Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
A |
T |
2: 69,069,540 (GRCm39) |
I1285N |
probably damaging |
Het |
Abcc8 |
G |
A |
7: 45,756,683 (GRCm39) |
R721* |
probably null |
Het |
Alox8 |
T |
C |
11: 69,077,394 (GRCm39) |
Y423C |
probably damaging |
Het |
Ankle2 |
T |
A |
5: 110,399,344 (GRCm39) |
|
probably null |
Het |
Cdc14a |
A |
G |
3: 116,217,109 (GRCm39) |
I9T |
probably benign |
Het |
Ceacam18 |
T |
C |
7: 43,291,328 (GRCm39) |
C257R |
probably damaging |
Het |
Cilp |
T |
C |
9: 65,186,980 (GRCm39) |
V1025A |
probably damaging |
Het |
Clcn7 |
G |
T |
17: 25,372,539 (GRCm39) |
|
probably benign |
Het |
Csnk1d |
A |
T |
11: 120,874,014 (GRCm39) |
|
probably benign |
Het |
Cyp11b2 |
A |
G |
15: 74,724,995 (GRCm39) |
S285P |
probably benign |
Het |
Dip2b |
T |
A |
15: 100,093,665 (GRCm39) |
|
probably null |
Het |
Dmrt1 |
T |
A |
19: 25,483,219 (GRCm39) |
M1K |
probably null |
Het |
Dnajc14 |
T |
C |
10: 128,653,219 (GRCm39) |
V684A |
probably benign |
Het |
Dnmt3b |
A |
G |
2: 153,512,284 (GRCm39) |
Q335R |
probably benign |
Het |
Exoc3l2 |
T |
A |
7: 19,229,117 (GRCm39) |
C772S |
unknown |
Het |
F2rl1 |
A |
T |
13: 95,650,492 (GRCm39) |
F130Y |
probably damaging |
Het |
Galk2 |
C |
G |
2: 125,771,557 (GRCm39) |
S194* |
probably null |
Het |
Garre1 |
C |
A |
7: 33,984,312 (GRCm39) |
V104L |
possibly damaging |
Het |
Gpbp1l1 |
A |
G |
4: 116,430,714 (GRCm39) |
T62A |
probably benign |
Het |
H2-Q10 |
A |
T |
17: 35,781,357 (GRCm39) |
D53V |
probably damaging |
Het |
H2-T22 |
T |
C |
17: 36,349,924 (GRCm39) |
K356R |
probably benign |
Het |
Insrr |
G |
A |
3: 87,718,911 (GRCm39) |
V956M |
probably damaging |
Het |
Ints7 |
A |
G |
1: 191,328,443 (GRCm39) |
T239A |
probably damaging |
Het |
Isl1 |
A |
G |
13: 116,444,806 (GRCm39) |
|
probably benign |
Het |
Kcng2 |
A |
G |
18: 80,366,083 (GRCm39) |
C90R |
probably benign |
Het |
Kif3c |
C |
T |
12: 3,451,735 (GRCm39) |
P171S |
probably damaging |
Het |
Knl1 |
A |
G |
2: 118,911,994 (GRCm39) |
T1704A |
probably benign |
Het |
Lats1 |
A |
G |
10: 7,581,549 (GRCm39) |
Y778C |
probably damaging |
Het |
Limd2 |
T |
C |
11: 106,050,215 (GRCm39) |
M1V |
probably null |
Het |
Mcm10 |
A |
T |
2: 5,008,970 (GRCm39) |
I333N |
probably damaging |
Het |
Mipep |
T |
A |
14: 61,040,329 (GRCm39) |
L283* |
probably null |
Het |
Mixl1 |
A |
G |
1: 180,522,237 (GRCm39) |
S215P |
probably benign |
Het |
Mmp21 |
A |
G |
7: 133,280,406 (GRCm39) |
L188P |
probably damaging |
Het |
Mob1a |
T |
C |
6: 83,317,221 (GRCm39) |
S213P |
probably benign |
Het |
Mplkipl1 |
C |
T |
19: 61,164,364 (GRCm39) |
G24R |
unknown |
Het |
Ndufaf6 |
T |
C |
4: 11,060,917 (GRCm39) |
T220A |
probably benign |
Het |
Nr4a3 |
A |
T |
4: 48,051,651 (GRCm39) |
Y135F |
possibly damaging |
Het |
Ntn1 |
