Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
A |
G |
6: 142,540,448 (GRCm39) |
V1497A |
possibly damaging |
Het |
Adam15 |
T |
C |
3: 89,255,817 (GRCm39) |
|
probably benign |
Het |
Angel2 |
T |
A |
1: 190,674,360 (GRCm39) |
S371T |
probably benign |
Het |
Atr |
T |
A |
9: 95,743,509 (GRCm39) |
N49K |
probably benign |
Het |
Bace2 |
G |
A |
16: 97,213,335 (GRCm39) |
M228I |
probably damaging |
Het |
Bdp1 |
A |
C |
13: 100,163,941 (GRCm39) |
|
probably null |
Het |
Calr |
A |
T |
8: 85,570,748 (GRCm39) |
D302E |
probably benign |
Het |
Camta1 |
T |
C |
4: 151,164,228 (GRCm39) |
D340G |
probably benign |
Het |
Car11 |
C |
T |
7: 45,352,949 (GRCm39) |
T236I |
possibly damaging |
Het |
Cfap69 |
A |
T |
5: 5,636,409 (GRCm39) |
S275T |
probably benign |
Het |
Cib2 |
G |
A |
9: 54,455,653 (GRCm39) |
R104W |
probably damaging |
Het |
CN725425 |
T |
C |
15: 91,130,018 (GRCm39) |
S294P |
possibly damaging |
Het |
Coro7 |
G |
A |
16: 4,446,097 (GRCm39) |
S876F |
possibly damaging |
Het |
Cspg4 |
G |
A |
9: 56,804,687 (GRCm39) |
V1833M |
probably damaging |
Het |
Dennd6b |
C |
A |
15: 89,069,540 (GRCm39) |
|
probably benign |
Het |
Dhx30 |
A |
T |
9: 109,914,341 (GRCm39) |
Y979N |
possibly damaging |
Het |
Dnaaf9 |
G |
A |
2: 130,554,299 (GRCm39) |
P187S |
probably damaging |
Het |
Dnah8 |
A |
T |
17: 30,944,098 (GRCm39) |
I1772F |
probably damaging |
Het |
Dync2h1 |
A |
T |
9: 6,993,942 (GRCm39) |
I3976N |
possibly damaging |
Het |
Ebi3 |
T |
C |
17: 56,261,479 (GRCm39) |
I125T |
probably damaging |
Het |
Elfn2 |
C |
T |
15: 78,556,568 (GRCm39) |
A660T |
probably benign |
Het |
F12 |
C |
T |
13: 55,569,346 (GRCm39) |
C209Y |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fgfr2 |
T |
A |
7: 129,782,187 (GRCm39) |
D413V |
probably damaging |
Het |
Gdf10 |
T |
A |
14: 33,654,000 (GRCm39) |
I169N |
possibly damaging |
Het |
Gdnf |
T |
C |
15: 7,845,130 (GRCm39) |
V41A |
probably benign |
Het |
Gm9857 |
A |
T |
3: 108,847,478 (GRCm39) |
|
probably benign |
Het |
Gpatch11 |
A |
G |
17: 79,146,529 (GRCm39) |
E58G |
possibly damaging |
Het |
Gpr55 |
A |
G |
1: 85,869,137 (GRCm39) |
V148A |
possibly damaging |
Het |
Gucy1b1 |
A |
G |
3: 81,952,767 (GRCm39) |
I222T |
probably benign |
Het |
Hnf4a |
T |
C |
2: 163,404,496 (GRCm39) |
S227P |
probably damaging |
Het |
Hsfy2 |
A |
G |
1: 56,675,548 (GRCm39) |
S330P |
possibly damaging |
Het |
Hycc1 |
T |
A |
5: 24,204,989 (GRCm39) |
M1L |
possibly damaging |
Het |
Ift122 |
T |
C |
6: 115,900,844 (GRCm39) |
V1054A |
probably benign |
Het |
Il27 |
T |
A |
7: 126,188,647 (GRCm39) |
E175D |
probably benign |
Het |
Lactb2 |
A |
T |
1: 13,730,641 (GRCm39) |
S12T |
probably damaging |
Het |
Lrfn2 |
T |
C |
17: 49,403,605 (GRCm39) |
V576A |
probably benign |
Het |
Mansc4 |
C |
G |
6: 146,976,689 (GRCm39) |
R309T |
possibly damaging |
Het |
Med12l |
AACAGCA |
AACAGCAACAGCA |
3: 59,183,379 (GRCm39) |
|
probably benign |
Het |
Mrpl16 |
C |
T |
19: 11,751,959 (GRCm39) |
R240* |
probably null |
Het |
Muc17 |
A |
G |
5: 137,172,843 (GRCm39) |
V70A |
probably benign |
Het |
Ndnf |
A |
G |
6: 65,680,054 (GRCm39) |
D111G |
probably benign |
Het |
Nek4 |
T |
C |
14: 30,704,384 (GRCm39) |
F688S |
probably damaging |
Het |
Nkx2-6 |
T |
A |
14: 69,412,126 (GRCm39) |
M98K |
probably benign |
Het |
Nup188 |
T |
C |
