Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg5 |
T |
G |
17: 84,983,523 (GRCm39) |
T144P |
possibly damaging |
Het |
Adhfe1 |
A |
G |
1: 9,628,417 (GRCm39) |
N263S |
probably null |
Het |
Aebp2 |
A |
T |
6: 140,583,453 (GRCm39) |
Q309L |
possibly damaging |
Het |
Akap7 |
A |
G |
10: 25,047,054 (GRCm39) |
Y281H |
probably damaging |
Het |
Atg2a |
G |
A |
19: 6,299,859 (GRCm39) |
A588T |
probably damaging |
Het |
Calcoco1 |
T |
C |
15: 102,624,228 (GRCm39) |
D236G |
probably damaging |
Het |
Camsap2 |
A |
T |
1: 136,208,077 (GRCm39) |
D470E |
probably benign |
Het |
Capn8 |
G |
T |
1: 182,392,698 (GRCm39) |
V25L |
probably benign |
Het |
Card10 |
A |
G |
15: 78,660,884 (GRCm39) |
V1041A |
probably damaging |
Het |
Ccr1 |
T |
A |
9: 123,764,119 (GRCm39) |
H137L |
probably damaging |
Het |
Cdh23 |
A |
T |
10: 60,151,435 (GRCm39) |
D2483E |
probably damaging |
Het |
Chd2 |
G |
T |
7: 73,085,532 (GRCm39) |
Q1701K |
probably benign |
Het |
Cimap2 |
C |
T |
4: 106,448,859 (GRCm39) |
G400S |
probably damaging |
Het |
Ckmt2 |
T |
A |
13: 92,007,335 (GRCm39) |
R286S |
probably damaging |
Het |
Cyp27a1 |
A |
T |
1: 74,771,214 (GRCm39) |
D133V |
probably benign |
Het |
Dusp9 |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
X: 72,684,217 (GRCm39) |
|
probably benign |
Het |
Eml1 |
A |
T |
12: 108,476,458 (GRCm39) |
I283F |
probably damaging |
Het |
Fat3 |
A |
G |
9: 15,901,887 (GRCm39) |
V3046A |
possibly damaging |
Het |
Fbxw20 |
A |
G |
9: 109,063,763 (GRCm39) |
V3A |
probably benign |
Het |
Fcgr2b |
A |
G |
1: 170,795,702 (GRCm39) |
S76P |
possibly damaging |
Het |
Fgg |
C |
T |
3: 82,917,477 (GRCm39) |
Q169* |
probably null |
Het |
Gm4779 |
G |
C |
X: 100,837,390 (GRCm39) |
T171S |
possibly damaging |
Het |
Incenp |
A |
G |
19: 9,870,993 (GRCm39) |
L212P |
unknown |
Het |
Incenp |
G |
C |
19: 9,871,005 (GRCm39) |
T208R |
unknown |
Het |
Mctp1 |
T |
A |
13: 76,949,666 (GRCm39) |
|
probably null |
Het |
Megf8 |
T |
C |
7: 25,057,848 (GRCm39) |
M2095T |
probably benign |
Het |
Mroh2b |
G |
A |
15: 4,941,391 (GRCm39) |
V308I |
probably benign |
Het |
Muc1 |
T |
A |
3: 89,139,341 (GRCm39) |
H580Q |
probably damaging |
Het |
Naip6 |
A |
T |
13: 100,452,920 (GRCm39) |
M47K |
probably benign |
Het |
Nrxn1 |
C |
A |
17: 90,471,249 (GRCm39) |
R1260L |
probably damaging |
Het |
Nynrin |
A |
G |
14: 56,100,815 (GRCm39) |
I202V |
possibly damaging |
Het |
Or14j7 |
T |
C |
17: 38,234,847 (GRCm39) |
L130P |
probably damaging |
Het |
Or5ac17 |
T |
C |
16: 59,036,458 (GRCm39) |
I173V |
probably benign |
Het |
Or5b98 |
T |
C |
19: 12,931,727 (GRCm39) |
M258T |
possibly damaging |
Het |
Pard3 |
G |
A |
8: 128,098,021 (GRCm39) |
W354* |
probably null |
Het |
Pcnx3 |
C |
T |
19: 5,715,412 (GRCm39) |
G1946E |
probably damaging |
Het |
Peak1 |
A |
G |
9: 56,166,677 (GRCm39) |
V417A |
probably damaging |
Het |
Prune2 |
A |
G |
19: 17,189,672 (GRCm39) |
R3052G |
unknown |
Het |
Prx |
T |
C |
7: 27,218,808 (GRCm39) |
L1242P |
probably damaging |
Het |
Pxylp1 |
A |
G |
9: 96,707,633 (GRCm39) |
I183T |
probably benign |
Het |
Ranbp2 |
A |
G |
10: 58,291,755 (GRCm39) |
E254G |
probably benign |
Het |
Rhot2 |
C |
A |
17: 26,058,864 (GRCm39) |
R512L |
probably benign |
Het |
Rpa1 |
T |
C |
11: 75,193,550 (GRCm39) |
N594D |
probably benign |
Het |
Rxfp2 |
T |
A |
5: 149,983,365 (GRCm39) |
I300K |
probably damaging |
Het |
Scarf1 |
