Mutagenetix > Incidental Mutations

Incidental Mutation 'IGL02428:Flnc'

292987

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Flnc

Ensembl Gene

ENSMUSG00000068699

Gene Name

filamin C, gamma

Synonyms

1110055E19Rik, actin binding protein 280, Fln2

Accession Numbers

Is this an essential gene?

Essential (E-score: 1.000) question?

Stock #

IGL02428

Quality Score

Status

Chromosome

Chromosomal Location

29433256-29461883 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 29451485 bp

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 1566 (D1566G)

Ref Sequence

ENSEMBL: ENSMUSP00000099139 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000065090] [ENSMUST00000101617]

Predicted Effect

probably damaging
Transcript: ENSMUST00000065090
AA Change: D1566G

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000064163
Gene: ENSMUSG00000068699
AA Change: D1566G

Domain	Start	End	E-Value	Type
CH	39	141	1.17e-25	SMART
CH	162	258	2.09e-22	SMART
IG_FLMN	275	372	3.84e-38	SMART
IG_FLMN	375	472	3.73e-36	SMART
IG_FLMN	474	569	4.41e-38	SMART
IG_FLMN	571	662	3.61e-34	SMART
IG_FLMN	667	762	2.48e-41	SMART
IG_FLMN	764	865	6.7e-29	SMART
IG_FLMN	867	964	3.42e-35	SMART
IG_FLMN	966	1060	2.92e-29	SMART
IG_FLMN	1062	1153	3.69e-40	SMART
IG_FLMN	1155	1248	6.53e-41	SMART
IG_FLMN	1250	1348	7.23e-34	SMART
IG_FLMN	1350	1441	2.04e-42	SMART
IG_FLMN	1443	1537	1.75e-41	SMART
IG_FLMN	1539	1634	1.31e-40	SMART
IG_FLMN	1636	1738	1.05e-30	SMART
IG_FLMN	1777	1858	2.93e-11	SMART
IG_FLMN	1859	1950	2.55e-43	SMART
IG_FLMN	1951	2037	2.43e-17	SMART
IG_FLMN	2041	2132	1.52e-41	SMART
PDB:2E9I\|A	2133	2162	3e-7	PDB
IG_FLMN	2217	2310	2.93e-11	SMART
IG_FLMN	2314	2405	1.67e-38	SMART
IG_FLMN	2408	2500	2.56e-25	SMART
IG_FLMN	2505	2596	9.54e-34	SMART
low complexity region	2618	2628	N/A	INTRINSIC
IG_FLMN	2635	2737	2.11e-26	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000101617
AA Change: D1566G

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000099139
Gene: ENSMUSG00000068699
AA Change: D1566G

Domain	Start	End	E-Value	Type
CH	39	141	1.17e-25	SMART
CH	162	258	2.09e-22	SMART
IG_FLMN	275	372	3.84e-38	SMART
IG_FLMN	375	472	3.73e-36	SMART
IG_FLMN	474	569	4.41e-38	SMART
IG_FLMN	571	662	3.61e-34	SMART
IG_FLMN	667	762	2.48e-41	SMART
IG_FLMN	764	865	6.7e-29	SMART
IG_FLMN	867	964	3.42e-35	SMART
IG_FLMN	966	1060	2.92e-29	SMART
IG_FLMN	1062	1153	3.69e-40	SMART
IG_FLMN	1155	1248	6.53e-41	SMART
IG_FLMN	1250	1348	7.23e-34	SMART
IG_FLMN	1350	1441	2.04e-42	SMART
IG_FLMN	1443	1537	1.75e-41	SMART
IG_FLMN	1539	1634	1.31e-40	SMART
IG_FLMN	1636	1738	6.11e-32	SMART
IG_FLMN	1744	1825	2.93e-11	SMART
IG_FLMN	1826	1917	2.55e-43	SMART
IG_FLMN	1918	2004	2.43e-17	SMART
IG_FLMN	2008	2099	1.52e-41	SMART
PDB:2E9I\|A	2100	2129	3e-7	PDB
IG_FLMN	2184	2277	2.93e-11	SMART
IG_FLMN	2281	2372	1.67e-38	SMART
IG_FLMN	2375	2467	2.56e-25	SMART
IG_FLMN	2472	2563	9.54e-34	SMART
low complexity region	2585	2595	N/A	INTRINSIC
IG_FLMN	2602	2704	2.11e-26	SMART

