Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810459M11Rik |
T |
C |
1: 85,974,231 (GRCm39) |
S183P |
possibly damaging |
Het |
2900092C05Rik |
A |
G |
7: 12,249,391 (GRCm39) |
T75A |
possibly damaging |
Het |
Abhd8 |
A |
G |
8: 71,914,406 (GRCm39) |
V74A |
probably benign |
Het |
Agrn |
A |
C |
4: 156,256,758 (GRCm39) |
S1282R |
possibly damaging |
Het |
Atf5 |
T |
C |
7: 44,462,380 (GRCm39) |
N248S |
possibly damaging |
Het |
Atp2a3 |
A |
G |
11: 72,869,576 (GRCm39) |
Y497C |
probably damaging |
Het |
Bpifa2 |
T |
G |
2: 153,851,739 (GRCm39) |
S58R |
probably benign |
Het |
Cacna1h |
C |
T |
17: 25,604,600 (GRCm39) |
E1238K |
possibly damaging |
Het |
Ccdc71 |
T |
A |
9: 108,340,523 (GRCm39) |
L112* |
probably null |
Het |
Cd300e |
A |
T |
11: 114,946,128 (GRCm39) |
I111N |
probably damaging |
Het |
Cdkl3 |
A |
T |
11: 51,924,369 (GRCm39) |
E552D |
probably benign |
Het |
Chst5 |
A |
G |
8: 112,617,245 (GRCm39) |
V125A |
probably benign |
Het |
Clock |
A |
T |
5: 76,414,692 (GRCm39) |
M1K |
probably null |
Het |
Cops7b |
T |
A |
1: 86,528,852 (GRCm39) |
L193Q |
probably benign |
Het |
Csmd1 |
T |
C |
8: 16,338,707 (GRCm39) |
T467A |
probably damaging |
Het |
Ctr9 |
A |
G |
7: 110,652,615 (GRCm39) |
E971G |
unknown |
Het |
Dcp2 |
A |
G |
18: 44,543,254 (GRCm39) |
T271A |
probably benign |
Het |
Dsp |
A |
G |
13: 38,381,172 (GRCm39) |
N2639S |
possibly damaging |
Het |
Fhip1a |
T |
C |
3: 85,637,784 (GRCm39) |
I172V |
probably benign |
Het |
Gm11168 |
C |
G |
9: 3,006,912 (GRCm39) |
C212W |
probably benign |
Het |
Gpr179 |
G |
T |
11: 97,242,420 (GRCm39) |
D141E |
probably damaging |
Het |
H2bc4 |
A |
G |
13: 23,868,342 (GRCm39) |
Y43C |
probably damaging |
Het |
Hdhd2 |
C |
T |
18: 77,031,811 (GRCm39) |
T89M |
probably benign |
Het |
Krt6b |
T |
G |
15: 101,587,513 (GRCm39) |
T194P |
probably benign |
Het |
Lrp1b |
T |
C |
2: 41,266,030 (GRCm39) |
|
probably null |
Het |
Maneal |
A |
T |
4: 124,754,161 (GRCm39) |
I214N |
possibly damaging |
Het |
Map1lc3b |
T |
A |
8: 122,317,355 (GRCm39) |
C11S |
unknown |
Het |
Mapt |
G |
A |
11: 104,213,350 (GRCm39) |
G296E |
possibly damaging |
Het |
Mgam |
A |
G |
6: 40,640,459 (GRCm39) |
N509S |
probably benign |
Het |
Mrgprx1 |
T |
A |
7: 47,671,733 (GRCm39) |
I5F |
possibly damaging |
Het |
Mroh5 |
T |
C |
15: 73,659,583 (GRCm39) |
D416G |
probably benign |
Het |
Ncan |
T |
G |
8: 70,562,749 (GRCm39) |
D503A |
probably benign |
Het |
Nedd1 |
A |
T |
10: 92,547,185 (GRCm39) |
|
probably null |
Het |
Ogdh |
A |
G |
11: 6,298,351 (GRCm39) |
T641A |
probably benign |
Het |
Or2b6 |
T |
C |
13: 21,823,316 (GRCm39) |
I126V |
probably benign |
Het |
Or4k2 |
T |
A |
14: 50,424,015 (GRCm39) |
I221F |
probably damaging |
Het |
Or6c219 |
A |
T |
10: 129,781,435 (GRCm39) |
D50E |
probably benign |
Het |
Or8b1b |
T |
