Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg5 |
G |
A |
17: 84,976,425 (GRCm39) |
H471Y |
probably damaging |
Het |
Adam3 |
A |
G |
8: 25,213,517 (GRCm39) |
L61P |
probably damaging |
Het |
Ank2 |
T |
A |
3: 126,733,744 (GRCm39) |
D622V |
probably damaging |
Het |
Antxr2 |
G |
A |
5: 98,151,973 (GRCm39) |
S166F |
probably damaging |
Het |
Asph |
C |
T |
4: 9,474,928 (GRCm39) |
G682D |
possibly damaging |
Het |
Asz1 |
T |
C |
6: 18,054,561 (GRCm39) |
E414G |
probably benign |
Het |
Cabp2 |
G |
A |
19: 4,135,597 (GRCm39) |
D96N |
probably damaging |
Het |
Cc2d2a |
T |
A |
5: 43,860,563 (GRCm39) |
D546E |
probably benign |
Het |
Cdca2 |
T |
A |
14: 67,917,762 (GRCm39) |
R545S |
probably benign |
Het |
Chrna7 |
G |
A |
7: 62,757,357 (GRCm39) |
Q181* |
probably null |
Het |
Cib1 |
T |
C |
7: 79,877,751 (GRCm39) |
D182G |
probably damaging |
Het |
Cib4 |
T |
C |
5: 30,655,477 (GRCm39) |
H76R |
probably benign |
Het |
Cop1 |
T |
G |
1: 159,067,187 (GRCm39) |
F157V |
probably damaging |
Het |
Cspg4b |
C |
T |
13: 113,505,374 (GRCm39) |
P2168S |
|
Het |
Dap3 |
T |
A |
3: 88,837,861 (GRCm39) |
T130S |
probably benign |
Het |
Ddb2 |
T |
A |
2: 91,064,593 (GRCm39) |
K106* |
probably null |
Het |
Derl3 |
G |
A |
10: 75,730,443 (GRCm39) |
V169I |
probably benign |
Het |
Dusp6 |
T |
A |
10: 99,102,074 (GRCm39) |
C353* |
probably null |
Het |
Efcab3 |
A |
T |
11: 104,736,360 (GRCm39) |
D2110V |
probably damaging |
Het |
Fry |
A |
G |
5: 150,269,525 (GRCm39) |
N217S |
probably damaging |
Het |
Gabrb2 |
A |
G |
11: 42,482,693 (GRCm39) |
T184A |
probably damaging |
Het |
Gfpt1 |
G |
A |
6: 87,053,248 (GRCm39) |
V403I |
probably benign |
Het |
Gm7276 |
A |
G |
18: 77,273,147 (GRCm39) |
S196P |
unknown |
Het |
Grik1 |
T |
A |
16: 87,852,956 (GRCm39) |
T76S |
|
Het |
Hrnr |
A |
G |
3: 93,238,863 (GRCm39) |
N3034D |
unknown |
Het |
Kmt2c |
T |
C |
5: 25,489,194 (GRCm39) |
T4582A |
possibly damaging |
Het |
Mroh9 |
T |
C |
1: 162,875,412 (GRCm39) |
I496V |
probably benign |
Het |
Muc3a |
A |
G |
5: 137,245,210 (GRCm39) |
L115P |
probably damaging |
Het |
Nfe2 |
A |
G |
15: 103,157,871 (GRCm39) |
L40P |
probably damaging |
Het |
Nipsnap3b |
A |
T |
4: 53,021,177 (GRCm39) |
D216V |
probably damaging |
Het |
Or5d14 |
C |
T |
2: 87,880,294 (GRCm39) |
V225M |
probably damaging |
Het |
Or8b49 |
T |
A |
9: 38,506,108 (GRCm39) |
I197K |
probably damaging |
Het |
Otx1 |
G |
A |
11: 21,949,458 (GRCm39) |
Q7* |
probably null |
Het |
Piezo2 |
A |
G |
18: 63,178,589 (GRCm39) |
I1776T |
probably benign |
Het |
Pira12 |
T |
A |
7: 3,900,021 (GRCm39) |
I194L |
possibly damaging |
Het |
Ppp1r37 |
T |
C |
7: 19,269,014 (GRCm39) |
D162G |
probably benign |
Het |
Ppp4c |
T |
A |
7: 126,386,739 (GRCm39) |
E116V |
probably damaging |
Het |
Pramel17 |
A |
G |
4: 101,694,073 (GRCm39) |
V270A |
probably benign |
Het |
Prorp |
A |
T |
12: 55,355,611 (GRCm39) |
D372V |
possibly damaging |
Het |
Psme2 |
T |
A |
14: 55,828,302 (GRCm39) |
K15N |
possibly damaging |
Het |
Retreg1 |
C |
T |
15: 25,968,618 (GRCm39) |
R125C |
probably damaging |
Het |
Rgs16 |
A |
G |
1: 153,617,874 (GRCm39) |
E128G |
probably null |
Het |
Rnf145 |
G |
T |
11: 44,450,819 (GRCm39) |
R381L |
probably damaging |
Het |
Rnf2 |
T |
C |
1: 151,347,433 (GRCm39) |
K289E |
probably benign |
Het |
Rsf1 |
CG |
CGACGGCGGGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,669,292 (GRCm39) |
V3504A |
probably benign |
Het |
Selp |
T |
A |
1: 163,951,356 (GRCm39) |
I30N |
probably benign |
Het |
Serpinb5 |
C |
T |
1: 106,798,137 (GRCm39) |
A42V |
probably benign |
