Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
A |
G |
1: 130,671,041 (GRCm39) |
D421G |
probably benign |
Het |
Adamts1 |
T |
G |
16: 85,599,333 (GRCm39) |
Q89P |
probably benign |
Het |
Arhgef10l |
T |
G |
4: 140,297,601 (GRCm39) |
N277T |
possibly damaging |
Het |
Atp2c1 |
G |
A |
9: 105,295,320 (GRCm39) |
R669* |
probably null |
Het |
Brip1 |
T |
C |
11: 86,029,971 (GRCm39) |
T558A |
possibly damaging |
Het |
Cbr2 |
G |
A |
11: 120,621,255 (GRCm39) |
T148I |
probably benign |
Het |
Ccdc110 |
C |
A |
8: 46,395,114 (GRCm39) |
T335K |
probably damaging |
Het |
Cd44 |
T |
G |
2: 102,644,629 (GRCm39) |
D731A |
probably damaging |
Het |
Cnot1 |
T |
C |
8: 96,501,986 (GRCm39) |
D44G |
probably damaging |
Het |
Cnrip1 |
T |
C |
11: 17,002,237 (GRCm39) |
V23A |
probably damaging |
Het |
Cntnap5c |
A |
T |
17: 58,505,995 (GRCm39) |
H673L |
probably benign |
Het |
Col3a1 |
C |
T |
1: 45,372,150 (GRCm39) |
A493V |
probably damaging |
Het |
Crem |
A |
T |
18: 3,299,256 (GRCm39) |
V19E |
probably damaging |
Het |
Cyp2g1 |
A |
G |
7: 26,518,858 (GRCm39) |
D418G |
probably benign |
Het |
Dmrta1 |
A |
T |
4: 89,579,742 (GRCm39) |
H234L |
probably benign |
Het |
Drc3 |
C |
T |
11: 60,261,310 (GRCm39) |
R154W |
probably damaging |
Het |
Drgx |
C |
T |
14: 32,369,112 (GRCm39) |
|
probably benign |
Het |
Eef1d |
A |
G |
15: 75,774,550 (GRCm39) |
S370P |
probably benign |
Het |
Fdx2 |
T |
C |
9: 20,984,720 (GRCm39) |
H28R |
probably benign |
Het |
Fmo5 |
A |
G |
3: 97,553,194 (GRCm39) |
I381V |
probably benign |
Het |
Fpr-rs4 |
CAGGAA |
CA |
17: 18,242,596 (GRCm39) |
|
probably null |
Het |
Fras1 |
T |
C |
5: 96,929,062 (GRCm39) |
L3822P |
probably damaging |
Het |
Gm3604 |
G |
T |
13: 62,517,420 (GRCm39) |
H313N |
possibly damaging |
Het |
Heatr4 |
T |
C |
12: 84,021,855 (GRCm39) |
E460G |
possibly damaging |
Het |
Ino80 |
T |
A |
2: 119,257,151 (GRCm39) |
H834L |
possibly damaging |
Het |
Insr |
A |
T |
8: 3,254,762 (GRCm39) |
C331S |
probably damaging |
Het |
Itih4 |
C |
T |
14: 30,613,694 (GRCm39) |
L304F |
probably damaging |
Het |
Klhdc3 |
C |
T |
17: 46,988,879 (GRCm39) |
V104I |
probably benign |
Het |
Lrp2 |
C |
T |
2: 69,366,365 (GRCm39) |
D245N |
probably benign |
Het |
Map1b |
T |
C |
13: 99,566,178 (GRCm39) |
E2181G |
unknown |
Het |
Map2 |
T |
C |
1: 66,438,599 (GRCm39) |
V41A |
probably damaging |
Het |
Mical3 |
A |
T |
6: 121,017,347 (GRCm39) |
H156Q |
probably damaging |
Het |
Mrgpra2b |
C |
T |
7: 47,113,908 (GRCm39) |
V249I |
probably benign |
Het |
Myo5b |
T |
A |
18: 74,892,263 (GRCm39) |
L1669Q |
probably damaging |
Het |
Nme8 |
G |
A |
13: 19,835,042 (GRCm39) |
S548F |
probably damaging |
Het |
Npas1 |
A |
T |
7: 16,193,202 (GRCm39) |
N408K |
probably benign |
Het |
Or1j11 |
A |
T |
2: 36,311,941 (GRCm39) |
Y177F |
probably benign |
Het |
Or8k30 |
A |
C |
2: 86,339,587 (GRCm39) |
Q261H |
probably damaging |
Het |
Pcnx4 |
T |
C |
12: 72,626,216 (GRCm39) |
Y1141H |
probably damaging |
Het |
Pmaip1 |
C |
A |
18: 66,594,052 (GRCm39) |
P64Q |
probably damaging |
Het |
Rbm4 |
A |
G |
19: 4,837,792 (GRCm39) |
Y231H |
probably damaging |
Het |
Rpgrip1l |
T |
C |
8: 91,996,760 (GRCm39) |
S105G |
possibly damaging |
Het |
Rsf1 |
CG |
CGACGGCGGGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Rtn3 |
A |
T |
19: 7,434,215 (GRCm39) |
D573E |
probably damaging |
Het |
Rxrg |
T |
C |
1: 167,454,893 (GRCm39) |
C159R |
probably damaging |
Het |
Sdk2 |
T |
C |
11: 113,833,948 (GRCm39) |
Y78C |
probably damaging |
Het |
Smu1 |
A |
G |
4: 40,738,438 (GRCm39) |
