Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
A |
T |
5: 88,118,518 (GRCm39) |
M1L |
probably benign |
Het |
Adgrf4 |
C |
A |
17: 42,980,606 (GRCm39) |
A160S |
probably damaging |
Het |
Adgrl1 |
T |
C |
8: 84,656,426 (GRCm39) |
V243A |
possibly damaging |
Het |
Adgrl4 |
G |
T |
3: 151,198,064 (GRCm39) |
|
probably null |
Het |
Alg8 |
A |
G |
7: 97,027,423 (GRCm39) |
Y97C |
probably damaging |
Het |
Ankrd12 |
T |
A |
17: 66,292,754 (GRCm39) |
D893V |
probably damaging |
Het |
Anxa6 |
T |
A |
11: 54,885,791 (GRCm39) |
T385S |
probably benign |
Het |
Art4 |
A |
T |
6: 136,831,365 (GRCm39) |
C259S |
probably damaging |
Het |
Ccer2 |
T |
C |
7: 28,456,561 (GRCm39) |
S102P |
possibly damaging |
Het |
Cdhr3 |
A |
G |
12: 33,132,320 (GRCm39) |
F101S |
probably damaging |
Het |
Cyp24a1 |
T |
C |
2: 170,338,277 (GRCm39) |
Y89C |
probably damaging |
Het |
Cyp2d34 |
T |
C |
15: 82,504,901 (GRCm39) |
D53G |
probably damaging |
Het |
Dnah7a |
A |
C |
1: 53,560,326 (GRCm39) |
I2115S |
possibly damaging |
Het |
Exoc4 |
T |
A |
6: 33,895,359 (GRCm39) |
I792N |
possibly damaging |
Het |
Gm4353 |
A |
G |
7: 115,683,006 (GRCm39) |
F192L |
probably damaging |
Het |
Hps4 |
G |
A |
5: 112,525,905 (GRCm39) |
S642N |
possibly damaging |
Het |
Ift140 |
T |
C |
17: 25,317,839 (GRCm39) |
V1441A |
probably benign |
Het |
Ighv1-49 |
A |
T |
12: 115,019,073 (GRCm39) |
C41S |
probably damaging |
Het |
Lgalsl |
A |
T |
11: 20,779,306 (GRCm39) |
I113N |
possibly damaging |
Het |
Lrp1b |
T |
C |
2: 41,401,460 (GRCm39) |
D398G |
|
Het |
Lrrc4b |
A |
G |
7: 44,112,099 (GRCm39) |
H657R |
possibly damaging |
Het |
Map2k2 |
T |
C |
10: 80,955,193 (GRCm39) |
V228A |
possibly damaging |
Het |
Mdn1 |
A |
G |
4: 32,694,612 (GRCm39) |
I1112V |
probably benign |
Het |
Mipep |
T |
A |
14: 61,068,692 (GRCm39) |
M488K |
possibly damaging |
Het |
Myo15b |
A |
G |
11: 115,750,924 (GRCm39) |
T565A |
|
Het |
Nfat5 |
T |
C |
8: 108,095,401 (GRCm39) |
L1214P |
probably damaging |
Het |
Nphp3 |
A |
G |
9: 103,885,328 (GRCm39) |
T223A |
probably benign |
Het |
Or10s1 |
A |
G |
9: 39,986,187 (GRCm39) |
I199V |
probably benign |
Het |
Or52s19 |
A |
G |
7: 103,008,092 (GRCm39) |
M103T |
probably damaging |
Het |
Pkn2 |
G |
A |
3: 142,499,709 (GRCm39) |
R939W |
probably damaging |
Het |
Pla2g4c |
T |
C |
7: 13,059,671 (GRCm39) |
C3R |
possibly damaging |
Het |
Plxnd1 |
A |
T |
6: 115,934,524 (GRCm39) |
I1803N |
probably damaging |
Het |
Pygb |
C |
A |
2: 150,662,781 (GRCm39) |
H583N |
possibly damaging |
Het |
Rbm20 |
A |
G |
19: 53,839,645 (GRCm39) |
D878G |
possibly damaging |
Het |
Rdx |
C |
A |
9: 51,992,468 (GRCm39) |
Q414K |
probably benign |
Het |
Scara3 |
T |
C |
14: 66,169,233 (GRCm39) |
E128G |
possibly damaging |
Het |
Sel1l2 |
T |
C |
2: 140,097,222 (GRCm39) |
