Mutagenetix > Incidental Mutations

Incidental Mutation 'BB011:Fcrls'

642616

Institutional Source

Beutler Lab

Gene Symbol

Fcrls

Ensembl Gene

ENSMUSG00000015852

Gene Name

Fc receptor-like S, scavenger receptor

Synonyms

IFGP2, Msr2, Fcrh2, moFcRH2sc, 2810439C17Rik

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.053) question?

Stock #

BB011

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

87250758-87263738 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 87259533 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 51 (Y51C)

Ref Sequence

ENSEMBL: ENSMUSP00000088508 (fasta)

Gene Model

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

AlphaFold

Q9EQY5

Predicted Effect

probably damaging
Transcript: ENSMUST00000090986
AA Change: Y51C

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000088508
Gene: ENSMUSG00000015852
AA Change: Y51C

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 damaging
Transcript: ENSMUST00000146512
AA Change: Y51C

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000115780
Gene: ENSMUSG00000015852
AA Change: Y51C

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

0.3619

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

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
4930435E12Rik	G	A	16: 38,812,464	Q369*	probably null	Het
Acacb	A	G	5: 114,245,220	K2155E	possibly damaging	Het
Adgre5	G	A	8: 83,729,400	P256S	possibly damaging	Het
Adipor1	T	A	1: 134,425,993	V172D	probably damaging	Het
Ahsa1	T	C	12: 87,270,456		probably null	Het
Ankrd11	T	C	8: 122,895,902	I404V	possibly damaging	Het
Asxl3	G	A	18: 22,525,545	R2204Q	probably damaging	Het
Barhl2	A	G	5: 106,457,649	S65P	unknown	Het
Bbx	A	T	16: 50,224,308	L630H	probably damaging	Het
Cars	T	C	7: 143,569,871	T531A	possibly damaging	Het
Catsperb	T	A	12: 101,520,565	H450Q	probably benign	Het
Cdt1	T	C	8: 122,569,352	L135P	probably damaging	Het
Cfap206	T	A	4: 34,728,833	H24L	probably benign	Het
Cnga4	T	A	7: 105,407,821	V480E	probably benign	Het
Cnot1	ACG	A	8: 95,745,647		probably null	Het
Ctcfl	G	A	2: 173,113,656	T271I	possibly damaging	Het
Dlc1	T	C	8: 36,571,416	R1003G	probably benign	Het
Dnah7b	A	G	1: 46,219,430	D1927G	probably benign	Het
Dscc1	A	T	15: 55,082,176	D374E	probably benign	Het
Eci2	G	A	13: 34,993,070	Q69*	probably null	Het
Ep300	C	A	15: 81,649,502	P1920Q	unknown	Het
Epha5	A	G	5: 84,084,846	Y629H	possibly damaging	Het
Fam208b	A	T	13: 3,594,331	F129Y	possibly damaging	Het
Fat2	G	A	11: 55,262,787	T3533I	probably benign	Het
Fat3	T	C	9: 15,999,297	N1803S	probably damaging	Het
G530012D18Rik	C	G	1: 85,577,214	D113E	unknown	Het
Gcnt2	A	T	13: 40,918,564	K228*	probably null	Het
Gucy2c	A	T	6: 136,763,055	V258E	probably benign	Het
Hecw1	C	A	13: 14,322,528	L298F	probably damaging	Het
Hydin	T	G	8: 110,418,471	V818G	possibly damaging	Het
Hykk	A	G	9: 54,922,240	Y131C	probably damaging	Het
Ick	T	C	9: 78,155,464	L260P	probably damaging	Het
Mpo	A	G	11: 87,794,840	D48G	probably damaging	Het
Mrps10	T	C	17: 47,378,283	*202Q	probably null	Het
Mrps14	T	C	1: 160,196,989	V30A	probably benign	Het
Mtmr7	G	A	8: 40,606,884	A62V	possibly damaging	Het
Muc2	G	T	7: 141,695,388	G497W	probably damaging	Het
Nnt	A	T	13: 119,386,645	V237D	probably damaging	Het
Nox4	G	T	7: 87,374,381	V492L	probably benign	Het
Obscn	C	G	11: 59,112,555	E1306Q	probably benign	Het
Olfr303	A	G	7: 86,394,730	I256T	probably damaging	Het
Olfr993	T	C	2: 85,414,219	Y220C	probably benign	Het
Pard3	A	G	8: 127,410,750	N861S	probably benign	Het
Pdlim4	G	A	11: 54,055,222	R230*	probably null	Het
Pinlyp	C	T	7: 24,542,125	V159M	possibly damaging	Het
Plcb1	A	T	2: 135,359,693	T855S	probably benign	Het
Pot1a	T	A	6: 25,753,310	D409V	possibly damaging	Het
Prom1	T	C	5: 44,029,769	D382G	probably benign	Het
Prss16	A	T	13: 22,008,664	N83K	probably damaging	Het
Ptprn2	A	G	12: 116,841,264	D133G	probably benign	Het
Rasef	C	T	4: 73,740,929		probably null	Het
Rbak	A	G	5: 143,174,486	S271P	probably damaging	Het
Rbm20	A	T	19: 53,677,585	I60F	possibly damaging	Het
Rftn1	G	T	17: 50,047,380	A318D	probably damaging	Het
Rsf1	G	GACGGCCGCC	7: 97,579,909		probably benign	Het
Serpinb3c	A	G	1: 107,273,174	L171P	probably damaging	Het
Slc25a19	T	C	11: 115,615,550	Y211C	unknown	Het
Sorbs2	C	T	8: 45,795,470	S586L	probably damaging	Het
Spesp1	A	T	9: 62,273,451	S58R	probably benign	Het
Spryd3	A	G	15: 102,118,327	I329T	probably benign	Het
St8sia2	G	A	7: 73,966,952	L113F	probably damaging	Het
Star	T	C	8: 25,809,855	I75T	possibly damaging	Het
Tdrd6	T	A	17: 43,627,806	I784F	possibly damaging	Het
Tsc22d4	A	G	5: 137,768,011	I144V	unknown	Het
Tspan8	T	C	10: 115,833,324		probably null	Het
Ttll9	C	T	2: 152,962,487		probably benign	Het
Ubr4	T	G	4: 139,467,276	L1160R	unknown	Het
Ufd1	A	G	16: 18,823,285	Y162C	possibly damaging	Het
Unc13c	A	T	9: 73,734,408	F1268I	probably benign	Het
Uvssa	T	C	5: 33,410,951	I561T	probably damaging	Het
Vmn2r15	A	T	5: 109,286,388	S817T	probably damaging	Het
Ybx1	T	C	4: 119,282,279	E173G	probably damaging	Het
Zc3h6	T	C	2: 129,015,480	S640P	possibly damaging	Het

