Incidental Mutation 'IGL02526:Atp2a3'
| ID |
297109 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Atp2a3
|
| Ensembl Gene |
ENSMUSG00000020788 |
| Gene Name |
ATPase, Ca++ transporting, ubiquitous |
| Synonyms |
Serca3 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.130)
|
| Stock # |
IGL02526
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
72851995-72883869 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 72866165 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Asparagine
at position 262
(H262N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000104125
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021142]
[ENSMUST00000108484]
[ENSMUST00000108485]
[ENSMUST00000108486]
[ENSMUST00000163326]
|
| AlphaFold |
Q64518 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000021142
AA Change: H262N
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000021142
Gene: ENSMUSG00000020788
AA Change: H262N
| Domain | Start | End | E-Value | Type |
|---|
|
Cation_ATPase_N
|
3 |
77 |
4.43e-12 |
SMART |
|
Pfam:E1-E2_ATPase
|
92 |
340 |
3.1e-66 |
PFAM |
|
Pfam:Hydrolase
|
345 |
715 |
5.2e-22 |
PFAM |
|
Pfam:HAD
|
348 |
712 |
3e-19 |
PFAM |
|
Pfam:Cation_ATPase
|
418 |
528 |
4.4e-23 |
PFAM |
|
Pfam:Hydrolase_3
|
684 |
747 |
4.5e-8 |
PFAM |
|
Pfam:Cation_ATPase_C
|
784 |
987 |
1.8e-48 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000108484
AA Change: H262N
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000104124
Gene: ENSMUSG00000020788
AA Change: H262N
| Domain | Start | End | E-Value | Type |
|---|
|
Cation_ATPase_N
|
3 |
77 |
3.4e-16 |
SMART |
|
Pfam:E1-E2_ATPase
|
93 |
341 |
8.9e-67 |
PFAM |
|
Pfam:Hydrolase
|
345 |
697 |
8.1e-27 |
PFAM |
|
Pfam:HAD
|
348 |
694 |
4.1e-14 |
PFAM |
|
Pfam:Hydrolase_like2
|
418 |
528 |
2.1e-21 |
PFAM |
|
Pfam:Hydrolase_3
|
666 |
729 |
2.6e-6 |
PFAM |
|
transmembrane domain
|
742 |
764 |
N/A |
INTRINSIC |
|
Pfam:Cation_ATPase_C
|
766 |
969 |
4.2e-46 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000108485
AA Change: H262N
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000104125
Gene: ENSMUSG00000020788
AA Change: H262N
| Domain | Start | End | E-Value | Type |
|---|
|
Cation_ATPase_N
|
3 |
77 |
4.43e-12 |
SMART |
|
Pfam:E1-E2_ATPase
|
93 |
341 |
1.1e-68 |
PFAM |
|
Pfam:Hydrolase
|
345 |
715 |
2.7e-33 |
PFAM |
|
Pfam:HAD
|
348 |
712 |
1.3e-17 |
PFAM |
|
Pfam:Hydrolase_like2
|
418 |
528 |
2.2e-23 |
PFAM |
|
Pfam:Hydrolase_3
|
684 |
747 |
1.8e-8 |
PFAM |
|
Pfam:Cation_ATPase_C
|
784 |
987 |
2.6e-48 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000108486
AA Change: H262N
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000104126
Gene: ENSMUSG00000020788
AA Change: H262N
| Domain | Start | End | E-Value | Type |
|---|
|
Cation_ATPase_N
|
3 |
77 |
4.43e-12 |
SMART |
|
Pfam:E1-E2_ATPase
|
93 |
341 |
1.4e-68 |
PFAM |
|
Pfam:Hydrolase
|
345 |
697 |
2.8e-28 |
PFAM |
|
Pfam:HAD
|
348 |
694 |
1.1e-15 |
PFAM |
|
Pfam:Hydrolase_like2
|
418 |
528 |
1.7e-23 |
PFAM |
|
Pfam:Hydrolase_3
|
666 |
729 |
5.1e-8 |
PFAM |
|
Pfam:Cation_ATPase_C
|
766 |
969 |
2.5e-48 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000149493
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000163326
AA Change: H262N
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000127036
Gene: ENSMUSG00000020788
AA Change: H262N
| Domain | Start | End | E-Value | Type |
|---|
|
Cation_ATPase_N
|
3 |
77 |
4.43e-12 |
SMART |
|
Pfam:E1-E2_ATPase
|
93 |
341 |
1.4e-68 |
PFAM |
|
Pfam:Hydrolase
|
345 |
715 |
6.5e-33 |
PFAM |
|
Pfam:HAD
|
348 |
712 |
2.5e-17 |
PFAM |
|
Pfam:Hydrolase_like2
|
418 |
528 |
1.7e-23 |
PFAM |
|
Pfam:Hydrolase_3
|
684 |
747 |
5.1e-8 |
PFAM |
|
Pfam:Cation_ATPase_C
|
784 |
987 |
2.5e-48 |
PFAM |
|
