Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510009E07Rik |
CCGGAAGGGGAGGAGCAGTGACCCAGTTTCGGA |
CCGGA |
16: 21,472,148 (GRCm39) |
|
probably null |
Het |
Adcy1 |
T |
G |
11: 7,059,075 (GRCm39) |
L327R |
probably damaging |
Het |
Ajm1 |
A |
T |
2: 25,467,914 (GRCm39) |
S666T |
probably benign |
Het |
Amotl1 |
T |
C |
9: 14,469,861 (GRCm39) |
Q624R |
probably damaging |
Het |
Ampd1 |
A |
G |
3: 102,988,374 (GRCm39) |
T106A |
probably benign |
Het |
Aqr |
T |
A |
2: 113,967,474 (GRCm39) |
I514F |
probably damaging |
Het |
Atp2b1 |
A |
G |
10: 98,804,866 (GRCm39) |
T30A |
possibly damaging |
Het |
Atp9a |
A |
T |
2: 168,547,097 (GRCm39) |
Y186N |
probably benign |
Het |
Bub1 |
T |
A |
2: 127,671,622 (GRCm39) |
N21I |
possibly damaging |
Het |
Cachd1 |
G |
A |
4: 100,810,363 (GRCm39) |
D322N |
probably damaging |
Het |
Ccdc38 |
A |
G |
10: 93,411,197 (GRCm39) |
E402G |
probably damaging |
Het |
Ccl27a |
A |
T |
4: 41,774,194 (GRCm39) |
|
probably null |
Het |
Clec4a4 |
T |
C |
6: 122,990,836 (GRCm39) |
|
probably benign |
Het |
Clic5 |
A |
T |
17: 44,552,992 (GRCm39) |
K82M |
probably benign |
Het |
Cnot10 |
A |
T |
9: 114,430,423 (GRCm39) |
S566T |
probably benign |
Het |
Cul9 |
T |
C |
17: 46,831,427 (GRCm39) |
T1596A |
probably damaging |
Het |
Cyp2c55 |
A |
G |
19: 39,022,816 (GRCm39) |
E318G |
|
Het |
Entpd8 |
A |
C |
2: 24,973,575 (GRCm39) |
|
probably benign |
Het |
Epb41l5 |
A |
G |
1: 119,547,936 (GRCm39) |
F156L |
probably damaging |
Het |
Ephb4 |
T |
A |
5: 137,369,067 (GRCm39) |
M819K |
probably damaging |
Het |
Esr1 |
A |
G |
10: 4,696,654 (GRCm39) |
R168G |
possibly damaging |
Het |
Fbxw10 |
C |
A |
11: 62,765,831 (GRCm39) |
Y700* |
probably null |
Het |
Fras1 |
G |
T |
5: 96,929,138 (GRCm39) |
R3847S |
probably benign |
Het |
Gm11110 |
T |
C |
17: 57,410,439 (GRCm39) |
T20A |
unknown |
Het |
Gpr150 |
G |
T |
13: 76,204,528 (GRCm39) |
S139* |
probably null |
Het |
Grm1 |
A |
T |
10: 10,595,281 (GRCm39) |
N782K |
probably damaging |
Het |
Hmcn2 |
A |
G |
2: 31,323,404 (GRCm39) |
S4173G |
possibly damaging |
Het |
Hmx1 |
T |
A |
5: 35,549,511 (GRCm39) |
V268D |
probably damaging |
Het |
Hsbp1l1 |
T |
C |
18: 80,278,685 (GRCm39) |
T33A |
possibly damaging |
Het |
Hsd17b3 |
T |
C |
13: 64,212,194 (GRCm39) |
T161A |
probably damaging |
Het |
Igll1 |
A |
T |
16: 16,681,576 (GRCm39) |
W60R |
probably benign |
Het |
Itga11 |
A |
G |
9: 62,664,893 (GRCm39) |
T593A |
probably benign |
Het |
Kat6a |
A |
G |
8: 23,428,824 (GRCm39) |
D1393G |
possibly damaging |
Het |
Krt36 |
A |
G |
11: 99,996,173 (GRCm39) |
F84L |
probably benign |
Het |
Macrod1 |
T |
C |
19: 7,174,385 (GRCm39) |
S266P |
probably damaging |
Het |
Mib2 |
A |
G |
4: 155,744,173 (GRCm39) |
V163A |
probably damaging |
Het |
Mmut |
A |
G |
17: 41,248,284 (GRCm39) |
T104A |
probably damaging |
Het |
Mpl |
A |
G |
4: 118,301,263 (GRCm39) |
L534P |
|
Het |
Myo3b |
C |
A |
2: 70,257,252 (GRCm39) |
H1317N |
probably benign |
Het |
Nkx2-6 |
A |
G |
14: 69,409,420 (GRCm39) |
D57G |
probably benign |
Het |
Or1ab2 |
A |
G |
8: 72,864,276 (GRCm39) |
I289V |
probably damaging |
Het |
Or5b24 |
T |
C |
19: 12,912,192 (GRCm39) |
V30A |
probably benign |
