Mutagenetix > Incidental Mutation

Incidental Mutation 'R7023:Fcgbpl1'

545768

Institutional Source

Beutler Lab

Gene Symbol

Fcgbpl1

Ensembl Gene

ENSMUSG00000078776

Gene Name

Fc fragment of IgG binding protein like 1

Synonyms

9530053A07Rik

MMRRC Submission

045124-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.103) question?

Stock #

R7023 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

27828891-27864236 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

T to A at 27839463 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Stop codon at position 425 (C425*)

Ref Sequence

ENSEMBL: ENSMUSP00000114986 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000059886] [ENSMUST00000150948]

AlphaFold

E9PVG8

Predicted Effect

probably null
Transcript: ENSMUST00000059886
AA Change: C425*

SMART Domains

Protein: ENSMUSP00000056479
Gene: ENSMUSG00000078776
AA Change: C425*

Domain	Start	End	E-Value	Type
low complexity region	8	24	N/A	INTRINSIC
FOLN	27	49	1.23e-4	SMART
VWD	46	211	1.5e-40	SMART
C8	251	326	4.31e-33	SMART
Pfam:TIL	329	383	2e-13	PFAM
VWC	385	448	1.02e0	SMART
VWD	439	603	4.32e-32	SMART
C8	640	715	4.54e-9	SMART
Pfam:TIL	718	771	1.6e-12	PFAM
VWC	773	826	1.1e0	SMART
FOLN	805	827	6.87e1	SMART
VWD	825	988	7.92e-40	SMART
C8	1033	1108	5.1e-35	SMART
Pfam:TIL	1111	1164	7.6e-11	PFAM
VWC	1166	1224	1.1e-2	SMART
FOLN	1197	1219	9.55e-1	SMART
FOLN	1223	1245	5.38e1	SMART
VWD	1241	1410	9.04e-35	SMART
C8	1450	1526	9.54e-26	SMART
low complexity region	1540	1550	N/A	INTRINSIC
EGF_like	1557	1580	5.34e1	SMART
VWC	1588	1681	3.21e-3	SMART
VWD	1639	1806	7.3e-30	SMART
C8	1838	1913	2.44e-32	SMART
EGF_like	1941	1964	4.46e1	SMART
VWC	1971	2062	2.85e-1	SMART
VWD	2022	2178	1.32e-27	SMART
low complexity region	2199	2212	N/A	INTRINSIC
C8	2219	2294	1.43e-29	SMART
Pfam:TIL	2297	2350	1.1e-11	PFAM
FOLN	2383	2405	5.68e1	SMART
VWD	2402	2564	4.58e-4	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129051

