Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921517D22Rik |
T |
C |
13: 59,837,470 (GRCm39) |
K205R |
possibly damaging |
Het |
9630041A04Rik |
A |
T |
9: 101,819,934 (GRCm39) |
N118I |
probably damaging |
Het |
AAdacl4fm3 |
A |
G |
4: 144,429,765 (GRCm39) |
V408A |
probably benign |
Het |
Acsm2 |
G |
A |
7: 119,174,969 (GRCm39) |
D245N |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,534,072 (GRCm39) |
H5836Q |
probably benign |
Het |
Ahcyl2 |
T |
C |
6: 29,886,167 (GRCm39) |
V391A |
probably damaging |
Het |
Alcam |
A |
T |
16: 52,130,227 (GRCm39) |
M41K |
probably benign |
Het |
Aldh3b3 |
A |
C |
19: 4,016,472 (GRCm39) |
E363D |
probably benign |
Het |
Alk |
A |
G |
17: 72,910,526 (GRCm39) |
V60A |
probably damaging |
Het |
Als2cl |
G |
A |
9: 110,727,152 (GRCm39) |
R906H |
probably damaging |
Het |
Apba2 |
T |
A |
7: 64,393,156 (GRCm39) |
I547N |
probably benign |
Het |
Apol10b |
A |
T |
15: 77,469,840 (GRCm39) |
D112E |
probably damaging |
Het |
Ash1l |
C |
A |
3: 88,965,896 (GRCm39) |
R2433S |
probably damaging |
Het |
Cachd1 |
T |
C |
4: 100,810,402 (GRCm39) |
F335L |
probably damaging |
Het |
Cbfa2t3 |
G |
T |
8: 123,365,690 (GRCm39) |
Q181K |
probably benign |
Het |
Cct6b |
A |
G |
11: 82,630,506 (GRCm39) |
M265T |
probably benign |
Het |
Cd151 |
G |
A |
7: 141,050,304 (GRCm39) |
V180I |
probably damaging |
Het |
Ces1h |
T |
A |
8: 94,083,706 (GRCm39) |
N412I |
unknown |
Het |
Chmp7 |
T |
C |
14: 69,969,905 (GRCm39) |
T12A |
probably benign |
Het |
Clasp1 |
A |
G |
1: 118,467,061 (GRCm39) |
T534A |
possibly damaging |
Het |
Cldn15 |
T |
A |
5: 136,997,052 (GRCm39) |
V31E |
possibly damaging |
Het |
Col16a1 |
G |
A |
4: 129,966,902 (GRCm39) |
G583D |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,396,652 (GRCm39) |
N426S |
probably damaging |
Het |
Dapp1 |
C |
T |
3: 137,641,398 (GRCm39) |
C199Y |
possibly damaging |
Het |
Dchs1 |
A |
G |
7: 105,407,745 (GRCm39) |
L2029P |
probably damaging |
Het |
Dmc1 |
A |
G |
15: 79,472,973 (GRCm39) |
F158S |
probably damaging |
Het |
Dst |
C |
T |
1: 34,228,200 (GRCm39) |
P1606L |
probably damaging |
Het |
Dthd1 |
T |
A |
5: 62,971,676 (GRCm39) |
N166K |
possibly damaging |
Het |
Enam |
A |
T |
5: 88,649,367 (GRCm39) |
Y292F |
probably damaging |
Het |
Esrrg |
A |
T |
1: 187,930,832 (GRCm39) |
I285F |
probably damaging |
Het |
Fam50b |
A |
G |
13: 34,931,220 (GRCm39) |
D232G |
probably damaging |
Het |
Fam91a1 |
T |
A |
15: 58,326,641 (GRCm39) |
S792T |
probably benign |
Het |
Fbxw22 |
A |
C |
9: 109,210,753 (GRCm39) |
C419W |
probably damaging |
Het |
Flt4 |
G |
A |
11: 49,521,170 (GRCm39) |
S393N |
probably benign |
Het |
Fras1 |
A |
T |
5: 96,917,512 (GRCm39) |
T3511S |
possibly damaging |
Het |
Frat2 |
A |
C |
