Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110032F04Rik |
T |
A |
3: 68,777,345 (GRCm39) |
I102N |
probably damaging |
Het |
2610008E11Rik |
A |
T |
10: 78,903,406 (GRCm39) |
C303* |
probably null |
Het |
A430033K04Rik |
T |
A |
5: 138,644,547 (GRCm39) |
V144D |
possibly damaging |
Het |
Adamts13 |
T |
A |
2: 26,883,024 (GRCm39) |
M858K |
probably benign |
Het |
Ankrd29 |
T |
C |
18: 12,408,760 (GRCm39) |
|
probably benign |
Het |
Arg1 |
A |
C |
10: 24,796,655 (GRCm39) |
D57E |
probably benign |
Het |
Bend4 |
G |
A |
5: 67,557,415 (GRCm39) |
T467M |
probably damaging |
Het |
C1s1 |
T |
C |
6: 124,517,758 (GRCm39) |
D74G |
probably damaging |
Het |
Cacnb2 |
G |
A |
2: 14,972,773 (GRCm39) |
G227S |
possibly damaging |
Het |
Cbs |
T |
C |
17: 31,844,889 (GRCm39) |
D137G |
probably damaging |
Het |
Ccdc136 |
A |
G |
6: 29,418,070 (GRCm39) |
E846G |
probably damaging |
Het |
Cd6 |
A |
T |
19: 10,776,855 (GRCm39) |
S57T |
probably benign |
Het |
Cep20 |
G |
A |
16: 14,135,222 (GRCm39) |
|
probably benign |
Het |
Col11a2 |
T |
A |
17: 34,273,119 (GRCm39) |
|
probably benign |
Het |
Col7a1 |
T |
C |
9: 108,789,274 (GRCm39) |
S829P |
unknown |
Het |
Ctsj |
T |
C |
13: 61,149,249 (GRCm39) |
Y264C |
probably damaging |
Het |
Dennd3 |
T |
A |
15: 73,429,463 (GRCm39) |
N915K |
probably damaging |
Het |
E2f2 |
A |
T |
4: 135,908,595 (GRCm39) |
|
probably null |
Het |
Eme1 |
T |
C |
11: 94,538,855 (GRCm39) |
T342A |
possibly damaging |
Het |
Epc1 |
A |
T |
18: 6,453,266 (GRCm39) |
|
probably benign |
Het |
Fat1 |
T |
C |
8: 45,405,682 (GRCm39) |
V811A |
possibly damaging |
Het |
Fbxo2 |
A |
G |
4: 148,250,166 (GRCm39) |
E232G |
probably damaging |
Het |
Flnb |
G |
T |
14: 7,817,996 (GRCm38) |
|
probably benign |
Het |
Fmn1 |
A |
C |
2: 113,271,973 (GRCm39) |
N114H |
unknown |
Het |
Foxp2 |
A |
T |
6: 15,286,711 (GRCm39) |
Q67L |
possibly damaging |
Het |
Galntl5 |
A |
T |
5: 25,415,353 (GRCm39) |
I295L |
possibly damaging |
Het |
Gjd4 |
T |
A |
18: 9,280,095 (GRCm39) |
T328S |
probably benign |
Het |
Hint2 |
A |
G |
4: 43,654,952 (GRCm39) |
I59T |
probably damaging |
Het |
Hpn |
C |
T |
7: 30,802,043 (GRCm39) |
R252Q |
probably benign |
Het |
Hspa12a |
T |
G |
19: 58,793,890 (GRCm39) |
T324P |
probably damaging |
Het |
Ighv4-1 |
A |
T |
12: 113,912,000 (GRCm39) |
D84E |
possibly damaging |
Het |
Il1r2 |
T |
A |
1: 40,151,258 (GRCm39) |
I171N |
probably damaging |
Het |
Il31ra |
C |
T |
13: 112,670,276 (GRCm39) |
E371K |
probably benign |
Het |
Klhl24 |
C |
T |
16: 19,936,690 (GRCm39) |
R433C |
probably damaging |
Het |
Klra5 |
C |
T |
6: 129,886,911 (GRCm39) |
C39Y |
probably benign |
Het |
Lypd8l |
T |
A |
11: 58,499,338 (GRCm39) |
D160V |
probably benign |
Het |
Macc1 |
T |
C |
12: 119,414,091 (GRCm39) |
S756P |
possibly damaging |
Het |
Mael |
A |
G |
1: 166,029,259 (GRCm39) |
V388A |
probably benign |
Het |
Mast3 |
A |
G |
8: 71,233,091 (GRCm39) |
S1074P |
probably damaging |
Het |
Med13 |
A |
G |
11: 86,192,297 (GRCm39) |
C823R |
probably benign |
Het |
Megf6 |
A |
G |
4: 154,339,130 (GRCm39) |
T556A |
probably benign |
Het |
Mlip |
A |
G |
9: 77,045,694 (GRCm39) |
F14L |
possibly damaging |
Het |
Moxd2 |
C |
A |
6: 40,860,978 (GRCm39) |
C271F |
probably damaging |
Het |
Myo1e |
A |
T |
