Incidental Mutation 'R7216:Atp2c1'
ID |
561482 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Atp2c1
|
Ensembl Gene |
ENSMUSG00000032570 |
Gene Name |
ATPase, Ca++-sequestering |
Synonyms |
ATP2C1A, D930003G21Rik, SPCA, 1700121J11Rik, PMR1 |
MMRRC Submission |
045288-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.403)
|
Stock # |
R7216 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
105288561-105398456 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 105344930 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 102
(D102E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000082220
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000038118]
[ENSMUST00000085133]
[ENSMUST00000112558]
[ENSMUST00000163879]
[ENSMUST00000176036]
[ENSMUST00000176190]
[ENSMUST00000176363]
[ENSMUST00000176651]
[ENSMUST00000176770]
[ENSMUST00000177074]
[ENSMUST00000177334]
|
AlphaFold |
Q80XR2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000038118
AA Change: D68E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000039103 Gene: ENSMUSG00000032570 AA Change: D68E
Domain | Start | End | E-Value | Type |
Cation_ATPase_N
|
25 |
99 |
1.85e-14 |
SMART |
Pfam:E1-E2_ATPase
|
105 |
339 |
2.3e-75 |
PFAM |
Pfam:Hydrolase
|
343 |
655 |
2.9e-31 |
PFAM |
Pfam:HAD
|
346 |
652 |
7.7e-15 |
PFAM |
Pfam:Hydrolase_like2
|
408 |
492 |
9.5e-20 |
PFAM |
low complexity region
|
706 |
721 |
N/A |
INTRINSIC |
Pfam:Cation_ATPase_C
|
725 |
897 |
4e-47 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000085133
AA Change: D102E
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000082220 Gene: ENSMUSG00000032570 AA Change: D102E
Domain | Start | End | E-Value | Type |
Cation_ATPase_N
|
59 |
133 |
1.85e-14 |
SMART |
Pfam:E1-E2_ATPase
|
138 |
372 |
3.4e-62 |
PFAM |
Pfam:Hydrolase
|
377 |
689 |
2.6e-23 |
PFAM |
Pfam:HAD
|
380 |
686 |
7.8e-14 |
PFAM |
Pfam:Cation_ATPase
|
442 |
526 |
3.2e-19 |
PFAM |
low complexity region
|
740 |
755 |
N/A |
INTRINSIC |
Pfam:Cation_ATPase_C
|
759 |
931 |
3.8e-48 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000112558
AA Change: D68E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000108177 Gene: ENSMUSG00000032570 AA Change: D68E
Domain | Start | End | E-Value | Type |
Cation_ATPase_N
|
25 |
99 |
1.85e-14 |
SMART |
Pfam:E1-E2_ATPase
|
105 |
339 |
2.3e-75 |
PFAM |
Pfam:Hydrolase
|
343 |
655 |
2.9e-31 |
PFAM |
Pfam:HAD
|
346 |
652 |
7.7e-15 |
PFAM |
Pfam:Hydrolase_like2
|
408 |
492 |
9.5e-20 |
PFAM |
low complexity region
|
706 |
721 |
N/A |
INTRINSIC |
Pfam:Cation_ATPase_C
|
725 |
897 |
4e-47 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000163879
AA Change: D52E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000129617 Gene: ENSMUSG00000032570 AA Change: D52E
Domain | Start | End | E-Value | Type |
Cation_ATPase_N
|
9 |
83 |
1.85e-14 |
SMART |
Pfam:E1-E2_ATPase
|
89 |
323 |
5.2e-76 |
PFAM |
Pfam:Hydrolase
|
327 |
639 |
5.6e-32 |
PFAM |
Pfam:HAD
|
330 |
636 |