T |
A |
11: 75,414,689 (GRCm39) |
S486T |
probably damaging |
Het |
Slc24a4 |
T |
C |
12: 102,220,928 (GRCm39) |
V455A |
probably damaging |
Het |
Slitrk1 |
A |
G |
14: 109,148,653 (GRCm39) |
V686A |
probably benign |
Het |
Spata31e2 |
T |
C |
1: 26,721,562 (GRCm39) |
E1206G |
probably benign |
Het |
Syne2 |
C |
A |
12: 75,996,143 (GRCm39) |
Q2228K |
possibly damaging |
Het |
Tenm4 |
G |
A |
7: 96,517,198 (GRCm39) |
G1430S |
probably damaging |
Het |
Tlr12 |
C |
A |
4: 128,511,492 (GRCm39) |
A253S |
probably benign |
Het |
Trpm1 |
G |
A |
7: 63,918,777 (GRCm39) |
A1590T |
probably benign |
Het |
Vmn1r184 |
T |
A |
7: 25,966,686 (GRCm39) |
M144K |
probably benign |
Het |
Wee2 |
A |
G |
6: 40,421,114 (GRCm39) |
D68G |
probably benign |
Het |
|
Other mutations in Ggt5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01503:Ggt5
|
APN |
10 |
75,445,944 (GRCm39) |
splice site |
probably benign |
|
IGL01926:Ggt5
|
APN |
10 |
75,439,935 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02095:Ggt5
|
APN |
10 |
75,444,637 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02252:Ggt5
|
APN |
10 |
75,438,566 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02393:Ggt5
|
APN |
10 |
75,446,071 (GRCm39) |
splice site |
probably benign |
|
IGL02515:Ggt5
|
APN |
10 |
75,425,604 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02528:Ggt5
|
APN |
10 |
75,446,254 (GRCm39) |
splice site |
probably benign |
|
IGL02964:Ggt5
|
APN |
10 |
75,439,962 (GRCm39) |
missense |
probably benign |
0.08 |
R0646:Ggt5
|
UTSW |
10 |
75,438,482 (GRCm39) |
missense |
probably damaging |
0.99 |
R0834:Ggt5
|
UTSW |
10 |
75,440,604 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1454:Ggt5
|
UTSW |
10 |
75,445,742 (GRCm39) |
missense |
probably benign |
0.01 |
R1650:Ggt5
|
UTSW |
10 |
75,440,595 (GRCm39) |
missense |
probably benign |
0.00 |
R1846:Ggt5
|
UTSW |
10 |
75,446,376 (GRCm39) |
splice site |
probably null |
|
R1896:Ggt5
|
UTSW |
10 |
75,440,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R2044:Ggt5
|
UTSW |
10 |
75,439,921 (GRCm39) |
missense |
probably damaging |
0.97 |
R2357:Ggt5
|
UTSW |
10 |
75,445,075 (GRCm39) |
missense |
probably benign |
0.19 |
R3151:Ggt5
|
UTSW |
10 |
75,445,076 (GRCm39) |
missense |
probably benign |
0.35 |
R4667:Ggt5
|
UTSW |
10 |
75,438,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R4669:Ggt5
|
UTSW |
10 |
75,438,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R5060:Ggt5
|
UTSW |
10 |
75,440,608 (GRCm39) |
missense |
probably benign |
|
R5756:Ggt5
|
UTSW |
10 |
75,440,607 (GRCm39) |
missense |
probably benign |
|
R6156:Ggt5
|
UTSW |
10 |
75,445,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R6162:Ggt5
|
UTSW |
10 |
75,425,626 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6900:Ggt5
|
UTSW |
10 |
75,446,371 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8259:Ggt5
|
UTSW |
10 |
75,450,666 (GRCm39) |
missense |
probably benign |
0.04 |
R9001:Ggt5
|
UTSW |
10 |
75,445,992 (GRCm39) |
missense |
probably benign |
0.21 |
R9510:Ggt5
|
UTSW |
10 |
75,445,139 (GRCm39) |
missense |
probably benign |
|
R9655:Ggt5
|
UTSW |
10 |
75,444,635 (GRCm39) |
missense |
probably benign |
|
Z1088:Ggt5
|
UTSW |
10 |
75,444,593 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1176:Ggt5
|
UTSW |
10 |
75,438,452 (GRCm39) |
critical splice acceptor site |
probably null |
|
|