Incidental Mutation 'R4720:Atp10b'
| ID |
354384 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Atp10b
|
| Ensembl Gene |
ENSMUSG00000055415 |
| Gene Name |
ATPase, class V, type 10B |
| Synonyms |
9030605H24Rik, 5930426O13Rik |
| MMRRC Submission |
041958-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.105)
|
| Stock # |
R4720 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
43040704-43153112 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 43093949 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Glycine
at position 498
(S498G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000076844
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077659]
|
| AlphaFold |
B1AWN4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000077659
AA Change: S498G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000076844
Gene: ENSMUSG00000055415
AA Change: S498G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:PhoLip_ATPase_N
|
47 |
118 |
3.8e-26 |
PFAM |
|
Pfam:E1-E2_ATPase
|
123 |
393 |
2.9e-7 |
PFAM |
|
low complexity region
|
621 |
638 |
N/A |
INTRINSIC |
|
Pfam:Cation_ATPase
|
692 |
799 |
7.1e-9 |
PFAM |
|
Pfam:HAD
|
705 |
1062 |
6.7e-12 |
PFAM |
|
Pfam:PhoLip_ATPase_C
|
1079 |
1324 |
1.9e-79 |
PFAM |
|
low complexity region
|
1353 |
1366 |
N/A |
INTRINSIC |
|
low complexity region
|
1457 |
1471 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127604
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000137991
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.0%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 91 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca9 |
A |
G |
11: 110,018,248 (GRCm39) |
I1124T |
probably damaging |
Het |
| Acacb |
A |
G |
5: 114,367,975 (GRCm39) |
T1658A |
possibly damaging |
Het |
| Acvrl1 |
C |
A |
15: 101,033,654 (GRCm39) |
P112Q |
probably damaging |
Het |
| Ankar |
A |
T |
1: 72,738,170 (GRCm39) |
I4K |
possibly damaging |
Het |
| Ankfn1 |
G |
C |
11: 89,332,252 (GRCm39) |
D431E |
possibly damaging |
Het |
| Apobec4 |
T |
C |
1: 152,632,425 (GRCm39) |
V151A |
possibly damaging |
Het |
| Azin1 |
A |
G |
15: 38,493,744 (GRCm39) |
V293A |
probably benign |
Het |
| Ccdc88b |
T |
C |
19: 6,835,083 (GRCm39) |
E46G |
probably damaging |
Het |
| Ccdc96 |
T |
C |
5: 36,642,219 (GRCm39) |
|
probably benign |
Het |
| Ccnyl1 |
A |
G |
1: 64,752,290 (GRCm39) |
D169G |
probably benign |
Het |
| Cdca3 |
T |
A |
6: 124,809,127 (GRCm39) |
V89E |
probably damaging |
Het |
| Cdh19 |
A |
T |
1: 110,823,111 (GRCm39) |
|
probably null |
Het |
| Chka |
G |
A |
19: 3,936,375 (GRCm39) |
V238I |
probably damaging |
Het |
| Cntn3 |
T |
C |
6: 102,218,983 (GRCm39) |
K546E |
possibly damaging |
Het |
| Crybg3 |
A |
G |
16: 59,360,180 (GRCm39) |
V787A |
probably damaging |
Het |
| Dlgap3 |
T |
C |
4: 127,089,508 (GRCm39) |
|
probably null |
Het |
| Dnah8 |
C |
T |
17: 30,902,608 (GRCm39) |
L889F |
probably benign |
Het |
| Dnah9 |
T |
C |
11: 65,967,184 (GRCm39) |
E1658G |
probably damaging |
Het |
| Dnajc11 |
A |
G |
4: 152,052,996 (GRCm39) |
D102G |
probably damaging |
Het |
| Dync1i2 |
T |
G |
2: 71,064,018 (GRCm39) |
S121A |
probably damaging |
Het |
| Ece1 |
G |
A |
4: 137,684,486 (GRCm39) |
E591K |
probably damaging |
Het |
| Enthd1 |
G |
A |
15: 80,444,510 (GRCm39) |
S15L |
probably damaging |
Het |
| Epb41l2 |
T |
A |
10: 25,347,524 (GRCm39) |
H372Q |
probably damaging |
Het |
| Errfi1 |
T |
A |
4: 150,951,204 (GRCm39) |
Y211N |
probably damaging |
Het |
| Fam193b |
G |
