Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrd1 |
G |
A |
5: 129,216,688 (GRCm39) |
D384N |
probably benign |
Het |
Aqp8 |
T |
C |
7: 123,065,883 (GRCm39) |
F226S |
possibly damaging |
Het |
Arl6ip6 |
A |
G |
2: 53,107,339 (GRCm39) |
Y207C |
probably damaging |
Het |
Bltp1 |
C |
A |
3: 37,002,562 (GRCm39) |
C1502* |
probably null |
Het |
Cbfa2t2 |
A |
G |
2: 154,342,365 (GRCm39) |
E27G |
possibly damaging |
Het |
Cdc42bpb |
T |
G |
12: 111,261,206 (GRCm39) |
E201A |
unknown |
Het |
Cfap54 |
A |
C |
10: 92,792,806 (GRCm39) |
V1769G |
unknown |
Het |
Dmxl2 |
C |
T |
9: 54,379,502 (GRCm39) |
G7S |
probably damaging |
Het |
Dnah6 |
G |
T |
6: 73,101,742 (GRCm39) |
F1927L |
possibly damaging |
Het |
Dnajc6 |
A |
G |
4: 101,497,688 (GRCm39) |
E942G |
probably damaging |
Het |
Fam170a |
A |
G |
18: 50,415,969 (GRCm39) |
R324G |
probably benign |
Het |
Gapdhs |
G |
A |
7: 30,438,756 (GRCm39) |
T9I |
unknown |
Het |
Gm10320 |
T |
A |
13: 98,626,232 (GRCm39) |
R51* |
probably null |
Het |
Gm19410 |
A |
T |
8: 36,277,501 (GRCm39) |
T1776S |
possibly damaging |
Het |
Ighv2-5 |
G |
A |
12: 113,649,358 (GRCm39) |
Q32* |
probably null |
Het |
Klc2 |
T |
C |
19: 5,161,660 (GRCm39) |
E310G |
probably damaging |
Het |
Krt75 |
A |
G |
15: 101,478,707 (GRCm39) |
M309T |
probably damaging |
Het |
Lrp11 |
G |
A |
10: 7,465,936 (GRCm39) |
G41R |
unknown |
Het |
Lrrc52 |
G |
T |
1: 167,293,664 (GRCm39) |
P207Q |
probably benign |
Het |
Lrrc52 |
G |
T |
1: 167,293,665 (GRCm39) |
P207T |
probably benign |
Het |
Lrrk2 |
A |
T |
15: 91,696,526 (GRCm39) |
D2438V |
probably damaging |
Het |
Mycbp |
C |
T |
4: 123,799,094 (GRCm39) |
T28M |
probably damaging |
Het |
Myh14 |
A |
G |
7: 44,281,846 (GRCm39) |
V804A |
probably benign |
Het |
Myo16 |
A |
G |
8: 10,426,238 (GRCm39) |
I332V |
unknown |
Het |
Ncor1 |
G |
T |
11: 62,208,794 (GRCm39) |
Q1359K |
probably benign |
Het |
Oog3 |
T |
C |
4: 143,884,889 (GRCm39) |
D349G |
probably benign |
Het |
Or12e1 |
A |
T |
2: 87,022,594 (GRCm39) |
I188L |
probably benign |
Het |
Or1j21 |
A |
G |
2: 36,683,943 (GRCm39) |
K232E |
probably benign |
Het |
Or52b4i |
A |
G |
7: 102,191,830 (GRCm39) |
H229R |
probably benign |
Het |
Or8k53 |
A |
G |
2: 86,178,006 (GRCm39) |
Y35H |
possibly damaging |
Het |
Pate4 |
A |
G |
9: 35,519,595 (GRCm39) |
S32P |
possibly damaging |
Het |
Pcdhb7 |
A |
C |
18: 37,475,514 (GRCm39) |
S217R |
probably benign |
Het |
Pde1c |
G |
A |
6: 56,103,910 (GRCm39) |
R580C |
probably damaging |
Het |
Pi4ka |
C |
A |
16: 17,111,841 (GRCm39) |
A1545S |
|
Het |
Pign |
G |
T |
1: 105,575,842 (GRCm39) |
T266K |
possibly damaging |
Het |
Pitpnm2 |
A |
G |
5: 124,260,090 (GRCm39) |
I1134T |
probably benign |
Het |
Ppfia2 |
G |
A |
10: 106,666,520 (GRCm39) |
V409I |
possibly damaging |
Het |
Prr7 |
A |
G |
13: 55,620,609 (GRCm39) |
T206A |
probably benign |
Het |
Rnf13 |
A |
T |
3: 57,727,955 (GRCm39) |
R212* |
probably null |
Het |
Rwdd2b |
T |
C |
16: 87,231,500 (GRCm39) |
N218S |
probably benign |
Het |
Serpina3m |
A |
G |
12: 104,355,834 (GRCm39) |
D167G |
possibly damaging |
Het |
Slit2 |
A |
T |
5: 48,142,547 (GRCm39) |
N56Y |
probably damaging |
Het |
Sprr3 |
G |
T |
3: 92,364,592 (GRCm39) |
T84K |
probably damaging |
Het |
Stab2 |
A |
T |
10: 86,709,766 (GRCm39) |
H1626Q |
possibly damaging |
Het |
Tex2 |
C |
A |
11: 106,437,721 (GRCm39) |
D650Y |
unknown |
Het |
Tmprss6 |
A |
G |
15: 78,330,926 (GRCm39) |
