Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
G |
C |
3: 121,926,344 (GRCm39) |
S1260T |
probably damaging |
Het |
Adgra2 |
A |
G |
8: 27,576,094 (GRCm39) |
I41V |
probably benign |
Het |
Agtrap |
A |
G |
4: 148,165,019 (GRCm39) |
I136T |
probably damaging |
Het |
Arhgef7 |
C |
T |
8: 11,867,736 (GRCm39) |
T601I |
probably damaging |
Het |
Asb7 |
T |
C |
7: 66,328,987 (GRCm39) |
I18V |
possibly damaging |
Het |
C1rl |
T |
C |
6: 124,485,322 (GRCm39) |
V231A |
probably benign |
Het |
Cachd1 |
A |
T |
4: 100,832,057 (GRCm39) |
T740S |
probably benign |
Het |
Ccdc146 |
T |
A |
5: 21,508,135 (GRCm39) |
I638F |
probably damaging |
Het |
Ccser2 |
T |
C |
14: 36,601,163 (GRCm39) |
N407S |
probably benign |
Het |
Clec7a |
G |
A |
6: 129,442,514 (GRCm39) |
S126L |
probably damaging |
Het |
Copb1 |
C |
T |
7: 113,848,182 (GRCm39) |
G118R |
probably damaging |
Het |
Cpne3 |
A |
T |
4: 19,525,148 (GRCm39) |
M449K |
probably damaging |
Het |
Cttnbp2 |
A |
T |
6: 18,423,880 (GRCm39) |
C815S |
probably damaging |
Het |
Cyp27b1 |
T |
C |
10: 126,886,006 (GRCm39) |
L253P |
probably damaging |
Het |
Cyp3a44 |
C |
A |
5: 145,740,548 (GRCm39) |
G31* |
probably null |
Het |
Dcp2 |
C |
T |
18: 44,538,361 (GRCm39) |
R173C |
probably damaging |
Het |
Dmgdh |
A |
T |
13: 93,880,813 (GRCm39) |
I748L |
probably benign |
Het |
Drc1 |
T |
A |
5: 30,502,938 (GRCm39) |
W154R |
probably benign |
Het |
E330034G19Rik |
T |
A |
14: 24,358,387 (GRCm39) |
|
probably null |
Het |
Gbp7 |
T |
A |
3: 142,248,718 (GRCm39) |
V327E |
probably damaging |
Het |
Gm11564 |
G |
A |
11: 99,706,065 (GRCm39) |
P122S |
unknown |
Het |
Grid2ip |
C |
A |
5: 143,367,435 (GRCm39) |
S615R |
|
Het |
Kcp |
T |
A |
6: 29,489,151 (GRCm39) |
Q1045L |
probably benign |
Het |
Lgals3bp |
T |
A |
11: 118,284,751 (GRCm39) |
E276V |
probably damaging |
Het |
Lrit1 |
T |
C |
14: 36,784,208 (GRCm39) |
V512A |
possibly damaging |
Het |
Mecom |
T |
A |
3: 30,039,597 (GRCm39) |
H154L |
probably benign |
Het |
Mmp14 |
C |
A |
14: 54,677,804 (GRCm39) |
T475K |
probably damaging |
Het |
Mmp1a |
T |
G |
9: 7,476,210 (GRCm39) |
F436V |
probably damaging |
Het |
Notch4 |
A |
G |
17: 34,795,801 (GRCm39) |
S830G |
probably benign |
Het |
Oas1b |
T |
C |
5: 120,955,693 (GRCm39) |
L158P |
probably benign |
Het |
Odf4 |
A |
G |
11: 68,813,810 (GRCm39) |
V126A |
probably benign |
Het |
Olfml2a |
A |
G |
2: 38,847,721 (GRCm39) |
T427A |
probably damaging |
Het |
Or2b28 |
A |
G |
13: 21,531,473 (GRCm39) |
Y125C |
probably damaging |
Het |
Or4c102 |
C |
A |
2: 88,422,877 (GRCm39) |
T243K |
probably damaging |
Het |
Or5b121 |
C |
T |
19: 13,507,222 (GRCm39) |
L106F |
probably damaging |
Het |
Or6d12 |
G |
A |
6: 116,493,574 (GRCm39) |
E279K |
possibly damaging |
Het |
Or8b42 |
A |
G |
9: 38,342,286 (GRCm39) |
K236R |
possibly damaging |
Het |
Panx3 |
G |
A |
9: 37,572,393 (GRCm39) |
H386Y |
probably benign |
Het |
Papss1 |
C |
A |
3: 131,270,708 (GRCm39) |
C8* |
probably null |
Het |
Papss2 |
G |
T |
19: 32,615,750 (GRCm39) |