| 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 one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is involved in calcium sequestration associated with muscular excitation and contraction. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutation of this gene results in reduced endothelial-dependent relaxation in the aorta. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 39 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acad10 |
A |
G |
5: 121,784,923 (GRCm39) |
V231A |
probably damaging |
Het |
| Aff4 |
T |
C |
11: 53,297,509 (GRCm39) |
|
probably benign |
Het |
| Ano2 |
G |
A |
6: 125,849,714 (GRCm39) |
|
probably null |
Het |
| Aspm |
A |
G |
1: 139,417,457 (GRCm39) |
E2818G |
probably benign |
Het |
| Caprin1 |
T |
C |
2: 103,605,948 (GRCm39) |
|
probably benign |
Het |
| Clca3a2 |
T |
C |
3: 144,793,779 (GRCm39) |
H292R |
probably benign |
Het |
| Dnah11 |
G |
A |
12: 118,143,353 (GRCm39) |
T430M |
possibly damaging |
Het |
| Fgd6 |
A |
G |
10: 93,936,373 (GRCm39) |
N902S |
probably benign |
Het |
| Grm3 |
A |
G |
5: 9,639,847 (GRCm39) |
I66T |
probably damaging |
Het |
| H13 |
T |
A |
2: 152,530,602 (GRCm39) |
F158L |
probably damaging |
Het |
| Kcnb2 |
A |
G |
1: 15,780,979 (GRCm39) |
E617G |
probably damaging |
Het |
| Kcnh7 |
T |
C |
2: 62,680,781 (GRCm39) |
S269G |
possibly damaging |
Het |
| Krit1 |
T |
A |
5: 3,872,103 (GRCm39) |
I376N |
probably damaging |
Het |
| Lonrf2 |
T |
A |
1: 38,839,791 (GRCm39) |
M435L |
probably benign |
Het |
| Map2 |
A |
T |
1: 66,419,876 (GRCm39) |
D69V |
possibly damaging |
Het |
| Mon1b |
G |
T |
8: 114,365,455 (GRCm39) |
R261L |
possibly damaging |
Het |
| Myh3 |
C |
T |
11: 66,978,371 (GRCm39) |
P453S |
probably benign |
Het |
| Or51d1 |
T |
A |
7: 102,348,291 (GRCm39) |
V282D |
possibly damaging |
Het |
| Pi4k2b |
T |
C |
5: 52,925,081 (GRCm39) |
F442L |
probably damaging |
Het |
| Pla2g12b |
T |
A |
10: 59,252,275 (GRCm39) |
C49S |
probably damaging |
Het |
| Polr2a |
C |
T |
11: 69,630,293 (GRCm39) |
R1258Q |
probably benign |
Het |
| Prmt8 |
A |
C |
6: 127,688,786 (GRCm39) |
S195A |
probably damaging |
Het |
| Pwp1 |
T |
A |
10: 85,717,967 (GRCm39) |
|
probably null |
Het |
| Rxfp1 |
C |
A |
3: 79,578,153 (GRCm39) |
|
probably null |
Het |
| Skor1 |
A |
T |
9: 63,053,159 (GRCm39) |
M270K |
probably damaging |
Het |
| Slc12a4 |
T |
C |
8: 106,676,438 (GRCm39) |
N495D |
possibly damaging |
Het |
| Slc26a3 |
T |
C |
12: 31,507,095 (GRCm39) |
V350A |
probably damaging |
Het |
| Slc44a4 |
T |
A |
17: 35,147,463 (GRCm39) |
V430D |
probably damaging |
Het |
| Slit2 |
C |
A |
5: 48,461,565 (GRCm39) |
C1537* |
probably null |
Het |
| Tas2r135 |
A |
T |
6: 42,383,214 (GRCm39) |
H251L |
probably damaging |
Het |
| Tbr1 |
T |
C |
2: 61,642,042 (GRCm39) |
F436L |
probably benign |
Het |
| Them6 |
A |
T |
15: 74,593,504 (GRCm39) |
T121S |
possibly damaging |
Het |
| Tmem145 |
G |
A |
7: 25,007,657 (GRCm39) |
M221I |
probably benign |
Het |
| Trrap |
T |
C |
5: 144,761,360 (GRCm39) |
V2300A |
probably benign |
Het |
| Usf3 |
C |
A |
16: 44,040,674 (GRCm39) |
A1718D |
possibly damaging |
Het |
| Usp10 |
C |
A |
8: 120,675,514 (GRCm39) |
S511Y |
probably damaging |
Het |
| Wdr38 |
A |
T |
2: 38,888,424 (GRCm39) |
N7I |
probably damaging |
Het |
| Wnt9a |
T |
C |
11: 59,219,331 (GRCm39) |
F119S |
probably damaging |
Het |
| Zc3h7b |
G |
A |
15: 81,677,338 (GRCm39) |
G880S |
probably benign |
Het |
|
| Other mutations in Atp2a3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00834:Atp2a3
|
APN |
11 |
72,873,613 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01141:Atp2a3
|
APN |
11 |
72,873,491 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01949:Atp2a3
|
APN |
11 |
72,872,723 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02267:Atp2a3
|
APN |
11 |
