Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
CTGTAGGAAATCTTCAATGT |
CTGT |
11: 110,101,019 (GRCm39) |
|
probably null |
Het |
Adcy8 |
C |
T |
15: 64,792,783 (GRCm39) |
G58S |
probably benign |
Het |
Adgra2 |
T |
A |
8: 27,604,232 (GRCm39) |
L24* |
probably null |
Het |
Ampd2 |
C |
A |
3: 107,992,685 (GRCm39) |
|
probably benign |
Het |
Ankrd26 |
T |
G |
6: 118,502,752 (GRCm39) |
E806A |
probably damaging |
Het |
Apol9b |
A |
G |
15: 77,619,639 (GRCm39) |
D145G |
probably benign |
Het |
Ash1l |
T |
A |
3: 88,892,726 (GRCm39) |
M1535K |
probably benign |
Het |
B3glct |
A |
T |
5: 149,677,621 (GRCm39) |
M417L |
probably damaging |
Het |
Cep192 |
A |
T |
18: 67,953,431 (GRCm39) |
T483S |
probably damaging |
Het |
Cep290 |
G |
A |
10: 100,354,657 (GRCm39) |
E914K |
probably damaging |
Het |
Chst15 |
C |
T |
7: 131,872,114 (GRCm39) |
A56T |
probably damaging |
Het |
Col27a1 |
A |
T |
4: 63,143,661 (GRCm39) |
T450S |
probably benign |
Het |
Cpsf2 |
A |
G |
12: 101,951,594 (GRCm39) |
N177S |
probably damaging |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
Ctc1 |
C |
T |
11: 68,926,441 (GRCm39) |
A859V |
possibly damaging |
Het |
Dcakd |
A |
G |
11: 102,888,183 (GRCm39) |
Y134H |
possibly damaging |
Het |
Dctn3 |
G |
T |
4: 41,723,065 (GRCm39) |
Y22* |
probably null |
Het |
Dync2h1 |
T |
A |
9: 7,124,797 (GRCm39) |
D2025V |
probably damaging |
Het |
Dync2li1 |
T |
C |
17: 84,943,702 (GRCm39) |
S92P |
probably damaging |
Het |
Eml5 |
A |
G |
12: 98,853,356 (GRCm39) |
V81A |
probably damaging |
Het |
Espl1 |
C |
T |
15: 102,228,023 (GRCm39) |
R1625C |
probably damaging |
Het |
Fam181a |
T |
C |
12: 103,282,785 (GRCm39) |
V230A |
probably benign |
Het |
Fanci |
T |
A |
7: 79,045,743 (GRCm39) |
D28E |
probably benign |
Het |
Fmn1 |
A |
G |
2: 113,195,962 (GRCm39) |
N554S |
unknown |
Het |
Frem2 |
T |
C |
3: 53,444,751 (GRCm39) |
Y2460C |
probably damaging |
Het |
Fscb |
G |
A |
12: 64,520,567 (GRCm39) |
P300S |
probably damaging |
Het |
Gm28042 |
A |
G |
2: 119,867,229 (GRCm39) |
D438G |
probably benign |
Het |
Ldaf1 |
A |
G |
7: 119,719,462 (GRCm39) |
E157G |
possibly damaging |
Het |
Map1b |
C |
T |
13: 99,565,846 (GRCm39) |
V2292M |
unknown |
Het |
Nbas |
A |
G |
12: 13,380,647 (GRCm39) |
D635G |
possibly damaging |
Het |
Ncapg2 |
A |
G |
12: 116,414,095 (GRCm39) |
|
probably null |
Het |
Nrp2 |
A |
T |
1: 62,783,514 (GRCm39) |
E205V |
probably damaging |
Het |
Pcdhb3 |
A |
T |
18: 37,435,239 (GRCm39) |
T402S |
possibly damaging |
Het |
Phc1 |
T |
C |
6: 122,299,296 (GRCm39) |
N638D |
possibly damaging |
Het |
Plcb1 |
A |
G |
2: 135,188,250 (GRCm39) |
N781S |
possibly damaging |
Het |
Prkdc |
T |
A |
16: 15,523,071 (GRCm39) |
D1164E |
probably damaging |
Het |
Proser2 |
T |
A |
2: 6,105,506 (GRCm39) |
R353W |
possibly damaging |
Het |
Prxl2b |
T |
G |
4: 154,982,606 (GRCm39) |
Y56S |
probably damaging |
Het |
Ptges |
T |
A |
2: 30,782,708 (GRCm39) |
T115S |
probably benign |
Het |
Ptprk |
A |
T |
10: 28,436,138 (GRCm39) |
D833V |
probably damaging |
Het |
Pum1 |
T |
A |
4: 130,455,394 (GRCm39) |
L173* |
probably null |
Het |
Pum1 |
G |
T |
4: 130,455,395 (GRCm39) |
L269F |
probably damaging |
Het |
Rasgrp4 |
A |
G |
7: 28,838,470 (GRCm39) |
Y106C |
probably damaging |
Het |
Rbbp6 |
T |
A |
7: 122,598,697 (GRCm39) |
|
probably benign |
Het |
Rdh1 |
A |
G |
10: 127,596,041 (GRCm39) |
T79A |
possibly damaging |
Het |
Relb |
A |
C |
7: 19,347,686 (GRCm39) |
|
probably null |
Het |
Rnf122 |
G |
A |
8: 31,602,192 (GRCm39) |
W6* |
probably null |
Het |
Rnf31 |
A |
G |
14: 55,829,994 (GRCm39) |
E138G |
possibly damaging |
Het |
Scaf8 |
G |
A |
17: 3,247,485 (GRCm39) |
R936Q |
probably damaging |
Het |
Scube3 |
T |
A |
17: 28,385,108 (GRCm39) |
V686D |
possibly damaging |
Het |
Snrnp27 |
A |
T |
6: 86,653,196 (GRCm39) |
C141S |
probably benign |
Het |
Spns2 |
C |
T |
11: 72,349,497 (GRCm39) |
V252M |
possibly damaging |
Het |
Tomm40l |
C |
T |
1: 171,047,703 (GRCm39) |
S220N |