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of three related filamin genes, specifically gamma filamin. These filamin proteins crosslink actin filaments into orthogonal networks in cortical cytoplasm and participate in the anchoring of membrane proteins for the actin cytoskeleton. Three functional domains exist in filamin: an N-terminal filamentous actin-binding domain, a C-terminal self-association domain, and a membrane glycoprotein-binding domain. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a hypomorphic allele display neonatal lethality, respiratory failure, reduced skeletal muscle mass, and abnormal skeletal muscle fiber morphology. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 39 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700024G13Rik	T	C	14: 32,388,248		probably benign	Het
AB124611	C	T	9: 21,528,925	S69L	possibly damaging	Het
Abca6	G	A	11: 110,178,792	A1566V	possibly damaging	Het
Ahnak	A	G	19: 9,014,833	I4494V	possibly damaging	Het
Ascc3	T	A	10: 50,845,695	Y2081*	probably null	Het
Cdc42bpb	T	C	12: 111,323,127	T423A	probably benign	Het
Cdh6	T	A	15: 13,064,430	I125F	possibly damaging	Het
Csgalnact1	C	A	8: 68,401,492	G219V	probably damaging	Het
Csmd2	T	C	4: 128,474,816	L1845P	possibly damaging	Het
Epha4	A	G	1: 77,506,748	V208A	possibly damaging	Het
Fanci	A	G	7: 79,444,516		probably benign	Het
Fezf2	T	C	14: 12,344,494	E231G	probably damaging	Het
Gm11565	A	G	11: 99,914,985	T68A	probably benign	Het
Ifng	G	A	10: 118,445,254	R154H	probably damaging	Het
Il1r1	G	A	1: 40,313,232	E521K	possibly damaging	Het
Irf3	G	T	7: 44,998,739	L9F	probably damaging	Het
Jade1	T	G	3: 41,613,939	I814S	probably benign	Het
Kcnh1	G	A	1: 192,337,543	W365*	probably null	Het
Kif16b	T	C	2: 142,672,360	T1209A	possibly damaging	Het
Mcur1	A	T	13: 43,541,727	S324T	probably damaging	Het
Mgat2	C	A	12: 69,184,784	A44E	probably benign	Het
Mgea5	A	T	19: 45,765,501	W645R	probably damaging	Het
Nox1	A	G	X: 134,107,834		probably benign	Het
Olfr608	A	T	7: 103,470,383	I115F	probably benign	Het
Olfr993	A	G	2: 85,414,193	S229P	probably benign	Het
Pcnt	A	T	10: 76,429,256	I340N	probably damaging	Het
Pde11a	T	C	2: 76,046,845	E760G	possibly damaging	Het
Per3	C	T	4: 151,018,217		probably null	Het
Rabep1	G	A	11: 70,917,480	A421T	probably benign	Het
Rint1	C	T	5: 23,794,452	Q80*	probably null	Het
Rnaset2b	G	A	17: 6,981,169		probably null	Het
Sccpdh	T	C	1: 179,680,505	Y237H	probably benign	Het
Scn10a	T	A	9: 119,691,562	T91S	probably damaging	Het
Spock1	A	G	13: 57,444,432		probably benign	Het
Stat1	A	G	1: 52,142,966		probably benign	Het
Svil	A	G	18: 5,118,203	E2212G	probably damaging	Het
Taok1	T	A	11: 77,549,277	R635W	probably benign	Het
Vmn1r39	A	G	6: 66,804,962	I124T	probably benign	Het
Vmn2r32	T	C	7: 7,474,284	I369M	probably benign	Het