A |
9: 38,375,439 (GRCm39) |
M34K |
possibly damaging |
Het |
Pcdhga8 |
A |
C |
18: 37,859,238 (GRCm39) |
Q98P |
possibly damaging |
Het |
Pik3c2a |
A |
G |
7: 115,953,242 (GRCm39) |
Y1218H |
probably damaging |
Het |
Ppp3cc |
A |
T |
14: 70,483,387 (GRCm39) |
S229T |
possibly damaging |
Het |
Prss43 |
T |
G |
9: 110,657,764 (GRCm39) |
I221S |
probably damaging |
Het |
Rasal1 |
A |
T |
5: 120,801,002 (GRCm39) |
T221S |
probably benign |
Het |
Serpinb9f |
G |
T |
13: 33,518,543 (GRCm39) |
E348* |
probably null |
Het |
Sfxn5 |
A |
G |
6: 85,244,889 (GRCm39) |
Y169H |
probably damaging |
Het |
Skint9 |
T |
C |
4: 112,246,428 (GRCm39) |
N228S |
probably benign |
Het |
Slx4ip |
A |
T |
2: 136,842,162 (GRCm39) |
D29V |
probably damaging |
Het |
Snx29 |
G |
T |
16: 11,573,180 (GRCm39) |
G474V |
probably damaging |
Het |
Spata6 |
T |
A |
4: 111,638,017 (GRCm39) |
D282E |
possibly damaging |
Het |
Srek1 |
A |
T |
13: 103,905,890 (GRCm39) |
V77E |
probably damaging |
Het |
Timd6 |
A |
G |
11: 46,468,285 (GRCm39) |
T120A |
possibly damaging |
Het |
Tmt1a3 |
T |
C |
15: 100,233,289 (GRCm39) |
V160A |
probably benign |
Het |
Tnfrsf22 |
T |
C |
7: 143,194,564 (GRCm39) |
D121G |
probably damaging |
Het |
Ucma |
G |
A |
2: 4,990,170 (GRCm39) |
W122* |
probably null |
Het |
Vmn2r124 |
T |
C |
17: 18,282,306 (GRCm39) |
M113T |
unknown |
Het |
Vmn2r54 |
A |
T |
7: 12,350,150 (GRCm39) |
|
probably null |
Het |
Vmn2r8 |
A |
G |
5: 108,948,442 (GRCm39) |
L482S |
probably benign |
Het |
Vwa3a |
T |
A |
7: 120,378,138 (GRCm39) |
I476N |
probably damaging |
Het |
Vwa8 |
A |
C |
14: 79,219,674 (GRCm39) |
|
probably null |
Het |
Wdr26 |
A |
T |
1: 181,015,240 (GRCm39) |
S390R |
probably damaging |
Het |
|
Other mutations in Zbtb40 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00473:Zbtb40
|
APN |
4 |
136,714,651 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00573:Zbtb40
|
APN |
4 |
136,745,389 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00774:Zbtb40
|
APN |
4 |
136,721,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Zbtb40
|
UTSW |
4 |
136,714,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Zbtb40
|
UTSW |
4 |
136,714,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Zbtb40
|
UTSW |
4 |
136,713,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R0393:Zbtb40
|
UTSW |
4 |
136,745,842 (GRCm39) |
missense |
probably benign |
0.09 |
R0482:Zbtb40
|
UTSW |
4 |
136,710,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R1457:Zbtb40
|
UTSW |
4 |
136,712,148 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1846:Zbtb40
|
UTSW |
4 |
136,735,150 (GRCm39) |
missense |
probably benign |
0.00 |
R2153:Zbtb40
|
UTSW |
4 |
136,718,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Zbtb40
|
UTSW |
4 |
136,744,596 (GRCm39) |
nonsense |
probably null |
|