CCTTCTTCT |
CCTTCT |
11: 68,103,852 (GRCm39) |
|
probably benign |
Het |
Obscn |
A |
T |
11: 59,027,032 (GRCm39) |
L57Q |
probably damaging |
Het |
Or52e19b |
T |
A |
7: 103,032,840 (GRCm39) |
D123V |
probably damaging |
Het |
Or5d35 |
T |
C |
2: 87,855,804 (GRCm39) |
L246P |
probably damaging |
Het |
Pirb |
T |
A |
7: 3,715,661 (GRCm39) |
M839L |
probably benign |
Het |
Plcl2 |
A |
G |
17: 50,914,254 (GRCm39) |
E421G |
possibly damaging |
Het |
Ppp1r12b |
T |
C |
1: 134,876,771 (GRCm39) |
N99S |
probably benign |
Het |
Ptpro |
A |
G |
6: 137,354,130 (GRCm39) |
K169E |
probably damaging |
Het |
Rita1 |
T |
A |
5: 120,749,448 (GRCm39) |
K88N |
probably damaging |
Het |
Rptn |
A |
T |
3: 93,303,776 (GRCm39) |
K370* |
probably null |
Het |
Simc1 |
A |
G |
13: 54,687,576 (GRCm39) |
D115G |
probably null |
Het |
Stab1 |
T |
A |
14: 30,864,000 (GRCm39) |
N136I |
probably benign |
Het |
Syt4 |
T |
A |
18: 31,580,409 (GRCm39) |
|
probably benign |
Het |
Sytl2 |
A |
T |
7: 90,038,106 (GRCm39) |
N522I |
probably damaging |
Het |
Tax1bp1 |
A |
G |
6: 52,706,478 (GRCm39) |
|
probably benign |
Het |
Tenm2 |
A |
T |
11: 35,969,396 (GRCm39) |
D847E |
probably damaging |
Het |
Th |
G |
T |
7: 142,447,834 (GRCm39) |
D321E |
probably benign |
Het |
Tmem44 |
A |
T |
16: 30,359,591 (GRCm39) |
L46Q |
probably damaging |
Het |
Trp53bp1 |
A |
G |
2: 121,087,122 (GRCm39) |
L178P |
probably damaging |
Het |
Trp63 |
A |
G |
16: 25,684,968 (GRCm39) |
*285W |
probably null |
Het |
Tsen34 |
T |
C |
7: 3,697,380 (GRCm39) |
|
probably benign |
Het |
Tssk4 |
C |
T |
14: 55,889,272 (GRCm39) |
T256I |
probably benign |
Het |
Ttc17 |
A |
T |
2: 94,196,954 (GRCm39) |
N464K |
probably damaging |
Het |
Ttll2 |
C |
T |
17: 7,618,998 (GRCm39) |
V310I |
probably benign |
Het |
Ubn1 |
A |
G |
16: 4,895,177 (GRCm39) |
E741G |
probably damaging |
Het |
Urad |
T |
A |
5: 147,252,264 (GRCm39) |
I63F |
probably damaging |
Het |
Vcan |
T |
C |
13: 89,852,858 (GRCm39) |
T701A |
probably benign |
Het |
Vmn2r58 |
A |
G |
7: 41,486,639 (GRCm39) |
V752A |
possibly damaging |
Het |
Vmn2r69 |
C |
A |
7: 85,060,793 (GRCm39) |
V264L |
possibly damaging |
Het |
Zfp292 |
A |
G |
4: 34,808,917 (GRCm39) |
S1376P |
probably damaging |
Het |
Znfx1 |
A |
C |
2: 166,897,189 (GRCm39) |
F578L |
probably benign |
Het |
|
Other mutations in Zfp955a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01115:Zfp955a
|
APN |
17 |
33,461,554 (GRCm39) |
nonsense |
probably null |
|
IGL01859:Zfp955a
|
APN |
17 |
33,462,693 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02612:Zfp955a
|
APN |
17 |
33,463,039 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02894:Zfp955a
|
APN |
17 |
33,461,426 (GRCm39) |
nonsense |
probably null |
|
IGL02933:Zfp955a
|
APN |
17 |
33,462,683 (GRCm39) |
