Mutagenetix > Incidental Mutation

Incidental Mutation 'R5191:Fyb2'

398128

Institutional Source

Beutler Lab

Gene Symbol

Fyb2

Ensembl Gene

ENSMUSG00000078612

Gene Name

FYN binding protein 2

Synonyms

1700024P16Rik

MMRRC Submission

043263-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.083) question?

Stock #

R5191 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

104770653-104874060 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 104852994 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Phenylalanine at position 558 (C558F)

Ref Sequence

ENSEMBL: ENSMUSP00000102415 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000106803] [ENSMUST00000106804]

AlphaFold

A2A995

Predicted Effect

possibly damaging
Transcript: ENSMUST00000106803
AA Change: C558F

PolyPhen 2 Score 0.877 (Sensitivity: 0.83; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000102415
Gene: ENSMUSG00000078612
AA Change: C558F

Domain	Start	End	E-Value	Type
low complexity region	120	132	N/A	INTRINSIC
low complexity region	340	349	N/A	INTRINSIC
low complexity region	442	459	N/A	INTRINSIC
low complexity region	537	549	N/A	INTRINSIC
low complexity region	567	578	N/A	INTRINSIC
low complexity region	682	697	N/A	INTRINSIC
SH3	735	791	3.82e0	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000106804
AA Change: C494F

PolyPhen 2 Score 0.778 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000102416
Gene: ENSMUSG00000078612
AA Change: C494F

Domain	Start	End	E-Value	Type
low complexity region	56	68	N/A	INTRINSIC
low complexity region	276	285	N/A	INTRINSIC
low complexity region	378	395	N/A	INTRINSIC
low complexity region	473	485	N/A	INTRINSIC
low complexity region	503	514	N/A	INTRINSIC
low complexity region	618	633	N/A	INTRINSIC
SH3	671	727	3.82e0	SMART

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.4%

Validation Efficiency

100% (69/69)