A |
13: 55,691,250 (GRCm39) |
T208M |
probably benign |
Het |
| Flacc1 |
T |
C |
1: 58,717,507 (GRCm39) |
I135V |
possibly damaging |
Het |
| Fmnl2 |
C |
T |
2: 52,997,552 (GRCm39) |
T501M |
possibly damaging |
Het |
| Gkn3 |
C |
T |
6: 87,360,507 (GRCm39) |
A163T |
probably damaging |
Het |
| Gm4841 |
G |
T |
18: 60,403,135 (GRCm39) |
D319E |
probably benign |
Het |
| Gucd1 |
A |
G |
10: 75,345,494 (GRCm39) |
F187S |
probably damaging |
Het |
| Hcar2 |
GCGGATGCGCAC |
GC |
5: 124,002,752 (GRCm39) |
|
probably null |
Het |
| Helz2 |
T |
C |
2: 180,880,210 (GRCm39) |
D502G |
probably damaging |
Het |
| Hspa2 |
A |
G |
12: 76,451,639 (GRCm39) |
E111G |
possibly damaging |
Het |
| Htr2a |
T |
A |
14: 74,882,499 (GRCm39) |
S162T |
probably damaging |
Het |
| Ift80 |
A |
G |
3: 68,869,623 (GRCm39) |
Y223H |
possibly damaging |
Het |
| Il1rl1 |
A |
G |
1: 40,485,838 (GRCm39) |
K330E |
probably benign |
Het |
| Il23r |
A |
T |
6: 67,400,645 (GRCm39) |
F562I |
probably damaging |
Het |
| Isx |
T |
C |
8: 75,600,487 (GRCm39) |
|
probably null |
Het |
| Jcad |
G |
A |
18: 4,674,055 (GRCm39) |
V606I |
probably benign |
Het |
| Kcnn2 |
A |
T |
18: 45,816,187 (GRCm39) |
T333S |
possibly damaging |
Het |
| Kcnq5 |
C |
T |
1: 21,473,274 (GRCm39) |
A630T |
probably damaging |
Het |
| Kif2c |
T |
C |
4: 117,028,946 (GRCm39) |
M188V |
probably benign |
Het |
| Kntc1 |
T |
C |
5: 123,903,086 (GRCm39) |
V321A |
possibly damaging |
Het |
| Krtap4-8 |
A |
T |
11: 99,671,271 (GRCm39) |
|
probably benign |
Het |
| Lcor |
G |
C |
19: 41,574,334 (GRCm39) |
A1030P |
probably benign |
Het |
| Lgals3bp |
A |
C |
11: 118,289,295 (GRCm39) |
L52R |
probably damaging |
Het |
| Lipk |
C |
A |
19: 33,999,099 (GRCm39) |
H126Q |
probably damaging |
Het |
| Lpgat1 |
T |
C |
1: 191,495,779 (GRCm39) |
Y323H |
probably damaging |
Het |
| Lrp2 |
T |
G |
2: 69,311,517 (GRCm39) |
N2654H |
probably damaging |
Het |
| Lsm14b |
C |
T |
2: 179,669,774 (GRCm39) |
Q6* |
probably null |
Het |
| Lysmd3 |
C |
T |
13: 81,817,584 (GRCm39) |
A187V |
possibly damaging |
Het |
| Map2k5 |
A |
G |
9: 63,201,001 (GRCm39) |
S211P |
probably damaging |
Het |
| Mlph |
A |
T |
1: 90,869,419 (GRCm39) |
I474F |
probably damaging |
Het |
| Mpped2 |
T |
C |
2: 106,614,091 (GRCm39) |
S142P |
probably damaging |
Het |
| Nemf |
A |
C |
12: 69,371,062 (GRCm39) |
M678R |
probably benign |
Het |
| Nfe2l1 |
A |
T |
11: 96,718,515 (GRCm39) |
Y7N |
probably damaging |
Het |
| Nfkbie |
T |
G |
17: 45,867,232 (GRCm39) |
D122E |
probably benign |
Het |
| Noc3l |
C |
A |
19: 38,778,066 (GRCm39) |
A783S |
probably benign |
Het |
| Nol8 |
T |
C |
13: 49,816,229 (GRCm39) |
V761A |
probably damaging |
Het |
| Nvl |
A |
G |
1: 180,929,152 (GRCm39) |
L743P |
probably damaging |
Het |
| Or1j1 |
T |
A |
2: 36,702,484 (GRCm39) |
I207F |
probably benign |
Het |
| Plcb1 |
A |
G |
2: 135,093,667 (GRCm39) |
K160R |
possibly damaging |
Het |
| Plekhg3 |
G |
T |
12: 76,625,096 (GRCm39) |
G1313C |
possibly damaging |
Het |
| Plekhh1 |
GTCAAA |
G |
12: 79,122,194 (GRCm39) |
|
probably null |
Het |
| Popdc3 |
G |
A |
10: 45,191,002 (GRCm39) |
V38I |
probably benign |
Het |
| Prdx3 |
A |
T |
19: 60,858,551 (GRCm39) |
V114D |
possibly damaging |
Het |
| Prkdc |
T |
A |
16: 15,485,579 (GRCm39) |
S469T |
probably benign |
Het |
| Rbm22 |
G |
A |
18: 60,697,463 (GRCm39) |
R56H |
probably damaging |
Het |
| Reln |
A |
T |
5: 22,491,894 (GRCm39) |
F113I |
possibly damaging |
Het |
| Rims1 |
A |
G |
1: 22,497,731 (GRCm39) |
Y808H |
