Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310011J03Rik |
T |
A |
10: 80,155,361 (GRCm39) |
R51W |
probably damaging |
Het |
Adam3 |
A |
G |
8: 25,197,453 (GRCm39) |
I326T |
probably benign |
Het |
Alpk3 |
A |
G |
7: 80,743,470 (GRCm39) |
K1096E |
probably benign |
Het |
Aph1a |
T |
C |
3: 95,802,150 (GRCm39) |
V44A |
possibly damaging |
Het |
Ash1l |
T |
A |
3: 88,971,014 (GRCm39) |
|
probably null |
Het |
Atg2b |
A |
G |
12: 105,629,199 (GRCm39) |
M410T |
probably damaging |
Het |
Castor2 |
T |
C |
5: 134,165,936 (GRCm39) |
F228S |
possibly damaging |
Het |
Ccdc15 |
C |
T |
9: 37,226,753 (GRCm39) |
G407D |
probably benign |
Het |
Cd200r4 |
T |
A |
16: 44,653,504 (GRCm39) |
N137K |
probably damaging |
Het |
Clec18a |
A |
G |
8: 111,798,683 (GRCm39) |
L438P |
probably damaging |
Het |
Clip1 |
A |
G |
5: 123,768,782 (GRCm39) |
S606P |
probably benign |
Het |
Col11a2 |
G |
A |
17: 34,280,230 (GRCm39) |
G1193E |
unknown |
Het |
Col6a4 |
A |
G |
9: 105,945,097 (GRCm39) |
S1006P |
possibly damaging |
Het |
Ctsc |
A |
T |
7: 87,951,416 (GRCm39) |
D221V |
probably benign |
Het |
Ctse |
T |
C |
1: 131,600,249 (GRCm39) |
Y333H |
probably damaging |
Het |
Cyp2c23 |
T |
C |
19: 44,010,066 (GRCm39) |
N93S |
probably benign |
Het |
Daam1 |
A |
T |
12: 71,999,263 (GRCm39) |
D633V |
probably damaging |
Het |
Dlg2 |
G |
A |
7: 92,036,140 (GRCm39) |
R607H |
probably damaging |
Het |
Dsg2 |
T |
A |
18: 20,713,606 (GRCm39) |
D192E |
probably damaging |
Het |
Dync2h1 |
A |
T |
9: 7,001,473 (GRCm39) |
N3838K |
possibly damaging |
Het |
Ephx2 |
A |
C |
14: 66,345,506 (GRCm39) |
S153A |
probably damaging |
Het |
Eprs1 |
C |
A |
1: 185,130,591 (GRCm39) |
H651N |
probably benign |
Het |
Fat2 |
T |
C |
11: 55,142,910 (GRCm39) |
D4313G |
possibly damaging |
Het |
Fras1 |
A |
G |
5: 96,702,714 (GRCm39) |
K252R |
probably benign |
Het |
Galt |
A |
T |
4: 41,757,226 (GRCm39) |
Q193L |
probably benign |
Het |
Gm7356 |
T |
C |
17: 14,221,583 (GRCm39) |
K149E |
probably damaging |
Het |
Gmcl1 |
G |
T |
6: 86,698,408 (GRCm39) |
A163E |
probably damaging |
Het |
Hectd1 |
T |
A |
12: 51,838,073 (GRCm39) |
R696S |
possibly damaging |
Het |
Hydin |
A |
G |
8: 111,178,668 (GRCm39) |
I1088V |
probably benign |
Het |
Igkv4-68 |
A |
T |
6: 69,282,306 (GRCm39) |
S14R |
probably benign |
Het |
Lamb2 |
C |
T |
9: 108,357,845 (GRCm39) |
R123W |
probably damaging |
Het |
Ldlrad4 |
C |
T |
18: 68,387,293 (GRCm39) |
R202* |
probably null |
Het |
Lrit3 |
T |
C |
3: 129,594,284 (GRCm39) |
T98A |
probably benign |
Het |
Macc1 |
A |
G |
12: 119,409,728 (GRCm39) |
I165M |
probably benign |
Het |
Mapre2 |
T |
A |
18: 23,991,218 (GRCm39) |
M162K |
probably benign |
Het |
Naa30 |
T |
A |
14: 49,410,865 (GRCm39) |
N264K |
probably benign |
Het |
Or5ac17 |
A |
G |
16: 59,036,352 (GRCm39) |
V208A |
probably benign |
Het |
Or8d2 |
T |
A |
9: 38,759,762 (GRCm39) |
Y117* |
probably null |
Het |
Osr2 |
T |
C |
15: 35,302,063 (GRCm39) |
I221T |
probably benign |
Het |
Pcdh12 |
A |
T |
18: 38,415,850 (GRCm39) |
I425K |
probably benign |
Het |
Pcdhb3 |
T |
G |
18: 37,436,292 (GRCm39) |
Y753D |
probably damaging |
Het |
Pcdhb9 |
T |
A |
18: 37,536,208 (GRCm39) |
V734E |
probably damaging |
Het |
Pibf1 |
T |
A |
14: 99,433,831 (GRCm39) |
L593I |
probably benign |
Het |
Prag1 |
G |
A |
8: 36,614,393 (GRCm39) |
C1315Y |
probably damaging |
Het |
Prl3c1 |
T |
C |
13: 27,383,330 (GRCm39) |
S19P |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 23,002,539 (GRCm39) |
D1543V |
probably damaging |
Het |
Ripor2 |
A |
G |
13: 24,879,600 (GRCm39) |
N356S |
probably benign |
Het |
Rmc1 |
T |
C |
18: 12,321,690 (GRCm39) |
V497A |
possibly damaging |
Het |
Saxo4 |
A |
T |
19: 10,455,629 (GRCm39) |
F207I |
probably damaging |
Het |
