Mutagenetix > Incidental Mutation

Incidental Mutation 'R1760:Gsn'

192655

Institutional Source

Beutler Lab

Gene Symbol

Gsn

Ensembl Gene

ENSMUSG00000026879

Gene Name

gelsolin

Synonyms

MMRRC Submission

039792-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.558) question?

Stock #

R1760 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

35146392-35197904 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 35174835 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 127 (Y127N)

Ref Sequence

ENSEMBL: ENSMUSP00000144296 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028239] [ENSMUST00000139867] [ENSMUST00000142324] [ENSMUST00000201185] [ENSMUST00000202899] [ENSMUST00000202990]

AlphaFold

P13020

Predicted Effect

probably damaging
Transcript: ENSMUST00000028239
AA Change: Y165N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000028239
Gene: ENSMUSG00000026879
AA Change: Y165N

Domain	Start	End	E-Value	Type
low complexity region	6	21	N/A	INTRINSIC
GEL	64	162	7.31e-30	SMART
GEL	183	275	1.53e-32	SMART
GEL	299	394	2.59e-30	SMART
GEL	443	540	9.28e-32	SMART
GEL	561	646	1.67e-24	SMART
GEL	666	761	4.04e-32	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000124323

Predicted Effect

probably damaging
Transcript: ENSMUST00000139867
AA Change: Y127N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000144217
Gene: ENSMUSG00000026879
AA Change: Y127N

Domain	Start	End	E-Value	Type
GEL	26	124	4.9e-32	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000142324
AA Change: Y116N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000118120
Gene: ENSMUSG00000026879
AA Change: Y116N

Domain	Start	End	E-Value	Type
GEL	15	113	7.31e-30	SMART
GEL	134	226	1.53e-32	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000201185
AA Change: Y116N

PolyPhen 2 Score 0.978 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000144561
Gene: ENSMUSG00000026879
AA Change: Y116N

Domain	Start	End	E-Value	Type
GEL	15	113	4.9e-32	SMART
GEL	134	226	9.6e-35	SMART
GEL	250	345	1.6e-32	SMART
GEL	394	491	5.8e-34	SMART
GEL	512	597	1.1e-26	SMART
GEL	617	712	2.7e-34	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000202212

Predicted Effect

probably damaging
Transcript: ENSMUST00000202899
AA Change: Y116N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000144470
Gene: ENSMUSG00000026879
AA Change: Y116N

Domain	Start	End	E-Value	Type
GEL	15	113	4.9e-32	SMART
GEL	134	226	9.6e-35	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000202990
AA Change: Y127N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000144296
Gene: ENSMUSG00000026879
AA Change: Y127N

Domain	Start	End	E-Value	Type
GEL	26	124	4.9e-32	SMART
GEL	145	237	9.6e-35	SMART
GEL	261	356	1.6e-32	SMART
GEL	405	502	5.8e-34	SMART