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000130693

Predicted Effect

probably null
Transcript: ENSMUST00000150948
AA Change: C425*

SMART Domains

Protein: ENSMUSP00000114986
Gene: ENSMUSG00000078776
AA Change: C425*

Domain	Start	End	E-Value	Type
low complexity region	8	24	N/A	INTRINSIC
FOLN	27	49	1.23e-4	SMART
VWD	46	211	1.5e-40	SMART
C8	251	326	4.31e-33	SMART
Pfam:TIL	329	383	2e-13	PFAM
VWC	385	448	1.02e0	SMART
VWD	439	603	4.32e-32	SMART
C8	640	715	4.54e-9	SMART
Pfam:TIL	718	771	1.6e-12	PFAM
VWC	773	826	1.1e0	SMART
FOLN	805	827	6.87e1	SMART
VWD	825	988	7.92e-40	SMART
C8	1033	1108	5.1e-35	SMART
Pfam:TIL	1111	1164	7.6e-11	PFAM
VWC	1166	1224	1.1e-2	SMART
FOLN	1197	1219	9.55e-1	SMART
FOLN	1223	1245	5.38e1	SMART
VWD	1241	1410	9.04e-35	SMART
C8	1450	1526	9.54e-26	SMART
low complexity region	1540	1550	N/A	INTRINSIC
EGF_like	1557	1580	5.34e1	SMART
VWC	1588	1681	3.21e-3	SMART
VWD	1639	1806	7.3e-30	SMART
C8	1838	1913	2.44e-32	SMART
EGF_like	1941	1964	4.46e1	SMART
VWC	1971	2062	2.85e-1	SMART
VWD	2022	2178	1.32e-27	SMART
low complexity region	2199	2212	N/A	INTRINSIC
C8	2219	2294	1.43e-29	SMART
Pfam:TIL	2297	2350	1.1e-11	PFAM
FOLN	2383	2405	5.68e1	SMART
VWD	2402	2564	4.58e-4	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 98.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 85 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4833420G17Rik	A	G	13: 119,610,443 (GRCm39)	H372R	probably benign	Het
4933405O20Rik	T	C	7: 50,250,001 (GRCm39)	I345T	probably damaging	Het
4933427D14Rik	A	G	11: 72,069,229 (GRCm39)		probably null	Het
6430548M08Rik	T	C	8: 120,872,096 (GRCm39)	V8A	probably damaging	Het
Adam2	A	T	14: 66,280,505 (GRCm39)	D501E	probably benign	Het
Agbl3	T	C	6: 34,791,704 (GRCm39)	V602A	probably benign	Het
Akap12	T	C	10: 4,306,895 (GRCm39)	M1235T	probably benign	Het
Arid5a	G	A	1: 36,356,631 (GRCm39)		probably benign	Het
Asxl1	T	A	2: 153,242,469 (GRCm39)	D1006E	probably benign	Het
AY074887	T	C	9: 54,858,149 (GRCm39)		probably benign	Het
Btbd9	T	A	17: 30,746,546 (GRCm39)	R93S	probably benign	Het
Cabp2	A	T	19: 4,132,658 (GRCm39)		probably null	Het
Cacna1e	T	C	1: 154,601,439 (GRCm39)	D76G	probably null	Het
