Incidental Mutation 'IGL02146:Nexn'
| ID |
281774 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Nexn
|
| Ensembl Gene |
ENSMUSG00000039103 |
| Gene Name |
nexilin |
| Synonyms |
1110046H09Rik, nF actin binding protein |
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.392)
|
| Stock # |
IGL02146
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
3 |
| Chromosomal Location |
151942619-151971987 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 151952885 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 278
(D278E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000142559
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000046045]
[ENSMUST00000196504]
[ENSMUST00000196815]
[ENSMUST00000198460]
[ENSMUST00000199423]
[ENSMUST00000198750]
[ENSMUST00000199470]
[ENSMUST00000200589]
[ENSMUST00000199685]
[ENSMUST00000198648]
|
| AlphaFold |
Q7TPW1 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000046045
AA Change: D228E
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000037120
Gene: ENSMUSG00000039103
AA Change: D228E
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
40 |
92 |
N/A |
INTRINSIC |
|
coiled coil region
|
176 |
358 |
N/A |
INTRINSIC |
|
coiled coil region
|
391 |
419 |
N/A |
INTRINSIC |
|
low complexity region
|
452 |
470 |
N/A |
INTRINSIC |
|
low complexity region
|
487 |
493 |
N/A |
INTRINSIC |
|
IG
|
519 |
603 |
4.82e-6 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000196504
|
| SMART Domains |
Protein: ENSMUSP00000143180
Gene: ENSMUSG00000039103
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
40 |
92 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000196529
AA Change: D94E
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000196815
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000197507
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000198404
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000198460
|
| SMART Domains |
Protein: ENSMUSP00000143573
Gene: ENSMUSG00000039103
| Domain | Start | End | E-Value | Type |
|---|
|
internal_repeat_1
|
14 |
35 |
1.01e-5 |
PROSPERO |
|
low complexity region
|
36 |
53 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
86 |
106 |
1.01e-5 |
PROSPERO |
|
low complexity region
|
108 |
131 |
N/A |
INTRINSIC |
|
coiled coil region
|
226 |
345 |
N/A |
INTRINSIC |
|
coiled coil region
|
378 |
406 |
N/A |
INTRINSIC |
|
coiled coil region
|
429 |
480 |
N/A |
INTRINSIC |
|
IG
|
506 |
590 |
2.1e-8 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000199423
AA Change: D292E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000142936
Gene: ENSMUSG00000039103
AA Change: D292E
| Domain | Start | End | E-Value | Type |
|---|
|
internal_repeat_1
|
14 |
35 |
4.74e-6 |
PROSPERO |
|
low complexity region
|
36 |
53 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
86 |
106 |
4.74e-6 |
PROSPERO |
|
low complexity region
|
108 |
131 |
N/A |
INTRINSIC |
|
coiled coil region
|
240 |
422 |
N/A |
INTRINSIC |
|
coiled coil region
|
455 |
483 |
N/A |
INTRINSIC |
|
coiled coil region
|
506 |
557 |
N/A |
INTRINSIC |
|
IG
|
583 |
667 |
2e-8 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000198750
AA Change: D214E
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000142574
Gene: ENSMUSG00000039103
AA Change: D214E
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
40 |
86 |
N/A |
INTRINSIC |
|
coiled coil region
|
162 |
269 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000199470
AA Change: D158E
PolyPhen 2
Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
|
| SMART Domains |
Protein: ENSMUSP00000143133
Gene: ENSMUSG00000039103
AA Change: D158E
| Domain | Start | End | E-Value | Type |
|---|
|
internal_repeat_1
|
14 |
35 |
5.77e-6 |
PROSPERO |
|
low complexity region
|
36 |
53 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
86 |
106 |
5.77e-6 |
PROSPERO |
|
low complexity region
|
108 |
131 |
N/A |
INTRINSIC |
|
low complexity region
|
176 |
210 |
N/A |
INTRINSIC |
|
low complexity region
|
248 |
259 |
N/A |
INTRINSIC |
|
coiled coil region
|
321 |
349 |
N/A |
INTRINSIC |
|
coiled coil region
|
372 |
423 |
N/A |
