Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700008O03Rik |
A |
G |
7: 44,009,704 (GRCm39) |
L135S |
probably damaging |
Het |
A2ml1 |
C |
T |
6: 128,557,349 (GRCm39) |
A115T |
probably benign |
Het |
Alpi |
G |
T |
1: 87,028,316 (GRCm39) |
T169N |
probably damaging |
Het |
Ccdc15 |
T |
C |
9: 37,226,801 (GRCm39) |
D378G |
possibly damaging |
Het |
Cpb2 |
T |
G |
14: 75,505,490 (GRCm39) |
V162G |
probably damaging |
Het |
Dnmbp |
T |
C |
19: 43,890,759 (GRCm39) |
E336G |
probably benign |
Het |
Dok6 |
G |
C |
18: 89,432,988 (GRCm39) |
R274G |
probably null |
Het |
Eef1d |
G |
A |
15: 75,768,166 (GRCm39) |
R199C |
probably damaging |
Het |
Epha8 |
T |
C |
4: 136,660,321 (GRCm39) |
Y714C |
probably damaging |
Het |
Fyb1 |
T |
C |
15: 6,681,388 (GRCm39) |
|
probably benign |
Het |
Gfpt2 |
A |
G |
11: 49,698,542 (GRCm39) |
N46D |
probably benign |
Het |
Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably benign |
Het |
Gm11596 |
C |
A |
11: 99,684,082 (GRCm39) |
E13* |
probably null |
Het |
Gsx2 |
T |
C |
5: 75,237,713 (GRCm39) |
F222L |
probably damaging |
Het |
Hpca |
T |
A |
4: 129,012,237 (GRCm39) |
K100* |
probably null |
Het |
Iqsec1 |
A |
G |
6: 90,671,636 (GRCm39) |
S89P |
probably damaging |
Het |
Kif12 |
T |
A |
4: 63,086,796 (GRCm39) |
T347S |
possibly damaging |
Het |
Knop1 |
A |
G |
7: 118,452,440 (GRCm39) |
L93S |
probably damaging |
Het |
Mib1 |
A |
G |
18: 10,812,045 (GRCm39) |
T981A |
probably damaging |
Het |
N4bp2l1 |
C |
T |
5: 150,496,246 (GRCm39) |
E123K |
probably damaging |
Het |
Npr2 |
C |
T |
4: 43,650,432 (GRCm39) |
R976W |
probably damaging |
Het |
Rbpj |
T |
C |
5: 53,799,537 (GRCm39) |
|
probably benign |
Het |
Ro60 |
C |
A |
1: 143,646,620 (GRCm39) |
E42* |
probably null |
Het |
Ruvbl1 |
T |
C |
6: 88,462,779 (GRCm39) |
V301A |
possibly damaging |
Het |
Sgip1 |
T |
C |
4: 102,766,988 (GRCm39) |
|
probably null |
Het |
Sh3bp2 |
T |
C |
5: 34,716,840 (GRCm39) |
I361T |
probably benign |
Het |
Skint1 |
T |
A |
4: 111,876,348 (GRCm39) |
Y90N |
probably damaging |
Het |
Slc25a45 |
G |
A |
19: 5,934,580 (GRCm39) |
V183I |
probably benign |
Het |
Slco4c1 |
T |
A |
1: 96,748,925 (GRCm39) |
H664L |
probably benign |
Het |
Sult2a4 |
T |
A |
7: 13,649,225 (GRCm39) |
I194L |
probably benign |
Het |
Tecta |
C |
A |
9: 42,299,570 (GRCm39) |
D173Y |
probably damaging |
Het |
Tnrc18 |
T |
A |
5: 142,745,459 (GRCm39) |
|
probably benign |
Het |
Use1 |
T |
C |
8: 71,821,823 (GRCm39) |
L169P |
possibly damaging |
Het |
Zfp451 |
A |
T |
1: 33,819,133 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Zfp335 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Zfp335
|
APN |
2 |
164,734,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00921:Zfp335
|
APN |
2 |
164,736,696 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL00980:Zfp335
|
APN |
2 |
164,744,594 (GRCm39) |
nonsense |
probably null |
|
IGL01145:Zfp335
|
APN |
2 |
164,749,422 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01568:Zfp335
|
APN |
2 |
164,736,708 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01612:Zfp335
|
APN |
2 |
164,752,540 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02138:Zfp335
|
APN |
2 |
164,735,724 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02675:Zfp335
|
APN |
2 |
164,752,609 (GRCm39) |
missense |
probably benign |
|
IGL03206:Zfp335
|
APN |
2 |
164,734,601 (GRCm39) |
splice site |
probably benign |
|
IGL03269:Zfp335
|
APN |
2 |
164,742,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03306:Zfp335
|
APN |
2 |
164,737,904 (GRCm39) |
splice site |
probably benign |
|
FR4342:Zfp335
|
UTSW |
2 |
164,749,397 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Zfp335
|
UTSW |
2 |
164,749,385 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Zfp335
|
UTSW |
2 |
164,749,403 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Zfp335
|
UTSW |
2 |
164,749,397 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Zfp335
|
UTSW |
2 |
164,749,392 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Zfp335
|
UTSW |
2 |
164,749,404 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Zfp335
|
UTSW |
2 |
164,749,395 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Zfp335
|
UTSW |
2 |
164,749,394 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Zfp335
|
UTSW |
2 |
164,749,398 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Zfp335
|
UTSW |
2 |
164,749,394 (GRCm39) |
small insertion |
probably benign |
|
PIT4403001:Zfp335
|
UTSW |
2 |
164,735,636 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0005:Zfp335
|
UTSW |
2 |
164,751,222 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0101:Zfp335