probably damaging |
Het |
| Rsbn1 |
C |
A |
3: 103,836,336 (GRCm39) |
T458N |
possibly damaging |
Het |
| Serpina3b |
A |
G |
12: 104,096,889 (GRCm39) |
S57G |
possibly damaging |
Het |
| Skor2 |
G |
T |
18: 76,948,878 (GRCm39) |
|
probably null |
Het |
| Slc22a4 |
A |
T |
11: 53,879,719 (GRCm39) |
Y447N |
probably damaging |
Het |
| Slco1a7 |
C |
A |
6: 141,668,948 (GRCm39) |
A495S |
probably damaging |
Het |
| Stx19 |
G |
T |
16: 62,642,682 (GRCm39) |
R166L |
probably damaging |
Het |
| Svep1 |
T |
C |
4: 58,205,869 (GRCm39) |
T170A |
possibly damaging |
Het |
| Sycp2 |
T |
G |
2: 178,016,225 (GRCm39) |
S746R |
probably benign |
Het |
| Tchh |
G |
T |
3: 93,355,189 (GRCm39) |
R1543L |
unknown |
Het |
| Tjp2 |
T |
C |
19: 24,078,169 (GRCm39) |
D908G |
probably damaging |
Het |
| Ttc8 |
C |
A |
12: 98,946,068 (GRCm39) |
A452E |
possibly damaging |
Het |
| Unc5a |
T |
A |
13: 55,151,696 (GRCm39) |
W709R |
probably null |
Het |
| Unc80 |
T |
A |
1: 66,549,951 (GRCm39) |
S736R |
possibly damaging |
Het |
| Vmn2r100 |
C |
A |
17: 19,742,788 (GRCm39) |
H387Q |
probably benign |
Het |
| Vmn2r39 |
C |
T |
7: 9,026,469 (GRCm39) |
|
probably null |
Het |
| Vmn2r88 |
T |
A |
14: 51,650,702 (GRCm39) |
D138E |
probably benign |
Het |
| Vwce |
T |
C |
19: 10,625,831 (GRCm39) |
F448L |
possibly damaging |
Het |
| Wdr75 |
C |
T |
1: 45,861,645 (GRCm39) |
S695F |
probably benign |
Het |
| Zfand4 |
T |
C |
6: 116,265,122 (GRCm39) |
|
probably null |
Het |
| Zfp511 |
T |
A |
7: 139,617,424 (GRCm39) |
|
probably null |
Het |
| Zfyve9 |
T |
C |
4: 108,501,565 (GRCm39) |
K584E |
possibly damaging |
Het |
|
| Other mutations in Atp10b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00944:Atp10b
|
APN |
11 |
43,092,988 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01385:Atp10b
|
APN |
11 |
43,125,256 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01524:Atp10b
|
APN |
11 |
43,150,672 (GRCm39) |
missense |
probably benign |
0.18 |
|
IGL01575:Atp10b
|
APN |
11 |
43,063,548 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01588:Atp10b
|
APN |
11 |
43,063,548 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01590:Atp10b
|
APN |
11 |
43,063,548 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01832:Atp10b
|
APN |
11 |
43,125,262 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01927:Atp10b
|
APN |
11 |
43,150,231 (GRCm39) |
splice site |
probably benign |
|
|
IGL01933:Atp10b
|
APN |
11 |
43,085,457 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02182:Atp10b
|
APN |
11 |
43,139,774 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02215:Atp10b
|
APN |
11 |
43,085,492 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02216:Atp10b
|
APN |
11 |
43,150,616 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02973:Atp10b
|
APN |
11 |
43,088,336 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03012:Atp10b
|
APN |
11 |
43,085,482 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03106:Atp10b
|
APN |
11 |
43,138,304 (GRCm39) |
missense |
probably benign |
0.32 |
|
IGL03123:Atp10b
|
APN |
11 |
43,044,110 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03202:Atp10b
|
APN |
11 |
43,125,268 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03339:Atp10b
|
APN |
11 |
43,121,442 (GRCm39) |
missense |
probably null |
0.71 |
|
R0053:Atp10b
|
UTSW |
11 |
43,107,391 (GRCm39) |
splice site |
probably benign |
|
|
R0053:Atp10b
|
UTSW |
11 |
43,107,391 (GRCm39) |
splice site |
probably benign |
|
|
R0098:Atp10b
|
