Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts3 |
G |
A |
5: 89,849,525 (GRCm39) |
H632Y |
probably damaging |
Het |
Adgre5 |
T |
A |
8: 84,455,030 (GRCm39) |
M221L |
probably benign |
Het |
Apba2 |
A |
T |
7: 64,386,689 (GRCm39) |
I439F |
possibly damaging |
Het |
Arid1b |
C |
A |
17: 5,371,559 (GRCm39) |
N632K |
probably damaging |
Het |
Bcas3 |
A |
T |
11: 85,256,417 (GRCm39) |
I60L |
probably damaging |
Het |
Brd9 |
T |
C |
13: 74,086,666 (GRCm39) |
S56P |
probably damaging |
Het |
Ccna1 |
A |
G |
3: 54,958,076 (GRCm39) |
V143A |
probably damaging |
Het |
Cdhr3 |
T |
C |
12: 33,102,208 (GRCm39) |
T410A |
probably benign |
Het |
Cimap3 |
A |
G |
3: 105,921,824 (GRCm39) |
V33A |
probably benign |
Het |
Ddx60 |
G |
T |
8: 62,411,680 (GRCm39) |
D511Y |
probably damaging |
Het |
Drc7 |
C |
A |
8: 95,782,629 (GRCm39) |
|
probably benign |
Het |
Dysf |
A |
G |
6: 84,118,933 (GRCm39) |
E1290G |
probably benign |
Het |
Fam168b |
T |
C |
1: 34,875,883 (GRCm39) |
M1V |
probably null |
Het |
Farsa |
A |
G |
8: 85,590,886 (GRCm39) |
K208R |
probably damaging |
Het |
Fnip2 |
A |
G |
3: 79,425,368 (GRCm39) |
|
probably benign |
Het |
Gm17535 |
A |
T |
9: 3,035,111 (GRCm39) |
H170L |
probably benign |
Het |
Gm4553 |
T |
C |
7: 141,718,964 (GRCm39) |
S155G |
unknown |
Het |
Gm5852 |
T |
C |
3: 93,634,501 (GRCm39) |
|
noncoding transcript |
Het |
Gnb2 |
T |
C |
5: 137,528,968 (GRCm39) |
|
probably benign |
Het |
Gpr158 |
A |
G |
2: 21,373,494 (GRCm39) |
N143S |
probably damaging |
Het |
Hcn1 |
C |
A |
13: 117,739,513 (GRCm39) |
Q92K |
unknown |
Het |
Helb |
T |
C |
10: 119,934,150 (GRCm39) |
I678V |
possibly damaging |
Het |
Hnrnpl |
C |
A |
7: 28,512,798 (GRCm39) |
A118D |
probably damaging |
Het |
Klhl14 |
G |
A |
18: 21,784,921 (GRCm39) |
P169S |
probably benign |
Het |
Kndc1 |
T |
C |
7: 139,481,904 (GRCm39) |
|
probably benign |
Het |
Lmod2 |
A |
G |
6: 24,598,051 (GRCm39) |
E57G |
probably damaging |
Het |
Lrch4 |
T |
C |
5: 137,636,009 (GRCm39) |
I300T |
possibly damaging |
Het |
Lrp6 |
A |
G |
6: 134,433,053 (GRCm39) |
V1426A |
probably benign |
Het |
Lrrc39 |
A |
G |
3: 116,364,630 (GRCm39) |
|
probably benign |
Het |
Mamstr |
G |
A |
7: 45,293,709 (GRCm39) |
V262I |
probably benign |
Het |
Mob1b |
A |
T |
5: 88,904,014 (GRCm39) |
T217S |
probably benign |
Het |
Mocs3 |
G |
A |
2: 168,073,411 (GRCm39) |
R286H |
possibly damaging |
Het |
Mpo |
A |
T |
11: 87,693,443 (GRCm39) |
Q27L |
probably benign |
Het |
Ncdn |
A |
T |
4: 126,640,981 (GRCm39) |
D506E |
probably benign |
Het |
Noxa1 |
A |
G |
2: 24,984,914 (GRCm39) |
I8T |
probably benign |
Het |
Oma1 |
G |
T |
4: 103,176,565 (GRCm39) |
A110S |
probably benign |
Het |
Or10a48 |
C |
T |
7: 108,424,280 (GRCm39) |
V309I |