Meta Mutation Damage Score

0.9526

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.3%
20x: 92.6%

Validation Efficiency

97% (95/98)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene binds to the "plus" ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for disruptions in this gene display abnormalities in the immune system, platelet and platelet function, bone density, nervous and circulatory system. In addition, there are background related effects on viability and mammary gland development. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 92 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca2	T	C	2: 25,333,055 (GRCm39)	S1585P	probably benign	Het
Abhd16b	T	C	2: 181,135,197 (GRCm39)	F33S	probably damaging	Het
Adgra2	G	A	8: 27,609,795 (GRCm39)	R856Q	probably damaging	Het
Aff3	A	T	1: 38,368,945 (GRCm39)		probably benign	Het
Anxa2	A	T	9: 69,397,049 (GRCm39)	Y251F	probably benign	Het
Arid1b	A	G	17: 5,392,088 (GRCm39)	T1873A	probably damaging	Het
Baz1b	C	A	5: 135,271,378 (GRCm39)	D1320E	probably benign	Het
Bbs1	A	T	19: 4,944,350 (GRCm39)	S426R	probably benign	Het
Bid	A	G	6: 120,877,209 (GRCm39)	V44A	possibly damaging	Het
Ccdc60	T	A	5: 116,310,532 (GRCm39)	M177L	probably damaging	Het
Cdh23	G	A	10: 60,161,855 (GRCm39)	T1997M	probably damaging	Het
Cdh5	T	A	8: 104,854,801 (GRCm39)	M243K	probably benign	Het
Clpb	T	A	7: 101,435,905 (GRCm39)	V578E	possibly damaging	Het
Cngb1	C	A	8: 96,026,328 (GRCm39)	C151F	probably benign	Het
Cntnap5b	T	C	1: 99,700,535 (GRCm39)	S16P	probably benign	Het
Cr1l	T	A	1: 194,797,123 (GRCm39)	M305L	probably benign	Het
Ctnnal1	A	T	4: 56,838,988 (GRCm39)	M235K	probably damaging	Het
Ddx55	A	T	5: 124,706,176 (GRCm39)	R534W	probably damaging	Het
Dip2b	T	A	15: 100,109,910 (GRCm39)	L1465Q	probably damaging	Het
Dnah9	G	T	11: 65,872,048 (GRCm39)	D2727E	probably benign	Het
Dph3b-ps	A	C	13: 106,683,497 (GRCm39)		noncoding transcript	Het
Dst	T	A	1: 34,267,684 (GRCm39)	L2702Q	probably damaging	Het
Efnb2	T	C	8: 8,673,184 (GRCm39)	T158A	possibly damaging	Het
Exosc10	A	T	4: 148,662,926 (GRCm39)	K712*	probably null	Het
Fgr	T	C	4: 132,725,653 (GRCm39)	V354A	possibly damaging	Het
Fsip2	A	G	2: 82,830,185 (GRCm39)	D6893G	possibly damaging	Het
Fsip2	G	A	2: 82,815,240 (GRCm39)	V3658M	probably benign	Het
Fsip2	A	T	2: 82,818,055 (GRCm39)	H4596L	possibly damaging	Het
Gm1527	G	A	3: 28,949,699 (GRCm39)		probably benign	Het
Gm5150	G	T	3: 16,060,468 (GRCm39)	Q7K	probably benign	Het
Gpr155	C	T	2: 73,212,279 (GRCm39)	V115M	probably damaging	Het
Gpr75	T	C	11: 30,841,527 (GRCm39)	L144P	probably damaging	Het
Hk1	A	G	10: 62,117,678 (GRCm39)	L615S	probably damaging	Het
Igsf9b	A	G	9: 27,229,123 (GRCm39)	T194A	possibly damaging	Het
Il17rd	C	T	14: 26,813,763 (GRCm39)	Q46*	probably null	Het
Jak1	T	A	4: 101,020,126 (GRCm39)	M678L	probably benign	Het
Kif6	T	C	17: 49,922,311 (GRCm39)	V16A	probably benign	Het
Kpna3	T	C	14: 61,607,990 (GRCm39)	E405G	probably benign	Het
Lmtk2	C	A	5: 144,110,993 (GRCm39)	T571K	probably damaging	Het
Mucl2	T	C	15: 103,927,838 (GRCm39)	T40A	possibly damaging	Het
Myh11	G	A	16: 14,051,559 (GRCm39)		probably benign	Het
