Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alas1 |
T |
C |
9: 106,118,480 (GRCm39) |
N214S |
probably benign |
Het |
Antxr1 |
A |
G |
6: 87,165,820 (GRCm39) |
|
probably benign |
Het |
Atxn7l3 |
A |
T |
11: 102,185,818 (GRCm39) |
|
probably null |
Het |
Cab39l |
A |
G |
14: 59,737,060 (GRCm39) |
E60G |
probably damaging |
Het |
Cdc5l |
G |
T |
17: 45,704,142 (GRCm39) |
|
probably benign |
Het |
Cux2 |
T |
C |
5: 121,998,671 (GRCm39) |
E1423G |
probably benign |
Het |
Dbndd1 |
G |
T |
8: 124,233,512 (GRCm39) |
Q165K |
probably damaging |
Het |
Drd1 |
C |
A |
13: 54,208,082 (GRCm39) |
C37F |
probably damaging |
Het |
Elp3 |
G |
A |
14: 65,828,042 (GRCm39) |
P11L |
probably benign |
Het |
F830045P16Rik |
A |
G |
2: 129,314,777 (GRCm39) |
Y167H |
probably damaging |
Het |
Gimap3 |
G |
A |
6: 48,742,664 (GRCm39) |
Q89* |
probably null |
Het |
H2ac25 |
C |
A |
11: 58,845,685 (GRCm39) |
S41* |
probably null |
Het |
Herc1 |
G |
A |
9: 66,371,981 (GRCm39) |
|
probably null |
Het |
Ipo11 |
A |
G |
13: 107,007,271 (GRCm39) |
V603A |
probably benign |
Het |
Kifap3 |
G |
A |
1: 163,624,833 (GRCm39) |
A130T |
probably damaging |
Het |
Klhl23 |
A |
G |
2: 69,664,241 (GRCm39) |
Y530C |
probably damaging |
Het |
Map4k1 |
C |
T |
7: 28,699,186 (GRCm39) |
|
probably benign |
Het |
Mroh2b |
T |
A |
15: 4,960,600 (GRCm39) |
L778M |
probably damaging |
Het |
Mtdh |
T |
C |
15: 34,118,247 (GRCm39) |
S344P |
possibly damaging |
Het |
Ncoa3 |
T |
G |
2: 165,896,211 (GRCm39) |
N371K |
probably damaging |
Het |
Ncor2 |
C |
A |
5: 125,111,408 (GRCm39) |
|
probably benign |
Het |
Nrn1l |
A |
G |
8: 106,621,052 (GRCm39) |
E48G |
probably benign |
Het |
Or1e17 |
A |
T |
11: 73,831,593 (GRCm39) |
I174F |
possibly damaging |
Het |
Or2t1 |
T |
C |
14: 14,328,498 (GRCm38) |
L129P |
probably damaging |
Het |
Pard3b |
A |
G |
1: 62,269,371 (GRCm39) |
N653S |
probably benign |
Het |
Plekhg1 |
A |
C |
10: 3,914,419 (GRCm39) |
K1380N |
probably damaging |
Het |
Ppara |
T |
A |
15: 85,675,161 (GRCm39) |
I210N |
probably damaging |
Het |
Ppp2r5b |
A |
G |
19: 6,279,077 (GRCm39) |
|
probably benign |
Het |
Prkn |
T |
C |
17: 11,286,027 (GRCm39) |
F6L |
probably damaging |
Het |
Prr14l |
A |
G |
5: 32,985,337 (GRCm39) |
L1386P |
probably damaging |
Het |
Ralgapa1 |
A |
G |
12: 55,829,685 (GRCm39) |
|
probably benign |
Het |
Reln |
A |
T |
5: 22,134,240 (GRCm39) |
L2563I |
probably damaging |
Het |
Rps7 |
A |
G |
12: 28,681,200 (GRCm39) |
|
probably benign |
Het |
Rslcan18 |
T |
C |
13: 67,246,686 (GRCm39) |
K309E |
probably damaging |
Het |
Sec14l5 |
C |
T |
16: 4,984,930 (GRCm39) |
T92M |
probably damaging |
Het |
Slc22a8 |
G |
A |
19: 8,585,514 (GRCm39) |
|
