Mutagenetix > Incidental Mutation

Incidental Mutation 'R7110:Fscn2'

551465

Institutional Source

Beutler Lab

Gene Symbol

Fscn2

Ensembl Gene

ENSMUSG00000025380

Gene Name

fascin actin-bundling protein 2

Synonyms

ahl8, C630046B20Rik

MMRRC Submission

045202-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.137) question?

Stock #

R7110 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

120252360-120258994 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 120257580 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Serine at position 314 (T314S)

Ref Sequence

ENSEMBL: ENSMUSP00000026445 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000026445] [ENSMUST00000026448]

AlphaFold

Q32M02

Predicted Effect

probably benign
Transcript: ENSMUST00000026445
AA Change: T314S

PolyPhen 2 Score 0.191 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000026445
Gene: ENSMUSG00000025380
AA Change: T314S

Domain	Start	End	E-Value	Type
Pfam:Fascin	20	133	4.9e-34	PFAM
Pfam:Fascin	141	254	1.2e-26	PFAM
Pfam:Fascin	266	376	8.9e-35	PFAM
Pfam:Fascin	389	492	4.1e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000026448

SMART Domains

Protein: ENSMUSP00000026448
Gene: ENSMUSG00000025384

Domain	Start	End	E-Value	Type
Pfam:FANCAA	447	879	1.4e-196	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (62/62)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the fascin protein family. Fascins crosslink actin into filamentous bundles within dynamic cell extensions. This family member is proposed to play a role in photoreceptor disk morphogenesis. A mutation in this gene results in one form of autosomal dominant retinitis pigmentosa and macular degeneration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for disruptions in this gene display retinal generation with structural abnormalities of the outer segment and depressed rod and cone ERGs that worsen with age. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810065E05Rik	A	G	11: 58,316,571 (GRCm39)	T184A	possibly damaging	Het
Abca4	T	A	3: 121,926,292 (GRCm39)	Y1243N	probably damaging	Het
Adamts7	A	G	9: 90,076,017 (GRCm39)	T1250A	possibly damaging	Het
Adgrg3	T	C	8: 95,761,591 (GRCm39)	V118A	possibly damaging	Het
Agrn	A	G	4: 156,263,332 (GRCm39)	V364A	possibly damaging	Het
Cacna2d1	C	A	5: 16,562,782 (GRCm39)	L853I	probably damaging	Het
Ccdc25	A	G	14: 66,094,165 (GRCm39)	K124R	probably benign	Het
Ccdc73	A	G	2: 104,803,569 (GRCm39)	M236V	probably benign	Het
Cdh1	G	A	8: 107,395,176 (GRCm39)	D862N	possibly damaging	Het
Cdh5	A	G	8: 104,867,400 (GRCm39)	D559G	probably damaging	Het
Celsr2	C	A	3: 108,305,181 (GRCm39)	G2133C	probably damaging	Het
Chd5	A	G	4: 152,469,896 (GRCm39)	N1823S	probably damaging	Het
Cog7	T	C	7: 121,534,999 (GRCm39)	N562S	probably damaging	Het
Dcaf6	A	T	1: 165,179,537 (GRCm39)	S534R	probably benign	Het
Donson	G	A	16: 91,479,009 (GRCm39)	R436*	probably null	Het
Fam53c	T	A	18: 34,895,523 (GRCm39)		probably null	Het
Foxi3	A	G	6: 70,937,730 (GRCm39)	T321A	probably benign	Het
Frmd4b	A	T	6: 97,273,192 (GRCm39)	Y733*	probably null	Het
Gfral	A	G	9: 76,072,112 (GRCm39)	I386T	possibly damaging	Het