Cd177	A	G	7: 24,459,187 (GRCm39)	I74T	probably benign	Het
Chchd1	G	A	14: 20,753,310 (GRCm39)		probably benign	Het
Col28a1	T	C	6: 8,083,763 (GRCm39)	R565G	possibly damaging	Het
Cpvl	T	A	6: 53,944,797 (GRCm39)	I80F	probably benign	Het
Csgalnact1	T	C	8: 68,811,081 (GRCm39)	T530A	probably benign	Het
Cybrd1	A	G	2: 70,968,922 (GRCm39)	D265G	probably benign	Het
Cyp2c69	A	T	19: 39,865,986 (GRCm39)	N202K	probably benign	Het
D1Pas1	A	G	1: 186,700,205 (GRCm39)	N45D	probably damaging	Het
Dclre1a	A	G	19: 56,528,638 (GRCm39)	V839A	probably damaging	Het
Degs1	A	T	1: 182,106,630 (GRCm39)	Y210N	probably damaging	Het
Doc2g	A	G	19: 4,054,778 (GRCm39)	S220G	probably benign	Het
Epb41l2	T	A	10: 25,388,875 (GRCm39)	L885Q	probably damaging	Het
Fabp1	A	T	6: 71,180,069 (GRCm39)		probably null	Het
Fat2	G	A	11: 55,201,328 (GRCm39)	S582L	probably benign	Het
Fras1	A	G	5: 96,857,943 (GRCm39)	N2079S	probably benign	Het
Gdf6	T	C	4: 9,860,210 (GRCm39)	Y431H	probably damaging	Het
Gfra1	A	T	19: 58,442,764 (GRCm39)	L6Q	probably damaging	Het
Gm45861	T	G	8: 28,071,034 (GRCm39)	S1305A	unknown	Het
Gse1	T	C	8: 120,957,387 (GRCm39)		probably benign	Het
Kmt2e	A	G	5: 23,705,485 (GRCm39)	H1303R	possibly damaging	Het
Lck	T	C	4: 129,442,658 (GRCm39)	D499G	possibly damaging	Het
Lepr	A	T	4: 101,646,484 (GRCm39)	Y805F	probably damaging	Het
Lin7a	A	T	10: 107,218,489 (GRCm39)	Y11F	possibly damaging	Het
Lrrc43	A	G	5: 123,641,826 (GRCm39)	K559E	probably damaging	Het
Megf6	T	C	4: 154,338,602 (GRCm39)	L467P	possibly damaging	Het
Mprip	G	A	11: 59,628,215 (GRCm39)	G221R	probably damaging	Het
Myo5c	T	C	9: 75,208,738 (GRCm39)	V1683A	probably damaging	Het
Nbeal2	G	A	9: 110,467,686 (GRCm39)	R501W	probably damaging	Het
Ncf1	G	T	5: 134,254,116 (GRCm39)	A219E	possibly damaging	Het
Nckap1l	T	C	15: 103,384,493 (GRCm39)	I616T	probably benign	Het
Nlrp2	A	T	7: 5,331,228 (GRCm39)	C389*	probably null	Het
Nrg3	T	C	14: 38,098,333 (GRCm39)	E507G	probably damaging	Het
Or4p19	A	G	2: 88,242,759 (GRCm39)	L81P	probably damaging	Het
P4ha2	A	T	11: 54,022,072 (GRCm39)	T532S	probably benign	Het
Pappa	A	T	4: 65,269,955 (GRCm39)	H1623L	probably benign	Het
Paqr6	A	G	3: 88,273,353 (GRCm39)	Y115C	probably damaging	Het
Pcolce2	A	T	9: 95,560,521 (GRCm39)	Q190L	probably benign	Het
