Mutagenetix > Incidental Mutation

Incidental Mutation 'R4866:Fcrl2'

374895

Institutional Source

Beutler Lab

Gene Symbol

Fcrl2

Ensembl Gene

ENSMUSG00000015852

Gene Name

Fc receptor like 2

Synonyms

Fcrls, IFGP2, 2810439C17Rik, Msr2, Fcrh2, moFcRH2sc

MMRRC Submission

042476-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.063) question?

Stock #

R4866 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

87158318-87171046 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 87170773 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 4 (C4S)

Ref Sequence

ENSEMBL: ENSMUSP00000088508 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000090986] [ENSMUST00000146512]

AlphaFold

Q9EQY5

Predicted Effect

possibly damaging
Transcript: ENSMUST00000090986
AA Change: C4S

PolyPhen 2 Score 0.655 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000088508
Gene: ENSMUSG00000015852
AA Change: C4S

Domain	Start	End	E-Value	Type
IG	23	106	1.32e-3	SMART
IGc2	122	186	2.77e-6	SMART
IGc2	226	291	1.09e-4	SMART
IG	315	396	1e-3	SMART
SR	402	503	7.29e-36	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000146512
AA Change: C4S

PolyPhen 2 Score 0.258 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000115780
Gene: ENSMUSG00000015852
AA Change: C4S

Domain	Start	End	E-Value	Type
IG	23	106	1.32e-3	SMART
Pfam:Ig_2	111	176	6.1e-6	PFAM
Pfam:Ig_3	111	176	1.4e-4	PFAM

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.9%
20x: 94.0%

Validation Efficiency

99% (79/80)

