Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02957:Fcrls'

365184

Institutional Source

Australian Phenomics Network (link to record)

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: 0.065) question?

Stock #

IGL02957

Quality Score

Status

Chromosome

Chromosomal Location

87250758-87263738 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 87262194 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Phenylalanine at position 13 (V13F)

Ref Sequence

ENSEMBL: ENSMUSP00000115780 (fasta)

Gene Model

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

AlphaFold

Q9EQY5

Predicted Effect

probably benign
Transcript: ENSMUST00000090986
AA Change: V13F

PolyPhen 2 Score 0.338 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000088508
Gene: ENSMUSG00000015852
AA Change: V13F

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

possibly damaging
Transcript: ENSMUST00000146512
AA Change: V13F

PolyPhen 2 Score 0.593 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000115780
Gene: ENSMUSG00000015852
AA Change: V13F

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

Coding Region Coverage

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: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A630095E13Rik	G	T	9: 36,637,850	T38K	probably benign	Het
Abi2	A	G	1: 60,470,786	D262G	probably damaging	Het
Ahcyl1	G	T	3: 107,667,642	Q462K	probably damaging	Het
Btbd11	T	A	10: 85,633,837	M405K	probably damaging	Het
Btbd11	C	T	10: 85,631,286		probably benign	Het
C8b	A	G	4: 104,766,455	T20A	probably benign	Het
Casd1	T	A	6: 4,634,068	Y594N	possibly damaging	Het
Crtc2	C	T	3: 90,262,533	P412L	probably damaging	Het
Cyp3a44	T	A	5: 145,779,662	R373*	probably null	Het
Dnah10	A	G	5: 124,763,133	D1277G	probably benign	Het
Dnah2	A	T	11: 69,448,507	V3058E	possibly damaging	Het
Eif3l	T	C	15: 79,089,828	L481P	probably benign	Het
Fbxw7	A	T	3: 84,976,237	T573S	probably benign	Het
Fcgbp	C	A	7: 28,091,847	Y844*	probably null	Het
Gbx2	T	G	1: 89,930,653	S35R	probably benign	Het
Gm10767	A	T	13: 66,908,213		probably benign	Het
H2-M9	A	G	17: 36,642,157	L86S	probably benign	Het
Hebp1	C	T	6: 135,137,992	G157D	probably benign	Het
Igf2bp3	C	A	6: 49,087,404	V560L	probably benign	Het
Igsf10	A	G	3: 59,330,864	I632T	probably damaging	Het
Kcnab2	A	T	4: 152,435,869	S5T	possibly damaging	Het
Kcnh5	T	C	12: 75,007,665	S502G	probably benign	Het
Lpcat2	T	A	8: 92,875,584	Y224*	probably null	Het
Mcrip2	A	G	17: 25,868,525	V24A	probably damaging	Het
Mttp	T	C	3: 138,109,081	K493E	possibly damaging	Het
Myl7	A	G	11: 5,897,137	S139P	possibly damaging	Het
Npepps	C	T	11: 97,242,652	R268H	probably damaging	Het
Oas1c	C	T	5: 120,805,413	W18*	probably null	Het
Olfr1328	G	T	4: 118,934,119	T241N	probably damaging	Het
P4ha3	T	C	7: 100,318,905		probably benign	Het
Pkd1l2	G	A	8: 117,065,745	T436I	probably benign	Het
Pkhd1l1	T	A	15: 44,512,908	W989R	probably damaging	Het
Podxl	A	G	6: 31,528,449		probably benign	Het
Pot1b	T	C	17: 55,700,009	Y36C	probably damaging	Het
Ppme1	A	T	7: 100,338,440	I103K	possibly damaging	Het
Ppp1r12a	T	C	10: 108,198,918	I108T	probably damaging	Het
Pramel1	A	G	4: 143,397,598	H281R	probably benign	Het
Prep	T	C	10: 45,126,030	V427A	probably benign	Het
Prkce	A	G	17: 86,496,026	D451G	possibly damaging	Het
Prrc2c	A	G	1: 162,706,535		probably benign	Het
Rrm2	A	G	12: 24,708,441	N32S	probably damaging	Het
Sema6a	A	G	18: 47,249,224	L752P	probably damaging	Het
Sik3	T	A	9: 46,195,845	I429N	possibly damaging	Het
Slc22a29	A	G	19: 8,169,990	L336P	probably benign	Het
Stk32a	A	T	18: 43,311,992	M284L	probably benign	Het
Syde2	T	C	3: 145,989,179		probably benign	Het
Tcta	G	A	9: 108,305,332	S91F	possibly damaging	Het
Traf3ip2	A	T	10: 39,654,410	T517S	probably damaging	Het
Trpv3	A	G	11: 73,285,872	Y359C	probably damaging	Het
Vmn1r66	A	G	7: 10,274,810	S99P	probably damaging	Het
Vmn2r8	G	A	5: 108,802,225	T252M	probably benign	Het
Wdr27	A	T	17: 14,910,110		probably benign	Het
Yipf1	A	G	4: 107,336,150	T78A	probably damaging	Het
Zfp735	A	T	11: 73,710,929	Y233F	probably benign	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
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
BB011: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
R9477:Fcrls	UTSW	3	87252496	missense	probably damaging	0.98
R9522:Fcrls	UTSW	3	87256794	missense	possibly damaging	0.95

Posted On

2015-12-18