Mutagenetix > Incidental Mutation

Incidental Mutation 'R3806:Fcrlb'

274575

Institutional Source

Beutler Lab

Gene Symbol

Fcrlb

Ensembl Gene

ENSMUSG00000070524

Gene Name

Fc receptor-like B

Synonyms

Fcry, FcRL2, FREB2, mFCRL2, FREB-2

MMRRC Submission

040763-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R3806 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

170734842-170740510 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 170735183 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 315 (T315A)

Ref Sequence

ENSEMBL: ENSMUSP00000091895 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000094337]

AlphaFold

Q5DRQ8

Predicted Effect

probably benign
Transcript: ENSMUST00000094337
AA Change: T315A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000091895
Gene: ENSMUSG00000070524
AA Change: T315A

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
IG_like	29	101	1.17e1	SMART
IG	109	191	9.34e-4	SMART
Blast:IG_like	209	281	2e-38	BLAST
low complexity region	290	306	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.5%
20x: 95.6%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] FCRL2 belongs to the Fc receptor family. Fc receptors are involved in phagocytosis, antibody-dependent cell cytotoxicity, immediate hypersensitivity, and transcytosis of immunoglobulins via their ability to bind immunoglobulin (Ig) constant regions (Chikaev et al., 2005 [PubMed 15676285]).[supplied by OMIM, Mar 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit an enhanced antibody response to a T-dependent antigen. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700012B07Rik	G	T	11: 109,684,980 (GRCm39)	C172*	probably null	Het
Akap9	A	G	5: 4,004,410 (GRCm39)	N108S	probably benign	Het
Ankmy1	A	G	1: 92,811,480 (GRCm39)	I636T	possibly damaging	Het
Bbs9	T	A	9: 22,798,926 (GRCm39)	D851E	probably damaging	Het
Bicd1	T	A	6: 149,420,489 (GRCm39)	L780M	probably damaging	Het
Ccdc175	T	C	12: 72,227,598 (GRCm39)	T62A	possibly damaging	Het
Cfhr4	T	A	1: 139,680,773 (GRCm39)	K248N	probably damaging	Het
Clcnka	T	C	4: 141,114,601 (GRCm39)	E615G	probably null	Het
Col1a2	G	A	6: 4,518,822 (GRCm39)		probably benign	Het
Cpxm2	C	T	7: 131,681,820 (GRCm39)	M236I	probably benign	Het
Dhrs2	A	T	14: 55,472,205 (GRCm39)	N32I	probably benign	Het
Fam131a	G	A	16: 20,514,608 (GRCm39)	V70M	probably benign	Het
Fat3	G	A	9: 15,909,567 (GRCm39)	S2145F	probably damaging	Het
Fbxl15	G	C	19: 46,317,891 (GRCm39)	R191P	possibly damaging	Het
Fer1l4	C	T	2: 155,887,603 (GRCm39)	G531D	probably damaging	Het
Gem	C	T	4: 11,705,965 (GRCm39)	Q18*	probably null	Het
Hemk1	T	A	9: 107,214,229 (GRCm39)	I68F	probably damaging	Het
Herc3	C	A	6: 58,893,835 (GRCm39)	H970Q	probably damaging	Het
Ighv5-17	C	A	12: 113,822,918 (GRCm39)	A68S	probably benign	Het
Ip6k3	T	C	17: 27,363,974 (GRCm39)	H358R	probably damaging	Het
Itpr2	T	C	6: 146,133,789 (GRCm39)		probably null	Het
Kmt2a	C	T	9: 44,731,653 (GRCm39)		probably benign	Het
Krt16	G	T	11: 100,139,566 (GRCm39)	R51S	unknown	Het
Lamtor1	G	A	7: 101,560,552 (GRCm39)	V156I	probably damaging	Het
Lingo4	A	G	3: 94,309,407 (GRCm39)	D115G	probably damaging	Het
Lrrc7	T	C	3: 157,891,130 (GRCm39)	I346V	probably benign	Het
Maco1	C	T	4: 134,557,891 (GRCm39)	M207I	probably benign	Het
Man1c1	A	T	4: 134,430,662 (GRCm39)	L40Q	probably damaging	Het
Mgat4c	A	G	10: 102,224,221 (GRCm39)	N145S	probably benign	Het
Morf4l1	A	G	9: 89,977,196 (GRCm39)	S203P	probably benign	Het
Muc5ac	T	C	7: 141,367,471 (GRCm39)	I2964T	possibly damaging	Het
Naip2	T	A	13: 100,289,142 (GRCm39)	Q1196L	possibly damaging	Het
Nbas	G	A	12: 13,532,505 (GRCm39)	G1738S	probably damaging	Het
Nlrp5	A	G	7: 23,104,271 (GRCm39)	E44G	probably benign	Het
Nolc1	CCAGCAGCAGCAGCAGCAGCAGCAGC	CCAGCAGCAGCAGCAGCAGCAGCAGCAGC	19: 46,069,791 (GRCm39)		probably benign	Het
Or4ac1-ps1	A	T	2: 88,370,700 (GRCm39)		noncoding transcript	Het
Or5d18	A	G	2: 87,864,911 (GRCm39)	S191P	possibly damaging	Het
Otof	T	A	5: 30,543,843 (GRCm39)		probably null	Het
Pcdha2	G	A	18: 37,072,582 (GRCm39)	R71H	probably benign	Het
Pcdha2	G	T	18: 37,074,744 (GRCm39)	E792*	probably null	Het
Pcnx1	A	G	12: 81,996,911 (GRCm39)	T936A	possibly damaging	Het
Pofut2	T	C	10: 77,096,640 (GRCm39)	Y122H	probably damaging	Het
Psg16	A	G	7: 16,824,609 (GRCm39)	E131G	probably benign	Het
Psmd12	T	G	11: 107,386,591 (GRCm39)	D387E	probably benign	Het
Rab6a	A	G	7: 100,257,431 (GRCm39)	M1V	probably null	Het
Ripk3	T	C	14: 56,023,725 (GRCm39)	R29G	probably benign	Het
Robo4	A	T	9: 37,315,734 (GRCm39)	D329V	possibly damaging	Het
Ruvbl2	A	G	7: 45,071,614 (GRCm39)	V423A	possibly damaging	Het
Rxylt1	A	T	10: 121,917,514 (GRCm39)	V333E	possibly damaging	Het
Scgb2b18	T	G	7: 32,872,563 (GRCm39)	M81L	probably benign	Het
Slc24a2	A	T	4: 87,146,021 (GRCm39)	L11H	possibly damaging	Het
Slc4a1	T	C	11: 102,248,019 (GRCm39)	E325G	probably benign	Het
Syt16	A	G	12: 74,276,172 (GRCm39)	E212G	possibly damaging	Het
Them6	A	G	15: 74,593,367 (GRCm39)	D75G	probably damaging	Het
Tnrc18	G	A	5: 142,773,029 (GRCm39)	A417V	unknown	Het
Vmn2r115	ATCTTCT	ATCT	17: 23,578,962 (GRCm39)		probably benign	Het
Zbtb22	C	T	17: 34,135,920 (GRCm39)		probably benign	Het
Zfp235	A	G	7: 23,840,046 (GRCm39)	D225G	probably benign	Het

