Mutagenetix > Incidental Mutation

Incidental Mutation 'R1874:Ffar2'

211038

Institutional Source

Beutler Lab

Gene Symbol

Ffar2

Ensembl Gene

ENSMUSG00000051314

Gene Name

free fatty acid receptor 2

Synonyms

Gpr43

MMRRC Submission

039896-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1874 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

30517778-30523200 bp(-) (GRCm39)

Type of Mutation

splice site (272 bp from exon)

DNA Base Change (assembly)

A to G at 30518839 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000140215 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000053156] [ENSMUST00000163504] [ENSMUST00000168528] [ENSMUST00000186059] [ENSMUST00000186339] [ENSMUST00000186534]

AlphaFold

Q8VCK6

Predicted Effect

probably damaging
Transcript: ENSMUST00000053156
AA Change: C234R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000052600
Gene: ENSMUSG00000051314
AA Change: C234R

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srv	10	284	3.1e-8	PFAM
Pfam:7tm_1	24	273	1.7e-37	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000163504
AA Change: C234R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000127758
Gene: ENSMUSG00000051314
AA Change: C234R

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srv	10	284	3.2e-8	PFAM
Pfam:7tm_1	24	277	1.2e-28	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000168528
AA Change: C234R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000129398
Gene: ENSMUSG00000051314
AA Change: C234R

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srv	10	284	3.1e-8	PFAM
Pfam:7tm_1	24	273	1.7e-37	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000186059

SMART Domains

Protein: ENSMUSP00000140484
Gene: ENSMUSG00000051314

Domain	Start	End	E-Value	Type
Pfam:7tm_1	24	133	1.4e-19	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000186339

SMART Domains

Protein: ENSMUSP00000140493
Gene: ENSMUSG00000051314

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srv	8	175	1.9e-4	PFAM
Pfam:7tm_1	24	179	1.4e-25	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000186534

