Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl3 |
T |
A |
5: 81,942,780 (GRCm39) |
V1538E |
probably damaging |
Het |
Ank1 |
T |
C |
8: 23,631,253 (GRCm39) |
V1833A |
probably benign |
Het |
Apc2 |
G |
A |
10: 80,150,733 (GRCm39) |
R1929Q |
probably damaging |
Het |
Asb1 |
A |
G |
1: 91,474,708 (GRCm39) |
I85V |
probably damaging |
Het |
Bco2 |
A |
T |
9: 50,445,938 (GRCm39) |
I486K |
probably damaging |
Het |
Braf |
T |
A |
6: 39,591,084 (GRCm39) |
I792F |
probably damaging |
Het |
Cacng2 |
T |
C |
15: 77,879,399 (GRCm39) |
K308E |
possibly damaging |
Het |
Ccr6 |
G |
T |
17: 8,475,821 (GRCm39) |
R342L |
possibly damaging |
Het |
Cdh16 |
T |
A |
8: 105,341,108 (GRCm39) |
I802F |
probably benign |
Het |
Cftr |
T |
C |
6: 18,313,649 (GRCm39) |
I1291T |
probably damaging |
Het |
CN725425 |
T |
A |
15: 91,120,030 (GRCm39) |
D50E |
possibly damaging |
Het |
Cnga1 |
T |
C |
5: 72,762,170 (GRCm39) |
Y448C |
probably benign |
Het |
Cntnap1 |
T |
C |
11: 101,072,178 (GRCm39) |
I477T |
probably damaging |
Het |
Col18a1 |
G |
A |
10: 76,916,578 (GRCm39) |
Q366* |
probably null |
Het |
Csf3 |
C |
A |
11: 98,592,949 (GRCm39) |
A104D |
probably benign |
Het |
Dmbt1 |
A |
G |
7: 130,660,015 (GRCm39) |
H422R |
unknown |
Het |
Dnah12 |
A |
G |
14: 26,590,871 (GRCm39) |
D3325G |
probably null |
Het |
Dnah17 |
T |
C |
11: 117,963,731 (GRCm39) |
D2514G |
probably damaging |
Het |
Fgf9 |
T |
A |
14: 58,310,680 (GRCm39) |
H56Q |
probably damaging |
Het |
Fgfr3 |
A |
T |
5: 33,892,248 (GRCm39) |
Y689F |
probably damaging |
Het |
Fhip2a |
G |
A |
19: 57,369,710 (GRCm39) |
V418I |
probably benign |
Het |
Gar1 |
A |
T |
3: 129,624,269 (GRCm39) |
D74E |
probably damaging |
Het |
Helq |
T |
C |
5: 100,934,927 (GRCm39) |
K488E |
possibly damaging |
Het |
Hmg20a |
A |
G |
9: 56,381,823 (GRCm39) |
H33R |
possibly damaging |
Het |
Igsf10 |
T |
C |
3: 59,233,624 (GRCm39) |
D1703G |
probably damaging |
Het |
Jph3 |
A |
T |
8: 122,480,377 (GRCm39) |
I352F |
probably benign |
Het |
Kng1 |
T |
C |
16: 22,879,224 (GRCm39) |
F96S |
probably damaging |
Het |
Krtap5-2 |
C |
A |
7: 141,729,029 (GRCm39) |
S217I |
unknown |
Het |
Lamp3 |
T |
C |
16: 19,518,455 (GRCm39) |
S261G |
possibly damaging |
Het |
Macf1 |
A |
G |
4: 123,365,654 (GRCm39) |
F3036L |
probably benign |
Het |
Map4k4 |
G |
A |
1: 40,058,722 (GRCm39) |
R972H |
possibly damaging |
Het |
Mccc1 |
C |
T |
3: 36,030,903 (GRCm39) |
D388N |
probably benign |
Het |
Mcoln1 |
T |
A |
8: 3,557,436 (GRCm39) |
Y147* |
probably null |
Het |
Mei1 |
T |
C |
15: 81,997,129 (GRCm39) |
S622P |
|
Het |
Ms4a5 |
T |
C |
19: 11,254,058 (GRCm39) |
I136M |
possibly damaging |
Het |
Nav3 |
A |
G |
10: 109,605,034 (GRCm39) |
L1013P |