Myh7	C	T	14: 55,210,170 (GRCm39)	R1845Q	probably damaging	Het
Myo1f	T	A	17: 33,805,172 (GRCm39)	L480Q	probably benign	Het
Nek9	T	G	12: 85,352,364 (GRCm39)	D833A	possibly damaging	Het
Nek9	T	C	12: 85,357,184 (GRCm39)	E660G	probably benign	Het
Or10z1	C	T	1: 174,077,926 (GRCm39)	C189Y	probably damaging	Het
Or2a12	A	G	6: 42,904,431 (GRCm39)	I89V	possibly damaging	Het
Or2t45	A	G	11: 58,669,195 (GRCm39)	M81V	possibly damaging	Het
Or5h18	T	C	16: 58,847,350 (GRCm39)	R307G	probably benign	Het
Or6c65	T	A	10: 129,603,417 (GRCm39)	D17E	probably benign	Het
Or6f2	G	A	7: 139,756,188 (GRCm39)	V52M	probably damaging	Het
Or7s1a-ps1	T	A	9: 18,843,791 (GRCm39)		probably benign	Het
Otud3	G	T	4: 138,623,092 (GRCm39)	T383K	possibly damaging	Het
Pkp4	T	C	2: 59,142,185 (GRCm39)	L496P	probably damaging	Het
Pla2g4e	C	A	2: 120,000,527 (GRCm39)	A737S	possibly damaging	Het
Pla2g4f	T	C	2: 120,144,547 (GRCm39)		probably benign	Het
Plxnd1	A	T	6: 115,944,740 (GRCm39)	V1018E	possibly damaging	Het
Ppp1r21	T	G	17: 88,869,653 (GRCm39)	V402G	possibly damaging	Het
Prkcq	T	G	2: 11,304,881 (GRCm39)	M690R	probably damaging	Het
Ptpra	T	C	2: 130,391,747 (GRCm39)	I719T	probably damaging	Het
Rab3ip	C	T	10: 116,773,415 (GRCm39)	D133N	probably damaging	Het
Relch	T	G	1: 105,647,169 (GRCm39)		probably benign	Het
Rsbn1	T	A	3: 103,867,347 (GRCm39)	Y563N	probably damaging	Het
Rtf1	A	C	2: 119,558,889 (GRCm39)	D530A	probably benign	Het
Rybp	G	T	6: 100,209,224 (GRCm39)	S199R	probably benign	Het
Sema5a	T	G	15: 32,641,252 (GRCm39)	C689G	probably damaging	Het
Senp6	T	A	9: 80,025,911 (GRCm39)	V314E	probably benign	Het
Setd1a	T	A	7: 127,385,062 (GRCm39)	C47S	possibly damaging	Het
Slamf1	C	A	1: 171,604,734 (GRCm39)	T168K	probably benign	Het
Slc12a5	T	C	2: 164,838,048 (GRCm39)	S937P	probably damaging	Het
Slc38a11	C	T	2: 65,185,663 (GRCm39)		probably null	Het
Slc6a2	C	T	8: 93,687,846 (GRCm39)		probably benign	Het
Snw1	A	T	12: 87,511,459 (GRCm39)	F64Y	probably benign	Het
Spata9	A	C	13: 76,146,643 (GRCm39)	I172L	probably benign	Het
Sphkap	T	C	1: 83,255,265 (GRCm39)	H828R	probably benign	Het
Spmip6	T	A	4: 41,507,330 (GRCm39)		probably null	Het
Tmem94	A	T	11: 115,687,580 (GRCm39)	K1146N	probably damaging	Het
Trdn	A	G	10: 33,109,883 (GRCm39)	T294A	possibly damaging	Het
Tsc22d1	T	C	14: 76,654,388 (GRCm39)	V289A	possibly damaging	Het
Tti1	C	A	2: 157,834,955 (GRCm39)	V1002L	possibly damaging	Het
Tubgcp4	T	A	2: 121,019,952 (GRCm39)		probably null	Het
Ush2a	G	A	1: 188,643,180 (GRCm39)	E4181K	possibly damaging	Het
Uvrag	A	G	7: 98,537,555 (GRCm39)	S547P	probably benign	Het
Vav3	T	C	3: 109,248,443 (GRCm39)	V30A	possibly damaging	Het
Vegfa	A	G	17: 46,336,395 (GRCm39)	Y242H	probably damaging	Het
Vmn2r75	G	T	7: 85,798,019 (GRCm39)	T598K	probably damaging	Het
Vps13b	C	T	15: 35,884,765 (GRCm39)	S3146L	possibly damaging	Het
Vrk3	A	G	7: 44,417,895 (GRCm39)	Y310C	probably damaging	Het
Zfhx4	A	G	3: 5,447,676 (GRCm39)	K1100R	probably benign	Het
Zfp748	T	A	13: 67,693,540 (GRCm39)		probably null	Het
Zfp760	A	T	17: 21,941,311 (GRCm39)	D162V	probably damaging	Het
Znfx1	T	A	2: 166,881,786 (GRCm39)	M1068L	probably damaging	Het

