Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300003K06Rik |
A |
T |
11: 99,728,667 (GRCm39) |
C59S |
possibly damaging |
Het |
Abca5 |
A |
T |
11: 110,166,107 (GRCm39) |
N1556K |
possibly damaging |
Het |
Ackr1 |
T |
C |
1: 173,160,052 (GRCm39) |
N156D |
probably benign |
Het |
Aco2 |
C |
T |
15: 81,779,465 (GRCm39) |
R57C |
probably benign |
Het |
Adamtsl3 |
A |
T |
7: 82,255,766 (GRCm39) |
S1593C |
probably benign |
Het |
Adgrb2 |
G |
A |
4: 129,900,647 (GRCm39) |
G333D |
probably damaging |
Het |
Arhgef7 |
T |
A |
8: 11,865,010 (GRCm39) |
F374Y |
possibly damaging |
Het |
Atxn7 |
T |
A |
14: 14,013,268 (GRCm38) |
M62K |
possibly damaging |
Het |
C87436 |
G |
A |
6: 86,422,582 (GRCm39) |
R52H |
probably damaging |
Het |
Cacna1g |
T |
A |
11: 94,306,762 (GRCm39) |
E1842V |
probably damaging |
Het |
Cdh4 |
T |
C |
2: 179,532,640 (GRCm39) |
S701P |
probably damaging |
Het |
Cecr2 |
C |
T |
6: 120,733,702 (GRCm39) |
S563L |
probably benign |
Het |
Cfap276 |
A |
G |
3: 108,449,819 (GRCm39) |
N33D |
possibly damaging |
Het |
Col12a1 |
A |
T |
9: 79,542,709 (GRCm39) |
V2352E |
probably damaging |
Het |
Col9a2 |
C |
G |
4: 120,911,455 (GRCm39) |
R599G |
probably damaging |
Het |
Crygs |
C |
T |
16: 22,624,301 (GRCm39) |
G102D |
possibly damaging |
Het |
Csad |
G |
T |
15: 102,095,557 (GRCm39) |
R167S |
probably damaging |
Het |
Dnlz |
A |
T |
2: 26,241,483 (GRCm39) |
C82S |
probably damaging |
Het |
Ehmt2 |
T |
A |
17: 35,129,691 (GRCm39) |
N951K |
possibly damaging |
Het |
Emilin1 |
C |
T |
5: 31,075,082 (GRCm39) |
P441L |
possibly damaging |
Het |
Enpp2 |
A |
C |
15: 54,761,190 (GRCm39) |
Y221D |
probably damaging |
Het |
Exoc3l |
A |
T |
8: 106,017,079 (GRCm39) |
|
probably null |
Het |
F11 |
T |
C |
8: 45,705,184 (GRCm39) |
D119G |
possibly damaging |
Het |
Faiml |
T |
C |
9: 99,111,612 (GRCm39) |
Y149C |
probably benign |
Het |
Fn1 |
C |
T |
1: 71,653,102 (GRCm39) |
G1296R |
probably null |
Het |
Glg1 |
A |
T |
8: 111,895,353 (GRCm39) |
Y819* |
probably null |
Het |
Gm11568 |
A |
G |
11: 99,749,070 (GRCm39) |
S92G |
unknown |
Het |
Gm28042 |
A |
C |
2: 119,867,310 (GRCm39) |
Q465P |
probably damaging |
Het |
Gpatch1 |
A |
T |
7: 34,988,103 (GRCm39) |
S678T |
probably benign |
Het |
Gpr158 |
A |
T |
2: 21,831,674 (GRCm39) |
M925L |
probably benign |
Het |
Hecw1 |
T |
C |
13: 14,520,653 (GRCm39) |
T195A |
probably benign |
Het |
Hoxd1 |
A |
G |
2: 74,594,501 (GRCm39) |
K252R |
probably damaging |
Het |
Iqck |
G |
A |
7: 118,498,880 (GRCm39) |
D173N |
possibly damaging |
Het |
Kcnh1 |
T |
G |
1: 192,019,829 (GRCm39) |
V358G |
probably damaging |
Het |
Kifap3 |
T |
A |
1: 163,696,327 (GRCm39) |
V652D |
possibly damaging |
Het |
Knl1 |
C |
A |
2: 118,902,762 (GRCm39) |
Q1488K |
probably damaging |
Het |
Map4k1 |
T |
A |
7: 28,701,382 (GRCm39) |
H729Q |
probably damaging |
Het |
Marchf1 |
T |
A |
8: 66,840,151 (GRCm39) |
N311K |
probably benign |
Het |
Mypn |
A |
G |
10: 62,966,848 (GRCm39) |
F943L |
probably damaging |
Het |
Nkpd1 |
A |
G |
7: 19,257,822 (GRCm39) |
I534V |
probably benign |
Het |
Nrarp |
T |
C |
2: 25,071,421 (GRCm39) |
V100A |
possibly damaging |
Het |
Nt5c1a |
T |
C |
4: 123,109,873 (GRCm39) |
F324S |
probably damaging |
Het |
Ntrk2 |
T |
A |
13: 59,009,165 (GRCm39) |
Y319N |
probably damaging |
Het |
Odad2 |
C |
A |
18: 7,223,676 (GRCm39) |
G456W |
probably benign |
Het |
Or5d41 |
A |
G |
2: 88,055,167 (GRCm39) |
F70L |
probably benign |
Het |
Parg |
A |
G |
14: 32,017,195 (GRCm39) |
D384G |
probably damaging |
Het |
Pde7b |
T |
A |
10: 20,276,165 (GRCm39) |
*460L |
