Mutagenetix > Incidental Mutation

Incidental Mutation 'R2513:Fcgbpl1'

253609

Institutional Source

Beutler Lab

Gene Symbol

Fcgbpl1

Ensembl Gene

ENSMUSG00000078776

Gene Name

Fc fragment of IgG binding protein like 1

Synonyms

9530053A07Rik

MMRRC Submission

040419-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.120) question?

Stock #

R2513 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

28129466-28164811 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to G at 28131635 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Cysteine at position 91 (S91C)

Ref Sequence

ENSEMBL: ENSMUSP00000114986 (fasta)

Gene Model

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

AlphaFold

E9PVG8

Predicted Effect

probably damaging
Transcript: ENSMUST00000059886
AA Change: S91C

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000056479
Gene: ENSMUSG00000078776
AA Change: S91C

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 damaging
Transcript: ENSMUST00000150948
AA Change: S91C

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000114986
Gene: ENSMUSG00000078776
AA Change: S91C

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: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 90 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	T	C	14: 32,661,852 (GRCm38)	T719A	possibly damaging	Het
Abcc1	A	G	16: 14,473,009 (GRCm38)		probably null	Het
Aftph	C	T	11: 20,708,676 (GRCm38)		probably null	Het
Als2	C	A	1: 59,215,117 (GRCm38)	K360N	probably benign	Het
Atg2a	T	A	19: 6,258,046 (GRCm38)		probably null	Het
Axl	T	C	7: 25,787,516 (GRCm38)	D22G	probably benign	Het
Baiap2	G	A	11: 119,999,226 (GRCm38)	A438T	probably benign	Het
Bean1	G	C	8: 104,182,011 (GRCm38)	A7P	probably benign	Het
Birc6	C	G	17: 74,647,729 (GRCm38)	P3431R	probably damaging	Het
Camk1d	A	G	2: 5,714,236 (GRCm38)	M1T	probably null	Het
Carmil3	T	C	14: 55,503,838 (GRCm38)	Y1027H	probably damaging	Het
Ccdc6	G	A	10: 70,187,828 (GRCm38)		probably benign	Het
Cemip	C	A	7: 83,942,025 (GRCm38)	V1280L	probably benign	Het
Cfap58	C	A	19: 47,962,542 (GRCm38)	N447K	probably benign	Het
Chd3	A	G	11: 69,360,645 (GRCm38)	L520P	probably damaging	Het
Col1a2	T	A	6: 4,531,223 (GRCm38)		probably null	Het
Cpne7	A	C	8: 123,117,667 (GRCm38)		probably null	Het
Ctla4	T	C	1: 60,912,564 (GRCm38)	V84A	probably damaging	Het
Dap3	A	G	3: 88,928,258 (GRCm38)	V263A	probably benign	Het
Dhx57	T	A	17: 80,241,949 (GRCm38)		probably null	Het
Dlg5	C	A	14: 24,164,525 (GRCm38)	K663N	probably damaging	Het
Dsg3	C	A	18: 20,523,662 (GRCm38)	F196L	possibly damaging	Het
Eif2ak4	C	A	2: 118,426,583 (GRCm38)	D402E	probably damaging	Het
Fance	T	C	17: 28,318,094 (GRCm38)	V24A	probably benign	Het
Fasn	A	T	11: 120,814,748 (GRCm38)	L1149Q	probably damaging	Het
Flg	T	A	3: 93,279,786 (GRCm38)	S182T	possibly damaging	Het
Gm128	T	A	3: 95,239,982 (GRCm38)	S334C	possibly damaging	Het
Gm3727	A	C	14: 7,264,561 (GRCm38)	H31Q	probably damaging	Het
Gm4841	T	G	18: 60,270,905 (GRCm38)	T39P	probably damaging	Het
Golgb1	G	T	16: 36,915,151 (GRCm38)	V1587L	possibly damaging	Het
Golm1	G	A	13: 59,642,258 (GRCm38)	P243S	probably benign	Het
Gstcd	C	A	3: 133,082,320 (GRCm38)	A206S	possibly damaging	Het
Gstcd	C	A	3: 133,082,321 (GRCm38)	K205N	possibly damaging	Het
Gtf3c1	A	G	7: 125,681,173 (GRCm38)	V355A	probably benign	Het
