Mutagenetix > Incidental Mutation

Incidental Mutation 'R5156:Fzd10'

396724

Institutional Source

Beutler Lab

Gene Symbol

Fzd10

Ensembl Gene

ENSMUSG00000081683

Gene Name

frizzled class receptor 10

Synonyms

Fz-10

MMRRC Submission

042738-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5156 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

128678170-128681157 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 128678366 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Serine at position 29 (R29S)

Ref Sequence

ENSEMBL: ENSMUSP00000114114 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000117102]

AlphaFold

Q8BKG4

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000091324

Predicted Effect

possibly damaging
Transcript: ENSMUST00000117102
AA Change: R29S

PolyPhen 2 Score 0.679 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000114114
Gene: ENSMUSG00000081683
AA Change: R29S

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
FRI	34	153	7.83e-68	SMART
Frizzled	218	542	2.62e-207	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126472

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000134673

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154305

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000199981

Meta Mutation Damage Score

0.1035

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 94.0%

Validation Efficiency

100% (52/52)

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 frizzled gene family. Members of this family encode 7-transmembrane domain proteins that are receptors for the Wingless type MMTV integration site family of signaling proteins. Most frizzled receptors are coupled to the beta-catenin canonical signaling pathway. Using array analysis, expression of this intronless gene is significantly up-regulated in two cases of primary colon cancer. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous 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: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921513D11Rik	G	T	17: 79,935,638 (GRCm39)		probably benign	Het
Apeh	C	T	9: 107,971,486 (GRCm39)	A29T	probably damaging	Het
Arap2	A	T	5: 62,826,524 (GRCm39)	Y1013*	probably null	Het
Arhgef4	A	G	1: 34,762,355 (GRCm39)	E537G	unknown	Het
Asf1b	T	C	8: 84,682,540 (GRCm39)	F28S	probably damaging	Het
Cd46	T	A	1: 194,767,693 (GRCm39)	I123L	possibly damaging	Het
Cdca7	A	T	2: 72,309,370 (GRCm39)	T48S	probably damaging	Het
Cfap53	T	A	18: 74,492,838 (GRCm39)		probably benign	Het
Clca3a2	T	A	3: 144,511,599 (GRCm39)	T599S	probably benign	Het
Csf1	T	A	3: 107,656,252 (GRCm39)	T148S	probably benign	Het
Dmbt1	T	C	7: 130,699,400 (GRCm39)		probably null	Het
Dmpk	A	G	7: 18,818,050 (GRCm39)	D44G	probably damaging	Het
Dnajb12	T	A	10: 59,728,782 (GRCm39)	N223K	probably damaging	Het
Dync1h1	T	A	12: 110,595,264 (GRCm39)	M1392K	probably benign	Het
Edrf1	C	T	7: 133,261,908 (GRCm39)	A867V	probably damaging	Het
Efemp2	T	A	19: 5,527,706 (GRCm39)	C94S	possibly damaging	Het
Epha8	C	T	4: 136,666,037 (GRCm39)	S373N	probably benign	Het
Foxk1	A	G	5: 142,434,588 (GRCm39)	D284G	possibly damaging	Het
Gm13991	T	C	2: 116,358,665 (GRCm39)		noncoding transcript	Het
Gm6818	A	T	7: 38,101,471 (GRCm39)		noncoding transcript	Het
Hydin	T	A	8: 111,336,333 (GRCm39)	C5037S	probably benign	Het
Ikzf1	T	A	11: 11,719,448 (GRCm39)	M492K	probably damaging	Het
Krt20	G	T	11: 99,320,879 (GRCm39)	S394R	possibly damaging	Het
Lrrc71	T	A	3: 87,653,094 (GRCm39)	R107S	probably benign	Het
Mia2	A	G	12: 59,219,323 (GRCm39)	T436A	possibly damaging	Het
Muc19	T	A	15: 91,784,614 (GRCm39)		noncoding transcript	Het
Neu4	T	C	1: 93,952,177 (GRCm39)	V182A	probably damaging	Het
Notch2	T	G	3: 98,031,626 (GRCm39)	F1167V	possibly damaging	Het
Nrap	A	G	19: 56,360,277 (GRCm39)	M189T	possibly damaging	Het
Nt5m	A	T	11: 59,765,487 (GRCm39)	I172F	probably damaging	Het
Or5b118	G	T	19: 13,449,037 (GRCm39)	K234N	probably damaging	Het
Or5w15	G	A	2: 87,568,119 (GRCm39)	P183L	possibly damaging	Het
Or8k41	A	T	2: 86,313,362 (GRCm39)	C241*	probably null	Het
Plekha5	C	T	6: 140,372,254 (GRCm39)	T68M	probably damaging	Het
Ppef2	A	G	5: 92,392,461 (GRCm39)		probably null	Het
Ppp1r37	T	C	7: 19,295,900 (GRCm39)		probably benign	Het
Rfx4	T	C	10: 84,704,218 (GRCm39)	Y238H	probably damaging	Het
Sanbr	A	G	11: 23,543,424 (GRCm39)		probably null	Het
Sec13	G	A	6: 113,707,837 (GRCm39)	A161V	probably benign	Het
Serhl	G	A	15: 82,986,895 (GRCm39)		probably benign	Het
Slco4a1	T	C	2: 180,114,572 (GRCm39)	V588A	probably benign	Het
Slitrk3	T	C	3: 72,956,592 (GRCm39)	T727A	probably benign	Het
Sp100	T	A	1: 85,601,404 (GRCm39)	D241E	probably damaging	Het
Spata2	G	T	2: 167,325,494 (GRCm39)	H442N	probably damaging	Het
Speg	T	C	1: 75,404,731 (GRCm39)	V2588A	probably damaging	Het
Tnfsf12	A	G	11: 69,578,155 (GRCm39)	S141P	probably damaging	Het
Trank1	A	G	9: 111,219,762 (GRCm39)	I2166M	probably damaging	Het
Trim10	T	A	17: 37,187,948 (GRCm39)	V388E	probably damaging	Het
Ttc23l	G	T	15: 10,551,636 (GRCm39)	T30K	possibly damaging	Het
Vmn2r10	A	G	5: 109,143,466 (GRCm39)	V828A	probably benign	Het
Vmn2r75	T	A	7: 85,813,436 (GRCm39)	L455F	possibly damaging	Het
Vwa8	T	A	14: 79,221,666 (GRCm39)	S541T	probably benign	Het