probably null |
Het |
Pigr |
G |
T |
1: 130,774,207 (GRCm39) |
V396L |
probably benign |
Het |
Pkhd1 |
A |
G |
1: 20,271,073 (GRCm39) |
I3160T |
possibly damaging |
Het |
Ppl |
T |
C |
16: 4,912,416 (GRCm39) |
S722G |
probably benign |
Het |
Ppp1r26 |
A |
G |
2: 28,342,713 (GRCm39) |
E781G |
possibly damaging |
Het |
Rptor |
T |
A |
11: 119,647,148 (GRCm39) |
C246* |
probably null |
Het |
Rusc2 |
G |
A |
4: 43,416,260 (GRCm39) |
R522H |
probably damaging |
Het |
Senp7 |
T |
C |
16: 56,005,146 (GRCm39) |
S927P |
probably damaging |
Het |
Serpinb6d |
A |
T |
13: 33,855,411 (GRCm39) |
M362L |
probably benign |
Het |
Setx |
GTGGCT |
GT |
2: 29,044,073 (GRCm39) |
1814 |
probably null |
Het |
Slc12a3 |
T |
A |
8: 95,059,915 (GRCm39) |
I187N |
possibly damaging |
Het |
Slc46a1 |
T |
G |
11: 78,357,249 (GRCm39) |
S101A |
probably benign |
Het |
Slc4a8 |
A |
G |
15: 100,705,283 (GRCm39) |
M830V |
probably benign |
Het |
Slco4a1 |
T |
C |
2: 180,106,529 (GRCm39) |
L237P |
possibly damaging |
Het |
Sned1 |
T |
A |
1: 93,209,364 (GRCm39) |
|
probably null |
Het |
Tia1 |
A |
G |
6: 86,404,659 (GRCm39) |
N298S |
probably benign |
Het |
Tsr1 |
A |
T |
11: 74,795,653 (GRCm39) |
|
probably null |
Het |
Ttc6 |
G |
A |
12: 57,749,084 (GRCm39) |
V1339I |
probably benign |
Het |
Tyrp1 |
A |
T |
4: 80,755,771 (GRCm39) |
E180V |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 69,846,685 (GRCm39) |
V1636A |
probably benign |
Het |
Usp1 |
T |
C |
4: 98,818,079 (GRCm39) |
L139P |
probably damaging |
Het |
Vmn1r228 |
A |
G |
17: 20,996,807 (GRCm39) |
L237P |
probably damaging |
Het |
Vmn1r232 |
A |
G |
17: 21,134,465 (GRCm39) |
L45P |
probably benign |
Het |
Vmn2r2 |
T |
C |
3: 64,023,930 (GRCm39) |
R884G |
probably benign |
Het |
Vmn2r60 |
T |
A |
7: 41,786,251 (GRCm39) |
Y351* |
probably null |
Het |
Zbtb7a |
G |
A |
10: 80,980,831 (GRCm39) |
V342I |
possibly damaging |
Het |
Zdhhc11 |
C |
A |
13: 74,121,871 (GRCm39) |
N127K |
probably damaging |
Het |
|
Other mutations in Cdr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01659:Cdr2
|
APN |
7 |
120,557,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R0394:Cdr2
|
UTSW |
7 |
120,557,954 (GRCm39) |
missense |
probably benign |
0.00 |
R0975:Cdr2
|
UTSW |
7 |
120,557,614 (GRCm39) |
missense |
probably benign |
0.07 |
R1781:Cdr2
|
UTSW |
7 |
120,557,268 (GRCm39) |
missense |
probably benign |
0.01 |
R1906:Cdr2
|
UTSW |
7 |
120,581,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R2124:Cdr2
|
UTSW |
7 |
120,581,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R2273:Cdr2
|
UTSW |
7 |
120,557,732 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2274:Cdr2
|
UTSW |
7 |
120,557,732 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2362:Cdr2
|
UTSW |
7 |
120,569,554 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4783:Cdr2
|
UTSW |
7 |
120,557,644 (GRCm39) |
missense |
probably benign |
0.00 |
R5269:Cdr2
|
UTSW |
7 |
120,557,557 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5403:Cdr2
|
UTSW |
7 |
120,557,968 (GRCm39) |
nonsense |
probably null |
|
R5650:Cdr2
|
UTSW |
7 |
120,557,559 (GRCm39) |
missense |
probably damaging |
0.96 |
R5923:Cdr2
|
UTSW |
7 |
120,581,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R6384:Cdr2
|
UTSW |
7 |
120,581,351 (GRCm39) |
splice site |
probably null |
|
R7073:Cdr2
|
UTSW |
7 |
120,581,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Cdr2
|
UTSW |
7 |
120,557,722 (GRCm39) |
missense |
probably benign |
0.01 |
R9111:Cdr2
|
UTSW |
7 |
120,559,345 (GRCm39) |
missense |
possibly damaging |
0.53 |
|