INTRINSIC |
|
IG
|
449 |
533 |
2e-8 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000200589
AA Change: D278E
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
| SMART Domains |
Protein: ENSMUSP00000142559
Gene: ENSMUSG00000039103
AA Change: D278E
| Domain | Start | End | E-Value | Type |
|---|
|
internal_repeat_1
|
14 |
35 |
8.44e-7 |
PROSPERO |
|
low complexity region
|
36 |
53 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
86 |
106 |
8.44e-7 |
PROSPERO |
|
low complexity region
|
108 |
131 |
N/A |
INTRINSIC |
|
coiled coil region
|
226 |
333 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000198734
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000199983
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000199685
|
| SMART Domains |
Protein: ENSMUSP00000142569
Gene: ENSMUSG00000039103
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
40 |
92 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000198648
|
| SMART Domains |
Protein: ENSMUSP00000143294
Gene: ENSMUSG00000039103
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
40 |
92 |
N/A |
INTRINSIC |
|
| 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 a filamentous actin-binding protein that may function in cell adhesion and migration. Mutations in this gene have been associated with dilated cardiomyopathy, also known as CMD1CC. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit postnatal lethality with endomyocardial fibroelastosis, cardiac hypertrophy and dilated cardiomyopathy. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 54 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700017B05Rik |
A |
G |
9: 57,164,023 (GRCm39) |
C784R |
possibly damaging |
Het |
| Akp3 |
A |
T |
1: 87,054,297 (GRCm39) |
D278V |
probably benign |
Het |
| Atxn7l1 |
G |
T |
12: 33,418,030 (GRCm39) |
R730S |
probably benign |
Het |
| Bag6 |
A |
G |
17: 35,355,191 (GRCm39) |
T30A |
probably damaging |
Het |
| Blk |
G |
T |
14: 63,611,648 (GRCm39) |
P429H |
probably damaging |
Het |
| Bmp2k |
T |
A |
5: 97,212,689 (GRCm39) |
M524K |
unknown |
Het |
| Bst1 |
T |
A |
5: 43,983,678 (GRCm39) |
H221Q |
probably damaging |
Het |
| Ces2g |
T |
C |
8: 105,693,576 (GRCm39) |
I419T |
possibly damaging |
Het |
| Cnep1r1 |
T |
C |
8: 88,856,326 (GRCm39) |
V34A |
probably benign |
Het |
| Ctnnbl1 |
A |
G |
2: 157,661,414 (GRCm39) |
E308G |
probably damaging |
Het |
| Cyp20a1 |
A |
T |
1: 60,410,410 (GRCm39) |
K237I |
possibly damaging |
Het |
| Dlg5 |
T |
C |
14: 24,252,429 (GRCm39) |
T104A |
probably damaging |
Het |
| Dnaaf11 |
C |
T |
15: 66,361,374 (GRCm39) |
W42* |
probably null |
Het |
| Dnaaf11 |
C |
A |
15: 66,361,375 (GRCm39) |
W42L |
probably benign |
Het |
| Dnah9 |
C |
T |
11: 65,818,526 (GRCm39) |
V3271M |
probably damaging |
Het |
| Eed |
T |
A |
7: 89,618,803 (GRCm39) |
N204Y |
possibly damaging |
Het |
| Fat3 |
A |
G |
9: 15,910,878 (GRCm39) |
V1708A |
probably benign |
Het |
| Fcrl6 |
T |
C |
1: 172,426,264 (GRCm39) |
T178A |
probably benign |
Het |
| Galnt4 |
A |
C |
10: 98,945,563 (GRCm39) |
K429N |
possibly damaging |
Het |
| Ints6 |
T |
A |
14: 62,996,709 (GRCm39) |
T94S |
possibly damaging |
Het |
| Iqsec3 |
A |
T |
6: 121,360,916 (GRCm39) |
S981T |
probably damaging |
Het |
| Itga9 |
T |
A |
9: 118,663,400 (GRCm39) |
S146T |
possibly damaging |
Het |
| Itpr3 |
A |
G |
17: 27,336,249 (GRCm39) |
Y2325C |
probably damaging |
Het |
| Kng2 |
T |
A |
16: 22,806,582 (GRCm39) |
Q539L |
probably damaging |
Het |
| Lmtk3 |
T |
A |
7: 45,444,371 (GRCm39) |
|
probably benign |
Het |
| Map1a |
T |
C |
2: 121,129,927 (GRCm39) |
Y248H |
probably damaging |
Het |
| Mroh1 |
A |
G |
15: 76,318,879 (GRCm39) |
|
probably benign |
Het |
| Mroh2b |
T |
C |
15: 4,980,776 (GRCm39) |
|
probably null |
Het |
| Myo18b |
A |
T |
5: 112,991,151 (GRCm39) |
M942K |
probably damaging |
Het |
| Myzap |
T |
A |
9: 71,471,730 (GRCm39) |
T94S |
probably benign |
Het |
| Nebl |
C |
A |
2: 17,353,679 (GRCm39) |
R957S |
probably damaging |
Het |
| Nlgn1 |
A |
T |
3: 25,966,846 (GRCm39) |
N222K |
probably damaging |
Het |
| Or6c76 |
T |
A |
10: 129,612,727 (GRCm39) |
|
probably benign |
Het |
