Mutagenetix > Incidental Mutation

Incidental Mutation 'R6333:Fcgr4'

513216

Institutional Source

Beutler Lab

Gene Symbol

Fcgr4

Ensembl Gene

ENSMUSG00000059089

Gene Name

Fc receptor, IgG, low affinity IV

Synonyms

CD16-2, 4833442P21Rik, Fcgr3a, FcgammaRIV

MMRRC Submission

044487-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.055) question?

Stock #

R6333 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

170846495-170857330 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 170856838 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 235 (Y235C)

Ref Sequence

ENSEMBL: ENSMUSP00000077873 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078825]

AlphaFold

A0A0B4J1G0

Predicted Effect

probably damaging
Transcript: ENSMUST00000078825
AA Change: Y235C

PolyPhen 2 Score 0.967 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000077873
Gene: ENSMUSG00000059089
AA Change: Y235C

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
IG	31	104	5.79e-9	SMART
IG	112	188	1.44e-4	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000083971

Meta Mutation Damage Score

0.6329

Coding Region Coverage

1x: 100.0%
3x: 99.7%
10x: 97.9%
20x: 93.2%

Validation Efficiency

98% (50/51)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit decreased susceptibility to induced arthritis and nephrotoxic nephritis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4931406C07Rik	T	C	9: 15,203,372 (GRCm39)	K111R	probably benign	Het
Abhd18	A	G	3: 40,888,218 (GRCm39)	Y354C	probably benign	Het
Acap1	T	C	11: 69,774,427 (GRCm39)	I424V	possibly damaging	Het
AI182371	A	T	2: 34,975,281 (GRCm39)	I306K	probably damaging	Het
Asb4	G	A	6: 5,423,597 (GRCm39)	R248H	probably damaging	Het
Brd7	T	C	8: 89,071,819 (GRCm39)	T349A	probably damaging	Het
Bub1b	T	C	2: 118,428,944 (GRCm39)		probably null	Het
Cep85l	G	A	10: 53,225,197 (GRCm39)	Q131*	probably null	Het
Chmp2b	T	A	16: 65,337,136 (GRCm39)	M178L	possibly damaging	Het
Chrnb3	A	G	8: 27,883,355 (GRCm39)	N84D	probably damaging	Het
Clec4b2	A	T	6: 123,177,637 (GRCm39)		probably null	Het
Defa34	T	C	8: 22,155,862 (GRCm39)	V17A	probably benign	Het
Dnah3	A	T	7: 119,653,856 (GRCm39)	L947Q	probably damaging	Het
Dynlt2a1	G	A	17: 15,261,717 (GRCm39)		probably benign	Het
Ell	A	G	8: 71,044,188 (GRCm39)	Y578C	probably damaging	Het
Esp36	T	A	17: 38,728,135 (GRCm39)	M49L	probably benign	Het
Fbxw19	A	T	9: 109,323,751 (GRCm39)	W75R	probably benign	Het
Gm10110	A	C	14: 90,135,733 (GRCm39)		noncoding transcript	Het
Gm13030	A	T	4: 138,598,708 (GRCm39)		probably null	Het
Hdac9	T	C	12: 34,102,323 (GRCm39)	M1058V	probably damaging	Het
Hsd3b6	A	G	3: 98,713,540 (GRCm39)	F253S	probably damaging	Het
Hspg2	T	C	4: 137,289,266 (GRCm39)	Y3794H	probably damaging	Het
Mark4	G	A	7: 19,177,208 (GRCm39)	T207M	probably damaging	Het
Mme	A	G	3: 63,249,382 (GRCm39)	T304A	probably benign	Het
Neb	A	G	2: 52,148,275 (GRCm39)	L2657P	probably damaging	Het
Nufip1	A	C	14: 76,349,425 (GRCm39)	K152N	probably damaging	Het
Pcdh1	A	G	18: 38,331,860 (GRCm39)	V381A	probably benign	Het
Pdss1	A	G	2: 22,791,778 (GRCm39)	T30A	probably damaging	Het
Plrg1	A	G	3: 82,964,102 (GRCm39)	T12A	probably damaging	Het
Ppig	C	T	2: 69,579,902 (GRCm39)	H479Y	unknown	Het
Prokr2	A	G	2: 132,215,898 (GRCm39)	F188L	probably damaging	Het
Prss39	A	G	1: 34,539,150 (GRCm39)	N130S	probably benign	Het
Ptar1	G	A	19: 23,671,686 (GRCm39)	D30N	possibly damaging	Het
Rai14	G	T	15: 10,575,022 (GRCm39)	Y645*	probably null	Het
Rnasek	T	C	11: 70,129,252 (GRCm39)	Y67C	probably damaging	Het
Rnd2	C	T	11: 101,359,825 (GRCm39)	L57F	probably damaging	Het
Rnf213	T	C	11: 119,354,192 (GRCm39)	V4023A	probably damaging	Het
Sash3	C	T	X: 47,248,398 (GRCm39)	L307F	probably damaging	Homo
Sctr	T	C	1: 119,984,182 (GRCm39)	F357L	probably damaging	Het
Sec14l5	G	A	16: 4,984,908 (GRCm39)	V85I	probably benign	Het
Shld2	G	A	14: 33,989,565 (GRCm39)	T447M	probably damaging	Het
Sirpd	T	C	3: 15,385,671 (GRCm39)	Y77C	probably damaging	Het
Spag8	T	C	4: 43,653,186 (GRCm39)		probably benign	Het
Tbc1d2	T	C	4: 46,620,736 (GRCm39)	D358G	possibly damaging	Het
Tenm4	A	G	7: 96,423,331 (GRCm39)	T672A	probably damaging	Het
Tent2	G	A	13: 93,322,821 (GRCm39)	Q43*	probably null	Het
Trmt1l	T	A	1: 151,329,685 (GRCm39)	S543T	probably benign	Het
Ube4b	A	G	4: 149,432,494 (GRCm39)	F810S	probably damaging	Het
Vmn2r104	C	T	17: 20,249,848 (GRCm39)	V808I	probably benign	Het
Zfp3	T	A	11: 70,662,266 (GRCm39)	I75N	probably benign	Het
Zwint	A	G	10: 72,490,784 (GRCm39)		probably benign	Het

