Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930533K18Rik |
A |
G |
10: 70,708,032 (GRCm39) |
|
noncoding transcript |
Het |
Abca3 |
G |
T |
17: 24,595,447 (GRCm39) |
C328F |
possibly damaging |
Het |
Aldh5a1 |
T |
C |
13: 25,102,495 (GRCm39) |
N323D |
possibly damaging |
Het |
Atp5f1c |
T |
C |
2: 10,073,477 (GRCm39) |
Y32C |
probably damaging |
Het |
Capn3 |
T |
G |
2: 120,332,667 (GRCm39) |
|
probably null |
Het |
Ccdc113 |
C |
A |
8: 96,277,866 (GRCm39) |
D275E |
probably benign |
Het |
Ccdc40 |
T |
A |
11: 119,133,545 (GRCm39) |
F562I |
possibly damaging |
Het |
Ccn6 |
A |
G |
10: 39,034,306 (GRCm39) |
Y99H |
probably damaging |
Het |
Cd96 |
T |
C |
16: 45,929,490 (GRCm39) |
T152A |
possibly damaging |
Het |
Cdh20 |
T |
A |
1: 109,988,870 (GRCm39) |
D257E |
probably damaging |
Het |
Cilp2 |
T |
C |
8: 70,333,854 (GRCm39) |
D1048G |
probably benign |
Het |
Clrn2 |
T |
G |
5: 45,617,408 (GRCm39) |
L93R |
probably damaging |
Het |
Crat |
C |
A |
2: 30,299,978 (GRCm39) |
G134V |
probably damaging |
Het |
Dis3 |
A |
T |
14: 99,335,181 (GRCm39) |
N140K |
probably benign |
Het |
Dmxl2 |
T |
A |
9: 54,352,660 (GRCm39) |
|
probably benign |
Het |
Dus1l |
T |
A |
11: 120,683,905 (GRCm39) |
Q181L |
probably damaging |
Het |
Ece1 |
A |
G |
4: 137,675,855 (GRCm39) |
T410A |
probably benign |
Het |
Gcc1 |
T |
A |
6: 28,421,047 (GRCm39) |
H90L |
probably damaging |
Het |
Gpr152 |
T |
A |
19: 4,192,951 (GRCm39) |
V164E |
probably damaging |
Het |
Grik3 |
A |
C |
4: 125,587,829 (GRCm39) |
I650L |
possibly damaging |
Het |
Gvin3 |
T |
C |
7: 106,201,744 (GRCm39) |
D500G |
probably damaging |
Het |
Gzmm |
A |
T |
10: 79,530,896 (GRCm39) |
T233S |
probably benign |
Het |
H2-Q4 |
T |
A |
17: 35,602,288 (GRCm39) |
V341D |
probably benign |
Het |
Igsf21 |
A |
G |
4: 139,755,029 (GRCm39) |
|
probably benign |
Het |
Kmt2d |
T |
C |
15: 98,758,538 (GRCm39) |
|
probably benign |
Het |
Kntc1 |
T |
G |
5: 123,919,721 (GRCm39) |
V864G |
probably damaging |
Het |
Lnx1 |
T |
C |
5: 74,780,816 (GRCm39) |
E235G |
possibly damaging |
Het |
Man2b1 |
G |
T |
8: 85,824,059 (GRCm39) |
K985N |
probably benign |
Het |
Map4k1 |
C |
A |
7: 28,701,044 (GRCm39) |
P670Q |
probably damaging |
Het |
Mapk8ip1 |
C |
A |
2: 92,219,319 (GRCm39) |
|
probably null |
Het |
Mettl16 |
T |
A |
11: 74,683,093 (GRCm39) |
Y178* |
probably null |
Het |
Mrpl11 |
T |
A |
19: 5,013,449 (GRCm39) |
|
probably null |
Het |
Nup85 |
T |
C |
11: 115,460,540 (GRCm39) |
S140P |
possibly damaging |
Het |
Or14c44 |
T |
C |
7: 86,062,167 (GRCm39) |
L199P |
possibly damaging |
Het |
Or1j20 |
T |
C |
2: 36,760,532 (GRCm39) |
|
probably benign |
Het |
Or4k51 |
T |
A |
2: 111,585,350 (GRCm39) |
V252E |
probably damaging |
Het |
Or5w16 |
T |
C |
2: 87,576,942 (GRCm39) |
V134A |
probably benign |
Het |
Pcdhb2 |
T |
A |
18: 37,428,375 (GRCm39) |
L116* |
probably null |
Het |
Pdcd7 |
C |
A |
9: 65,253,985 (GRCm39) |
R188S |
probably damaging |
Het |
Pdk2 |
T |
C |
11: 94,918,111 (GRCm39) |
