Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agfg1 |
T |
C |
1: 82,860,030 (GRCm39) |
F299S |
probably damaging |
Het |
Arhgap32 |
A |
T |
9: 32,157,220 (GRCm39) |
E72D |
probably benign |
Het |
Arid1a |
G |
T |
4: 133,408,391 (GRCm39) |
Q1654K |
unknown |
Het |
Atp6v1f |
A |
C |
6: 29,470,194 (GRCm39) |
H96P |
probably damaging |
Het |
Cast |
A |
G |
13: 74,887,960 (GRCm39) |
V161A |
probably damaging |
Het |
Ccdc186 |
A |
T |
19: 56,796,610 (GRCm39) |
C320S |
probably damaging |
Het |
Cgn |
T |
A |
3: 94,670,362 (GRCm39) |
K1031* |
probably null |
Het |
Cnot10 |
T |
C |
9: 114,460,894 (GRCm39) |
N92S |
probably benign |
Het |
Crat |
C |
T |
2: 30,294,577 (GRCm39) |
R497Q |
probably benign |
Het |
Cstf2t |
T |
C |
19: 31,060,593 (GRCm39) |
V43A |
possibly damaging |
Het |
D930020B18Rik |
T |
C |
10: 121,525,739 (GRCm39) |
L547P |
probably damaging |
Het |
Dennd1a |
G |
A |
2: 37,742,184 (GRCm39) |
|
probably null |
Het |
Dtnb |
T |
A |
12: 3,694,272 (GRCm39) |
|
probably null |
Het |
Entpd1 |
A |
G |
19: 40,727,309 (GRCm39) |
N486D |
possibly damaging |
Het |
Fes |
G |
A |
7: 80,028,410 (GRCm39) |
R736C |
probably damaging |
Het |
Galr1 |
T |
G |
18: 82,411,990 (GRCm39) |
Y292S |
probably damaging |
Het |
Gda |
T |
A |
19: 21,405,988 (GRCm39) |
D80V |
probably damaging |
Het |
Ghr |
A |
G |
15: 3,377,054 (GRCm39) |
C56R |
probably benign |
Het |
Golgb1 |
A |
G |
16: 36,718,909 (GRCm39) |
T313A |
probably damaging |
Het |
Gpaa1 |
A |
T |
15: 76,217,193 (GRCm39) |
D236V |
probably damaging |
Het |
Gsdmc |
A |
G |
15: 63,676,315 (GRCm39) |
S43P |
probably benign |
Het |
Gsdmd |
A |
G |
15: 75,738,202 (GRCm39) |
E295G |
probably damaging |
Het |
Htatip2 |
A |
G |
7: 49,409,534 (GRCm39) |
K96R |
probably benign |
Het |
Insm1 |
T |
A |
2: 146,064,711 (GRCm39) |
F176I |
probably benign |
Het |
Itih1 |
T |
C |
14: 30,665,117 (GRCm39) |
E36G |
probably benign |
Het |
Jak1 |
A |
G |
4: 101,032,379 (GRCm39) |
V409A |
probably damaging |
Het |
Knl1 |
A |
G |
2: 118,901,073 (GRCm39) |
I925V |
possibly damaging |
Het |
Lcmt2 |
A |
G |
2: 120,969,185 (GRCm39) |
S413P |
probably benign |
Het |
Lmo7 |
T |
C |
14: 102,118,389 (GRCm39) |
S205P |
probably damaging |
Het |
Lrch3 |
C |
A |
16: 32,807,113 (GRCm39) |
S462* |
probably null |
Het |
Lrrtm2 |
T |
C |
18: 35,346,688 (GRCm39) |
I205V |
possibly damaging |
Het |
Mark3 |
T |
G |
12: 111,600,223 (GRCm39) |
N479K |
probably damaging |
Het |
Mrpl19 |
C |
T |
6: 81,942,793 (GRCm39) |
G39D |
possibly damaging |
Het |
Msh4 |
A |
G |
3: 153,582,382 (GRCm39) |
Y497H |
probably benign |
Het |
Msl2 |
T |
A |
9: 100,979,316 (GRCm39) |
D563E |
probably benign |
Het |
Mta1 |
G |
A |
12: 113,095,088 (GRCm39) |
|
probably null |
Het |
Ncapg |
T |
C |
5: 45,853,135 (GRCm39) |
L867P |
probably benign |
Het |
Nkapl |
T |
C |
13: 21,652,013 (GRCm39) |
D200G |
unknown |
Het |
Nos1 |
A |
C |
5: 118,005,583 (GRCm39) |
E101A |
probably damaging |
Het |
Npat |
T |
C |
9: 53,481,216 (GRCm39) |
S1008P |
probably damaging |
Het |
Ntng1 |
A |
G |
3: 109,760,398 (GRCm39) |
I358T |
probably benign |
Het |
Or11h6 |
A |
G |
14: 50,879,852 (GRCm39) |
E32G |
probably benign |
Het |
Or13p4 |
C |
T |
4: 118,546,859 (GRCm39) |
M263I |
probably damaging |
Het |
Or2d2b |
A |
G |
7: 106,705,274 (GRCm39) |
S265P |
