Mutagenetix > Incidental Mutation

Incidental Mutation 'R0458:Fzd6'

41334

Institutional Source

Beutler Lab

Gene Symbol

Fzd6

Ensembl Gene

ENSMUSG00000022297

Gene Name

frizzled class receptor 6

Synonyms

rst, Fz6

MMRRC Submission

038658-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0458 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

38869673-38901587 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 38894676 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Threonine at position 281 (A281T)

Ref Sequence

ENSEMBL: ENSMUSP00000136328 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000022906] [ENSMUST00000179165]

AlphaFold

Q61089

Predicted Effect

probably damaging
Transcript: ENSMUST00000022906
AA Change: A281T

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000022906
Gene: ENSMUSG00000022297
AA Change: A281T

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
FRI	23	134	9.66e-59	SMART
Frizzled	188	513	4.88e-184	SMART
low complexity region	532	543	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000179165
AA Change: A281T

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000136328
Gene: ENSMUSG00000022297
AA Change: A281T

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
FRI	23	134	9.66e-59	SMART
Frizzled	188	513	4.88e-184	SMART
low complexity region	532	543	N/A	INTRINSIC

Meta Mutation Damage Score

0.1446

Coding Region Coverage

1x: 99.7%
3x: 98.9%
10x: 97.0%
20x: 94.3%

Validation Efficiency

100% (79/79)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene represents a member of the 'frizzled' gene family, which encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The protein encoded by this family member contains a signal peptide, a cysteine-rich domain in the N-terminal extracellular region, and seven transmembrane domains, but unlike other family members, this protein does not contain a C-terminal PDZ domain-binding motif. This protein functions as a negative regulator of the canonical Wnt/beta-catenin signaling cascade, thereby inhibiting the processes that trigger oncogenic transformation, cell proliferation, and inhibition of apoptosis. Alternative splicing results in multiple transcript variants, some of which do not encode a protein with a predicted signal peptide.[provided by RefSeq, Aug 2011]
PHENOTYPE: Homozygous mice for one mutation display abnormal hair follicle orientation. Another mutation of this gene does not appear to result in a phenotype. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933407L21Rik	A	G	1: 85,856,747 (GRCm39)	E8G	unknown	Het
9130008F23Rik	T	C	17: 41,191,127 (GRCm39)	T101A	probably benign	Het
Abcb8	C	T	5: 24,611,231 (GRCm39)	T455I	probably benign	Het
Abcb9	C	A	5: 124,220,209 (GRCm39)		probably null	Het
Akp3	T	G	1: 87,054,259 (GRCm39)	Y265*	probably null	Het
Atp6v1b1	A	T	6: 83,729,390 (GRCm39)	D109V	probably damaging	Het
Aurka	C	A	2: 172,212,366 (GRCm39)	E4*	probably null	Het
Cacna1g	T	A	11: 94,300,266 (GRCm39)	Q2168L	probably damaging	Het
Cdc45	T	A	16: 18,600,722 (GRCm39)		probably benign	Het
Cfap61	T	C	2: 145,850,837 (GRCm39)	V325A	probably benign	Het
Clasp2	T	A	9: 113,735,292 (GRCm39)		probably null	Het
Crim1	T	A	17: 78,620,655 (GRCm39)	I365N	probably damaging	Het
Dcaf8	A	G	1: 172,001,610 (GRCm39)	N269S	probably benign	Het
Dnaaf5	T	C	5: 139,147,633 (GRCm39)	V399A	possibly damaging	Het
Ear2	A	G	14: 44,340,705 (GRCm39)	Y121C	probably damaging	Het
Eef2k	T	C	7: 120,502,513 (GRCm39)	Y692H	probably damaging	Het
Elavl2	A	T	4: 91,197,104 (GRCm39)		probably benign	Het
