Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
A |
T |
6: 146,854,606 (GRCm39) |
F145L |
probably benign |
Het |
Abcc9 |
T |
C |
6: 142,551,645 (GRCm39) |
D1221G |
possibly damaging |
Het |
Adamtsl4 |
T |
C |
3: 95,584,864 (GRCm39) |
K935E |
probably benign |
Het |
Ago4 |
A |
T |
4: 126,409,655 (GRCm39) |
|
probably benign |
Het |
Arhgef28 |
T |
C |
13: 98,130,575 (GRCm39) |
D421G |
probably benign |
Het |
Armh4 |
T |
A |
14: 50,011,444 (GRCm39) |
M88L |
probably benign |
Het |
Atl2 |
T |
C |
17: 80,157,588 (GRCm39) |
*413W |
probably null |
Het |
B4galt7 |
C |
A |
13: 55,756,152 (GRCm39) |
|
probably null |
Het |
Bltp3b |
A |
G |
10: 89,651,917 (GRCm39) |
N247S |
probably benign |
Het |
C8g |
A |
T |
2: 25,389,425 (GRCm39) |
S147T |
probably damaging |
Het |
Clstn3 |
A |
T |
6: 124,426,792 (GRCm39) |
Y510N |
possibly damaging |
Het |
Cnot2 |
A |
G |
10: 116,373,301 (GRCm39) |
V34A |
possibly damaging |
Het |
Cyb5d2 |
A |
T |
11: 72,686,606 (GRCm39) |
|
probably benign |
Het |
Dnah5 |
T |
C |
15: 28,421,144 (GRCm39) |
I3827T |
probably damaging |
Het |
Dnah7a |
G |
T |
1: 53,464,376 (GRCm39) |
Q3672K |
probably benign |
Het |
Dock1 |
A |
T |
7: 134,717,021 (GRCm39) |
Y1219F |
possibly damaging |
Het |
Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
Fat1 |
A |
T |
8: 45,478,518 (GRCm39) |
E2521D |
probably benign |
Het |
Gm10719 |
G |
T |
9: 3,019,043 (GRCm39) |
W96L |
probably damaging |
Het |
H2-M2 |
G |
A |
17: 37,792,399 (GRCm39) |
H291Y |
probably damaging |
Het |
Hmgcl |
T |
C |
4: 135,686,035 (GRCm39) |
Y167H |
probably damaging |
Het |
Il22ra2 |
A |
T |
10: 19,502,400 (GRCm39) |
D73V |
possibly damaging |
Het |
Incenp |
A |
T |
19: 9,861,142 (GRCm39) |
M480K |
unknown |
Het |
Irag1 |
G |
T |
7: 110,522,984 (GRCm39) |
A359D |
probably benign |
Het |
Kdm6a |
A |
G |
X: 18,117,114 (GRCm39) |
T266A |
probably benign |
Het |
Lipf |
A |
G |
19: 33,942,965 (GRCm39) |
N91S |
probably benign |
Het |
M1ap |
A |
T |
6: 82,980,756 (GRCm39) |
N214I |
probably damaging |
Het |
Mast3 |
A |
G |
8: 71,233,838 (GRCm39) |
V969A |
probably damaging |
Het |
Mdga1 |
A |
G |
17: 30,057,005 (GRCm39) |
C826R |
probably damaging |
Het |
Msx1 |
C |
A |
5: 37,981,365 (GRCm39) |
A105S |
probably benign |
Het |
Or5ac23 |
A |
C |
16: 59,149,243 (GRCm39) |
S210A |
probably benign |
Het |
Otogl |
A |
T |
10: 107,626,510 (GRCm39) |
D1451E |
probably benign |
Het |
Otop2 |
G |
A |
11: 115,220,201 (GRCm39) |
G347D |
probably damaging |
Het |
Ppp1r13l |
A |
T |
7: 19,103,978 (GRCm39) |
H153L |
probably benign |
Het |
Pramel29 |
T |
C |
4: 143,935,265 (GRCm39) |
K161E |
possibly damaging |
Het |
Proz |
A |
G |
8: 13,114,621 (GRCm39) |
Y85C |
probably damaging |
Het |
Prss50 |
A |
G |
9: 110,687,480 (GRCm39) |
D141G |
probably benign |
Het |
Rad54l2 |
T |
A |
9: 106,597,613 (GRCm39) |
Q131L |
probably benign |
Het |
Sdha |
A |
G |
13: 74,472,077 (GRCm39) |
|
probably benign |
Het |
Sema3d |
T |
A |
5: 12,635,091 (GRCm39) |
I719N |
probably benign |
Het |
Slc18b1 |
A |
T |
10: 23,681,879 (GRCm39) |
I148L |
probably benign |
Het |
Tacc2 |
G |
T |
7: 130,330,852 (GRCm39) |
D2086Y |
probably damaging |
Het |
Tchh |
T |
C |
3: 93,354,298 (GRCm39) |
L1246P |
unknown |
Het |
Tmprss11d |
T |
C |
5: 86,457,177 (GRCm39) |
I161V |
probably benign |
Het |
Trpc3 |
T |
C |
3: 36,725,172 (GRCm39) |
D268G |
probably damaging |
Het |
Trpm8 |
G |
A |
1: 88,289,727 (GRCm39) |
R895H |
probably damaging |
Het |
Txndc2 |
A |
G |
17: 65,945,079 (GRCm39) |
I366T |
possibly damaging |
Het |
Ugt2a3 |
T |
C |
5: 87,484,725 (GRCm39) |
I100V |
probably benign |
Het |
Upp1 |
C |
A |
11: 9,081,709 (GRCm39) |
P82Q |
probably damaging |
Het |
Vim |
A |
G |
2: 13,584,827 (GRCm39) |
