Mutagenetix > Incidental Mutation

Incidental Mutation 'R5788:Fzd2'

448169

Institutional Source

Beutler Lab

Gene Symbol

Fzd2

Ensembl Gene

ENSMUSG00000050288

Gene Name

frizzled class receptor 2

Synonyms

Fz10, Mfz10a, Mfz10

MMRRC Submission

043382-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.737) question?

Stock #

R5788 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

102495257-102498884 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 102496293 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Serine at position 246 (T246S)

Ref Sequence

ENSEMBL: ENSMUSP00000091463 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057893]

AlphaFold

Q9JIP6

Predicted Effect

probably benign
Transcript: ENSMUST00000057893
AA Change: T246S

PolyPhen 2 Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000091463
Gene: ENSMUSG00000050288
AA Change: T246S

Domain	Start	End	E-Value	Type
signal peptide	1	27	N/A	INTRINSIC
FRI	43	160	7.47e-74	SMART
low complexity region	176	195	N/A	INTRINSIC
Frizzled	239	563	3.32e-218	SMART

Meta Mutation Damage Score

0.1655

Coding Region Coverage

1x: 99.4%
3x: 98.8%
10x: 97.6%
20x: 96.2%

Validation Efficiency

98% (62/63)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This intronless gene is a member of the frizzled gene family. Members of this family encode seven-transmembrane domain proteins that are receptors for the wingless type MMTV integration site family of signaling proteins. This gene encodes a protein that is coupled to the beta-catenin canonical signaling pathway. Competition between the wingless-type MMTV integration site family, member 3A and wingless-type MMTV integration site family, member 5A gene products for binding of this protein is thought to regulate the beta-catenin-dependent and -independent pathways. [provided by RefSeq, Dec 2010]
PHENOTYPE: About 50% of mice homozygous for a reporter allele display a cleft palate and die as neonates; the remaining 50% survive exhibiting a variable degree of postnatal runting and reduced olfactory sensitivity to various odorants. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acadsb	A	G	7: 131,045,328 (GRCm39)	Y420C	probably benign	Het
Acot11	C	T	4: 106,617,327 (GRCm39)	G240R	probably damaging	Het
Amfr	T	A	8: 94,726,942 (GRCm39)	R90S	probably damaging	Het
Ankrd60	TGGCCACGCGG	TGG	2: 173,419,882 (GRCm39)		probably null	Het
Ano5	G	A	7: 51,216,066 (GRCm39)	D348N	possibly damaging	Het
Atp8a2	T	A	14: 60,258,242 (GRCm39)	D440V	probably damaging	Het
Bahcc1	A	G	11: 120,177,178 (GRCm39)	D2022G	probably damaging	Het
Bicd1	T	C	6: 149,385,498 (GRCm39)	F77S	probably benign	Het
Ccdc66	C	T	14: 27,220,448 (GRCm39)	R255H	probably benign	Het
Ckm	A	G	7: 19,153,372 (GRCm39)	D152G	probably benign	Het
Cpsf7	T	G	19: 10,518,082 (GRCm39)	S431A	possibly damaging	Het
Csmd1	T	C	8: 16,251,980 (GRCm39)	T959A	probably damaging	Het
Dkk4	T	C	8: 23,115,347 (GRCm39)	C66R	probably damaging	Het
Espl1	T	A	15: 102,232,465 (GRCm39)	W2058R	probably damaging	Het
Evi5l	A	T	8: 4,256,800 (GRCm39)		probably benign	Het
Fancg	A	T	4: 43,007,130 (GRCm39)		probably benign	Het
Flg2	A	T	3: 93,108,296 (GRCm39)	H108L	probably benign	Het
Gm10428	T	G	11: 62,644,107 (GRCm39)		probably benign	Het
Gm1988	T	A	7: 38,821,627 (GRCm39)		noncoding transcript	Het
Gm4787	G	C	12: 81,424,604 (GRCm39)	T518S	probably benign	Het
Gm7133	A	T	1: 97,171,201 (GRCm39)		noncoding transcript	Het
Grin2b	T	C	6: 135,717,962 (GRCm39)	N710S	probably benign	Het
Hcn2	T	C	10: 79,552,945 (GRCm39)	V148A	possibly damaging	Het
Hephl1	A	G	9: 14,995,579 (GRCm39)	L483S	possibly damaging	Het
Hinfp	C	T	9: 44,209,105 (GRCm39)	E338K	possibly damaging	Het
Hsd17b4	G	A	18: 50,306,776 (GRCm39)	D494N	probably damaging	Het
Ipo4	C	T	14: 55,866,277 (GRCm39)	V801M	probably benign	Het
Kcns2	A	C	15: 34,839,000 (GRCm39)	Y121S	probably benign	Het
Kif1c	T	A	11: 70,599,654 (GRCm39)	L462H	probably damaging	Het
Lrrk2	T	G	15: 91,648,851 (GRCm39)	V1615G	possibly damaging	Het
Naca	G	A	10: 127,876,011 (GRCm39)		probably benign	Het
Naip6	G	T	13: 100,436,724 (GRCm39)	Q600K	probably benign	Het
Ndufs2	A	G	1: 171,066,954 (GRCm39)	Y135H	probably damaging	Het
Nwd2	T	C	5: 63,965,114 (GRCm39)	V1566A	probably benign	Het
Or52d13	C	T	7: 103,110,086 (GRCm39)	V110I	possibly damaging	Het
Or52n4b	T	C	7: 108,144,551 (GRCm39)	I271T	probably damaging	Het
Or5t17	A	G	2: 86,832,645 (GRCm39)	T111A	probably benign	Het
Or6c75	A	G	10: 129,336,779 (GRCm39)	M1V	probably null	Het
Or6c75	A	T	10: 129,336,763 (GRCm39)	L3F	probably benign	Het
Pcid2	C	T	8: 13,150,320 (GRCm39)		probably null	Het
Pld4	A	C	12: 112,730,551 (GRCm39)	I145L	probably benign	Het
Pogk	A	T	1: 166,236,580 (GRCm39)		probably benign	Het
Rhbg	C	T	3: 88,152,874 (GRCm39)	V280I	probably benign	Het
Rnd2	C	T	11: 101,359,825 (GRCm39)	L57F	probably damaging	Het
Rxfp3	A	G	15: 11,036,250 (GRCm39)	F374S	possibly damaging	Het
Son	A	G	16: 91,456,940 (GRCm39)		probably benign	Het
Specc1l	G	T	10: 75,112,755 (GRCm39)	R994L	probably damaging	Het
Tas2r135	T	A	6: 42,382,531 (GRCm39)	D23E	probably damaging	Het
Teddm2	A	T	1: 153,726,810 (GRCm39)	H21Q	probably benign	Het
Tet1	T	C	10: 62,675,737 (GRCm39)	T780A	possibly damaging	Het
Thbs1	T	A	2: 117,952,989 (GRCm39)	D866E	probably damaging	Het
Tmed4	A	G	11: 6,221,743 (GRCm39)	W198R	probably damaging	Het
Ttn	A	T	2: 76,749,575 (GRCm39)	C3825S	probably benign	Het
Uchl1	T	A	5: 66,833,754 (GRCm39)		probably benign	Het
Wsb2	A	G	5: 117,515,483 (GRCm39)	T363A	possibly damaging	Het
Zfp266	A	G	9: 20,417,332 (GRCm39)	Y19H	probably damaging	Het
Zkscan17	A	G	11: 59,378,086 (GRCm39)	C366R	probably damaging	Het