|
UTSW |
2 |
164,741,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R0196:Zfp335
|
UTSW |
2 |
164,738,065 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0211:Zfp335
|
UTSW |
2 |
164,749,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R0211:Zfp335
|
UTSW |
2 |
164,749,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R0533:Zfp335
|
UTSW |
2 |
164,749,842 (GRCm39) |
nonsense |
probably null |
|
R0865:Zfp335
|
UTSW |
2 |
164,741,415 (GRCm39) |
splice site |
probably null |
|
R1023:Zfp335
|
UTSW |
2 |
164,734,505 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1029:Zfp335
|
UTSW |
2 |
164,734,598 (GRCm39) |
splice site |
probably benign |
|
R1052:Zfp335
|
UTSW |
2 |
164,749,388 (GRCm39) |
small deletion |
probably benign |
|
R1106:Zfp335
|
UTSW |
2 |
164,749,471 (GRCm39) |
small deletion |
probably benign |
|
R1146:Zfp335
|
UTSW |
2 |
164,738,043 (GRCm39) |
missense |
probably benign |
0.01 |
R1146:Zfp335
|
UTSW |
2 |
164,738,043 (GRCm39) |
missense |
probably benign |
0.01 |
R1274:Zfp335
|
UTSW |
2 |
164,749,388 (GRCm39) |
small deletion |
probably benign |
|
R1386:Zfp335
|
UTSW |
2 |
164,740,161 (GRCm39) |
missense |
probably benign |
0.00 |
R1433:Zfp335
|
UTSW |
2 |
164,741,376 (GRCm39) |
missense |
probably damaging |
0.99 |
R1813:Zfp335
|
UTSW |
2 |
164,734,525 (GRCm39) |
missense |
probably damaging |
0.99 |
R1959:Zfp335
|
UTSW |
2 |
164,736,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R3847:Zfp335
|
UTSW |
2 |
164,742,026 (GRCm39) |
splice site |
probably null |
|
R3937:Zfp335
|
UTSW |
2 |
164,752,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R3946:Zfp335
|
UTSW |
2 |
164,734,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R3979:Zfp335
|
UTSW |
2 |
164,752,558 (GRCm39) |
missense |
probably benign |
0.00 |
R4019:Zfp335
|
UTSW |
2 |
164,743,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R4020:Zfp335
|
UTSW |
2 |
164,743,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R4668:Zfp335
|
UTSW |
2 |
164,742,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:Zfp335
|
UTSW |
2 |
164,736,588 (GRCm39) |
missense |
probably benign |
|
R5038:Zfp335
|
UTSW |
2 |
164,752,564 (GRCm39) |
nonsense |
probably null |
|
R5245:Zfp335
|
UTSW |
2 |
164,736,678 (GRCm39) |
missense |
probably benign |
|
R5411:Zfp335
|
UTSW |
2 |
164,744,165 (GRCm39) |
missense |
probably damaging |
0.99 |
R5422:Zfp335
|
UTSW |
2 |
164,749,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R5968:Zfp335
|
UTSW |
2 |
164,734,314 (GRCm39) |
missense |
probably damaging |
0.99 |
R6056:Zfp335
|
UTSW |
2 |
164,737,018 (GRCm39) |
splice site |
probably null |
|
R6551:Zfp335
|
UTSW |
2 |
164,751,285 (GRCm39) |
missense |
probably benign |
|
R6927:Zfp335
|
UTSW |
2 |
164,735,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R6943:Zfp335
|
UTSW |
2 |
164,736,795 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6995:Zfp335
|
UTSW |
2 |
164,735,210 (GRCm39) |
nonsense |
probably null |
|
R7174:Zfp335
|
UTSW |
2 |
164,744,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R7185:Zfp335
|
UTSW |
2 |
164,735,164 (GRCm39) |
critical splice donor site |
probably null |
|
R7296:Zfp335
|
UTSW |
2 |
164,742,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R7322:Zfp335
|
UTSW |
2 |
164,752,741 (GRCm39) |
start codon destroyed |
probably null |
0.90 |
R7504:Zfp335
|
UTSW |
2 |
164,751,338 (GRCm39) |
missense |
probably benign |
0.27 |
R7560:Zfp335
|
UTSW |
2 |
164,737,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R7637:Zfp335
|
UTSW |
2 |
164,734,459 (GRCm39) |
critical splice donor site |
probably null |
|
R8064:Zfp335
|
UTSW |
2 |
164,749,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R8208:Zfp335
|
UTSW |
2 |
164,735,536 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8228:Zfp335
|
UTSW |
2 |
164,746,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R8271:Zfp335
|
UTSW |
2 |
164,739,973 (GRCm39) |
missense |
probably damaging |
0.98 |
R8688:Zfp335
|
UTSW |
2 |
164,734,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R8803:Zfp335
|
UTSW |
2 |
164,751,290 (GRCm39) |
missense |
probably benign |
0.14 |
R9266:Zfp335
|
UTSW |
2 |
164,738,007 (GRCm39) |
missense |
probably benign |
0.33 |
R9352:Zfp335
|
UTSW |
2 |
164,742,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R9487:Zfp335
|
UTSW |
2 |
164,735,395 (GRCm39) |
missense |
probably damaging |
0.99 |
R9752:Zfp335
|
UTSW |
2 |
164,749,347 (GRCm39) |
critical splice donor site |
probably null |
|
RF031:Zfp335
|
UTSW |
2 |
164,749,383 (GRCm39) |
small insertion |
probably benign |
|
|