Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
A |
G |
6: 142,571,726 (GRCm39) |
V1121A |
probably benign |
Het |
Adamtsl3 |
A |
C |
7: 82,261,006 (GRCm39) |
K1647Q |
possibly damaging |
Het |
Adgrb1 |
A |
T |
15: 74,415,550 (GRCm39) |
Q710L |
probably null |
Het |
Alox12 |
T |
C |
11: 70,145,243 (GRCm39) |
E110G |
probably damaging |
Het |
Cep152 |
T |
A |
2: 125,429,544 (GRCm39) |
M738L |
probably benign |
Het |
Cma2 |
T |
C |
14: 56,209,532 (GRCm39) |
V38A |
probably benign |
Het |
Dlc1 |
C |
T |
8: 37,405,552 (GRCm39) |
G79D |
probably damaging |
Het |
Dmpk |
C |
G |
7: 18,821,944 (GRCm39) |
L301V |
probably benign |
Het |
Dus3l |
A |
G |
17: 57,076,574 (GRCm39) |
I585V |
probably benign |
Het |
Etl4 |
A |
G |
2: 20,718,198 (GRCm39) |
Y313C |
probably damaging |
Het |
Fbxw15 |
C |
A |
9: 109,387,242 (GRCm39) |
S251I |
probably benign |
Het |
Gata4 |
G |
A |
14: 63,437,900 (GRCm39) |
S417L |
probably benign |
Het |
Gdpd5 |
T |
A |
7: 99,087,515 (GRCm39) |
Y60N |
probably damaging |
Het |
Gm17669 |
T |
C |
18: 67,695,626 (GRCm39) |
M57T |
probably benign |
Het |
Gpr39 |
A |
T |
1: 125,605,173 (GRCm39) |
I34F |
probably benign |
Het |
Iffo2 |
T |
A |
4: 139,302,528 (GRCm39) |
D90E |
probably benign |
Het |
Il17c |
A |
G |
8: 123,149,108 (GRCm39) |
D84G |
possibly damaging |
Het |
Itih3 |
T |
C |
14: 30,634,606 (GRCm39) |
T134A |
probably benign |
Het |
Lama2 |
G |
A |
10: 27,222,999 (GRCm39) |
A429V |
probably damaging |
Het |
Muc6 |
G |
T |
7: 141,218,685 (GRCm39) |
T1996N |
possibly damaging |
Het |
Mug1 |
G |
A |
6: 121,851,521 (GRCm39) |
R806H |
probably damaging |
Het |
Naaa |
G |
A |
5: 92,415,904 (GRCm39) |
R65* |
probably null |
Het |
Nemf |
A |
G |
12: 69,402,821 (GRCm39) |
S72P |
probably damaging |
Het |
Nudt7 |
G |
A |
8: 114,862,185 (GRCm39) |
|
probably null |
Het |
Or4b1b |
T |
C |
2: 90,126,737 (GRCm39) |
Q156R |
probably damaging |
Het |
Or52z15 |
T |
C |
7: 103,331,936 (GRCm39) |
S4P |
probably benign |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pacs1 |
T |
C |
19: 5,189,325 (GRCm39) |
D757G |
probably benign |
Het |
Pkd2 |
A |
C |
5: 104,630,958 (GRCm39) |
I461L |
probably benign |
Het |
Potegl |
G |
A |
2: 23,102,473 (GRCm39) |
C121Y |
probably damaging |
Het |
Pramel5 |
T |
G |
4: 144,000,064 (GRCm39) |
|
probably benign |
Het |
Ptgdr |
G |
C |
14: 45,096,300 (GRCm39) |
F137L |
probably damaging |
Het |
Pum1 |
T |
A |
4: 130,507,190 (GRCm39) |
C1085* |
probably null |
Het |
Rfx3 |
T |
C |
19: 27,808,176 (GRCm39) |
D189G |
probably damaging |
Het |
Rlf |
T |
A |
4: 121,005,750 (GRCm39) |
K1077* |
probably null |
Het |
Slc25a30 |
C |
A |
14: 76,007,056 (GRCm39) |
D147Y |
probably benign |
Het |
Smap2 |
T |
C |
4: 120,873,984 (GRCm39) |
E22G |
possibly damaging |
Het |
Szt2 |
T |
C |
4: 118,245,519 (GRCm39) |
T1098A |
probably benign |
Het |
Tbcc |
T |
C |
17: 47,201,788 (GRCm39) |