Other mutations in Flnc

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00952:Flnc	APN	6	29459547	nonsense	probably null
IGL01099:Flnc	APN	6	29433618	missense	probably damaging	0.99
IGL01656:Flnc	APN	6	29443508	splice site	probably benign
IGL01659:Flnc	APN	6	29448671	missense	probably damaging	0.98
IGL01780:Flnc	APN	6	29438493	nonsense	probably null
IGL01935:Flnc	APN	6	29454280	missense	probably damaging	1.00
IGL02039:Flnc	APN	6	29450719	missense	probably benign	0.05
IGL02119:Flnc	APN	6	29447512	missense	probably damaging	0.98
IGL02122:Flnc	APN	6	29444336	missense	possibly damaging	0.70
IGL02236:Flnc	APN	6	29454376	missense	probably damaging	1.00
IGL02350:Flnc	APN	6	29438493	nonsense	probably null
IGL02357:Flnc	APN	6	29438493	nonsense	probably null
IGL02496:Flnc	APN	6	29440685	missense	probably damaging	0.98
IGL02516:Flnc	APN	6	29450841	missense	probably damaging	0.99
IGL02696:Flnc	APN	6	29446698	missense	probably damaging	0.98
IGL03165:Flnc	APN	6	29449378	missense	probably damaging	1.00
IGL03190:Flnc	APN	6	29445637	splice site	probably benign
I1329:Flnc	UTSW	6	29451415	missense	probably damaging	1.00
R0111:Flnc	UTSW	6	29454340	missense	probably damaging	0.99
R0665:Flnc	UTSW	6	29455531	missense	probably damaging	1.00
R0748:Flnc	UTSW	6	29446344	missense	probably damaging	0.99
R0960:Flnc	UTSW	6	29441512	missense	probably damaging	1.00
R1328:Flnc	UTSW	6	29438613	missense	probably damaging	1.00
R1502:Flnc	UTSW	6	29438694	missense	probably benign	0.45
R1544:Flnc	UTSW	6	29444080	missense	probably benign	0.00
R1565:Flnc	UTSW	6	29455171	missense	probably damaging	1.00
R1640:Flnc	UTSW	6	29433807	missense	possibly damaging	0.78
R1691:Flnc	UTSW	6	29441214	missense	probably benign	0.09
R1818:Flnc	UTSW	6	29457448	missense	probably damaging	1.00
R1826:Flnc	UTSW	6	29455185	missense	probably damaging	0.99
R1851:Flnc	UTSW	6	29443479	missense	probably damaging	1.00
R1898:Flnc	UTSW	6	29438666	nonsense	probably null
R1905:Flnc	UTSW	6	29459460	missense	probably damaging	1.00
R1985:Flnc	UTSW	6	29444416	splice site	probably benign
R2016:Flnc	UTSW	6	29443797	critical splice donor site	probably null
R2017:Flnc	UTSW	6	29443797	critical splice donor site	probably null
R2020:Flnc	UTSW	6	29444363	missense	probably damaging	0.97
R2104:Flnc	UTSW	6	29450735	critical splice donor site	probably null
R2132:Flnc	UTSW	6	29443676	missense	probably damaging	1.00
R2141:Flnc	UTSW	6	29448675	missense	probably damaging	1.00
R2197:Flnc	UTSW	6	29459135	missense	probably damaging	1.00
R2202:Flnc	UTSW	6	29459508	missense	probably damaging	1.00
R2203:Flnc	UTSW	6	29459508	missense	probably damaging	1.00
R2204:Flnc	UTSW	6	29459508	missense	probably damaging	1.00
R2205:Flnc	UTSW	6	29459508	missense	probably damaging	1.00
R2209:Flnc	UTSW	6	29455845	missense	possibly damaging	0.91
R2248:Flnc	UTSW	6	29451401	missense	probably damaging	0.99
R2258:Flnc	UTSW	6	29438666	nonsense	probably null
R2259:Flnc	UTSW	6	29438666	nonsense	probably null
R2280:Flnc	UTSW	6	29438666	nonsense	probably null
R2281:Flnc	UTSW	6	29438666	nonsense	probably null
R2873:Flnc	UTSW	6	29447543	missense	probably damaging	0.96
R2900:Flnc	UTSW	6	29448585	missense	probably damaging	0.98
R3788:Flnc	UTSW	6	29454057	missense	probably damaging	0.99
R3799:Flnc	UTSW	6	29443739	missense	probably damaging	1.00
R3801:Flnc	UTSW	6	29447404	missense	probably damaging	0.98
R3851:Flnc	UTSW	6	29453719	missense	probably damaging	1.00
R3910:Flnc	UTSW	6	29459427	missense	probably damaging	1.00
