Incidental Mutation 'IGL02362:Serpina12'
| ID |
290550 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Serpina12
|
| Ensembl Gene |
ENSMUSG00000041567 |
| Gene Name |
serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 |
| Synonyms |
vaspin |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL02362
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
12 |
| Chromosomal Location |
103995028-104010702 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 104004140 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Proline
at position 164
(L164P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000045572
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043915]
|
| AlphaFold |
Q7TMF5 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000043915
AA Change: L164P
PolyPhen 2
Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
|
| SMART Domains |
Protein: ENSMUSP00000045572
Gene: ENSMUSG00000041567
AA Change: L164P
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
SERPIN
|
57 |
411 |
1.02e-139 |
SMART |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Mice hmomozygous for a knock-out allele exhibit increased body weight, epididymal fat pad weight, liver weight, fat cell size, serum total and small density LDL cholesterol, serum leptin, liver triglyceride and insulin resistance when fed a high fat, high sucrose diet. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam3 |
C |
A |
8: 25,187,207 (GRCm39) |
C428F |
probably damaging |
Het |
| Alas1 |
T |
C |
9: 106,113,838 (GRCm39) |
Y469C |
probably damaging |
Het |
| Asxl1 |
C |
T |
2: 153,243,706 (GRCm39) |
L1419F |
probably benign |
Het |
| Bcan |
C |
T |
3: 87,901,449 (GRCm39) |
D418N |
possibly damaging |
Het |
| Cdc42bpg |
A |
G |
19: 6,360,839 (GRCm39) |
D199G |
possibly damaging |
Het |
| Chst15 |
T |
C |
7: 131,868,401 (GRCm39) |
N340D |
probably benign |
Het |
| Col12a1 |
T |
G |
9: 79,537,993 (GRCm39) |
|
probably benign |
Het |
| Cyp2c67 |
T |
A |
19: 39,631,849 (GRCm39) |
H116L |
probably benign |
Het |
| Cyp2c67 |
G |
A |
19: 39,605,826 (GRCm39) |
R357* |
probably null |
Het |
| Ears2 |
T |
C |
7: 121,643,773 (GRCm39) |
D395G |
probably benign |
Het |
| Fam227a |
A |
T |
15: 79,528,139 (GRCm39) |
|
probably benign |
Het |
| Fap |
A |
G |
2: 62,403,842 (GRCm39) |
V11A |
probably benign |
Het |
| Ganc |
A |
G |
2: 120,264,238 (GRCm39) |
D397G |
probably damaging |
Het |
| Gjb6 |
C |
A |
14: 57,361,752 (GRCm39) |
G170C |
possibly damaging |
Het |
| Gria2 |
A |
T |
3: 80,614,244 (GRCm39) |
W599R |
probably damaging |
Het |
| Gvin-ps5 |
T |
C |
7: 105,929,480 (GRCm39) |
|
noncoding transcript |
Het |
| Ighv1-64 |
A |
G |
12: 115,471,236 (GRCm39) |
S94P |
probably benign |
Het |
| Kifc3 |
C |
T |
8: 95,836,507 (GRCm39) |
A85T |
probably damaging |
Het |
| Lifr |
G |
A |
15: 7,194,174 (GRCm39) |
|
probably null |
Het |
| Lonp2 |
T |
G |
8: 87,350,874 (GRCm39) |
S21R |
probably benign |
Het |
| Nxpe3 |
A |
G |
16: 55,710,949 (GRCm39) |
V30A |
probably benign |
Het |
| Olfml1 |
T |
C |
7: 107,167,010 (GRCm39) |
V13A |
probably benign |
Het |
| Or10w1 |
T |
C |
19: 13,632,597 (GRCm39) |
V268A |
probably benign |
Het |
| Or1af1 |
A |
G |
2: 37,109,681 (GRCm39) |
Y60C |
probably damaging |
Het |
| Pcnt |
G |
A |
10: 76,210,996 (GRCm39) |
Q2376* |
probably null |
Het |
| Pglyrp2 |
A |
G |
17: 32,635,996 (GRCm39) |
L380P |
probably damaging |
Het |
| Plin3 |
A |
G |
17: 56,593,636 (GRCm39) |
V26A |
probably benign |
Het |
| Potefam1 |
T |
C |
2: 111,041,996 (GRCm39) |
|
probably benign |
Het |
| Pramel25 |
A |
G |
4: 143,519,580 (GRCm39) |
S114G |
probably damaging |
Het |
| Rims1 |
A |
G |
1: 22,522,288 (GRCm39) |
I470T |
probably damaging |
Het |
| Rora |
T |
C |
9: 69,281,374 (GRCm39) |
Y329H |
probably damaging |
Het |
| Scnn1b |
G |
A |
7: 121,516,770 (GRCm39) |
R503H |
probably damaging |
Het |
| Sec14l1 |
A |
G |
11: 117,035,675 (GRCm39) |
D237G |
possibly damaging |
Het |
| Selplg |
A |
G |