Y374C |
probably damaging |
Het |
Ppp1r12a |
G |
T |
10: 108,069,882 (GRCm39) |
D224Y |
probably damaging |
Het |
Ppp2r2d |
T |
A |
7: 138,478,364 (GRCm39) |
Y169N |
probably damaging |
Het |
Prcp |
A |
C |
7: 92,559,421 (GRCm39) |
T162P |
probably benign |
Het |
Prkd1 |
A |
G |
12: 50,388,925 (GRCm39) |
S873P |
probably benign |
Het |
Ptpn2 |
T |
C |
18: 67,814,623 (GRCm39) |
T129A |
probably benign |
Het |
Rtkn |
G |
A |
6: 83,123,042 (GRCm39) |
R68H |
probably damaging |
Het |
Sall4 |
C |
T |
2: 168,597,776 (GRCm39) |
D355N |
probably damaging |
Het |
Scn7a |
A |
G |
2: 66,534,196 (GRCm39) |
V493A |
probably benign |
Het |
Sema4b |
G |
A |
7: 79,865,444 (GRCm39) |
A140T |
probably damaging |
Het |
Shisa6 |
C |
A |
11: 66,108,654 (GRCm39) |
G408C |
possibly damaging |
Het |
Slc7a9 |
G |
T |
7: 35,153,589 (GRCm39) |
V197F |
probably damaging |
Het |
Spata2 |
A |
T |
2: 167,326,071 (GRCm39) |
D249E |
probably damaging |
Het |
Stk36 |
T |
A |
1: 74,672,797 (GRCm39) |
V1013E |
probably benign |
Het |
Tcp10a |
T |
C |
17: 7,610,899 (GRCm39) |
V336A |
probably damaging |
Het |
Tfb2m |
A |
T |
1: 179,365,409 (GRCm39) |
V185D |
possibly damaging |
Het |
Tgm7 |
T |
A |
2: 120,937,396 (GRCm39) |
Y76F |
probably benign |
Het |
Tph1 |
T |
C |
7: 46,303,177 (GRCm39) |
Y267C |
probably damaging |
Het |
Trgv1 |
G |
A |
13: 19,520,740 (GRCm39) |
|
probably benign |
Het |
Vmn2r12 |
C |
A |
5: 109,239,716 (GRCm39) |
R282S |
probably damaging |
Het |
Vps4a |
A |
G |
8: 107,763,556 (GRCm39) |
D72G |
probably benign |
Het |
Wipf2 |
T |
A |
11: 98,781,629 (GRCm39) |
V56D |
possibly damaging |
Het |
Zfp750 |
C |
A |
11: 121,402,991 (GRCm39) |
V586L |
probably benign |
Het |
Zfp831 |
A |
G |
2: 174,486,399 (GRCm39) |
E358G |
possibly damaging |
Het |
|
Other mutations in Ube2d1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01695:Ube2d1
|
APN |
10 |
71,098,082 (GRCm39) |
missense |
probably damaging |
0.99 |
R0669:Ube2d1
|
UTSW |
10 |
71,097,940 (GRCm39) |
missense |
probably benign |
0.00 |
R1616:Ube2d1
|
UTSW |
10 |
71,092,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Ube2d1
|
UTSW |
10 |
71,120,953 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
R4177:Ube2d1
|
UTSW |
10 |
71,094,033 (GRCm39) |
missense |
probably damaging |
0.98 |
R5440:Ube2d1
|
UTSW |
10 |
71,091,682 (GRCm39) |
missense |
probably damaging |
0.98 |
R5889:Ube2d1
|
UTSW |
10 |
71,095,699 (GRCm39) |
intron |
probably benign |
|
R6562:Ube2d1
|
UTSW |
10 |
71,098,071 (GRCm39) |
missense |
probably benign |
0.27 |
R6644:Ube2d1
|
UTSW |
10 |
71,092,530 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7227:Ube2d1
|
UTSW |
10 |
71,091,702 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8707:Ube2d1
|
UTSW |
10 |
71,092,478 (GRCm39) |
missense |
probably benign |
0.17 |
R9237:Ube2d1
|
UTSW |
10 |
71,097,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R9505:Ube2d1
|
UTSW |
10 |
71,098,094 (GRCm39) |
critical splice acceptor site |
probably null |
|
|