Poll	A	G	19: 45,547,277 (GRCm39)	I65T	probably benign	Het
Prmt9	T	C	8: 78,276,086 (GRCm39)		probably benign	Het
Prpf39	T	C	12: 65,100,074 (GRCm39)	V130A	possibly damaging	Het
Prpf6	A	G	2: 181,262,433 (GRCm39)	D144G	probably damaging	Het
Rgs6	T	A	12: 83,138,878 (GRCm39)		probably benign	Het
Rimbp2	A	G	5: 128,879,847 (GRCm39)		probably null	Het
Ripor2	A	G	13: 24,855,829 (GRCm39)	T90A	probably benign	Het
Rnf150	T	C	8: 83,590,706 (GRCm39)	F23S	probably damaging	Het
Rpp40	G	A	13: 36,082,889 (GRCm39)	R200W	possibly damaging	Het
Rtp3	G	A	9: 110,815,714 (GRCm39)	S217L	probably benign	Het
Sacs	A	C	14: 61,446,264 (GRCm39)	K2770T	probably benign	Het
Scn10a	A	T	9: 119,442,610 (GRCm39)	I1545N	probably damaging	Het
Scn2b	G	T	9: 45,037,438 (GRCm39)	V162L	probably damaging	Het
Sema6d	A	G	2: 124,506,831 (GRCm39)	T880A	probably damaging	Het
Slc36a4	A	G	9: 15,630,929 (GRCm39)	D16G	probably benign	Het
Slc4a8	T	A	15: 100,689,524 (GRCm39)	I378K	probably benign	Het
Smco2	T	A	6: 146,760,354 (GRCm39)	L70*	probably null	Het
Sptb	C	T	12: 76,671,862 (GRCm39)	V364I	probably damaging	Het
Susd4	A	G	1: 182,592,613 (GRCm39)	H3R	probably damaging	Het
Tbc1d16	T	C	11: 119,049,617 (GRCm39)	Q293R	probably damaging	Het
Tnfsf9	T	A	17: 57,414,317 (GRCm39)	M248K	possibly damaging	Het
Toporsl	A	G	4: 52,611,211 (GRCm39)	N368S	possibly damaging	Het
Trip11	T	C	12: 101,852,126 (GRCm39)	E361G	probably benign	Het
Trrap	T	A	5: 144,728,964 (GRCm39)	M626K	possibly damaging	Het
Ttn	A	T	2: 76,773,218 (GRCm39)	S2395T	probably damaging	Het
Ubqln3	T	C	7: 103,790,630 (GRCm39)	R487G	probably damaging	Het
Vdac1	A	G	11: 52,265,193 (GRCm39)	Y22C	probably damaging	Het
Vmn1r59	C	T	7: 5,457,477 (GRCm39)	M94I	probably benign	Het
Vmn2r10	G	T	5: 109,149,894 (GRCm39)	D383E	probably damaging	Het
Vmn2r115	T	C	17: 23,578,785 (GRCm39)	Y753H	probably damaging	Het
Vmn2r97	G	T	17: 19,134,663 (GRCm39)	C27F	probably damaging	Het
Wasf1	T	A	10: 40,812,471 (GRCm39)	V420E	unknown	Het
Zfp94	A	T	7: 24,002,821 (GRCm39)	L201Q	probably damaging	Het
Zgpat	TGGAGGAGGAGGAGGAGGA	TGGAGGAGGAGGAGGA	2: 181,007,811 (GRCm39)		probably benign	Het
Zmym4	C	A	4: 126,762,593 (GRCm39)	R1410L	probably damaging	Het