Hhatl	T	C	9: 121,789,170 (GRCm38)	D173G	probably benign	Het
Kcnu1	T	A	8: 25,905,966 (GRCm38)	C660S	probably benign	Het
Kctd8	T	C	5: 69,110,645 (GRCm38)	D374G	probably benign	Het
Kif21a	T	C	15: 90,994,391 (GRCm38)	I229V	possibly damaging	Het
L3mbtl1	A	T	2: 162,967,585 (GRCm38)	I702F	probably benign	Het
Lce1d	T	C	3: 92,685,759 (GRCm38)		probably benign	Het
Lrig1	C	T	6: 94,617,366 (GRCm38)		probably null	Het
Lrp12	A	T	15: 39,876,111 (GRCm38)	D563E	probably damaging	Het
Lrp2	C	T	2: 69,506,374 (GRCm38)		probably null	Het
Map3k5	G	A	10: 20,094,455 (GRCm38)	V703I	possibly damaging	Het
Mecr	A	G	4: 131,853,765 (GRCm38)	R110G	probably benign	Het
Mtrr	T	A	13: 68,566,973 (GRCm38)	K445*	probably null	Het
Nanos1	T	A	19: 60,756,552 (GRCm38)	L96Q	probably benign	Het
Or13a24	T	G	7: 140,574,156 (GRCm38)	M1R	probably null	Het
Or51t4	T	A	7: 102,949,493 (GRCm38)	F333I	probably benign	Het
Or6c214	T	A	10: 129,755,152 (GRCm38)	L99F	probably damaging	Het
Otog	T	C	7: 46,305,590 (GRCm38)		probably null	Het
Pcdhb3	G	T	18: 37,301,241 (GRCm38)	V87F	probably benign	Het
Pcdhb3	A	T	18: 37,301,240 (GRCm38)	L86F	probably damaging	Het
Pcdhb3	T	A	18: 37,301,239 (GRCm38)	L86*	probably null	Het
Pdgfd	A	G	9: 6,359,894 (GRCm38)	K322E	probably damaging	Het
Picalm	T	C	7: 90,197,009 (GRCm38)	S648P	probably damaging	Het
Pigr	T	C	1: 130,846,620 (GRCm38)	S446P	possibly damaging	Het
Pik3cb	A	C	9: 99,061,842 (GRCm38)	L636W	probably damaging	Het
Pla2g2f	A	T	4: 138,754,162 (GRCm38)	L92Q	probably damaging	Het
Plod3	G	C	5: 136,988,146 (GRCm38)	A50P	probably benign	Het
Prkar2b	C	T	12: 31,975,929 (GRCm38)	V191I	possibly damaging	Het
Prune1	C	A	3: 95,258,119 (GRCm38)	A281S	probably benign	Het
Ptges3l	A	T	11: 101,424,042 (GRCm38)	C42S	possibly damaging	Het
Reg3b	A	T	6: 78,371,819 (GRCm38)	I33L	probably benign	Het
Rel	A	G	11: 23,745,823 (GRCm38)	I188T	probably damaging	Het
Rif1	GCCACCA	GCCA	2: 52,110,324 (GRCm38)		probably benign	Het
Ripor1	G	T	8: 105,617,622 (GRCm38)	V463L	probably benign	Het
Rrm1	T	A	7: 102,460,689 (GRCm38)	D510E	probably damaging	Het
Setd7	A	G	3: 51,533,015 (GRCm38)	S202P	probably damaging	Het
Shank3	T	A	15: 89,548,686 (GRCm38)	D1211E	probably benign	Het
Slc30a1	A	T	1: 191,907,562 (GRCm38)	T186S	possibly damaging	Het
Slc4a4	G	A	5: 89,156,398 (GRCm38)	V523I	probably benign	Het
Slc9a2	T	A	1: 40,742,608 (GRCm38)		probably null	Het
Smg6	A	G	11: 74,929,676 (GRCm38)	T258A	probably damaging	Het
Sptlc1	C	T	13: 53,337,640 (GRCm38)	D408N	possibly damaging	Het
Tasor2	G	T	13: 3,582,150 (GRCm38)	L784I	possibly damaging	Het
Tbl3	T	C	17: 24,704,550 (GRCm38)		probably null	Het
Tdo2	T	C	3: 81,969,505 (GRCm38)	D139G	possibly damaging	Het
Ticam1	T	A	17: 56,271,612 (GRCm38)	H161L	possibly damaging	Het
Tnfaip3	T	A	10: 19,005,659 (GRCm38)	D293V	probably benign	Het
Trim72	G	A	7: 128,004,706 (GRCm38)	V75M	possibly damaging	Het
Trip11	T	A	12: 101,837,727 (GRCm38)	N1632I	possibly damaging	Het
Tspan18	A	T	2: 93,220,095 (GRCm38)	M61K	possibly damaging	Het
Tuba8	A	T	6: 121,225,973 (GRCm38)	E415V	probably damaging	Het
Ung	A	G	5: 114,137,192 (GRCm38)	H214R	probably benign	Het
Uqcrc1	T	C	9: 108,936,768 (GRCm38)	L17P	probably damaging	Het
Usp24	A	G	4: 106,379,405 (GRCm38)		probably null	Het
Vps39	A	C	2: 120,338,787 (GRCm38)	Y245D	probably damaging	Het
Whrn	T	A	4: 63,435,412 (GRCm38)	T373S	probably benign	Het
Zc2hc1a	C	T	3: 7,516,536 (GRCm38)		probably null	Het

