Mutagenetix > Incidental Mutation

Incidental Mutation 'R4924:Wnt2'

378857

Institutional Source

Beutler Lab

Gene Symbol

Wnt2

Ensembl Gene

ENSMUSG00000010797

Gene Name

wingless-type MMTV integration site family, member 2

Synonyms

Mirp, 2610510E18Rik, Int1l1, m-irp, Irp, Wnt2a, Wnt-2

MMRRC Submission

042526-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.530) question?

Stock #

R4924 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

17988939-18030584 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 18023239 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Arginine at position 137 (C137R)

Ref Sequence

ENSEMBL: ENSMUSP00000010941 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000010941]

AlphaFold

P21552

Predicted Effect

probably damaging
Transcript: ENSMUST00000010941
AA Change: C137R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000010941
Gene: ENSMUSG00000010797
AA Change: C137R

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
WNT1	43	349	5.1e-213	SMART

Coding Region Coverage

1x: 99.0%
3x: 98.2%
10x: 96.0%
20x: 91.6%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the WNT gene family. The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutants exhibit impaired placental vascularization, runting and 50% perinatal mortality resulting from difficulties in breathing and nursing. Survivors of the perinatal period tend to recover, and adults are healthy and fertile. [provided by MGI curators]

Allele List at MGI

All alleles(4) : Targeted, knock-out(1) Targeted, other(3)

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aatk	G	A	11: 119,902,351 (GRCm39)	H625Y	probably damaging	Het
Adamts4	C	T	1: 171,086,643 (GRCm39)	R812W	probably damaging	Het
Ajuba	A	C	14: 54,809,056 (GRCm39)		probably null	Het
Aox1	T	A	1: 58,344,503 (GRCm39)	V532D	probably damaging	Het
Arpc1b	G	A	5: 145,063,625 (GRCm39)	S295N	probably benign	Het
Baiap2	A	G	11: 119,887,850 (GRCm39)	S335G	probably damaging	Het
Brap	T	G	5: 121,803,318 (GRCm39)	N155K	probably damaging	Het
Btn1a1	A	G	13: 23,648,396 (GRCm39)		probably benign	Het
Ccl12	G	A	11: 81,993,475 (GRCm39)	V38I	probably benign	Het
Cemip	T	C	7: 83,602,146 (GRCm39)	Y881C	probably damaging	Het
Cep128	T	C	12: 90,989,174 (GRCm39)		silent	Het
Chd5	A	C	4: 152,450,886 (GRCm39)	D670A	possibly damaging	Het
Cmip	T	C	8: 117,983,994 (GRCm39)	Y52H	probably benign	Het
Dmtn	A	G	14: 70,855,399 (GRCm39)	I30T	probably benign	Het
Dscaml1	T	A	9: 45,656,487 (GRCm39)	M1609K	probably damaging	Het
Edar	C	A	10: 58,465,197 (GRCm39)	E55D	probably damaging	Het
Ehmt1	A	T	2: 24,729,734 (GRCm39)	I601N	probably damaging	Het
Fam120a	A	T	13: 49,055,572 (GRCm39)	N705K	probably benign	Het
Gm21718	G	T	14: 51,550,292 (GRCm39)		noncoding transcript	Het
Gnaz	A	G	10: 74,827,545 (GRCm39)	D99G	probably benign	Het
Helz	G	A	11: 107,493,165 (GRCm39)	G196D	probably damaging	Het
Hif1a	T	C	12: 73,986,331 (GRCm39)	S341P	probably damaging	Het
Hivep1	G	T	13: 42,311,792 (GRCm39)	S1344I	probably benign	Het
Hspa1l	T	A	17: 35,196,832 (GRCm39)	Y290*	probably null	Het
Ift81	A	G	5: 122,732,679 (GRCm39)	L285S	possibly damaging	Het
Inpp4b	T	A	8: 82,849,253 (GRCm39)	N891K	probably damaging	Het
Irx6	C	T	8: 93,404,981 (GRCm39)	T283M	probably benign	Het
Kdm5b	A	G	1: 134,559,089 (GRCm39)	K1538E	probably benign	Het
Kif13a	A	G	13: 47,083,075 (GRCm39)	V8A	probably damaging	Het
Krtap15-1	T	A	16: 88,626,036 (GRCm39)	N34K	probably damaging	Het
Lama2	T	G	10: 27,245,137 (GRCm39)	I215L	probably damaging	Het
Ldlrad3	C	T	2: 101,900,328 (GRCm39)	R58H	possibly damaging	Het
Lvrn	C	T	18: 47,027,792 (GRCm39)	P869L	probably damaging	Het
Myo1d	A	G	11: 80,565,504 (GRCm39)	F411S	probably damaging	Het
Myo5b	T	A	18: 74,828,455 (GRCm39)	H702Q	probably benign	Het
Nat8f4	G	T	6: 85,878,401 (GRCm39)	Q41K	probably benign	Het
Nckap5	C	A	1: 125,954,765 (GRCm39)	E596*	probably null	Het
Nek10	T	A	14: 14,846,594 (GRCm38)		probably null	Het
Notch3	T	C	17: 32,363,705 (GRCm39)	Y1145C	probably damaging	Het
Nr4a2	A	T	2: 57,002,035 (GRCm39)	H76Q	probably benign	Het
Nup98	T	C	7: 101,784,185 (GRCm39)	Q1049R	probably damaging	Het
Or4k48	A	T	2: 111,476,121 (GRCm39)	S74T	possibly damaging	Het
Or5k1b	T	A	16: 58,580,982 (GRCm39)	R186*	probably null	Het
Or8k33	A	T	2: 86,383,853 (GRCm39)	F205Y	probably damaging	Het
Pepd	T	C	7: 34,720,409 (GRCm39)	Y231H	probably benign	Het
Plagl1	G	T	10: 13,003,301 (GRCm39)	A190S	possibly damaging	Het
Plat	T	A	8: 23,268,269 (GRCm39)	I345N	probably damaging	Het
Pnmt	A	G	11: 98,278,286 (GRCm39)	E120G	probably damaging	Het
Prkrip1	C	A	5: 136,227,797 (GRCm39)		probably null	Het
Pygm	G	A	19: 6,443,754 (GRCm39)	A572T	probably damaging	Het
Rbm4b	T	C	19: 4,807,400 (GRCm39)	F39L	probably damaging	Het
Rpe65	A	G	3: 159,328,268 (GRCm39)	H388R	probably benign	Het
Scn4a	G	T	11: 106,210,914 (GRCm39)	A1701E	possibly damaging	Het
Sdk2	C	A	11: 113,748,584 (GRCm39)	W616L	probably damaging	Het
Serpina3m	T	A	12: 104,357,729 (GRCm39)	S218T	probably benign	Het
Siglece	C	T	7: 43,309,297 (GRCm39)	R87H	probably damaging	Het
Sim1	C	A	10: 50,785,998 (GRCm39)	L284M	probably damaging	Het
Smok3c	G	T	5: 138,063,844 (GRCm39)	E444*	probably null	Het
Snx4	T	C	16: 33,115,100 (GRCm39)	V427A	probably benign	Het
Srp68	A	T	11: 116,151,684 (GRCm39)	V304E	probably damaging	Het
Stag1	A	T	9: 100,678,808 (GRCm39)	H243L	possibly damaging	Het
Stx6	T	C	1: 155,049,737 (GRCm39)	V14A	probably damaging	Het
Sv2b	T	A	7: 74,786,169 (GRCm39)	Y417F	probably benign	Het
Tas2r103	A	G	6: 133,013,161 (GRCm39)	Y302H	probably benign	Het
Thop1	T	C	10: 80,916,028 (GRCm39)	S404P	probably benign	Het
Trp53bp1	G	T	2: 121,051,701 (GRCm39)	C988*	probably null	Het
Tsbp1	C	T	17: 34,678,951 (GRCm39)	P221L	probably damaging	Het
Ube3c	A	G	5: 29,836,269 (GRCm39)	E630G	possibly damaging	Het
Usf3	T	C	16: 44,037,718 (GRCm39)	S733P	probably benign	Het
Vmn1r195	A	G	13: 22,463,189 (GRCm39)	T220A	probably benign	Het
Vmn1r201	A	T	13: 22,658,882 (GRCm39)	H32L	probably benign	Het
Ythdc2	T	C	18: 44,980,871 (GRCm39)	S489P	probably damaging	Het
Zfp248	A	G	6: 118,406,033 (GRCm39)	C418R	probably damaging	Het
Zfp946	T	G	17: 22,674,502 (GRCm39)	F419V	probably damaging	Het
Zfp994	C	T	17: 22,419,738 (GRCm39)	E404K	probably damaging	Het
Zfpm1	T	C	8: 123,061,347 (GRCm39)	V304A	possibly damaging	Het

