging	Het
Dnah8	A	T	17: 30,955,121 (GRCm39)	Q2050L	probably damaging	Het
Etnppl	T	A	3: 130,423,141 (GRCm39)	M274K	probably benign	Het
Farp2	G	T	1: 93,504,614 (GRCm39)		probably null	Het
Fbxo46	G	A	7: 18,870,469 (GRCm39)	G363R	probably damaging	Het
Fiz1	A	G	7: 5,015,909 (GRCm39)	V27A	probably benign	Het
Fndc3b	T	A	3: 27,494,144 (GRCm39)	M994L	probably benign	Het
G3bp1	T	G	11: 55,389,457 (GRCm39)	D384E	possibly damaging	Het
Galnt2	C	T	8: 125,061,025 (GRCm39)	R306*	probably null	Het
Gle1	T	C	2: 29,832,556 (GRCm39)	Y304H	possibly damaging	Het
Gm3415	G	A	5: 146,493,407 (GRCm39)	R84H	probably benign	Het
Gm7694	A	C	1: 170,129,209 (GRCm39)	S107A	possibly damaging	Het
Gpc6	A	G	14: 117,673,232 (GRCm39)	D163G	probably damaging	Het
Gtpbp6	G	A	5: 110,251,892 (GRCm39)	H514Y	possibly damaging	Het
Hdgfl2	A	G	17: 56,406,370 (GRCm39)	E595G	possibly damaging	Het
Hoxc11	G	A	15: 102,863,186 (GRCm39)	G76S	possibly damaging	Het
Hoxc4	T	C	15: 102,943,440 (GRCm39)	C98R	possibly damaging	Het
Hydin	A	T	8: 111,329,878 (GRCm39)	I4871F	possibly damaging	Het
Ifnar1	A	G	16: 91,292,187 (GRCm39)	D176G	probably benign	Het
Inafm1	A	G	7: 16,007,055 (GRCm39)	I54T	probably damaging	Het
Inpp5b	G	A	4: 124,678,967 (GRCm39)	G458D	probably damaging	Het
Irs2	A	T	8: 11,054,974 (GRCm39)	S1153T	probably damaging	Het
Kcnj15	A	G	16: 95,096,609 (GRCm39)	Y77C	probably damaging	Het
Klhl35	C	A	7: 99,121,062 (GRCm39)	D10E	probably damaging	Het
Lef1	A	T	3: 130,906,461 (GRCm39)	M1L	probably benign	Het
Lima1	T	C	15: 99,678,753 (GRCm39)	T403A	probably benign	Het
Magi3	T	A	3: 103,958,531 (GRCm39)	N518I	probably damaging	Het
Mcoln3	T	C	3: 145,836,974 (GRCm39)	C269R	probably damaging	Het
Mis18a	A	T	16: 90,523,919 (GRCm39)	L81*	probably null	Het
Mug2	A	T	6: 122,049,192 (GRCm39)	K903*	probably null	Het
Nhsl3	G	A	4: 129,117,699 (GRCm39)	R322C	probably damaging	Het
Pex6	T	C	17: 47,034,039 (GRCm39)	S656P	probably benign	Het
Pgr	C	A	9: 8,922,602 (GRCm39)	Q591K	probably benign	Het
Phactr3	T	C	2: 177,897,935 (GRCm39)	S50P	probably benign	Het
Plscr4	C	T	9: 92,372,843 (GRCm39)	R322*	probably null	Het
Sipa1l1	T	A	12: 82,443,045 (GRCm39)	N778K	probably benign	Het
Slc22a6	C	G	19: 8,599,169 (GRCm39)	R267G	probably damaging	Het
Slc5a7	A	G	17: 54,583,655 (GRCm39)	V545A	possibly damaging	Het
Snf8	A	G	11: 95,925,877 (GRCm39)	K13R	probably benign	Het
St3gal1	G	A	15: 66,985,511 (GRCm39)	R48C	probably damaging	Het
Tacc2	A	C	7: 130,225,019 (GRCm39)	K568T	possibly damaging	Het
Tnxb	C	A	17: 34,929,102 (GRCm39)	T2715K	possibly damaging	Het
Vegfb	T	C	19: 6,962,856 (GRCm39)	I140V	probably benign	Het
Vmn2r89	A	C	14: 51,692,548 (GRCm39)	D117A	possibly damaging	Het
Vps13c	C	T	9: 67,786,385 (GRCm39)	T284I	possibly damaging	Het
Wnk1	T	C	6: 119,906,960 (GRCm39)		probably null	Het
Zfp69	A	T	4: 120,787,834 (GRCm39)	C494S	probably damaging	Het
Zfp715	T	C	7: 42,949,361 (GRCm39)	T200A	possibly damaging	Het

