Mutagenetix > Incidental Mutation

Incidental Mutation 'R0981:Fcgbp'

97154

Institutional Source

Beutler Lab

Gene Symbol

Fcgbp

Ensembl Gene

ENSMUSG00000047730

Gene Name

Fc fragment of IgG binding protein

Synonyms

A430096B05Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0981 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

28071236-28120862 bp(+) (GRCm38)

Type of Mutation

nonsense

DNA Base Change (assembly)

T to A at 28085110 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 198 (Y198*)

Ref Sequence

ENSEMBL: ENSMUSP00000114271 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000076648] [ENSMUST00000138392]

AlphaFold

E9Q0B5

Predicted Effect

probably null
Transcript: ENSMUST00000076648
AA Change: Y198*

SMART Domains

Protein: ENSMUSP00000075945
Gene: ENSMUSG00000047730
AA Change: Y198*

Domain	Start	End	E-Value	Type
signal peptide	1	26	N/A	INTRINSIC
FOLN	27	49	2.3e-4	SMART
VWD	46	211	5.26e-45	SMART
low complexity region	226	237	N/A	INTRINSIC
C8	251	326	1.17e-34	SMART
Pfam:TIL	329	383	1.2e-12	PFAM
VWC	385	431	2.34e-1	SMART
FOLN	418	441	3.48e1	SMART
VWD	438	603	6.85e-35	SMART
C8	642	717	1.4e-32	SMART
Pfam:TIL	720	773	4.7e-14	PFAM
VWC	775	829	9.42e-1	SMART
VWD	824	990	7.86e-44	SMART
C8	1034	1109	1.66e-34	SMART
Pfam:TIL	1112	1165	6.7e-13	PFAM
VWC	1167	1225	9.8e-3	SMART
FOLN	1198	1220	9.55e-1	SMART
FOLN	1224	1246	2.41e0	SMART
VWD	1243	1411	6.59e-37	SMART
C8	1451	1527	5.6e-32	SMART
low complexity region	1541	1551	N/A	INTRINSIC
EGF_like	1558	1581	6.15e1	SMART
VWC	1589	1682	1.6e-2	SMART
VWD	1640	1807	5.15e-39	SMART
C8	1839	1914	4.62e-33	SMART
EGF_like	1942	1965	4.46e1	SMART
VWC	1972	2064	1.92e-1	SMART
VWD	2024	2180	6.34e-39	SMART
low complexity region	2201	2214	N/A	INTRINSIC
C8	2221	2296	3.7e-32	SMART
Pfam:TIL	2299	2352	5e-12	PFAM
VWC	2354	2413	8.29e-1	SMART
FOLN	2385	2407	4.96e1	SMART
VWD	2404	2566	1.89e-5	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000138392
AA Change: Y198*

SMART Domains

Protein: ENSMUSP00000114271
Gene: ENSMUSG00000047730
AA Change: Y198*

Domain	Start	End	E-Value	Type
signal peptide	1	26	N/A	INTRINSIC
FOLN	27	49	2.3e-4	SMART
VWD	46	211	5.26e-45	SMART
low complexity region	226	237	N/A	INTRINSIC
C8	251	326	1.17e-34	SMART
Pfam:TIL	329	383	8.4e-13	PFAM
VWC	385	431	2.34e-1	SMART
FOLN	418	441	3.48e1	SMART
VWD	438	603	7.99e-36	SMART
C8	642	717	1.4e-32	SMART
Pfam:TIL	720	773	3.3e-14	PFAM
VWC	775	829	9.42e-1	SMART
VWD	824	990	7.86e-44	SMART
C8	1034	1109	1.66e-34	SMART
Pfam:TIL	1112	1165	6.9e-13	PFAM
VWC	1167	1225	9.8e-3	SMART
FOLN	1198	1220	9.55e-1	SMART
FOLN	1224	1246	2.41e0	SMART
VWD	1243	1411	6.59e-37	SMART
C8	1451	1527	5.6e-32	SMART
low complexity region	1541	1551	N/A	INTRINSIC
EGF_like	1558	1581	6.15e1	SMART
VWC	1589	1682	1.6e-2	SMART
VWD	1640	1807	5.15e-39	SMART
C8	1839	1914	4.62e-33	SMART
EGF_like	1942	1965	4.46e1	SMART
VWC	1972	2064	1.92e-1	SMART
VWD	2024	2180	6.34e-39	SMART
low complexity region	2201	2214	N/A	INTRINSIC
C8	2221	2296	3.7e-32	SMART
Pfam:TIL	2299	2352	1e-11	PFAM
VWC	2354	2413	8.29e-1	SMART
FOLN	2385	2407	4.96e1	SMART
VWD	2404	2566	1.89e-5	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000140004