V161L |
possibly damaging |
Het |
Pcdh18 |
G |
T |
3: 49,709,051 (GRCm39) |
H755N |
possibly damaging |
Het |
Pilrb2 |
G |
C |
5: 137,866,964 (GRCm39) |
H180D |
probably benign |
Het |
Pla2g4f |
T |
C |
2: 120,133,264 (GRCm39) |
D645G |
possibly damaging |
Het |
Pnlip |
A |
T |
19: 58,669,290 (GRCm39) |
K430* |
probably null |
Het |
Ralbp1 |
C |
A |
17: 66,171,506 (GRCm39) |
A156S |
possibly damaging |
Het |
Rnf4 |
C |
T |
5: 34,508,641 (GRCm39) |
R168C |
probably benign |
Het |
Slc17a5 |
C |
T |
9: 78,484,457 (GRCm39) |
G127E |
probably damaging |
Het |
Slc22a27 |
A |
T |
19: 7,874,156 (GRCm39) |
N306K |
probably damaging |
Het |
Slc5a9 |
G |
A |
4: 111,734,803 (GRCm39) |
R664C |
probably damaging |
Het |
Slco1b2 |
T |
A |
6: 141,603,249 (GRCm39) |
I210K |
possibly damaging |
Het |
Snx16 |
C |
T |
3: 10,499,520 (GRCm39) |
R170H |
probably damaging |
Het |
Speer4e1 |
T |
C |
5: 14,987,136 (GRCm39) |
I90V |
possibly damaging |
Het |
Stxbp5l |
T |
C |
16: 36,994,706 (GRCm39) |
D733G |
possibly damaging |
Het |
Tbc1d24 |
A |
G |
17: 24,404,382 (GRCm39) |
V254A |
probably benign |
Het |
Tmf1 |
A |
G |
6: 97,149,293 (GRCm39) |
F485L |
probably benign |
Het |
Tnks |
G |
A |
8: 35,340,819 (GRCm39) |
L396F |
probably damaging |
Het |
Trabd |
T |
C |
15: 88,969,496 (GRCm39) |
C230R |
probably damaging |
Het |
Trp53rkb |
C |
T |
2: 166,637,542 (GRCm39) |
A166V |
probably benign |
Het |
Upf1 |
A |
T |
8: 70,792,003 (GRCm39) |
D418E |
probably benign |
Het |
Ust |
A |
C |
10: 8,205,873 (GRCm39) |
S137A |
probably damaging |
Het |
Zfp513 |
T |
A |
5: 31,357,695 (GRCm39) |
H228L |
possibly damaging |
Het |
Zfp827 |
C |
A |
8: 79,905,588 (GRCm39) |
A855E |
probably damaging |
Het |
|
Other mutations in Adgrf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01343:Adgrf1
|
APN |
17 |
43,624,086 (GRCm39) |
missense |
probably null |
0.92 |
IGL01359:Adgrf1
|
APN |
17 |
43,621,577 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02131:Adgrf1
|
APN |
17 |
43,614,638 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02692:Adgrf1
|
APN |
17 |
43,614,669 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02891:Adgrf1
|
APN |
17 |
43,622,052 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03027:Adgrf1
|
APN |
17 |
43,607,605 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03296:Adgrf1
|
APN |
17 |
43,632,044 (GRCm39) |
splice site |
probably benign |
|
R0211:Adgrf1
|
UTSW |
17 |
43,607,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R0211:Adgrf1
|
UTSW |
17 |
43,607,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R0389:Adgrf1
|
UTSW |
17 |
43,614,679 (GRCm39) |
critical splice donor site |
probably null |
|
R0488:Adgrf1
|
UTSW |
17 |
43,621,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R1591:Adgrf1
|
UTSW |
17 |
43,621,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R1817:Adgrf1
|
UTSW |
17 |
43,620,924 (GRCm39) |
missense |
probably benign |
0.01 |
R1819:Adgrf1
|
UTSW |
17 |
43,620,924 (GRCm39) |
missense |
probably benign |
0.01 |