Other mutations in Fcgbpl1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00435:Fcgbpl1	APN	7	27,863,953 (GRCm39)	missense	probably damaging	1.00
IGL00757:Fcgbpl1	APN	7	27,853,870 (GRCm39)	missense	probably damaging	1.00
IGL01015:Fcgbpl1	APN	7	27,854,743 (GRCm39)	missense	probably damaging	1.00
IGL01079:Fcgbpl1	APN	7	27,839,203 (GRCm39)	missense	probably damaging	0.99
IGL01343:Fcgbpl1	APN	7	27,850,127 (GRCm39)	missense	probably benign	0.19
IGL01420:Fcgbpl1	APN	7	27,839,558 (GRCm39)	missense	probably benign	0.28
IGL01604:Fcgbpl1	APN	7	27,854,749 (GRCm39)	missense	probably benign	0.11
IGL01666:Fcgbpl1	APN	7	27,852,717 (GRCm39)	missense	probably damaging	1.00
IGL02002:Fcgbpl1	APN	7	27,852,221 (GRCm39)	missense	probably damaging	1.00
IGL02036:Fcgbpl1	APN	7	27,836,950 (GRCm39)	missense	possibly damaging	0.82
IGL02126:Fcgbpl1	APN	7	27,839,281 (GRCm39)	missense	probably damaging	1.00
IGL02150:Fcgbpl1	APN	7	27,846,204 (GRCm39)	nonsense	probably null
IGL02219:Fcgbpl1	APN	7	27,854,060 (GRCm39)	missense	probably damaging	1.00
IGL02563:Fcgbpl1	APN	7	27,857,317 (GRCm39)	missense	probably benign
IGL02804:Fcgbpl1	APN	7	27,852,795 (GRCm39)	missense	probably benign	0.00
IGL02830:Fcgbpl1	APN	7	27,862,348 (GRCm39)	missense	probably damaging	1.00
IGL02943:Fcgbpl1	APN	7	27,846,613 (GRCm39)	missense	probably damaging	1.00
IGL02977:Fcgbpl1	APN	7	27,863,797 (GRCm39)	missense	possibly damaging	0.83
IGL03231:Fcgbpl1	APN	7	27,853,147 (GRCm39)	missense	possibly damaging	0.95
IGL03304:Fcgbpl1	APN	7	27,841,667 (GRCm39)	missense	probably damaging	0.99
herz	UTSW	7	27,853,264 (GRCm39)	missense	possibly damaging	0.72
pulse	UTSW	7	27,853,174 (GRCm39)	missense	probably damaging	1.00
Sinusoidal	UTSW	7	27,839,555 (GRCm39)	missense	probably damaging	1.00
PIT4378001:Fcgbpl1	UTSW	7	27,853,889 (GRCm39)	missense	possibly damaging	0.61
R0023:Fcgbpl1	UTSW	7	27,852,837 (GRCm39)	missense	probably benign	0.00
R0131:Fcgbpl1	UTSW	7	27,837,040 (GRCm39)	missense	probably damaging	1.00
R0131:Fcgbpl1	UTSW	7	27,837,040 (GRCm39)	missense	probably damaging	1.00
R0132:Fcgbpl1	UTSW	7	27,837,040 (GRCm39)	missense	probably damaging	1.00
R0158:Fcgbpl1	UTSW	7	27,854,917 (GRCm39)	missense	probably damaging	1.00
R0230:Fcgbpl1	UTSW	7	27,856,250 (GRCm39)	missense	probably damaging	1.00
R0310:Fcgbpl1	UTSW	7	27,841,699 (GRCm39)	missense	probably benign	0.04
R0448:Fcgbpl1	UTSW	7	27,839,660 (GRCm39)	missense	probably benign	0.03
R0462:Fcgbpl1	UTSW	7	27,836,765 (GRCm39)	missense	probably damaging	1.00
R0481:Fcgbpl1	UTSW	7	27,853,174 (GRCm39)	missense	probably damaging	1.00
R0497:Fcgbpl1	UTSW	7	27,846,890 (GRCm39)	missense	probably damaging	1.00
R0556:Fcgbpl1	UTSW	7	27,858,803 (GRCm39)	missense	probably benign
R0562:Fcgbpl1	UTSW	7	27,862,115 (GRCm39)	missense	probably benign	0.30
R0586:Fcgbpl1	UTSW	7	27,836,516 (GRCm39)	missense	probably damaging	0.99