Coding Region Coverage

1x: 99.5%
3x: 98.4%
10x: 95.4%
20x: 89.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 42 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aars2	T	A	17: 45,520,331 (GRCm38)	C942S	probably damaging	Het
Alpk1	T	C	3: 127,679,402 (GRCm38)	N984S	possibly damaging	Het
Ankrd55	T	C	13: 112,323,076 (GRCm38)	V68A	possibly damaging	Het
Asap2	T	C	12: 21,265,960 (GRCm38)	S960P	probably damaging	Het
Atp2b1	T	A	10: 99,015,629 (GRCm38)	N66K	probably damaging	Het
Cckar	C	T	5: 53,706,290 (GRCm38)	G39R	probably damaging	Het
Col11a1	G	A	3: 114,138,765 (GRCm38)	R113H	unknown	Het
Cpb1	C	A	3: 20,275,490 (GRCm38)	R24L	probably benign	Het
Dlg5	T	G	14: 24,154,631 (GRCm38)	R1258S	probably damaging	Het
Fam71e2	T	A	7: 4,757,589 (GRCm38)		probably null	Het
Fanci	A	G	7: 79,405,166 (GRCm38)	Q148R	probably benign	Het
Gapt	G	C	13: 110,353,739 (GRCm38)	T130R	probably damaging	Het
Glis1	A	G	4: 107,615,042 (GRCm38)	E272G	probably damaging	Het
Gm13741	T	C	2: 87,656,234 (GRCm38)	N229S	probably benign	Het
Gsdmc4	T	A	15: 63,892,073 (GRCm38)	I392F	probably damaging	Het
H2-M2	T	C	17: 37,482,630 (GRCm38)	T162A	probably benign	Het
Hk2	G	A	6: 82,743,968 (GRCm38)	R190W	probably damaging	Het
Irf1	T	C	11: 53,773,722 (GRCm38)	*52R	probably null	Het
Lman2l	T	A	1: 36,445,233 (GRCm38)	M1L	unknown	Het
Mgat1	C	T	11: 49,261,055 (GRCm38)	R122C	probably damaging	Het
Mtrf1	T	C	14: 79,401,590 (GRCm38)	L54S	probably benign	Het
Myo5c	A	T	9: 75,271,591 (GRCm38)	L676F	probably damaging	Het
Odf3	A	G	7: 140,848,295 (GRCm38)	M7V	probably benign	Het
Ofcc1	A	G	13: 40,072,698 (GRCm38)	I786T	probably damaging	Het
Olfr488	GGTAG	GG	7: 108,256,022 (GRCm38)		probably benign	Het
Olfr488	AGGT	A	7: 108,256,021 (GRCm38)		probably benign	Het
Pfn1	G	A	11: 70,652,138 (GRCm38)	R137C	probably benign	Het
Pgbd5	G	A	8: 124,384,293 (GRCm38)	R129*	probably null	Het
Pibf1	T	C	14: 99,150,743 (GRCm38)		probably null	Het
Pkd2l1	A	G	19: 44,154,422 (GRCm38)		probably null	Het
Plin5	C	A	17: 56,114,020 (GRCm38)	R215L	probably damaging	Het
Prrc2c	C	T	1: 162,705,981 (GRCm38)		probably benign	Het
Rnasel	T	G	1: 153,759,599 (GRCm38)	C608G	probably benign	Het
Slc28a2	T	A	2: 122,450,984 (GRCm38)	V218D	probably damaging	Het
Snx1	T	C	9: 66,109,559 (GRCm38)	I29V	probably benign	Het
Tenm3	A	G	8: 48,298,965 (GRCm38)	W939R	probably damaging	Het
Tmem237	C	A	1: 59,118,005 (GRCm38)	R15L	probably damaging	Het
Tmx3	T	C	18: 90,537,200 (GRCm38)	V347A	probably benign	Het
Vmn1r191	T	C	13: 22,179,219 (GRCm38)	T122A	probably benign	Het
Wdfy4	G	T	14: 33,147,092 (GRCm38)	N326K	probably benign	Het
Zfp408	A	G	2: 91,645,183 (GRCm38)	L642P	probably benign	Het
Zfp808	C	A	13: 62,171,673 (GRCm38)	H239N	possibly damaging	Het