Gm21698	T	C	5: 26,190,175 (GRCm39)	E174G	probably damaging	Het
Gm40460	CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG	CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG	7: 141,794,554 (GRCm39)		probably benign	Het
Gprin1	T	C	13: 54,887,056 (GRCm39)	D406G	probably benign	Het
Habp2	A	T	19: 56,299,596 (GRCm39)	R128*	probably null	Het
Hoxc10	A	T	15: 102,879,356 (GRCm39)	Y292F	probably damaging	Het
Hydin	A	T	8: 111,081,583 (GRCm39)		probably null	Het
Igkv12-89	T	C	6: 68,812,115 (GRCm39)	D18G	probably damaging	Het
Jhy	T	C	9: 40,828,556 (GRCm39)	N450S	probably damaging	Het
Klhl18	T	A	9: 110,279,833 (GRCm39)	Q119L	probably damaging	Het
Krt1	AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC	AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC	15: 101,758,813 (GRCm39)		probably benign	Het
Lsmem1	A	T	12: 40,235,272 (GRCm39)		probably null	Het
Ly75	A	G	2: 60,206,528 (GRCm39)	I47T	probably benign	Het
Med12l	C	A	3: 59,169,645 (GRCm39)	T1603K	possibly damaging	Het
Mgat5	A	G	1: 127,310,716 (GRCm39)	D210G	possibly damaging	Het
Mgmt	G	T	7: 136,687,715 (GRCm39)	G55W	probably damaging	Het
Mrpl57	G	A	14: 58,063,754 (GRCm39)		probably benign	Het
Mtg1	G	A	7: 139,726,779 (GRCm39)	R209Q	probably benign	Het
Muc21	CGGGGTGGGTGTAGATCCTGAGGCAGTGCTGGATACAGGGGTGGTTGGGGTGGGTGAAGAGCCTGAGGCAGTGCTGGATGCAGGGGTGGTCGGGGTAGGTGTAGATCCTGAGGCAGTGCT	CGGGGTGGGTGAAGAGCCTGAGGCAGTGCTGGATGCAGGGGTGGTCGGGGTAGGTGTAGATCCTGAGGCAGTGCT	17: 35,933,510 (GRCm39)		probably benign	Het
Muc5ac	T	G	7: 141,353,559 (GRCm39)	C826W	possibly damaging	Het
Myot	A	G	18: 44,474,453 (GRCm39)	D146G	probably damaging	Het
Nlrp4f	T	A	13: 65,347,160 (GRCm39)	I11F	probably damaging	Het
Nsun5	T	A	5: 135,400,104 (GRCm39)	Y76N	probably damaging	Het
Or7a42	A	T	10: 78,791,284 (GRCm39)	M82L	possibly damaging	Het
Pcdhb3	A	G	18: 37,435,975 (GRCm39)	N647S	possibly damaging	Het
Pdgfra	T	A	5: 75,349,895 (GRCm39)	Y926*	probably null	Het
Pdzd2	A	T	15: 12,368,099 (GRCm39)	L2630H	probably damaging	Het
Phox2b	G	A	5: 67,253,505 (GRCm39)	S297L	unknown	Het
Polr3e	T	A	7: 120,539,510 (GRCm39)		probably null	Het
Ppp4r2	T	A	6: 100,842,823 (GRCm39)	V238E	probably damaging	Het
Proc	A	T	18: 32,266,441 (GRCm39)	F129I	probably benign	Het
Sgca	T	A	11: 94,854,227 (GRCm39)		probably null	Het
Slc7a10	A	G	7: 34,899,009 (GRCm39)	H360R	probably benign	Het
Slurp2	G	A	15: 74,614,964 (GRCm39)	T59I	probably benign	Het
Son	A	G	16: 91,453,406 (GRCm39)	T718A	probably benign	Het
Sorbs1	G	C	19: 40,365,244 (GRCm39)	R180G	probably benign	Het
Spink7	T	C	18: 62,727,338 (GRCm39)	N62S	probably damaging	Het
Stxbp3	C	A	3: 108,723,649 (GRCm39)	R195S	probably damaging	Het
Sulf1	G	A	1: 12,908,825 (GRCm39)	V613M	probably damaging	Het
Tbc1d9b	A	T	11: 50,054,657 (GRCm39)	I934F	probably benign	Het
Tecpr2	T	G	12: 110,885,406 (GRCm39)	L195R	probably damaging	Het
Tns2	G	C	15: 102,013,801 (GRCm39)	C71S	probably damaging	Het
Tulp4	C	T	17: 6,282,055 (GRCm39)	H695Y	probably damaging	Het
Usp40	G	T	1: 87,913,884 (GRCm39)	T403K	probably benign	Het
Vat1	G	T	11: 101,356,539 (GRCm39)	R141S	possibly damaging	Het
Vmn2r28	T	G	7: 5,493,733 (GRCm39)	N71T	probably benign	Het

