Incidental Mutation 'IGL01820:Nf2'
| ID |
154528 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Nf2
|
| Ensembl Gene |
ENSMUSG00000009073 |
| Gene Name |
neurofibromin 2 |
| Synonyms |
schwannomin, merlin, moesin-ezrin-radixin-like protein |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL01820
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
4715845-4799536 bp(-) (GRCm39) |
| Type of Mutation |
splice site (1546 bp from exon) |
| DNA Base Change (assembly) |
A to T
at 4739655 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000129388
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053079]
[ENSMUST00000056290]
[ENSMUST00000109910]
[ENSMUST00000152656]
[ENSMUST00000164190]
|
| AlphaFold |
P46662 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000053079
|
| SMART Domains |
Protein: ENSMUSP00000055033
Gene: ENSMUSG00000009073
| Domain | Start | End | E-Value | Type |
|---|
|
B41
|
18 |
222 |
5.26e-81 |
SMART |
|
FERM_C
|
226 |
315 |
1.08e-30 |
SMART |
|
Pfam:ERM
|
347 |
585 |
6.3e-63 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000056290
|
| SMART Domains |
Protein: ENSMUSP00000055061
Gene: ENSMUSG00000009073
| Domain | Start | End | E-Value | Type |
|---|
|
B41
|
18 |
222 |
5.26e-81 |
SMART |
|
FERM_C
|
226 |
315 |
1.08e-30 |
SMART |
|
Pfam:ERM
|
347 |
585 |
6.3e-63 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000093374
|
| SMART Domains |
Protein: ENSMUSP00000091066
Gene: ENSMUSG00000009073
| Domain | Start | End | E-Value | Type |
|---|
|
B41
|
2 |
152 |
2.21e-33 |
SMART |
|
FERM_C
|
156 |
245 |
1.08e-30 |
SMART |
|
Pfam:ERM
|
277 |
515 |
1.7e-66 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000109908
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109910
|
| SMART Domains |
Protein: ENSMUSP00000105536
Gene: ENSMUSG00000009073
| Domain | Start | End | E-Value | Type |
|---|
|
B41
|
18 |
222 |
5.26e-81 |
SMART |
|
FERM_C
|
226 |
315 |
1.08e-30 |
SMART |
|
Pfam:ERM
|
347 |
596 |
5.5e-74 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000137926
|
| SMART Domains |
Protein: ENSMUSP00000116505
Gene: ENSMUSG00000009073
| Domain | Start | End | E-Value | Type |
|---|
|
B41
|
2 |
116 |
1.53e-4 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141342
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000155600
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000152656
|
| SMART Domains |
Protein: ENSMUSP00000128494
Gene: ENSMUSG00000009073
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:B41
|
1 |
28 |
2e-9 |
BLAST |
|
PDB:1E5W|A
|
1 |
28 |
7e-6 |
PDB |
|
FERM_C
|
29 |
118 |
1.08e-30 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000164190
|
| SMART Domains |
Protein: ENSMUSP00000129388
Gene: ENSMUSG00000009073
| Domain | Start | End | E-Value | Type |
|---|
|
B41
|
18 |
181 |
1.24e-45 |
SMART |
|
FERM_C
|
160 |
229 |
1.23e0 |
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 a protein that is similar to some members of the ERM (ezrin, radixin, moesin) family of proteins that are thought to link cytoskeletal components with proteins in the cell membrane. This gene product has been shown to interact with cell-surface proteins, proteins involved in cytoskeletal dynamics and proteins involved in regulating ion transport. This gene is expressed at high levels during embryonic development; in adults, significant expression is found in Schwann cells, meningeal cells, lens and nerve. Mutations in this gene are associated with neurofibromatosis type II which is characterized by nervous system and skin tumors and ocular abnormalities. Two predominant isoforms and a number of minor isoforms are produced by alternatively spliced transcripts. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous targeted null mutants lack extraembryonic ectoderm, do not initiate gastrulation and die by embryonic day 7. Heterozygotes develop malignant tumors, especially osteosarcomas. Conditional Schwann cell knockouts resemble neurofibromatosis type 2. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 48 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb1a |