72,878,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02385:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02390:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02391:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02392:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02487:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02525:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02527:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02581:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02643:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02644:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02646:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02647:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02649:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02650:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02651:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02667:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02668:Atp2a3
|
APN |
11 |
72,866,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02819:Atp2a3
|
APN |
11 |
72,868,033 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02888:Atp2a3
|
APN |
11 |
72,867,954 (GRCm39) |
splice site |
probably benign |
|
|
Aplomb
|
UTSW |
11 |
72,871,274 (GRCm39) |
missense |
probably damaging |
1.00 |
|
flair
|
UTSW |
11 |
72,866,223 (GRCm39) |
missense |
probably damaging |
1.00 |
|
panache
|
UTSW |
11 |
72,872,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0193:Atp2a3
|
UTSW |
11 |
72,863,046 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R0357:Atp2a3
|
UTSW |
11 |
72,861,757 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0376:Atp2a3
|
UTSW |
11 |
72,873,528 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0452:Atp2a3
|
UTSW |
11 |
72,868,058 (GRCm39) |
splice site |
probably null |
|
|
R0494:Atp2a3
|
UTSW |
11 |
72,872,731 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0588:Atp2a3
|
UTSW |
11 |
72,863,850 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R0674:Atp2a3
|
UTSW |
11 |
72,872,711 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1586:Atp2a3
|
UTSW |
11 |
72,882,570 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1666:Atp2a3
|
UTSW |
11 |
72,869,633 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1994:Atp2a3
|
UTSW |
11 |
72,866,240 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2087:Atp2a3
|
UTSW |
11 |
72,871,274 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4675:Atp2a3
|
UTSW |
11 |
72,872,623 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4795:Atp2a3
|
UTSW |
11 |
72,863,855 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4898:Atp2a3
|
UTSW |
11 |
72,873,506 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5083:Atp2a3
|
UTSW |
11 |
72,873,652 (GRCm39) |
missense |
probably null |
0.49 |
|
R5174:Atp2a3
|
UTSW |
11 |
72,871,041 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5266:Atp2a3
|
UTSW |
11 |
72,866,223 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5304:Atp2a3
|
UTSW |
11 |
72,879,383 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5802:Atp2a3
|
UTSW |
11 |
72,863,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6107:Atp2a3
|
UTSW |
11 |
72,879,287 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R6157:Atp2a3
|
UTSW |
11 |
72,871,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6760:Atp2a3
|
UTSW |
11 |
72,873,566 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7406:Atp2a3
|
UTSW |
11 |
72,869,576 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8818:Atp2a3
|
UTSW |
11 |
72,872,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9376:Atp2a3
|
UTSW |
11 |
72,863,290 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9456:Atp2a3
|
UTSW |
11 |
72,871,131 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9562:Atp2a3
|
UTSW |
11 |
72,873,578 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9608:Atp2a3
|
UTSW |
11 |
72,879,866 (GRCm39) |
missense |
probably benign |
0.40 |
|
Z1176:Atp2a3
|
UTSW |
11 |
72,880,366 (GRCm39) |
missense |
probably benign |
|
|
Z1176:Atp2a3
|
UTSW |
11 |
72,871,448 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
Z1177:Atp2a3
|
UTSW |
11 |
72,871,153 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
| Posted On |
2015-04-16 |
Incidental Mutation