2: 30,230,667 (GRCm39) |
S1402P |
probably benign |
Het |
Or10j2 |
T |
A |
1: 173,098,467 (GRCm39) |
S242T |
probably damaging |
Het |
Or2t48 |
A |
T |
11: 58,420,237 (GRCm39) |
S192T |
probably damaging |
Het |
Or4f14b |
C |
T |
2: 111,775,264 (GRCm39) |
C179Y |
probably damaging |
Het |
Or52i2 |
A |
G |
7: 102,319,609 (GRCm39) |
T161A |
possibly damaging |
Het |
Or5ac23 |
A |
T |
16: 59,149,607 (GRCm39) |
N88K |
probably benign |
Het |
Or5ac24 |
T |
C |
16: 59,165,790 (GRCm39) |
I91M |
possibly damaging |
Het |
Or5m9b |
T |
A |
2: 85,905,594 (GRCm39) |
V170D |
probably benign |
Het |
Parp10 |
A |
T |
15: 76,126,270 (GRCm39) |
V306E |
probably benign |
Het |
Pcnx3 |
A |
G |
19: 5,723,343 (GRCm39) |
L1284P |
probably damaging |
Het |
Pld1 |
A |
T |
3: 28,103,389 (GRCm39) |
I365F |
probably benign |
Het |
Pnisr |
A |
G |
4: 21,865,893 (GRCm39) |
D294G |
probably damaging |
Het |
Pogz |
C |
T |
3: 94,786,160 (GRCm39) |
T863I |
probably benign |
Het |
Ptprn2 |
A |
C |
12: 116,685,792 (GRCm39) |
T84P |
possibly damaging |
Het |
Rln1 |
C |
T |
19: 29,309,468 (GRCm39) |
E104K |
possibly damaging |
Het |
Rnf38 |
A |
G |
4: 44,138,681 (GRCm39) |
S271P |
probably damaging |
Het |
Rngtt |
A |
G |
4: 33,368,660 (GRCm39) |
T398A |
probably benign |
Het |
Rprd2 |
G |
T |
3: 95,672,115 (GRCm39) |
T1096K |
probably damaging |
Het |
Sema5a |
T |
A |
15: 32,548,945 (GRCm39) |
C140S |
probably damaging |
Het |
Shpk |
A |
C |
11: 73,113,757 (GRCm39) |
D390A |
probably benign |
Het |
Slc22a20 |
C |
T |
19: 6,022,876 (GRCm39) |
|
probably benign |
Het |
Steap2 |
A |
G |
5: 5,727,393 (GRCm39) |
V314A |
possibly damaging |
Het |
Stxbp5l |
A |
G |
16: 37,111,289 (GRCm39) |
|
probably null |
Het |
Tgm3 |
G |
T |
2: 129,883,688 (GRCm39) |
E449* |
probably null |
Het |
Tmem68 |
A |
C |
4: 3,560,627 (GRCm39) |
L186V |
probably damaging |
Het |
Ttc41 |
T |
A |
10: 86,612,116 (GRCm39) |
W1130R |
possibly damaging |
Het |
Ttpal |
T |
C |
2: 163,457,286 (GRCm39) |
F253L |
possibly damaging |
Het |
Vmn2r99 |
G |
T |
17: 19,582,514 (GRCm39) |
V40F |
probably benign |
Het |
Xkr9 |
G |
A |
1: 13,771,167 (GRCm39) |
V228M |
probably damaging |
Het |
Zc3h7b |
C |
T |
15: 81,661,268 (GRCm39) |
A369V |
probably benign |
Het |
|
Other mutations in Sema3e |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00503:Sema3e
|
APN |
5 |
14,290,586 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01068:Sema3e
|
APN |
5 |
14,283,732 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01128:Sema3e
|
APN |
5 |
14,282,129 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01134:Sema3e
|
APN |
5 |
14,302,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02013:Sema3e
|
APN |
5 |
14,280,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02051:Sema3e
|
APN |
5 |
14,274,324 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02309:Sema3e
|
APN |
5 |
14,274,404 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02636:Sema3e
|
APN |
5 |
14,275,670 (GRCm39) |
missense |
probably benign |
|
IGL02702:Sema3e
|
APN |
5 |
14,283,740 (GRCm39) |
splice site |
probably benign |
|
IGL03001:Sema3e
|
APN |
5 |
14,291,057 (GRCm39) |
missense |
probably benign |
0.19 |
R0011:Sema3e
|
UTSW |
5 |
14,194,025 (GRCm39) |
nonsense |
probably null |
|
R0098:Sema3e
|
UTSW |
5 |