Het |
Or5d46 |
T |
G |
2: 88,169,949 (GRCm39) |
F13L |
possibly damaging |
Het |
Or5p79 |
A |
G |
7: 108,221,919 (GRCm39) |
N300S |
probably damaging |
Het |
Or6s1 |
A |
G |
14: 51,308,665 (GRCm39) |
Y62H |
probably damaging |
Het |
Or7g33 |
A |
T |
9: 19,448,760 (GRCm39) |
D155E |
possibly damaging |
Het |
Osbpl11 |
T |
A |
16: 33,047,607 (GRCm39) |
H523Q |
probably damaging |
Het |
Pde1c |
A |
T |
6: 56,156,128 (GRCm39) |
S148T |
possibly damaging |
Het |
Pign |
G |
A |
1: 105,519,359 (GRCm39) |
A521V |
possibly damaging |
Het |
Pprc1 |
A |
G |
19: 46,060,183 (GRCm39) |
M1536V |
possibly damaging |
Het |
Prg4 |
C |
A |
1: 150,331,810 (GRCm39) |
A288S |
possibly damaging |
Het |
Prkdc |
T |
C |
16: 15,545,590 (GRCm39) |
V1902A |
probably benign |
Het |
Prss40 |
C |
T |
1: 34,595,045 (GRCm39) |
|
probably benign |
Het |
Ret |
C |
T |
6: 118,157,174 (GRCm39) |
|
probably benign |
Het |
Rgs22 |
A |
T |
15: 36,026,127 (GRCm39) |
C1056S |
probably damaging |
Het |
Schip1 |
T |
C |
3: 68,402,436 (GRCm39) |
L199P |
possibly damaging |
Het |
Sema4d |
A |
T |
13: 51,854,935 (GRCm39) |
L54* |
probably null |
Het |
Sgsm1 |
C |
T |
5: 113,421,495 (GRCm39) |
G531R |
probably benign |
Het |
Tas1r2 |
T |
C |
4: 139,394,714 (GRCm39) |
F519S |
probably damaging |
Het |
Tnfsf11 |
C |
T |
14: 78,516,119 (GRCm39) |
R283Q |
possibly damaging |
Het |
Tril |
C |
T |
6: 53,797,202 (GRCm39) |
V7M |
possibly damaging |
Het |
Tsr1 |
T |
A |
11: 74,790,217 (GRCm39) |
Y137* |
probably null |
Het |
Ubr5 |
A |
G |
15: 38,042,153 (GRCm39) |
S148P |
|
Het |
Unc13b |
A |
G |
4: 43,178,531 (GRCm39) |
|
probably benign |
Het |
Zfp606 |
A |
G |
7: 12,223,506 (GRCm39) |
T64A |
possibly damaging |
Het |
|
Other mutations in Prim2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00921:Prim2
|
APN |
1 |
33,551,241 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02576:Prim2
|
APN |
1 |
33,523,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R0398:Prim2
|
UTSW |
1 |
33,523,757 (GRCm39) |
splice site |
probably benign |
|
R0686:Prim2
|
UTSW |
1 |
33,553,270 (GRCm39) |
missense |
probably benign |
|
R1452:Prim2
|
UTSW |
1 |
33,669,485 (GRCm39) |
missense |
probably benign |
|
R3925:Prim2
|
UTSW |
1 |
33,572,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R4398:Prim2
|
UTSW |
1 |
33,551,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831:Prim2
|
UTSW |
1 |
33,709,217 (GRCm39) |
unclassified |
probably benign |
|
R4832:Prim2
|
UTSW |
1 |
33,503,145 (GRCm39) |
missense |
probably benign |
|
R5057:Prim2
|
UTSW |
1 |
33,669,441 (GRCm39) |
nonsense |
probably null |
|
R5240:Prim2
|
UTSW |
1 |
33,519,397 (GRCm39) |
intron |
probably benign |
|
R5294:Prim2
|
UTSW |
1 |
33,707,974 (GRCm39) |
missense |
probably benign |
0.11 |
R5771:Prim2
|
UTSW |
1 |
33,493,232 (GRCm39) |
missense |
unknown |
|
R5807:Prim2
|
UTSW |
1 |
33,519,487 (GRCm39) |
intron |
probably benign |
|
R6307:Prim2
|
UTSW |
1 |
33,701,373 (GRCm39) |
missense |
probably benign |
0.00 |
R7165:Prim2
|
UTSW |
1 |
33,667,474 (GRCm39) |
critical splice donor site |
probably null |
|
R9435:Prim2
|
UTSW |
1 |
33,523,876 (GRCm39) |
missense |
probably damaging |
1.00 |
|