Incidental Mutation 'IGL00091:Pdia3'
| ID |
1853 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Pdia3
|
| Ensembl Gene |
ENSMUSG00000027248 |
| Gene Name |
protein disulfide isomerase associated 3 |
| Synonyms |
PDI-Q2, ERp57, ERp60, ERp61, Grp58, PDI, Plca, Erp |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL00091
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
121244383-121269168 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 121244659 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Proline
at position 47
(L47P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000028683
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028683]
[ENSMUST00000038073]
[ENSMUST00000135079]
[ENSMUST00000154604]
|
| AlphaFold |
P27773 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000028683
AA Change: L47P
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000028683
Gene: ENSMUSG00000027248
AA Change: L47P
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
|
Pfam:Thioredoxin
|
26 |
131 |
5.2e-36 |
PFAM |
|
Pfam:Thioredoxin_6
|
160 |
355 |
2e-29 |
PFAM |
|
Pfam:Thioredoxin
|
377 |
483 |
9.5e-33 |
PFAM |
|
low complexity region
|
487 |
503 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000038073
|
| SMART Domains |
Protein: ENSMUSP00000037222
Gene: ENSMUSG00000033486
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
78 |
91 |
N/A |
INTRINSIC |
|
Pfam:Ion_trans
|
105 |
350 |
1e-35 |
PFAM |
|
low complexity region
|
422 |
447 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
450 |
473 |
3.72e-11 |
PROSPERO |
|
internal_repeat_1
|
465 |
488 |
3.72e-11 |
PROSPERO |
|
low complexity region
|
491 |
502 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000123982
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000135079
AA Change: L24P
PolyPhen 2
Score 0.112 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000119337
Gene: ENSMUSG00000027248
AA Change: L24P
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Thioredoxin
|
3 |
105 |
5.1e-35 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153378
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000154604
|
| SMART Domains |
Protein: ENSMUSP00000119091
Gene: ENSMUSG00000033486
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
78 |
91 |
N/A |
INTRINSIC |
|
| 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 of the endoplasmic reticulum that interacts with lectin chaperones calreticulin and calnexin to modulate folding of newly synthesized glycoproteins. The protein was once thought to be a phospholipase; however, it has been demonstrated that the protein actually has protein disulfide isomerase activity. It is thought that complexes of lectins and this protein mediate protein folding by promoting formation of disulfide bonds in their glycoprotein substrates. This protein also functions as a molecular chaperone that prevents the formation of protein aggregates. [provided by RefSeq, Dec 2016]
PHENOTYPE: Mice homozygous for a knock-out allele die by E13.5 with minor changes in ER calcium capacity and unfolded protein response in mouse embryonic fibroblasts. Mice homozygous for a gene trap allele die prior to birth while heterozygous mice exhibit abnormalbone volume bone morphology. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 47 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abraxas2 |
A |
T |
7: 132,485,157 (GRCm39) |
Y400F |
probably benign |
Het |
| Adamts8 |
C |
A |
9: 30,864,796 (GRCm39) |
T429K |
probably damaging |
Het |
| Adgrv1 |
C |
T |
13: 81,726,220 (GRCm39) |
D602N |
probably damaging |
Het |
| Ano7 |
A |
T |
1: 93,329,888 (GRCm39) |
H775L |
probably benign |
Het |
| Apoo-ps |
A |
T |
13: 107,551,134 (GRCm39) |
|
noncoding transcript |
Het |
| Arid2 |
T |
C |
15: 96,270,183 (GRCm39) |
V1432A |
probably benign |
Het |
| Atoh1 |
T |
C |
6: 64,706,568 (GRCm39) |
S88P |
possibly damaging |
Het |
| C130050O18Rik |
A |
G |
5: 139,400,601 (GRCm39) |
E218G |
probably damaging |
Het |
| Cacna2d1 |
T |
A |
5: 16,417,942 (GRCm39) |
F155L |
probably damaging |
Het |
| Car4 |
C |
T |
11: 84,856,593 (GRCm39) |
P294S |
probably damaging |
Het |
| Cyp1a2 |
G |
T |
9: 57,589,352 (GRCm39) |
S154* |
probably null |
Het |
| Cyp3a25 |
A |
T |
5: 145,938,273 (GRCm39) |
Y68* |
probably null |
Het |
| Dmbt1 |
C |
A |
7: 130,681,270 (GRCm39) |
|
probably benign |
Het |
| Dnajc22 |
T |
A |
15: 98,999,059 (GRCm39) |
F81L |
possibly damaging |
Het |
| Eml5 |
G |
A |
12: 98,839,468 (GRCm39) |
|
probably benign |
Het |
| Fpgs |
A |
T |
2: 32,576,559 (GRCm39) |
|
probably benign |
Het |
| Gab2 |
T |
C |
7: 96,951,650 (GRCm39) |
S537P |
possibly damaging |
Het |
| Gmds |
G |
A |
13: 32,418,373 (GRCm39) |
S37L |
probably damaging |
Het |
| Ipo13 |
T |
C |
