Incidental Mutation 'IGL01567:Anxa9'
| ID |
91030 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Anxa9
|
| Ensembl Gene |
ENSMUSG00000015702 |
| Gene Name |
annexin A9 |
| Synonyms |
2310069F17Rik |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL01567
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
3 |
| Chromosomal Location |
95203407-95214487 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
G to A
at 95209743 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000127424
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000015846]
[ENSMUST00000107183]
[ENSMUST00000123365]
[ENSMUST00000164406]
|
| AlphaFold |
Q9JHQ0 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000015846
|
| SMART Domains |
Protein: ENSMUSP00000015846
Gene: ENSMUSG00000015702
| Domain | Start | End | E-Value | Type |
|---|
|
ANX
|
58 |
110 |
1.48e-17 |
SMART |
|
ANX
|
130 |
182 |
6.56e-10 |
SMART |
|
ANX
|
212 |
264 |
1.52e-1 |
SMART |
|
ANX
|
287 |
339 |
1.03e-11 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000107183
|
| SMART Domains |
Protein: ENSMUSP00000102801
Gene: ENSMUSG00000015702
| Domain | Start | End | E-Value | Type |
|---|
|
ANX
|
58 |
110 |
1.48e-17 |
SMART |
|
ANX
|
130 |
182 |
6.56e-10 |
SMART |
|
ANX
|
212 |
264 |
1.52e-1 |
SMART |
|
ANX
|
287 |
339 |
1.03e-11 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000123365
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000164406
|
| SMART Domains |
Protein: ENSMUSP00000127424
Gene: ENSMUSG00000015702
| Domain | Start | End | E-Value | Type |
|---|
|
ANX
|
58 |
110 |
1.48e-17 |
SMART |
|
ANX
|
130 |
182 |
6.56e-10 |
SMART |
|
ANX
|
212 |
264 |
1.52e-1 |
SMART |
|
ANX
|
287 |
339 |
1.03e-11 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000198947
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The annexins are a family of calcium-dependent phospholipid-binding proteins. Members of the annexin family contain 4 internal repeat domains, each of which includes a type II calcium-binding site. The calcium-binding sites are required for annexins to aggregate and cooperatively bind anionic phospholipids and extracellular matrix proteins. This gene encodes a divergent member of the annexin protein family in which all four homologous type II calcium-binding sites in the conserved tetrad core contain amino acid substitutions that ablate their function. However, structural analysis suggests that the conserved putative ion channel formed by the tetrad core is intact. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 30 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Agbl1 |
A |
G |
7: 76,071,628 (GRCm39) |
S317G |
probably benign |
Het |
| Akna |
T |
C |
4: 63,300,087 (GRCm39) |
T652A |
probably benign |
Het |
| Bpifb4 |
T |
A |
2: 153,789,198 (GRCm39) |
|
probably benign |
Het |
| Bptf |
A |
G |
11: 106,949,600 (GRCm39) |
S2125P |
probably damaging |
Het |
| Capns2 |
C |
A |
8: 93,628,634 (GRCm39) |
H174Q |
probably benign |
Het |
| Cd200 |
A |
C |
16: 45,215,054 (GRCm39) |
L199R |
probably damaging |
Het |
| Clasp2 |
T |
C |
9: 113,709,164 (GRCm39) |
V651A |
probably damaging |
Het |
| Cox18 |
G |
A |
5: 90,365,447 (GRCm39) |
Q251* |
probably null |
Het |
| Depdc1a |
T |
C |
3: 159,232,183 (GRCm39) |
S645P |
probably damaging |
Het |
| Dio3 |
T |
A |
12: 110,245,861 (GRCm39) |
C66S |
possibly damaging |
Het |
| Dock9 |
A |
T |
14: 121,890,496 (GRCm39) |
L258Q |
probably damaging |
Het |
| Ghrhr |
A |
G |
6: 55,361,108 (GRCm39) |
D274G |