Scrib |
T |
C |
15: 75,931,037 (GRCm39) |
H914R |
possibly damaging |
Het |
Sema6b |
G |
A |
17: 56,435,448 (GRCm39) |
A265V |
probably damaging |
Het |
Tdrd9 |
C |
G |
12: 111,951,500 (GRCm39) |
L97V |
probably benign |
Het |
Tle7 |
A |
G |
8: 110,835,493 (GRCm39) |
M24V |
probably benign |
Het |
Trabd |
T |
A |
15: 88,970,024 (GRCm39) |
L340H |
probably damaging |
Het |
Trpm1 |
T |
C |
7: 63,849,017 (GRCm39) |
W88R |
probably damaging |
Het |
Txndc12 |
G |
T |
4: 108,710,419 (GRCm39) |
|
probably null |
Het |
Vmn1r175 |
T |
C |
7: 23,508,523 (GRCm39) |
I35V |
probably benign |
Het |
Vmn1r48 |
A |
T |
6: 90,012,994 (GRCm39) |
V277E |
probably damaging |
Het |
Vmn2r72 |
G |
A |
7: 85,400,441 (GRCm39) |
H203Y |
probably benign |
Het |
Zbtb7c |
A |
G |
18: 76,270,398 (GRCm39) |
E162G |
probably benign |
Het |
Zfp93 |
T |
A |
7: 23,975,885 (GRCm39) |
C623* |
probably null |
Het |
Zzz3 |
A |
G |
3: 152,155,285 (GRCm39) |
I645V |
probably null |
Het |
|
Other mutations in Mzf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00418:Mzf1
|
APN |
7 |
12,778,543 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01728:Mzf1
|
APN |
7 |
12,785,654 (GRCm39) |
splice site |
probably benign |
|
IGL02194:Mzf1
|
APN |
7 |
12,777,647 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02256:Mzf1
|
APN |
7 |
12,786,664 (GRCm39) |
splice site |
probably benign |
|
IGL02584:Mzf1
|
APN |
7 |
12,786,744 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02678:Mzf1
|
APN |
7 |
12,786,836 (GRCm39) |
missense |
probably benign |
0.00 |
R0903:Mzf1
|
UTSW |
7 |
12,786,698 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0904:Mzf1
|
UTSW |
7 |
12,786,698 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0905:Mzf1
|
UTSW |
7 |
12,786,698 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1128:Mzf1
|
UTSW |
7 |
12,786,698 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1131:Mzf1
|
UTSW |
7 |
12,786,698 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1280:Mzf1
|
UTSW |
7 |
12,787,010 (GRCm39) |
missense |
probably damaging |
0.96 |
R1400:Mzf1
|
UTSW |
7 |
12,786,698 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1640:Mzf1
|
UTSW |
7 |
12,777,197 (GRCm39) |
makesense |
probably null |
|
R1687:Mzf1
|
UTSW |
7 |
12,786,698 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4014:Mzf1
|
UTSW |
7 |
12,777,883 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4721:Mzf1
|
UTSW |
7 |
12,777,448 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4721:Mzf1
|
UTSW |
7 |
12,777,223 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5511:Mzf1
|
UTSW |
7 |
12,785,526 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5611:Mzf1
|
UTSW |
7 |
12,778,554 (GRCm39) |
utr 3 prime |
probably benign |
|
R5728:Mzf1
|
UTSW |
7 |
12,777,985 (GRCm39) |
missense |
probably benign |
0.00 |
R5868:Mzf1
|
UTSW |
7 |
12,787,116 (GRCm39) |
missense |
probably benign |
0.00 |
R6283:Mzf1
|
UTSW |
7 |
12,787,296 (GRCm39) |
intron |
probably benign |
|
R7059:Mzf1
|
UTSW |
7 |
12,786,985 (GRCm39) |
missense |
probably damaging |
0.96 |
R7066:Mzf1
|
UTSW |
7 |
12,777,490 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7763:Mzf1
|
UTSW |
7 |
12,778,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R8870:Mzf1
|
UTSW |
7 |
12,786,836 (GRCm39) |
missense |
probably benign |
0.00 |
R9063:Mzf1
|
UTSW |
7 |
12,787,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R9113:Mzf1
|
UTSW |
7 |
12,778,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R9252:Mzf1
|
UTSW |
7 |
12,777,647 (GRCm39) |
missense |
probably benign |
0.33 |
R9289:Mzf1
|
UTSW |
7 |
12,785,534 (GRCm39) |
missense |
probably benign |
0.02 |
R9792:Mzf1
|
UTSW |
7 |
12,786,131 (GRCm39) |
missense |
probably benign |
0.02 |
|