probably benign |
Het |
Or4b1 |
T |
A |
2: 89,980,188 (GRCm39) |
H54L |
probably benign |
Het |
Or6c88 |
A |
G |
10: 129,406,493 (GRCm39) |
|
probably benign |
Het |
Pex1 |
A |
G |
5: 3,680,222 (GRCm39) |
D948G |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,755,218 (GRCm39) |
I1660N |
possibly damaging |
Het |
Pkp2 |
T |
A |
16: 16,079,537 (GRCm39) |
Y540N |
possibly damaging |
Het |
Pkp4 |
T |
C |
2: 59,142,110 (GRCm39) |
L471P |
probably damaging |
Het |
Plekhm3 |
A |
T |
1: 64,977,143 (GRCm39) |
M109K |
probably benign |
Het |
Plekhn1 |
T |
C |
4: 156,318,418 (GRCm39) |
N68S |
probably benign |
Het |
Pramel7 |
T |
A |
2: 87,321,189 (GRCm39) |
D282V |
possibly damaging |
Het |
Pxdn |
T |
C |
12: 30,040,944 (GRCm39) |
Y407H |
probably benign |
Het |
Rab3ip |
T |
C |
10: 116,773,546 (GRCm39) |
D89G |
possibly damaging |
Het |
Rad17 |
G |
A |
13: 100,766,019 (GRCm39) |
Q370* |
probably null |
Het |
Robo4 |
T |
C |
9: 37,322,277 (GRCm39) |
C751R |
probably benign |
Het |
Sez6 |
A |
G |
11: 77,844,356 (GRCm39) |
T60A |
probably damaging |
Het |
Socs4 |
A |
G |
14: 47,527,296 (GRCm39) |
H77R |
probably benign |
Het |
Srrm3 |
T |
A |
5: 135,881,060 (GRCm39) |
M120K |
probably benign |
Het |
Steap4 |
A |
T |
5: 8,028,453 (GRCm39) |
I344F |
probably benign |
Het |
Stk36 |
T |
A |
1: 74,672,725 (GRCm39) |
F989Y |
probably damaging |
Het |
Toporsl |
A |
T |
4: 52,612,108 (GRCm39) |
Q667L |
probably benign |
Het |
Tspan17 |
T |
C |
13: 54,937,466 (GRCm39) |
F20S |
probably benign |
Het |
Tubgcp3 |
G |
A |
8: 12,711,359 (GRCm39) |
Q65* |
probably null |
Het |
Ush2a |
A |
T |
1: 188,465,726 (GRCm39) |
I2765F |
probably benign |
Het |
Vwa8 |
A |
C |
14: 79,219,674 (GRCm39) |
|
probably null |
Het |
Wdfy4 |
A |
G |
14: 32,800,264 (GRCm39) |
V1954A |
|
Het |
Xrn2 |
T |
A |
2: 146,884,017 (GRCm39) |
|
probably null |
Het |
Zfp687 |
C |
T |
3: 94,914,841 (GRCm39) |
R1220H |
probably damaging |
Het |
|
Other mutations in Nalcn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00952:Nalcn
|
APN |
14 |
123,586,201 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00964:Nalcn
|
APN |
14 |
123,532,796 (GRCm39) |
splice site |
probably benign |
|
IGL01310:Nalcn
|
APN |
14 |
123,554,661 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01578:Nalcn
|
APN |
14 |
123,809,503 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01925:Nalcn
|
APN |
14 |
123,529,260 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02072:Nalcn
|
APN |
14 |
123,560,770 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02096:Nalcn
|
APN |
14 |
123,831,915 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02212:Nalcn
|
APN |
14 |
123,752,742 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02306:Nalcn
|
APN |
14 |
123,560,750 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02471:Nalcn
|
APN |
14 |
123,560,726 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02478:Nalcn
|
APN |
14 |
123,558,717 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02551:Nalcn
|
APN |
14 |
123,560,750 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02630:Nalcn
|
APN |
14 |
123,555,291 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02632:Nalcn
|
APN |
14 |
123,555,265 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02661:Nalcn
|