R3982:Flnc	UTSW	6	29442941	missense	probably damaging	1.00
R3983:Flnc	UTSW	6	29442941	missense	probably damaging	1.00
R4023:Flnc	UTSW	6	29451635	missense	possibly damaging	0.95
R4676:Flnc	UTSW	6	29445154	splice site	probably null
R4694:Flnc	UTSW	6	29443448	missense	probably damaging	1.00
R4695:Flnc	UTSW	6	29440429	missense	probably damaging	0.99
R4735:Flnc	UTSW	6	29455813	missense	probably damaging	1.00
R4773:Flnc	UTSW	6	29445039	missense	possibly damaging	0.96
R4828:Flnc	UTSW	6	29455167	missense	probably damaging	1.00
R4856:Flnc	UTSW	6	29447890	missense	probably damaging	1.00
R4879:Flnc	UTSW	6	29460806	missense	probably damaging	0.99
R4899:Flnc	UTSW	6	29446843	missense	probably benign	0.17
R4906:Flnc	UTSW	6	29447525	missense	probably damaging	0.99
R5089:Flnc	UTSW	6	29447813	missense	probably damaging	0.96
R5173:Flnc	UTSW	6	29455538	missense	probably damaging	1.00
R5174:Flnc	UTSW	6	29448894	missense	possibly damaging	0.91
R5290:Flnc	UTSW	6	29457554	missense	probably damaging	1.00
R5338:Flnc	UTSW	6	29444064	missense	possibly damaging	0.47
R5352:Flnc	UTSW	6	29449318	missense	possibly damaging	0.85
R5397:Flnc	UTSW	6	29441161	missense	possibly damaging	0.87
R5431:Flnc	UTSW	6	29456384	missense	possibly damaging	0.74
R5481:Flnc	UTSW	6	29441217	missense	probably damaging	1.00
R5511:Flnc	UTSW	6	29458898	missense	probably damaging	1.00
R5539:Flnc	UTSW	6	29446230	missense	probably damaging	1.00
R5549:Flnc	UTSW	6	29453691	missense	probably damaging	1.00
R5567:Flnc	UTSW	6	29444045	nonsense	probably null
R5584:Flnc	UTSW	6	29446628	missense	probably damaging	0.98
R5689:Flnc	UTSW	6	29441592	missense	probably benign	0.03
R5753:Flnc	UTSW	6	29433489	missense	probably benign
R5786:Flnc	UTSW	6	29459537	nonsense	probably null
R5822:Flnc	UTSW	6	29459430	missense	probably damaging	0.98
R5823:Flnc	UTSW	6	29461202	missense	probably damaging	0.99
R5933:Flnc	UTSW	6	29441106	missense	probably damaging	0.99
R6043:Flnc	UTSW	6	29446608	missense	probably damaging	1.00
R6320:Flnc	UTSW	6	29459063	missense	probably damaging	1.00
R6337:Flnc	UTSW	6	29454319	missense	probably damaging	0.99
R6399:Flnc	UTSW	6	29458883	missense	probably damaging	1.00
R6423:Flnc	UTSW	6	29445156	splice site	probably null
R6540:Flnc	UTSW	6	29446377	missense	possibly damaging	0.96
R6547:Flnc	UTSW	6	29448608	missense	probably damaging	0.98
R6717:Flnc	UTSW	6	29450902	small deletion	probably benign
R6875:Flnc	UTSW	6	29445749	missense	probably damaging	1.00
R7193:Flnc	UTSW	6	29450871	missense	probably damaging	1.00
R7255:Flnc	UTSW	6	29445766	missense	probably damaging	1.00
R7303:Flnc	UTSW	6	29460850	missense	probably benign	0.31
R7413:Flnc	UTSW	6	29452259	missense	probably damaging	1.00
R7422:Flnc	UTSW	6	29455471	missense	probably damaging	1.00
R7559:Flnc	UTSW	6	29459010	missense	probably damaging	1.00
R7632:Flnc	UTSW	6	29446985	missense	probably damaging	0.98
R7651:Flnc	UTSW	6	29444050	missense	probably benign	0.08
R7679:Flnc	UTSW	6	29456790	missense	probably benign	0.00
R7697:Flnc	UTSW	6	29456517	missense	probably damaging	0.98
R7788:Flnc	UTSW	6	29456444	missense	possibly damaging	0.67
R7852:Flnc	UTSW	6	29440898	missense	probably damaging	1.00
R7870:Flnc	UTSW	6	29454307	missense	probably damaging	1.00
R7873:Flnc	UTSW	6	29456991	missense	possibly damaging	0.88
R7935:Flnc	UTSW	6	29440898	missense	probably damaging	1.00
R7953:Flnc	UTSW	6	29454307	missense	probably damaging	1.00
R7956:Flnc	UTSW	6	29456991	missense	possibly damaging	0.88
Z1088:Flnc	UTSW	6	29457151	missense	probably damaging	1.00

Posted On

2015-04-16