Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,775,362 (GRCm39) |
V1517A |
probably benign |
Het |
Adam17 |
C |
A |
12: 21,390,493 (GRCm39) |
G410C |
probably damaging |
Het |
Adcy3 |
A |
G |
12: 4,254,762 (GRCm39) |
D698G |
probably damaging |
Het |
Afap1 |
T |
A |
5: 36,131,742 (GRCm39) |
N356K |
possibly damaging |
Het |
Afm |
A |
G |
5: 90,671,713 (GRCm39) |
N132D |
probably benign |
Het |
Bsdc1 |
T |
A |
4: 129,359,141 (GRCm39) |
|
probably null |
Het |
Ccdc121rt2 |
T |
G |
5: 112,597,698 (GRCm39) |
Y82D |
not run |
Het |
Cit |
T |
G |
5: 116,001,027 (GRCm39) |
F142C |
probably benign |
Het |
Cnga3 |
A |
G |
1: 37,300,852 (GRCm39) |
D524G |
probably damaging |
Het |
Cpne8 |
T |
A |
15: 90,424,450 (GRCm39) |
D313V |
probably damaging |
Het |
Ell3 |
TCTCCTC |
TCTC |
2: 121,269,937 (GRCm39) |
|
probably benign |
Het |
Flrt1 |
C |
A |
19: 7,073,229 (GRCm39) |
L439F |
possibly damaging |
Het |
Gkn1 |
A |
T |
6: 87,325,163 (GRCm39) |
I82N |
probably damaging |
Het |
Gm14410 |
C |
A |
2: 176,885,613 (GRCm39) |
C217F |
probably damaging |
Het |
Gm14412 |
G |
T |
2: 177,007,590 (GRCm39) |
H102N |
probably benign |
Het |
Gm3159 |
A |
T |
14: 4,397,585 (GRCm38) |
|
probably benign |
Het |
Golm2 |
T |
C |
2: 121,764,022 (GRCm39) |
V434A |
probably benign |
Het |
Helz2 |
A |
G |
2: 180,879,782 (GRCm39) |
M612T |
probably benign |
Het |
Iars1 |
T |
A |
13: 49,876,494 (GRCm39) |
I853N |
probably damaging |
Het |
Kcna4 |
A |
C |
2: 107,126,237 (GRCm39) |
I324L |
possibly damaging |
Het |
Kcnh1 |
T |
C |
1: 192,117,183 (GRCm39) |
S690P |
probably damaging |
Het |
Kpna3 |
T |
C |
14: 61,622,182 (GRCm39) |
Y194C |
probably damaging |
Het |
Lrrc56 |
T |
C |
7: 140,789,515 (GRCm39) |
S511P |
probably damaging |
Het |
Ltbp1 |
A |
G |
17: 75,559,351 (GRCm39) |
Y280C |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,420,906 (GRCm39) |
I116T |
probably benign |
Het |
Mmp16 |
A |
T |
4: 18,112,112 (GRCm39) |
N496I |
probably damaging |
Het |
Mon2 |
T |
C |
10: 122,878,236 (GRCm39) |
D229G |
probably benign |
Het |
Or2b2 |
T |
A |
13: 21,887,369 (GRCm39) |
L66Q |
probably damaging |
Het |
Or2j6 |
A |
T |
7: 139,980,377 (GRCm39) |
M194K |
probably damaging |
Het |
Or52s1 |
A |
G |
7: 102,861,186 (GRCm39) |
I40V |
probably benign |
Het |
Or5p61 |
T |
A |
7: 107,758,637 (GRCm39) |
I148F |
probably benign |
Het |
Or5w14 |
G |
T |
2: 87,541,428 (GRCm39) |
T274K |
possibly damaging |
Het |
Pkp1 |
A |
G |
1: 135,817,695 (GRCm39) |
F147L |
possibly damaging |
Het |
Ppp1r3e |
T |
C |
14: 55,114,672 (GRCm39) |
Q30R |
probably damaging |
Het |
Ppp2r5b |
C |
A |
19: 6,282,628 (GRCm39) |
R174L |
probably benign |
Het |
Pramel58 |
A |
G |
5: 94,831,287 (GRCm39) |
D98G |
possibly damaging |
Het |
Qrfprl |
G |
T |
6: 65,433,121 (GRCm39) |
A314S |
possibly damaging |
Het |
Rbm15 |
C |
T |
3: 107,239,459 (GRCm39) |
R313H |
probably damaging |
Het |
Rgs18 |
A |
G |
1: 144,629,603 (GRCm39) |
F219L |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,702,985 (GRCm39) |
|
probably null |
Het |
Sirpd |
T |
A |
3: 15,361,723 (GRCm39) |
|
probably null |
Het |
Sirt4 |
T |
G |
5: 115,617,805 (GRCm39) |
I284L |
probably benign |
Het |
Slc25a11 |
A |
G |
11: 70,536,005 (GRCm39) |
V243A |
probably benign |
Het |
Syde1 |
A |
G |
10: 78,425,741 (GRCm39) |
I142T |
probably benign |
Het |
Synj2 |
A |
G |