Other mutations in Fcrlb

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00324:Fcrlb	APN	1	170,736,393 (GRCm39)	missense	possibly damaging	0.81
IGL02124:Fcrlb	APN	1	170,734,927 (GRCm39)	missense	probably benign	0.15
IGL02142:Fcrlb	APN	1	170,736,248 (GRCm39)	missense	probably damaging	1.00
IGL02385:Fcrlb	APN	1	170,735,168 (GRCm39)	missense	probably damaging	0.99
R0928:Fcrlb	UTSW	1	170,735,509 (GRCm39)	missense	possibly damaging	0.87
R1460:Fcrlb	UTSW	1	170,739,853 (GRCm39)	splice site	probably benign
R1735:Fcrlb	UTSW	1	170,734,901 (GRCm39)	missense	probably benign
R1806:Fcrlb	UTSW	1	170,735,096 (GRCm39)	missense	probably benign	0.01
R2078:Fcrlb	UTSW	1	170,735,650 (GRCm39)	missense	probably damaging	1.00
R4570:Fcrlb	UTSW	1	170,740,189 (GRCm39)	critical splice donor site	probably null
R5457:Fcrlb	UTSW	1	170,739,726 (GRCm39)	missense	probably damaging	0.99
R5854:Fcrlb	UTSW	1	170,735,530 (GRCm39)	missense	probably damaging	1.00
R6233:Fcrlb	UTSW	1	170,736,458 (GRCm39)	missense	probably damaging	1.00
R7502:Fcrlb	UTSW	1	170,736,210 (GRCm39)	missense	probably damaging	0.98
R7579:Fcrlb	UTSW	1	170,735,416 (GRCm39)	splice site	probably null
R7879:Fcrlb	UTSW	1	170,736,365 (GRCm39)	missense	probably damaging	1.00
R8287:Fcrlb	UTSW	1	170,739,653 (GRCm39)	missense	probably damaging	1.00
R8696:Fcrlb	UTSW	1	170,739,648 (GRCm39)	missense	probably damaging	1.00
R8957:Fcrlb	UTSW	1	170,735,536 (GRCm39)	missense	probably benign	0.28
R9036:Fcrlb	UTSW	1	170,734,938 (GRCm39)	missense	probably benign
R9629:Fcrlb	UTSW	1	170,739,735 (GRCm39)	missense	probably benign	0.13
R9706:Fcrlb	UTSW	1	170,735,474 (GRCm39)	missense	possibly damaging	0.86

Predicted Primers

PCR Primer
(F):5'- TTTGAGCAGCTGCATCTCGC -3'
(R):5'- CTCGAATCGTACTGGTGTGAGG -3'

Sequencing Primer
(F):5'- CGAAGCAGGAGGTCCACC -3'
(R):5'- TGAGTGGCAGCTCAGCATCAC -3'

Posted On

2015-04-02