Other mutations in Fcgbp

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00309:Fcgbp	APN	7	28,085,130 (GRCm38)	missense	probably damaging	1.00
IGL00331:Fcgbp	APN	7	28,101,541 (GRCm38)	splice site	probably benign
IGL00335:Fcgbp	APN	7	28,086,135 (GRCm38)	missense	possibly damaging	0.90
IGL00470:Fcgbp	APN	7	28,075,086 (GRCm38)	nonsense	probably null
IGL00491:Fcgbp	APN	7	28,093,402 (GRCm38)	missense	probably damaging	1.00
IGL00498:Fcgbp	APN	7	28,091,797 (GRCm38)	missense	probably damaging	1.00
IGL01296:Fcgbp	APN	7	28,089,647 (GRCm38)	missense	probably benign	0.15
IGL01582:Fcgbp	APN	7	28,093,642 (GRCm38)	missense	probably benign	0.19
IGL01929:Fcgbp	APN	7	28,103,963 (GRCm38)	missense	probably damaging	1.00
IGL02024:Fcgbp	APN	7	28,106,374 (GRCm38)	missense	probably damaging	1.00
IGL02027:Fcgbp	APN	7	28,075,204 (GRCm38)	missense	probably damaging	1.00
IGL02140:Fcgbp	APN	7	28,091,954 (GRCm38)	missense	probably damaging	1.00
IGL02162:Fcgbp	APN	7	28,075,235 (GRCm38)	missense	probably damaging	1.00
IGL02345:Fcgbp	APN	7	28,071,643 (GRCm38)	splice site	probably benign
IGL02377:Fcgbp	APN	7	28,106,970 (GRCm38)	missense	possibly damaging	0.67
IGL02389:Fcgbp	APN	7	28,075,171 (GRCm38)	missense	probably damaging	1.00
IGL02423:Fcgbp	APN	7	28,089,953 (GRCm38)	missense	probably benign	0.02
IGL02523:Fcgbp	APN	7	28,104,732 (GRCm38)	missense	possibly damaging	0.89
IGL02561:Fcgbp	APN	7	28,101,174 (GRCm38)	intron	probably benign
IGL02631:Fcgbp	APN	7	28,085,298 (GRCm38)	missense	probably damaging	1.00
IGL02716:Fcgbp	APN	7	28,101,434 (GRCm38)	missense	probably damaging	0.98
IGL02836:Fcgbp	APN	7	28,117,358 (GRCm38)	missense	possibly damaging	0.91
IGL02957:Fcgbp	APN	7	28,091,847 (GRCm38)	nonsense	probably null
IGL02971:Fcgbp	APN	7	28,101,473 (GRCm38)	missense	probably damaging	1.00
IGL03284:Fcgbp	APN	7	28,085,432 (GRCm38)	missense	possibly damaging	0.93
IGL03379:Fcgbp	APN	7	28,089,917 (GRCm38)	missense	possibly damaging	0.76
bilge	UTSW	7	28,117,337 (GRCm38)	missense	probably benign	0.00
R6548_fcgbp_365	UTSW	7	28,091,918 (GRCm38)	missense	probably benign	0.00
swill	UTSW	7	28,089,734 (GRCm38)	missense	probably damaging	1.00
G1citation:Fcgbp	UTSW	7	28,107,356 (GRCm38)	missense	probably damaging	1.00
IGL02796:Fcgbp	UTSW	7	28,101,151 (GRCm38)	intron	probably benign
PIT4486001:Fcgbp	UTSW	7	28,075,273 (GRCm38)	missense	possibly damaging	0.52