17: 6,088,098 (GRCm39) |
E1383G |
probably benign |
Het |
Syt4 |
A |
T |
18: 31,573,245 (GRCm39) |
C423* |
probably null |
Het |
Tfr2 |
T |
A |
5: 137,569,986 (GRCm39) |
Y131N |
possibly damaging |
Het |
Tgm1 |
C |
T |
14: 55,949,932 (GRCm39) |
R92Q |
unknown |
Het |
Thoc1 |
A |
T |
18: 9,984,441 (GRCm39) |
D309V |
probably damaging |
Het |
Vmn2r24 |
C |
T |
6: 123,757,422 (GRCm39) |
H97Y |
probably benign |
Het |
Wbp1 |
A |
T |
6: 83,097,176 (GRCm39) |
Y89* |
probably null |
Het |
Wnk1 |
A |
G |
6: 119,926,137 (GRCm39) |
L1358P |
probably benign |
Het |
Zfp14 |
T |
C |
7: 29,738,368 (GRCm39) |
T206A |
possibly damaging |
Het |
Zfp748 |
T |
C |
13: 67,689,608 (GRCm39) |
T551A |
probably benign |
Het |
Zfp9 |
A |
T |
6: 118,441,843 (GRCm39) |
V273E |
probably damaging |
Het |
|
Other mutations in Ccdc47 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00952:Ccdc47
|
APN |
11 |
106,094,358 (GRCm39) |
splice site |
probably null |
|
IGL01890:Ccdc47
|
APN |
11 |
106,096,277 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02026:Ccdc47
|
APN |
11 |
106,095,853 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03343:Ccdc47
|
APN |
11 |
106,095,788 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4677001:Ccdc47
|
UTSW |
11 |
106,099,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R1508:Ccdc47
|
UTSW |
11 |
106,093,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R2239:Ccdc47
|
UTSW |
11 |
106,092,960 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3103:Ccdc47
|
UTSW |
11 |
106,093,667 (GRCm39) |
missense |
probably benign |
0.00 |
R3935:Ccdc47
|
UTSW |
11 |
106,092,823 (GRCm39) |
unclassified |
probably benign |
|
R4783:Ccdc47
|
UTSW |
11 |
106,094,430 (GRCm39) |
missense |
probably benign |
0.03 |
R5150:Ccdc47
|
UTSW |
11 |
106,096,265 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5331:Ccdc47
|
UTSW |
11 |
106,101,176 (GRCm39) |
missense |
probably benign |
0.17 |
R5362:Ccdc47
|
UTSW |
11 |
106,099,039 (GRCm39) |
splice site |
probably null |
|
R5417:Ccdc47
|
UTSW |
11 |
106,101,176 (GRCm39) |
missense |
probably benign |
0.17 |
R5420:Ccdc47
|
UTSW |
11 |
106,101,176 (GRCm39) |
missense |
probably benign |
0.17 |
R5473:Ccdc47
|
UTSW |
11 |
106,095,855 (GRCm39) |
missense |
probably damaging |
0.98 |
R6297:Ccdc47
|
UTSW |
11 |
106,094,427 (GRCm39) |
missense |
probably damaging |
0.99 |
R6449:Ccdc47
|
UTSW |
11 |
106,095,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R6981:Ccdc47
|
UTSW |
11 |
106,093,563 (GRCm39) |
missense |
probably benign |
0.04 |
R7136:Ccdc47
|
UTSW |
11 |
106,095,830 (GRCm39) |
missense |
probably benign |
0.01 |
R7170:Ccdc47
|
UTSW |
11 |
106,093,304 (GRCm39) |
missense |
probably benign |
0.01 |
R7340:Ccdc47
|
UTSW |
11 |
106,091,799 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8335:Ccdc47
|
UTSW |
11 |
106,099,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R8335:Ccdc47
|
UTSW |
11 |
106,099,084 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8487:Ccdc47
|
UTSW |
11 |
106,092,971 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8752:Ccdc47
|
UTSW |
11 |
106,095,818 (GRCm39) |
missense |
probably damaging |
0.99 |
R9157:Ccdc47
|
UTSW |
11 |
106,093,208 (GRCm39) |
critical splice donor site |
probably null |
|
R9504:Ccdc47
|
UTSW |
11 |
106,101,155 (GRCm39) |
missense |
probably benign |
0.01 |
|