probably damaging |
Het |
Ndrg2 |
T |
C |
14: 52,146,071 (GRCm39) |
N170S |
probably damaging |
Het |
Ndufa12 |
G |
A |
10: 94,035,832 (GRCm39) |
G40D |
probably damaging |
Het |
Ogdhl |
T |
A |
14: 32,059,523 (GRCm39) |
V390E |
probably damaging |
Het |
Or10ak12 |
A |
C |
4: 118,666,999 (GRCm39) |
S21A |
probably benign |
Het |
Or1e26 |
T |
C |
11: 73,479,686 (GRCm39) |
R293G |
probably damaging |
Het |
Or4d10 |
A |
T |
19: 12,051,567 (GRCm39) |
I143K |
possibly damaging |
Het |
Or4f6 |
T |
A |
2: 111,839,124 (GRCm39) |
M136L |
probably benign |
Het |
Or8g37 |
A |
T |
9: 39,731,801 (GRCm39) |
I289F |
possibly damaging |
Het |
Osgin1 |
A |
G |
8: 120,172,247 (GRCm39) |
D347G |
possibly damaging |
Het |
Oxct2a |
A |
T |
4: 123,216,687 (GRCm39) |
N231K |
probably damaging |
Het |
Pak6 |
C |
T |
2: 118,520,243 (GRCm39) |
T78M |
probably benign |
Het |
Pde4dip |
T |
C |
3: 97,649,841 (GRCm39) |
Y1006C |
probably damaging |
Het |
Psg18 |
A |
G |
7: 18,084,880 (GRCm39) |
I193T |
probably benign |
Het |
Psmd2 |
C |
A |
16: 20,479,173 (GRCm39) |
H677Q |
probably benign |
Het |
Resf1 |
T |
A |
6: 149,229,766 (GRCm39) |
C937* |
probably null |
Het |
Scaf11 |
C |
T |
15: 96,316,195 (GRCm39) |
R1123H |
probably damaging |
Het |
Setx |
A |
T |
2: 29,051,555 (GRCm39) |
S2036C |
probably damaging |
Het |
Skint6 |
A |
G |
4: 113,093,546 (GRCm39) |
F199S |
probably damaging |
Het |
Slc3a2 |
A |
T |
19: 8,686,594 (GRCm39) |
S367R |
probably damaging |
Het |
Spidr |
T |
C |
16: 15,871,304 (GRCm39) |
D222G |
probably damaging |
Het |
Styxl1 |
T |
C |
5: 135,799,190 (GRCm39) |
E8G |
probably null |
Het |
Syk |
A |
C |
13: 52,778,808 (GRCm39) |
K298T |
probably benign |
Het |
Tcp11 |
T |
A |
17: 28,286,028 (GRCm39) |
Q529L |
possibly damaging |
Het |
Tgfbi |
A |
G |
13: 56,762,100 (GRCm39) |
Y61C |
probably damaging |
Het |
Tlr9 |
G |
A |
9: 106,100,721 (GRCm39) |
R4H |
probably benign |
Het |
Top2a |
A |
C |
11: 98,914,883 (GRCm39) |
S4A |
probably benign |
Het |
Ttc4 |
G |
T |
4: 106,528,919 (GRCm39) |
H166N |
probably benign |
Het |
Ube2o |
C |
A |
11: 116,435,639 (GRCm39) |
R383L |
possibly damaging |
Het |
Umod |
A |
G |
7: 119,076,517 (GRCm39) |
V83A |
possibly damaging |
Het |
|
Other mutations in Sycp2l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
PIT4531001:Sycp2l
|
UTSW |
13 |
41,300,148 (GRCm39) |
missense |
probably null |
0.00 |
R0016:Sycp2l
|
UTSW |
13 |
41,310,976 (GRCm39) |
intron |
probably benign |
|
R0024:Sycp2l
|
UTSW |
13 |
41,295,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R0024:Sycp2l
|
UTSW |
13 |
41,295,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R0099:Sycp2l
|
UTSW |
13 |
41,283,001 (GRCm39) |
splice site |