A |
G |
5: 8,765,896 (GRCm39) |
|
probably benign |
Het |
| Adcy2 |
T |
C |
13: 68,886,664 (GRCm39) |
|
probably null |
Het |
| Akna |
G |
T |
4: 63,304,495 (GRCm39) |
T553N |
probably benign |
Het |
| Boc |
A |
G |
16: 44,312,235 (GRCm39) |
I609T |
possibly damaging |
Het |
| Btbd9 |
C |
T |
17: 30,746,383 (GRCm39) |
V148I |
possibly damaging |
Het |
| Cacna1d |
A |
T |
14: 29,764,823 (GRCm39) |
I2049N |
possibly damaging |
Het |
| Cdhr1 |
A |
T |
14: 36,807,536 (GRCm39) |
M368K |
probably benign |
Het |
| Cftr |
A |
G |
6: 18,226,138 (GRCm39) |
Y362C |
probably damaging |
Het |
| Cnppd1 |
G |
T |
1: 75,116,236 (GRCm39) |
|
probably null |
Het |
| Col3a1 |
T |
C |
1: 45,360,768 (GRCm39) |
I66T |
unknown |
Het |
| Col5a2 |
C |
A |
1: 45,481,985 (GRCm39) |
M46I |
unknown |
Het |
| Csmd3 |
G |
T |
15: 47,470,538 (GRCm39) |
C3379* |
probably null |
Het |
| Ctla2b |
T |
A |
13: 61,044,503 (GRCm39) |
*28C |
probably null |
Het |
| Ddhd2 |
C |
T |
8: 26,239,781 (GRCm39) |
E33K |
possibly damaging |
Het |
| Dock3 |
T |
C |
9: 106,773,092 (GRCm39) |
H387R |
probably damaging |
Het |
| Dyrk1b |
T |
A |
7: 27,881,025 (GRCm39) |
|
probably benign |
Het |
| Fam131c |
T |
C |
4: 141,107,648 (GRCm39) |
C53R |
probably damaging |
Het |
| Fat1 |
T |
A |
8: 45,463,539 (GRCm39) |
F1360L |
probably damaging |
Het |
| Gm10320 |
G |
T |
13: 98,626,045 (GRCm39) |
S113* |
probably null |
Het |
| Ifih1 |
T |
C |
2: 62,447,657 (GRCm39) |
D349G |
probably damaging |
Het |
| Il12a |
T |
C |
3: 68,599,495 (GRCm39) |
|
probably benign |
Het |
| Ivl |
A |
T |
3: 92,478,940 (GRCm39) |
M375K |
possibly damaging |
Het |
| Krt82 |
C |
A |
15: 101,451,887 (GRCm39) |
|
probably benign |
Het |
| Mc4r |
C |
T |
18: 66,992,226 (GRCm39) |
V296I |
probably benign |
Het |
| Met |
T |
A |
6: 17,534,230 (GRCm39) |
I691N |
possibly damaging |
Het |
| Mycbp2 |
A |
T |
14: 103,425,937 (GRCm39) |
I2396K |
probably damaging |
Het |
| Napg |
C |
A |
18: 63,119,516 (GRCm39) |
Q135K |
probably benign |
Het |
| Nrxn1 |
G |
T |
17: 90,950,531 (GRCm39) |
H549Q |
probably damaging |
Het |
| P4ha1 |
T |
A |
10: 59,197,736 (GRCm39) |
I321K |
probably damaging |
Het |
| Prl5a1 |
T |
C |
13: 28,332,683 (GRCm39) |
S94P |
probably benign |
Het |
| Prnp |
T |
C |
2: 131,778,990 (GRCm39) |
V214A |
probably benign |
Het |
| Ptprc |
A |
T |
1: 137,993,936 (GRCm39) |
F1165I |
probably damaging |
Het |
| Rdh10 |
T |
C |
1: 16,198,483 (GRCm39) |
V207A |
possibly damaging |
Het |
| Rel |
A |
T |
11: 23,703,218 (GRCm39) |
N131K |
probably benign |
Het |
| Rgs14 |
A |
T |
13: 55,531,338 (GRCm39) |
D448V |
probably benign |
Het |
| Spag5 |
T |
G |
11: 78,195,085 (GRCm39) |
S131A |
probably benign |
Het |
| Styxl1 |
C |
T |
5: 135,794,604 (GRCm39) |
D88N |
probably damaging |
Het |
| Tlr3 |
C |
T |
8: 45,851,376 (GRCm39) |
R507H |
probably benign |
Het |
| Ttn |
C |
T |
2: 76,616,670 (GRCm39) |
E16528K |
possibly damaging |
Het |
| Txlnb |
T |
C |
10: 17,682,606 (GRCm39) |
|
probably null |
Het |
| Unc13a |
A |
G |
8: 72,107,591 (GRCm39) |
V567A |
probably damaging |
Het |
| Vmn1r8 |
T |
C |
6: 57,013,653 (GRCm39) |
S235P |
