Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
T |
13: 77,451,573 (GRCm39) |
I886F |
possibly damaging |
Het |
3100002H09Rik |
A |
G |
4: 124,504,151 (GRCm39) |
S134P |
unknown |
Het |
Abcf2 |
A |
G |
5: 24,770,940 (GRCm39) |
L604P |
possibly damaging |
Het |
Arih2 |
C |
G |
9: 108,488,938 (GRCm39) |
R260P |
probably damaging |
Het |
Atg14 |
G |
T |
14: 47,783,138 (GRCm39) |
H373Q |
probably damaging |
Het |
Atmin |
C |
T |
8: 117,681,537 (GRCm39) |
H179Y |
probably damaging |
Het |
Catsperg1 |
G |
T |
7: 28,897,777 (GRCm39) |
P197T |
possibly damaging |
Het |
Ccdc7b |
C |
T |
8: 129,837,473 (GRCm39) |
Q155* |
probably null |
Het |
Cep85l |
T |
G |
10: 53,224,875 (GRCm39) |
E238A |
possibly damaging |
Het |
Cfap119 |
T |
C |
7: 127,184,087 (GRCm39) |
|
probably null |
Het |
Cntln |
G |
A |
4: 84,897,630 (GRCm39) |
V406I |
probably benign |
Het |
Csf2rb2 |
C |
A |
15: 78,168,965 (GRCm39) |
G730V |
probably benign |
Het |
Cyp3a59 |
T |
A |
5: 146,034,997 (GRCm39) |
L225Q |
probably damaging |
Het |
Dock1 |
T |
A |
7: 134,367,962 (GRCm39) |
F511I |
probably damaging |
Het |
Dsg1b |
A |
T |
18: 20,531,008 (GRCm39) |
Y453F |
|
Het |
Dync1h1 |
T |
C |
12: 110,625,137 (GRCm39) |
F3829L |
probably benign |
Het |
Epha8 |
G |
T |
4: 136,665,897 (GRCm39) |
L420M |
probably damaging |
Het |
Esco2 |
C |
A |
14: 66,068,657 (GRCm39) |
G218* |
probably null |
Het |
Gale |
C |
T |
4: 135,692,574 (GRCm39) |
|
probably benign |
Het |
Grid1 |
G |
A |
14: 35,043,664 (GRCm39) |
D340N |
probably damaging |
Het |
Hgf |
A |
G |
5: 16,766,029 (GRCm39) |
D55G |
possibly damaging |
Het |
Inha |
A |
G |
1: 75,486,562 (GRCm39) |
S286G |
probably benign |
Het |
Kif1b |
C |
T |
4: 149,345,616 (GRCm39) |
|
probably null |
Het |
Klhl24 |
T |
G |
16: 19,941,763 (GRCm39) |
S570R |
possibly damaging |
Het |
Krt87 |
G |
A |
15: 101,385,449 (GRCm39) |
R308W |
probably benign |
Het |
Lama2 |
T |
A |
10: 26,891,478 (GRCm39) |
E2545V |
probably damaging |
Het |
Lztfl1 |
T |
C |
9: 123,537,167 (GRCm39) |
K165E |
possibly damaging |
Het |
Mab21l3 |
A |
T |
3: 101,725,987 (GRCm39) |
D336E |
probably damaging |
Het |
Matn2 |
T |
C |
15: 34,345,242 (GRCm39) |
I83T |
probably damaging |
Het |
Mfsd9 |
T |
C |
1: 40,812,941 (GRCm39) |
D458G |
probably benign |
Het |
Ncbp3 |
A |
G |
11: 72,968,768 (GRCm39) |
D513G |
probably damaging |
Het |
Neb |
T |
A |
2: 52,078,788 (GRCm39) |
K5818N |
probably benign |
Het |
Nol4 |
G |
A |
18: 23,053,934 (GRCm39) |
P120S |
probably damaging |
Het |
Oit3 |
C |
A |
10: 59,274,464 (GRCm39) |
C112F |
probably damaging |
Het |
Or11g27 |
A |
T |
14: 50,771,051 (GRCm39) |
T61S |
probably benign |
Het |
Or4b1 |
C |
A |
2: 89,979,595 (GRCm39) |
A252S |
possibly damaging |
Het |
Or5p52 |
G |
A |
7: 107,502,238 (GRCm39) |
V105M |
probably damaging |
Het |
Or6c6 |
T |
A |
10: 129,186,960 (GRCm39) |
M176K |
possibly damaging |
Het |
Pank4 |
G |
A |
4: 155,064,565 (GRCm39) |
R708Q |
probably benign |
Het |
Plch1 |
T |
A |
3: 63,606,825 (GRCm39) |
L1026F |
probably benign |
Het |
Poglut3 |
T |
C |
9: 53,303,236 (GRCm39) |
F232L |
probably damaging |
Het |
Ptpn3 |
A |
T |
4: 57,197,573 (GRCm39) |
I772N |
probably damaging |
Het |
Purb |
A |
G |
11: 6,425,424 (GRCm39) |
F155L |
probably damaging |
Het |
Rcor2 |
C |
T |
19: 7,248,794 (GRCm39) |
R256W |
probably damaging |
Het |
Rp1 |
A |
G |
1: 4,417,545 (GRCm39) |
L1189P |
probably benign |
Het |
Scn1a |
T |
C |
2: 66,156,493 (GRCm39) |
E472G |
probably benign |
Het |
Sema3e |
T |
C |
5: 14,286,386 (GRCm39) |
Y536H |
probably damaging |
Het |
Serpina3n |
A |
T |
12: 104,378,672 (GRCm39) |
I331F |
possibly damaging |
Het |
Sertad3 |
T |
C |
7: 27,175,679 (GRCm39) |
S38P |
probably damaging |
Het |
Sfrp4 |
G |
T |
13: 19,807,610 (GRCm39) |
R3L |
unknown |
Het |
Slc35a5 |
T |
C |
16: 44,964,426 (GRCm39) |
E269G |
probably damaging |
Het |
Snrnp200 |
G |
A |
2: 127,076,993 (GRCm39) |
|