SMART Domains

Protein: ENSMUSP00000140215
Gene: ENSMUSG00000051314

Domain	Start	End	E-Value	Type
Pfam:7tm_1	24	142	1.5e-22	PFAM

Meta Mutation Damage Score

0.9405

Coding Region Coverage

1x: 97.5%
3x: 97.0%
10x: 95.8%
20x: 94.1%

Validation Efficiency

96% (105/109)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the GP40 family of G protein-coupled receptors that are clustered together on chromosome 19. The encoded protein is a receptor for short chain free fatty acids and may be involved in the inflammatory response and in regulating lipid plasma levels. [provided by RefSeq, Apr 2009]
PHENOTYPE: Mice homozygous for a null allele show altered granulocyte and neutrophil physiology and increased inflammation in models of induced colitis, arthritis and asthma, whereas homozygotes for a different null allele show reduced neutrophil recruitment and decreased susceptibility to induced colitis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 104 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
AA986860	A	G	1: 130,670,428 (GRCm39)	S217G	probably benign	Het
Adrb3	C	A	8: 27,717,591 (GRCm39)	R286L	probably damaging	Het
Akap11	T	A	14: 78,749,306 (GRCm39)	D1027V	probably benign	Het
Ank3	A	T	10: 69,733,913 (GRCm39)	I726F	probably damaging	Het
Ankmy2	T	A	12: 36,215,930 (GRCm39)	D43E	possibly damaging	Het
Ankrd34b	A	G	13: 92,576,064 (GRCm39)	D432G	probably damaging	Het
Ano3	A	C	2: 110,715,217 (GRCm39)	S74A	probably benign	Het
B4galnt4	T	A	7: 140,650,439 (GRCm39)	S769T	probably damaging	Het
Bicral	T	A	17: 47,136,104 (GRCm39)	T369S	probably benign	Het
Blm	A	G	7: 80,147,166 (GRCm39)	L738P	probably damaging	Het
Bpifb3	A	G	2: 153,767,760 (GRCm39)	T278A	probably benign	Het
Bpifb5	A	G	2: 154,069,122 (GRCm39)		probably benign	Het
Brd8	G	C	18: 34,743,527 (GRCm39)	P266R	probably damaging	Het
Btaf1	A	T	19: 36,957,983 (GRCm39)	M587L	probably benign	Het
Casz1	C	G	4: 149,027,668 (GRCm39)	T1015S	probably damaging	Het
Cdh23	A	G	10: 60,272,597 (GRCm39)	I524T	possibly damaging	Het
Celsr3	T	C	9: 108,713,037 (GRCm39)	V1825A	probably benign	Het
Cenpf	A	G	1: 189,416,013 (GRCm39)	L104P	probably damaging	Het
Clasp1	G	T	1: 118,528,315 (GRCm39)		probably null	Het
Coprs	A	G	8: 13,935,112 (GRCm39)	W148R	probably damaging	Het
Cpne1	A	G	2: 155,920,302 (GRCm39)	S168P	probably damaging	Het
Cpxm2	T	C	7: 131,661,563 (GRCm39)	Y408C	probably damaging	Het
Ctnna3	A	G	10: 63,339,886 (GRCm39)	E24G	possibly damaging	Het
Cubn	T	A	2: 13,327,813 (GRCm39)	S2671C	probably damaging	Het
Cyp4f39	T	A	17: 32,702,298 (GRCm39)	F265Y	probably damaging	Het
Dgkq	C	A	5: 108,808,461 (GRCm39)	R34L	probably benign	Het
Dnajc7	C	T	11: 100,490,139 (GRCm39)		probably benign	Het
Eml6	T	G	11: 29,781,136 (GRCm39)	D632A	probably damaging	Het
Fbxl18	G	A	5: 142,871,978 (GRCm39)	A419V	probably damaging	Het
Fbxw22	A	T	9: 109,214,179 (GRCm39)	C212*	probably null	Het
Fga	A	T	3: 82,940,028 (GRCm39)	T561S	probably damaging	Het
Fry	A	G	5: 150,269,386 (GRCm39)	Y159C	probably damaging	Het
Gal3st1	A	G	11: 3,948,231 (GRCm39)	Y146C	probably damaging	Het
Gapvd1	A	T	2: 34,596,033 (GRCm39)	H788Q	probably damaging	Het
Gimap7	G	A	6: 48,700,449 (GRCm39)	V12I	possibly damaging	Het
Gli2	C	A	1: 118,929,779 (GRCm39)	A43S	possibly damaging	Het
Gm15446	T	C	5: 110,090,419 (GRCm39)	F224L	probably damaging	Het
Gm21738	C	T	14: 19,418,824 (GRCm38)	V35I	possibly damaging	Het
Grhl1	T	C	12: 24,636,155 (GRCm39)		probably benign	Het
Grk6	T	C	13: 55,598,086 (GRCm39)	Y53H	probably damaging	Het
Hcar1	C	T	5: 124,017,328 (GRCm39)	R121K	probably damaging	Het
Hmcn1	A	C	1: 150,596,446 (GRCm39)	S1797A	probably damaging	Het
Hsd17b7	A	T	1: 169,783,562 (GRCm39)	L282Q	possibly damaging	Het
Irs1	TTCTCTGAGTGGCCACAGCGTCT	TTCT	1: 82,267,574 (GRCm39)		probably null	Het
Kif1b	C	T	4: 149,272,089 (GRCm39)	V1571I	probably benign	Het
Lpl	T	A	8: 69,349,271 (GRCm39)	C266S	probably damaging	Het
Mag	G	A	7: 30,608,476 (GRCm39)	H213Y	probably benign	Het
Mansc4	T	G	6: 146,976,688 (GRCm39)	R309S	probably benign	Het
Mlh3	A	G	12: 85,284,287 (GRCm39)		probably null	Het
Mndal	G	A	1: 173,687,933 (GRCm39)		probably benign	Het
Mrgpra2b	T	A	7: 47,113,742 (GRCm39)	E330V	probably damaging	Het
Myh3	A	G	11: 66,984,005 (GRCm39)	I990V	probably benign	Het
Myoz2	A	T	3: 122,819,765 (GRCm39)	S65T	probably damaging	Het
Naa16	T	C	14: 79,593,183 (GRCm39)	E463G	possibly damaging	Het
Nadsyn1	A	G	7: 143,351,581 (GRCm39)	F684S	probably damaging	Het
Notch1	T	C	2: 26,371,591 (GRCm39)	E286G	possibly damaging	Het
Nynrin	A	T	14: 56,100,950 (GRCm39)	I247L	probably benign	Het
Oprm1	A	G	10: 6,739,035 (GRCm39)	H54R	probably benign	Het
Or10g6	T	A	9: 39,934,151 (GRCm39)	I154N	possibly damaging	Het
Or2n1d	C	T	17: 38,646,860 (GRCm39)	P271S	probably damaging	Het
Or51a43	T	C	7: 103,717,336 (GRCm39)	I301V	probably null	Het
P4hb	C	T	11: 120,452,992 (GRCm39)	D483N	probably benign	Het
Pak1	T	C	7: 97,520,787 (GRCm39)	S149P	probably benign	Het
Pars2	T	C	4: 106,510,913 (GRCm39)	F232L	possibly damaging	Het
Pih1d2	A	G	9: 50,532,245 (GRCm39)	M88V	possibly damaging	Het
Pms1	A	T	1: 53,246,392 (GRCm39)	N382K	probably benign	Het
Pnliprp2	G	T	19: 58,751,821 (GRCm39)	V189L	probably benign	Het
Pole	G	A	5: 110,471,530 (GRCm39)	V1425M	possibly damaging	Het
Pot1b	T	A	17: 55,961,805 (GRCm39)	Q591L	probably benign	Het
Ppp1r9a	C	T	6: 4,906,348 (GRCm39)	T301M	possibly damaging	Het
Psg21	T	C	7: 18,384,741 (GRCm39)	E335G	probably benign	Het
Ptpru	T	A	4: 131,497,066 (GRCm39)	M1416L	probably benign	Het
Pxn	T	C	5: 115,683,049 (GRCm39)	V117A	probably damaging	Het
Qsox1	C	T	1: 155,688,385 (GRCm39)	R54H	possibly damaging	Het
Rad1	A	G	15: 10,488,092 (GRCm39)	E42G	probably damaging	Het
Rpp14	A	G	14: 8,090,145 (GRCm38)	Y23C	probably benign	Het
Sdk2	C	T	11: 113,725,782 (GRCm39)	V1156I	probably benign	Het
Serpina3j	G	T	12: 104,285,958 (GRCm39)	R371L	probably benign	Het
Serpinb9d	T	A	13: 33,381,946 (GRCm39)		probably null	Het
Sirt5	C	T	13: 43,524,267 (GRCm39)	S13F	possibly damaging	Het
Slc6a7	T	A	18: 61,134,470 (GRCm39)		probably benign	Het
Slx4	A	G	16: 3,804,712 (GRCm39)	S701P	probably benign	Het
Snx29	A	G	16: 11,185,545 (GRCm39)	T43A	probably benign	Het
Speg	T	C	1: 75,400,550 (GRCm39)	V2570A	probably benign	Het
Srrm4	T	A	5: 116,591,565 (GRCm39)		probably benign	Het
Stk32a	A	G	18: 43,394,381 (GRCm39)	Y110C	probably damaging	Het
Tbc1d31	G	A	15: 57,779,506 (GRCm39)	G73E	probably benign	Het
Thsd7a	A	T	6: 12,555,434 (GRCm39)	I150N	possibly damaging	Het
Tjp1	A	T	7: 64,969,001 (GRCm39)	D699E	probably damaging	Het
Tmem143	A	G	7: 45,565,988 (GRCm39)	D437G	possibly damaging	Het
Tmem45a2	A	G	16: 56,867,447 (GRCm39)	Y85H	possibly damaging	Het
Tmem45b	T	A	9: 31,340,383 (GRCm39)	T7S	probably damaging	Het
Tut4	T	A	4: 108,407,922 (GRCm39)	V1397D	probably damaging	Het
Ube4b	A	G	4: 149,432,428 (GRCm39)	L832P	probably damaging	Het
Ugp2	G	T	11: 21,279,048 (GRCm39)	F379L	probably damaging	Het
Ugt3a1	A	T	15: 9,365,437 (GRCm39)	D350V	probably damaging	Het
Vmn2r8	T	A	5: 108,950,284 (GRCm39)	T188S	possibly damaging	Het
Vwa7	C	G	17: 35,236,088 (GRCm39)	P14R	probably benign	Het
Vwc2	C	A	11: 11,211,495 (GRCm39)	T317K	probably damaging	Het
Vwf	A	T	6: 125,605,335 (GRCm39)	Q906L	probably benign	Het
Wdr49	A	G	3: 75,336,654 (GRCm39)	V351A	probably damaging	Het
Wdr7	A	G	18: 63,861,575 (GRCm39)	S196G	probably benign	Het
Xkr6	C	A	14: 64,035,745 (GRCm39)	A26E	unknown	Het
Zfp955b	T	C	17: 33,524,427 (GRCm39)	I47V	probably benign	Het