R0924:Fcgbpl1	UTSW	7	27,839,555 (GRCm39)	missense	probably damaging	1.00
R0930:Fcgbpl1	UTSW	7	27,839,555 (GRCm39)	missense	probably damaging	1.00
R1103:Fcgbpl1	UTSW	7	27,853,945 (GRCm39)	missense	probably damaging	1.00
R1213:Fcgbpl1	UTSW	7	27,857,098 (GRCm39)	missense	probably damaging	1.00
R1292:Fcgbpl1	UTSW	7	27,842,219 (GRCm39)	splice site	probably benign
R1368:Fcgbpl1	UTSW	7	27,858,903 (GRCm39)	missense	possibly damaging	0.89
R1451:Fcgbpl1	UTSW	7	27,836,582 (GRCm39)	missense	probably damaging	1.00
R1477:Fcgbpl1	UTSW	7	27,856,518 (GRCm39)	missense	probably benign	0.01
R1538:Fcgbpl1	UTSW	7	27,854,917 (GRCm39)	missense	probably damaging	1.00
R1655:Fcgbpl1	UTSW	7	27,846,535 (GRCm39)	missense	probably damaging	0.98
R1697:Fcgbpl1	UTSW	7	27,853,772 (GRCm39)	missense	probably damaging	1.00
R1741:Fcgbpl1	UTSW	7	27,857,279 (GRCm39)	missense	probably damaging	0.98
R1796:Fcgbpl1	UTSW	7	27,854,797 (GRCm39)	missense	probably damaging	1.00
R1853:Fcgbpl1	UTSW	7	27,854,971 (GRCm39)	nonsense	probably null
R1861:Fcgbpl1	UTSW	7	27,854,157 (GRCm39)	missense	probably damaging	1.00
R1909:Fcgbpl1	UTSW	7	27,843,773 (GRCm39)	missense	possibly damaging	0.52
R1971:Fcgbpl1	UTSW	7	27,830,937 (GRCm39)	missense	possibly damaging	0.90
R1990:Fcgbpl1	UTSW	7	27,853,785 (GRCm39)	missense	probably damaging	0.98
R2020:Fcgbpl1	UTSW	7	27,855,019 (GRCm39)	missense	probably benign
R2084:Fcgbpl1	UTSW	7	27,856,960 (GRCm39)	missense	probably damaging	1.00
R2125:Fcgbpl1	UTSW	7	27,857,447 (GRCm39)	missense	probably benign	0.00
R2132:Fcgbpl1	UTSW	7	27,854,899 (GRCm39)	missense	probably damaging	1.00
R2513:Fcgbpl1	UTSW	7	27,831,060 (GRCm39)	missense	probably damaging	0.99
R2913:Fcgbpl1	UTSW	7	27,863,732 (GRCm39)	missense	probably damaging	1.00
R3150:Fcgbpl1	UTSW	7	27,853,620 (GRCm39)	missense	probably benign	0.21
R3499:Fcgbpl1	UTSW	7	27,853,980 (GRCm39)	missense	probably benign	0.42
R3702:Fcgbpl1	UTSW	7	27,857,203 (GRCm39)	missense	probably damaging	1.00
R3881:Fcgbpl1	UTSW	7	27,839,463 (GRCm39)	nonsense	probably null
R3938:Fcgbpl1	UTSW	7	27,853,719 (GRCm39)	missense	probably damaging	1.00
R4050:Fcgbpl1	UTSW	7	27,852,410 (GRCm39)	missense	possibly damaging	0.55
R4152:Fcgbpl1	UTSW	7	27,856,322 (GRCm39)	missense	possibly damaging	0.47
R4168:Fcgbpl1	UTSW	7	27,836,534 (GRCm39)	missense	probably benign	0.05
R4235:Fcgbpl1	UTSW	7	27,856,073 (GRCm39)	missense	probably damaging	0.99
R4241:Fcgbpl1	UTSW	7	27,853,760 (GRCm39)	missense	probably damaging	1.00
R4363:Fcgbpl1	UTSW	7	27,846,331 (GRCm39)	missense	probably damaging	1.00
R4460:Fcgbpl1	UTSW	7	27,852,281 (GRCm39)	missense	probably benign	0.17
R4463:Fcgbpl1	UTSW	7	27,850,144 (GRCm39)	missense	probably benign
R4841:Fcgbpl1	UTSW	7	27,850,147 (GRCm39)	missense	probably damaging	1.00
R4842:Fcgbpl1	UTSW	7	27,850,147 (GRCm39)	missense	probably damaging	1.00