R0277:Fcgbp	UTSW	7	28,085,493 (GRCm38)	critical splice donor site	probably null
R0387:Fcgbp	UTSW	7	28,091,454 (GRCm38)	splice site	probably benign
R0586:Fcgbp	UTSW	7	28,089,713 (GRCm38)	missense	probably damaging	1.00
R0987:Fcgbp	UTSW	7	28,094,174 (GRCm38)	missense	probably damaging	1.00
R1240:Fcgbp	UTSW	7	28,120,525 (GRCm38)	missense	probably damaging	1.00
R1394:Fcgbp	UTSW	7	28,093,379 (GRCm38)	missense	probably damaging	0.98
R1395:Fcgbp	UTSW	7	28,093,379 (GRCm38)	missense	probably damaging	0.98
R1438:Fcgbp	UTSW	7	28,103,733 (GRCm38)	nonsense	probably null
R1474:Fcgbp	UTSW	7	28,091,848 (GRCm38)	missense	probably benign	0.00
R1521:Fcgbp	UTSW	7	28,075,160 (GRCm38)	missense	probably benign	0.00
R1740:Fcgbp	UTSW	7	28,101,249 (GRCm38)	missense	possibly damaging	0.87
R1750:Fcgbp	UTSW	7	28,093,443 (GRCm38)	nonsense	probably null
R1772:Fcgbp	UTSW	7	28,105,175 (GRCm38)	missense	possibly damaging	0.90
R1804:Fcgbp	UTSW	7	28,086,139 (GRCm38)	missense	probably benign
R1808:Fcgbp	UTSW	7	28,085,090 (GRCm38)	missense	probably benign	0.04
R1819:Fcgbp	UTSW	7	28,085,283 (GRCm38)	missense	probably benign	0.00
R1934:Fcgbp	UTSW	7	28,107,093 (GRCm38)	missense	probably damaging	1.00
R1972:Fcgbp	UTSW	7	28,094,192 (GRCm38)	missense	probably benign	0.11
R2051:Fcgbp	UTSW	7	28,120,360 (GRCm38)	missense	probably damaging	0.97
R2072:Fcgbp	UTSW	7	28,120,389 (GRCm38)	missense	probably damaging	0.98
R2074:Fcgbp	UTSW	7	28,120,389 (GRCm38)	missense	probably damaging	0.98
R2124:Fcgbp	UTSW	7	28,092,019 (GRCm38)	missense	probably benign	0.03
R2155:Fcgbp	UTSW	7	28,107,203 (GRCm38)	missense	probably benign	0.00
R3015:Fcgbp	UTSW	7	28,075,413 (GRCm38)	splice site	probably benign
R3037:Fcgbp	UTSW	7	28,102,702 (GRCm38)	missense	possibly damaging	0.62
R3151:Fcgbp	UTSW	7	28,117,240 (GRCm38)	missense	probably damaging	1.00
R3176:Fcgbp	UTSW	7	28,091,661 (GRCm38)	missense	probably damaging	0.99
R3177:Fcgbp	UTSW	7	28,091,661 (GRCm38)	missense	probably damaging	0.99
R3276:Fcgbp	UTSW	7	28,091,661 (GRCm38)	missense	probably damaging	0.99
R3277:Fcgbp	UTSW	7	28,091,661 (GRCm38)	missense	probably damaging	0.99
R3623:Fcgbp	UTSW	7	28,101,276 (GRCm38)	missense	probably damaging	1.00
R3730:Fcgbp	UTSW	7	28,085,457 (GRCm38)	missense	possibly damaging	0.82
R3935:Fcgbp	UTSW	7	28,075,399 (GRCm38)	missense	probably benign	0.00