|
probably null |
Het |
Vmn2r12 |
A |
T |
5: 109,240,058 (GRCm39) |
N168K |
possibly damaging |
Het |
Zdhhc14 |
G |
T |
17: 5,802,983 (GRCm39) |
C362F |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,810,863 (GRCm39) |
V727A |
probably damaging |
Het |
Zswim5 |
G |
A |
4: 116,735,177 (GRCm39) |
G174D |
unknown |
Het |
|
Other mutations in Pramel21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02052:Pramel21
|
APN |
4 |
143,341,643 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02390:Pramel21
|
APN |
4 |
143,341,895 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02676:Pramel21
|
APN |
4 |
143,342,667 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL03381:Pramel21
|
APN |
4 |
143,343,625 (GRCm39) |
splice site |
probably benign |
|
IGL03410:Pramel21
|
APN |
4 |
143,341,851 (GRCm39) |
missense |
probably benign |
0.02 |
H8562:Pramel21
|
UTSW |
4 |
143,341,920 (GRCm39) |
splice site |
probably benign |
|
PIT4151001:Pramel21
|
UTSW |
4 |
143,342,722 (GRCm39) |
nonsense |
probably null |
|
R0157:Pramel21
|
UTSW |
4 |
143,342,366 (GRCm39) |
missense |
probably damaging |
0.98 |
R0352:Pramel21
|
UTSW |
4 |
143,342,559 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0494:Pramel21
|
UTSW |
4 |
143,342,726 (GRCm39) |
missense |
probably benign |
0.33 |
R0688:Pramel21
|
UTSW |
4 |
143,343,927 (GRCm39) |
missense |
probably benign |
0.00 |
R0884:Pramel21
|
UTSW |
4 |
143,341,754 (GRCm39) |
missense |
probably benign |
0.01 |
R1267:Pramel21
|
UTSW |
4 |
143,342,304 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1418:Pramel21
|
UTSW |
4 |
143,342,604 (GRCm39) |
missense |
probably benign |
0.15 |
R1761:Pramel21
|
UTSW |
4 |
143,342,438 (GRCm39) |
missense |
probably benign |
0.00 |
R3148:Pramel21
|
UTSW |
4 |
143,344,047 (GRCm39) |
missense |
probably benign |
0.30 |
R4115:Pramel21
|
UTSW |
4 |
143,344,026 (GRCm39) |
missense |
probably benign |
0.06 |
R4760:Pramel21
|
UTSW |
4 |
143,343,801 (GRCm39) |
missense |
probably benign |
0.04 |
R5516:Pramel21
|
UTSW |
4 |
143,342,253 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5603:Pramel21
|
UTSW |
4 |
143,344,066 (GRCm39) |
nonsense |
probably null |
|
R5724:Pramel21
|
UTSW |
4 |
143,344,026 (GRCm39) |
missense |
probably benign |
0.06 |
R5796:Pramel21
|
UTSW |
4 |
143,341,778 (GRCm39) |
missense |
probably benign |
0.12 |
R5879:Pramel21
|
UTSW |
4 |
143,344,161 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6181:Pramel21
|
UTSW |
4 |
143,342,828 (GRCm39) |
critical splice donor site |
probably null |
|
R7155:Pramel21
|
UTSW |
4 |
143,342,735 (GRCm39) |
missense |
probably benign |
0.01 |
R7492:Pramel21
|
UTSW |
4 |
143,342,744 (GRCm39) |
missense |
not run |
|
R7913:Pramel21
|
UTSW |
4 |
143,341,615 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7995:Pramel21
|
UTSW |
4 |
143,342,570 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8126:Pramel21
|
UTSW |
4 |
143,343,635 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8901:Pramel21
|
UTSW |
4 |
143,343,677 (GRCm39) |
missense |
probably benign |
0.00 |
R9061:Pramel21
|
UTSW |
4 |
143,342,741 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9095:Pramel21
|
UTSW |
4 |
143,341,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R9170:Pramel21
|
UTSW |
4 |
143,341,600 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9445:Pramel21
|
UTSW |
4 |
143,343,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R9666:Pramel21
|
UTSW |
4 |
143,341,699 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Pramel21
|
UTSW |
4 |
143,341,802 (GRCm39) |
missense |
possibly damaging |
0.78 |
Z1177:Pramel21
|
UTSW |
4 |
143,342,730 (GRCm39) |
missense |
probably benign |
0.05 |
|