Epn2	C	A	11: 61,437,281 (GRCm39)	R97L	possibly damaging	Het
Fam243	T	C	16: 92,117,995 (GRCm39)	I98V	probably benign	Het
Garem2	T	A	5: 30,319,180 (GRCm39)	I214N	probably damaging	Het
Glg1	A	G	8: 111,887,238 (GRCm39)		probably benign	Het
Golm1	T	C	13: 59,812,178 (GRCm39)	E48G	probably damaging	Het
Gpaa1	G	T	15: 76,216,233 (GRCm39)	R12L	probably benign	Het
Gstm1	T	A	3: 107,924,679 (GRCm39)	T34S	probably benign	Het
Gtf3c1	G	A	7: 125,243,306 (GRCm39)	P1766L	possibly damaging	Het
Herc1	A	T	9: 66,383,663 (GRCm39)	Q3709L	probably benign	Het
Hoxa13	CCG	CCGCG	6: 52,237,618 (GRCm39)		probably null	Het
Icam1	A	G	9: 20,939,157 (GRCm39)		probably null	Het
Itga9	T	C	9: 118,510,096 (GRCm39)		probably null	Het
Kif15	T	C	9: 122,838,424 (GRCm39)	F1121L	probably benign	Het
Klhl30	T	A	1: 91,288,718 (GRCm39)		probably benign	Het
Ldlrad1	T	C	4: 107,073,387 (GRCm39)	C141R	probably damaging	Het
Lemd2	T	C	17: 27,409,627 (GRCm39)	D508G	probably damaging	Het
Lilra5	A	C	7: 4,241,218 (GRCm39)	T52P	probably benign	Het
Lrtm2	G	A	6: 119,294,229 (GRCm39)	P301S	probably damaging	Het
Mcoln2	A	G	3: 145,855,768 (GRCm39)		probably benign	Het
Mkrn2os	A	G	6: 115,563,631 (GRCm39)	S135P	probably damaging	Het
Mlxipl	T	C	5: 135,162,224 (GRCm39)	V607A	probably benign	Het
Mmadhc	T	C	2: 50,171,173 (GRCm39)	Y213C	probably benign	Het
Mpo	C	A	11: 87,687,123 (GRCm39)	A223E	probably benign	Het
Mthfd2l	C	G	5: 91,168,036 (GRCm39)	I310M	probably damaging	Het
Muc5b	C	A	7: 141,418,709 (GRCm39)	A3885D	probably benign	Het
Mvp	A	G	7: 126,597,663 (GRCm39)	W152R	probably damaging	Het
Nmur2	A	T	11: 55,931,394 (GRCm39)	F106I	possibly damaging	Het
Nr3c2	T	A	8: 77,636,167 (GRCm39)	F423I	probably damaging	Het
Or1l8	A	G	2: 36,817,349 (GRCm39)	V259A	probably damaging	Het
Or5m5	A	G	2: 85,814,600 (GRCm39)	S139G	probably benign	Het
Or8c16	G	A	9: 38,130,344 (GRCm39)	C75Y	probably damaging	Het
Or9q1	G	T	19: 13,805,593 (GRCm39)	H56N	probably benign	Het
Pappa	A	G	4: 65,074,119 (GRCm39)	I224M	probably damaging	Het
Prex1	A	C	2: 166,427,743 (GRCm39)	S800A	probably damaging	Het
Prkaca	T	C	8: 84,721,911 (GRCm39)		probably benign	Het
Ptpru	A	T	4: 131,526,986 (GRCm39)	V662E	possibly damaging	Het
Rabep1	T	A	11: 70,777,824 (GRCm39)		probably null	Het
Rbms2	C	T	10: 127,987,058 (GRCm39)	C50Y	probably damaging	Het
Rd3	C	T	1: 191,709,414 (GRCm39)	P25S	probably damaging	Het
Rnf148	T	G	6: 23,654,256 (GRCm39)	I247L	probably benign	Het
Sf3b3	A	G	8: 111,538,768 (GRCm39)		probably benign	Het
Slc35c1	A	T	2: 92,284,858 (GRCm39)	F252Y	probably damaging	Het
Slc38a11	T	C	2: 65,193,813 (GRCm39)		probably null	Het
Snx6	G	T	12: 54,814,921 (GRCm39)	Y17*	probably null	Het
Sox6	C	A	7: 115,089,029 (GRCm39)	R611L	probably damaging	Het
Spata13	G	A	14: 60,929,492 (GRCm39)	R350H	probably damaging	Het
Sppl2a	G	T	2: 126,746,879 (GRCm39)	A483D	probably damaging	Het
Stat1	C	T	1: 52,188,211 (GRCm39)		probably benign	Het
Tab2	A	T	10: 7,795,319 (GRCm39)	Y314N	probably damaging	Het
Tor1aip1	T	C	1: 155,906,153 (GRCm39)	N213S	probably damaging	Het
Trim39	T	C	17: 36,572,404 (GRCm39)	K300E	probably damaging	Het
Tubal3	T	C	13: 3,983,137 (GRCm39)	S306P	probably damaging	Het
Ufm1	A	G	3: 53,768,655 (GRCm39)	L33P	probably damaging	Het
Washc4	G	A	10: 83,382,663 (GRCm39)	V26I	possibly damaging	Het
Wfs1	A	G	5: 37,126,013 (GRCm39)	Y293H	probably damaging	Het
Zbtb41	T	C	1: 139,351,214 (GRCm39)	V109A	probably damaging	Het
Zfp667	T	C	7: 6,307,844 (GRCm39)	S171P	probably benign	Het
Zkscan5	T	A	5: 145,142,281 (GRCm39)	H59Q	probably damaging	Het
Zswim8	C	T	14: 20,768,965 (GRCm39)	R1128W	probably damaging	Het

