Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
A |
G |
12: 71,265,963 (GRCm39) |
|
probably null |
Het |
Abca16 |
T |
C |
7: 120,026,409 (GRCm39) |
S124P |
probably damaging |
Het |
Acan |
A |
T |
7: 78,736,090 (GRCm39) |
S179C |
probably damaging |
Het |
Atg2b |
A |
C |
12: 105,630,967 (GRCm39) |
H319Q |
probably damaging |
Het |
Bptf |
G |
A |
11: 106,945,635 (GRCm39) |
Q2535* |
probably null |
Het |
Brpf3 |
T |
C |
17: 29,055,665 (GRCm39) |
*1205R |
probably null |
Het |
Cabyr |
C |
A |
18: 12,884,815 (GRCm39) |
P434Q |
probably damaging |
Het |
Cacna1g |
C |
A |
11: 94,300,057 (GRCm39) |
D2268Y |
possibly damaging |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Cct4 |
A |
G |
11: 22,947,111 (GRCm39) |
T201A |
probably benign |
Het |
Cdyl2 |
A |
C |
8: 117,350,733 (GRCm39) |
S133A |
probably benign |
Het |
Cep76 |
A |
G |
18: 67,774,204 (GRCm39) |
L14P |
possibly damaging |
Het |
Cert1 |
T |
A |
13: 96,767,341 (GRCm39) |
|
probably null |
Het |
Crybg3 |
A |
T |
16: 59,379,956 (GRCm39) |
S433T |
possibly damaging |
Het |
Cul9 |
T |
C |
17: 46,849,423 (GRCm39) |
K574R |
probably damaging |
Het |
Cyp2u1 |
T |
C |
3: 131,084,792 (GRCm39) |
I527V |
probably benign |
Het |
Dnaaf9 |
C |
A |
2: 130,648,708 (GRCm39) |
R258L |
unknown |
Het |
Eif4a3l1 |
A |
T |
6: 136,306,213 (GRCm39) |
I225F |
probably damaging |
Het |
F5 |
A |
G |
1: 164,046,966 (GRCm39) |
N2142S |
probably damaging |
Het |
Fam50b |
G |
A |
13: 34,931,084 (GRCm39) |
E187K |
possibly damaging |
Het |
Flnc |
A |
G |
6: 29,450,870 (GRCm39) |
Y1506C |
probably damaging |
Het |
Foxred2 |
T |
A |
15: 77,836,230 (GRCm39) |
S376C |
probably damaging |
Het |
Gbe1 |
T |
C |
16: 70,292,258 (GRCm39) |
L530P |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,525,331 (GRCm39) |
R3398G |
probably null |
Het |
Igf1r |
T |
C |
7: 67,836,905 (GRCm39) |
L587P |
probably damaging |
Het |
Ints15 |
A |
G |
5: 143,293,598 (GRCm39) |
V293A |
probably benign |
Het |
Kcna3 |
T |
C |
3: 106,943,853 (GRCm39) |
Y39H |
probably benign |
Het |
Krtap5-2 |
GCCACAGCCTCCCTTGCAACCCCCACAGGAGCCACAGCCCCCACAGGAACTACAGCCTCCCTTGCA |
GCTACAGCCTCCCTTGCA |
7: 141,728,980 (GRCm39) |
|
probably benign |
Het |
Mbl1 |
T |
C |
14: 40,880,669 (GRCm39) |
F186L |
probably damaging |
Het |
Ncam2 |
A |
T |
16: 81,386,683 (GRCm39) |
K687N |
probably damaging |
Het |
Nedd4l |
T |
C |
18: 65,130,441 (GRCm39) |
V24A |
probably damaging |
Het |
Nek1 |
A |
G |
8: 61,526,612 (GRCm39) |
E661G |
probably damaging |
Het |
Nudt14 |
G |
T |
12: 112,902,940 (GRCm39) |
D28E |
probably benign |
Het |
Or13n4 |
T |
C |
7: 106,423,798 (GRCm39) |
|
probably benign |
Het |
Or1j15 |
T |
A |
2: 36,459,248 (GRCm39) |
C213S |
probably benign |
Het |
Or2n1 |
T |
A |
17: 38,485,987 (GRCm39) |
I4N |
probably benign |
Het |
Or4k47 |
A |
T |
2: 111,451,600 (GRCm39) |
V273E |
probably damaging |
Het |
Pdk4 |
A |
T |
6: 5,487,089 (GRCm39) |
M319K |
probably benign |
Het |
Pfkp |
T |
C |
13: 6,643,252 (GRCm39) |
N522S |
probably benign |
Het |
Pias2 |
T |
C |
18: 77,207,817 (GRCm39) |
V234A |
possibly damaging |
Het |
Pik3c2b |
C |
A |
1: 133,007,512 (GRCm39) |
H625Q |
probably benign |
Het |
Pnpla7 |
T |
C |
2: 24,941,627 (GRCm39) |