5: 113,957,467 (GRCm39) |
S280P |
probably benign |
Het |
| Sik2 |
C |
T |
9: 50,828,903 (GRCm39) |
W176* |
probably null |
Het |
| Slc2a1 |
T |
C |
4: 118,993,612 (GRCm39) |
F483S |
possibly damaging |
Het |
| Speg |
A |
G |
1: 75,400,559 (GRCm39) |
D2573G |
possibly damaging |
Het |
| Stil |
C |
T |
4: 114,867,308 (GRCm39) |
S239L |
probably damaging |
Het |
| Tmem94 |
C |
A |
11: 115,685,571 (GRCm39) |
S941R |
probably damaging |
Het |
| Tnfrsf11b |
T |
A |
15: 54,115,778 (GRCm39) |
D273V |
probably damaging |
Het |
| Tns2 |
A |
G |
15: 102,020,725 (GRCm39) |
T864A |
probably benign |
Het |
| Zfpm2 |
A |
G |
15: 40,962,890 (GRCm39) |
H184R |
probably damaging |
Het |
|
| Other mutations in Serpina12 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00598:Serpina12
|
APN |
12 |
103,997,373 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL00976:Serpina12
|
APN |
12 |
103,998,787 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01592:Serpina12
|
APN |
12 |
104,004,381 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02355:Serpina12
|
APN |
12 |
104,004,140 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02648:Serpina12
|
APN |
12 |
104,004,267 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL03011:Serpina12
|
APN |
12 |
103,997,397 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL03156:Serpina12
|
APN |
12 |
104,004,158 (GRCm39) |
missense |
probably damaging |
1.00 |
|
sabina
|
UTSW |
12 |
104,004,179 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4305001:Serpina12
|
UTSW |
12 |
104,001,976 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0038:Serpina12
|
UTSW |
12 |
104,004,216 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0038:Serpina12
|
UTSW |
12 |
104,004,216 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0448:Serpina12
|
UTSW |
12 |
104,004,354 (GRCm39) |
missense |
probably benign |
0.20 |
|
R0465:Serpina12
|
UTSW |
12 |
104,004,104 (GRCm39) |
missense |
probably benign |
0.04 |
|
R0480:Serpina12
|
UTSW |
12 |
104,001,960 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0498:Serpina12
|
UTSW |
12 |
104,002,048 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0503:Serpina12
|
UTSW |
12 |
103,997,418 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0581:Serpina12
|
UTSW |
12 |
103,997,399 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1393:Serpina12
|
UTSW |
12 |
104,004,009 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R1847:Serpina12
|
UTSW |
12 |
103,998,769 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1956:Serpina12
|
UTSW |
12 |
104,002,048 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3125:Serpina12
|
UTSW |
12 |
104,004,242 (GRCm39) |
missense |
probably benign |
|
|
R4093:Serpina12
|
UTSW |
12 |
104,004,183 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4584:Serpina12
|
UTSW |
12 |
104,004,611 (GRCm39) |
missense |
unknown |
|
|
R4897:Serpina12
|
UTSW |
12 |
104,004,056 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R5117:Serpina12
|
UTSW |
12 |
104,004,009 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5167:Serpina12
|
UTSW |
12 |
104,004,179 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5344:Serpina12
|
UTSW |
12 |
104,001,807 (GRCm39) |
splice site |
probably null |
|
|
R5720:Serpina12
|
UTSW |
12 |
104,004,563 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6011:Serpina12
|
UTSW |
12 |
104,001,993 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6027:Serpina12
|
UTSW |
12 |
103,997,336 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6170:Serpina12
|
UTSW |
12 |
104,004,500 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7538:Serpina12
|
UTSW |
12 |
104,004,587 (GRCm39) |
missense |
unknown |
|
|
R7899:Serpina12
|
UTSW |
12 |
104,004,524 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9649:Serpina12
|
UTSW |
12 |
104,004,317 (GRCm39) |
missense |
probably benign |
0.01 |
|
| Posted On |
2015-04-16 |
Incidental Mutation