probably benign |
Het |
Or13a18 |
T |
A |
7: 140,190,666 (GRCm39) |
S196T |
probably damaging |
Het |
Or8b4 |
A |
G |
9: 37,830,346 (GRCm39) |
Y131C |
probably damaging |
Het |
Pde4a |
A |
C |
9: 21,122,357 (GRCm39) |
K694T |
probably benign |
Het |
Phc1 |
A |
G |
6: 122,299,958 (GRCm39) |
|
probably benign |
Het |
Pias1 |
A |
G |
9: 62,830,578 (GRCm39) |
V187A |
probably damaging |
Het |
Pigf |
C |
A |
17: 87,327,876 (GRCm39) |
L130F |
probably null |
Het |
Pkd1 |
G |
T |
17: 24,799,069 (GRCm39) |
V2763L |
probably damaging |
Het |
Potefam1 |
G |
T |
2: 111,051,107 (GRCm39) |
L230I |
probably damaging |
Het |
Ppp1r8 |
T |
C |
4: 132,561,992 (GRCm39) |
Y76C |
probably damaging |
Het |
Ppp6r3 |
C |
A |
19: 3,568,324 (GRCm39) |
G158V |
probably damaging |
Het |
Ptpn13 |
A |
G |
5: 103,698,924 (GRCm39) |
I1136V |
probably damaging |
Het |
Ptprq |
T |
C |
10: 107,412,790 (GRCm39) |
I1770V |
probably damaging |
Het |
Rhpn2 |
A |
T |
7: 35,070,185 (GRCm39) |
I148F |
probably damaging |
Het |
Stard3 |
T |
C |
11: 98,268,285 (GRCm39) |
Y239H |
probably damaging |
Het |
Stau1 |
T |
C |
2: 166,792,729 (GRCm39) |
Y412C |
probably benign |
Het |
Sucnr1 |
A |
G |
3: 59,994,053 (GRCm39) |
I194V |
probably benign |
Het |
Tanc1 |
A |
G |
2: 59,621,185 (GRCm39) |
T335A |
possibly damaging |
Het |
Tmem126a |
T |
C |
7: 90,101,963 (GRCm39) |
T79A |
probably benign |
Het |
Trav9-2 |
A |
T |
14: 53,828,840 (GRCm39) |
Y70F |
probably benign |
Het |
Tspear |
A |
G |
10: 77,709,070 (GRCm39) |
E432G |
probably benign |
Het |
Ube2o |
T |
C |
11: 116,435,580 (GRCm39) |
R403G |
probably benign |
Het |
Unc80 |
C |
A |
1: 66,645,618 (GRCm39) |
S1431R |
possibly damaging |
Het |
Usp24 |
G |
A |
4: 106,258,336 (GRCm39) |
C1578Y |
probably damaging |
Het |
Vsig10 |
A |
T |
5: 117,489,652 (GRCm39) |
M473L |
probably benign |
Het |
Xpot |
T |
A |
10: 121,441,549 (GRCm39) |
M559L |
probably benign |
Het |
|
Other mutations in Ccdc57 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01069:Ccdc57
|
APN |
11 |
120,752,085 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02065:Ccdc57
|
APN |
11 |
120,764,586 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02143:Ccdc57
|
APN |
11 |
120,752,069 (GRCm39) |
nonsense |
probably null |
|
R0265:Ccdc57
|
UTSW |
11 |
120,812,637 (GRCm39) |
missense |
probably benign |
0.00 |
R1184:Ccdc57
|
UTSW |
11 |
120,764,637 (GRCm39) |
splice site |
probably benign |
|
R1792:Ccdc57
|
UTSW |
11 |
120,788,707 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1834:Ccdc57
|
UTSW |
11 |
120,752,045 (GRCm39) |
missense |
probably benign |
0.07 |
R1852:Ccdc57
|
UTSW |
11 |
120,812,499 (GRCm39) |
missense |
probably damaging |
0.98 |
R1914:Ccdc57
|
UTSW |
11 |
120,794,134 (GRCm39) |