R3936:Fcgbp	UTSW	7	28,075,399 (GRCm38)	missense	probably benign	0.00
R4041:Fcgbp	UTSW	7	28,113,979 (GRCm38)	missense	probably benign	0.01
R4056:Fcgbp	UTSW	7	28,104,116 (GRCm38)	missense	probably benign	0.09
R4057:Fcgbp	UTSW	7	28,104,116 (GRCm38)	missense	probably benign	0.09
R4705:Fcgbp	UTSW	7	28,107,296 (GRCm38)	missense	probably benign	0.44
R4708:Fcgbp	UTSW	7	28,094,961 (GRCm38)	missense	probably benign	0.00
R4710:Fcgbp	UTSW	7	28,094,961 (GRCm38)	missense	probably benign	0.00
R4779:Fcgbp	UTSW	7	28,094,937 (GRCm38)	missense	probably damaging	1.00
R4820:Fcgbp	UTSW	7	28,113,958 (GRCm38)	missense	probably damaging	1.00
R4863:Fcgbp	UTSW	7	28,086,344 (GRCm38)	missense	probably benign	0.33
R4926:Fcgbp	UTSW	7	28,086,235 (GRCm38)	missense	probably damaging	0.99
R4947:Fcgbp	UTSW	7	28,089,812 (GRCm38)	missense	probably benign	0.00
R4979:Fcgbp	UTSW	7	28,117,570 (GRCm38)	missense	probably benign	0.06
R5002:Fcgbp	UTSW	7	28,086,103 (GRCm38)	splice site	probably null
R5219:Fcgbp	UTSW	7	28,104,085 (GRCm38)	missense	probably damaging	1.00
R5241:Fcgbp	UTSW	7	28,085,199 (GRCm38)	missense	probably damaging	1.00
R5301:Fcgbp	UTSW	7	28,093,674 (GRCm38)	missense	possibly damaging	0.93
R5306:Fcgbp	UTSW	7	28,091,818 (GRCm38)	missense	probably damaging	1.00
R5335:Fcgbp	UTSW	7	28,089,734 (GRCm38)	missense	probably damaging	1.00
R5399:Fcgbp	UTSW	7	28,105,055 (GRCm38)	missense	probably benign	0.05
R5418:Fcgbp	UTSW	7	28,085,313 (GRCm38)	missense	probably damaging	1.00
R5527:Fcgbp	UTSW	7	28,093,635 (GRCm38)	missense	probably benign
R5583:Fcgbp	UTSW	7	28,091,579 (GRCm38)	missense	probably damaging	1.00
R5698:Fcgbp	UTSW	7	28,092,022 (GRCm38)	missense	possibly damaging	0.95
R5780:Fcgbp	UTSW	7	28,085,218 (GRCm38)	missense	probably benign	0.02
R5813:Fcgbp	UTSW	7	28,101,494 (GRCm38)	missense	possibly damaging	0.64
R5910:Fcgbp	UTSW	7	28,085,503 (GRCm38)	splice site	probably benign
R5936:Fcgbp	UTSW	7	28,086,692 (GRCm38)	missense	probably damaging	0.98
R5992:Fcgbp	UTSW	7	28,120,534 (GRCm38)	missense	probably benign	0.05
R6091:Fcgbp	UTSW	7	28,104,965 (GRCm38)	missense	possibly damaging	0.90
R6372:Fcgbp	UTSW	7	28,107,008 (GRCm38)	missense	probably damaging	1.00
R6488:Fcgbp	UTSW	7	28,093,538 (GRCm38)	missense	probably damaging	0.96
R6548:Fcgbp	UTSW	7	28,091,918 (GRCm38)	missense	probably benign	0.00