splice site |
probably null |
|
R0145:Zfp955a
|
UTSW |
17 |
33,461,430 (GRCm39) |
missense |
probably damaging |
0.98 |
R0577:Zfp955a
|
UTSW |
17 |
33,461,068 (GRCm39) |
missense |
probably damaging |
0.99 |
R0963:Zfp955a
|
UTSW |
17 |
33,462,726 (GRCm39) |
missense |
probably benign |
0.00 |
R1588:Zfp955a
|
UTSW |
17 |
33,460,791 (GRCm39) |
missense |
probably benign |
0.00 |
R1614:Zfp955a
|
UTSW |
17 |
33,461,306 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1704:Zfp955a
|
UTSW |
17 |
33,460,699 (GRCm39) |
nonsense |
probably null |
|
R1994:Zfp955a
|
UTSW |
17 |
33,460,620 (GRCm39) |
missense |
probably damaging |
0.99 |
R2043:Zfp955a
|
UTSW |
17 |
33,461,527 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2091:Zfp955a
|
UTSW |
17 |
33,461,731 (GRCm39) |
nonsense |
probably null |
|
R2091:Zfp955a
|
UTSW |
17 |
33,461,731 (GRCm39) |
nonsense |
probably null |
|
R4077:Zfp955a
|
UTSW |
17 |
33,460,675 (GRCm39) |
missense |
probably benign |
0.15 |
R4078:Zfp955a
|
UTSW |
17 |
33,460,675 (GRCm39) |
missense |
probably benign |
0.15 |
R4689:Zfp955a
|
UTSW |
17 |
33,461,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R4735:Zfp955a
|
UTSW |
17 |
33,460,696 (GRCm39) |
missense |
probably benign |
0.09 |
R4904:Zfp955a
|
UTSW |
17 |
33,461,162 (GRCm39) |
nonsense |
probably null |
|
R5180:Zfp955a
|
UTSW |
17 |
33,461,592 (GRCm39) |
missense |
probably benign |
0.15 |
R6006:Zfp955a
|
UTSW |
17 |
33,460,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R7132:Zfp955a
|
UTSW |
17 |
33,460,589 (GRCm39) |
nonsense |
probably null |
|
R7403:Zfp955a
|
UTSW |
17 |
33,462,720 (GRCm39) |
missense |
probably benign |
0.01 |
R7457:Zfp955a
|
UTSW |
17 |
33,463,025 (GRCm39) |
nonsense |
probably null |
|
R7547:Zfp955a
|
UTSW |
17 |
33,461,797 (GRCm39) |
missense |
probably benign |
0.05 |
R8263:Zfp955a
|
UTSW |
17 |
33,463,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R8265:Zfp955a
|
UTSW |
17 |
33,463,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R8330:Zfp955a
|
UTSW |
17 |
33,463,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R8947:Zfp955a
|
UTSW |
17 |
33,460,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R9052:Zfp955a
|
UTSW |
17 |
33,461,279 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9352:Zfp955a
|
UTSW |
17 |
33,461,335 (GRCm39) |
missense |
probably benign |
0.01 |
R9557:Zfp955a
|
UTSW |
17 |
33,461,107 (GRCm39) |
nonsense |
probably null |
|
R9683:Zfp955a
|
UTSW |
17 |
33,461,587 (GRCm39) |
missense |
probably benign |
0.01 |
R9784:Zfp955a
|
UTSW |
17 |
33,461,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R9797:Zfp955a
|
UTSW |
17 |
33,461,888 (GRCm39) |
missense |
possibly damaging |
0.59 |
X0062:Zfp955a
|
UTSW |
17 |
33,460,976 (GRCm39) |
missense |
probably benign |
0.37 |
|