Incidental Mutation 'IGL01947:Serpina1b'
| ID |
181260 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Serpina1b
|
| Ensembl Gene |
ENSMUSG00000071178 |
| Gene Name |
serine (or cysteine) preptidase inhibitor, clade A, member 1B |
| Synonyms |
PI2, D12Ucla2, Spi1-2 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.176)
|
| Stock # |
IGL01947
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
12 |
| Chromosomal Location |
103694415-103704448 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 103695576 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Glycine
at position 322
(S322G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000139941
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000095450]
[ENSMUST00000164454]
[ENSMUST00000186166]
[ENSMUST00000187220]
|
| AlphaFold |
P22599 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000095450
AA Change: S322G
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000093101
Gene: ENSMUSG00000071178
AA Change: S322G
| Domain | Start | End | E-Value | Type |
|---|
|
SERPIN
|
53 |
410 |
7.62e-203 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000164454
AA Change: S322G
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000127266
Gene: ENSMUSG00000071178
AA Change: S322G
| Domain | Start | End | E-Value | Type |
|---|
|
SERPIN
|
53 |
410 |
7.62e-203 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000186166
AA Change: S322G
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000139941
Gene: ENSMUSG00000071178
AA Change: S322G
| Domain | Start | End | E-Value | Type |
|---|
|
SERPIN
|
53 |
410 |
7.62e-203 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000187220
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Targeted disruption of this gene leads to significantly fewer than expected heterozygous and homozygous offspring from heterozygous matings. Homozygotes are healthy with no obvious changes in major organs while heterozygotes show a 30% decrease in serum anti-elastase and anti-chymotrypsin activity. [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 |
|---|
| Adgrl4 |
T |
C |
3: 151,216,428 (GRCm39) |
|
probably null |
Het |
| Aloxe3 |
T |
A |
11: 69,033,847 (GRCm39) |
|
probably benign |
Het |
| Atic |
C |
T |
1: 71,609,996 (GRCm39) |
|
probably benign |
Het |
| Avpr1a |
T |
C |
10: 122,288,087 (GRCm39) |
V365A |
probably benign |
Het |
| Brd7 |
A |
G |
8: 89,059,503 (GRCm39) |
|
probably benign |
Het |
| Cc2d2a |
A |
G |
5: 43,845,579 (GRCm39) |
N332D |
probably damaging |
Het |
| Cdh20 |
C |
T |
1: 104,921,649 (GRCm39) |
P649S |
possibly damaging |
Het |
| Cgnl1 |
T |
C |
9: 71,632,326 (GRCm39) |
T342A |
probably damaging |
Het |
| Chst10 |
A |
G |
1: 38,904,646 (GRCm39) |
L349P |
probably damaging |
Het |
| Cox6b2 |
T |
A |
7: 4,754,929 (GRCm39) |
K77* |
probably null |
Het |
| Crnkl1 |
G |
A |
2: 145,763,744 (GRCm39) |
A498V |
probably benign |
Het |
| Cux1 |
A |
G |
5: 136,303,979 (GRCm39) |
L1394P |
probably benign |
Het |
| Dapp1 |
T |
C |
3: 137,641,404 (GRCm39) |
Y197C |
probably damaging |
Het |
| Dcc |
A |
G |
18: 71,959,280 (GRCm39) |
I164T |
probably benign |
Het |
| Disp3 |
T |
A |
4: 148,344,976 (GRCm39) |
I472F |
probably damaging |
Het |
| Gm10392 |
A |
T |
11: 77,408,306 (GRCm39) |
D104E |
probably benign |
Het |
| Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
| Gpd1 |
A |
G |
15: 99,618,112 (GRCm39) |
I143V |
possibly damaging |
Het |
| Hmcn1 |
T |
A |
1: 150,608,643 (GRCm39) |
N1513I |
possibly damaging |
Het |
| Jakmip2 |
T |
C |
18: 43,680,159 (GRCm39) |
I733V |
probably benign |
Het |
| Klhl12 |
T |
A |
1: 134,391,689 (GRCm39) |
L107H |
probably damaging |
Het |
| Lcn8 |
A |
G |
2: 25,545,157 (GRCm39) |
D109G |
probably damaging |
Het |
| Maz |
A |
T |
7: 126,623,614 (GRCm39) |
|
probably null |
Het |
| Mttp |
T |
A |
3: 137,812,890 (GRCm39) |
D595V |
probably damaging |
Het |
| Mymk |
A |
C |
2: 26,956,406 (GRCm39) |
L58R |
possibly damaging |
