Incidental Mutation 'R2259:Atp10b'
| ID |
243657 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Atp10b
|
| Ensembl Gene |
ENSMUSG00000055415 |
| Gene Name |
ATPase, class V, type 10B |
| Synonyms |
9030605H24Rik, 5930426O13Rik |
| MMRRC Submission |
040259-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.105)
|
| Stock # |
R2259 (G1)
|
| Quality Score |
220 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
43040704-43153112 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 43080440 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Methionine
at position 239
(V239M)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000076844
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077659]
|
| AlphaFold |
B1AWN4 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000077659
AA Change: V239M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000076844
Gene: ENSMUSG00000055415
AA Change: V239M
| 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: ENSMUST00000137991
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 94.9%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrd1 |
T |
G |
5: 129,189,375 (GRCm39) |
S91A |
possibly damaging |
Het |
| Ankrd13b |
T |
G |
11: 77,367,168 (GRCm39) |
N247T |
probably damaging |
Het |
| Cflar |
C |
T |
1: 58,768,280 (GRCm39) |
T121I |
probably benign |
Het |
| Clca3b |
T |
C |
3: 144,552,142 (GRCm39) |
N180D |
possibly damaging |
Het |
| Cnbd2 |
T |
A |
2: 156,177,192 (GRCm39) |
I62N |
probably damaging |
Het |
| Col11a2 |
A |
G |
17: 34,258,651 (GRCm39) |
H8R |
probably benign |
Het |
| Cyp2a4 |
C |
T |
7: 26,008,460 (GRCm39) |
L201F |
probably damaging |
Het |
| D630003M21Rik |
A |
T |
2: 158,046,631 (GRCm39) |
L782Q |
probably damaging |
Het |
| Dctn1 |
C |
A |
6: 83,174,568 (GRCm39) |
H1065N |
possibly damaging |
Het |
| Dgcr2 |
A |
T |
16: 17,662,841 (GRCm39) |
|
probably null |
Het |
| Dlg4 |
T |
C |
11: 69,922,196 (GRCm39) |
I143T |
probably damaging |
Het |
| E2f7 |
T |
G |
10: 110,582,204 (GRCm39) |
N4K |
probably damaging |
Het |
| Eef2kmt |
C |
T |
16: 5,063,172 (GRCm39) |
V323I |
probably benign |
Het |
| Eif2ak4 |
A |
C |
2: 118,286,264 (GRCm39) |
I1017L |
probably damaging |
Het |
| Eln |
C |
A |
5: 134,758,508 (GRCm39) |
A126S |
unknown |
Het |
| Exoc7 |
T |
C |
11: 116,197,237 (GRCm39) |
S35G |
probably damaging |
Het |
| Fam187a |
A |
G |
11: 102,776,124 (GRCm39) |
|
probably benign |
Het |
| Fkbp6 |
C |
T |
5: 135,366,468 (GRCm39) |
|
probably null |
Het |
| Flnc |
G |
A |
6: 29,438,665 (GRCm39) |
W186* |
probably null |
Het |
| Fmn2 |
T |
A |
1: 174,330,498 (GRCm39) |
L296H |
unknown |
Het |
| Galnt14 |
C |
A |
17: 73,801,261 (GRCm39) |
M520I |
probably benign |
Het |
| Gba2 |
A |
