Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01634:Fscn3'

93526

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Fscn3

Ensembl Gene

ENSMUSG00000029707

Gene Name

fascin actin-bundling protein 3

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.195) question?

Stock #

IGL01634

Quality Score

Status

Chromosome

Chromosomal Location

28427888-28438621 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 28430537 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 236 (Y236N)

Ref Sequence

ENSEMBL: ENSMUSP00000031719 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000020717] [ENSMUST00000031719] [ENSMUST00000064377] [ENSMUST00000169841]

AlphaFold

Q9QXW4

Predicted Effect

probably benign
Transcript: ENSMUST00000020717

SMART Domains

Protein: ENSMUSP00000020717
Gene: ENSMUSG00000020440

Domain	Start	End	E-Value	Type
ARF	1	180	5.83e-121	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000031719
AA Change: Y236N

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000031719
Gene: ENSMUSG00000029707
AA Change: Y236N

Domain	Start	End	E-Value	Type
Pfam:Fascin	24	138	1e-29	PFAM
SCOP:d1dfca2	146	260	2e-48	SMART
Pfam:Fascin	271	381	2.1e-26	PFAM
SCOP:d1dfca4	386	498	3e-53	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000064377

SMART Domains

Protein: ENSMUSP00000067395
Gene: ENSMUSG00000029708

Domain	Start	End	E-Value	Type
coiled coil region	13	61	N/A	INTRINSIC
low complexity region	93	109	N/A	INTRINSIC
low complexity region	130	153	N/A	INTRINSIC
coiled coil region	156	315	N/A	INTRINSIC
low complexity region	408	418	N/A	INTRINSIC
low complexity region	432	443	N/A	INTRINSIC
low complexity region	479	491	N/A	INTRINSIC
Blast:H2B	492	590	3e-8	BLAST
low complexity region	613	631	N/A	INTRINSIC
coiled coil region	659	701	N/A	INTRINSIC
Grip	719	766	8.28e-20	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000147036