Het |
Sfpq |
G |
A |
4: 126,915,633 (GRCm39) |
G142S |
unknown |
Het |
Sh2d1b2 |
T |
C |
1: 170,075,751 (GRCm39) |
Y62H |
possibly damaging |
Het |
Sipa1l3 |
C |
T |
7: 29,086,656 (GRCm39) |
E645K |
probably damaging |
Het |
Slc22a1 |
T |
A |
17: 12,878,598 (GRCm39) |
T372S |
probably benign |
Het |
Smarca2 |
T |
A |
19: 26,693,583 (GRCm39) |
D1262E |
possibly damaging |
Het |
Speer4a3 |
T |
C |
5: 26,156,596 (GRCm39) |
M128V |
possibly damaging |
Het |
Sptbn2 |
A |
T |
19: 4,784,241 (GRCm39) |
Q661L |
probably benign |
Het |
Tarbp1 |
G |
T |
8: 127,174,202 (GRCm39) |
T868K |
possibly damaging |
Het |
Tnfrsf8 |
A |
G |
4: 145,023,531 (GRCm39) |
S101P |
probably damaging |
Het |
Tnfsf10 |
A |
C |
3: 27,380,028 (GRCm39) |
|
probably benign |
Het |
Tsc2 |
C |
T |
17: 24,823,802 (GRCm39) |
R1001K |
probably null |
Het |
Unc80 |
T |
A |
1: 66,718,740 (GRCm39) |
S2988T |
probably benign |
Het |
Vmn1r195 |
A |
G |
13: 22,463,335 (GRCm39) |
I268M |
possibly damaging |
Het |
Vmn1r27 |
G |
A |
6: 58,192,416 (GRCm39) |
T196I |
probably benign |
Het |
Vmn2r80 |
T |
A |
10: 78,984,760 (GRCm39) |
D37E |
probably benign |
Het |
Vmn2r9 |
A |
T |
5: 108,996,047 (GRCm39) |
H200Q |
|
Het |
Washc5 |
T |
C |
15: 59,209,134 (GRCm39) |
Y1030C |
probably damaging |
Het |
Wdr47 |
T |
C |
3: 108,526,106 (GRCm39) |
F210L |
probably damaging |
Het |
|
Other mutations in Wscd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Wscd2
|
APN |
5 |
113,689,236 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01113:Wscd2
|
APN |
5 |
113,708,800 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01476:Wscd2
|
APN |
5 |
113,710,382 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01894:Wscd2
|
APN |
5 |
113,710,357 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02560:Wscd2
|
APN |
5 |
113,699,045 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02755:Wscd2
|
APN |
5 |
113,712,092 (GRCm39) |
missense |
possibly damaging |
0.66 |
froggie
|
UTSW |
5 |
113,726,206 (GRCm39) |
makesense |
probably null |
|
R0381:Wscd2
|
UTSW |
5 |
113,689,192 (GRCm39) |
missense |
probably damaging |
0.96 |
R1144:Wscd2
|
UTSW |
5 |
113,699,151 (GRCm39) |
splice site |
probably null |
|
R1858:Wscd2
|
UTSW |
5 |
113,689,231 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3695:Wscd2
|
UTSW |
5 |
113,689,078 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4231:Wscd2
|
UTSW |
5 |
113,699,045 (GRCm39) |
missense |
probably benign |
0.00 |
R4232:Wscd2
|
UTSW |
5 |
113,699,045 (GRCm39) |
missense |
probably benign |
0.00 |
R4667:Wscd2
|
UTSW |
5 |
113,715,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R4696:Wscd2
|
UTSW |
5 |
113,689,240 (GRCm39) |
missense |
probably benign |
|
R5727:Wscd2
|
UTSW |
5 |
113,715,411 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6401:Wscd2
|
UTSW |
5 |
113,726,206 (GRCm39) |
makesense |
probably null |
|
R7413:Wscd2
|
UTSW |
5 |
113,715,402 (GRCm39) |
missense |
probably benign |
0.02 |
R7642:Wscd2
|
UTSW |
5 |
113,715,475 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7837:Wscd2
|
UTSW |
5 |
113,710,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R8046:Wscd2
|
UTSW |
5 |
113,689,176 (GRCm39) |
missense |
probably benign |
0.05 |
R8331:Wscd2
|
UTSW |
5 |
113,688,996 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R8348:Wscd2
|
UTSW |
5 |
113,710,371 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8680:Wscd2
|
UTSW |
5 |
113,712,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Wscd2
|
UTSW |
5 |
113,715,401 (GRCm39) |
missense |
possibly damaging |
0.90 |
|