MGI Phenotype

PHENOTYPE: Female homozygous mutant mice are larger than controls and show increased mean body weight, total tissue mass, lean body mass and total body fat. Homozygous mutant mice eshow a decreased mean percentage of CD8 cells in the peripheral blood. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca3	C	T	17: 24,593,274 (GRCm39)	R224C	probably damaging	Het
Abcc5	A	T	16: 20,241,182 (GRCm39)	M1K	probably null	Het
Ablim2	C	T	5: 35,959,766 (GRCm39)	R73C	possibly damaging	Het
Adam5	A	C	8: 25,232,172 (GRCm39)		probably null	Het
Adam5	G	A	8: 25,271,619 (GRCm39)	T596I	probably damaging	Het
Apoa2	T	C	1: 171,053,369 (GRCm39)		probably null	Het
Atad1	A	T	19: 32,679,964 (GRCm39)	H79Q	probably benign	Het
Atp8a2	T	C	14: 59,928,916 (GRCm39)	D1046G	probably damaging	Het
Bcam	A	G	7: 19,499,397 (GRCm39)	Y209H	probably benign	Het
Brpf1	G	A	6: 113,299,431 (GRCm39)	V1120I	probably damaging	Het
Catsperb	G	A	12: 101,474,208 (GRCm39)	C302Y	probably damaging	Het
Cbl	A	G	9: 44,064,166 (GRCm39)	V790A	probably benign	Het
Ccdc60	T	C	5: 116,310,549 (GRCm39)	D171G	probably damaging	Het
Cd300c2	A	T	11: 114,891,807 (GRCm39)	C22*	probably null	Het
Cdan1	C	A	2: 120,561,928 (GRCm39)		probably benign	Het
Cdk5rap1	C	T	2: 154,212,876 (GRCm39)		probably null	Het
Cfap410	T	A	10: 77,817,413 (GRCm39)		probably null	Het
Cfap65	T	C	1: 74,964,716 (GRCm39)	D479G	probably damaging	Het
Cmbl	A	G	15: 31,585,490 (GRCm39)	K113E	probably benign	Het
Cog6	G	A	3: 52,918,019 (GRCm39)	T173I	probably benign	Het
Cts6	T	A	13: 61,350,090 (GRCm39)		probably null	Het
Cyp11a1	G	A	9: 57,933,380 (GRCm39)	V413M	probably damaging	Het
Cyp2c39	G	A	19: 39,502,020 (GRCm39)	M136I	probably benign	Het
Dclre1b	A	T	3: 103,715,412 (GRCm39)	Y29N	probably damaging	Het
Depdc1a	T	A	3: 159,221,764 (GRCm39)	I236K	probably damaging	Het
Dhx36	A	T	3: 62,380,198 (GRCm39)	Y833N	probably damaging	Het
Dop1b	G	T	16: 93,560,318 (GRCm39)		probably null	Het
Elovl3	A	G	19: 46,120,603 (GRCm39)	E32G	possibly damaging	Het
Entrep1	A	G	19: 23,952,790 (GRCm39)	S507P	possibly damaging	Het
Epcam	T	C	17: 87,951,049 (GRCm39)	V212A	possibly damaging	Het
Galnt16	T	C	12: 80,630,851 (GRCm39)	Y310H	probably damaging	Het
Gm12789	G	A	4: 101,846,182 (GRCm39)		probably benign	Het
Gspt1	C	T	16: 11,040,529 (GRCm39)	R593H	possibly damaging	Het
Hmcn2	A	T	2: 31,279,403 (GRCm39)	T1802S	possibly damaging	Het
Igha	A	G	12: 113,223,129 (GRCm39)	V166A	probably benign	Het
Itfg2	A	G	6: 128,393,279 (GRCm39)		probably benign	Het
Jund	T	C	8: 71,152,254 (GRCm39)	V183A	probably damaging	Het
Katnb1	T	C	8: 95,824,132 (GRCm39)	S471P	possibly damaging	Het
Kazn	A	G	4: 141,832,216 (GRCm39)	F661S	unknown	Het
Kif19a	G	A	11: 114,658,053 (GRCm39)	M37I	probably benign	Het
Lgr5	C	T	10: 115,288,590 (GRCm39)	V661I	probably benign	Het
Lvrn	G	T	18: 47,026,768 (GRCm39)	A789S	probably damaging	Het
Mapk10	T	C	5: 103,111,391 (GRCm39)	D351G	probably damaging	Het
Mga	T	A	2: 119,794,535 (GRCm39)	C2622S	possibly damaging	Het
Mios	T	G	6: 8,214,857 (GRCm39)	F18V	probably damaging	Het
Mllt6	A	G	11: 97,565,285 (GRCm39)	D575G	probably damaging	Het
Mmp10	G	A	9: 7,508,190 (GRCm39)	V439M	probably damaging	Het
Myh4	A	G	11: 67,139,453 (GRCm39)	D590G	probably benign	Het
Ndufs2	C	T	1: 171,074,618 (GRCm39)	G14R	probably benign	Het
Or10ad1b	T	A	15: 98,125,371 (GRCm39)	I52F	probably damaging	Het
Or51a7	A	T	7: 102,614,927 (GRCm39)	M207L	probably benign	Het
Or56a4	T	C	7: 104,806,514 (GRCm39)	Y125C	possibly damaging	Het
Or8g26	A	G	9: 39,096,367 (GRCm39)	K298E	probably damaging	Het
Plau	G	T	14: 20,887,872 (GRCm39)	V39L	probably benign	Het
Ppp3cb	A	G	14: 20,573,911 (GRCm39)	C275R	probably damaging	Het
Ppp4r4	T	G	12: 103,566,706 (GRCm39)	M51R	possibly damaging	Het
Prr5	A	G	15: 84,626,105 (GRCm39)	Y60C	probably damaging	Het
Ptprt	T	C	2: 161,402,159 (GRCm39)	D1023G	probably damaging	Het
Raly	T	A	2: 154,703,816 (GRCm39)	V129E	probably damaging	Het
Rsph10b	A	G	5: 143,885,347 (GRCm39)	E249G	probably benign	Het
Sart1	A	C	19: 5,432,248 (GRCm39)	L577W	probably damaging	Het
Senp1	T	C	15: 97,964,729 (GRCm39)	E189G	possibly damaging	Het
Slc22a2	G	T	17: 12,803,316 (GRCm39)	C50F	probably damaging	Het
Spem1	A	T	11: 69,711,755 (GRCm39)	V303E	probably damaging	Het
Tgfb3	A	G	12: 86,124,588 (GRCm39)	V40A	possibly damaging	Het
Ttl	T	C	2: 128,923,147 (GRCm39)	S163P	probably damaging	Het
Ttll9	C	A	2: 152,844,920 (GRCm39)	N429K	probably benign	Het
Uggt1	G	A	1: 36,241,936 (GRCm39)	R333*	probably null	Het
Zfhx2	A	G	14: 55,302,993 (GRCm39)	S1664P	possibly damaging	Het
Zfp51	T	A	17: 21,682,012 (GRCm39)	D70E	possibly damaging	Het
Zfp592	T	A	7: 80,691,607 (GRCm39)	V1262E	probably damaging	Het
Zfp595	C	A	13: 67,465,760 (GRCm39)	G168C	probably damaging	Het
Zswim9	A	T	7: 12,995,095 (GRCm39)	S354T	probably damaging	Het