Predicted Effect

probably benign
Transcript: ENSMUST00000169841

SMART Domains

Protein: ENSMUSP00000127281
Gene: ENSMUSG00000020440

Domain	Start	End	E-Value	Type
ARF	1	180	5.83e-121	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700034H15Rik	A	T	1: 191,633,016 (GRCm39)		noncoding transcript	Het
4933421I07Rik	C	T	7: 42,097,123 (GRCm39)	D63N	probably benign	Het
Alg9	C	A	9: 50,686,677 (GRCm39)		probably null	Het
Anln	T	C	9: 22,271,771 (GRCm39)	T695A	probably benign	Het
Aox4	G	T	1: 58,261,089 (GRCm39)	D141Y	possibly damaging	Het
Arhgap21	C	A	2: 20,919,455 (GRCm39)	Q84H	probably benign	Het
Arnt	G	A	3: 95,377,709 (GRCm39)		probably benign	Het
Atp8a2	T	A	14: 60,235,511 (GRCm39)	Y677F	probably benign	Het
Car6	C	T	4: 150,282,610 (GRCm39)	V12M	probably benign	Het
Cd209d	A	T	8: 3,927,974 (GRCm39)		probably null	Het
Ctnna1	T	A	18: 35,356,501 (GRCm39)	V390E	probably damaging	Het
Cypt4	T	A	9: 24,536,952 (GRCm39)	N147K	possibly damaging	Het
Dnah10	C	A	5: 124,898,405 (GRCm39)	A3729E	probably damaging	Het
Dusp8	A	G	7: 141,638,160 (GRCm39)	V156A	probably benign	Het
Ecm1	G	A	3: 95,642,211 (GRCm39)	P458L	probably damaging	Het
Fat3	T	G	9: 15,909,654 (GRCm39)	Y2116S	probably damaging	Het
Gaa	G	A	11: 119,164,902 (GRCm39)	S265N	possibly damaging	Het
Gas7	T	C	11: 67,565,057 (GRCm39)		probably benign	Het
Gbp8	T	C	5: 105,166,438 (GRCm39)	K297R	probably damaging	Het
Gm1818	G	A	12: 48,602,992 (GRCm39)		noncoding transcript	Het
Gm5114	G	T	7: 39,058,071 (GRCm39)	T516K	probably benign	Het
Hectd1	A	G	12: 51,850,562 (GRCm39)	S165P	probably damaging	Het
Hoxb4	G	T	11: 96,209,726 (GRCm39)	R44L	probably damaging	Het
Ivd	G	A	2: 118,706,863 (GRCm39)	R285H	probably damaging	Het
Krtap20-2	T	C	16: 89,002,977 (GRCm39)	F59S	unknown	Het
Megf8	G	A	7: 25,058,206 (GRCm39)		probably benign	Het
Mgat4d	A	T	8: 84,094,745 (GRCm39)	M261L	possibly damaging	Het
Mlc1	A	T	15: 88,858,921 (GRCm39)		probably benign	Het
Mmp20	T	A	9: 7,635,149 (GRCm39)	Y43*	probably null	Het
Morc3	G	A	16: 93,670,125 (GRCm39)	V767I	probably benign	Het
Myo15a	A	G	11: 60,386,298 (GRCm39)	T1808A	probably damaging	Het
Notch4	T	C	17: 34,791,562 (GRCm39)	F574L	probably damaging	Het
Npas3	G	A	12: 53,993,946 (GRCm39)	V164M	probably damaging	Het
Nptx1	A	G	11: 119,435,498 (GRCm39)	Y273H	probably damaging	Het
Oaf	T	C	9: 43,135,301 (GRCm39)	N159S	probably damaging	Het
Or10a3n	A	T	7: 108,493,292 (GRCm39)	F107L	probably benign	Het
Or4c111	T	A	2: 88,843,788 (GRCm39)	I207F	probably damaging	Het
Or5ak24	A	T	2: 85,260,783 (GRCm39)	L130H	probably damaging	Het
Pgm2	T	C	5: 64,258,317 (GRCm39)	F101L	probably benign	Het
Pkd1l3	A	C	8: 110,394,157 (GRCm39)		probably null	Het
Plcd1	C	T	9: 118,902,857 (GRCm39)	R527H	probably damaging	Het
Rexo2	C	T	9: 48,380,215 (GRCm39)	E206K	probably damaging	Het
Ropn1	C	A	16: 34,487,148 (GRCm39)	T28N	possibly damaging	Het
Ropn1	A	T	16: 34,487,141 (GRCm39)	I26F	probably damaging	Het
Rpgrip1l	C	A	8: 91,979,171 (GRCm39)	S998I	probably benign	Het
Rpgrip1l	T	A	8: 91,979,172 (GRCm39)	S998C	probably benign	Het
Scap	T	C	9: 110,207,857 (GRCm39)		probably null	Het
Sec23b	T	C	2: 144,401,150 (GRCm39)	Y4H	probably damaging	Het
Sfrp4	C	A	13: 19,807,800 (GRCm39)	D66E	possibly damaging	Het
Slc25a36	T	C	9: 96,962,534 (GRCm39)	T13A	probably benign	Het
Synpr	A	T	14: 13,608,576 (GRCm38)	I119F	possibly damaging	Het
Tamm41	A	C	6: 114,993,059 (GRCm39)	H109Q	probably benign	Het
Tet1	A	T	10: 62,714,367 (GRCm39)	I476K	possibly damaging	Het
Tg	A	T	15: 66,601,415 (GRCm39)	I142F	probably benign	Het
Thada	A	T	17: 84,700,786 (GRCm39)		probably null	Het
Triobp	T	C	15: 78,877,568 (GRCm39)	L1654P	probably damaging	Het
Trpm7	A	G	2: 126,668,738 (GRCm39)	V726A	probably damaging	Het
Txndc15	T	G	13: 55,869,438 (GRCm39)	V197G	probably damaging	Het
Ubr3	A	T	2: 69,803,916 (GRCm39)	T1169S	probably benign	Het
Uhmk1	C	T	1: 170,034,682 (GRCm39)		probably null	Het
Vmn2r16	T	A	5: 109,488,177 (GRCm39)	M350K	probably benign	Het
Vmn2r77	G	A	7: 86,460,857 (GRCm39)	V728I	probably benign	Het
Wipf1	G	A	2: 73,278,225 (GRCm39)	P7S	unknown	Het
Zswim3	A	G	2: 164,661,922 (GRCm39)	D134G	probably damaging	Het