Other mutations in Fcgr4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01015:Fcgr4	APN	1	170,853,358 (GRCm39)	missense	possibly damaging	0.72
R0193:Fcgr4	UTSW	1	170,853,329 (GRCm39)	missense	possibly damaging	0.76
R0526:Fcgr4	UTSW	1	170,856,760 (GRCm39)	missense	probably damaging	0.98
R1164:Fcgr4	UTSW	1	170,856,739 (GRCm39)	missense	possibly damaging	0.75
R1544:Fcgr4	UTSW	1	170,847,523 (GRCm39)	missense	probably damaging	1.00
R1716:Fcgr4	UTSW	1	170,847,672 (GRCm39)	missense	probably damaging	1.00
R1905:Fcgr4	UTSW	1	170,856,874 (GRCm39)	missense	probably damaging	0.99
R6012:Fcgr4	UTSW	1	170,853,233 (GRCm39)	missense	possibly damaging	0.80
R6043:Fcgr4	UTSW	1	170,847,699 (GRCm39)	missense	probably damaging	1.00
R7034:Fcgr4	UTSW	1	170,847,657 (GRCm39)	missense	probably benign	0.00
R7036:Fcgr4	UTSW	1	170,847,657 (GRCm39)	missense	probably benign	0.00
R8123:Fcgr4	UTSW	1	170,847,572 (GRCm39)	missense	probably benign
R8791:Fcgr4	UTSW	1	170,847,477 (GRCm39)	missense	probably damaging	1.00
R9325:Fcgr4	UTSW	1	170,847,711 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACCCCTGCCTTAATGACAGC -3'
(R):5'- CCTGAGATAGTCCATTGGAGAG -3'

Sequencing Primer
(F):5'- GCCTTAATGACAGCCATCTTTC -3'
(R):5'- TAGTCCATTGGAGAGAGACAAAC -3'

Posted On

2018-04-27