probably damaging |
Het |
Trim17 |
A |
G |
11: 58,862,237 (GRCm39) |
D423G |
probably damaging |
Het |
Trpc6 |
A |
AT |
9: 8,610,466 (GRCm39) |
|
probably null |
Het |
Tut4 |
G |
A |
4: 108,360,226 (GRCm39) |
R481Q |
possibly damaging |
Het |
Uba5 |
A |
T |
9: 103,937,442 (GRCm39) |
M89K |
probably damaging |
Het |
Vav2 |
T |
C |
2: 27,163,718 (GRCm39) |
D628G |
probably damaging |
Het |
Vmn2r107 |
T |
C |
17: 20,595,904 (GRCm39) |
L819P |
probably damaging |
Het |
Vmn2r25 |
A |
T |
6: 123,816,518 (GRCm39) |
D354E |
possibly damaging |
Het |
Xrn1 |
A |
G |
9: 95,888,873 (GRCm39) |
E984G |
possibly damaging |
Het |
Zbtb17 |
T |
C |
4: 141,191,557 (GRCm39) |
V223A |
probably benign |
Het |
Zfp592 |
T |
C |
7: 80,691,186 (GRCm39) |
S1122P |
possibly damaging |
Het |
|
Other mutations in Atf6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01327:Atf6
|
APN |
1 |
170,616,175 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01431:Atf6
|
APN |
1 |
170,680,571 (GRCm39) |
splice site |
probably benign |
|
IGL01755:Atf6
|
APN |
1 |
170,616,180 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02060:Atf6
|
APN |
1 |
170,646,989 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02416:Atf6
|
APN |
1 |
170,574,726 (GRCm39) |
nonsense |
probably null |
|
IGL02903:Atf6
|
APN |
1 |
170,627,283 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02989:Atf6
|
APN |
1 |
170,616,252 (GRCm39) |
splice site |
probably benign |
|
IGL03209:Atf6
|
APN |
1 |
170,662,463 (GRCm39) |
missense |
probably benign |
|
R0455:Atf6
|
UTSW |
1 |
170,662,492 (GRCm39) |
missense |
probably benign |
0.00 |
R0467:Atf6
|
UTSW |
1 |
170,621,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R0491:Atf6
|
UTSW |
1 |
170,614,913 (GRCm39) |
critical splice donor site |
probably null |
|
R0784:Atf6
|
UTSW |
1 |
170,537,516 (GRCm39) |
missense |
probably benign |
0.19 |
R1486:Atf6
|
UTSW |
1 |
170,622,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1850:Atf6
|
UTSW |
1 |
170,646,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R1945:Atf6
|
UTSW |
1 |
170,682,710 (GRCm39) |
missense |
probably benign |
0.00 |
R3782:Atf6
|
UTSW |
1 |
170,622,336 (GRCm39) |
nonsense |
probably null |
|
R4454:Atf6
|
UTSW |
1 |
170,621,608 (GRCm39) |
missense |
probably damaging |
0.99 |
R4631:Atf6
|
UTSW |
1 |
170,574,766 (GRCm39) |
splice site |
probably null |
|
R4676:Atf6
|
UTSW |
1 |
170,614,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Atf6
|
UTSW |
1 |
170,574,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R5860:Atf6
|
UTSW |
1 |
170,669,345 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5860:Atf6
|
UTSW |
1 |
170,669,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R5950:Atf6
|
UTSW |
1 |
170,662,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Atf6
|
UTSW |
1 |
170,621,545 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6520:Atf6
|
UTSW |
1 |
170,695,238 (GRCm39) |
missense |
probably benign |
0.00 |
R7032:Atf6
|
UTSW |
1 |
170,627,181 (GRCm39) |
critical splice donor site |
probably null |
|
R7472:Atf6
|
UTSW |
1 |
170,643,060 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7923:Atf6
|
UTSW |
1 |
170,622,275 (GRCm39) |
missense |
probably benign |
|
R8002:Atf6
|
UTSW |
1 |
170,646,823 (GRCm39) |
missense |
probably benign |
0.43 |
R8860:Atf6
|
UTSW |
1 |
170,680,535 (GRCm39) |
missense |
probably null |
0.95 |
R8956:Atf6
|
UTSW |
1 |
170,621,576 (GRCm39) |
missense |
probably damaging |
0.98 |
R9090:Atf6
|
UTSW |
1 |
170,622,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R9271:Atf6
|
UTSW |
1 |
170,622,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R9323:Atf6
|
UTSW |
1 |
170,682,682 (GRCm39) |
nonsense |
probably null |
|
R9500:Atf6
|
UTSW |
1 |
170,574,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R9594:Atf6
|
UTSW |
1 |
170,668,402 (GRCm39) |
missense |
probably benign |
0.18 |
R9733:Atf6
|
UTSW |
1 |
170,662,402 (GRCm39) |
missense |
probably benign |
0.00 |
|