R4876:Fcgbpl1	UTSW	7	27,842,225 (GRCm39)	intron	probably benign
R4905:Fcgbpl1	UTSW	7	27,856,408 (GRCm39)	missense	possibly damaging	0.93
R4997:Fcgbpl1	UTSW	7	27,843,349 (GRCm39)	missense	possibly damaging	0.77
R5091:Fcgbpl1	UTSW	7	27,856,383 (GRCm39)	missense	probably benign	0.44
R5159:Fcgbpl1	UTSW	7	27,852,733 (GRCm39)	missense	probably benign	0.09
R5326:Fcgbpl1	UTSW	7	27,854,914 (GRCm39)	missense	probably damaging	0.98
R5396:Fcgbpl1	UTSW	7	27,839,608 (GRCm39)	missense	probably benign
R5441:Fcgbpl1	UTSW	7	27,856,339 (GRCm39)	missense	probably damaging	1.00
R5480:Fcgbpl1	UTSW	7	27,857,424 (GRCm39)	nonsense	probably null
R5542:Fcgbpl1	UTSW	7	27,854,914 (GRCm39)	missense	probably damaging	0.98
R5571:Fcgbpl1	UTSW	7	27,855,994 (GRCm39)	missense	probably damaging	0.99
R5613:Fcgbpl1	UTSW	7	27,842,303 (GRCm39)	intron	probably benign
R5637:Fcgbpl1	UTSW	7	27,852,277 (GRCm39)	missense	probably benign	0.00
R5766:Fcgbpl1	UTSW	7	27,836,754 (GRCm39)	nonsense	probably null
R6174:Fcgbpl1	UTSW	7	27,839,384 (GRCm39)	missense	probably damaging	0.96
R6233:Fcgbpl1	UTSW	7	27,830,885 (GRCm39)	missense	probably damaging	0.99
R6250:Fcgbpl1	UTSW	7	27,850,139 (GRCm39)	missense	probably damaging	1.00
R6379:Fcgbpl1	UTSW	7	27,857,017 (GRCm39)	missense	probably damaging	1.00
R6442:Fcgbpl1	UTSW	7	27,843,611 (GRCm39)	missense	possibly damaging	0.88
R6478:Fcgbpl1	UTSW	7	27,854,798 (GRCm39)	missense	probably damaging	1.00
R6699:Fcgbpl1	UTSW	7	27,843,793 (GRCm39)	missense	probably damaging	1.00
R6852:Fcgbpl1	UTSW	7	27,846,560 (GRCm39)	missense	probably damaging	1.00
R6883:Fcgbpl1	UTSW	7	27,852,260 (GRCm39)	missense	possibly damaging	0.89
R6902:Fcgbpl1	UTSW	7	27,836,638 (GRCm39)	missense	probably damaging	1.00
R6903:Fcgbpl1	UTSW	7	27,836,638 (GRCm39)	missense	probably damaging	1.00
R6904:Fcgbpl1	UTSW	7	27,836,638 (GRCm39)	missense	probably damaging	1.00
R6992:Fcgbpl1	UTSW	7	27,839,608 (GRCm39)	missense	probably benign	0.04
R7039:Fcgbpl1	UTSW	7	27,839,573 (GRCm39)	missense	possibly damaging	0.80
R7171:Fcgbpl1	UTSW	7	27,853,944 (GRCm39)	nonsense	probably null
R7282:Fcgbpl1	UTSW	7	27,843,833 (GRCm39)	missense	probably benign	0.02
R7291:Fcgbpl1	UTSW	7	27,839,645 (GRCm39)	missense	probably benign
R7344:Fcgbpl1	UTSW	7	27,852,185 (GRCm39)	missense	possibly damaging	0.46
R7344:Fcgbpl1	UTSW	7	27,839,704 (GRCm39)	missense	possibly damaging	0.79
R7392:Fcgbpl1	UTSW	7	27,863,797 (GRCm39)	missense	possibly damaging	0.83
R7531:Fcgbpl1	UTSW	7	27,839,656 (GRCm39)	missense	probably benign
R7541:Fcgbpl1	UTSW	7	27,843,681 (GRCm39)	nonsense	probably null
R7577:Fcgbpl1	UTSW	7	27,853,848 (GRCm39)	missense	possibly damaging	0.65
R7594:Fcgbpl1	UTSW	7	27,830,885 (GRCm39)	missense	probably damaging	0.99
R7647:Fcgbpl1	UTSW	7	27,839,470 (GRCm39)	missense	probably benign	0.00
R7718:Fcgbpl1	UTSW	7	27,846,626 (GRCm39)	missense	probably damaging	1.00