Other mutations in Fscn2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01684:Fscn2	APN	11	120,258,131 (GRCm39)	missense	probably damaging	0.99
IGL01767:Fscn2	APN	11	120,258,576 (GRCm39)	missense	possibly damaging	0.82
IGL02212:Fscn2	APN	11	120,252,881 (GRCm39)	missense	probably damaging	1.00
IGL02299:Fscn2	APN	11	120,253,025 (GRCm39)	missense	probably benign	0.09
IGL02494:Fscn2	APN	11	120,253,228 (GRCm39)	missense	probably benign	0.02
IGL02716:Fscn2	APN	11	120,257,550 (GRCm39)	missense	probably benign	0.00
IGL02882:Fscn2	APN	11	120,253,325 (GRCm39)	missense	probably benign
IGL02986:Fscn2	APN	11	120,258,176 (GRCm39)	missense	possibly damaging	0.74
bundle	UTSW	11	120,258,852 (GRCm39)	missense	probably damaging	1.00
R0513_Fscn2_038	UTSW	11	120,252,706 (GRCm39)	missense	probably damaging	1.00
R7170_Fscn2_209	UTSW	11	120,253,335 (GRCm39)	missense	probably damaging	0.98
ANU74:Fscn2	UTSW	11	120,253,162 (GRCm39)	missense	probably damaging	1.00
R0277:Fscn2	UTSW	11	120,258,837 (GRCm39)	missense	probably damaging	1.00
R0323:Fscn2	UTSW	11	120,258,837 (GRCm39)	missense	probably damaging	1.00
R0513:Fscn2	UTSW	11	120,252,706 (GRCm39)	missense	probably damaging	1.00
R1451:Fscn2	UTSW	11	120,252,848 (GRCm39)	missense	probably damaging	0.98
R1620:Fscn2	UTSW	11	120,257,511 (GRCm39)	missense	probably damaging	1.00
R1736:Fscn2	UTSW	11	120,258,852 (GRCm39)	missense	probably damaging	1.00
R2212:Fscn2	UTSW	11	120,252,417 (GRCm39)	start gained	probably benign
R2327:Fscn2	UTSW	11	120,257,527 (GRCm39)	missense	probably damaging	1.00
R2384:Fscn2	UTSW	11	120,257,559 (GRCm39)	missense	possibly damaging	0.48
R2397:Fscn2	UTSW	11	120,252,995 (GRCm39)	missense	probably damaging	1.00
R4624:Fscn2	UTSW	11	120,258,169 (GRCm39)	missense	probably benign	0.21
R4634:Fscn2	UTSW	11	120,258,546 (GRCm39)	missense	possibly damaging	0.65
R4784:Fscn2	UTSW	11	120,258,813 (GRCm39)	missense	possibly damaging	0.82
R5062:Fscn2	UTSW	11	120,257,575 (GRCm39)	missense	probably damaging	1.00
R5084:Fscn2	UTSW	11	120,252,686 (GRCm39)	missense	probably damaging	0.96
R5514:Fscn2	UTSW	11	120,258,858 (GRCm39)	missense	probably damaging	1.00
R5780:Fscn2	UTSW	11	120,257,494 (GRCm39)	missense	probably benign	0.14
R6073:Fscn2	UTSW	11	120,252,613 (GRCm39)	nonsense	probably null
R6345:Fscn2	UTSW	11	120,252,853 (GRCm39)	missense	probably damaging	0.99
R7170:Fscn2	UTSW	11	120,253,335 (GRCm39)	missense	probably damaging	0.98
R7171:Fscn2	UTSW	11	120,253,335 (GRCm39)	missense	probably damaging	0.98
R7538:Fscn2	UTSW	11	120,258,152 (GRCm39)	missense	possibly damaging	0.55
R7917:Fscn2	UTSW	11	120,258,082 (GRCm39)	missense	possibly damaging	0.79
R9468:Fscn2	UTSW	11	120,253,283 (GRCm39)	missense	probably damaging	1.00
R9541:Fscn2	UTSW	11	120,258,771 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGACTTCATGCTACCCCAAAG -3'
(R):5'- ATGACCGAAGTGACAGTGGTC -3'

Sequencing Primer
(F):5'- AAAGCACACTTCCCCATCCTTCTC -3'
(R):5'- CAGATCTCTGGGTTGGAAACTAC -3'

Posted On

2019-05-15