Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
C |
T |
2: 68,490,222 (GRCm39) |
|
probably benign |
Het |
Abl1 |
T |
C |
2: 31,691,708 (GRCm39) |
Y1076H |
probably damaging |
Het |
Adamts7 |
C |
T |
9: 90,076,063 (GRCm39) |
T1265I |
possibly damaging |
Het |
Adgb |
T |
C |
10: 10,283,209 (GRCm39) |
I166V |
probably benign |
Het |
Axin2 |
T |
A |
11: 108,833,402 (GRCm39) |
I529N |
possibly damaging |
Het |
Bbof1 |
T |
C |
12: 84,455,957 (GRCm39) |
M1T |
probably null |
Het |
Cmpk2 |
G |
T |
12: 26,519,570 (GRCm39) |
A74S |
probably benign |
Het |
Colgalt1 |
G |
A |
8: 72,075,350 (GRCm39) |
V419I |
probably benign |
Het |
Crybg3 |
A |
G |
16: 59,364,414 (GRCm39) |
S2403P |
probably damaging |
Het |
D930048N14Rik |
G |
A |
11: 51,545,632 (GRCm39) |
|
probably benign |
Het |
Dnah7b |
T |
A |
1: 46,176,578 (GRCm39) |
C733S |
possibly damaging |
Het |
Drc1 |
G |
A |
5: 30,504,490 (GRCm39) |
V211M |
possibly damaging |
Het |
Ephx2 |
T |
C |
14: 66,322,393 (GRCm39) |
T525A |
probably damaging |
Het |
Eya4 |
A |
G |
10: 23,102,698 (GRCm39) |
|
probably null |
Het |
Foxc1 |
T |
C |
13: 31,991,690 (GRCm39) |
F167S |
probably damaging |
Het |
Fsip2 |
C |
T |
2: 82,805,493 (GRCm39) |
T604I |
probably damaging |
Het |
Gm6370 |
C |
A |
5: 146,430,734 (GRCm39) |
F306L |
possibly damaging |
Het |
Hmgcr |
A |
G |
13: 96,796,729 (GRCm39) |
V187A |
probably damaging |
Het |
Igkv9-129 |
T |
A |
6: 67,817,242 (GRCm39) |
S114R |
possibly damaging |
Het |
Ikbke |
T |
A |
1: 131,191,085 (GRCm39) |
I519F |
probably damaging |
Het |
Ikzf3 |
T |
C |
11: 98,381,313 (GRCm39) |
Y89C |
probably benign |
Het |
Inpp5j |
T |
G |
11: 3,451,107 (GRCm39) |
H514P |
probably damaging |
Het |
Iqsec3 |
T |
C |
6: 121,389,999 (GRCm39) |
|
probably benign |
Het |
Itga3 |
C |
A |
11: 94,953,449 (GRCm39) |
V298L |
probably benign |
Het |
Kel |
C |
T |
6: 41,675,359 (GRCm39) |
W297* |
probably null |
Het |
Larp7 |
T |
A |
3: 127,340,603 (GRCm39) |
R112S |
probably benign |
Het |
Lbh |
T |
A |
17: 73,228,178 (GRCm39) |
|
probably null |
Het |
Lrba |
G |
A |
3: 86,267,433 (GRCm39) |
G1708S |
probably damaging |
Het |
Lrig2 |
C |
T |
3: 104,374,620 (GRCm39) |
V154I |
probably benign |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,875,713 (GRCm39) |
F1318L |
probably damaging |
Het |
Ncam2 |
T |
C |
16: 81,323,991 (GRCm39) |
V545A |
probably benign |
Het |
Numa1 |
T |
G |
7: 101,658,945 (GRCm39) |
L356R |
probably damaging |
Het |
Or2w1 |
A |
T |
13: 21,317,607 (GRCm39) |
I221L |
possibly damaging |
Het |
Or6n2 |
G |
A |
1: 173,897,574 (GRCm39) |
A237T |
probably damaging |
Het |
Pcgf5 |
C |
A |
19: 36,414,740 (GRCm39) |
N26K |
possibly damaging |
Het |
Pdlim4 |
T |
G |
11: 53,946,744 (GRCm39) |
D181A |
possibly damaging |
Het |
Phtf1 |
G |
A |
3: 103,910,919 (GRCm39) |
|
probably null |
Het |
Pik3r4 |
G |
A |
9: 105,527,957 (GRCm39) |
A437T |
possibly damaging |
Het |
Proser3 |
G |
A |
7: 30,245,525 (GRCm39) |
|
probably benign |
Het |
Rax |
T |
A |
18: 66,068,152 (GRCm39) |
N318Y |
unknown |
Het |
Rnf152 |
A |
G |
1: 105,212,077 (GRCm39) |
V160A |
probably benign |
Het |
Serpina3a |
A |
T |
12: 104,084,902 (GRCm39) |
D99V |
probably benign |
Het |
Sidt2 |
T |
C |
9: 45,854,073 (GRCm39) |
T652A |
probably benign |
Het |
Slc12a7 |
A |
G |
13: 73,962,962 (GRCm39) |
Y1054C |
probably damaging |
Het |
Slc9a5 |
A |
G |
8: 106,085,103 (GRCm39) |
N535D |
possibly damaging |
Het |
Sspo |
C |
A |
6: 48,441,835 (GRCm39) |
H1948Q |
probably benign |
Het |
Stap2 |
G |
T |
17: 56,304,827 (GRCm39) |
Y318* |
probably null |
Het |
Sytl1 |
T |
C |
4: 132,980,876 (GRCm39) |
D421G |