19: 41,836,263 (GRCm39) |
S30A |
probably damaging |
Het |
Glp1r |
T |
A |
17: 31,155,312 (GRCm39) |
M433K |
probably benign |
Het |
Gm10300 |
G |
A |
4: 131,802,299 (GRCm39) |
|
probably benign |
Het |
Gpatch4 |
A |
G |
3: 87,961,661 (GRCm39) |
|
probably benign |
Het |
Gpr22 |
A |
T |
12: 31,759,461 (GRCm39) |
S220R |
possibly damaging |
Het |
Grn |
T |
C |
11: 102,327,049 (GRCm39) |
V549A |
probably benign |
Het |
Gtf3c5 |
T |
C |
2: 28,467,930 (GRCm39) |
D177G |
probably damaging |
Het |
Htr1b |
A |
T |
9: 81,513,704 (GRCm39) |
M301K |
probably benign |
Het |
Ifi207 |
A |
T |
1: 173,557,431 (GRCm39) |
S436T |
possibly damaging |
Het |
Ifnb1 |
A |
T |
4: 88,440,766 (GRCm39) |
N82K |
possibly damaging |
Het |
Ina |
T |
G |
19: 47,010,358 (GRCm39) |
N384K |
probably damaging |
Het |
Kirrel2 |
T |
C |
7: 30,149,883 (GRCm39) |
N541D |
possibly damaging |
Het |
Lrp2 |
A |
T |
2: 69,263,421 (GRCm39) |
I4377N |
possibly damaging |
Het |
Lrrc37a |
A |
G |
11: 103,355,221 (GRCm39) |
V2532A |
unknown |
Het |
Mast4 |
T |
C |
13: 102,871,781 (GRCm39) |
E2529G |
probably damaging |
Het |
Myh6 |
T |
C |
14: 55,183,777 (GRCm39) |
H1719R |
possibly damaging |
Het |
Myo5a |
A |
T |
9: 75,101,259 (GRCm39) |
H150L |
probably benign |
Het |
Naglu |
C |
T |
11: 100,964,933 (GRCm39) |
|
probably benign |
Het |
Nags |
G |
A |
11: 102,036,530 (GRCm39) |
A40T |
unknown |
Het |
Nav1 |
G |
T |
1: 135,460,359 (GRCm39) |
Y321* |
probably null |
Het |
Nav1 |
A |
T |
1: 135,460,361 (GRCm39) |
Y321N |
probably damaging |
Het |
Neu3 |
C |
T |
7: 99,462,985 (GRCm39) |
S246N |
probably benign |
Het |
Npy5r |
C |
T |
8: 67,134,625 (GRCm39) |
G56D |
probably benign |
Het |
Nrxn1 |
A |
G |
17: 91,395,742 (GRCm39) |
V138A |
possibly damaging |
Het |
Nuggc |
C |
T |
14: 65,850,921 (GRCm39) |
Q264* |
probably null |
Het |
Ogfod1 |
G |
A |
8: 94,790,156 (GRCm39) |
|
probably null |
Het |
Or1o11 |
T |
A |
17: 37,756,757 (GRCm39) |
F115Y |
probably damaging |
Het |
Or2t45 |
A |
T |
11: 58,669,195 (GRCm39) |
M81L |
probably benign |
Het |
Or5b101 |
A |
G |
19: 13,005,663 (GRCm39) |
F10S |
probably damaging |
Het |
Or5p66 |
A |
G |
7: 107,885,478 (GRCm39) |
V285A |
probably benign |
Het |
Per1 |
T |
A |
11: 68,993,103 (GRCm39) |
I340N |
probably damaging |
Het |
Pkhd1 |
C |
T |
1: 20,451,771 (GRCm39) |
A2175T |
probably benign |
Het |
Pogk |
A |
G |
1: 166,231,171 (GRCm39) |
V52A |
probably damaging |
Het |
Pou2af3 |
C |
T |
9: 51,191,834 (GRCm39) |
|
probably benign |
Het |
Ppib |
A |
T |
9: 65,973,601 (GRCm39) |
T185S |
possibly damaging |
Het |
Ptar1 |
G |
T |
19: 23,697,563 (GRCm39) |
M358I |
probably damaging |
Het |
Qser1 |
A |
C |
2: 104,593,226 (GRCm39) |
I1597S |
probably damaging |
Het |
Ranbp17 |
T |
C |
11: 33,424,896 (GRCm39) |
I487V |
