Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm4 |
G |
A |
4: 144,396,683 (GRCm39) |
R350C |
possibly damaging |
Het |
Acsm3 |
T |
A |
7: 119,374,392 (GRCm39) |
S281R |
probably damaging |
Het |
Adipor2 |
G |
T |
6: 119,340,447 (GRCm39) |
|
probably benign |
Het |
Alk |
T |
C |
17: 72,204,936 (GRCm39) |
S1079G |
probably damaging |
Het |
Ankrd27 |
T |
C |
7: 35,302,009 (GRCm39) |
|
probably null |
Het |
Anxa6 |
C |
A |
11: 54,892,108 (GRCm39) |
E283* |
probably null |
Het |
Bnc2 |
T |
C |
4: 84,194,550 (GRCm39) |
H858R |
possibly damaging |
Het |
Btnl6 |
T |
C |
17: 34,727,043 (GRCm39) |
S496G |
probably benign |
Het |
Ccdc88a |
T |
C |
11: 29,410,860 (GRCm39) |
S449P |
probably benign |
Het |
Cdh23 |
A |
T |
10: 60,246,689 (GRCm39) |
D916E |
probably damaging |
Het |
Cfap43 |
A |
T |
19: 47,736,456 (GRCm39) |
L1345H |
possibly damaging |
Het |
Cyld |
A |
T |
8: 89,456,138 (GRCm39) |
H396L |
probably benign |
Het |
Czib |
A |
G |
4: 107,752,796 (GRCm39) |
N152D |
unknown |
Het |
Dera |
A |
T |
6: 137,807,202 (GRCm39) |
I217F |
probably damaging |
Het |
Dnah11 |
A |
G |
12: 118,154,539 (GRCm39) |
L247P |
probably damaging |
Het |
Eftud2 |
G |
A |
11: 102,759,447 (GRCm39) |
T152M |
probably damaging |
Het |
Entrep1 |
T |
C |
19: 23,965,858 (GRCm39) |
K214E |
probably damaging |
Het |
Epb41l2 |
C |
T |
10: 25,319,674 (GRCm39) |
T169M |
probably benign |
Het |
Fam186a |
T |
C |
15: 99,845,023 (GRCm39) |
D407G |
unknown |
Het |
Gli3 |
T |
A |
13: 15,889,619 (GRCm39) |
C578S |
probably damaging |
Het |
Gm6408 |
A |
G |
5: 146,419,237 (GRCm39) |
N84S |
probably benign |
Het |
Heatr5a |
AGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGTGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGAGCACACTGCAGGAAGCTCA |
AGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGAGCACACTGCAGGAAGCTCA |
12: 51,934,702 (GRCm39) |
|
probably benign |
Het |
Herc2 |
C |
A |
7: 55,838,361 (GRCm39) |
T3296K |
probably damaging |
Het |
Hnf4g |
A |
T |
3: 3,708,133 (GRCm39) |
|
probably benign |
Het |
Hyal4 |
C |
A |
6: 24,755,826 (GRCm39) |
Q15K |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kcna3 |
A |
G |
3: 106,943,908 (GRCm39) |
E57G |
probably damaging |
Het |
Kcnc3 |
C |
A |
7: 44,241,020 (GRCm39) |
D237E |
probably benign |
Het |
Map3k8 |
A |
G |
18: 4,343,137 (GRCm39) |
V130A |
probably benign |
Het |
Mpp7 |
A |
G |
18: 7,440,430 (GRCm39) |
|
probably null |
Het |
Mtres1 |
A |
G |
10: 43,408,933 (GRCm39) |
L70S |
probably benign |
Het |
Myh13 |
T |
A |
11: 67,233,311 (GRCm39) |
L610Q |
probably damaging |
Het |
Or13p5 |
C |
A |
4: 118,592,235 (GRCm39) |
P170T |
probably damaging |
Het |
Or5ap2 |
T |
A |
2: 85,680,246 (GRCm39) |
M150K |
probably benign |
Het |
Or8b52 |
T |
C |
9: 38,577,064 (GRCm39) |
I25M |
probably benign |
Het |
Pcdhb5 |
A |
T |
18: 37,454,129 (GRCm39) |
T170S |
probably benign |
Het |
Polr3b |
T |
A |
10: 84,516,251 (GRCm39) |
H626Q |
probably benign |
Het |
Prkg1 |
A |
T |
19: 31,742,146 (GRCm39) |
L26Q |
probably damaging |
Het |
Prob1 |
T |
C |
18: 35,787,039 (GRCm39) |
N405S |
possibly damaging |
Het |
Proz |
T |
G |
8: 13,123,630 (GRCm39) |
S300R |
probably damaging |
Het |
Psg19 |
A |
G |
7: 18,527,990 (GRCm39) |
I251T |
probably benign |
Het |
Rcbtb1 |
T |
C |
14: 59,467,401 (GRCm39) |
I413T |
possibly damaging |
Het |
Rnf144b |
T |
A |
13: 47,382,452 (GRCm39) |
Y103N |
probably damaging |
Het |
Rspry1 |
G |
C |
8: 95,358,747 (GRCm39) |
G194R |
probably benign |
Het |
Scn2b |
A |
G |
9: 45,036,917 (GRCm39) |
I142V |
probably damaging |
Het |
Spata20 |
A |
T |
11: 94,372,607 (GRCm39) |
L588H |
probably damaging |
Het |
Stk32b |
T |
A |
5: 37,614,503 (GRCm39) |
H335L |
probably benign |
Het |
Taar4 |