Y361C |
probably damaging |
Het |
Sfmbt2 |
T |
C |
2: 10,442,860 (GRCm39) |
I179T |
probably benign |
Het |
Sgsm2 |
C |
T |
11: 74,748,960 (GRCm39) |
V567M |
possibly damaging |
Het |
Sirt4 |
G |
A |
5: 115,618,372 (GRCm39) |
T234M |
probably damaging |
Het |
Stab1 |
T |
G |
14: 30,867,812 (GRCm39) |
K1653Q |
probably benign |
Het |
Strn4 |
T |
C |
7: 16,559,722 (GRCm39) |
|
probably benign |
Het |
Stxbp5l |
C |
A |
16: 37,076,206 (GRCm39) |
S280I |
probably damaging |
Het |
Tex30 |
G |
A |
1: 44,126,133 (GRCm39) |
R199W |
probably damaging |
Het |
Tjp3 |
A |
C |
10: 81,110,420 (GRCm39) |
F731V |
probably damaging |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tmco3 |
A |
G |
8: 13,360,143 (GRCm39) |
|
probably null |
Het |
Tmem94 |
C |
A |
11: 115,683,191 (GRCm39) |
A658E |
probably damaging |
Het |
Tnxb |
T |
A |
17: 34,904,766 (GRCm39) |
L1177Q |
probably damaging |
Het |
Trim28 |
G |
A |
7: 12,763,490 (GRCm39) |
A544T |
probably benign |
Het |
Upf2 |
T |
A |
2: 6,051,845 (GRCm39) |
V1169D |
unknown |
Het |
Usp20 |
C |
A |
2: 30,907,412 (GRCm39) |
A648D |
probably damaging |
Het |
Vmn2r108 |
T |
G |
17: 20,691,330 (GRCm39) |
N398H |
probably benign |
Het |
Whamm |
A |
T |
7: 81,243,655 (GRCm39) |
S626C |
probably damaging |
Het |
Zbtb44 |
A |
G |
9: 30,975,524 (GRCm39) |
S385G |
possibly damaging |
Het |
Zfp580 |
C |
T |
7: 5,056,137 (GRCm39) |
Q166* |
probably null |
Het |
|
Other mutations in Ctdsp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01954:Ctdsp1
|
APN |
1 |
74,433,242 (GRCm39) |
unclassified |
probably benign |
|
IGL02011:Ctdsp1
|
APN |
1 |
74,433,175 (GRCm39) |
splice site |
probably benign |
|
IGL02014:Ctdsp1
|
APN |
1 |
74,433,175 (GRCm39) |
splice site |
probably benign |
|
IGL02205:Ctdsp1
|
APN |
1 |
74,432,993 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL03011:Ctdsp1
|
APN |
1 |
74,434,606 (GRCm39) |
unclassified |
probably benign |
|
budgie
|
UTSW |
1 |
74,434,676 (GRCm39) |
missense |
possibly damaging |
0.90 |
lorikeet
|
UTSW |
1 |
74,433,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R0811:Ctdsp1
|
UTSW |
1 |
74,433,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R0812:Ctdsp1
|
UTSW |
1 |
74,433,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Ctdsp1
|
UTSW |
1 |
74,433,823 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5777:Ctdsp1
|
UTSW |
1 |
74,433,227 (GRCm39) |
missense |
probably damaging |
0.96 |
R7328:Ctdsp1
|
UTSW |
1 |
74,433,199 (GRCm39) |
missense |
probably damaging |
0.98 |
R9020:Ctdsp1
|
UTSW |
1 |
74,434,676 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9106:Ctdsp1
|
UTSW |
1 |
74,433,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R9163:Ctdsp1
|
UTSW |
1 |
74,434,126 (GRCm39) |
missense |
possibly damaging |
0.93 |
|