probably benign |
Het |
Repin1 |
C |
A |
6: 48,574,459 (GRCm39) |
R460S |
probably damaging |
Het |
Sfmbt1 |
T |
C |
14: 30,509,574 (GRCm39) |
|
probably benign |
Het |
Sh3rf1 |
C |
T |
8: 61,846,696 (GRCm39) |
|
probably benign |
Het |
Shroom3 |
C |
T |
5: 92,928,762 (GRCm39) |
R106C |
probably damaging |
Het |
Siglecf |
T |
A |
7: 43,005,399 (GRCm39) |
V453D |
probably damaging |
Het |
Slc2a9 |
A |
G |
5: 38,610,512 (GRCm39) |
S96P |
probably damaging |
Het |
Slc5a2 |
A |
G |
7: 127,866,654 (GRCm39) |
Y124C |
probably damaging |
Het |
Slf1 |
A |
G |
13: 77,254,088 (GRCm39) |
|
probably benign |
Het |
Smad1 |
T |
G |
8: 80,076,411 (GRCm39) |
K269T |
probably benign |
Het |
Srp54b |
G |
A |
12: 55,296,884 (GRCm39) |
R194H |
probably damaging |
Het |
St8sia6 |
T |
A |
2: 13,670,247 (GRCm39) |
S238C |
probably damaging |
Het |
Stat3 |
A |
T |
11: 100,780,763 (GRCm39) |
|
probably benign |
Het |
Tafa2 |
A |
T |
10: 123,429,497 (GRCm39) |
H37L |
probably benign |
Het |
Tas1r2 |
T |
A |
4: 139,382,665 (GRCm39) |
M101K |
possibly damaging |
Het |
Tesc |
A |
G |
5: 118,191,647 (GRCm39) |
|
probably null |
Het |
Tle3 |
T |
A |
9: 61,317,353 (GRCm39) |
M334K |
probably damaging |
Het |
Tmem151a |
A |
T |
19: 5,132,261 (GRCm39) |
V315E |
probably damaging |
Het |
Tmprss2 |
T |
C |
16: 97,368,245 (GRCm39) |
D480G |
probably damaging |
Het |
Trmt1 |
C |
A |
8: 85,423,741 (GRCm39) |
|
probably null |
Het |
Tsr3 |
T |
C |
17: 25,461,198 (GRCm39) |
|
probably null |
Het |
Ube2u |
A |
G |
4: 100,338,845 (GRCm39) |
K37E |
probably benign |
Het |
Usp16 |
T |
A |
16: 87,272,334 (GRCm39) |
D382E |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,340,053 (GRCm39) |
F1442Y |
probably damaging |
Het |
Utp20 |
A |
T |
10: 88,654,457 (GRCm39) |
M210K |
probably damaging |
Het |
Utp25 |
T |
C |
1: 192,805,984 (GRCm39) |
E187G |
possibly damaging |
Het |
V1ra8 |
C |
T |
6: 90,179,991 (GRCm39) |
L65F |
possibly damaging |
Het |
Vmn2r10 |
T |
C |
5: 109,149,859 (GRCm39) |
N395S |
probably damaging |
Het |
Vmn2r100 |
C |
A |
17: 19,742,382 (GRCm39) |
P252Q |
possibly damaging |
Het |
Zfp217 |
C |
T |
2: 169,957,382 (GRCm39) |
A539T |
probably benign |
Het |
Zfp330 |
G |
A |
8: 83,491,511 (GRCm39) |
Q221* |
probably null |
Het |
|
Other mutations in Ap5z1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01382:Ap5z1
|
APN |
5 |
142,458,006 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01456:Ap5z1
|
APN |
5 |
142,453,791 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01656:Ap5z1
|
APN |
5 |
142,456,069 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02079:Ap5z1
|
APN |
5 |
142,462,868 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02134:Ap5z1
|
APN |
5 |