9: 70,283,830 (GRCm39) |
D842V |
probably damaging |
Het |
Ndst4 |
C |
T |
3: 125,231,722 (GRCm39) |
A97V |
probably damaging |
Het |
Nherf4 |
A |
G |
9: 44,160,676 (GRCm39) |
C240R |
probably damaging |
Het |
Nos1 |
G |
C |
5: 118,017,402 (GRCm39) |
R255P |
probably benign |
Het |
Nptx2 |
A |
G |
5: 144,492,980 (GRCm39) |
T356A |
probably benign |
Het |
Nup160 |
A |
G |
2: 90,533,489 (GRCm39) |
D646G |
probably damaging |
Het |
Nup98 |
C |
A |
7: 101,788,037 (GRCm39) |
R1011L |
probably benign |
Het |
Nxt2 |
C |
T |
X: 141,020,747 (GRCm39) |
A118V |
possibly damaging |
Het |
Or1j19 |
A |
G |
2: 36,676,938 (GRCm39) |
T134A |
probably benign |
Het |
Or1p1 |
A |
C |
11: 74,180,169 (GRCm39) |
Q232H |
probably damaging |
Het |
Or5c1 |
T |
C |
2: 37,222,017 (GRCm39) |
L86P |
possibly damaging |
Het |
Or7h8 |
T |
A |
9: 20,124,358 (GRCm39) |
F238I |
probably damaging |
Het |
Or8k24 |
A |
G |
2: 86,216,324 (GRCm39) |
V146A |
probably benign |
Het |
Osbp2 |
A |
G |
11: 3,665,143 (GRCm39) |
L67P |
probably damaging |
Het |
Pabpc6 |
C |
T |
17: 9,886,937 (GRCm39) |
S538N |
probably benign |
Het |
Pcdhga1 |
C |
A |
18: 37,796,433 (GRCm39) |
A479D |
possibly damaging |
Het |
Pdgfd |
A |
T |
9: 6,333,328 (GRCm39) |
D172V |
probably benign |
Het |
Pfpl |
A |
T |
19: 12,405,804 (GRCm39) |
E18D |
possibly damaging |
Het |
Plat |
A |
G |
8: 23,268,466 (GRCm39) |
T373A |
probably damaging |
Het |
Plekhg1 |
G |
A |
10: 3,907,527 (GRCm39) |
D870N |
|
Het |
Ppp1r13b |
T |
C |
12: 111,800,268 (GRCm39) |
H626R |
probably benign |
Het |
Ppp6r3 |
A |
T |
19: 3,543,974 (GRCm39) |
V347D |
probably damaging |
Het |
Prr12 |
G |
T |
7: 44,697,242 (GRCm39) |
P891H |
unknown |
Het |
Psg22 |
T |
A |
7: 18,460,682 (GRCm39) |
I437K |
probably benign |
Het |
Ptpra |
T |
A |
2: 30,328,255 (GRCm39) |
M192K |
probably damaging |
Het |
Ptpra |
G |
T |
2: 30,328,256 (GRCm39) |
M192I |
probably benign |
Het |
Ptprj |
G |
A |
2: 90,288,562 (GRCm39) |
S801L |
probably benign |
Het |
Relb |
T |
C |
7: 19,350,276 (GRCm39) |
Y228C |
probably damaging |
Het |
Rfx3 |
A |
T |
19: 27,878,207 (GRCm39) |
V30E |
possibly damaging |
Het |
Rgs2 |
A |
G |
1: 143,877,925 (GRCm39) |
S124P |
probably damaging |
Het |
Rph3a |
T |
C |
5: 121,086,880 (GRCm39) |
N440S |
possibly damaging |
Het |
Ryr2 |
T |
C |
13: 11,900,424 (GRCm39) |
T104A |
probably benign |
Het |
Scn7a |
T |
C |
2: 66,514,507 (GRCm39) |
D1089G |
possibly damaging |
Het |
Sebox |
A |
G |
11: 78,395,222 (GRCm39) |
D188G |
possibly damaging |
Het |
Serpinf2 |
A |
T |
11: 75,323,418 (GRCm39) |
F429L |
probably damaging |
Het |
Six4 |
A |
C |
12: 73,155,681 (GRCm39) |
S429A |
probably benign |
Het |
Slc2a10 |
A |
T |
2: 165,357,543 (GRCm39) |
H401L |
possibly damaging |
Het |
Spag16 |
G |
C |
1: 70,420,459 (GRCm39) |
L482F |
probably damaging |
Het |
Ssbp2 |
T |
C |
13: 91,842,141 (GRCm39) |
S321P |
probably damaging |
Het |
Syne2 |
A |
G |
12: 75,937,158 (GRCm39) |
E252G |
probably damaging |
Het |
Synj2 |
T |
C |
17: 6,084,172 (GRCm39) |
I1178T |
probably damaging |
Het |
Tafa5 |
T |
C |
15: 87,428,775 (GRCm39) |
I28T |
probably benign |
Het |
Tmem132b |
C |
A |
5: 125,864,167 (GRCm39) |
Q758K |
probably damaging |
Het |
Tril |
A |
G |
6: 53,795,137 (GRCm39) |
L695P |
probably damaging |
Het |
Ubap1l |
T |