R2009:Adgrf1
|
UTSW |
17 |
43,632,112 (GRCm39) |
nonsense |
probably null |
|
R2032:Adgrf1
|
UTSW |
17 |
43,622,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R2140:Adgrf1
|
UTSW |
17 |
43,611,693 (GRCm39) |
missense |
probably damaging |
0.99 |
R3953:Adgrf1
|
UTSW |
17 |
43,621,098 (GRCm39) |
missense |
probably benign |
0.08 |
R4679:Adgrf1
|
UTSW |
17 |
43,621,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R4775:Adgrf1
|
UTSW |
17 |
43,622,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R4858:Adgrf1
|
UTSW |
17 |
43,614,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R4894:Adgrf1
|
UTSW |
17 |
43,609,975 (GRCm39) |
nonsense |
probably null |
|
R4895:Adgrf1
|
UTSW |
17 |
43,621,511 (GRCm39) |
missense |
probably benign |
0.33 |
R4935:Adgrf1
|
UTSW |
17 |
43,606,130 (GRCm39) |
missense |
probably benign |
0.00 |
R5027:Adgrf1
|
UTSW |
17 |
43,614,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R5373:Adgrf1
|
UTSW |
17 |
43,601,896 (GRCm39) |
start gained |
probably benign |
|
R5374:Adgrf1
|
UTSW |
17 |
43,601,896 (GRCm39) |
start gained |
probably benign |
|
R5455:Adgrf1
|
UTSW |
17 |
43,632,034 (GRCm39) |
splice site |
probably null |
|
R5579:Adgrf1
|
UTSW |
17 |
43,621,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R5985:Adgrf1
|
UTSW |
17 |
43,604,146 (GRCm39) |
missense |
probably benign |
0.00 |
R6038:Adgrf1
|
UTSW |
17 |
43,606,100 (GRCm39) |
missense |
probably benign |
0.00 |
R6038:Adgrf1
|
UTSW |
17 |
43,606,100 (GRCm39) |
missense |
probably benign |
0.00 |
R6160:Adgrf1
|
UTSW |
17 |
43,621,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R6227:Adgrf1
|
UTSW |
17 |
43,621,164 (GRCm39) |
missense |
probably benign |
0.05 |
R6500:Adgrf1
|
UTSW |
17 |
43,621,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R7066:Adgrf1
|
UTSW |
17 |
43,621,151 (GRCm39) |
missense |
probably benign |
0.05 |
R7099:Adgrf1
|
UTSW |
17 |
43,621,493 (GRCm39) |
missense |
probably benign |
0.00 |
R7561:Adgrf1
|
UTSW |
17 |
43,622,000 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8359:Adgrf1
|
UTSW |
17 |
43,621,286 (GRCm39) |
missense |
probably damaging |
0.99 |
R8480:Adgrf1
|
UTSW |
17 |
43,606,055 (GRCm39) |
missense |
probably benign |
0.08 |
R8543:Adgrf1
|
UTSW |
17 |
43,624,097 (GRCm39) |
missense |
probably null |
0.99 |
R9023:Adgrf1
|
UTSW |
17 |
43,614,651 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9074:Adgrf1
|
UTSW |
17 |
43,601,879 (GRCm39) |
start gained |
probably benign |
|
R9207:Adgrf1
|
UTSW |
17 |
43,621,164 (GRCm39) |
missense |
probably benign |
0.05 |
R9232:Adgrf1
|
UTSW |
17 |
43,621,295 (GRCm39) |
missense |
probably benign |
0.07 |
R9526:Adgrf1
|
UTSW |
17 |
43,616,237 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9697:Adgrf1
|
UTSW |
17 |
43,625,362 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9711:Adgrf1
|
UTSW |
17 |
43,621,580 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1177:Adgrf1
|
UTSW |
17 |
43,621,038 (GRCm39) |
missense |
probably benign |
0.14 |
|