Other mutations in Wscd2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00323:Wscd2	APN	5	113,689,236 (GRCm39)	missense	possibly damaging	0.56
IGL01113:Wscd2	APN	5	113,708,800 (GRCm39)	missense	probably damaging	1.00
IGL01476:Wscd2	APN	5	113,710,382 (GRCm39)	missense	probably damaging	0.99
IGL01894:Wscd2	APN	5	113,710,357 (GRCm39)	missense	probably damaging	0.96
IGL02560:Wscd2	APN	5	113,699,045 (GRCm39)	missense	probably benign	0.01
IGL02755:Wscd2	APN	5	113,712,092 (GRCm39)	missense	possibly damaging	0.66
froggie	UTSW	5	113,726,206 (GRCm39)	makesense	probably null
R0381:Wscd2	UTSW	5	113,689,192 (GRCm39)	missense	probably damaging	0.96
R1144:Wscd2	UTSW	5	113,699,151 (GRCm39)	splice site	probably null
R1858:Wscd2	UTSW	5	113,689,231 (GRCm39)	missense	possibly damaging	0.63
R3695:Wscd2	UTSW	5	113,689,078 (GRCm39)	missense	possibly damaging	0.82
R4231:Wscd2	UTSW	5	113,699,045 (GRCm39)	missense	probably benign	0.00
R4232:Wscd2	UTSW	5	113,699,045 (GRCm39)	missense	probably benign	0.00
R4667:Wscd2	UTSW	5	113,715,333 (GRCm39)	missense	probably damaging	1.00
R4696:Wscd2	UTSW	5	113,689,240 (GRCm39)	missense	probably benign
R5727:Wscd2	UTSW	5	113,715,411 (GRCm39)	missense	possibly damaging	0.89
R6401:Wscd2	UTSW	5	113,726,206 (GRCm39)	makesense	probably null
R7413:Wscd2	UTSW	5	113,715,402 (GRCm39)	missense	probably benign	0.02
R7642:Wscd2	UTSW	5	113,715,475 (GRCm39)	missense	possibly damaging	0.67
R7837:Wscd2	UTSW	5	113,710,394 (GRCm39)	missense	probably damaging	1.00
R8046:Wscd2	UTSW	5	113,689,176 (GRCm39)	missense	probably benign	0.05
R8331:Wscd2	UTSW	5	113,688,996 (GRCm39)	start codon destroyed	probably null	0.99
R8680:Wscd2	UTSW	5	113,712,235 (GRCm39)	missense	probably damaging	1.00
R8928:Wscd2	UTSW	5	113,715,401 (GRCm39)	missense	possibly damaging	0.90
R9125:Wscd2	UTSW	5	113,715,417 (GRCm39)	missense	probably benign	0.33

Predicted Primers

PCR Primer
(F):5'- GCCAAGTCTCTCCTGAAGTC -3'
(R):5'- GCTTCTCACTGCTGGCTTAG -3'

Sequencing Primer
(F):5'- TACTTCAGGTAAGGGAACAGATAAGC -3'
(R):5'- TTAGGGACCAACTGGCCATG -3'

Posted On

2021-01-18