Other mutations in Fcgbpl1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00435:Fcgbpl1	APN	7	28,164,528 (GRCm38)	missense	probably damaging	1.00
IGL00757:Fcgbpl1	APN	7	28,154,445 (GRCm38)	missense	probably damaging	1.00
IGL01015:Fcgbpl1	APN	7	28,155,318 (GRCm38)	missense	probably damaging	1.00
IGL01079:Fcgbpl1	APN	7	28,139,778 (GRCm38)	missense	probably damaging	0.99
IGL01343:Fcgbpl1	APN	7	28,150,702 (GRCm38)	missense	probably benign	0.19
IGL01420:Fcgbpl1	APN	7	28,140,133 (GRCm38)	missense	probably benign	0.28
IGL01604:Fcgbpl1	APN	7	28,155,324 (GRCm38)	missense	probably benign	0.11
IGL01666:Fcgbpl1	APN	7	28,153,292 (GRCm38)	missense	probably damaging	1.00
IGL02002:Fcgbpl1	APN	7	28,152,796 (GRCm38)	missense	probably damaging	1.00
IGL02036:Fcgbpl1	APN	7	28,137,525 (GRCm38)	missense	possibly damaging	0.82
IGL02126:Fcgbpl1	APN	7	28,139,856 (GRCm38)	missense	probably damaging	1.00
IGL02150:Fcgbpl1	APN	7	28,146,779 (GRCm38)	nonsense	probably null
IGL02219:Fcgbpl1	APN	7	28,154,635 (GRCm38)	missense	probably damaging	1.00
IGL02563:Fcgbpl1	APN	7	28,157,892 (GRCm38)	missense	probably benign
IGL02804:Fcgbpl1	APN	7	28,153,370 (GRCm38)	missense	probably benign	0.00
IGL02830:Fcgbpl1	APN	7	28,162,923 (GRCm38)	missense	probably damaging	1.00
IGL02943:Fcgbpl1	APN	7	28,147,188 (GRCm38)	missense	probably damaging	1.00
IGL02977:Fcgbpl1	APN	7	28,164,372 (GRCm38)	missense	possibly damaging	0.83
IGL03231:Fcgbpl1	APN	7	28,153,722 (GRCm38)	missense	possibly damaging	0.95
IGL03304:Fcgbpl1	APN	7	28,142,242 (GRCm38)	missense	probably damaging	0.99
herz	UTSW	7	28,153,839 (GRCm38)	missense	possibly damaging	0.72
pulse	UTSW	7	28,153,749 (GRCm38)	missense	probably damaging	1.00
Sinusoidal	UTSW	7	28,140,130 (GRCm38)	missense	probably damaging	1.00
PIT4378001:Fcgbpl1	UTSW	7	28,154,464 (GRCm38)	missense	possibly damaging	0.61
R0023:Fcgbpl1	UTSW	7	28,153,412 (GRCm38)	missense	probably benign	0.00
R0131:Fcgbpl1	UTSW	7	28,137,615 (GRCm38)	missense	probably damaging	1.00
R0131:Fcgbpl1	UTSW	7	28,137,615 (GRCm38)	missense	probably damaging	1.00
R0132:Fcgbpl1	UTSW	7	28,137,615 (GRCm38)	missense	probably damaging	1.00
R0158:Fcgbpl1	UTSW	7	28,155,492 (GRCm38)	missense	probably damaging	1.00
R0230:Fcgbpl1	UTSW	7	28,156,825 (GRCm38)	missense	probably damaging	1.00