C |
9: 65,276,603 (GRCm39) |
L35P |
probably damaging |
Het |
Vmn1r225 |
T |
A |
17: 20,722,577 (GRCm39) |
M6K |
possibly damaging |
Het |
Vmn1r229 |
T |
C |
17: 21,034,758 (GRCm39) |
M1T |
probably null |
Het |
Vmn2r80 |
A |
T |
10: 79,030,687 (GRCm39) |
I838F |
probably damaging |
Het |
Vmn2r98 |
T |
A |
17: 19,286,383 (GRCm39) |
W294R |
probably benign |
Het |
Wnk1 |
A |
G |
6: 119,925,631 (GRCm39) |
S1527P |
unknown |
Het |
Wnt11 |
G |
A |
7: 98,488,241 (GRCm39) |
|
probably benign |
Het |
Zdhhc17 |
A |
T |
10: 110,785,503 (GRCm39) |
S436R |
possibly damaging |
Het |
Zfp12 |
T |
C |
5: 143,230,389 (GRCm39) |
S271P |
probably damaging |
Het |
|
Other mutations in Nicn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02935:Nicn1
|
APN |
9 |
108,167,845 (GRCm39) |
missense |
probably benign |
|
R7148:Nicn1
|
UTSW |
9 |
108,172,306 (GRCm39) |
makesense |
probably null |
|
R8121:Nicn1
|
UTSW |
9 |
108,172,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Nicn1
|
UTSW |
9 |
108,170,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R8453:Nicn1
|
UTSW |
9 |
108,170,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R8925:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8927:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8937:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8951:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8962:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8965:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8967:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8987:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8988:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9079:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9145:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9245:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9246:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9248:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9249:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9253:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9254:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9255:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9272:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9273:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9274:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9282:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9320:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9321:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9326:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9379:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9380:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9467:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9507:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9508:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9581:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9582:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9624:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9625:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9628:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9629:Nicn1
|
UTSW |
9 |
108,171,708 (GRCm39) |
missense |
possibly damaging |
0.79 |
|