Incidental Mutation 'R9479:Gsn'
| ID |
716106 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Gsn
|
| Ensembl Gene |
ENSMUSG00000026879 |
| Gene Name |
gelsolin |
| Synonyms |
|
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.558)
|
| Stock # |
R9479 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
35146392-35197904 bp(+) (GRCm39) |
| Type of Mutation |
critical splice donor site (2 bp from exon) |
| DNA Base Change (assembly) |
T to C
at 35186227 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000028239
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028239]
[ENSMUST00000142324]
[ENSMUST00000201185]
[ENSMUST00000202899]
[ENSMUST00000202990]
|
| AlphaFold |
P13020 |
| PDB Structure |
Gelsolin Domains 4-6 in Active, Actin Free Conformation Identifies Sites of Regulatory Calcium Ions [X-RAY DIFFRACTION]
Crystal structure of Plasmodium falciparum actin I [X-RAY DIFFRACTION]
Crystal structure of Plasmodium berghei actin I with D-loop from muscle actin [X-RAY DIFFRACTION]
Crystal structure of Plasmodium berghei actin II [X-RAY DIFFRACTION]
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000028239
|
| SMART Domains |
Protein: ENSMUSP00000028239
Gene: ENSMUSG00000026879
| 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 |
probably benign
Transcript: ENSMUST00000142324
|
| SMART Domains |
Protein: ENSMUSP00000118120
Gene: ENSMUSG00000026879
| Domain | Start | End | E-Value | Type |
|---|
|
GEL
|
15 |
113 |
7.31e-30 |
SMART |
|
GEL
|
134 |
226 |
1.53e-32 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000201185
|
| SMART Domains |
Protein: ENSMUSP00000144561
Gene: ENSMUSG00000026879
| 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 |
probably benign
Transcript: ENSMUST00000202899
|
| SMART Domains |
Protein: ENSMUSP00000144470
Gene: ENSMUSG00000026879
| Domain | Start | End | E-Value | Type |
|---|
|
GEL
|
15 |
113 |
4.9e-32 |
SMART |
|
GEL
|
134 |
226 |
9.6e-35 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000202990
|
| SMART Domains |
Protein: ENSMUSP00000144296
Gene: ENSMUSG00000026879
| 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 |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.9%
|
| Validation Efficiency |
|
| 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: 51 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aox3 |
A |
G |
1: 58,177,568 (GRCm39) |
Y261C |
probably benign |
Het |
| Arhgef10 |
T |
C |
8: 15,047,632 (GRCm39) |
V1165A |
probably damaging |
Het |
| Arih2 |
C |
G |
9: 108,488,938 (GRCm39) |
R260P |
probably damaging |
Het |
| Bhmt2 |
G |
A |
13: 93,799,833 (GRCm39) |
A201V |
probably damaging |
Het |
| Ccdc115 |
A |
T |
1: 34,476,895 (GRCm39) |
S115T |
possibly damaging |
Het |
| Clca4b |
A |
G |
3: 144,617,100 (GRCm39) |
V850A |
probably benign |
Het |
| Commd8 |
A |
T |
5: 72,318,350 (GRCm39) |
H144Q |
probably benign |
Het |
| Creb3l1 |
C |
T |
2: 91,822,231 (GRCm39) |
|
probably null |
Het |
| Csnka2ip |
T |
C |
16: 64,298,262 (GRCm39) |
K701E |
unknown |
Het |
| Cyb5d2 |
A |
G |
11: 72,669,702 (GRCm39) |
C219R |
|
Het |
| Ep400 |
T |
C |
5: 110,877,730 (GRCm39) |
T835A |
unknown |
Het |
| Fam169a |
A |
G |
13: 97,246,543 (GRCm39) |
Y228C |
possibly damaging |
Het |
| Fam169a |
A |
G |
13: 97,250,695 (GRCm39) |
D342G |
possibly damaging |
Het |
| Fbxw21 |