R0310:Fcgbpl1	UTSW	7	28,142,274 (GRCm38)	missense	probably benign	0.04
R0448:Fcgbpl1	UTSW	7	28,140,235 (GRCm38)	missense	probably benign	0.03
R0462:Fcgbpl1	UTSW	7	28,137,340 (GRCm38)	missense	probably damaging	1.00
R0481:Fcgbpl1	UTSW	7	28,153,749 (GRCm38)	missense	probably damaging	1.00
R0497:Fcgbpl1	UTSW	7	28,147,465 (GRCm38)	missense	probably damaging	1.00
R0556:Fcgbpl1	UTSW	7	28,159,378 (GRCm38)	missense	probably benign
R0562:Fcgbpl1	UTSW	7	28,162,690 (GRCm38)	missense	probably benign	0.30
R0586:Fcgbpl1	UTSW	7	28,137,091 (GRCm38)	missense	probably damaging	0.99
R0924:Fcgbpl1	UTSW	7	28,140,130 (GRCm38)	missense	probably damaging	1.00
R0930:Fcgbpl1	UTSW	7	28,140,130 (GRCm38)	missense	probably damaging	1.00
R1103:Fcgbpl1	UTSW	7	28,154,520 (GRCm38)	missense	probably damaging	1.00
R1213:Fcgbpl1	UTSW	7	28,157,673 (GRCm38)	missense	probably damaging	1.00
R1292:Fcgbpl1	UTSW	7	28,142,794 (GRCm38)	splice site	probably benign
R1368:Fcgbpl1	UTSW	7	28,159,478 (GRCm38)	missense	possibly damaging	0.89
R1451:Fcgbpl1	UTSW	7	28,137,157 (GRCm38)	missense	probably damaging	1.00
R1477:Fcgbpl1	UTSW	7	28,157,093 (GRCm38)	missense	probably benign	0.01
R1538:Fcgbpl1	UTSW	7	28,155,492 (GRCm38)	missense	probably damaging	1.00
R1655:Fcgbpl1	UTSW	7	28,147,110 (GRCm38)	missense	probably damaging	0.98
R1697:Fcgbpl1	UTSW	7	28,154,347 (GRCm38)	missense	probably damaging	1.00
R1741:Fcgbpl1	UTSW	7	28,157,854 (GRCm38)	missense	probably damaging	0.98
R1796:Fcgbpl1	UTSW	7	28,155,372 (GRCm38)	missense	probably damaging	1.00
R1853:Fcgbpl1	UTSW	7	28,155,546 (GRCm38)	nonsense	probably null
R1861:Fcgbpl1	UTSW	7	28,154,732 (GRCm38)	missense	probably damaging	1.00
R1909:Fcgbpl1	UTSW	7	28,144,348 (GRCm38)	missense	possibly damaging	0.52
R1971:Fcgbpl1	UTSW	7	28,131,512 (GRCm38)	missense	possibly damaging	0.90
R1990:Fcgbpl1	UTSW	7	28,154,360 (GRCm38)	missense	probably damaging	0.98
R2020:Fcgbpl1	UTSW	7	28,155,594 (GRCm38)	missense	probably benign
R2084:Fcgbpl1	UTSW	7	28,157,535 (GRCm38)	missense	probably damaging	1.00
R2125:Fcgbpl1	UTSW	7	28,158,022 (GRCm38)	missense	probably benign	0.00
R2132:Fcgbpl1	UTSW	7	28,155,474 (GRCm38)	missense	probably damaging	1.00
R2913:Fcgbpl1	UTSW	7	28,164,307 (GRCm38)	missense	probably damaging	1.00
