Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932442E05Rik |
T |
A |
10: 118,697,371 (GRCm39) |
W210R |
possibly damaging |
Het |
Aknad1 |
T |
C |
3: 108,659,217 (GRCm39) |
M77T |
probably benign |
Het |
Aox1 |
A |
T |
1: 58,393,469 (GRCm39) |
I1210F |
possibly damaging |
Het |
Brd8 |
A |
T |
18: 34,747,858 (GRCm39) |
|
probably benign |
Het |
Cdh23 |
T |
C |
10: 60,139,292 (GRCm39) |
D3307G |
probably benign |
Het |
Chsy1 |
T |
C |
7: 65,821,058 (GRCm39) |
I431T |
probably damaging |
Het |
Cobl |
A |
G |
11: 12,204,980 (GRCm39) |
|
probably benign |
Het |
Col28a1 |
T |
C |
6: 8,158,134 (GRCm39) |
D308G |
probably damaging |
Het |
Csmd3 |
A |
G |
15: 48,048,700 (GRCm39) |
Y568H |
probably damaging |
Het |
Dmrt3 |
T |
C |
19: 25,599,947 (GRCm39) |
I264T |
probably damaging |
Het |
Dusp22 |
G |
T |
13: 30,880,235 (GRCm39) |
C52F |
probably damaging |
Het |
Fbxw22 |
A |
C |
9: 109,212,993 (GRCm39) |
M318R |
probably damaging |
Het |
Ffar4 |
C |
T |
19: 38,102,295 (GRCm39) |
T310M |
probably damaging |
Het |
Fn1 |
A |
G |
1: 71,658,644 (GRCm39) |
V1138A |
probably damaging |
Het |
Glt6d1 |
T |
A |
2: 25,684,505 (GRCm39) |
Y167F |
probably benign |
Het |
Hydin |
T |
A |
8: 111,217,421 (GRCm39) |
Y1436* |
probably null |
Het |
Il12a |
G |
A |
3: 68,598,888 (GRCm39) |
C2Y |
possibly damaging |
Het |
Inpp5a |
T |
C |
7: 139,034,006 (GRCm39) |
Y38H |
possibly damaging |
Het |
Jmy |
A |
C |
13: 93,596,159 (GRCm39) |
L490R |
probably damaging |
Het |
Kif26a |
T |
A |
12: 112,143,262 (GRCm39) |
L1172H |
probably benign |
Het |
Kmo |
A |
T |
1: 175,482,668 (GRCm39) |
M331L |
probably benign |
Het |
Lonp1 |
G |
A |
17: 56,923,026 (GRCm39) |
T627M |
probably damaging |
Het |
Lrrc41 |
T |
C |
4: 115,950,331 (GRCm39) |
|
probably null |
Het |
Mast4 |
A |
T |
13: 102,874,123 (GRCm39) |
S1556R |
probably damaging |
Het |
Mmel1 |
A |
G |
4: 154,976,408 (GRCm39) |
N490S |
probably benign |
Het |
Mpped2 |
A |
G |
2: 106,614,158 (GRCm39) |
D164G |
probably damaging |
Het |
Nap1l1 |
A |
G |
10: 111,328,760 (GRCm39) |
T230A |
probably benign |
Het |
Nrap |
C |
A |
19: 56,338,741 (GRCm39) |
A913S |
probably damaging |
Het |
Nudt16 |
G |
T |
9: 105,008,707 (GRCm39) |
Q65K |
probably benign |
Het |
Or1e23 |
C |
A |
11: 73,407,462 (GRCm39) |
A188S |
probably benign |
Het |
Or5ac17 |
T |
G |
16: 59,036,792 (GRCm39) |
L61F |
probably benign |
Het |
Or5ac19 |
T |
A |
16: 59,089,213 (GRCm39) |
K272N |
probably benign |
Het |
Or5al5 |
T |
A |
2: 85,962,012 (GRCm39) |
|
probably benign |
Het |
Or6c76b |
T |
A |
10: 129,692,671 (GRCm39) |
C95S |
probably benign |
Het |
Parp14 |
A |
G |
16: 35,678,970 (GRCm39) |
F333L |
probably benign |
Het |
Pi4ka |
G |
T |
16: 17,115,124 (GRCm39) |
Q1422K |
probably benign |
Het |
Polr3c |
T |
C |
3: 96,620,836 (GRCm39) |
E494G |
probably damaging |
Het |
Prss42 |
C |
A |
9: 110,627,411 (GRCm39) |
P49Q |
probably benign |
Het |
Ptpra |
C |
T |
2: 130,385,997 (GRCm39) |
T568I |
probably damaging |
Het |
Ring1 |
T |
C |
17: 34,242,294 (GRCm39) |
D71G |
probably damaging |
Het |
Siae |
T |
A |
9: 37,542,782 (GRCm39) |
S193T |
probably damaging |
Het |
Slf2 |
T |
C |
19: 44,961,706 (GRCm39) |
|
probably null |
Het |
Spinkl |
T |
A |
18: 44,307,639 (GRCm39) |
K7N |
possibly damaging |
Het |
Tbk1 |
G |
A |
10: 121,407,888 (GRCm39) |
R82* |
probably null |
Het |
Tcf12 |
T |
C |
9: 71,829,930 (GRCm39) |
|
probably null |
Het |
Thumpd3 |
C |
A |
6: 113,043,806 (GRCm39) |
T407K |
probably damaging |
Het |
Timm29 |
T |
C |
9: 21,505,031 (GRCm39) |
V233A |
probably damaging |
Het |
Tns3 |
A |
G |
11: 8,469,192 (GRCm39) |
|
probably benign |
Het |
Ubash3b |
T |
C |
9: 40,937,543 (GRCm39) |
|
probably benign |
Het |
Ugdh |
G |
T |
5: 65,580,031 (GRCm39) |
T253K |
probably benign |
Het |
Zfp143 |
T |
A |
7: 109,671,416 (GRCm39) |
|
probably benign |
Het |
Zfp738 |
A |
G |
13: 67,831,563 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Tcl1b5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00932:Tcl1b5
|
APN |
12 |
105,142,759 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02545:Tcl1b5
|
APN |
12 |
105,146,296 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02948:Tcl1b5
|
APN |
12 |
105,145,273 (GRCm39) |
missense |
probably benign |
0.15 |
IGL03037:Tcl1b5
|
APN |
12 |
105,145,273 (GRCm39) |
missense |
probably benign |
0.15 |
R0378:Tcl1b5
|
UTSW |
12 |
105,145,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R5424:Tcl1b5
|
UTSW |
12 |
105,146,275 (GRCm39) |
missense |
possibly damaging |
0.45 |
R6528:Tcl1b5
|
UTSW |
12 |
105,145,258 (GRCm39) |
missense |
probably benign |
0.43 |
R7033:Tcl1b5
|
UTSW |
12 |
105,142,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R7651:Tcl1b5
|
UTSW |
12 |
105,142,694 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7844:Tcl1b5
|
UTSW |
12 |
105,142,815 (GRCm39) |
critical splice donor site |
probably null |
|
R8127:Tcl1b5
|
UTSW |
12 |
105,146,262 (GRCm39) |
missense |
probably benign |
0.43 |
R8200:Tcl1b5
|
UTSW |
12 |
105,145,212 (GRCm39) |
missense |
probably benign |
|
|