V432A |
probably benign |
Het |
Spag1 |
T |
C |
15: 36,224,276 (GRCm39) |
L609P |
probably damaging |
Het |
Spata21 |
T |
G |
4: 140,824,277 (GRCm39) |
V180G |
probably benign |
Het |
Spata31e2 |
G |
T |
1: 26,721,222 (GRCm39) |
Y1319* |
probably null |
Het |
Sptlc3 |
A |
T |
2: 139,467,794 (GRCm39) |
I451F |
possibly damaging |
Het |
Srl |
A |
G |
16: 4,340,896 (GRCm39) |
C8R |
unknown |
Het |
Tmprss13 |
A |
G |
9: 45,256,340 (GRCm39) |
R485G |
probably damaging |
Het |
Trpv4 |
C |
T |
5: 114,773,565 (GRCm39) |
A266T |
probably damaging |
Het |
Vmn1r198 |
A |
G |
13: 22,538,855 (GRCm39) |
T25A |
probably benign |
Het |
Vmn2r77 |
T |
C |
7: 86,450,702 (GRCm39) |
V196A |
probably benign |
Het |
Vmn2r82 |
C |
T |
10: 79,231,813 (GRCm39) |
T604I |
probably benign |
Het |
Zfp268 |
C |
A |
4: 145,349,139 (GRCm39) |
T192N |
probably benign |
Het |
Zfp354a |
C |
T |
11: 50,960,551 (GRCm39) |
T254I |
probably damaging |
Het |
|
Other mutations in Ranbp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00423:Ranbp3
|
APN |
17 |
57,016,238 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02801:Ranbp3
|
APN |
17 |
57,017,766 (GRCm39) |
missense |
probably benign |
|
IGL03004:Ranbp3
|
APN |
17 |
57,014,207 (GRCm39) |
missense |
probably damaging |
1.00 |
Waif
|
UTSW |
17 |
56,984,208 (GRCm39) |
splice site |
probably null |
|
R0094:Ranbp3
|
UTSW |
17 |
57,016,338 (GRCm39) |
unclassified |
probably benign |
|
R0139:Ranbp3
|
UTSW |
17 |
57,016,272 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0419:Ranbp3
|
UTSW |
17 |
57,015,219 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0426:Ranbp3
|
UTSW |
17 |
57,014,169 (GRCm39) |
missense |
probably benign |
|
R0629:Ranbp3
|
UTSW |
17 |
57,015,200 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0632:Ranbp3
|
UTSW |
17 |
57,009,896 (GRCm39) |
splice site |
probably benign |
|
R1495:Ranbp3
|
UTSW |
17 |
57,012,527 (GRCm39) |
missense |
probably benign |
0.03 |
R1525:Ranbp3
|
UTSW |
17 |
57,017,865 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2044:Ranbp3
|
UTSW |
17 |
56,980,367 (GRCm39) |
start gained |
probably benign |
|
R4649:Ranbp3
|
UTSW |
17 |
57,003,640 (GRCm39) |
critical splice donor site |
probably null |
|
R4780:Ranbp3
|
UTSW |
17 |
56,980,346 (GRCm39) |
start gained |
probably benign |
|
R5568:Ranbp3
|
UTSW |
17 |
57,008,543 (GRCm39) |
critical splice donor site |
probably null |
|
R5642:Ranbp3
|
UTSW |
17 |
57,017,703 (GRCm39) |
missense |
probably benign |
0.01 |
R5806:Ranbp3
|
UTSW |
17 |
57,017,717 (GRCm39) |
missense |
probably benign |
0.01 |
R5875:Ranbp3
|
UTSW |
17 |
57,014,955 (GRCm39) |
critical splice donor site |
probably null |
|
R6142:Ranbp3
|
UTSW |
17 |
56,993,018 (GRCm39) |
missense |
probably benign |
0.33 |
R6250:Ranbp3
|
UTSW |
17 |
56,984,208 (GRCm39) |
splice site |
probably null |
|
R6745:Ranbp3
|
UTSW |
17 |
57,016,308 (GRCm39) |
missense |
probably benign |
0.24 |
R7222:Ranbp3
|
UTSW |
17 |
57,017,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R7571:Ranbp3
|
UTSW |
17 |
57,014,923 (GRCm39) |
missense |
probably benign |
0.01 |
R7718:Ranbp3
|
UTSW |
17 |
57,003,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R7744:Ranbp3
|
UTSW |
17 |
57,015,219 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8504:Ranbp3
|
UTSW |
17 |
57,015,273 (GRCm39) |
missense |
probably damaging |
0.98 |
R8746:Ranbp3
|
UTSW |
17 |
57,009,826 (GRCm39) |
missense |
probably benign |
|
R9133:Ranbp3
|
UTSW |
17 |
57,003,791 (GRCm39) |
critical splice donor site |
probably null |
|
|