S1117P |
probably damaging |
Het |
Prdm2 |
A |
T |
4: 142,907,464 (GRCm39) |
V36D |
probably damaging |
Het |
Prep |
C |
T |
10: 44,968,795 (GRCm39) |
R98C |
probably benign |
Het |
Rae1 |
T |
C |
2: 172,850,110 (GRCm39) |
|
probably null |
Het |
Rgs3 |
T |
A |
4: 62,533,573 (GRCm39) |
V138E |
probably damaging |
Het |
Rnf185 |
T |
C |
11: 3,375,329 (GRCm39) |
T142A |
possibly damaging |
Het |
Rsph6a |
C |
A |
7: 18,799,572 (GRCm39) |
P401Q |
probably damaging |
Het |
Runx3 |
A |
T |
4: 134,848,456 (GRCm39) |
T14S |
probably benign |
Het |
Scaf11 |
A |
G |
15: 96,317,042 (GRCm39) |
S841P |
probably damaging |
Het |
Spta1 |
T |
A |
1: 174,012,178 (GRCm39) |
L328Q |
probably damaging |
Het |
Sqor |
G |
A |
2: 122,645,929 (GRCm39) |
V318M |
probably damaging |
Het |
Stox2 |
T |
C |
8: 47,639,489 (GRCm39) |
T902A |
probably benign |
Het |
Susd3 |
T |
C |
13: 49,384,679 (GRCm39) |
H248R |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,183,406 (GRCm39) |
Y4133C |
probably damaging |
Het |
Tbc1d20 |
C |
T |
2: 152,153,337 (GRCm39) |
T289M |
probably benign |
Het |
Unc80 |
T |
A |
1: 66,588,943 (GRCm39) |
F1036Y |
possibly damaging |
Het |
Zeb1 |
A |
T |
18: 5,772,756 (GRCm39) |
D1015V |
probably damaging |
Het |
Zfp606 |
T |
G |
7: 12,227,966 (GRCm39) |
S696A |
probably benign |
Het |
|
Other mutations in Zbtb7c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00927:Zbtb7c
|
APN |
18 |
76,278,921 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02314:Zbtb7c
|
APN |
18 |
76,278,937 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02397:Zbtb7c
|
APN |
18 |
76,270,047 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0112:Zbtb7c
|
UTSW |
18 |
76,269,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Zbtb7c
|
UTSW |
18 |
76,270,464 (GRCm39) |
missense |
probably benign |
0.01 |
R1485:Zbtb7c
|
UTSW |
18 |
76,270,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Zbtb7c
|
UTSW |
18 |
76,270,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Zbtb7c
|
UTSW |
18 |
76,269,977 (GRCm39) |
missense |
probably benign |
0.16 |
R3737:Zbtb7c
|
UTSW |
18 |
76,270,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R4611:Zbtb7c
|
UTSW |
18 |
76,269,918 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4737:Zbtb7c
|
UTSW |
18 |
76,279,225 (GRCm39) |
missense |
probably benign |
0.15 |
R5080:Zbtb7c
|
UTSW |
18 |
76,270,413 (GRCm39) |
missense |
probably benign |
0.06 |
R6160:Zbtb7c
|
UTSW |
18 |
76,278,904 (GRCm39) |
missense |
probably benign |
0.05 |
R6262:Zbtb7c
|
UTSW |
18 |
76,270,413 (GRCm39) |
missense |
probably benign |
|
R7703:Zbtb7c
|
UTSW |
18 |
76,270,433 (GRCm39) |
missense |
probably benign |
0.02 |
R7849:Zbtb7c
|
UTSW |
18 |
76,278,772 (GRCm39) |
missense |
probably benign |
0.40 |
R8047:Zbtb7c
|
UTSW |
18 |
76,270,221 (GRCm39) |
missense |
probably damaging |
0.98 |
R8157:Zbtb7c
|
UTSW |
18 |
76,270,398 (GRCm39) |
missense |
probably benign |
0.05 |
R8809:Zbtb7c
|
UTSW |
18 |
76,270,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R8903:Zbtb7c
|
UTSW |
18 |
76,270,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R8982:Zbtb7c
|
UTSW |
18 |
76,279,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|