probably benign |
|
R0471:Sycp2l
|
UTSW |
13 |
41,304,006 (GRCm39) |
splice site |
probably null |
|
R0582:Sycp2l
|
UTSW |
13 |
41,291,431 (GRCm39) |
splice site |
probably benign |
|
R0605:Sycp2l
|
UTSW |
13 |
41,296,942 (GRCm39) |
missense |
probably benign |
0.22 |
R1311:Sycp2l
|
UTSW |
13 |
41,288,661 (GRCm39) |
nonsense |
probably null |
|
R1999:Sycp2l
|
UTSW |
13 |
41,271,780 (GRCm39) |
missense |
probably benign |
0.11 |
R3115:Sycp2l
|
UTSW |
13 |
41,302,274 (GRCm39) |
missense |
probably benign |
0.41 |
R3977:Sycp2l
|
UTSW |
13 |
41,295,440 (GRCm39) |
missense |
probably damaging |
0.99 |
R3979:Sycp2l
|
UTSW |
13 |
41,295,440 (GRCm39) |
missense |
probably damaging |
0.99 |
R4643:Sycp2l
|
UTSW |
13 |
41,296,941 (GRCm39) |
missense |
probably benign |
0.01 |
R5027:Sycp2l
|
UTSW |
13 |
41,283,247 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5037:Sycp2l
|
UTSW |
13 |
41,283,337 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5780:Sycp2l
|
UTSW |
13 |
41,282,976 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6216:Sycp2l
|
UTSW |
13 |
41,295,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R7035:Sycp2l
|
UTSW |
13 |
41,310,973 (GRCm39) |
missense |
unknown |
|
R7179:Sycp2l
|
UTSW |
13 |
41,283,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7267:Sycp2l
|
UTSW |
13 |
41,300,070 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7470:Sycp2l
|
UTSW |
13 |
41,316,580 (GRCm39) |
missense |
probably benign |
0.01 |
R7593:Sycp2l
|
UTSW |
13 |
41,326,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R8030:Sycp2l
|
UTSW |
13 |
41,326,146 (GRCm39) |
missense |
not run |
|
R8218:Sycp2l
|
UTSW |
13 |
41,271,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R8303:Sycp2l
|
UTSW |
13 |
41,283,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R8503:Sycp2l
|
UTSW |
13 |
41,306,952 (GRCm39) |
missense |
|
|
R8504:Sycp2l
|
UTSW |
13 |
41,291,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R8942:Sycp2l
|
UTSW |
13 |
41,277,522 (GRCm39) |
critical splice donor site |
probably null |
|
R9096:Sycp2l
|
UTSW |
13 |
41,300,070 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9097:Sycp2l
|
UTSW |
13 |
41,300,070 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9653:Sycp2l
|
UTSW |
13 |
41,295,381 (GRCm39) |
missense |
probably benign |
0.01 |
R9713:Sycp2l
|
UTSW |
13 |
41,326,183 (GRCm39) |
missense |
probably damaging |
0.99 |
R9729:Sycp2l
|
UTSW |
13 |
41,326,132 (GRCm39) |
missense |
|
|
R9763:Sycp2l
|
UTSW |
13 |
41,306,232 (GRCm39) |
missense |
|
|
Z1177:Sycp2l
|
UTSW |
13 |
41,300,058 (GRCm39) |
missense |
possibly damaging |
0.84 |
Z1177:Sycp2l
|
UTSW |
13 |
41,267,840 (GRCm39) |
unclassified |
probably benign |
|
|