APN |
14 |
123,830,321 (GRCm39) |
splice site |
probably benign |
|
IGL02830:Nalcn
|
APN |
14 |
123,530,881 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02939:Nalcn
|
APN |
14 |
123,536,284 (GRCm39) |
missense |
probably null |
1.00 |
IGL03035:Nalcn
|
APN |
14 |
123,515,630 (GRCm39) |
nonsense |
probably null |
|
IGL03226:Nalcn
|
APN |
14 |
123,518,527 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03242:Nalcn
|
APN |
14 |
123,558,899 (GRCm39) |
missense |
possibly damaging |
0.91 |
Narnia
|
UTSW |
14 |
123,528,459 (GRCm39) |
missense |
probably benign |
0.11 |
R0019:Nalcn
|
UTSW |
14 |
123,744,901 (GRCm39) |
missense |
probably benign |
0.18 |
R0144:Nalcn
|
UTSW |
14 |
123,647,251 (GRCm39) |
splice site |
probably benign |
|
R0144:Nalcn
|
UTSW |
14 |
123,608,948 (GRCm39) |
missense |
probably damaging |
0.96 |
R0359:Nalcn
|
UTSW |
14 |
123,536,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R0383:Nalcn
|
UTSW |
14 |
123,744,971 (GRCm39) |
missense |
probably benign |
0.01 |
R0400:Nalcn
|
UTSW |
14 |
123,528,372 (GRCm39) |
splice site |
probably benign |
|
R0467:Nalcn
|
UTSW |
14 |
123,528,459 (GRCm39) |
missense |
probably benign |
0.11 |
R0506:Nalcn
|
UTSW |
14 |
123,834,026 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0583:Nalcn
|
UTSW |
14 |
123,531,755 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0620:Nalcn
|
UTSW |
14 |
123,536,553 (GRCm39) |
splice site |
probably benign |
|
R0624:Nalcn
|
UTSW |
14 |
123,607,444 (GRCm39) |
missense |
probably benign |
|
R0883:Nalcn
|
UTSW |
14 |
123,702,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R1381:Nalcn
|
UTSW |
14 |
123,551,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Nalcn
|
UTSW |
14 |
123,702,068 (GRCm39) |
splice site |
probably benign |
|
R1689:Nalcn
|
UTSW |
14 |
123,522,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1726:Nalcn
|
UTSW |
14 |
123,545,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1774:Nalcn
|
UTSW |
14 |
123,515,678 (GRCm39) |
missense |
probably benign |
|
R1854:Nalcn
|
UTSW |
14 |
123,697,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R1869:Nalcn
|
UTSW |
14 |
123,831,965 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1871:Nalcn
|
UTSW |
14 |
123,831,965 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1873:Nalcn
|
UTSW |
14 |
123,521,013 (GRCm39) |
missense |
probably benign |
0.00 |
R1899:Nalcn
|
UTSW |
14 |
123,553,538 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1915:Nalcn
|
UTSW |
14 |
123,540,181 (GRCm39) |
missense |
probably benign |
0.08 |
R2016:Nalcn
|
UTSW |
14 |
123,831,993 (GRCm39) |
splice site |
probably null |
|
R2034:Nalcn
|
UTSW |
14 |
123,521,015 (GRCm39) |
missense |
probably benign |
0.01 |
R2087:Nalcn
|
UTSW |
14 |
123,518,557 (GRCm39) |
missense |
probably benign |
|
R2149:Nalcn
|
UTSW |
14 |
123,607,429 (GRCm39) |
missense |
probably benign |
0.01 |
R2157:Nalcn
|
UTSW |
14 |
123,647,164 (GRCm39) |
missense |
probably benign |
0.32 |
R2166:Nalcn
|
UTSW |
14 |
123,607,363 (GRCm39) |
missense |
probably benign |
0.00 |
R2932:Nalcn
|
UTSW |
14 |
123,830,430 (GRCm39) |
missense |
probably benign |
0.06 |
R3408:Nalcn
|
UTSW |
14 |
123,834,029 (GRCm39) |
missense |
probably null |
0.98 |
R3778:Nalcn
|
UTSW |
14 |