Het |
| Nckap1 |
A |
C |
2: 80,339,097 (GRCm39) |
I977S |
probably damaging |
Het |
| Nckap1l |
A |
T |
15: 103,399,442 (GRCm39) |
I1021F |
probably benign |
Het |
| Or12d2 |
A |
T |
17: 37,624,556 (GRCm39) |
C240S |
probably damaging |
Het |
| Or4f14b |
A |
T |
2: 111,775,339 (GRCm39) |
M154K |
probably benign |
Het |
| Or4f6 |
A |
T |
2: 111,839,361 (GRCm39) |
S57T |
possibly damaging |
Het |
| Or6c38 |
G |
A |
10: 128,929,747 (GRCm39) |
T32I |
possibly damaging |
Het |
| Pde5a |
T |
A |
3: 122,629,259 (GRCm39) |
F644L |
probably damaging |
Het |
| Pdzd2 |
A |
G |
15: 12,592,440 (GRCm39) |
I68T |
probably damaging |
Het |
| Pik3r4 |
T |
A |
9: 105,563,349 (GRCm39) |
V1242D |
possibly damaging |
Het |
| Ppp6r2 |
G |
T |
15: 89,162,929 (GRCm39) |
W517L |
probably damaging |
Het |
| Scrib |
A |
T |
15: 75,933,616 (GRCm39) |
I703K |
probably benign |
Het |
| Siglecg |
C |
A |
7: 43,058,187 (GRCm39) |
Q25K |
probably benign |
Het |
| Slc12a3 |
G |
A |
8: 95,092,447 (GRCm39) |
|
probably null |
Het |
| Slc6a13 |
G |
T |
6: 121,302,116 (GRCm39) |
|
probably null |
Het |
| Stard13 |
A |
T |
5: 150,986,309 (GRCm39) |
D282E |
probably damaging |
Het |
| Tpte |
A |
T |
8: 22,845,489 (GRCm39) |
Y513F |
possibly damaging |
Het |
| Ubox5 |
T |
A |
2: 130,442,579 (GRCm39) |
K36I |
possibly damaging |
Het |
|
| Other mutations in Serpina1b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00544:Serpina1b
|
APN |
12 |
103,695,555 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL00990:Serpina1b
|
APN |
12 |
103,694,525 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03258:Serpina1b
|
APN |
12 |
103,696,655 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03392:Serpina1b
|
APN |
12 |
103,698,329 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R1937:Serpina1b
|
UTSW |
12 |
103,698,420 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2383:Serpina1b
|
UTSW |
12 |
103,694,539 (GRCm39) |
missense |
probably benign |
|
|
R3789:Serpina1b
|
UTSW |
12 |
103,695,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4690:Serpina1b
|
UTSW |
12 |
103,698,639 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5164:Serpina1b
|
UTSW |
12 |
103,698,346 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5650:Serpina1b
|
UTSW |
12 |
103,694,694 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R6017:Serpina1b
|
UTSW |
12 |
103,695,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6241:Serpina1b
|
UTSW |
12 |
103,695,515 (GRCm39) |
splice site |
probably null |
|
|
R6522:Serpina1b
|
UTSW |
12 |
103,701,296 (GRCm39) |
splice site |
probably null |
|
|
R6745:Serpina1b
|
UTSW |
12 |
103,696,614 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R6884:Serpina1b
|
UTSW |
12 |
103,698,712 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7053:Serpina1b
|
UTSW |
12 |
103,698,688 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7208:Serpina1b
|
UTSW |
12 |
103,694,553 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7679:Serpina1b
|
UTSW |
12 |
103,696,774 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7908:Serpina1b
|
UTSW |
12 |
103,694,566 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R8056:Serpina1b
|
UTSW |
12 |
103,784,137 (GRCm39) |
intron |
probably benign |
|
|
R8237:Serpina1b
|
UTSW |
12 |
103,785,063 (GRCm39) |
splice site |
probably null |
|
|
R9092:Serpina1b
|
UTSW |
12 |
103,696,540 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9112:Serpina1b
|
UTSW |
12 |
103,698,699 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9123:Serpina1b
|
UTSW |
12 |
103,696,566 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9310:Serpina1b
|
UTSW |
12 |
103,698,756 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9358:Serpina1b
|
UTSW |
12 |
103,694,653 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R9409:Serpina1b
|
UTSW |
12 |
103,694,607 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2014-05-07 |
Incidental Mutation