R6553:Fcgbp	UTSW	7	28,113,979 (GRCm38)	missense	possibly damaging	0.79
R6585:Fcgbp	UTSW	7	28,113,979 (GRCm38)	missense	possibly damaging	0.79
R6695:Fcgbp	UTSW	7	28,086,270 (GRCm38)	nonsense	probably null
R6711:Fcgbp	UTSW	7	28,089,673 (GRCm38)	missense	probably damaging	0.99
R6803:Fcgbp	UTSW	7	28,103,212 (GRCm38)	missense	probably benign	0.00
R6822:Fcgbp	UTSW	7	28,107,356 (GRCm38)	missense	probably damaging	1.00
R6907:Fcgbp	UTSW	7	28,085,018 (GRCm38)	missense	probably damaging	1.00
R6912:Fcgbp	UTSW	7	28,089,704 (GRCm38)	missense	probably benign	0.15
R6924:Fcgbp	UTSW	7	28,093,823 (GRCm38)	missense	probably benign
R6943:Fcgbp	UTSW	7	28,092,052 (GRCm38)	missense	probably benign	0.22
R7060:Fcgbp	UTSW	7	28,091,933 (GRCm38)	missense	probably benign	0.20
R7103:Fcgbp	UTSW	7	28,084,962 (GRCm38)	missense	probably benign	0.00
R7208:Fcgbp	UTSW	7	28,104,021 (GRCm38)	missense	probably benign	0.01
R7291:Fcgbp	UTSW	7	28,101,392 (GRCm38)	missense	probably benign	0.00
R7301:Fcgbp	UTSW	7	28,093,436 (GRCm38)	missense	possibly damaging	0.65
R7404:Fcgbp	UTSW	7	28,101,507 (GRCm38)	missense	probably damaging	1.00
R7426:Fcgbp	UTSW	7	28,086,524 (GRCm38)	missense	probably benign	0.00
R7459:Fcgbp	UTSW	7	28,107,285 (GRCm38)	missense	possibly damaging	0.65
R7475:Fcgbp	UTSW	7	28,102,976 (GRCm38)	missense	probably damaging	0.99
R7505:Fcgbp	UTSW	7	28,089,674 (GRCm38)	missense	probably damaging	0.97
R7517:Fcgbp	UTSW	7	28,085,369 (GRCm38)	missense	probably damaging	1.00
R7519:Fcgbp	UTSW	7	28,086,299 (GRCm38)	missense	probably damaging	1.00
R7524:Fcgbp	UTSW	7	28,102,966 (GRCm38)	missense	probably damaging	1.00
R7649:Fcgbp	UTSW	7	28,091,503 (GRCm38)	missense	possibly damaging	0.88
R7782:Fcgbp	UTSW	7	28,085,035 (GRCm38)	nonsense	probably null
R7820:Fcgbp	UTSW	7	28,120,359 (GRCm38)	missense	probably benign	0.01
R7831:Fcgbp	UTSW	7	28,106,979 (GRCm38)	missense	probably damaging	0.98
R7835:Fcgbp	UTSW	7	28,117,207 (GRCm38)	missense	possibly damaging	0.64
R7947:Fcgbp	UTSW	7	28,104,170 (GRCm38)	critical splice donor site	probably null
R8086:Fcgbp	UTSW	7	28,113,964 (GRCm38)	missense	probably damaging	1.00
R8137:Fcgbp	UTSW	7	28,105,071 (GRCm38)	missense	probably damaging	1.00
R8154:Fcgbp	UTSW	7	28,085,082 (GRCm38)	missense	probably benign	0.00
R8169:Fcgbp	UTSW	7	28,085,494 (GRCm38)	critical splice donor site	probably null