123,702,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Nalcn
|
UTSW |
14 |
123,515,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R3835:Nalcn
|
UTSW |
14 |
123,530,834 (GRCm39) |
splice site |
probably benign |
|
R3937:Nalcn
|
UTSW |
14 |
123,607,357 (GRCm39) |
missense |
probably benign |
0.00 |
R4001:Nalcn
|
UTSW |
14 |
123,834,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4015:Nalcn
|
UTSW |
14 |
123,723,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R4033:Nalcn
|
UTSW |
14 |
123,837,401 (GRCm39) |
splice site |
probably benign |
|
R4231:Nalcn
|
UTSW |
14 |
123,837,325 (GRCm39) |
missense |
probably benign |
0.01 |
R4464:Nalcn
|
UTSW |
14 |
123,560,762 (GRCm39) |
missense |
probably benign |
|
R4512:Nalcn
|
UTSW |
14 |
123,532,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R4542:Nalcn
|
UTSW |
14 |
123,558,889 (GRCm39) |
synonymous |
silent |
|
R4557:Nalcn
|
UTSW |
14 |
123,558,647 (GRCm39) |
intron |
probably benign |
|
R4869:Nalcn
|
UTSW |
14 |
123,837,296 (GRCm39) |
missense |
probably benign |
0.44 |
R5083:Nalcn
|
UTSW |
14 |
123,560,706 (GRCm39) |
splice site |
probably null |
|
R5109:Nalcn
|
UTSW |
14 |
123,515,650 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5131:Nalcn
|
UTSW |
14 |
123,753,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R5158:Nalcn
|
UTSW |
14 |
123,753,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R5259:Nalcn
|
UTSW |
14 |
123,753,063 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5422:Nalcn
|
UTSW |
14 |
123,752,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R5514:Nalcn
|
UTSW |
14 |
123,521,123 (GRCm39) |
missense |
probably benign |
0.14 |
R5523:Nalcn
|
UTSW |
14 |
123,647,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R5551:Nalcn
|
UTSW |
14 |
123,515,698 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5667:Nalcn
|
UTSW |
14 |
123,532,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Nalcn
|
UTSW |
14 |
123,532,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R5750:Nalcn
|
UTSW |
14 |
123,809,450 (GRCm39) |
missense |
probably benign |
|
R5765:Nalcn
|
UTSW |
14 |
123,702,138 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6324:Nalcn
|
UTSW |
14 |
123,647,161 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6523:Nalcn
|
UTSW |
14 |
123,555,255 (GRCm39) |
missense |
probably benign |
0.00 |
R6558:Nalcn
|
UTSW |
14 |
123,723,919 (GRCm39) |
missense |
probably benign |
|
R6631:Nalcn
|
UTSW |
14 |
123,697,663 (GRCm39) |
missense |
probably benign |
0.17 |
R6667:Nalcn
|
UTSW |
14 |
123,558,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R6670:Nalcn
|
UTSW |
14 |
123,702,084 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6724:Nalcn
|
UTSW |
14 |
123,535,479 (GRCm39) |
missense |
probably damaging |
0.99 |
R6731:Nalcn
|
UTSW |
14 |
123,837,346 (GRCm39) |
missense |
probably benign |
0.22 |
R6957:Nalcn
|
UTSW |
14 |
123,744,966 (GRCm39) |
missense |
probably damaging |
0.96 |
R6970:Nalcn
|
UTSW |
14 |
123,551,506 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7010:Nalcn
|
UTSW |
14 |
123,530,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R7018:Nalcn
|
UTSW |
14 |
123,647,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R7040:Nalcn
|
UTSW |
14 |
123,525,267 (GRCm39) |
missense |
probably benign |
|
R7089:Nalcn