R3150:Fcgbpl1	UTSW	7	28,154,195 (GRCm38)	missense	probably benign	0.21
R3499:Fcgbpl1	UTSW	7	28,154,555 (GRCm38)	missense	probably benign	0.42
R3702:Fcgbpl1	UTSW	7	28,157,778 (GRCm38)	missense	probably damaging	1.00
R3881:Fcgbpl1	UTSW	7	28,140,038 (GRCm38)	nonsense	probably null
R3938:Fcgbpl1	UTSW	7	28,154,294 (GRCm38)	missense	probably damaging	1.00
R4050:Fcgbpl1	UTSW	7	28,152,985 (GRCm38)	missense	possibly damaging	0.55
R4152:Fcgbpl1	UTSW	7	28,156,897 (GRCm38)	missense	possibly damaging	0.47
R4168:Fcgbpl1	UTSW	7	28,137,109 (GRCm38)	missense	probably benign	0.05
R4235:Fcgbpl1	UTSW	7	28,156,648 (GRCm38)	missense	probably damaging	0.99
R4241:Fcgbpl1	UTSW	7	28,154,335 (GRCm38)	missense	probably damaging	1.00
R4363:Fcgbpl1	UTSW	7	28,146,906 (GRCm38)	missense	probably damaging	1.00
R4460:Fcgbpl1	UTSW	7	28,152,856 (GRCm38)	missense	probably benign	0.17
R4463:Fcgbpl1	UTSW	7	28,150,719 (GRCm38)	missense	probably benign
R4841:Fcgbpl1	UTSW	7	28,150,722 (GRCm38)	missense	probably damaging	1.00
R4842:Fcgbpl1	UTSW	7	28,150,722 (GRCm38)	missense	probably damaging	1.00
R4876:Fcgbpl1	UTSW	7	28,142,800 (GRCm38)	intron	probably benign
R4905:Fcgbpl1	UTSW	7	28,156,983 (GRCm38)	missense	possibly damaging	0.93
R4997:Fcgbpl1	UTSW	7	28,143,924 (GRCm38)	missense	possibly damaging	0.77
R5091:Fcgbpl1	UTSW	7	28,156,958 (GRCm38)	missense	probably benign	0.44
R5159:Fcgbpl1	UTSW	7	28,153,308 (GRCm38)	missense	probably benign	0.09
R5326:Fcgbpl1	UTSW	7	28,155,489 (GRCm38)	missense	probably damaging	0.98
R5396:Fcgbpl1	UTSW	7	28,140,183 (GRCm38)	missense	probably benign
R5441:Fcgbpl1	UTSW	7	28,156,914 (GRCm38)	missense	probably damaging	1.00
R5480:Fcgbpl1	UTSW	7	28,157,999 (GRCm38)	nonsense	probably null
R5542:Fcgbpl1	UTSW	7	28,155,489 (GRCm38)	missense	probably damaging	0.98
R5571:Fcgbpl1	UTSW	7	28,156,569 (GRCm38)	missense	probably damaging	0.99
R5613:Fcgbpl1	UTSW	7	28,142,878 (GRCm38)	intron	probably benign
R5637:Fcgbpl1	UTSW	7	28,152,852 (GRCm38)	missense	probably benign	0.00
R5766:Fcgbpl1	UTSW	7	28,137,329 (GRCm38)	nonsense	probably null
R6174:Fcgbpl1	UTSW	7	28,139,959 (GRCm38)	missense	probably damaging	0.96
R6233:Fcgbpl1	UTSW	7	28,131,460 (GRCm38)	missense	probably damaging	0.99
R6250:Fcgbpl1	UTSW	7	28,150,714 (GRCm38)	missense	probably damaging	1.00