1.4e-15 |
PFAM |
Pfam:Hydrolase_like2
|
392 |
476 |
3.2e-20 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176036
AA Change: D68E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000135010 Gene: ENSMUSG00000032570 AA Change: D68E
Domain | Start | End | E-Value | Type |
Cation_ATPase_N
|
25 |
99 |
1.85e-14 |
SMART |
Pfam:E1-E2_ATPase
|
105 |
177 |
1.1e-22 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176190
AA Change: D52E
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000135320 Gene: ENSMUSG00000032570 AA Change: D52E
Domain | Start | End | E-Value | Type |
Cation_ATPase_N
|
9 |
83 |
1.85e-14 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176363
AA Change: D72E
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000135170 Gene: ENSMUSG00000032570 AA Change: D72E
Domain | Start | End | E-Value | Type |
Cation_ATPase_N
|
29 |
103 |
1.85e-14 |
SMART |
Pfam:E1-E2_ATPase
|
109 |
231 |
3e-36 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176651
AA Change: D52E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000135732 Gene: ENSMUSG00000032570 AA Change: D52E
Domain | Start | End | E-Value | Type |
Cation_ATPase_N
|
9 |
83 |
1.85e-14 |
SMART |
Pfam:E1-E2_ATPase
|
89 |
253 |
6.4e-51 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176770
|
SMART Domains |
Protein: ENSMUSP00000134764 Gene: ENSMUSG00000032570
Domain | Start | End | E-Value | Type |
Pfam:E1-E2_ATPase
|
100 |
334 |
8.9e-76 |
PFAM |
Pfam:Hydrolase
|
338 |
650 |
1.1e-31 |
PFAM |
Pfam:HAD
|
341 |
647 |
2.7e-15 |
PFAM |
Pfam:Hydrolase_like2
|
403 |
487 |
4.8e-20 |
PFAM |
low complexity region
|
701 |
716 |
N/A |
INTRINSIC |
Pfam:Cation_ATPase_C
|
720 |
892 |
1.6e-47 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000177074
AA Change: D68E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000135646 Gene: ENSMUSG00000032570 AA Change: D68E
Domain | Start | End | E-Value | Type |
Cation_ATPase_N
|
25 |
99 |
1.85e-14 |
SMART |
Pfam:E1-E2_ATPase
|
105 |
339 |
8.2e-76 |
PFAM |
Pfam:Hydrolase
|
343 |
655 |
1e-31 |
PFAM |
Pfam:HAD
|
346 |
652 |
2.5e-15 |
PFAM |
Pfam:Hydrolase_like2
|
408 |
492 |
4.5e-20 |
PFAM |
low complexity region
|
706 |
721 |
N/A |
INTRINSIC |
Pfam:Cation_ATPase_C
|
725 |
886 |
7e-44 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000177334
AA Change: D68E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000134902 Gene: ENSMUSG00000032570 AA Change: D68E
Domain | Start | End | E-Value | Type |
Cation_ATPase_N
|
25 |
99 |
1.85e-14 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011] PHENOTYPE: Mice homozygous for a knock-out allele show embryonic growth retardation, failure of rostral neural tube closure, Golgi and endoplasmic reticulum stress, increased apoptosis, accumulation of intracellular lipid droplets and midgestational lethality. Agedheterozygotes develop squamous cell tumors. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap6 |
T |
A |
12: 53,187,240 (GRCm39) |
N1551K |