G |
4: 43,570,107 (GRCm39) |
C396R |
probably benign |
Het |
| Gigyf1 |
C |
A |
5: 137,518,594 (GRCm39) |
A215E |
possibly damaging |
Het |
| Glb1 |
C |
T |
9: 114,272,100 (GRCm39) |
Q246* |
probably null |
Het |
| Gm11565 |
T |
G |
11: 99,805,844 (GRCm39) |
C79G |
possibly damaging |
Het |
| Gpr160 |
A |
G |
3: 30,950,444 (GRCm39) |
Y172C |
probably damaging |
Het |
| Ift52 |
A |
G |
2: 162,870,013 (GRCm39) |
N159S |
probably benign |
Het |
| Insrr |
A |
G |
3: 87,707,759 (GRCm39) |
D67G |
probably damaging |
Het |
| Insyn2a |
T |
A |
7: 134,519,396 (GRCm39) |
E378V |
probably damaging |
Het |
| Irf2 |
A |
G |
8: 47,290,868 (GRCm39) |
Y230C |
probably benign |
Het |
| Jmjd6 |
T |
C |
11: 116,732,140 (GRCm39) |
H187R |
probably damaging |
Het |
| Kdm2b |
C |
T |
5: 123,020,479 (GRCm39) |
G90S |
probably damaging |
Het |
| Kif7 |
C |
T |
7: 79,361,337 (GRCm39) |
G118D |
probably damaging |
Het |
| Klhl38 |
G |
C |
15: 58,178,374 (GRCm39) |
T532S |
possibly damaging |
Het |
| Kmt2a |
G |
T |
9: 44,792,440 (GRCm39) |
|
probably benign |
Het |
| Lama2 |
A |
G |
10: 26,907,123 (GRCm39) |
L2346S |
probably benign |
Het |
| Marveld2 |
A |
G |
13: 100,748,978 (GRCm39) |
S34P |
probably benign |
Het |
| Mllt6 |
T |
C |
11: 97,555,802 (GRCm39) |
V44A |
probably damaging |
Het |
| Muc5ac |
A |
G |
7: 141,344,745 (GRCm39) |
N72S |
probably benign |
Het |
| Myo7a |
T |
G |
7: 97,718,706 (GRCm39) |
D1388A |
probably damaging |
Het |
| Ncapd3 |
A |
G |
9: 26,967,368 (GRCm39) |
D568G |
probably benign |
Het |
| Ncoa1 |
A |
C |
12: 4,365,819 (GRCm39) |
H82Q |
probably damaging |
Het |
| Npbwr1 |
C |
A |
1: 5,986,877 (GRCm39) |
L212F |
probably damaging |
Het |
| Nptx1 |
T |
G |
11: 119,434,142 (GRCm39) |
I315L |
probably benign |
Het |
| Npy2r |
G |
T |
3: 82,448,661 (GRCm39) |
P38Q |
possibly damaging |
Het |
| Ocln |
A |
T |
13: 100,671,537 (GRCm39) |
D24E |
probably damaging |
Het |
| Or14c41 |
T |
A |
7: 86,235,092 (GRCm39) |
V203D |
possibly damaging |
Het |
| Or5bw2 |
A |
T |
7: 6,573,022 (GRCm39) |
I11F |
probably damaging |
Het |
| Or8d1b |
T |
C |
9: 38,887,296 (GRCm39) |
V108A |
probably benign |
Het |
| Pde2a |
A |
T |
7: 101,133,774 (GRCm39) |
D85V |
probably damaging |
Het |
| Phf3 |
A |
G |
1: 30,843,424 (GRCm39) |
V1845A |
probably benign |
Het |
| Plch1 |
T |
A |
3: 63,605,398 (GRCm39) |
Q1493L |
possibly damaging |
Het |
| Pold1 |
T |
C |
7: 44,190,908 (GRCm39) |
|
probably benign |
Het |
| Polq |
T |
C |
16: 36,882,459 (GRCm39) |
V1541A |
probably benign |
Het |
| Psmd3 |
T |
A |
11: 98,581,790 (GRCm39) |
M305K |
probably benign |
Het |
| Pura |
T |
C |
18: 36,420,803 (GRCm39) |
F197L |
possibly damaging |
Het |
| Rab3gap2 |
T |
A |
1: 184,954,056 (GRCm39) |
W43R |
probably damaging |
Het |
| Repin1 |
A |
G |
6: 48,573,464 (GRCm39) |
Q128R |
probably benign |
Het |
| Rnf208 |
G |
A |
2: 25,133,656 (GRCm39) |
V117I |
probably damaging |
Het |
| Rpe65 |
A |
G |
3: 159,321,208 (GRCm39) |
Y340C |
probably damaging |
Het |
| Ryr1 |
C |
A |
7: 28,719,166 (GRCm39) |
V4414L |
unknown |
Het |
| Sephs2 |
T |
C |
7: 126,872,649 (GRCm39) |
E148G |
possibly damaging |
Het |
| Spns2 |
T |
A |
11: 72,348,094 (GRCm39) |
Q291L |
probably benign |
Het |
| Ssc5d |
C |
T |
7: 4,946,915 (GRCm39) |
P1090S |
probably benign |
Het |
| Tasp1 |
A |
T |
2: 139,793,426 (GRCm39) |
V250D |
probably damaging |
Het |
| Tcaf3 |
A |
G |
6: 42,568,364 (GRCm39) |
I664T |
possibly damaging |
Het |
| Tg |
T |
C |
15: 66,555,747 (GRCm39) |
V813A |
probably benign |
Het |
| Tmem132c |
T |
C |
5: 127,581,988 (GRCm39) |
L401P |
probably benign |
Het |
| Tmem138 |
T |
C |
19: 10,548,967 (GRCm39) |
N101S |
probably benign |
Het |
| Tmem242 |
G |
T |
17: 5,483,745 (GRCm39) |
A99E |
probably damaging |
Het |
| Tmem30a |
C |
T |
9: 79,681,446 (GRCm39) |
R277H |
probably benign |
Het |
| Tmt1a |
A |
T |
15: 100,211,049 (GRCm39) |
I174F |
probably benign |
Het |
| Tnni3 |
T |
A |
7: 4,522,405 (GRCm39) |
I182F |
probably benign |
Het |
| Trim30a |
T |
A |
7: 104,060,711 (GRCm39) |
D355V |
probably damaging |
Het |
| Trim35 |
C |
T |
14: 66,546,711 (GRCm39) |
R493* |
probably null |
Het |
| Trip10 |
G |
C |
17: 57,562,135 (GRCm39) |
V254L |
probably benign |
Het |
| Tshz2 |
A |
T |
2: 169,728,326 (GRCm39) |
Q505L |
probably benign |
Het |
| Ttyh1 |
T |
C |
7: 4,131,183 (GRCm39) |
V218A |
probably damaging |
Het |
| Unc13b |
A |
T |
4: 43,182,780 (GRCm39) |
E3163V |
possibly damaging |
Het |
| Unc45b |
T |
A |
11: 82,808,625 (GRCm39) |
M237K |
probably benign |
Het |
| Usp8 |
A |
G |
2: 126,600,488 (GRCm39) |
T1080A |
probably benign |
Het |
| Vmn2r65 |
T |
A |
7: 84,590,119 (GRCm39) |
H599L |
possibly damaging |
Het |
| Vps13c |
A |
G |
9: 67,861,142 (GRCm39) |
N2891S |
probably benign |
Het |
| Xpo5 |
C |
T |
17: 46,551,822 (GRCm39) |
Q1050* |
probably null |
Het |
| Zfp407 |
G |
T |
18: 84,227,918 (GRCm39) |
T1897K |
probably damaging |
Het |
| Zzef1 |
C |
T |
11: 72,791,459 (GRCm39) |
R2188* |
probably null |
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 |
43,063,572 (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 |
|
R4720:Atp10b
|
UTSW |
11 |
43,093,949 (GRCm39) |
missense |
probably benign |
|
|
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'- GCATCATGGTGTGACAAAGGAC -3'
(R):5'- ATACAGTTTGGTTCTTAGGGAAGAG -3'
Sequencing Primer
(F):5'- ACAGTGGCCGCATGTGTG -3'
(R):5'- GGTCTGTAAGCCTCAAACATCTG -3'
|
| Posted On |
2014-10-16 |
Incidental Mutation