splice site |
probably benign |
|
R2146:Ccdc57
|
UTSW |
11 |
120,776,051 (GRCm39) |
splice site |
probably benign |
|
R2341:Ccdc57
|
UTSW |
11 |
120,751,349 (GRCm39) |
missense |
probably benign |
0.00 |
R3013:Ccdc57
|
UTSW |
11 |
120,752,025 (GRCm39) |
missense |
probably benign |
0.01 |
R4798:Ccdc57
|
UTSW |
11 |
120,772,683 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4821:Ccdc57
|
UTSW |
11 |
120,751,225 (GRCm39) |
critical splice donor site |
probably null |
|
R4869:Ccdc57
|
UTSW |
11 |
120,794,344 (GRCm39) |
splice site |
probably null |
|
R4964:Ccdc57
|
UTSW |
11 |
120,751,978 (GRCm39) |
missense |
probably benign |
0.17 |
R4966:Ccdc57
|
UTSW |
11 |
120,751,978 (GRCm39) |
missense |
probably benign |
0.17 |
R5204:Ccdc57
|
UTSW |
11 |
120,776,888 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5993:Ccdc57
|
UTSW |
11 |
120,785,550 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6072:Ccdc57
|
UTSW |
11 |
120,792,901 (GRCm39) |
missense |
probably damaging |
0.98 |
R6404:Ccdc57
|
UTSW |
11 |
120,785,538 (GRCm39) |
missense |
probably benign |
0.10 |
R6877:Ccdc57
|
UTSW |
11 |
120,764,528 (GRCm39) |
missense |
probably benign |
0.00 |
R7074:Ccdc57
|
UTSW |
11 |
120,794,200 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7102:Ccdc57
|
UTSW |
11 |
120,812,557 (GRCm39) |
nonsense |
probably null |
|
R7311:Ccdc57
|
UTSW |
11 |
120,764,567 (GRCm39) |
missense |
probably benign |
|
R8087:Ccdc57
|
UTSW |
11 |
120,788,705 (GRCm39) |
missense |
probably benign |
|
R8111:Ccdc57
|
UTSW |
11 |
120,769,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R8164:Ccdc57
|
UTSW |
11 |
120,788,788 (GRCm39) |
missense |
probably benign |
0.00 |
R8273:Ccdc57
|
UTSW |
11 |
120,812,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R8316:Ccdc57
|
UTSW |
11 |
120,776,742 (GRCm39) |
missense |
probably damaging |
0.98 |
R8323:Ccdc57
|
UTSW |
11 |
120,788,750 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8388:Ccdc57
|
UTSW |
11 |
120,717,744 (GRCm39) |
missense |
probably benign |
|
R8768:Ccdc57
|
UTSW |
11 |
120,788,788 (GRCm39) |
missense |
probably benign |
0.00 |
R8957:Ccdc57
|
UTSW |
11 |
120,776,861 (GRCm39) |
missense |
probably benign |
|
R9245:Ccdc57
|
UTSW |
11 |
120,812,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R9281:Ccdc57
|
UTSW |
11 |
120,751,413 (GRCm39) |
missense |
probably benign |
0.19 |
R9422:Ccdc57
|
UTSW |
11 |
120,764,444 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9704:Ccdc57
|
UTSW |
11 |
120,764,531 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Ccdc57
|
UTSW |
11 |
120,751,964 (GRCm39) |
missense |
probably null |
|
Z1176:Ccdc57
|
UTSW |
11 |
120,751,314 (GRCm39) |
missense |
possibly damaging |
0.89 |
|