R8176:Fcgbp	UTSW	7	28,091,749 (GRCm38)	missense	possibly damaging	0.88
R8193:Fcgbp	UTSW	7	28,104,851 (GRCm38)	missense	probably damaging	1.00
R8313:Fcgbp	UTSW	7	28,086,344 (GRCm38)	missense	probably benign	0.00
R8350:Fcgbp	UTSW	7	28,094,189 (GRCm38)	missense	probably benign	0.02
R8382:Fcgbp	UTSW	7	28,117,337 (GRCm38)	missense	probably benign	0.00
R8393:Fcgbp	UTSW	7	28,107,390 (GRCm38)	missense	probably benign	0.18
R8438:Fcgbp	UTSW	7	28,089,806 (GRCm38)	missense	probably benign	0.25
R8489:Fcgbp	UTSW	7	28,105,010 (GRCm38)	missense	possibly damaging	0.94
R8495:Fcgbp	UTSW	7	28,086,553 (GRCm38)	missense	probably damaging	1.00
R8707:Fcgbp	UTSW	7	28,120,495 (GRCm38)	missense	probably benign	0.01
R8736:Fcgbp	UTSW	7	28,106,196 (GRCm38)	missense	probably benign	0.05
R8816:Fcgbp	UTSW	7	28,084,987 (GRCm38)	missense	probably benign	0.09
R8905:Fcgbp	UTSW	7	28,086,509 (GRCm38)	missense	probably damaging	1.00
R9031:Fcgbp	UTSW	7	28,091,483 (GRCm38)	missense	possibly damaging	0.89
R9063:Fcgbp	UTSW	7	28,091,852 (GRCm38)	missense	probably damaging	1.00
R9180:Fcgbp	UTSW	7	28,103,773 (GRCm38)	nonsense	probably null
R9262:Fcgbp	UTSW	7	28,120,527 (GRCm38)	missense	probably damaging	1.00
R9439:Fcgbp	UTSW	7	28,104,011 (GRCm38)	missense	possibly damaging	0.60
R9526:Fcgbp	UTSW	7	28,091,512 (GRCm38)	missense	probably damaging	1.00
R9603:Fcgbp	UTSW	7	28,103,138 (GRCm38)	missense	probably damaging	1.00
R9635:Fcgbp	UTSW	7	28,101,407 (GRCm38)	missense	probably benign	0.40
R9703:Fcgbp	UTSW	7	28,106,975 (GRCm38)	missense	probably damaging	0.98
R9711:Fcgbp	UTSW	7	28,093,575 (GRCm38)	missense	probably benign	0.00
R9733:Fcgbp	UTSW	7	28,103,587 (GRCm38)	missense	probably damaging	1.00
RF002:Fcgbp	UTSW	7	28,089,755 (GRCm38)	missense	probably benign
X0028:Fcgbp	UTSW	7	28,104,020 (GRCm38)	missense	possibly damaging	0.48
Z1186:Fcgbp	UTSW	7	28,091,647 (GRCm38)	missense	probably benign
Z1186:Fcgbp	UTSW	7	28,089,755 (GRCm38)	missense	probably benign
Z1186:Fcgbp	UTSW	7	28,086,191 (GRCm38)	missense	probably benign
Z1186:Fcgbp	UTSW	7	28,103,884 (GRCm38)	missense	probably benign	0.09
Z1186:Fcgbp	UTSW	7	28,093,345 (GRCm38)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TGTAATGAGCTTGCCGTTCTGCC -3'
(R):5'- ACAGAGACGGTCTCCCTTGTAGTG -3'

Sequencing Primer
(F):5'- attgttggggtgggggg -3'
(R):5'- CTCCCTTGTAGTGTTGGGTC -3'

Posted On

2014-01-05