A |
T |
9: 108,968,612 (GRCm39) |
C455S |
probably benign |
Het |
| Fbxw26 |
A |
G |
9: 109,561,625 (GRCm39) |
S190P |
probably damaging |
Het |
| Gabra5 |
A |
G |
7: 57,058,440 (GRCm39) |
I436T |
|
Het |
| Gm9767 |
G |
A |
10: 25,954,916 (GRCm39) |
G156D |
|
Het |
| Grid1 |
G |
A |
14: 35,043,664 (GRCm39) |
D340N |
probably damaging |
Het |
| Hao1 |
A |
G |
2: 134,396,204 (GRCm39) |
S17P |
probably benign |
Het |
| Hspa1l |
A |
G |
17: 35,196,735 (GRCm39) |
N258S |
probably benign |
Het |
| Isyna1 |
C |
T |
8: 71,048,193 (GRCm39) |
R200C |
probably damaging |
Het |
| Itgb2 |
A |
T |
10: 77,396,942 (GRCm39) |
K659M |
probably benign |
Het |
| Klf11 |
T |
C |
12: 24,705,029 (GRCm39) |
M161T |
probably benign |
Het |
| Ktn1 |
A |
T |
14: 47,962,174 (GRCm39) |
K1114N |
probably damaging |
Het |
| Lonrf1 |
G |
A |
8: 36,697,668 (GRCm39) |
R439* |
probably null |
Het |
| Lrrc26 |
C |
T |
2: 25,180,571 (GRCm39) |
P191S |
probably benign |
Het |
| Ogdh |
T |
C |
11: 6,297,854 (GRCm39) |
I576T |
possibly damaging |
Het |
| Or10al4 |
T |
C |
17: 38,036,986 (GRCm39) |
S24P |
probably damaging |
Het |
| Or14c45 |
T |
C |
7: 86,176,285 (GRCm39) |
C107R |
possibly damaging |
Het |
| Or14j4 |
A |
G |
17: 37,920,718 (GRCm39) |
F308S |
probably damaging |
Het |
| Or4k40 |
A |
T |
2: 111,251,013 (GRCm39) |
F94L |
probably damaging |
Het |
| Or4p20 |
T |
C |
2: 88,253,677 (GRCm39) |
R231G |
probably damaging |
Het |
| Or7g20 |
G |
A |
9: 18,946,730 (GRCm39) |
V104I |
probably benign |
Het |
| Pcnt |
A |
G |
10: 76,217,963 (GRCm39) |
V2104A |
probably benign |
Het |
| Pds5a |
G |
A |
5: 65,792,747 (GRCm39) |
R729W |
probably damaging |
Het |
| Pgap1 |
G |
A |
1: 54,582,275 (GRCm39) |
Q191* |
probably null |
Het |
| Pglyrp3 |
A |
G |
3: 91,935,310 (GRCm39) |
I187V |
probably benign |
Het |
| Pkdrej |
T |
A |
15: 85,699,571 (GRCm39) |
I2122F |
possibly damaging |
Het |
| Pold1 |
G |
A |
7: 44,191,079 (GRCm39) |
R251W |
probably damaging |
Het |
| Prr22 |
A |
G |
17: 57,078,335 (GRCm39) |
M163V |
probably benign |
Het |
| Ptprc |
A |
T |
1: 138,001,388 (GRCm39) |
N814K |
probably benign |
Het |
| Rapgef2 |
G |
A |
3: 79,019,495 (GRCm39) |
L59F |
probably damaging |
Het |
| Rbm22 |
T |
C |
18: 60,699,492 (GRCm39) |
L147P |
probably damaging |
Het |
| Rgsl1 |
G |
A |
1: 153,657,445 (GRCm39) |
S391F |
unknown |
Het |
| Rnf13 |
A |
T |
3: 57,727,983 (GRCm39) |
D221V |
possibly damaging |
Het |
| Senp2 |
T |
A |
16: 21,842,398 (GRCm39) |
L154Q |
probably damaging |
Het |
| Srfbp1 |
A |
G |
18: 52,621,332 (GRCm39) |
Q131R |
possibly damaging |
Het |
| Tmprss11a |
A |
T |
5: 86,562,402 (GRCm39) |
Y314* |
probably null |
Het |
| Ttn |
G |
T |
2: 76,666,286 (GRCm39) |
P11590Q |
unknown |
Het |
| Txnrd3 |
C |
T |
6: 89,640,084 (GRCm39) |
T266M |
possibly damaging |
Het |
| Zfp810 |
T |
C |
9: 22,194,497 (GRCm39) |
S64G |
possibly 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 |
|
R1760:Gsn
|
UTSW |
2 |
35,174,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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 |
|
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'- TCTCTTGGAGCTAGGAACCCTC -3'
(R):5'- CTGGGAGAACTGAAACCTGG -3'
Sequencing Primer
(F):5'- CTCTGGCTATTGTCTAAATGTAAGG -3'
(R):5'- GAACTGAAACCTGGGAAGGG -3'
|
| Posted On |
2022-07-18 |
Incidental Mutation