UTSW |
11 |
43,080,431 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0098:Atp10b
|
UTSW |
11 |
43,080,431 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0281:Atp10b
|
UTSW |
11 |
43,044,131 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0379:Atp10b
|
UTSW |
11 |
43,145,141 (GRCm39) |
missense |
probably benign |
0.05 |
|
R0380:Atp10b
|
UTSW |
11 |
43,116,424 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0470:Atp10b
|
UTSW |
11 |
43,093,866 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1355:Atp10b
|
UTSW |
11 |
43,042,482 (GRCm39) |
nonsense |
probably null |
|
|
R1368:Atp10b
|
UTSW |
11 |
43,092,981 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1370:Atp10b
|
UTSW |
11 |
43,042,482 (GRCm39) |
nonsense |
probably null |
|
|
R1413:Atp10b
|
UTSW |
11 |
43,121,391 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1502:Atp10b
|
UTSW |
11 |
43,121,174 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1530:Atp10b
|
UTSW |
11 |
43,088,351 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1596:Atp10b
|
UTSW |
11 |
43,126,594 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1675:Atp10b
|
UTSW |
11 |
43,116,475 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1880:Atp10b
|
UTSW |
11 |
43,150,259 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1938:Atp10b
|
UTSW |
11 |
43,121,245 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1986:Atp10b
|
UTSW |
11 |
43,063,595 (GRCm39) |
missense |
probably benign |
0.12 |
|
R2081:Atp10b
|
UTSW |
11 |
43,092,955 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2083:Atp10b
|
UTSW |
11 |
43,103,250 (GRCm39) |
missense |
probably benign |
0.24 |
|
R2159:Atp10b
|
UTSW |
11 |
43,042,680 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R2255:Atp10b
|
UTSW |
11 |
43,125,207 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2259:Atp10b
|
UTSW |
11 |
43,080,440 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2259:Atp10b
|
UTSW |
11 |
43,063,572 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3741:Atp10b
|
UTSW |
11 |
43,126,489 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3942:Atp10b
|
UTSW |
11 |
43,063,581 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3971:Atp10b
|
UTSW |
11 |
43,107,339 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4007:Atp10b
|
UTSW |
11 |
43,150,679 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4050:Atp10b
|
UTSW |
11 |
43,150,363 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4078:Atp10b
|
UTSW |
11 |
43,044,110 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4567:Atp10b
|
UTSW |
11 |
43,088,384 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4651:Atp10b
|
UTSW |
11 |
43,085,472 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4652:Atp10b
|
UTSW |
11 |
43,085,472 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4667:Atp10b
|
UTSW |
11 |
43,138,345 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4987:Atp10b
|
UTSW |
11 |
43,042,440 (GRCm39) |
utr 5 prime |
probably benign |
|
|
R5232:Atp10b
|
UTSW |
11 |
43,093,006 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5233:Atp10b
|
UTSW |
11 |
43,121,387 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5281:Atp10b
|
UTSW |
11 |
43,145,163 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5307:Atp10b
|
UTSW |
11 |
43,103,302 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5460:Atp10b
|
UTSW |
11 |
43,121,282 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5518:Atp10b
|
UTSW |
11 |