Other mutations in Fcrl2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01568:Fcrl2	APN	3	87,163,986 (GRCm39)	missense	probably damaging	0.99
IGL01959:Fcrl2	APN	3	87,166,939 (GRCm39)	missense	probably damaging	0.97
IGL02409:Fcrl2	APN	3	87,160,030 (GRCm39)	missense	probably benign	0.00
IGL02677:Fcrl2	APN	3	87,166,694 (GRCm39)	missense	probably benign	0.01
IGL02957:Fcrl2	APN	3	87,169,501 (GRCm39)	missense	possibly damaging	0.59
IGL02974:Fcrl2	APN	3	87,164,704 (GRCm39)	missense	possibly damaging	0.89
IGL02992:Fcrl2	APN	3	87,166,773 (GRCm39)	missense	probably damaging	0.99
BB001:Fcrl2	UTSW	3	87,166,840 (GRCm39)	missense	probably damaging	0.99
BB011:Fcrl2	UTSW	3	87,166,840 (GRCm39)	missense	probably damaging	0.99
R0052:Fcrl2	UTSW	3	87,164,085 (GRCm39)	missense	possibly damaging	0.94
R0052:Fcrl2	UTSW	3	87,164,085 (GRCm39)	missense	possibly damaging	0.94
R0131:Fcrl2	UTSW	3	87,166,266 (GRCm39)	missense	possibly damaging	0.90
R1171:Fcrl2	UTSW	3	87,164,167 (GRCm39)	missense	probably benign	0.24
R1319:Fcrl2	UTSW	3	87,169,484 (GRCm39)	critical splice donor site	probably null
R1522:Fcrl2	UTSW	3	87,164,014 (GRCm39)	missense	possibly damaging	0.64
R1696:Fcrl2	UTSW	3	87,166,825 (GRCm39)	missense	possibly damaging	0.95
R1742:Fcrl2	UTSW	3	87,166,350 (GRCm39)	missense	possibly damaging	0.76
R2156:Fcrl2	UTSW	3	87,164,648 (GRCm39)	missense	probably benign	0.43
R2255:Fcrl2	UTSW	3	87,164,655 (GRCm39)	nonsense	probably null
R2257:Fcrl2	UTSW	3	87,166,928 (GRCm39)	missense	probably damaging	0.99
R2434:Fcrl2	UTSW	3	87,164,005 (GRCm39)	missense	probably damaging	1.00
R2680:Fcrl2	UTSW	3	87,164,656 (GRCm39)	missense	probably damaging	0.99
R3552:Fcrl2	UTSW	3	87,166,717 (GRCm39)	missense	possibly damaging	0.73
R4883:Fcrl2	UTSW	3	87,166,922 (GRCm39)	missense	possibly damaging	0.48
R5654:Fcrl2	UTSW	3	87,164,851 (GRCm39)	missense	probably benign
R5771:Fcrl2	UTSW	3	87,170,775 (GRCm39)	missense	probably damaging	0.98
R5917:Fcrl2	UTSW	3	87,164,094 (GRCm39)	missense	probably damaging	0.99
R6349:Fcrl2	UTSW	3	87,159,803 (GRCm39)	missense	probably damaging	0.99
R6562:Fcrl2	UTSW	3	87,164,635 (GRCm39)	missense	probably benign
R6954:Fcrl2	UTSW	3	87,170,983 (GRCm39)	critical splice donor site	probably benign
R7059:Fcrl2	UTSW	3	87,164,647 (GRCm39)	missense	possibly damaging	0.82
R7188:Fcrl2	UTSW	3	87,166,830 (GRCm39)	missense	probably benign	0.13
R7201:Fcrl2	UTSW	3	87,159,934 (GRCm39)	missense	probably damaging	0.99
R7369:Fcrl2	UTSW	3	87,164,008 (GRCm39)	missense	possibly damaging	0.59
R7431:Fcrl2	UTSW	3	87,166,233 (GRCm39)	missense	probably damaging	0.99
R7610:Fcrl2	UTSW	3	87,160,004 (GRCm39)	missense	probably damaging	1.00
R7924:Fcrl2	UTSW	3	87,166,840 (GRCm39)	missense	probably damaging	0.99
R8018:Fcrl2	UTSW	3	87,166,933 (GRCm39)	nonsense	probably null
R8280:Fcrl2	UTSW	3	87,166,364 (GRCm39)	nonsense	probably null
R8981:Fcrl2	UTSW	3	87,164,677 (GRCm39)	missense	probably damaging	1.00
R9368:Fcrl2	UTSW	3	87,164,906 (GRCm39)	missense	possibly damaging	0.59
R9477:Fcrl2	UTSW	3	87,159,803 (GRCm39)	missense	probably damaging	0.98
R9522:Fcrl2	UTSW	3	87,164,101 (GRCm39)	missense	possibly damaging	0.95

Predicted Primers

PCR Primer
(F):5'- GAGACAAATCACCAGCCTTTAG -3'
(R):5'- CTTTTGCAGCACCCATTGG -3'

Sequencing Primer
(F):5'- AGAGCCTTTTCCTTTTCTTGGGAAC -3'
(R):5'- CCATTGGGTTGGGGTATGGAC -3'

Posted On

2016-03-17