probably null |
Het |
Sumo1 |
A |
G |
1: 59,694,615 (GRCm39) |
|
probably null |
Het |
Syne2 |
A |
G |
12: 76,154,387 (GRCm39) |
K2020E |
probably damaging |
Het |
Tcp10a |
A |
T |
17: 7,601,740 (GRCm39) |
T247S |
probably benign |
Het |
Tgds |
T |
C |
14: 118,352,544 (GRCm39) |
D290G |
possibly damaging |
Het |
Trav7d-3 |
A |
T |
14: 52,982,054 (GRCm39) |
I32F |
possibly damaging |
Het |
Vps41 |
A |
G |
13: 19,046,913 (GRCm39) |
N788D |
|
Het |
Zfp521 |
G |
A |
18: 13,950,372 (GRCm39) |
T1194I |
probably damaging |
Het |
Zmynd8 |
C |
A |
2: 165,649,569 (GRCm39) |
K841N |
probably damaging |
Het |
|
Other mutations in Il17ra |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01367:Il17ra
|
APN |
6 |
120,458,426 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01413:Il17ra
|
APN |
6 |
120,452,542 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01418:Il17ra
|
APN |
6 |
120,452,542 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03215:Il17ra
|
APN |
6 |
120,449,075 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03047:Il17ra
|
UTSW |
6 |
120,458,187 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4305001:Il17ra
|
UTSW |
6 |
120,458,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R0042:Il17ra
|
UTSW |
6 |
120,449,086 (GRCm39) |
splice site |
probably benign |
|
R0042:Il17ra
|
UTSW |
6 |
120,449,086 (GRCm39) |
splice site |
probably benign |
|
R0365:Il17ra
|
UTSW |
6 |
120,455,410 (GRCm39) |
missense |
probably benign |
0.03 |
R0391:Il17ra
|
UTSW |
6 |
120,453,940 (GRCm39) |
splice site |
probably benign |
|
R0470:Il17ra
|
UTSW |
6 |
120,458,767 (GRCm39) |
missense |
probably benign |
0.01 |
R0599:Il17ra
|
UTSW |
6 |
120,458,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R1525:Il17ra
|
UTSW |
6 |
120,450,751 (GRCm39) |
missense |
probably damaging |
0.98 |
R1900:Il17ra
|
UTSW |
6 |
120,454,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1972:Il17ra
|
UTSW |
6 |
120,459,177 (GRCm39) |
missense |
probably benign |
0.01 |
R4192:Il17ra
|
UTSW |
6 |
120,458,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R4923:Il17ra
|
UTSW |
6 |
120,454,406 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5009:Il17ra
|
UTSW |
6 |
120,459,168 (GRCm39) |
missense |
probably benign |
0.00 |
R5133:Il17ra
|
UTSW |
6 |
120,458,514 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5411:Il17ra
|
UTSW |
6 |
120,458,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R5548:Il17ra
|
UTSW |
6 |
120,455,434 (GRCm39) |
missense |
probably benign |
0.23 |
R6137:Il17ra
|
UTSW |
6 |
120,452,543 (GRCm39) |
missense |
probably benign |
0.23 |
R6190:Il17ra
|
UTSW |
6 |
120,452,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R7202:Il17ra
|
UTSW |
6 |
120,452,572 (GRCm39) |
missense |
probably benign |
0.01 |
R7300:Il17ra
|
UTSW |
6 |
120,459,063 (GRCm39) |
missense |
probably benign |
0.00 |
R8130:Il17ra
|
UTSW |
6 |
120,455,416 (GRCm39) |
missense |
probably benign |
0.01 |
R8152:Il17ra
|
UTSW |
6 |
120,459,063 (GRCm39) |
missense |
probably benign |
0.00 |
R8213:Il17ra
|
UTSW |
6 |
120,449,995 (GRCm39) |
missense |
probably benign |
0.39 |
R8525:Il17ra
|
UTSW |
6 |
120,451,298 (GRCm39) |
nonsense |
probably null |
|
R8560:Il17ra
|
UTSW |
6 |
120,459,226 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8675:Il17ra
|
UTSW |
6 |
120,458,949 (GRCm39) |
missense |
probably benign |
0.05 |
R8754:Il17ra
|
UTSW |
6 |
120,458,417 (GRCm39) |
missense |
probably benign |
0.09 |
R8956:Il17ra
|
UTSW |
6 |
120,458,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R9419:Il17ra
|
UTSW |
6 |
120,458,255 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9742:Il17ra
|
UTSW |
6 |
120,458,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R9790:Il17ra
|
UTSW |
6 |
120,459,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R9791:Il17ra
|
UTSW |
6 |
120,459,240 (GRCm39) |
missense |
probably damaging |
1.00 |
|