A |
C |
10: 23,836,801 (GRCm39) |
D137A |
possibly damaging |
Het |
Tchh |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
3: 93,354,015 (GRCm39) |
|
probably benign |
Het |
Tek |
A |
T |
4: 94,738,074 (GRCm39) |
H708L |
probably benign |
Het |
Tmem89 |
C |
T |
9: 108,744,095 (GRCm39) |
L132F |
unknown |
Het |
Ugt2b38 |
T |
C |
5: 87,559,681 (GRCm39) |
I404V |
probably benign |
Het |
Vmn1r16 |
C |
T |
6: 57,299,814 (GRCm39) |
M269I |
probably benign |
Het |
Vmn1r201 |
A |
G |
13: 22,659,422 (GRCm39) |
K212R |
probably damaging |
Het |
Vmn2r11 |
A |
C |
5: 109,201,626 (GRCm39) |
F293V |
probably damaging |
Het |
Zdhhc17 |
A |
T |
10: 110,798,240 (GRCm39) |
|
probably benign |
Het |
Zfp423 |
C |
A |
8: 88,509,338 (GRCm39) |
M335I |
probably benign |
Het |
Zfp74 |
T |
C |
7: 29,634,079 (GRCm39) |
Y543C |
probably damaging |
Het |
Zfp975 |
A |
T |
7: 42,312,264 (GRCm39) |
S116R |
probably benign |
Het |
|
Other mutations in Cyp20a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02146:Cyp20a1
|
APN |
1 |
60,410,410 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02725:Cyp20a1
|
APN |
1 |
60,405,865 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03394:Cyp20a1
|
APN |
1 |
60,405,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R0003:Cyp20a1
|
UTSW |
1 |
60,426,285 (GRCm39) |
splice site |
probably benign |
|
R0098:Cyp20a1
|
UTSW |
1 |
60,426,413 (GRCm39) |
nonsense |
probably null |
|
R0098:Cyp20a1
|
UTSW |
1 |
60,426,413 (GRCm39) |
nonsense |
probably null |
|
R0217:Cyp20a1
|
UTSW |
1 |
60,382,625 (GRCm39) |
splice site |
probably benign |
|
R0491:Cyp20a1
|
UTSW |
1 |
60,410,486 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1543:Cyp20a1
|
UTSW |
1 |
60,415,353 (GRCm39) |
splice site |
probably benign |
|
R4519:Cyp20a1
|
UTSW |
1 |
60,426,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R4621:Cyp20a1
|
UTSW |
1 |
60,415,258 (GRCm39) |
missense |
probably benign |
|
R4930:Cyp20a1
|
UTSW |
1 |
60,405,878 (GRCm39) |
missense |
probably damaging |
0.98 |
R4980:Cyp20a1
|
UTSW |
1 |
60,402,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R5088:Cyp20a1
|
UTSW |
1 |
60,402,509 (GRCm39) |
missense |
probably damaging |
0.99 |
R5356:Cyp20a1
|
UTSW |
1 |
60,418,546 (GRCm39) |
missense |
probably benign |
0.08 |
R5545:Cyp20a1
|
UTSW |
1 |
60,415,241 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5897:Cyp20a1
|
UTSW |
1 |
60,392,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R5926:Cyp20a1
|
UTSW |
1 |
60,402,401 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6317:Cyp20a1
|
UTSW |
1 |
60,391,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R6320:Cyp20a1
|
UTSW |
1 |
60,391,331 (GRCm39) |
critical splice donor site |
probably null |
|
R7471:Cyp20a1
|
UTSW |
1 |
60,393,799 (GRCm39) |
missense |
probably damaging |
0.99 |
R7681:Cyp20a1
|
UTSW |
1 |
60,392,192 (GRCm39) |
missense |
probably benign |
0.01 |
R7715:Cyp20a1
|
UTSW |
1 |
60,411,764 (GRCm39) |
missense |
probably benign |
0.00 |
R8033:Cyp20a1
|
UTSW |
1 |
60,411,750 (GRCm39) |
missense |
probably benign |
0.02 |
R8259:Cyp20a1
|
UTSW |
1 |
60,391,330 (GRCm39) |
critical splice donor site |
probably null |
|
R8430:Cyp20a1
|
UTSW |
1 |
60,402,488 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8748:Cyp20a1
|
UTSW |
1 |
60,392,181 (GRCm39) |
missense |
probably damaging |
0.98 |
R8885:Cyp20a1
|
UTSW |
1 |
60,411,765 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8935:Cyp20a1
|
UTSW |
1 |
60,410,473 (GRCm39) |
missense |
probably damaging |
0.97 |
R9171:Cyp20a1
|
UTSW |
1 |
60,415,343 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cyp20a1
|
UTSW |
1 |
60,392,169 (GRCm39) |
missense |
probably damaging |
0.96 |
|