142,460,214 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02662:Ap5z1
|
APN |
5 |
142,462,644 (GRCm39) |
splice site |
probably null |
|
IGL02805:Ap5z1
|
APN |
5 |
142,456,038 (GRCm39) |
unclassified |
probably benign |
|
R0057:Ap5z1
|
UTSW |
5 |
142,456,144 (GRCm39) |
unclassified |
probably benign |
|
R0057:Ap5z1
|
UTSW |
5 |
142,456,144 (GRCm39) |
unclassified |
probably benign |
|
R0094:Ap5z1
|
UTSW |
5 |
142,462,567 (GRCm39) |
missense |
probably benign |
0.00 |
R0811:Ap5z1
|
UTSW |
5 |
142,461,546 (GRCm39) |
missense |
probably benign |
0.00 |
R0812:Ap5z1
|
UTSW |
5 |
142,461,546 (GRCm39) |
missense |
probably benign |
0.00 |
R1241:Ap5z1
|
UTSW |
5 |
142,455,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R1248:Ap5z1
|
UTSW |
5 |
142,460,255 (GRCm39) |
missense |
probably benign |
0.02 |
R1374:Ap5z1
|
UTSW |
5 |
142,456,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R1616:Ap5z1
|
UTSW |
5 |
142,457,991 (GRCm39) |
missense |
probably benign |
0.10 |
R1923:Ap5z1
|
UTSW |
5 |
142,458,096 (GRCm39) |
missense |
probably benign |
0.30 |
R2423:Ap5z1
|
UTSW |
5 |
142,462,532 (GRCm39) |
missense |
probably benign |
0.02 |
R3790:Ap5z1
|
UTSW |
5 |
142,456,168 (GRCm39) |
missense |
probably benign |
|
R4859:Ap5z1
|
UTSW |
5 |
142,459,748 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4965:Ap5z1
|
UTSW |
5 |
142,453,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R5147:Ap5z1
|
UTSW |
5 |
142,452,265 (GRCm39) |
missense |
probably benign |
0.02 |
R5311:Ap5z1
|
UTSW |
5 |
142,453,442 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5531:Ap5z1
|
UTSW |
5 |
142,453,536 (GRCm39) |
missense |
probably benign |
|
R5569:Ap5z1
|
UTSW |
5 |
142,460,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R5725:Ap5z1
|
UTSW |
5 |
142,454,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R7287:Ap5z1
|
UTSW |
5 |
142,459,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R7407:Ap5z1
|
UTSW |
5 |
142,452,330 (GRCm39) |
missense |
probably benign |
0.06 |
R7537:Ap5z1
|
UTSW |
5 |
142,463,053 (GRCm39) |
missense |
probably benign |
0.06 |
R7894:Ap5z1
|
UTSW |
5 |
142,456,191 (GRCm39) |
nonsense |
probably null |
|
R7894:Ap5z1
|
UTSW |
5 |
142,452,039 (GRCm39) |
missense |
probably benign |
0.34 |
R7895:Ap5z1
|
UTSW |
5 |
142,456,313 (GRCm39) |
critical splice donor site |
probably null |
|
R8022:Ap5z1
|
UTSW |
5 |
142,455,904 (GRCm39) |
critical splice donor site |
probably null |
|
R8244:Ap5z1
|
UTSW |
5 |
142,459,735 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8823:Ap5z1
|
UTSW |
5 |
142,460,191 (GRCm39) |
missense |
probably benign |
0.19 |
R8867:Ap5z1
|
UTSW |
5 |
142,463,011 (GRCm39) |
missense |
probably benign |
0.05 |
R9673:Ap5z1
|
UTSW |
5 |
142,463,113 (GRCm39) |
missense |
probably benign |
0.32 |
|