4: 117,760,602 (GRCm39) |
E626G |
probably benign |
Het |
| Kcng1 |
T |
C |
2: 168,110,684 (GRCm39) |
H160R |
probably benign |
Het |
| Lama3 |
A |
G |
18: 12,713,349 (GRCm39) |
T1608A |
probably benign |
Het |
| Lama4 |
A |
C |
10: 38,948,801 (GRCm39) |
S855R |
probably damaging |
Het |
| Ltbp1 |
C |
T |
17: 75,532,333 (GRCm39) |
H454Y |
probably damaging |
Het |
| Map3k14 |
C |
A |
11: 103,118,405 (GRCm39) |
G594C |
probably damaging |
Het |
| Mcph1 |
A |
G |
8: 18,682,636 (GRCm39) |
N591S |
possibly damaging |
Het |
| Moxd1 |
G |
A |
10: 24,155,762 (GRCm39) |
V289I |
probably damaging |
Het |
| Mptx2 |
T |
G |
1: 173,102,455 (GRCm39) |
N78T |
probably damaging |
Het |
| Muc4 |
G |
A |
16: 32,754,086 (GRCm38) |
G1321R |
probably benign |
Het |
| Muc6 |
A |
C |
7: 141,218,497 (GRCm39) |
S2059A |
probably benign |
Het |
| Nup50 |
T |
A |
15: 84,819,605 (GRCm39) |
F293Y |
probably benign |
Het |
| Ogn |
A |
G |
13: 49,774,514 (GRCm39) |
Y219C |
probably damaging |
Het |
| Piwil4 |
A |
T |
9: 14,614,393 (GRCm39) |
D786E |
probably damaging |
Het |
| Pspc1 |
A |
G |
14: 57,009,168 (GRCm39) |
L222P |
probably damaging |
Het |
| Ptchd3 |
T |
A |
11: 121,721,972 (GRCm39) |
Y282N |
probably damaging |
Het |
| Reln |
C |
A |
5: 22,244,563 (GRCm39) |
G805V |
possibly damaging |
Het |
| Serpini2 |
T |
C |
3: 75,156,549 (GRCm39) |
Y327C |
probably damaging |
Het |
| Spire2 |
A |
G |
8: 124,080,798 (GRCm39) |
D14G |
probably damaging |
Het |
| Stab2 |
A |
T |
10: 86,705,070 (GRCm39) |
|
probably null |
Het |
| Timeless |
T |
C |
10: 128,077,577 (GRCm39) |
L219P |
probably damaging |
Het |
| Tmem63a |
C |
T |
1: 180,790,653 (GRCm39) |
T437M |
probably damaging |
Het |
| Tslp |
A |
G |
18: 32,948,448 (GRCm39) |
|
probably benign |
Het |
| Ttbk2 |
C |
A |
2: 120,579,314 (GRCm39) |
G534* |
probably null |
Het |
| Uggt1 |
T |
C |
1: 36,218,633 (GRCm39) |
|
probably benign |
Het |
| Vmn2r118 |
T |
C |
17: 55,899,708 (GRCm39) |
E732G |
probably damaging |
Het |
| Zfhx2 |
G |
A |
14: 55,304,022 (GRCm39) |
P1321S |
possibly damaging |
Het |
| Zfp58 |
A |
G |
13: 67,639,114 (GRCm39) |
V459A |
probably benign |
Het |
| Zfp831 |
T |
C |
2: 174,487,451 (GRCm39) |
S709P |
possibly damaging |
Het |
|
| Other mutations in Pdia3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00777:Pdia3
|
APN |
2 |
121,260,037 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02020:Pdia3
|
APN |
2 |
121,266,900 (GRCm39) |
splice site |
probably null |
|
|
IGL02437:Pdia3
|
APN |
2 |
121,264,129 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02988:Pdia3
|
UTSW |
2 |
121,260,037 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4812001:Pdia3
|
UTSW |
2 |
121,264,011 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0242:Pdia3
|
UTSW |
2 |
121,244,592 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0242:Pdia3
|
UTSW |
2 |
121,244,592 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0606:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0612:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0658:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0724:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0730:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0880:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0882:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1157:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1160:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1238:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1619:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1853:Pdia3
|
UTSW |
2 |
121,262,144 (GRCm39) |
missense |
probably benign |
0.20 |
|
R1854:Pdia3
|
UTSW |
2 |
121,262,144 (GRCm39) |
missense |
probably benign |
0.20 |
|
R2014:Pdia3
|
UTSW |
2 |
121,265,301 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2103:Pdia3
|
UTSW |
2 |
121,264,474 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4160:Pdia3
|
UTSW |
2 |
121,244,596 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4628:Pdia3
|
UTSW |
2 |
121,244,620 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5032:Pdia3
|
UTSW |
2 |
121,244,620 (GRCm39) |
missense |
probably benign |
0.28 |
|
R5279:Pdia3
|
UTSW |
2 |
121,244,484 (GRCm39) |
unclassified |
probably benign |
|
|
R5598:Pdia3
|
UTSW |
2 |
121,244,611 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R5815:Pdia3
|
UTSW |
2 |
121,266,892 (GRCm39) |
nonsense |
probably null |
|
|
R7162:Pdia3
|
UTSW |
2 |
121,260,002 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7729:Pdia3
|
UTSW |
2 |
121,262,838 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
X0012:Pdia3
|
UTSW |
2 |
121,266,426 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
| Posted On |
2011-07-12 |
Incidental Mutation