| Or8d1 |
G |
A |
9: 38,766,654 (GRCm39) |
A99T |
probably benign |
Het |
| Osbpl6 |
A |
T |
2: 76,380,094 (GRCm39) |
R79S |
possibly damaging |
Het |
| Phip |
T |
C |
9: 82,763,771 (GRCm39) |
I1268M |
probably benign |
Het |
| Pkd2 |
G |
T |
5: 104,637,157 (GRCm39) |
R590L |
probably damaging |
Het |
| Reg2 |
G |
A |
6: 78,382,568 (GRCm39) |
|
probably benign |
Het |
| Scaf1 |
A |
T |
7: 44,662,934 (GRCm39) |
D26E |
probably damaging |
Het |
| Ska1 |
A |
G |
18: 74,329,981 (GRCm39) |
I253T |
possibly damaging |
Het |
| Slc11a2 |
T |
C |
15: 100,299,169 (GRCm39) |
N443D |
probably damaging |
Het |
| Slc6a12 |
A |
T |
6: 121,330,460 (GRCm39) |
T155S |
probably benign |
Het |
| Slit3 |
A |
G |
11: 35,125,675 (GRCm39) |
K118R |
possibly damaging |
Het |
| Snap23 |
T |
G |
2: 120,429,792 (GRCm39) |
N212K |
probably damaging |
Het |
| Snx13 |
T |
A |
12: 35,151,078 (GRCm39) |
D346E |
probably benign |
Het |
| Sumf1 |
C |
A |
6: 108,150,392 (GRCm39) |
|
probably null |
Het |
| Susd2 |
T |
C |
10: 75,474,267 (GRCm39) |
N479S |
possibly damaging |
Het |
| Tiam1 |
A |
G |
16: 89,646,569 (GRCm39) |
I821T |
probably benign |
Het |
| Tll2 |
C |
A |
19: 41,086,276 (GRCm39) |
V651L |
probably benign |
Het |
| Vmn2r1 |
A |
G |
3: 64,012,104 (GRCm39) |
D655G |
probably benign |
Het |
| Vmn2r72 |
T |
C |
7: 85,387,170 (GRCm39) |
Y798C |
probably damaging |
Het |
| Vps13b |
A |
C |
15: 35,646,479 (GRCm39) |
I1528L |
probably benign |
Het |
| Wdtc1 |
G |
A |
4: 133,029,076 (GRCm39) |
L337F |
probably benign |
Het |
| Zfp128 |
A |
C |
7: 12,623,959 (GRCm39) |
K109T |
possibly damaging |
Het |
|
| Other mutations in Nexn |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01316:Nexn
|
APN |
3 |
151,952,870 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01681:Nexn
|
APN |
3 |
151,949,507 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL02098:Nexn
|
APN |
3 |
151,949,540 (GRCm39) |
nonsense |
probably null |
|
|
IGL02151:Nexn
|
APN |
3 |
151,953,881 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0369:Nexn
|
UTSW |
3 |
151,953,894 (GRCm39) |
missense |
probably benign |
0.40 |
|
R0540:Nexn
|
UTSW |
3 |
151,953,879 (GRCm39) |
nonsense |
probably null |
|
|
R1501:Nexn
|
UTSW |
3 |
151,943,323 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R1828:Nexn
|
UTSW |
3 |
151,948,405 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1903:Nexn
|
UTSW |
3 |
151,953,818 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1990:Nexn
|
UTSW |
3 |
151,958,576 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2857:Nexn
|
UTSW |
3 |
151,953,680 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2858:Nexn
|
UTSW |
3 |
151,953,680 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4482:Nexn
|
UTSW |
3 |
151,948,390 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4593:Nexn
|
UTSW |
3 |
151,958,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4750:Nexn
|
UTSW |
3 |
151,943,359 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5113:Nexn
|
UTSW |
3 |
151,949,525 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5252:Nexn
|
UTSW |
3 |
151,943,590 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5289:Nexn
|
UTSW |
3 |
151,953,709 (GRCm39) |
missense |
probably benign |
0.13 |
|
R5502:Nexn
|
UTSW |
3 |
151,943,941 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5746:Nexn
|
UTSW |
3 |
151,948,513 (GRCm39) |
unclassified |
probably benign |
|
|
R6230:Nexn
|
UTSW |
3 |
151,943,912 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7251:Nexn
|
UTSW |
3 |
151,952,832 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7523:Nexn
|
UTSW |
3 |
151,952,815 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7571:Nexn
|
UTSW |
3 |
151,959,284 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R7587:Nexn
|
UTSW |
3 |
151,952,815 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8359:Nexn
|
UTSW |
3 |
151,953,998 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8898:Nexn
|
UTSW |
3 |
151,948,306 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9382:Nexn
|
UTSW |
3 |
151,959,401 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation