Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
A |
G |
2: 25,332,088 (GRCm39) |
D1400G |
probably benign |
Het |
Abca6 |
C |
T |
11: 110,073,852 (GRCm39) |
|
probably null |
Het |
Adh4 |
A |
G |
3: 138,134,901 (GRCm39) |
I358M |
possibly damaging |
Het |
Akap6 |
T |
G |
12: 52,934,147 (GRCm39) |
D546E |
probably benign |
Het |
Arap3 |
G |
A |
18: 38,106,616 (GRCm39) |
A1409V |
possibly damaging |
Het |
Arhgap22 |
C |
T |
14: 32,993,890 (GRCm39) |
R68* |
probably null |
Het |
Arhgef4 |
A |
T |
1: 34,846,273 (GRCm39) |
D207V |
probably damaging |
Het |
Asb15 |
A |
G |
6: 24,566,462 (GRCm39) |
T472A |
probably damaging |
Het |
Ascl1 |
A |
T |
10: 87,328,326 (GRCm39) |
S209T |
probably damaging |
Het |
Asxl1 |
T |
C |
2: 153,239,355 (GRCm39) |
V382A |
probably benign |
Het |
Calu |
C |
T |
6: 29,356,554 (GRCm39) |
R27* |
probably null |
Het |
Cdh20 |
A |
G |
1: 104,898,598 (GRCm39) |
T442A |
probably benign |
Het |
Chrm3 |
T |
A |
13: 9,927,869 (GRCm39) |
Q389L |
probably benign |
Het |
Cntnap1 |
A |
G |
11: 101,079,460 (GRCm39) |
T1233A |
probably benign |
Het |
Cwc15 |
G |
A |
9: 14,421,525 (GRCm39) |
C197Y |
probably damaging |
Het |
D6Ertd527e |
C |
G |
6: 87,088,506 (GRCm39) |
T223S |
unknown |
Het |
Dennd3 |
C |
T |
15: 73,429,459 (GRCm39) |
T914I |
probably damaging |
Het |
Dlx3 |
C |
A |
11: 95,011,276 (GRCm39) |
Y43* |
probably null |
Het |
Dnah17 |
A |
T |
11: 117,946,556 (GRCm39) |
|
probably null |
Het |
Dnah17 |
A |
G |
11: 117,994,182 (GRCm39) |
F1081S |
probably damaging |
Het |
Dpp10 |
G |
A |
1: 123,281,157 (GRCm39) |
Q631* |
probably null |
Het |
Dsel |
T |
A |
1: 111,789,506 (GRCm39) |
D343V |
probably damaging |
Het |
Efcab12 |
T |
C |
6: 115,787,997 (GRCm39) |
D655G |
possibly damaging |
Het |
Epha8 |
T |
A |
4: 136,673,224 (GRCm39) |
I187L |
probably damaging |
Het |
Exosc10 |
A |
G |
4: 148,664,834 (GRCm39) |
K781E |
probably damaging |
Het |
Exosc5 |
T |
C |
7: 25,365,751 (GRCm39) |
L200P |
probably benign |
Het |
Faiml |
T |
C |
9: 99,111,666 (GRCm39) |
E131G |
probably damaging |
Het |
Gm5145 |
G |
A |
17: 20,790,993 (GRCm39) |
V124I |
probably benign |
Het |
Grm7 |
T |
C |
6: 110,622,974 (GRCm39) |
V49A |
probably benign |
Het |
Gtf2e1 |
T |
C |
16: 37,356,427 (GRCm39) |
D35G |
probably damaging |
Het |
Heatr1 |
C |
T |
13: 12,435,941 (GRCm39) |
Q1160* |
probably null |
Het |
Herc2 |
T |
A |
7: 55,786,406 (GRCm39) |
C1584S |
probably benign |
Het |
Hsd17b3 |
T |
C |
13: 64,224,165 (GRCm39) |
I88V |
probably damaging |
Het |
Hspa14 |
A |
C |
2: 3,499,179 (GRCm39) |
L205R |
possibly damaging |
Het |
Ifna11 |
A |
C |
4: 88,738,662 (GRCm39) |
E156A |
possibly damaging |
Het |
Krt87 |
T |
C |
15: 101,387,528 (GRCm39) |
D170G |
probably benign |
Het |
Mas1 |
T |
C |
17: 13,060,745 (GRCm39) |
Y226C |
probably damaging |
Het |
Micall1 |
T |
C |
15: 79,005,097 (GRCm39) |
F190L |
unknown |
Het |
Msi2 |
A |
T |
11: 88,370,864 (GRCm39) |
L141Q |
probably damaging |
Het |
Nfkbib |
T |
C |
7: 28,465,768 (GRCm39) |
D27G |
probably benign |
Het |
Nlrp9b |
A |
G |
7: 19,783,438 (GRCm39) |
D927G |
possibly damaging |
Het |
Nrg3 |
T |
C |
14: 38,092,896 (GRCm39) |
D579G |
probably benign |
Het |
Nutm1 |
G |
A |
2: 112,080,401 (GRCm39) |
R505C |
probably damaging |
Het |
Or8d1 |
G |
A |
9: 38,767,245 (GRCm39) |
D296N |
probably damaging |
Het |
Or8h6 |
A |
T |
2: 86,703,980 (GRCm39) |
V29E |
probably damaging |
Het |
Parp4 |
C |
T |
14: 56,885,138 (GRCm39) |
P1406S |
not run |
Het |
Pkib |
A |
T |
10: 57,612,422 (GRCm39) |
Q101L |
possibly damaging |
Het |
Plat |
C |
T |
8: 23,265,713 (GRCm39) |
T252I |
probably benign |
Het |
Ppm1d |
A |
T |
11: 85,236,821 (GRCm39) |
E533D |
probably damaging |
Het |
Psd3 |
T |
C |
8: 68,573,686 (GRCm39) |
K165R |
probably damaging |
Het |
Psg29 |
T |
A |
7: 16,944,616 (GRCm39) |
Y375* |
probably null |
Het |
Pus7 |
A |
T |
5: 23,946,908 (GRCm39) |
I644N |
probably damaging |
Het |
Rbbp9 |
A |
T |
2: 144,385,722 (GRCm39) |
M181K |
probably benign |
Het |
Rell1 |
A |
T |
5: 64,093,418 (GRCm39) |
N112K |
possibly damaging |
Het |
Simc1 |
AATGCAGTCACCAAGAGATGTGATGCAGTCACCAAGAGATGTGATGCAGTCACCAAGAGATGTGATGCAGTCACCAAGAG |
AATGCAGTCACCAAGAGATGTGATGCAGTCACCAAGAGATGTGATGCAGTCACCAAGAG |
13: 54,673,048 (GRCm39) |
|
probably benign |
Het |
Skint5 |
G |
A |
4: 113,400,131 (GRCm39) |
T1184M |
unknown |
Het |
Slc27a2 |
T |
A |
2: 126,420,866 (GRCm39) |
D452E |
probably damaging |
Het |
Slc44a4 |
T |
A |
17: 35,146,888 (GRCm39) |
I489N |
probably damaging |
Het |
Slfn14 |
T |
A |
11: 83,169,821 (GRCm39) |
K608* |
probably null |
Het |
Snx15 |
T |
A |
19: 6,170,537 (GRCm39) |
I301F |
probably damaging |
Het |
Sost |
C |
T |
11: 101,854,929 (GRCm39) |
G127R |
probably damaging |
Het |
Stt3b |
A |
G |
9: 115,106,025 (GRCm39) |
I150T |
probably damaging |
Het |
Susd2 |
T |
C |
10: 75,478,402 (GRCm39) |
D58G |
probably benign |
Het |
Tex46 |
T |
G |
4: 136,340,212 (GRCm39) |
V99G |
probably damaging |
Het |
Tgfbi |
T |
A |
13: 56,779,926 (GRCm39) |
F492I |
possibly damaging |
Het |
Tmem132c |
G |
A |
5: 127,437,281 (GRCm39) |
A257T |
probably benign |
Het |
Trim2 |
A |
T |
3: 84,117,540 (GRCm39) |
I51K |
probably damaging |
Het |
Tsn |
A |
T |
1: 118,228,591 (GRCm39) |
Y210* |
probably null |
Het |
Umodl1 |
G |
A |
17: 31,227,639 (GRCm39) |
R1324H |
probably benign |
Het |
Utp3 |
G |
C |
5: 88,702,376 (GRCm39) |
|
probably benign |
Het |
Vmn1r5 |
A |
T |
6: 56,963,204 (GRCm39) |
N293I |
possibly damaging |
Het |
Vmn2r124 |
A |
T |
17: 18,293,835 (GRCm39) |
I641F |
probably damaging |
Het |
Vmn2r84 |
T |
C |
10: 130,227,119 (GRCm39) |
N240D |
probably benign |
Het |
Wbp1l |
A |
G |
19: 46,642,839 (GRCm39) |
D264G |
possibly damaging |
Het |
|
Other mutations in Atp11a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01160:Atp11a
|
APN |
8 |
12,894,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01397:Atp11a
|
APN |
8 |
12,862,321 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01712:Atp11a
|
APN |
8 |
12,901,138 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02113:Atp11a
|
APN |
8 |
12,915,048 (GRCm39) |
missense |
probably benign |
|
IGL02449:Atp11a
|
APN |
8 |
12,807,358 (GRCm39) |
splice site |
probably null |
|
IGL02550:Atp11a
|
APN |
8 |
12,866,997 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL03099:Atp11a
|
APN |
8 |
12,877,462 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0139:Atp11a
|
UTSW |
8 |
12,896,054 (GRCm39) |
missense |
probably benign |
0.00 |
R0265:Atp11a
|
UTSW |
8 |
12,906,930 (GRCm39) |
splice site |
probably benign |
|
R0294:Atp11a
|
UTSW |
8 |
12,877,524 (GRCm39) |
missense |
probably benign |
0.03 |
R0331:Atp11a
|
UTSW |
8 |
12,866,953 (GRCm39) |
nonsense |
probably null |
|
R0582:Atp11a
|
UTSW |
8 |
12,881,214 (GRCm39) |
missense |
probably benign |
0.10 |
R1033:Atp11a
|
UTSW |
8 |
12,878,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R1213:Atp11a
|
UTSW |
8 |
12,892,859 (GRCm39) |
missense |
probably benign |
0.04 |
R1551:Atp11a
|
UTSW |
8 |
12,862,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R1648:Atp11a
|
UTSW |
8 |
12,897,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R1752:Atp11a
|
UTSW |
8 |
12,863,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Atp11a
|
UTSW |
8 |
12,896,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R1887:Atp11a
|
UTSW |
8 |
12,862,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R2079:Atp11a
|
UTSW |
8 |
12,907,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R2106:Atp11a
|
UTSW |
8 |
12,885,228 (GRCm39) |
missense |
probably benign |
|
R2319:Atp11a
|
UTSW |
8 |
12,897,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R2966:Atp11a
|
UTSW |
8 |
12,897,853 (GRCm39) |
splice site |
probably null |
|
R4021:Atp11a
|
UTSW |
8 |
12,892,938 (GRCm39) |
missense |
probably benign |
0.01 |
R4183:Atp11a
|
UTSW |
8 |
12,866,990 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4640:Atp11a
|
UTSW |
8 |
12,878,434 (GRCm39) |
splice site |
probably benign |
|
R4705:Atp11a
|
UTSW |
8 |
12,863,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Atp11a
|
UTSW |
8 |
12,856,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R5777:Atp11a
|
UTSW |
8 |
12,882,522 (GRCm39) |
missense |
probably damaging |
0.99 |
R6152:Atp11a
|
UTSW |
8 |
12,896,100 (GRCm39) |
missense |
probably damaging |
0.97 |
R6171:Atp11a
|
UTSW |
8 |
12,882,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R6197:Atp11a
|
UTSW |
8 |
12,896,099 (GRCm39) |
missense |
probably benign |
0.01 |
R6335:Atp11a
|
UTSW |
8 |
12,909,481 (GRCm39) |
critical splice donor site |
probably null |
|
R6526:Atp11a
|
UTSW |
8 |
12,914,999 (GRCm39) |
missense |
probably benign |
|
R6792:Atp11a
|
UTSW |
8 |
12,911,939 (GRCm39) |
unclassified |
probably benign |
|
R6923:Atp11a
|
UTSW |
8 |
12,906,949 (GRCm39) |
missense |
probably damaging |
0.99 |
R6959:Atp11a
|
UTSW |
8 |
12,870,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R7499:Atp11a
|
UTSW |
8 |
12,882,575 (GRCm39) |
missense |
probably benign |
0.01 |
R7606:Atp11a
|
UTSW |
8 |
12,894,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R7844:Atp11a
|
UTSW |
8 |
12,901,039 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8099:Atp11a
|
UTSW |
8 |
12,911,973 (GRCm39) |
missense |
|
|
R8479:Atp11a
|
UTSW |
8 |
12,892,932 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8546:Atp11a
|
UTSW |
8 |
12,901,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R8803:Atp11a
|
UTSW |
8 |
12,875,721 (GRCm39) |
missense |
probably benign |
0.18 |
R8896:Atp11a
|
UTSW |
8 |
12,899,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R9047:Atp11a
|
UTSW |
8 |
12,878,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R9135:Atp11a
|
UTSW |
8 |
12,863,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R9225:Atp11a
|
UTSW |
8 |
12,867,005 (GRCm39) |
missense |
probably benign |
0.01 |
R9483:Atp11a
|
UTSW |
8 |
12,901,087 (GRCm39) |
missense |
probably damaging |
0.98 |
R9492:Atp11a
|
UTSW |
8 |
12,894,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R9674:Atp11a
|
UTSW |
8 |
12,877,525 (GRCm39) |
missense |
probably benign |
0.00 |
R9679:Atp11a
|
UTSW |
8 |
12,909,388 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0017:Atp11a
|
UTSW |
8 |
12,876,323 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0022:Atp11a
|
UTSW |
8 |
12,897,794 (GRCm39) |
missense |
probably damaging |
0.99 |
|