R7733:Fcgbpl1	UTSW	7	27,839,390 (GRCm39)	missense	probably damaging	1.00
R7737:Fcgbpl1	UTSW	7	27,856,498 (GRCm39)	missense	probably damaging	1.00
R7908:Fcgbpl1	UTSW	7	27,846,921 (GRCm39)	missense	probably benign	0.12
R8013:Fcgbpl1	UTSW	7	27,836,966 (GRCm39)	missense	probably benign	0.14
R8014:Fcgbpl1	UTSW	7	27,836,966 (GRCm39)	missense	probably benign	0.14
R8151:Fcgbpl1	UTSW	7	27,852,766 (GRCm39)	missense	possibly damaging	0.95
R8175:Fcgbpl1	UTSW	7	27,863,873 (GRCm39)	nonsense	probably null
R8254:Fcgbpl1	UTSW	7	27,846,774 (GRCm39)	missense	possibly damaging	0.63
R8345:Fcgbpl1	UTSW	7	27,854,785 (GRCm39)	missense	probably damaging	1.00
R8414:Fcgbpl1	UTSW	7	27,842,158 (GRCm39)	missense	probably damaging	1.00
R8419:Fcgbpl1	UTSW	7	27,843,346 (GRCm39)	missense	probably damaging	1.00
R8496:Fcgbpl1	UTSW	7	27,843,377 (GRCm39)	missense	possibly damaging	0.81
R8691:Fcgbpl1	UTSW	7	27,853,264 (GRCm39)	missense	possibly damaging	0.72
R8785:Fcgbpl1	UTSW	7	27,854,132 (GRCm39)	missense	probably damaging	1.00
R8863:Fcgbpl1	UTSW	7	27,831,006 (GRCm39)	missense	probably damaging	1.00
R8926:Fcgbpl1	UTSW	7	27,853,869 (GRCm39)	missense	probably damaging	1.00
R8950:Fcgbpl1	UTSW	7	27,863,751 (GRCm39)	missense	probably benign	0.32
R9014:Fcgbpl1	UTSW	7	27,854,876 (GRCm39)	missense	probably damaging	1.00
R9045:Fcgbpl1	UTSW	7	27,853,856 (GRCm39)	missense	probably damaging	1.00
R9115:Fcgbpl1	UTSW	7	27,853,754 (GRCm39)	missense	possibly damaging	0.74
R9233:Fcgbpl1	UTSW	7	27,839,519 (GRCm39)	missense	possibly damaging	0.83
R9330:Fcgbpl1	UTSW	7	27,856,410 (GRCm39)	missense	probably benign	0.02
R9426:Fcgbpl1	UTSW	7	27,843,281 (GRCm39)	missense	possibly damaging	0.92
R9477:Fcgbpl1	UTSW	7	27,852,265 (GRCm39)	missense	probably damaging	1.00
R9502:Fcgbpl1	UTSW	7	27,836,891 (GRCm39)	missense	probably benign	0.09
R9505:Fcgbpl1	UTSW	7	27,841,909 (GRCm39)	nonsense	probably null
R9601:Fcgbpl1	UTSW	7	27,853,805 (GRCm39)	missense	possibly damaging	0.78
R9630:Fcgbpl1	UTSW	7	27,836,624 (GRCm39)	missense	probably damaging	1.00
R9632:Fcgbpl1	UTSW	7	27,841,726 (GRCm39)	missense	probably benign
R9673:Fcgbpl1	UTSW	7	27,856,044 (GRCm39)	missense	probably benign	0.25
R9735:Fcgbpl1	UTSW	7	27,856,435 (GRCm39)	missense	probably damaging	1.00
Z1176:Fcgbpl1	UTSW	7	27,854,187 (GRCm39)	missense	probably benign	0.03
Z1176:Fcgbpl1	UTSW	7	27,841,811 (GRCm39)	missense	probably benign	0.06
Z1177:Fcgbpl1	UTSW	7	27,839,323 (GRCm39)	missense	probably benign	0.25
Z1186:Fcgbpl1	UTSW	7	27,856,411 (GRCm39)	missense	probably benign	0.01
Z1186:Fcgbpl1	UTSW	7	27,846,130 (GRCm39)	missense	probably benign	0.00
Z1186:Fcgbpl1	UTSW	7	27,830,997 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- AGACCGACCAACTGCTCTTC -3'
(R):5'- CACTTTGAAGTCGGGGAGAG -3'

Sequencing Primer
(F):5'- TGCGTGTGCCTTCCAGG -3'
(R):5'- AGAGATGGGTGCTGGCCAC -3'

Posted On

2019-05-13