R6379:Fcgbpl1	UTSW	7	28,157,592 (GRCm38)	missense	probably damaging	1.00
R6442:Fcgbpl1	UTSW	7	28,144,186 (GRCm38)	missense	possibly damaging	0.88
R6478:Fcgbpl1	UTSW	7	28,155,373 (GRCm38)	missense	probably damaging	1.00
R6699:Fcgbpl1	UTSW	7	28,144,368 (GRCm38)	missense	probably damaging	1.00
R6852:Fcgbpl1	UTSW	7	28,147,135 (GRCm38)	missense	probably damaging	1.00
R6883:Fcgbpl1	UTSW	7	28,152,835 (GRCm38)	missense	possibly damaging	0.89
R6902:Fcgbpl1	UTSW	7	28,137,213 (GRCm38)	missense	probably damaging	1.00
R6903:Fcgbpl1	UTSW	7	28,137,213 (GRCm38)	missense	probably damaging	1.00
R6904:Fcgbpl1	UTSW	7	28,137,213 (GRCm38)	missense	probably damaging	1.00
R6992:Fcgbpl1	UTSW	7	28,140,183 (GRCm38)	missense	probably benign	0.04
R7023:Fcgbpl1	UTSW	7	28,140,038 (GRCm38)	nonsense	probably null
R7039:Fcgbpl1	UTSW	7	28,140,148 (GRCm38)	missense	possibly damaging	0.80
R7171:Fcgbpl1	UTSW	7	28,154,519 (GRCm38)	nonsense	probably null
R7282:Fcgbpl1	UTSW	7	28,144,408 (GRCm38)	missense	probably benign	0.02
R7291:Fcgbpl1	UTSW	7	28,140,220 (GRCm38)	missense	probably benign
R7344:Fcgbpl1	UTSW	7	28,152,760 (GRCm38)	missense	possibly damaging	0.46
R7344:Fcgbpl1	UTSW	7	28,140,279 (GRCm38)	missense	possibly damaging	0.79
R7392:Fcgbpl1	UTSW	7	28,164,372 (GRCm38)	missense	possibly damaging	0.83
R7531:Fcgbpl1	UTSW	7	28,140,231 (GRCm38)	missense	probably benign
R7541:Fcgbpl1	UTSW	7	28,144,256 (GRCm38)	nonsense	probably null
R7577:Fcgbpl1	UTSW	7	28,154,423 (GRCm38)	missense	possibly damaging	0.65
R7594:Fcgbpl1	UTSW	7	28,131,460 (GRCm38)	missense	probably damaging	0.99
R7647:Fcgbpl1	UTSW	7	28,140,045 (GRCm38)	missense	probably benign	0.00
R7718:Fcgbpl1	UTSW	7	28,147,201 (GRCm38)	missense	probably damaging	1.00
R7733:Fcgbpl1	UTSW	7	28,139,965 (GRCm38)	missense	probably damaging	1.00
R7737:Fcgbpl1	UTSW	7	28,157,073 (GRCm38)	missense	probably damaging	1.00
R7908:Fcgbpl1	UTSW	7	28,147,496 (GRCm38)	missense	probably benign	0.12
R8013:Fcgbpl1	UTSW	7	28,137,541 (GRCm38)	missense	probably benign	0.14
R8014:Fcgbpl1	UTSW	7	28,137,541 (GRCm38)	missense	probably benign	0.14
R8151:Fcgbpl1	UTSW	7	28,153,341 (GRCm38)	missense	possibly damaging	0.95
R8175:Fcgbpl1	UTSW	7	28,164,448 (GRCm38)	nonsense	probably null
R8254:Fcgbpl1	UTSW	7	28,147,349 (GRCm38)	missense	possibly damaging	0.63
