Incidental Mutation 'IGL00339:Amz2'
| ID |
4476 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Amz2
|
| Ensembl Gene |
ENSMUSG00000020610 |
| Gene Name |
archaelysin family metallopeptidase 2 |
| Synonyms |
ESTM12 |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL00339
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
109316772-109328974 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 109324847 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Phenylalanine
at position 244
(I244F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000099350
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000020929]
[ENSMUST00000092500]
[ENSMUST00000103061]
|
| AlphaFold |
Q400C8 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000020929
AA Change: I244F
PolyPhen 2
Score 0.788 (Sensitivity: 0.85; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000020929
Gene: ENSMUSG00000020610
AA Change: I244F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Peptidase_M54
|
220 |
302 |
7.2e-17 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000092500
AA Change: I244F
PolyPhen 2
Score 0.967 (Sensitivity: 0.77; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000090157
Gene: ENSMUSG00000020610
AA Change: I244F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Peptidase_M54
|
232 |
302 |
2e-16 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000103061
AA Change: I244F
PolyPhen 2
Score 0.967 (Sensitivity: 0.77; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000099350
Gene: ENSMUSG00000020610
AA Change: I244F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Peptidase_M54
|
232 |
302 |
2e-16 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125108
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000131181
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141739
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148057
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000155036
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 38 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2700049A03Rik |
A |
G |
12: 71,213,893 (GRCm39) |
M707V |
probably benign |
Het |
| Atp4a |
T |
C |
7: 30,412,629 (GRCm39) |
C112R |
possibly damaging |
Het |
| Axin2 |
A |
G |
11: 108,814,816 (GRCm39) |
T235A |
probably benign |
Het |
| Barhl2 |
C |
T |
5: 106,603,365 (GRCm39) |
A265T |
possibly damaging |
Het |
| Brd8 |
C |
A |
18: 34,742,936 (GRCm39) |
G310* |
probably null |
Het |
| Capn11 |
A |
T |
17: 45,954,693 (GRCm39) |
I148N |
probably damaging |
Het |
| Caskin2 |
A |
G |
11: 115,694,425 (GRCm39) |
L392P |
probably benign |
Het |
| Cep72 |
C |
T |
13: 74,210,387 (GRCm39) |
|
probably benign |
Het |
| Chst11 |
A |
G |
10: 83,027,467 (GRCm39) |
Y298C |
possibly damaging |
Het |
| Cyp21a1 |
C |
T |
17: 35,023,108 (GRCm39) |
|
probably null |
Het |
| F830045P16Rik |
T |
C |
2: 129,302,449 (GRCm39) |
D381G |
probably damaging |
Het |
| Fnip2 |
T |
G |
3: 79,422,462 (GRCm39) |
H106P |
probably benign |
Het |
| Fosl1 |
T |
A |
19: 5,500,330 (GRCm39) |
I83K |
probably damaging |
Het |
| Foxk2 |
C |
T |
11: 121,190,560 (GRCm39) |
T567M |
probably damaging |
Het |
| Frmd4a |
A |
G |
2: 4,599,525 (GRCm39) |
N208S |
probably benign |
Het |
| Gm4553 |
T |
C |
7: 141,718,964 (GRCm39) |
S155G |
unknown |
Het |
| Heatr5a |
A |
T |
12: 51,935,684 (GRCm39) |
I1634N |
probably damaging |
Het |
| Hspg2 |
C |
T |
4: 137,266,506 (GRCm39) |
T1889M |
probably damaging |
Het |
| Kcnh6 |
C |
T |
11: 105,909,845 (GRCm39) |
P457S |
probably damaging |
Het |
| Kcnk18 |
G |
T |
19: 59,223,502 (GRCm39) |
A216S |
probably benign |
Het |
| Klhl42 |
A |
G |
6: 147,003,231 (GRCm39) |
Y335C |
probably damaging |
Het |
| Lrguk |
C |
T |
6: 34,020,364 (GRCm39) |
P36L |
probably damaging |
Het |
| Mmp1b |
T |
A |
9: 7,368,304 (GRCm39) |
R443S |
probably benign |
Het |
| Ncapd3 |
T |
C |
9: 26,963,649 (GRCm39) |
S501P |
probably benign |
Het |
| Neurl4 |
C |
T |
11: 69,795,413 (GRCm39) |
R422W |
probably damaging |
Het |
| Nol4 |
T |
C |
18: 22,956,469 (GRCm39) |
S311G |
probably benign |
Het |
| Oaf |
T |
C |
9: 43,135,313 (GRCm39) |
D155G |
probably damaging |
Het |
| Oas1g |
T |
A |
5: 121,024,109 (GRCm39) |
K67* |
probably null |
Het |
| Or1l4 |
T |
C |
2: 37,091,609 (GRCm39) |
S119P |
probably damaging |
Het |
| Or2a20 |
T |
G |
6: 43,194,782 (GRCm39) |
L312V |
probably benign |
Het |
| Rims2 |
C |
A |
15: 39,323,011 (GRCm39) |
T735K |
probably benign |
Het |
| Sema4f |
T |
C |
6: 82,914,155 (GRCm39) |
T68A |
probably benign |
Het |
| Snx19 |
T |
G |
9: 30,340,380 (GRCm39) |
V506G |
possibly damaging |
Het |
| Sp140 |
T |
A |
1: 85,569,543 (GRCm39) |
C107* |
probably null |
Het |
| Sspo |
G |
A |
6: 48,460,680 (GRCm39) |
|
probably benign |
Het |
| Syce1l |
T |
G |
8: 114,376,134 (GRCm39) |
L28R |
probably damaging |
Het |
| Tgm3 |
G |
A |
2: 129,880,333 (GRCm39) |
V380M |
probably damaging |
Het |
| Unc5a |
T |
A |
13: 55,143,628 (GRCm39) |
V104D |
possibly damaging |
Het |
|
| Other mutations in Amz2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02454:Amz2
|
APN |
11 |
109,324,887 (GRCm39) |
splice site |
probably benign |
|
|
IGL03163:Amz2
|
APN |
11 |
109,319,751 (GRCm39) |
missense |
probably benign |
0.00 |
|
BB004:Amz2
|
UTSW |
11 |
109,319,884 (GRCm39) |
missense |
probably damaging |
0.96 |
|
BB014:Amz2
|
UTSW |
11 |
109,319,884 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0546:Amz2
|
UTSW |
11 |
109,324,780 (GRCm39) |
missense |
probably benign |
|
|
R1617:Amz2
|
UTSW |
11 |
109,324,850 (GRCm39) |
missense |
probably benign |
0.11 |
|
R1913:Amz2
|
UTSW |
11 |
109,319,697 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2179:Amz2
|
UTSW |
11 |
109,320,658 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4291:Amz2
|
UTSW |
11 |
109,324,881 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4722:Amz2
|
UTSW |
11 |
109,325,457 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5797:Amz2
|
UTSW |
11 |
109,317,905 (GRCm39) |
start gained |
probably benign |
|
|
R5845:Amz2
|
UTSW |
11 |
109,324,755 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6341:Amz2
|
UTSW |
11 |
109,319,653 (GRCm39) |
missense |
probably benign |
0.10 |
|
R6384:Amz2
|
UTSW |
11 |
109,319,860 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7698:Amz2
|
UTSW |
11 |
109,319,833 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7896:Amz2
|
UTSW |
11 |
109,327,413 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R7927:Amz2
|
UTSW |
11 |
109,319,884 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9688:Amz2
|
UTSW |
11 |
109,320,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2012-04-20 |
Incidental Mutation