Other mutations in Fzd2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01667:Fzd2	APN	11	102,496,608 (GRCm39)	missense	possibly damaging	0.94
IGL02034:Fzd2	APN	11	102,495,730 (GRCm39)	missense	probably damaging	1.00
IGL02035:Fzd2	APN	11	102,497,270 (GRCm39)	makesense	probably null
frowzy	UTSW	11	102,495,955 (GRCm39)	missense	probably damaging	1.00
PIT4585001:Fzd2	UTSW	11	102,496,573 (GRCm39)	missense	probably damaging	0.99
R0201:Fzd2	UTSW	11	102,496,948 (GRCm39)	missense	probably damaging	1.00
R1146:Fzd2	UTSW	11	102,496,206 (GRCm39)	missense	possibly damaging	0.76
R1146:Fzd2	UTSW	11	102,496,206 (GRCm39)	missense	possibly damaging	0.76
R1530:Fzd2	UTSW	11	102,496,134 (GRCm39)	missense	probably benign	0.00
R1589:Fzd2	UTSW	11	102,497,154 (GRCm39)	missense	probably benign	0.06
R1676:Fzd2	UTSW	11	102,496,707 (GRCm39)	missense	probably damaging	1.00
R2057:Fzd2	UTSW	11	102,496,759 (GRCm39)	missense	probably damaging	1.00
R2219:Fzd2	UTSW	11	102,496,249 (GRCm39)	missense	probably benign	0.01
R2410:Fzd2	UTSW	11	102,496,453 (GRCm39)	missense	possibly damaging	0.71
R5058:Fzd2	UTSW	11	102,495,633 (GRCm39)	missense	probably damaging	0.99
R5296:Fzd2	UTSW	11	102,496,981 (GRCm39)	missense	probably damaging	0.96
R5580:Fzd2	UTSW	11	102,496,665 (GRCm39)	missense	probably damaging	0.99
R6104:Fzd2	UTSW	11	102,497,161 (GRCm39)	missense	probably damaging	1.00
R6452:Fzd2	UTSW	11	102,495,811 (GRCm39)	missense	probably damaging	1.00
R7454:Fzd2	UTSW	11	102,495,955 (GRCm39)	missense	probably damaging	1.00
R7774:Fzd2	UTSW	11	102,496,314 (GRCm39)	missense	possibly damaging	0.88
R9129:Fzd2	UTSW	11	102,496,465 (GRCm39)	missense	probably benign	0.06
R9246:Fzd2	UTSW	11	102,496,749 (GRCm39)	missense	possibly damaging	0.94
R9631:Fzd2	UTSW	11	102,496,916 (GRCm39)	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- CTCATGAACAAGTTCGGCTTCC -3'
(R):5'- GCAATGTAGGCCACTGACAC -3'

Sequencing Primer
(F):5'- ACAAGTTCGGCTTCCAATGG -3'
(R):5'- ATGTAGGCCACTGACACCATGG -3'

Posted On

2016-12-15