Other mutations in Ffar2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01508:Ffar2	APN	7	30,518,601 (GRCm39)	missense	probably benign	0.00
IGL01655:Ffar2	APN	7	30,519,012 (GRCm39)	missense	probably damaging	1.00
R3826:Ffar2	UTSW	7	30,519,510 (GRCm39)	missense	possibly damaging	0.77
R3827:Ffar2	UTSW	7	30,519,510 (GRCm39)	missense	possibly damaging	0.77
R3828:Ffar2	UTSW	7	30,519,510 (GRCm39)	missense	possibly damaging	0.77
R4156:Ffar2	UTSW	7	30,519,093 (GRCm39)	missense	probably damaging	1.00
R6377:Ffar2	UTSW	7	30,518,971 (GRCm39)	missense	probably benign	0.00
R6987:Ffar2	UTSW	7	30,519,108 (GRCm39)	missense	possibly damaging	0.94
R7270:Ffar2	UTSW	7	30,518,929 (GRCm39)	missense	probably benign	0.00
R7374:Ffar2	UTSW	7	30,519,465 (GRCm39)	missense	probably damaging	1.00
R7616:Ffar2	UTSW	7	30,519,357 (GRCm39)	missense	probably damaging	1.00
R7784:Ffar2	UTSW	7	30,518,683 (GRCm39)	missense	probably benign	0.01
R8494:Ffar2	UTSW	7	30,519,164 (GRCm39)	nonsense	probably null
R9117:Ffar2	UTSW	7	30,518,616 (GRCm39)	missense	probably damaging	0.97
R9371:Ffar2	UTSW	7	30,518,929 (GRCm39)	missense	probably benign	0.00
R9566:Ffar2	UTSW	7	30,518,847 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTGCGGATCAGTAGCAAACC -3'
(R):5'- TGGGCACTGAGAACCAAATAAC -3'

Sequencing Primer
(F):5'- GCGGATCAGTAGCAAACCTTTCC -3'
(R):5'- TTCACCCAAGAGCAGCTGGATG -3'

Posted On

2014-06-30