14,302,446 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0098:Sema3e
|
UTSW |
5 |
14,302,446 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0220:Sema3e
|
UTSW |
5 |
14,214,167 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0564:Sema3e
|
UTSW |
5 |
14,286,099 (GRCm39) |
critical splice donor site |
probably null |
|
R1079:Sema3e
|
UTSW |
5 |
14,275,669 (GRCm39) |
missense |
probably benign |
0.12 |
R1187:Sema3e
|
UTSW |
5 |
14,282,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1736:Sema3e
|
UTSW |
5 |
14,260,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R3433:Sema3e
|
UTSW |
5 |
14,302,728 (GRCm39) |
missense |
probably benign |
0.00 |
R3831:Sema3e
|
UTSW |
5 |
14,276,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4094:Sema3e
|
UTSW |
5 |
14,283,704 (GRCm39) |
missense |
probably benign |
0.12 |
R4580:Sema3e
|
UTSW |
5 |
14,283,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Sema3e
|
UTSW |
5 |
14,276,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R4855:Sema3e
|
UTSW |
5 |
14,280,144 (GRCm39) |
missense |
probably damaging |
0.99 |
R4884:Sema3e
|
UTSW |
5 |
14,275,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R4960:Sema3e
|
UTSW |
5 |
14,302,646 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5264:Sema3e
|
UTSW |
5 |
14,276,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R5389:Sema3e
|
UTSW |
5 |
14,286,099 (GRCm39) |
critical splice donor site |
probably benign |
|
R5512:Sema3e
|
UTSW |
5 |
14,280,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R5642:Sema3e
|
UTSW |
5 |
14,212,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R5647:Sema3e
|
UTSW |
5 |
14,275,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R5814:Sema3e
|
UTSW |
5 |
14,275,680 (GRCm39) |
missense |
probably benign |
0.01 |
R5993:Sema3e
|
UTSW |
5 |
14,274,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R6076:Sema3e
|
UTSW |
5 |
14,291,100 (GRCm39) |
missense |
probably benign |
0.01 |
R6906:Sema3e
|
UTSW |
5 |
14,290,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R7432:Sema3e
|
UTSW |
5 |
14,274,404 (GRCm39) |
missense |
probably damaging |
0.98 |
R8738:Sema3e
|
UTSW |
5 |
14,214,169 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8849:Sema3e
|
UTSW |
5 |
14,302,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R8879:Sema3e
|
UTSW |
5 |
14,282,108 (GRCm39) |
missense |
probably benign |
0.16 |
R8935:Sema3e
|
UTSW |
5 |
14,282,127 (GRCm39) |
missense |
probably damaging |
0.97 |
R9071:Sema3e
|
UTSW |
5 |
14,282,154 (GRCm39) |
missense |
probably benign |
0.00 |
R9100:Sema3e
|
UTSW |
5 |
14,282,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R9367:Sema3e
|
UTSW |
5 |
14,291,084 (GRCm39) |
missense |
probably benign |
0.00 |
R9444:Sema3e
|
UTSW |
5 |
14,302,625 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9478:Sema3e
|
UTSW |
5 |
14,286,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R9601:Sema3e
|
UTSW |
5 |
14,302,397 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9671:Sema3e
|
UTSW |
5 |
14,212,217 (GRCm39) |
missense |
probably benign |
0.00 |
X0064:Sema3e
|
UTSW |
5 |
14,280,156 (GRCm39) |
missense |
probably benign |
0.05 |
Z1088:Sema3e
|
UTSW |
5 |
14,276,470 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Sema3e
|
UTSW |
5 |
14,075,725 (GRCm39) |
start gained |
probably benign |
|
|