probably damaging |
Het |
Taar7e |
A |
T |
10: 23,913,932 (GRCm39) |
I141F |
probably damaging |
Het |
Taar7f |
T |
A |
10: 23,925,921 (GRCm39) |
W172R |
probably damaging |
Het |
Tcn2 |
T |
C |
11: 3,872,114 (GRCm39) |
K338E |
possibly damaging |
Het |
Tenm3 |
C |
T |
8: 48,802,439 (GRCm39) |
G374D |
probably damaging |
Het |
Terf2 |
A |
G |
8: 107,806,080 (GRCm39) |
S291P |
probably damaging |
Het |
Tex16 |
T |
A |
X: 111,030,640 (GRCm39) |
D1046E |
probably benign |
Het |
Tmod4 |
A |
G |
3: 95,035,140 (GRCm39) |
D215G |
probably benign |
Het |
Tnxb |
T |
C |
17: 34,929,951 (GRCm39) |
I2895T |
possibly damaging |
Het |
Tsbp1 |
G |
T |
17: 34,679,257 (GRCm39) |
|
probably benign |
Het |
Urgcp |
C |
A |
11: 5,665,878 (GRCm39) |
G820V |
probably damaging |
Het |
Uxs1 |
T |
A |
1: 43,789,398 (GRCm39) |
H419L |
possibly damaging |
Het |
Vmn1r152 |
A |
T |
7: 22,223,004 (GRCm39) |
T205S |
possibly damaging |
Het |
Vmn1r79 |
A |
G |
7: 11,910,415 (GRCm39) |
Y99C |
possibly damaging |
Het |
Zc3h14 |
A |
G |
12: 98,751,658 (GRCm39) |
H199R |
probably damaging |
Het |
Zfand2b |
A |
T |
1: 75,146,454 (GRCm39) |
M110L |
probably benign |
Het |
Zfp976 |
A |
G |
7: 42,265,749 (GRCm39) |
F12S |
probably damaging |
Het |
|
Other mutations in Clcc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01443:Clcc1
|
APN |
3 |
108,578,219 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01683:Clcc1
|
APN |
3 |
108,584,112 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02067:Clcc1
|
APN |
3 |
108,576,037 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02341:Clcc1
|
APN |
3 |
108,580,699 (GRCm39) |
missense |
possibly damaging |
0.60 |
B6584:Clcc1
|
UTSW |
3 |
108,580,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R0014:Clcc1
|
UTSW |
3 |
108,568,712 (GRCm39) |
nonsense |
probably null |
|
R0733:Clcc1
|
UTSW |
3 |
108,582,056 (GRCm39) |
missense |
probably benign |
0.00 |
R1151:Clcc1
|
UTSW |
3 |
108,575,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R1432:Clcc1
|
UTSW |
3 |
108,575,418 (GRCm39) |
missense |
probably benign |
0.11 |
R3546:Clcc1
|
UTSW |
3 |
108,575,429 (GRCm39) |
missense |
probably benign |
0.00 |
R3547:Clcc1
|
UTSW |
3 |
108,575,429 (GRCm39) |
missense |
probably benign |
0.00 |
R3548:Clcc1
|
UTSW |
3 |
108,575,429 (GRCm39) |
missense |
probably benign |
0.00 |
R3932:Clcc1
|
UTSW |
3 |
108,580,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R4211:Clcc1
|
UTSW |
3 |
108,570,907 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4756:Clcc1
|
UTSW |
3 |
108,580,236 (GRCm39) |
splice site |
probably null |
|
R4856:Clcc1
|
UTSW |
3 |
108,584,154 (GRCm39) |
missense |
probably benign |
0.02 |
R4886:Clcc1
|
UTSW |
3 |
108,584,154 (GRCm39) |
missense |
probably benign |
0.02 |
R5858:Clcc1
|
UTSW |
3 |
108,568,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R6258:Clcc1
|
UTSW |
3 |
108,580,624 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6301:Clcc1
|
UTSW |
3 |
108,580,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R6414:Clcc1
|
UTSW |
3 |
108,584,167 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6944:Clcc1
|
UTSW |
3 |
108,578,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R6965:Clcc1
|
UTSW |
3 |
108,580,625 (GRCm39) |
missense |
probably damaging |
0.99 |
R7331:Clcc1
|
UTSW |
3 |
108,575,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R7961:Clcc1
|
UTSW |
3 |
108,568,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R8009:Clcc1
|
UTSW |
3 |
108,568,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R9313:Clcc1
|
UTSW |
3 |
108,581,976 (GRCm39) |
missense |
probably benign |
0.03 |
|