Other mutations in Fcrls

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01568:Fcrls	APN	3	87256679	missense	probably damaging	0.99
IGL01959:Fcrls	APN	3	87259632	missense	probably damaging	0.97
IGL02409:Fcrls	APN	3	87252723	missense	probably benign	0.00
IGL02677:Fcrls	APN	3	87259387	missense	probably benign	0.01
IGL02957:Fcrls	APN	3	87262194	missense	possibly damaging	0.59
IGL02974:Fcrls	APN	3	87257397	missense	possibly damaging	0.89
IGL02992:Fcrls	APN	3	87259466	missense	probably damaging	0.99
BB001:Fcrls	UTSW	3	87259533	missense	probably damaging	0.99
R0052:Fcrls	UTSW	3	87256778	missense	possibly damaging	0.94
R0052:Fcrls	UTSW	3	87256778	missense	possibly damaging	0.94
R0131:Fcrls	UTSW	3	87258959	missense	possibly damaging	0.90
R1171:Fcrls	UTSW	3	87256860	missense	probably benign	0.24
R1319:Fcrls	UTSW	3	87262177	critical splice donor site	probably null
R1522:Fcrls	UTSW	3	87256707	missense	possibly damaging	0.64
R1696:Fcrls	UTSW	3	87259518	missense	possibly damaging	0.95
R1742:Fcrls	UTSW	3	87259043	missense	possibly damaging	0.76
R2156:Fcrls	UTSW	3	87257341	missense	probably benign	0.43
R2255:Fcrls	UTSW	3	87257348	nonsense	probably null
R2257:Fcrls	UTSW	3	87259621	missense	probably damaging	0.99
R2434:Fcrls	UTSW	3	87256698	missense	probably damaging	1.00
R2680:Fcrls	UTSW	3	87257349	missense	probably damaging	0.99
R3552:Fcrls	UTSW	3	87259410	missense	possibly damaging	0.73
R4866:Fcrls	UTSW	3	87263466	missense	possibly damaging	0.65
R4883:Fcrls	UTSW	3	87259615	missense	possibly damaging	0.48
R5654:Fcrls	UTSW	3	87257544	missense	probably benign
R5771:Fcrls	UTSW	3	87263468	missense	probably damaging	0.98
R5917:Fcrls	UTSW	3	87256787	missense	probably damaging	0.99
R6349:Fcrls	UTSW	3	87252496	missense	probably damaging	0.99
R6562:Fcrls	UTSW	3	87257328	missense	probably benign
R6954:Fcrls	UTSW	3	87263676	critical splice donor site	probably benign
R7059:Fcrls	UTSW	3	87257340	missense	possibly damaging	0.82
R7188:Fcrls	UTSW	3	87259523	missense	probably benign	0.13
R7201:Fcrls	UTSW	3	87252627	missense	probably damaging	0.99
R7369:Fcrls	UTSW	3	87256701	missense	possibly damaging	0.59
R7431:Fcrls	UTSW	3	87258926	missense	probably damaging	0.99
R7610:Fcrls	UTSW	3	87252697	missense	probably damaging	1.00
R7924:Fcrls	UTSW	3	87259533	missense	probably damaging	0.99
R8018:Fcrls	UTSW	3	87259626	nonsense	probably null
R8280:Fcrls	UTSW	3	87259057	nonsense	probably null
R8981:Fcrls	UTSW	3	87257370	missense	probably damaging	1.00
R9368:Fcrls	UTSW	3	87257599	missense	possibly damaging	0.59

Predicted Primers

PCR Primer
(F):5'- CCTTGGACATTCAGCCACTTAG -3'
(R):5'- AGTTAACAAAGCTGGTAGGGCTC -3'

Sequencing Primer
(F):5'- GGACATTCAGCCACTTAGATCCTG -3'
(R):5'- ACACATGTAGAGGATCTGTCTCC -3'

Posted On

2020-08-01