Other mutations in Fzd10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00155:Fzd10	APN	5	128,678,592 (GRCm39)	missense	probably damaging	1.00
IGL02354:Fzd10	APN	5	128,678,932 (GRCm39)	missense	possibly damaging	0.89
IGL02361:Fzd10	APN	5	128,678,932 (GRCm39)	missense	possibly damaging	0.89
IGL03088:Fzd10	APN	5	128,679,669 (GRCm39)	missense	possibly damaging	0.81
R0530:Fzd10	UTSW	5	128,679,077 (GRCm39)	missense	probably damaging	1.00
R0645:Fzd10	UTSW	5	128,679,662 (GRCm39)	missense	possibly damaging	0.94
R1515:Fzd10	UTSW	5	128,679,623 (GRCm39)	missense	probably damaging	1.00
R3930:Fzd10	UTSW	5	128,679,476 (GRCm39)	missense	probably damaging	1.00
R4467:Fzd10	UTSW	5	128,678,340 (GRCm39)	missense	probably benign	0.01
R4976:Fzd10	UTSW	5	128,679,178 (GRCm39)	nonsense	probably null
R5202:Fzd10	UTSW	5	128,679,180 (GRCm39)	missense	possibly damaging	0.78
R5874:Fzd10	UTSW	5	128,678,364 (GRCm39)	missense	probably benign	0.41
R6238:Fzd10	UTSW	5	128,679,995 (GRCm39)	missense	probably damaging	0.99
R6921:Fzd10	UTSW	5	128,678,646 (GRCm39)	missense	probably damaging	0.99
R7684:Fzd10	UTSW	5	128,678,480 (GRCm39)	missense	possibly damaging	0.73
R8093:Fzd10	UTSW	5	128,679,303 (GRCm39)	missense	probably benign	0.14
R9011:Fzd10	UTSW	5	128,679,369 (GRCm39)	missense	probably damaging	1.00
R9013:Fzd10	UTSW	5	128,679,369 (GRCm39)	missense	probably damaging	1.00
R9014:Fzd10	UTSW	5	128,679,369 (GRCm39)	missense	probably damaging	1.00
R9332:Fzd10	UTSW	5	128,678,316 (GRCm39)	missense	possibly damaging	0.92
R9603:Fzd10	UTSW	5	128,678,771 (GRCm39)	missense	probably benign	0.00
Z1088:Fzd10	UTSW	5	128,678,310 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- CCGTATTGTTTGCAAACTTCGC -3'
(R):5'- ATGATCGGCGAGCACTTGAG -3'

Sequencing Primer
(F):5'- CAGACTGGATGGGCATGC -3'
(R):5'- ACATGACCCGGCAAGCAGG -3'

Posted On

2016-06-21