Other mutations in Fzd6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02470:Fzd6	APN	15	38,899,952 (GRCm39)	utr 3 prime	probably benign
IGL02500:Fzd6	APN	15	38,894,781 (GRCm39)	missense	probably damaging	1.00
IGL02938:Fzd6	APN	15	38,897,285 (GRCm39)	missense	probably benign	0.03
IGL03219:Fzd6	APN	15	38,894,971 (GRCm39)	missense	probably damaging	1.00
R0314:Fzd6	UTSW	15	38,889,128 (GRCm39)	missense	possibly damaging	0.88
R0478:Fzd6	UTSW	15	38,897,429 (GRCm39)	splice site	probably null
R0961:Fzd6	UTSW	15	38,889,073 (GRCm39)	missense	probably damaging	1.00
R1473:Fzd6	UTSW	15	38,894,358 (GRCm39)	missense	probably damaging	1.00
R1479:Fzd6	UTSW	15	38,894,394 (GRCm39)	missense	probably damaging	1.00
R1533:Fzd6	UTSW	15	38,895,019 (GRCm39)	missense	probably damaging	1.00
R1731:Fzd6	UTSW	15	38,894,722 (GRCm39)	missense	probably damaging	1.00
R1836:Fzd6	UTSW	15	38,897,315 (GRCm39)	missense	probably damaging	1.00
R2241:Fzd6	UTSW	15	38,894,931 (GRCm39)	missense	probably damaging	0.96
R5089:Fzd6	UTSW	15	38,870,875 (GRCm39)	missense	probably damaging	1.00
R5526:Fzd6	UTSW	15	38,894,559 (GRCm39)	missense	possibly damaging	0.89
R5666:Fzd6	UTSW	15	38,894,510 (GRCm39)	missense	probably benign	0.32
R5670:Fzd6	UTSW	15	38,894,510 (GRCm39)	missense	probably benign	0.32
R5903:Fzd6	UTSW	15	38,870,783 (GRCm39)	start codon destroyed	probably null	0.99
R6221:Fzd6	UTSW	15	38,894,239 (GRCm39)	missense	probably benign	0.00
R6944:Fzd6	UTSW	15	38,889,212 (GRCm39)	missense	possibly damaging	0.69
R7731:Fzd6	UTSW	15	38,897,327 (GRCm39)	missense	probably damaging	1.00
R7922:Fzd6	UTSW	15	38,894,503 (GRCm39)	missense	probably damaging	1.00
R8195:Fzd6	UTSW	15	38,894,959 (GRCm39)	missense	probably damaging	1.00
R8985:Fzd6	UTSW	15	38,895,019 (GRCm39)	missense	probably damaging	1.00
R9196:Fzd6	UTSW	15	38,895,103 (GRCm39)	missense	probably damaging	1.00
R9196:Fzd6	UTSW	15	38,895,102 (GRCm39)	missense	probably damaging	1.00
R9212:Fzd6	UTSW	15	38,898,289 (GRCm39)	missense	probably damaging	0.97
R9276:Fzd6	UTSW	15	38,870,962 (GRCm39)	splice site	probably benign
R9350:Fzd6	UTSW	15	38,895,043 (GRCm39)	missense	probably damaging	1.00
R9384:Fzd6	UTSW	15	38,895,103 (GRCm39)	missense	probably damaging	1.00
R9384:Fzd6	UTSW	15	38,895,102 (GRCm39)	missense	probably damaging	1.00
R9650:Fzd6	UTSW	15	38,894,941 (GRCm39)	missense	probably damaging	1.00
Z1177:Fzd6	UTSW	15	38,894,736 (GRCm39)	missense	probably damaging	1.00
Z1177:Fzd6	UTSW	15	38,870,956 (GRCm39)	missense	possibly damaging	0.72

Predicted Primers

PCR Primer
(F):5'- AATTGAACAGTGTGCCCCTCCG -3'
(R):5'- CAAACGCCGCTAATGTTGTCTCC -3'

Sequencing Primer
(F):5'- AAAGTGATGAACTAGACTTTGCC -3'
(R):5'- CTTATTCATAGCGAGCAGCATGAC -3'

Posted On

2013-05-23