probably benign |
Het |
Amy2a1 |
T |
C |
3: 113,324,090 (GRCm39) |
D150G |
possibly damaging |
Het |
Atp2b1 |
T |
A |
10: 98,822,839 (GRCm39) |
C165S |
probably benign |
Het |
Capn8 |
C |
A |
1: 182,426,363 (GRCm39) |
R233S |
possibly damaging |
Het |
Cd48 |
T |
C |
1: 171,523,390 (GRCm39) |
S78P |
probably damaging |
Het |
Clasp1 |
T |
A |
1: 118,475,648 (GRCm39) |
D944E |
probably benign |
Het |
Clip2 |
A |
G |
5: 134,531,771 (GRCm39) |
M678T |
probably benign |
Het |
Clmp |
T |
C |
9: 40,672,205 (GRCm39) |
Y12H |
possibly damaging |
Het |
Col22a1 |
A |
T |
15: 71,845,694 (GRCm39) |
V356D |
probably damaging |
Het |
Copg2 |
A |
T |
6: 30,862,535 (GRCm39) |
D101E |
probably damaging |
Het |
Cpsf6 |
G |
A |
10: 117,197,928 (GRCm39) |
P229S |
unknown |
Het |
Dgke |
T |
C |
11: 88,941,163 (GRCm39) |
D340G |
probably benign |
Het |
Dlg1 |
TAAA |
TAA |
16: 31,615,736 (GRCm39) |
|
probably null |
Het |
Dlg5 |
G |
A |
14: 24,186,706 (GRCm39) |
Q1865* |
probably null |
Het |
Dnajc2 |
C |
T |
5: 21,981,777 (GRCm39) |
R123Q |
probably damaging |
Het |
Efcab3 |
A |
T |
11: 104,771,375 (GRCm39) |
K2633N |
possibly damaging |
Het |
Egln2 |
T |
C |
7: 26,859,254 (GRCm39) |
D365G |
probably damaging |
Het |
Epha4 |
T |
C |
1: 77,421,621 (GRCm39) |
D287G |
probably damaging |
Het |
Fat4 |
A |
G |
3: 38,945,192 (GRCm39) |
T1362A |
probably damaging |
Het |
Flt4 |
A |
G |
11: 49,525,508 (GRCm39) |
T685A |
possibly damaging |
Het |
Fras1 |
T |
C |
5: 96,887,173 (GRCm39) |
Y2652H |
probably damaging |
Het |
Gas2 |
A |
G |
7: 51,547,005 (GRCm39) |
E52G |
possibly damaging |
Het |
Gm5093 |
A |
T |
17: 46,751,014 (GRCm39) |
D4E |
not run |
Het |
Gm6370 |
A |
T |
5: 146,430,723 (GRCm39) |
T303S |
probably benign |
Het |
Gpr161 |
A |
G |
1: 165,134,115 (GRCm39) |
I126V |
probably benign |
Het |
Gpr63 |
T |
C |
4: 25,008,038 (GRCm39) |
L254P |
probably damaging |
Het |
H2-M9 |
C |
T |
17: 36,951,594 (GRCm39) |
V294I |
probably benign |
Het |
Insr |
T |
A |
8: 3,253,034 (GRCm39) |
N375I |
possibly damaging |
Het |
Ints1 |
T |
C |
5: 139,754,739 (GRCm39) |
N600S |
possibly damaging |
Het |
Ints10 |
A |
G |
8: 69,274,809 (GRCm39) |
N628S |
probably damaging |
Het |
Irf2 |
A |
G |
8: 47,246,591 (GRCm39) |
T20A |
probably benign |
Het |
Irs1 |
T |
A |
1: 82,267,476 (GRCm39) |
T247S |
probably damaging |
Het |
Islr |
C |
T |
9: 58,064,250 (GRCm39) |
S419N |
unknown |
Het |
Kcna2 |
T |
A |
3: 107,012,109 (GRCm39) |
I230N |
probably damaging |
Het |
Kif3c |
C |
A |
12: 3,416,126 (GRCm39) |
A49E |
probably benign |
Het |
Kifap3 |
A |
T |
1: 163,623,558 (GRCm39) |
K108N |
probably damaging |
Het |
Lama3 |
T |
A |
18: 12,563,057 (GRCm39) |
F527I |
probably damaging |
Het |
Layn |
A |
G |
9: 50,988,352 (GRCm39) |
|
probably benign |
Het |
Lims2 |
G |
T |
18: 32,090,315 (GRCm39) |
W276L |
probably damaging |
Het |
Lsp1 |
T |
C |
7: 142,042,179 (GRCm39) |
L133S |
probably damaging |
Het |
Map3k6 |
T |
G |
4: 132,974,211 (GRCm39) |
V536G |