Other mutations in Fscn3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01290:Fscn3	APN	6	28,430,505 (GRCm39)	missense	probably benign	0.43
IGL01312:Fscn3	APN	6	28,434,469 (GRCm39)	missense	probably damaging	0.99
IGL01899:Fscn3	APN	6	28,436,078 (GRCm39)	missense	probably damaging	1.00
IGL01928:Fscn3	APN	6	28,430,181 (GRCm39)	missense	possibly damaging	0.65
IGL02334:Fscn3	APN	6	28,428,153 (GRCm39)	splice site	probably null
IGL02959:Fscn3	APN	6	28,435,997 (GRCm39)	missense	possibly damaging	0.93
IGL03201:Fscn3	APN	6	28,430,604 (GRCm39)	missense	probably benign	0.07
IGL03202:Fscn3	APN	6	28,434,451 (GRCm39)	missense	probably benign	0.10
IGL03227:Fscn3	APN	6	28,434,429 (GRCm39)	missense	probably benign	0.00
0152:Fscn3	UTSW	6	28,429,966 (GRCm39)	unclassified	probably benign
R1478:Fscn3	UTSW	6	28,430,567 (GRCm39)	missense	probably benign
R1502:Fscn3	UTSW	6	28,435,622 (GRCm39)	missense	probably benign	0.05
R1955:Fscn3	UTSW	6	28,430,235 (GRCm39)	missense	possibly damaging	0.82
R2122:Fscn3	UTSW	6	28,430,388 (GRCm39)	missense	probably benign	0.18
R2135:Fscn3	UTSW	6	28,431,583 (GRCm39)	missense	probably benign	0.02
R3713:Fscn3	UTSW	6	28,428,091 (GRCm39)	missense	possibly damaging	0.89
R3715:Fscn3	UTSW	6	28,428,091 (GRCm39)	missense	possibly damaging	0.89
R3778:Fscn3	UTSW	6	28,430,031 (GRCm39)	missense	possibly damaging	0.72
R4572:Fscn3	UTSW	6	28,430,634 (GRCm39)	splice site	probably null
R4745:Fscn3	UTSW	6	28,435,627 (GRCm39)	missense	probably damaging	0.98
R4764:Fscn3	UTSW	6	28,436,200 (GRCm39)	makesense	probably null
R4794:Fscn3	UTSW	6	28,430,595 (GRCm39)	missense	probably damaging	1.00
R5738:Fscn3	UTSW	6	28,430,030 (GRCm39)	missense	possibly damaging	0.56
R5951:Fscn3	UTSW	6	28,436,173 (GRCm39)	missense	possibly damaging	0.88
R5994:Fscn3	UTSW	6	28,430,294 (GRCm39)	missense	probably benign
R6595:Fscn3	UTSW	6	28,430,174 (GRCm39)	missense	probably damaging	1.00
R7323:Fscn3	UTSW	6	28,431,544 (GRCm39)	missense	possibly damaging	0.53
R7738:Fscn3	UTSW	6	28,434,445 (GRCm39)	missense	probably benign	0.01
R7840:Fscn3	UTSW	6	28,430,175 (GRCm39)	missense	probably damaging	1.00
R8169:Fscn3	UTSW	6	28,430,328 (GRCm39)	missense	possibly damaging	0.79
R8991:Fscn3	UTSW	6	28,434,472 (GRCm39)	missense	probably benign
R9111:Fscn3	UTSW	6	28,430,310 (GRCm39)	missense	probably damaging	0.98
R9350:Fscn3	UTSW	6	28,430,432 (GRCm39)	nonsense	probably null
R9370:Fscn3	UTSW	6	28,434,535 (GRCm39)	missense	probably benign
R9410:Fscn3	UTSW	6	28,430,432 (GRCm39)	nonsense	probably null

Posted On

2013-12-09