probably damaging |
Het |
| Gm5129 |
A |
G |
5: 29,940,862 (GRCm39) |
|
probably benign |
Het |
| Grb7 |
A |
G |
11: 98,345,776 (GRCm39) |
N518S |
probably damaging |
Het |
| Kdm5b |
G |
A |
1: 134,530,278 (GRCm39) |
A430T |
probably damaging |
Het |
| Map10 |
C |
A |
8: 126,398,232 (GRCm39) |
Q542K |
probably benign |
Het |
| Metap1 |
T |
C |
3: 138,168,150 (GRCm39) |
T325A |
probably damaging |
Het |
| Ncan |
A |
T |
8: 70,560,984 (GRCm39) |
M661K |
probably benign |
Het |
| Or2f1b |
T |
C |
6: 42,739,661 (GRCm39) |
I225T |
probably benign |
Het |
| Or51h5 |
A |
G |
7: 102,577,623 (GRCm39) |
I263V |
probably benign |
Het |
| Otog |
T |
C |
7: 45,926,039 (GRCm39) |
|
probably benign |
Het |
| Pip4k2b |
T |
C |
11: 97,620,387 (GRCm39) |
D116G |
probably damaging |
Het |
| Rps15 |
T |
A |
10: 80,129,643 (GRCm39) |
L86Q |
probably benign |
Het |
| Sfxn4 |
G |
T |
19: 60,842,336 (GRCm39) |
T122K |
probably damaging |
Het |
| Slc4a3 |
T |
C |
1: 75,527,526 (GRCm39) |
V165A |
probably damaging |
Het |
| Spmip7 |
A |
G |
11: 11,465,015 (GRCm39) |
H122R |
possibly damaging |
Het |
| Synm |
A |
G |
7: 67,384,980 (GRCm39) |
V452A |
probably damaging |
Het |
| Tdpoz1 |
T |
C |
3: 93,578,013 (GRCm39) |
H257R |
possibly damaging |
Het |
| Tmem26 |
A |
G |
10: 68,587,061 (GRCm39) |
T170A |
probably damaging |
Het |
| Wdfy4 |
T |
G |
14: 32,873,618 (GRCm39) |
E230D |
probably benign |
Het |
|
| Other mutations in Anxa9 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01618:Anxa9
|
APN |
3 |
95,207,847 (GRCm39) |
splice site |
probably null |
|
|
IGL02272:Anxa9
|
APN |
3 |
95,213,205 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0012:Anxa9
|
UTSW |
3 |
95,215,406 (GRCm39) |
unclassified |
probably benign |
|
|
R0128:Anxa9
|
UTSW |
3 |
95,209,733 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0130:Anxa9
|
UTSW |
3 |
95,209,733 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0356:Anxa9
|
UTSW |
3 |
95,215,387 (GRCm39) |
unclassified |
probably benign |
|
|
R1656:Anxa9
|
UTSW |
3 |
95,207,884 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1967:Anxa9
|
UTSW |
3 |
95,207,919 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2180:Anxa9
|
UTSW |
3 |
95,213,735 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R2359:Anxa9
|
UTSW |
3 |
95,210,062 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3155:Anxa9
|
UTSW |
3 |
95,209,716 (GRCm39) |
missense |
probably benign |
0.04 |
|
R3156:Anxa9
|
UTSW |
3 |
95,209,716 (GRCm39) |
missense |
probably benign |
0.04 |
|
R3767:Anxa9
|
UTSW |
3 |
95,208,425 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4693:Anxa9
|
UTSW |
3 |
95,204,667 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4974:Anxa9
|
UTSW |
3 |
95,215,324 (GRCm39) |
unclassified |
probably benign |
|
|
R5435:Anxa9
|
UTSW |
3 |
95,204,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6342:Anxa9
|
UTSW |
3 |
95,204,101 (GRCm39) |
makesense |
probably null |
|
|
R7272:Anxa9
|
UTSW |
3 |
95,213,184 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8210:Anxa9
|
UTSW |
3 |
95,213,207 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8673:Anxa9
|
UTSW |
3 |
95,207,657 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8728:Anxa9
|
UTSW |
3 |
95,209,979 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9342:Anxa9
|
UTSW |
3 |
95,210,359 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9542:Anxa9
|
UTSW |
3 |
95,210,379 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2013-12-09 |
Incidental Mutation