probably damaging |
Het |
Med7 |
T |
A |
11: 46,331,681 (GRCm39) |
L92H |
probably damaging |
Het |
Mllt1 |
A |
G |
17: 57,234,042 (GRCm39) |
V48A |
probably damaging |
Het |
Mtcl2 |
T |
C |
2: 156,860,290 (GRCm39) |
R1650G |
possibly damaging |
Het |
Neurl4 |
T |
A |
11: 69,801,088 (GRCm39) |
V1153E |
probably damaging |
Het |
Nkx2-1 |
A |
C |
12: 56,581,587 (GRCm39) |
C87G |
probably damaging |
Het |
Nsun7 |
T |
C |
5: 66,436,000 (GRCm39) |
S291P |
probably damaging |
Het |
Or10n1 |
A |
T |
9: 39,525,790 (GRCm39) |
Q309L |
probably benign |
Het |
Or13a18 |
A |
T |
7: 140,190,373 (GRCm39) |
N90I |
possibly damaging |
Het |
Or1p1c |
A |
T |
11: 74,160,550 (GRCm39) |
I112F |
probably damaging |
Het |
Or4e1 |
G |
A |
14: 52,700,945 (GRCm39) |
P174S |
probably damaging |
Het |
Or7g17 |
T |
A |
9: 18,768,632 (GRCm39) |
M237K |
probably benign |
Het |
Pals1 |
G |
A |
12: 78,844,006 (GRCm39) |
R70H |
probably damaging |
Het |
Pbrm1 |
A |
G |
14: 30,767,379 (GRCm39) |
Y331C |
possibly damaging |
Het |
Pirb |
T |
A |
7: 3,719,273 (GRCm39) |
T539S |
probably benign |
Het |
Plch2 |
T |
G |
4: 155,068,685 (GRCm39) |
T1314P |
probably benign |
Het |
Polk |
T |
C |
13: 96,644,728 (GRCm39) |
S133G |
probably benign |
Het |
Pramel27 |
A |
G |
4: 143,578,399 (GRCm39) |
I220V |
probably damaging |
Het |
Prdm5 |
A |
T |
6: 65,904,967 (GRCm39) |
K533* |
probably null |
Het |
Prmt1 |
T |
A |
7: 44,632,997 (GRCm39) |
Q35H |
probably benign |
Het |
Pum3 |
A |
T |
19: 27,401,625 (GRCm39) |
W142R |
probably damaging |
Het |
Rest |
G |
A |
5: 77,430,455 (GRCm39) |
R958H |
probably benign |
Het |
Rictor |
C |
T |
15: 6,798,782 (GRCm39) |
T343M |
probably damaging |
Het |
Ripor2 |
G |
A |
13: 24,855,886 (GRCm39) |
G109R |
probably damaging |
Het |
Sec62 |
C |
T |
3: 30,872,978 (GRCm39) |
Q354* |
probably null |
Het |
Snx14 |
T |
C |
9: 88,263,844 (GRCm39) |
Y847C |
probably damaging |
Het |
Sox7 |
A |
T |
14: 64,185,438 (GRCm39) |
D158V |
probably benign |
Het |
Spag8 |
A |
G |
4: 43,652,034 (GRCm39) |
V350A |
possibly damaging |
Het |
Syngr1 |
A |
T |
15: 79,995,934 (GRCm39) |
I158F |
probably damaging |
Het |
Tacstd2 |
C |
A |
6: 67,511,979 (GRCm39) |
V238L |
probably benign |
Het |
Tex15 |
T |
C |
8: 34,063,014 (GRCm39) |
S815P |
possibly damaging |
Het |
Tmem117 |
A |
T |
15: 94,612,793 (GRCm39) |
T110S |
possibly damaging |
Het |
Tnrc6a |
T |
C |
7: 122,770,718 (GRCm39) |
I836T |
probably benign |
Het |
Trim30b |
C |
A |
7: 104,006,569 (GRCm39) |
V96L |
probably benign |
Het |
Tssk3 |
TGCTATCATGGGG |
TG |
4: 129,383,106 (GRCm39) |
|
probably null |
Het |
Tyk2 |
G |
T |
9: 21,031,822 (GRCm39) |
H418N |
probably benign |
Het |
Uap1 |
G |
T |
1: 169,986,472 (GRCm39) |
T170K |
probably damaging |
Het |
Vmn1r40 |
T |
C |
6: 89,691,606 (GRCm39) |
V141A |
not run |
Het |
Vmn1r54 |
T |
A |
6: 90,246,647 (GRCm39) |
I187K |
probably damaging |
Het |
Vmp1 |
C |
T |
11: 86,492,859 (GRCm39) |
V317M |
probably damaging |
Het |
Wnt8b |
