Mutagenetix > Incidental Mutation

Incidental Mutation 'R1368:Fcgbpl1'

155877

Institutional Source

Beutler Lab

Gene Symbol

Fcgbpl1

Ensembl Gene

ENSMUSG00000078776

Gene Name

Fc fragment of IgG binding protein like 1

Synonyms

9530053A07Rik

MMRRC Submission

039433-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.098) question?

Stock #

R1368 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

28129466-28164811 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 28159478 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Arginine at position 2341 (Q2341R)

Ref Sequence

ENSEMBL: ENSMUSP00000114986 (fasta)

Gene Model

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

AlphaFold

E9PVG8

Predicted Effect

possibly damaging
Transcript: ENSMUST00000059886
AA Change: Q2341R

PolyPhen 2 Score 0.895 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000056479
Gene: ENSMUSG00000078776
AA Change: Q2341R

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

possibly damaging
Transcript: ENSMUST00000150948
AA Change: Q2341R

PolyPhen 2 Score 0.895 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000114986
Gene: ENSMUSG00000078776
AA Change: Q2341R

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

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.1%
20x: 95.1%

Validation Efficiency

98% (55/56)

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca13	A	G	11: 9,291,836 (GRCm38)	D1233G	probably benign	Het
Abcc8	G	A	7: 46,122,860 (GRCm38)	R832W	probably damaging	Het
Atp10b	A	G	11: 43,202,154 (GRCm38)	T439A	probably damaging	Het
Brd10	C	A	19: 29,716,396 (GRCm38)	S1966I	probably damaging	Het
C130073F10Rik	T	A	4: 101,890,756 (GRCm38)	N74Y	possibly damaging	Het
Cct8	G	A	16: 87,491,312 (GRCm38)	S124L	probably damaging	Het
Cdh9	T	A	15: 16,848,482 (GRCm38)		probably benign	Het
Cep290	C	T	10: 100,494,966 (GRCm38)		probably benign	Het
Chrng	T	A	1: 87,205,853 (GRCm38)	L10H	probably damaging	Het
Cnn3	T	C	3: 121,457,137 (GRCm38)	L189S	probably benign	Het
Cog4	A	G	8: 110,858,525 (GRCm38)		probably benign	Het
Cxcl12	A	G	6: 117,176,150 (GRCm38)		probably benign	Het
Eif2b2	G	A	12: 85,223,456 (GRCm38)	A257T	probably damaging	Het
Entrep2	A	T	7: 64,819,877 (GRCm38)	V41E	probably damaging	Het
Fanca	G	A	8: 123,304,281 (GRCm38)		probably benign	Het
Fktn	G	A	4: 53,734,880 (GRCm38)	G173R	probably damaging	Het
Gabbr2	T	C	4: 46,674,464 (GRCm38)	N841S	probably benign	Het
Gm5622	T	A	14: 51,662,190 (GRCm38)	V167E	possibly damaging	Het
Gnaq	T	C	19: 16,378,287 (GRCm38)	V289A	probably benign	Het
Gpatch2l	T	G	12: 86,260,665 (GRCm38)	D272E	possibly damaging	Het
Gzmg	G	A	14: 56,157,806 (GRCm38)	T74I	probably benign	Het
Ikzf2	G	A	1: 69,539,315 (GRCm38)	A271V	possibly damaging	Het
Lig4	T	C	8: 9,971,176 (GRCm38)	D868G	possibly damaging	Het
Mfsd6	T	C	1: 52,708,605 (GRCm38)	E367G	possibly damaging	Het
Mpz	T	C	1: 171,159,964 (GRCm38)	L223P	probably damaging	Het
Muc17	T	C	5: 137,146,826 (GRCm38)		probably benign	Het
Or2f1b	C	A	6: 42,762,679 (GRCm38)	T209K	possibly damaging	Het
Pdcd2	G	T	17: 15,526,584 (GRCm38)	N104K	probably damaging	Het
Pigg	G	T	5: 108,317,288 (GRCm38)	G129V	probably damaging	Het
Ppp3cc	T	C	14: 70,245,862 (GRCm38)	Y254C	probably damaging	Het
Prl3b1	G	A	13: 27,243,865 (GRCm38)	A53T	probably benign	Het
Psg23	A	G	7: 18,614,720 (GRCm38)	V54A	probably benign	Het
Psmd3	A	G	11: 98,682,920 (GRCm38)	D64G	probably damaging	Het
Psmg2	CTTCAGTT	CTTCAGTTCAGTT	18: 67,646,025 (GRCm38)		probably null	Het
Ptgdr	T	A	14: 44,853,342 (GRCm38)	I320F	probably damaging	Het
Rad50	T	A	11: 53,683,245 (GRCm38)	K722*	probably null	Het
Rasl10b	G	A	11: 83,417,839 (GRCm38)		probably null	Het
Rgs9	G	A	11: 109,248,151 (GRCm38)	S255L	probably benign	Het
Ror1	C	T	4: 100,441,137 (GRCm38)	P569L	possibly damaging	Het
Rsad2	T	C	12: 26,447,148 (GRCm38)		probably null	Het
Scn8a	A	G	15: 101,035,541 (GRCm38)	D1501G	probably damaging	Het
Sema3c	A	G	5: 17,678,332 (GRCm38)	T313A	possibly damaging	Het
Serpinc1	T	A	1: 160,993,524 (GRCm38)	F59L	probably damaging	Het
Sike1	A	G	3: 102,996,184 (GRCm38)	D63G	possibly damaging	Het
Slc25a11	T	A	11: 70,645,526 (GRCm38)		probably null	Het
Slc32a1	A	G	2: 158,611,320 (GRCm38)	M27V	probably benign	Het
Smc5	A	G	19: 23,210,443 (GRCm38)	V1003A	probably damaging	Het
Tll2	G	A	19: 41,120,228 (GRCm38)	R328C	probably damaging	Het
Topaz1	A	G	9: 122,748,250 (GRCm38)	E75G	possibly damaging	Het
Tspan3	A	T	9: 56,147,499 (GRCm38)	V48E	probably benign	Het
Ugt1a6b	T	C	1: 88,107,636 (GRCm38)	I232T	probably benign	Het
Unc79	A	G	12: 103,156,513 (GRCm38)	K2290E	probably damaging	Het
Vmn1r19	T	C	6: 57,404,671 (GRCm38)	F70L	probably benign	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
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
R2513:Fcgbpl1	UTSW	7	28,131,635 (GRCm38)	missense	probably damaging	0.99
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'- TTGGAGACTGCCTGCCACATTCAC -3'
(R):5'- CTCACATTTGACCTGCTGAGCCTG -3'

Sequencing Primer
(F):5'- ACCTTGTCTCCTCTCCCTAACAG -3'
(R):5'- gggtgatcagtacagcgac -3'

Posted On

2014-02-11