R2291:Zbtb40
|
UTSW |
4 |
136,712,328 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2406:Zbtb40
|
UTSW |
4 |
136,725,879 (GRCm39) |
missense |
probably benign |
0.34 |
R3707:Zbtb40
|
UTSW |
4 |
136,726,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R4131:Zbtb40
|
UTSW |
4 |
136,722,707 (GRCm39) |
missense |
probably benign |
0.00 |
R4243:Zbtb40
|
UTSW |
4 |
136,745,860 (GRCm39) |
missense |
probably benign |
0.00 |
R4424:Zbtb40
|
UTSW |
4 |
136,726,005 (GRCm39) |
missense |
probably damaging |
0.96 |
R4725:Zbtb40
|
UTSW |
4 |
136,746,072 (GRCm39) |
utr 5 prime |
probably benign |
|
R4784:Zbtb40
|
UTSW |
4 |
136,734,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Zbtb40
|
UTSW |
4 |
136,725,953 (GRCm39) |
missense |
probably benign |
0.00 |
R4796:Zbtb40
|
UTSW |
4 |
136,725,953 (GRCm39) |
missense |
probably benign |
0.00 |
R4838:Zbtb40
|
UTSW |
4 |
136,728,527 (GRCm39) |
missense |
probably benign |
0.15 |
R4859:Zbtb40
|
UTSW |
4 |
136,716,070 (GRCm39) |
missense |
probably damaging |
0.98 |
R4883:Zbtb40
|
UTSW |
4 |
136,728,241 (GRCm39) |
missense |
probably benign |
0.09 |
R5001:Zbtb40
|
UTSW |
4 |
136,723,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R5030:Zbtb40
|
UTSW |
4 |
136,725,263 (GRCm39) |
missense |
probably benign |
0.00 |
R5060:Zbtb40
|
UTSW |
4 |
136,728,604 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5529:Zbtb40
|
UTSW |
4 |
136,710,474 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5536:Zbtb40
|
UTSW |
4 |
136,714,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R5589:Zbtb40
|
UTSW |
4 |
136,722,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R6114:Zbtb40
|
UTSW |
4 |
136,716,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Zbtb40
|
UTSW |
4 |
136,712,177 (GRCm39) |
missense |
probably null |
|
R7208:Zbtb40
|
UTSW |
4 |
136,726,937 (GRCm39) |
splice site |
probably null |
|
R7722:Zbtb40
|
UTSW |
4 |
136,718,829 (GRCm39) |
missense |
probably damaging |
0.98 |
R7803:Zbtb40
|
UTSW |
4 |
136,744,638 (GRCm39) |
missense |
probably benign |
|
R8292:Zbtb40
|
UTSW |
4 |
136,726,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R8735:Zbtb40
|
UTSW |
4 |
136,725,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R8890:Zbtb40
|
UTSW |
4 |
136,725,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R9003:Zbtb40
|
UTSW |
4 |
136,745,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R9290:Zbtb40
|
UTSW |
4 |
136,745,529 (GRCm39) |
missense |
probably benign |
0.00 |
R9328:Zbtb40
|
UTSW |
4 |
136,745,620 (GRCm39) |
missense |
probably benign |
0.00 |
RF014:Zbtb40
|
UTSW |
4 |
136,744,617 (GRCm39) |
missense |
probably benign |
0.20 |
Z1176:Zbtb40
|
UTSW |
4 |
136,722,774 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zbtb40
|
UTSW |
4 |
136,745,335 (GRCm39) |
nonsense |
probably null |
|
|