Other mutations in Gsn

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00797:Gsn	APN	2	35,174,049 (GRCm39)	missense	probably damaging	1.00
IGL02119:Gsn	APN	2	35,192,507 (GRCm39)	missense	probably damaging	1.00
IGL02512:Gsn	APN	2	35,173,962 (GRCm39)	nonsense	probably null
IGL02550:Gsn	APN	2	35,172,619 (GRCm39)	intron	probably benign
IGL02975:Gsn	APN	2	35,194,666 (GRCm39)	missense	probably benign	0.25
IGL03061:Gsn	APN	2	35,172,471 (GRCm39)	intron	probably benign
R0321:Gsn	UTSW	2	35,180,408 (GRCm39)	missense	probably benign	0.03
R0454:Gsn	UTSW	2	35,194,651 (GRCm39)	missense	probably damaging	1.00
R1446:Gsn	UTSW	2	35,196,598 (GRCm39)	missense	probably benign	0.04
R1974:Gsn	UTSW	2	35,191,483 (GRCm39)	missense	probably damaging	1.00
R2258:Gsn	UTSW	2	35,180,349 (GRCm39)	missense	probably damaging	1.00
R2260:Gsn	UTSW	2	35,180,349 (GRCm39)	missense	probably damaging	1.00
R2281:Gsn	UTSW	2	35,173,930 (GRCm39)	missense	probably benign	0.01
R2495:Gsn	UTSW	2	35,193,205 (GRCm39)	missense	probably damaging	1.00
R2516:Gsn	UTSW	2	35,173,965 (GRCm39)	missense	probably benign
R3896:Gsn	UTSW	2	35,192,650 (GRCm39)	missense	possibly damaging	0.92
R4003:Gsn	UTSW	2	35,173,995 (GRCm39)	missense	probably benign	0.38
R4006:Gsn	UTSW	2	35,197,633 (GRCm39)	nonsense	probably null
R4281:Gsn	UTSW	2	35,188,883 (GRCm39)	missense	probably damaging	1.00
R4291:Gsn	UTSW	2	35,180,432 (GRCm39)	missense	probably benign	0.14
R4692:Gsn	UTSW	2	35,188,883 (GRCm39)	missense	probably damaging	1.00
R4850:Gsn	UTSW	2	35,173,912 (GRCm39)	splice site	probably null
R4895:Gsn	UTSW	2	35,192,590 (GRCm39)	missense	probably damaging	1.00
R5011:Gsn	UTSW	2	35,188,933 (GRCm39)	missense	probably damaging	1.00
R5013:Gsn	UTSW	2	35,188,933 (GRCm39)	missense	probably damaging	1.00
R5290:Gsn	UTSW	2	35,186,484 (GRCm39)	missense	probably benign	0.01
R6472:Gsn	UTSW	2	35,180,463 (GRCm39)	splice site	probably null
R6764:Gsn	UTSW	2	35,174,056 (GRCm39)	missense	probably damaging	1.00
R7018:Gsn	UTSW	2	35,183,518 (GRCm39)	missense	probably benign	0.03
R7036:Gsn	UTSW	2	35,182,611 (GRCm39)	missense	probably damaging	1.00
R7097:Gsn	UTSW	2	35,185,061 (GRCm39)	nonsense	probably null
R7122:Gsn	UTSW	2	35,185,061 (GRCm39)	nonsense	probably null
R7183:Gsn	UTSW	2	35,184,960 (GRCm39)	missense	probably benign	0.00
R7203:Gsn	UTSW	2	35,188,807 (GRCm39)	missense	probably benign	0.00
R7456:Gsn	UTSW	2	35,172,718 (GRCm39)	missense	possibly damaging	0.84
R7488:Gsn	UTSW	2	35,186,433 (GRCm39)	missense	possibly damaging	0.65
R7880:Gsn	UTSW	2	35,173,939 (GRCm39)	missense	probably damaging	1.00
R8088:Gsn	UTSW	2	35,182,659 (GRCm39)	missense	possibly damaging	0.77
R9472:Gsn	UTSW	2	35,182,741 (GRCm39)	missense	probably damaging	1.00
R9479:Gsn	UTSW	2	35,186,227 (GRCm39)	critical splice donor site	probably null
R9568:Gsn	UTSW	2	35,174,003 (GRCm39)	missense	probably benign	0.02
R9777:Gsn	UTSW	2	35,194,600 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGAAGCCAGTCTCATGCTACCCTC -3'
(R):5'- AGAAGGTCTCCTGTGTGCTCACTC -3'

Sequencing Primer
(F):5'- AGTCTCATGCTACCCTCATGTTTC -3'
(R):5'- CCAGGCTGTAGAGAATCttttcattg -3'

Posted On

2014-05-23