R8345:Fcgbpl1	UTSW	7	28,155,360 (GRCm38)	missense	probably damaging	1.00
R8414:Fcgbpl1	UTSW	7	28,142,733 (GRCm38)	missense	probably damaging	1.00
R8419:Fcgbpl1	UTSW	7	28,143,921 (GRCm38)	missense	probably damaging	1.00
R8496:Fcgbpl1	UTSW	7	28,143,952 (GRCm38)	missense	possibly damaging	0.81
R8691:Fcgbpl1	UTSW	7	28,153,839 (GRCm38)	missense	possibly damaging	0.72
R8785:Fcgbpl1	UTSW	7	28,154,707 (GRCm38)	missense	probably damaging	1.00
R8863:Fcgbpl1	UTSW	7	28,131,581 (GRCm38)	missense	probably damaging	1.00
R8926:Fcgbpl1	UTSW	7	28,154,444 (GRCm38)	missense	probably damaging	1.00
R8950:Fcgbpl1	UTSW	7	28,164,326 (GRCm38)	missense	probably benign	0.32
R9014:Fcgbpl1	UTSW	7	28,155,451 (GRCm38)	missense	probably damaging	1.00
R9045:Fcgbpl1	UTSW	7	28,154,431 (GRCm38)	missense	probably damaging	1.00
R9115:Fcgbpl1	UTSW	7	28,154,329 (GRCm38)	missense	possibly damaging	0.74
R9233:Fcgbpl1	UTSW	7	28,140,094 (GRCm38)	missense	possibly damaging	0.83
R9330:Fcgbpl1	UTSW	7	28,156,985 (GRCm38)	missense	probably benign	0.02
R9426:Fcgbpl1	UTSW	7	28,143,856 (GRCm38)	missense	possibly damaging	0.92
R9477:Fcgbpl1	UTSW	7	28,152,840 (GRCm38)	missense	probably damaging	1.00
R9502:Fcgbpl1	UTSW	7	28,137,466 (GRCm38)	missense	probably benign	0.09
R9505:Fcgbpl1	UTSW	7	28,142,484 (GRCm38)	nonsense	probably null
R9601:Fcgbpl1	UTSW	7	28,154,380 (GRCm38)	missense	possibly damaging	0.78
R9630:Fcgbpl1	UTSW	7	28,137,199 (GRCm38)	missense	probably damaging	1.00
R9632:Fcgbpl1	UTSW	7	28,142,301 (GRCm38)	missense	probably benign
R9673:Fcgbpl1	UTSW	7	28,156,619 (GRCm38)	missense	probably benign	0.25
R9735:Fcgbpl1	UTSW	7	28,157,010 (GRCm38)	missense	probably damaging	1.00
Z1176:Fcgbpl1	UTSW	7	28,154,762 (GRCm38)	missense	probably benign	0.03
Z1176:Fcgbpl1	UTSW	7	28,142,386 (GRCm38)	missense	probably benign	0.06
Z1177:Fcgbpl1	UTSW	7	28,139,898 (GRCm38)	missense	probably benign	0.25
Z1186:Fcgbpl1	UTSW	7	28,156,986 (GRCm38)	missense	probably benign	0.01
Z1186:Fcgbpl1	UTSW	7	28,146,705 (GRCm38)	missense	probably benign	0.00
Z1186:Fcgbpl1	UTSW	7	28,131,572 (GRCm38)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- AAGGCATTCAGTGTGCACC -3'
(R):5'- GATGGTTTGGGGTCTAACACC -3'

Sequencing Primer
(F):5'- ATTCAGTGTGCACCTGGGC -3'
(R):5'- AACACCAAGGCTATAGCTCCTTTTG -3'

Posted On

2014-12-04