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acvrl1	A	G	15: 101,034,946 (GRCm39)	E235G	probably damaging	Het
Adam26b	T	C	8: 43,973,028 (GRCm39)	D658G	probably damaging	Het
Adamts12	A	G	15: 11,327,843 (GRCm39)	R1407G	probably benign	Het
Aknad1	T	C	3: 108,659,306 (GRCm39)	S107P	probably benign	Het
Aknad1	G	A	3: 108,659,867 (GRCm39)	V294I	probably benign	Het
Arfgef2	A	G	2: 166,718,431 (GRCm39)	T1407A	probably damaging	Het
Atp5f1a	C	T	18: 77,867,929 (GRCm39)	P318S	probably damaging	Het
Atp9a	C	T	2: 168,503,983 (GRCm39)	V494M	possibly damaging	Het
Ccdc69	A	T	11: 54,943,719 (GRCm39)		probably null	Het
Crh	T	C	3: 19,748,093 (GRCm39)	E183G	probably damaging	Het
Cyp2c40	A	C	19: 39,791,035 (GRCm39)	N265K	probably damaging	Het
D630003M21Rik	C	T	2: 158,042,955 (GRCm39)	A862T	probably benign	Het
Dact3	T	G	7: 16,609,375 (GRCm39)	V9G	probably damaging	Het
Dnaaf9	A	T	2: 130,579,323 (GRCm39)	I638N	possibly damaging	Het
Dnah8	A	G	17: 30,965,739 (GRCm39)	E2357G	probably damaging	Het
Dzip1	C	T	14: 119,148,805 (GRCm39)	M291I	probably damaging	Het
Etl4	G	T	2: 20,344,810 (GRCm39)	S38I	probably damaging	Het
Galnt3	T	C	2: 65,924,050 (GRCm39)	E406G	probably damaging	Het
Golga3	T	A	5: 110,332,173 (GRCm39)		probably benign	Het
Gpr179	T	A	11: 97,228,975 (GRCm39)	Q1060L	possibly damaging	Het
Havcr1	A	T	11: 46,647,024 (GRCm39)	I153F	probably benign	Het
Hnrnpc	A	T	14: 52,314,964 (GRCm39)	V141E	probably damaging	Het
Kcnj2	C	T	11: 110,963,297 (GRCm39)	Q230*	probably null	Het
Lgr6	C	T	1: 134,921,748 (GRCm39)	A199T	probably damaging	Het
Limch1	T	C	5: 67,184,904 (GRCm39)	L631P	probably damaging	Het
Lpin1	T	C	12: 16,630,829 (GRCm39)	N23S	possibly damaging	Het
Macf1	A	G	4: 123,366,755 (GRCm39)	S1104P	probably benign	Het
Man2b1	A	G	8: 85,811,088 (GRCm39)	D73G	probably damaging	Het
Marf1	A	G	16: 13,963,942 (GRCm39)	F454L	probably damaging	Het
Mcpt4	T	A	14: 56,298,466 (GRCm39)	I90L	probably benign	Het
Mfsd4b5	T	C	10: 39,846,668 (GRCm39)	E304G	probably damaging	Het
Mst1r	G	A	9: 107,788,750 (GRCm39)	R423H	probably damaging	Het
Muc20	G	A	16: 32,614,846 (GRCm39)	S177L	unknown	Het
Muc5b	A	G	7: 141,412,276 (GRCm39)	T1741A	unknown	Het
Myo1g	C	T	11: 6,465,105 (GRCm39)	A447T	probably benign	Het
Nr1h2	C	A	7: 44,199,840 (GRCm39)	A360S	probably damaging	Het
Nufip1	A	G	14: 76,349,429 (GRCm39)	K154E	probably damaging	Het
Or12k8	T	G	2: 36,974,990 (GRCm39)	M257L	probably benign	Het
Or2a54	T	A	6: 43,092,800 (GRCm39)	N41K	probably damaging	Het
Or7e166	G	A	9: 19,624,630 (GRCm39)	C169Y	probably damaging	Het
Pecr	A	T	1: 72,314,136 (GRCm39)		probably null	Het
Pkd2	G	A	5: 104,634,547 (GRCm39)	R526Q	probably benign	Het
Plec	T	C	15: 76,059,365 (GRCm39)	E3551G	probably damaging	Het
Rufy4	T	C	1: 74,186,822 (GRCm39)	C537R	probably damaging	Het
Sarm1	G	A	11: 78,387,945 (GRCm39)	Q114*	probably null	Het
Sec31a	T	C	5: 100,553,370 (GRCm39)	E112G	possibly damaging	Het
Slc22a30	G	A	19: 8,321,757 (GRCm39)	Q436*	probably null	Het
Slc9a2	G	T	1: 40,783,053 (GRCm39)	R439L	probably damaging	Het
Sptb	C	A	12: 76,659,608 (GRCm39)	E1097D	probably benign	Het
Stk38	A	C	17: 29,193,344 (GRCm39)	C362G	probably benign	Het
Stmn2	A	T	3: 8,610,635 (GRCm39)	M40L	probably benign	Het
Sytl2	A	T	7: 90,024,860 (GRCm39)	T283S	probably damaging	Het
Tcf4	A	G	18: 69,775,954 (GRCm39)	S48G	probably damaging	Het
Tlr4	A	T	4: 66,759,616 (GRCm39)	H803L	probably damaging	Het
Ttn	C	T	2: 76,709,432 (GRCm39)		probably benign	Het
Tyk2	G	T	9: 21,018,793 (GRCm39)	Q1099K	probably damaging	Het
Usp30	C	T	5: 114,203,755 (GRCm39)		probably benign	Het
Vmn1r175	A	G	7: 23,508,447 (GRCm39)	V60A	possibly damaging	Het
Zc3h12d	C	A	10: 7,743,582 (GRCm39)	P451T	possibly damaging	Het
Zeb2	T	C	2: 44,892,612 (GRCm39)	S146G	probably benign	Het
Zfp236	T	A	18: 82,639,548 (GRCm39)	N1233I	probably damaging	Het
Zfp954	A	G	7: 7,119,022 (GRCm39)	V174A	probably damaging	Het
Zswim1	G	A	2: 164,667,939 (GRCm39)	S397N	probably benign	Het