possibly damaging |
Het |
| Vmn2r51 |
T |
A |
7: 9,839,409 (GRCm39) |
N60Y |
probably damaging |
Het |
| Wbp1l |
T |
A |
19: 46,640,922 (GRCm39) |
L68Q |
probably damaging |
Het |
| Wdfy3 |
A |
T |
5: 102,071,947 (GRCm39) |
V981E |
probably benign |
Het |
| Zdhhc13 |
T |
C |
7: 48,458,613 (GRCm39) |
S316P |
probably damaging |
Het |
| Zfp516 |
C |
T |
18: 83,005,486 (GRCm39) |
R797C |
probably benign |
Het |
| Zp3r |
A |
G |
1: 130,526,657 (GRCm39) |
V182A |
probably benign |
Het |
|
| Other mutations in Nf2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00832:Nf2
|
APN |
11 |
4,741,123 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01072:Nf2
|
APN |
11 |
4,739,713 (GRCm39) |
missense |
probably null |
0.00 |
|
IGL01349:Nf2
|
APN |
11 |
4,734,472 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL01686:Nf2
|
APN |
11 |
4,768,613 (GRCm39) |
missense |
probably benign |
|
|
IGL02251:Nf2
|
APN |
11 |
4,798,873 (GRCm39) |
missense |
probably null |
1.00 |
|
IGL02755:Nf2
|
APN |
11 |
4,768,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02859:Nf2
|
APN |
11 |
4,741,209 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0331:Nf2
|
UTSW |
11 |
4,744,914 (GRCm39) |
missense |
probably benign |
0.21 |
|
R0513:Nf2
|
UTSW |
11 |
4,741,185 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R0606:Nf2
|
UTSW |
11 |
4,732,194 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0734:Nf2
|
UTSW |
11 |
4,770,409 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1749:Nf2
|
UTSW |
11 |
4,753,694 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R2192:Nf2
|
UTSW |
11 |
4,749,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4073:Nf2
|
UTSW |
11 |
4,798,958 (GRCm39) |
missense |
probably benign |
0.27 |
|
R4355:Nf2
|
UTSW |
11 |
4,730,613 (GRCm39) |
nonsense |
probably null |
|
|
R4629:Nf2
|
UTSW |
11 |
4,798,915 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5129:Nf2
|
UTSW |
11 |
4,766,145 (GRCm39) |
missense |
probably benign |
|
|
R5130:Nf2
|
UTSW |
11 |
4,779,862 (GRCm39) |
intron |
probably benign |
|
|
R5580:Nf2
|
UTSW |
11 |
4,753,689 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5599:Nf2
|
UTSW |
11 |
4,732,269 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5840:Nf2
|
UTSW |
11 |
4,766,146 (GRCm39) |
missense |
probably benign |
0.24 |
|
R6017:Nf2
|
UTSW |
11 |
4,766,137 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6029:Nf2
|
UTSW |
11 |
4,734,566 (GRCm39) |
splice site |
probably null |
|
|
R6230:Nf2
|
UTSW |
11 |
4,758,262 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R6897:Nf2
|
UTSW |
11 |
4,749,878 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6990:Nf2
|
UTSW |
11 |
4,749,944 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7155:Nf2
|
UTSW |
11 |
4,749,964 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7826:Nf2
|
UTSW |
11 |
4,739,750 (GRCm39) |
missense |
probably benign |
0.35 |
|
R8427:Nf2
|
UTSW |
11 |
4,741,118 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8717:Nf2
|
UTSW |
11 |
4,766,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9154:Nf2
|
UTSW |
11 |
4,744,873 (GRCm39) |
missense |
probably damaging |
1.00 |
|
RF028:Nf2
|
UTSW |
11 |
4,779,936 (GRCm39) |
frame shift |
probably null |
|
|
RF031:Nf2
|
UTSW |
11 |
4,779,936 (GRCm39) |
frame shift |
probably null |
|
|
RF032:Nf2
|
UTSW |
11 |
4,779,936 (GRCm39) |
frame shift |
probably null |
|
|
RF033:Nf2
|
UTSW |
11 |
4,779,936 (GRCm39) |
frame shift |
probably null |
|
|
RF041:Nf2
|
UTSW |
11 |
4,779,936 (GRCm39) |
frame shift |
probably null |
|
|
| Posted On |
2014-02-04 |
Incidental Mutation