A |
G |
19: 44,500,511 (GRCm39) |
K366R |
probably benign |
Het |
Zfp207 |
C |
T |
11: 80,286,004 (GRCm39) |
P415L |
unknown |
Het |
Zfp263 |
A |
G |
16: 3,562,435 (GRCm39) |
E66G |
probably damaging |
Het |
Zfp764l1 |
A |
G |
7: 126,990,695 (GRCm39) |
S431P |
probably benign |
Het |
Zfp985 |
T |
A |
4: 147,667,913 (GRCm39) |
H260Q |
probably damaging |
Het |
Zmiz1 |
GCC |
GC |
14: 25,576,624 (GRCm39) |
|
probably null |
Het |
Zmiz1 |
A |
G |
14: 25,576,633 (GRCm39) |
R47G |
probably damaging |
Het |
Zmiz1 |
A |
C |
14: 25,576,631 (GRCm39) |
Q46P |
probably damaging |
Het |
|
Other mutations in Atp2c1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00984:Atp2c1
|
APN |
9 |
105,295,778 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01682:Atp2c1
|
APN |
9 |
105,330,041 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01874:Atp2c1
|
APN |
9 |
105,326,024 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02299:Atp2c1
|
APN |
9 |
105,338,286 (GRCm39) |
unclassified |
probably benign |
|
IGL03186:Atp2c1
|
APN |
9 |
105,290,329 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03212:Atp2c1
|
APN |
9 |
105,322,466 (GRCm39) |
missense |
probably damaging |
1.00 |
BB002:Atp2c1
|
UTSW |
9 |
105,319,969 (GRCm39) |
missense |
possibly damaging |
0.92 |
BB012:Atp2c1
|
UTSW |
9 |
105,319,969 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02799:Atp2c1
|
UTSW |
9 |
105,290,242 (GRCm39) |
unclassified |
probably benign |
|
IGL03047:Atp2c1
|
UTSW |
9 |
105,398,206 (GRCm39) |
intron |
probably benign |
|
R0885:Atp2c1
|
UTSW |
9 |
105,298,772 (GRCm39) |
critical splice donor site |
probably null |
|
R1072:Atp2c1
|
UTSW |
9 |
105,336,943 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1469:Atp2c1
|
UTSW |
9 |
105,312,351 (GRCm39) |
nonsense |
probably null |
|
R1469:Atp2c1
|
UTSW |
9 |
105,312,351 (GRCm39) |
nonsense |
probably null |
|
R1611:Atp2c1
|
UTSW |
9 |
105,320,051 (GRCm39) |
missense |
probably damaging |
0.98 |
R1638:Atp2c1
|
UTSW |
9 |
105,309,897 (GRCm39) |
missense |
probably damaging |
0.96 |
R1667:Atp2c1
|
UTSW |
9 |
105,309,996 (GRCm39) |
missense |
probably null |
0.94 |
R1722:Atp2c1
|
UTSW |
9 |
105,316,599 (GRCm39) |
missense |
probably benign |
0.01 |
R1734:Atp2c1
|
UTSW |
9 |
105,291,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R1782:Atp2c1
|
UTSW |
9 |
105,308,786 (GRCm39) |
missense |
probably damaging |
0.99 |
R1964:Atp2c1
|
UTSW |
9 |
105,323,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R2008:Atp2c1
|
UTSW |
9 |
105,309,925 (GRCm39) |
missense |
probably benign |
0.00 |
R2093:Atp2c1
|
UTSW |
9 |
105,295,320 (GRCm39) |
nonsense |
probably null |
|
R3720:Atp2c1
|
UTSW |
9 |
105,300,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R4118:Atp2c1
|
UTSW |
9 |
105,343,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R4273:Atp2c1
|
UTSW |
9 |
105,312,339 (GRCm39) |
missense |
probably benign |
0.10 |
R4763:Atp2c1
|
UTSW |
9 |