|
UTSW |
14 |
123,515,761 (GRCm39) |
missense |
probably benign |
0.01 |
R7128:Nalcn
|
UTSW |
14 |
123,831,914 (GRCm39) |
missense |
probably damaging |
0.99 |
R7149:Nalcn
|
UTSW |
14 |
123,837,277 (GRCm39) |
missense |
probably benign |
0.02 |
R7361:Nalcn
|
UTSW |
14 |
123,529,251 (GRCm39) |
missense |
probably benign |
0.00 |
R7378:Nalcn
|
UTSW |
14 |
123,540,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7470:Nalcn
|
UTSW |
14 |
123,809,456 (GRCm39) |
missense |
probably benign |
0.09 |
R7483:Nalcn
|
UTSW |
14 |
123,551,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R7521:Nalcn
|
UTSW |
14 |
123,530,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R7558:Nalcn
|
UTSW |
14 |
123,723,797 (GRCm39) |
critical splice donor site |
probably null |
|
R7585:Nalcn
|
UTSW |
14 |
123,753,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R7591:Nalcn
|
UTSW |
14 |
123,561,297 (GRCm39) |
missense |
probably benign |
0.01 |
R7761:Nalcn
|
UTSW |
14 |
123,531,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R7761:Nalcn
|
UTSW |
14 |
123,531,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R7811:Nalcn
|
UTSW |
14 |
123,536,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R7983:Nalcn
|
UTSW |
14 |
123,830,409 (GRCm39) |
missense |
probably benign |
0.17 |
R8089:Nalcn
|
UTSW |
14 |
123,537,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R8110:Nalcn
|
UTSW |
14 |
123,702,113 (GRCm39) |
missense |
probably benign |
0.00 |
R8190:Nalcn
|
UTSW |
14 |
123,837,351 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8273:Nalcn
|
UTSW |
14 |
123,554,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R8407:Nalcn
|
UTSW |
14 |
123,554,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R8497:Nalcn
|
UTSW |
14 |
123,752,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R8544:Nalcn
|
UTSW |
14 |
123,608,935 (GRCm39) |
missense |
probably benign |
0.40 |
R8549:Nalcn
|
UTSW |
14 |
123,607,448 (GRCm39) |
missense |
probably benign |
0.01 |
R8731:Nalcn
|
UTSW |
14 |
123,837,266 (GRCm39) |
missense |
probably benign |
0.01 |
R8862:Nalcn
|
UTSW |
14 |
123,647,199 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8919:Nalcn
|
UTSW |
14 |
123,561,284 (GRCm39) |
missense |
probably benign |
0.00 |
R9072:Nalcn
|
UTSW |
14 |
123,532,863 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9073:Nalcn
|
UTSW |
14 |
123,532,863 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9182:Nalcn
|
UTSW |
14 |
123,834,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R9193:Nalcn
|
UTSW |
14 |
123,545,792 (GRCm39) |
nonsense |
probably null |
|
R9241:Nalcn
|
UTSW |
14 |
123,809,429 (GRCm39) |
missense |
probably benign |
0.00 |
R9267:Nalcn
|
UTSW |
14 |
123,518,567 (GRCm39) |
missense |
probably benign |
0.08 |
R9274:Nalcn
|
UTSW |
14 |
123,753,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R9277:Nalcn
|
UTSW |
14 |
123,518,523 (GRCm39) |
missense |
probably damaging |
0.98 |
R9376:Nalcn
|
UTSW |
14 |
123,515,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
X0060:Nalcn
|
UTSW |
14 |
123,522,653 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Nalcn
|
UTSW |
14 |
123,831,980 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Nalcn
|
UTSW |
14 |
123,531,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|