probably benign |
Het |
Smad2 |
G |
A |
18: 76,395,692 (GRCm39) |
A44T |
probably damaging |
Het |
Smcr8 |
T |
C |
11: 60,671,048 (GRCm39) |
V732A |
possibly damaging |
Het |
Spata2l |
A |
G |
8: 123,960,371 (GRCm39) |
F306S |
probably damaging |
Het |
Stab2 |
T |
C |
10: 86,677,491 (GRCm39) |
D2552G |
probably benign |
Het |
Tctn3 |
A |
T |
19: 40,595,711 (GRCm39) |
L358H |
possibly damaging |
Het |
Tk2 |
C |
T |
8: 104,975,146 (GRCm39) |
|
probably benign |
Het |
Tm6sf2 |
C |
T |
8: 70,530,564 (GRCm39) |
R215C |
probably damaging |
Het |
Tmbim6 |
T |
C |
15: 99,304,555 (GRCm39) |
I204T |
probably damaging |
Het |
Tubgcp2 |
C |
A |
7: 139,579,260 (GRCm39) |
W675C |
probably damaging |
Het |
Usp48 |
T |
A |
4: 137,321,794 (GRCm39) |
I62N |
probably damaging |
Het |
Vmn2r74 |
T |
C |
7: 85,601,491 (GRCm39) |
T716A |
probably benign |
Het |
Vps13b |
C |
A |
15: 35,879,949 (GRCm39) |
T3008K |
probably damaging |
Het |
Wnk1 |
G |
A |
6: 119,905,124 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Nudcd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Nudcd1
|
APN |
15 |
44,284,222 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01956:Nudcd1
|
APN |
15 |
44,263,612 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01996:Nudcd1
|
APN |
15 |
44,269,357 (GRCm39) |
missense |
probably benign |
0.41 |
R0960:Nudcd1
|
UTSW |
15 |
44,291,047 (GRCm39) |
unclassified |
probably benign |
|
R3409:Nudcd1
|
UTSW |
15 |
44,284,207 (GRCm39) |
missense |
probably benign |
0.17 |
R3410:Nudcd1
|
UTSW |
15 |
44,284,207 (GRCm39) |
missense |
probably benign |
0.17 |
R4771:Nudcd1
|
UTSW |
15 |
44,268,878 (GRCm39) |
missense |
probably damaging |
0.98 |
R4970:Nudcd1
|
UTSW |
15 |
44,240,039 (GRCm39) |
nonsense |
probably null |
|
R5112:Nudcd1
|
UTSW |
15 |
44,240,039 (GRCm39) |
nonsense |
probably null |
|
R5789:Nudcd1
|
UTSW |
15 |
44,251,879 (GRCm39) |
nonsense |
probably null |
|
R6353:Nudcd1
|
UTSW |
15 |
44,284,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R7045:Nudcd1
|
UTSW |
15 |
44,269,226 (GRCm39) |
missense |
probably benign |
0.00 |
R7483:Nudcd1
|
UTSW |
15 |
44,269,253 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7742:Nudcd1
|
UTSW |
15 |
44,268,754 (GRCm39) |
missense |
probably benign |
0.06 |
R8949:Nudcd1
|
UTSW |
15 |
44,251,971 (GRCm39) |
missense |
probably benign |
0.00 |
R9066:Nudcd1
|
UTSW |
15 |
44,243,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R9201:Nudcd1
|
UTSW |
15 |
44,263,473 (GRCm39) |
missense |
probably benign |
0.00 |
R9438:Nudcd1
|
UTSW |
15 |
44,269,321 (GRCm39) |
missense |
probably benign |
0.15 |
Z1177:Nudcd1
|
UTSW |
15 |
44,268,828 (GRCm39) |
missense |
probably benign |
0.01 |
|