105,295,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Atp2c1
|
UTSW |
9 |
105,320,149 (GRCm39) |
missense |
probably benign |
0.03 |
R5121:Atp2c1
|
UTSW |
9 |
105,326,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R5458:Atp2c1
|
UTSW |
9 |
105,291,924 (GRCm39) |
nonsense |
probably null |
|
R5551:Atp2c1
|
UTSW |
9 |
105,336,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R6198:Atp2c1
|
UTSW |
9 |
105,398,271 (GRCm39) |
missense |
probably benign |
0.00 |
R6414:Atp2c1
|
UTSW |
9 |
105,343,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R6432:Atp2c1
|
UTSW |
9 |
105,322,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R6675:Atp2c1
|
UTSW |
9 |
105,330,732 (GRCm39) |
critical splice donor site |
probably null |
|
R6719:Atp2c1
|
UTSW |
9 |
105,301,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R6777:Atp2c1
|
UTSW |
9 |
105,295,799 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6847:Atp2c1
|
UTSW |
9 |
105,295,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R6870:Atp2c1
|
UTSW |
9 |
105,347,261 (GRCm39) |
missense |
probably benign |
0.13 |
R7097:Atp2c1
|
UTSW |
9 |
105,341,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R7120:Atp2c1
|
UTSW |
9 |
105,297,385 (GRCm39) |
nonsense |
probably null |
|
R7284:Atp2c1
|
UTSW |
9 |
105,398,008 (GRCm39) |
splice site |
probably null |
|
R7365:Atp2c1
|
UTSW |
9 |
105,300,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Atp2c1
|
UTSW |
9 |
105,329,982 (GRCm39) |
missense |
probably damaging |
0.98 |
R7818:Atp2c1
|
UTSW |
9 |
105,291,956 (GRCm39) |
missense |
probably benign |
0.06 |
R7921:Atp2c1
|
UTSW |
9 |
105,291,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R7925:Atp2c1
|
UTSW |
9 |
105,319,969 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8088:Atp2c1
|
UTSW |
9 |
105,329,768 (GRCm39) |
splice site |
probably null |
|
R8257:Atp2c1
|
UTSW |
9 |
105,308,756 (GRCm39) |
missense |
probably benign |
0.40 |
R8260:Atp2c1
|
UTSW |
9 |
105,295,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R8265:Atp2c1
|
UTSW |
9 |
105,347,315 (GRCm39) |
missense |
probably benign |
0.01 |
R8307:Atp2c1
|
UTSW |
9 |
105,320,030 (GRCm39) |
missense |
probably benign |
|
R9052:Atp2c1
|
UTSW |
9 |
105,330,032 (GRCm39) |
missense |
probably damaging |
0.99 |
R9066:Atp2c1
|
UTSW |
9 |
105,330,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R9177:Atp2c1
|
UTSW |
9 |
105,336,858 (GRCm39) |
critical splice donor site |
probably null |
|
R9257:Atp2c1
|
UTSW |
9 |
105,291,851 (GRCm39) |
nonsense |
probably null |
|
R9566:Atp2c1
|
UTSW |
9 |
105,343,828 (GRCm39) |
missense |
probably damaging |
0.97 |
R9779:Atp2c1
|
UTSW |
9 |
105,291,919 (GRCm39) |
missense |
probably damaging |
0.98 |
X0053:Atp2c1
|
UTSW |
9 |
105,295,883 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GCCCTGTAAGCTACACTCACTC -3'
(R):5'- GGTCCCATACAAACACTCTAGGG -3'
Sequencing Primer
(F):5'- CTCAGAGCCTTTTGCCTAAAATCAG -3'
(R):5'- ATTTCAGCAGATTGAGTGCCC -3'
|
Posted On |
2019-06-26 |