Other mutations in Fyb2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00664:Fyb2	APN	4	104,872,913 (GRCm39)	missense	probably damaging	1.00
IGL01155:Fyb2	APN	4	104,856,583 (GRCm39)	missense	probably benign	0.00
IGL01632:Fyb2	APN	4	104,853,008 (GRCm39)	missense	probably benign
IGL01746:Fyb2	APN	4	104,802,404 (GRCm39)	missense	probably benign	0.01
IGL02381:Fyb2	APN	4	104,805,863 (GRCm39)	splice site	probably benign
IGL02590:Fyb2	APN	4	104,836,250 (GRCm39)	missense	probably damaging	1.00
IGL02885:Fyb2	APN	4	104,861,118 (GRCm39)	missense	probably damaging	0.99
IGL03114:Fyb2	APN	4	104,852,975 (GRCm39)	missense	probably damaging	0.97
IGL03189:Fyb2	APN	4	104,872,939 (GRCm39)	missense	probably damaging	1.00
IGL03231:Fyb2	APN	4	104,843,460 (GRCm39)	nonsense	probably null
R0076:Fyb2	UTSW	4	104,802,661 (GRCm39)	missense	possibly damaging	0.46
R0662:Fyb2	UTSW	4	104,852,895 (GRCm39)	missense	possibly damaging	0.46
R0723:Fyb2	UTSW	4	104,873,063 (GRCm39)	missense	probably benign	0.00
R1216:Fyb2	UTSW	4	104,852,903 (GRCm39)	missense	possibly damaging	0.86
R1672:Fyb2	UTSW	4	104,808,059 (GRCm39)	missense	probably benign	0.10
R1710:Fyb2	UTSW	4	104,861,113 (GRCm39)	missense	probably damaging	1.00
R1900:Fyb2	UTSW	4	104,802,652 (GRCm39)	missense	probably benign	0.06
R1965:Fyb2	UTSW	4	104,770,846 (GRCm39)	missense	probably benign	0.00
R2106:Fyb2	UTSW	4	104,802,769 (GRCm39)	missense	probably benign	0.01
R5236:Fyb2	UTSW	4	104,805,957 (GRCm39)	missense	probably benign	0.00
R5277:Fyb2	UTSW	4	104,872,876 (GRCm39)	missense	probably damaging	1.00
R5502:Fyb2	UTSW	4	104,802,521 (GRCm39)	missense	probably damaging	1.00
R5769:Fyb2	UTSW	4	104,872,841 (GRCm39)	missense	probably damaging	1.00
R5769:Fyb2	UTSW	4	104,870,518 (GRCm39)	missense	probably damaging	1.00
R6167:Fyb2	UTSW	4	104,802,661 (GRCm39)	missense	possibly damaging	0.46
R6169:Fyb2	UTSW	4	104,857,713 (GRCm39)	missense	probably benign	0.16
R6371:Fyb2	UTSW	4	104,852,975 (GRCm39)	missense	probably damaging	0.97
R6582:Fyb2	UTSW	4	104,802,739 (GRCm39)	missense	probably benign	0.00
R6713:Fyb2	UTSW	4	104,847,432 (GRCm39)	missense	probably benign	0.16
R6719:Fyb2	UTSW	4	104,867,656 (GRCm39)	missense	probably benign	0.07
R7484:Fyb2	UTSW	4	104,870,499 (GRCm39)	missense	probably benign	0.01
R7534:Fyb2	UTSW	4	104,856,545 (GRCm39)	nonsense	probably null
R7590:Fyb2	UTSW	4	104,802,443 (GRCm39)	missense	probably benign	0.01
R7699:Fyb2	UTSW	4	104,867,651 (GRCm39)	missense	probably benign	0.07
R7700:Fyb2	UTSW	4	104,867,651 (GRCm39)	missense	probably benign	0.07
R8041:Fyb2	UTSW	4	104,857,681 (GRCm39)	missense	possibly damaging	0.82
R8298:Fyb2	UTSW	4	104,806,028 (GRCm39)	missense	probably damaging	0.99
R8300:Fyb2	UTSW	4	104,857,689 (GRCm39)	missense	probably damaging	1.00
R8755:Fyb2	UTSW	4	104,861,086 (GRCm39)	missense	unknown
R8817:Fyb2	UTSW	4	104,802,652 (GRCm39)	missense	probably benign	0.06
R8873:Fyb2	UTSW	4	104,856,538 (GRCm39)	missense	probably damaging	1.00
R8914:Fyb2	UTSW	4	104,857,700 (GRCm39)	missense	probably benign	0.09
R9224:Fyb2	UTSW	4	104,853,105 (GRCm39)	missense	probably benign	0.44
R9434:Fyb2	UTSW	4	104,847,534 (GRCm39)	missense	probably damaging	0.99
R9512:Fyb2	UTSW	4	104,853,100 (GRCm39)	missense	probably benign	0.00
R9589:Fyb2	UTSW	4	104,872,833 (GRCm39)	missense	probably damaging	1.00
R9634:Fyb2	UTSW	4	104,856,579 (GRCm39)	nonsense	probably null
R9758:Fyb2	UTSW	4	104,802,961 (GRCm39)	missense	probably benign	0.01
X0018:Fyb2	UTSW	4	104,802,407 (GRCm39)	missense	probably benign	0.04
Z1176:Fyb2	UTSW	4	104,770,857 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- ATTGCCAGGGATGAGTGCAG -3'
(R):5'- ACCATTGAAAATGTGCCCAAG -3'

Sequencing Primer
(F):5'- GAGTGCAGCTATGTCTCTAATAGC -3'
(R):5'- CCCAAGTAAAAGGCTGTGGTCAC -3'

Posted On

2016-07-06