Other mutations in Wnt2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03264:Wnt2	APN	6	17,989,959 (GRCm39)	missense	probably benign	0.22
1mM(1):Wnt2	UTSW	6	18,008,622 (GRCm39)	missense	probably damaging	1.00
R1165:Wnt2	UTSW	6	17,989,946 (GRCm39)	missense	probably benign
R1771:Wnt2	UTSW	6	18,008,696 (GRCm39)	missense	probably damaging	0.97
R1782:Wnt2	UTSW	6	18,008,639 (GRCm39)	missense	possibly damaging	0.65
R1836:Wnt2	UTSW	6	18,023,234 (GRCm39)	missense	probably damaging	1.00
R1921:Wnt2	UTSW	6	18,030,252 (GRCm39)	missense	unknown
R2009:Wnt2	UTSW	6	18,030,208 (GRCm39)	missense	probably damaging	0.98
R3749:Wnt2	UTSW	6	18,023,167 (GRCm39)	missense	probably benign	0.00
R4831:Wnt2	UTSW	6	18,023,285 (GRCm39)	missense	probably benign	0.19
R4888:Wnt2	UTSW	6	18,023,125 (GRCm39)	missense	possibly damaging	0.89
R5121:Wnt2	UTSW	6	18,023,125 (GRCm39)	missense	possibly damaging	0.89
R5660:Wnt2	UTSW	6	18,028,145 (GRCm39)	missense	probably benign	0.09
R5767:Wnt2	UTSW	6	17,990,027 (GRCm39)	missense	probably damaging	0.97
R6005:Wnt2	UTSW	6	18,030,322 (GRCm39)	start gained	probably benign
R6670:Wnt2	UTSW	6	18,028,091 (GRCm39)	missense	possibly damaging	0.90
R7205:Wnt2	UTSW	6	18,028,046 (GRCm39)	missense	probably benign	0.11
R7711:Wnt2	UTSW	6	17,990,036 (GRCm39)	missense	probably benign	0.44
R7732:Wnt2	UTSW	6	18,023,335 (GRCm39)	missense	probably damaging	1.00
R8249:Wnt2	UTSW	6	18,030,284 (GRCm39)	start codon destroyed	probably null
R9145:Wnt2	UTSW	6	18,030,397 (GRCm39)	start gained	probably benign

Predicted Primers

PCR Primer
(F):5'- AGTCACAAGAGCACAGGGTC -3'
(R):5'- TTCACCATAGGAAAGCTATGCAG -3'

Sequencing Primer
(F):5'- CAAGAGCACAGGGTCCTCAG -3'
(R):5'- CAGAACACTTGGAGAGACGCTC -3'

Posted On

2016-04-15