S436P |
probably benign |
Het |
Uba2 |
A |
C |
7: 33,864,860 (GRCm39) |
F63L |
probably damaging |
Het |
Ubxn2b |
C |
T |
4: 6,214,692 (GRCm39) |
S242L |
probably damaging |
Het |
Vmn1r86 |
T |
G |
7: 12,836,685 (GRCm39) |
I64L |
probably benign |
Het |
Vmn2r67 |
A |
T |
7: 84,785,662 (GRCm39) |
V781E |
probably damaging |
Het |
Vmn2r80 |
T |
A |
10: 79,030,097 (GRCm39) |
F641Y |
probably damaging |
Het |
Wdfy4 |
A |
T |
14: 32,800,231 (GRCm39) |
I1965K |
|
Het |
Wdr25 |
G |
A |
12: 108,958,819 (GRCm39) |
G344S |
possibly damaging |
Het |
Wdr90 |
G |
T |
17: 26,073,083 (GRCm39) |
F837L |
probably benign |
Het |
Xpo4 |
A |
G |
14: 57,834,468 (GRCm39) |
V704A |
possibly damaging |
Het |
Zc3h12d |
A |
G |
10: 7,743,033 (GRCm39) |
K268E |
probably damaging |
Het |
|
Other mutations in Gm4846 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02682:Gm4846
|
APN |
1 |
166,322,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02975:Gm4846
|
APN |
1 |
166,311,449 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0504:Gm4846
|
UTSW |
1 |
166,319,114 (GRCm39) |
missense |
probably benign |
0.04 |
R0989:Gm4846
|
UTSW |
1 |
166,314,689 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1836:Gm4846
|
UTSW |
1 |
166,311,492 (GRCm39) |
missense |
probably benign |
0.17 |
R1965:Gm4846
|
UTSW |
1 |
166,314,533 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3120:Gm4846
|
UTSW |
1 |
166,319,117 (GRCm39) |
missense |
probably benign |
0.11 |
R4013:Gm4846
|
UTSW |
1 |
166,322,249 (GRCm39) |
splice site |
probably null |
|
R4617:Gm4846
|
UTSW |
1 |
166,323,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R4641:Gm4846
|
UTSW |
1 |
166,311,462 (GRCm39) |
missense |
probably damaging |
0.99 |
R4825:Gm4846
|
UTSW |
1 |
166,319,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R4952:Gm4846
|
UTSW |
1 |
166,311,503 (GRCm39) |
missense |
probably damaging |
0.97 |
R5135:Gm4846
|
UTSW |
1 |
166,311,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R5230:Gm4846
|
UTSW |
1 |
166,317,748 (GRCm39) |
missense |
probably benign |
0.26 |
R5335:Gm4846
|
UTSW |
1 |
166,325,022 (GRCm39) |
nonsense |
probably null |
|
R5711:Gm4846
|
UTSW |
1 |
166,311,594 (GRCm39) |
missense |
probably benign |
0.12 |
R5957:Gm4846
|
UTSW |
1 |
166,314,522 (GRCm39) |
missense |
probably benign |
|
R6024:Gm4846
|
UTSW |
1 |
166,317,696 (GRCm39) |
missense |
probably benign |
0.00 |
R6460:Gm4846
|
UTSW |
1 |
166,325,082 (GRCm39) |
missense |
probably benign |
0.00 |
R6764:Gm4846
|
UTSW |
1 |
166,319,121 (GRCm39) |
missense |
probably benign |
|
R6833:Gm4846
|
UTSW |
1 |
166,322,147 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6834:Gm4846
|
UTSW |
1 |
166,322,147 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7161:Gm4846
|
UTSW |
1 |
166,314,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7275:Gm4846
|
UTSW |
1 |
166,314,648 (GRCm39) |
missense |
probably benign |
0.01 |
R7890:Gm4846
|
UTSW |
1 |
166,322,228 (GRCm39) |
missense |
probably benign |
|
R8072:Gm4846
|
UTSW |
1 |
166,322,241 (GRCm39) |
missense |
probably benign |
0.06 |
R8558:Gm4846
|
UTSW |
1 |
166,314,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Gm4846
|
UTSW |
1 |
166,322,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R9221:Gm4846
|
UTSW |
1 |
166,324,959 (GRCm39) |
missense |
probably benign |
0.02 |
R9251:Gm4846
|
UTSW |
1 |
166,311,307 (GRCm39) |
missense |
probably benign |
0.02 |
|