43,042,463 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R5659:Atp10b
|
UTSW |
11 |
43,136,252 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5688:Atp10b
|
UTSW |
11 |
43,092,000 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5735:Atp10b
|
UTSW |
11 |
43,042,601 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6153:Atp10b
|
UTSW |
11 |
43,145,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6251:Atp10b
|
UTSW |
11 |
43,126,573 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6259:Atp10b
|
UTSW |
11 |
43,092,065 (GRCm39) |
missense |
probably benign |
0.24 |
|
R6394:Atp10b
|
UTSW |
11 |
43,116,464 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6492:Atp10b
|
UTSW |
11 |
43,109,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6769:Atp10b
|
UTSW |
11 |
43,094,079 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6771:Atp10b
|
UTSW |
11 |
43,094,079 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6775:Atp10b
|
UTSW |
11 |
43,113,040 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R7134:Atp10b
|
UTSW |
11 |
43,136,291 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7322:Atp10b
|
UTSW |
11 |
43,103,374 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7367:Atp10b
|
UTSW |
11 |
43,138,328 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7538:Atp10b
|
UTSW |
11 |
43,116,373 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7708:Atp10b
|
UTSW |
11 |
43,092,970 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7787:Atp10b
|
UTSW |
11 |
43,150,700 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R8145:Atp10b
|
UTSW |
11 |
43,092,949 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8406:Atp10b
|
UTSW |
11 |
43,093,984 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8503:Atp10b
|
UTSW |
11 |
43,113,066 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R8542:Atp10b
|
UTSW |
11 |
43,121,208 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8744:Atp10b
|
UTSW |
11 |
43,121,177 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8815:Atp10b
|
UTSW |
11 |
43,093,978 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R8833:Atp10b
|
UTSW |
11 |
43,112,986 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8880:Atp10b
|
UTSW |
11 |
43,106,811 (GRCm39) |
missense |
probably benign |
|
|
R8989:Atp10b
|
UTSW |
11 |
43,136,269 (GRCm39) |
nonsense |
probably null |
|
|
R8998:Atp10b
|
UTSW |
11 |
43,150,726 (GRCm39) |
makesense |
probably null |
|
|
R9255:Atp10b
|
UTSW |
11 |
43,107,148 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9281:Atp10b
|
UTSW |
11 |
43,116,458 (GRCm39) |
missense |
probably benign |
0.11 |
|
R9345:Atp10b
|
UTSW |
11 |
43,094,024 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9357:Atp10b
|
UTSW |
11 |
43,150,711 (GRCm39) |
missense |
probably benign |
0.18 |
|
R9393:Atp10b
|
UTSW |
11 |
43,063,608 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9516:Atp10b
|
UTSW |
11 |
43,121,224 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9644:Atp10b
|
UTSW |
11 |
43,042,659 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9747:Atp10b
|
UTSW |
11 |
43,088,339 (GRCm39) |
missense |
probably benign |
|
|
Z1177:Atp10b
|
UTSW |
11 |
43,044,176 (GRCm39) |
missense |
probably benign |
0.05 |
|
| Predicted Primers |
PCR Primer
(F):5'- ACCCCTGAAGTCTAGCATCC -3'
(R):5'- TCAGGGTTTATAGAGGCTCTGC -3'
Sequencing Primer
(F):5'- TGAAGTCTAGCATCCCCCAAAC -3'
(R):5'- AGAGGCTCTGCTATATCCTAGAGC -3'
|
| Posted On |
2015-10-21 |
Incidental Mutation