F58S |
probably damaging |
Het |
Tekt3 |
G |
A |
11: 62,961,134 (GRCm39) |
R101H |
probably damaging |
Het |
Vcan |
T |
A |
13: 89,838,991 (GRCm39) |
E2184D |
probably damaging |
Het |
Vkorc1 |
T |
C |
7: 127,493,760 (GRCm39) |
E18G |
probably benign |
Het |
Vmn1r68 |
T |
C |
7: 10,261,723 (GRCm39) |
H125R |
probably benign |
Het |
Vmn2r63 |
C |
A |
7: 42,553,169 (GRCm39) |
V696L |
probably benign |
Het |
Wdr59 |
G |
A |
8: 112,208,620 (GRCm39) |
H421Y |
probably benign |
Het |
Xkr7 |
T |
C |
2: 152,896,873 (GRCm39) |
Y576H |
probably damaging |
Het |
Zfp112 |
T |
C |
7: 23,824,281 (GRCm39) |
V83A |
possibly damaging |
Het |
Zfp616 |
G |
A |
11: 73,974,336 (GRCm39) |
V293I |
probably benign |
Het |
|
Other mutations in Nacc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00571:Nacc2
|
APN |
2 |
25,979,702 (GRCm39) |
missense |
probably benign |
|
IGL00906:Nacc2
|
APN |
2 |
25,951,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02122:Nacc2
|
APN |
2 |
25,979,960 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02836:Nacc2
|
APN |
2 |
25,980,329 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03355:Nacc2
|
APN |
2 |
25,952,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Nacc2
|
UTSW |
2 |
25,952,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Nacc2
|
UTSW |
2 |
25,952,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0326:Nacc2
|
UTSW |
2 |
25,950,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R0553:Nacc2
|
UTSW |
2 |
25,979,602 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1743:Nacc2
|
UTSW |
2 |
25,950,155 (GRCm39) |
missense |
probably benign |
|
R2172:Nacc2
|
UTSW |
2 |
25,950,235 (GRCm39) |
missense |
probably benign |
0.00 |
R2497:Nacc2
|
UTSW |
2 |
25,979,580 (GRCm39) |
nonsense |
probably null |
|
R4027:Nacc2
|
UTSW |
2 |
25,950,348 (GRCm39) |
missense |
probably benign |
0.11 |
R4724:Nacc2
|
UTSW |
2 |
25,980,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Nacc2
|
UTSW |
2 |
25,980,150 (GRCm39) |
splice site |
probably null |
|
R5151:Nacc2
|
UTSW |
2 |
25,980,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Nacc2
|
UTSW |
2 |
25,951,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R6028:Nacc2
|
UTSW |
2 |
25,951,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Nacc2
|
UTSW |
2 |
25,950,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R6924:Nacc2
|
UTSW |
2 |
25,980,041 (GRCm39) |
missense |
probably damaging |
0.97 |
R8263:Nacc2
|
UTSW |
2 |
25,952,240 (GRCm39) |
missense |
probably damaging |
0.99 |
R8936:Nacc2
|
UTSW |
2 |
25,952,216 (GRCm39) |
missense |
probably benign |
0.16 |
R9035:Nacc2
|
UTSW |
2 |
25,951,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R9200:Nacc2
|
UTSW |
2 |
25,980,118 (GRCm39) |
missense |
probably damaging |
0.98 |
R9395:Nacc2
|
UTSW |
2 |
25,950,128 (GRCm39) |
missense |
probably damaging |
1.00 |
|