Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef38 |
T |
G |
3: 132,866,529 (GRCm39) |
K203Q |
|
Het |
Cacna1d |
G |
A |
14: 29,796,925 (GRCm39) |
R1517W |
probably damaging |
Het |
Ccdc80 |
T |
A |
16: 44,915,949 (GRCm39) |
M235K |
probably damaging |
Het |
Cdc42bpg |
T |
C |
19: 6,372,149 (GRCm39) |
S1414P |
probably damaging |
Het |
Dab2ip |
A |
G |
2: 35,602,891 (GRCm39) |
D395G |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,358,945 (GRCm39) |
E255G |
probably benign |
Het |
Dnaja1 |
T |
A |
4: 40,724,133 (GRCm39) |
M98K |
probably benign |
Het |
Dnajb7 |
G |
A |
15: 81,292,266 (GRCm39) |
R24C |
probably benign |
Het |
Dscc1 |
C |
A |
15: 54,947,505 (GRCm39) |
W225L |
probably damaging |
Het |
Dsg2 |
T |
A |
18: 20,727,223 (GRCm39) |
V590D |
probably benign |
Het |
Epcam |
A |
G |
17: 87,947,960 (GRCm39) |
|
probably benign |
Het |
Fbn2 |
T |
C |
18: 58,257,344 (GRCm39) |
Y341C |
probably damaging |
Het |
Fry |
T |
G |
5: 150,322,728 (GRCm39) |
L1040R |
probably damaging |
Het |
Gm9639 |
C |
T |
10: 77,630,828 (GRCm39) |
C28Y |
unknown |
Het |
Hsd17b7 |
A |
G |
1: 169,794,833 (GRCm39) |
S69P |
probably damaging |
Het |
Igsf1 |
A |
G |
X: 48,884,191 (GRCm39) |
M2T |
possibly damaging |
Het |
Katnip |
T |
A |
7: 125,469,867 (GRCm39) |
D1445E |
probably damaging |
Het |
Kmt2d |
TGCTGCTGCTGCTGCTGCTGG |
TG |
15: 98,747,499 (GRCm39) |
|
probably null |
Het |
Lrp5 |
T |
C |
19: 3,654,190 (GRCm39) |
Y1079C |
probably damaging |
Het |
Lrp6 |
T |
C |
6: 134,457,467 (GRCm39) |
D779G |
probably damaging |
Het |
Nbea |
AC |
A |
3: 55,998,393 (GRCm39) |
|
probably null |
Het |
Pacsin1 |
A |
G |
17: 27,923,924 (GRCm39) |
D106G |
probably damaging |
Het |
Pcm1 |
T |
A |
8: 41,732,790 (GRCm39) |
D682E |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,023,231 (GRCm39) |
D269G |
probably benign |
Het |
Rcor1 |
T |
A |
12: 111,078,327 (GRCm39) |
V474E |
|
Het |
Rdh16 |
A |
G |
10: 127,649,306 (GRCm39) |
D254G |
probably benign |
Het |
Rp1 |
A |
T |
1: 4,418,675 (GRCm39) |
D812E |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,419,160 (GRCm39) |
S651P |
probably benign |
Het |
Sec16b |
G |
A |
1: 157,359,748 (GRCm39) |
|
probably benign |
Het |
Sephs2 |
C |
T |
7: 126,872,122 (GRCm39) |
G324S |
probably damaging |
Het |
Sirpb1a |
T |
C |
3: 15,481,992 (GRCm39) |
D112G |
probably damaging |
Het |
Slc25a47 |
C |
G |
12: 108,820,215 (GRCm39) |
T73S |
probably benign |
Het |
Slco4c1 |
A |
T |
1: 96,799,509 (GRCm39) |
L109H |
probably damaging |
Het |
Smc2 |
A |
G |
4: 52,470,848 (GRCm39) |
E845G |
possibly damaging |
Het |
Sstr3 |
G |
T |
15: 78,423,792 (GRCm39) |
N318K |
probably damaging |
Het |
Suz12 |
A |
G |
11: 79,904,087 (GRCm39) |
|
probably benign |
Het |
Sycp2 |
A |
G |
2: 178,035,931 (GRCm39) |
I252T |
probably damaging |
Het |
Syne3 |
T |
C |
12: 104,934,415 (GRCm39) |
Y118C |
probably damaging |
Het |
Tbx18 |
C |
A |
9: 87,611,521 (GRCm39) |
A170S |
probably damaging |
Het |
Trak2 |
T |
C |
1: 58,985,481 (GRCm39) |
N6D |
probably benign |
Het |
Ttn |
G |
A |
2: 76,720,868 (GRCm39) |
T6852I |
unknown |
Het |
Tufm |
A |
G |
7: 126,088,100 (GRCm39) |
E201G |
probably damaging |
Het |
Vwa3b |
C |
A |
1: 37,099,493 (GRCm39) |
P236Q |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,345,289 (GRCm39) |
Y2510C |
possibly damaging |
Het |
|
Other mutations in Akr1c14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01759:Akr1c14
|
APN |
13 |
4,131,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02085:Akr1c14
|
APN |
13 |
4,128,035 (GRCm39) |
nonsense |
probably null |
|
IGL02201:Akr1c14
|
APN |
13 |
4,131,022 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02419:Akr1c14
|
APN |
13 |
4,130,617 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03293:Akr1c14
|
APN |
13 |
4,129,130 (GRCm39) |
nonsense |
probably null |
|
PIT4362001:Akr1c14
|
UTSW |
13 |
4,129,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R0518:Akr1c14
|
UTSW |
13 |
4,131,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R2168:Akr1c14
|
UTSW |
13 |
4,131,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R4751:Akr1c14
|
UTSW |
13 |
4,115,338 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4812:Akr1c14
|
UTSW |
13 |
4,129,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R5030:Akr1c14
|
UTSW |
13 |
4,129,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R6329:Akr1c14
|
UTSW |
13 |
4,137,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R6590:Akr1c14
|
UTSW |
13 |
4,113,713 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6612:Akr1c14
|
UTSW |
13 |
4,115,331 (GRCm39) |
missense |
probably benign |
0.00 |
R6690:Akr1c14
|
UTSW |
13 |
4,113,713 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7033:Akr1c14
|
UTSW |
13 |
4,129,178 (GRCm39) |
critical splice donor site |
probably null |
|
R7200:Akr1c14
|
UTSW |
13 |
4,131,051 (GRCm39) |
missense |
probably benign |
0.00 |
R7257:Akr1c14
|
UTSW |
13 |
4,138,966 (GRCm39) |
missense |
probably benign |
0.03 |
R7432:Akr1c14
|
UTSW |
13 |
4,138,952 (GRCm39) |
missense |
probably benign |
|
R7536:Akr1c14
|
UTSW |
13 |
4,113,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R7769:Akr1c14
|
UTSW |
13 |
4,109,644 (GRCm39) |
missense |
probably benign |
0.00 |
R7941:Akr1c14
|
UTSW |
13 |
4,109,713 (GRCm39) |
missense |
probably benign |
|
R8292:Akr1c14
|
UTSW |
13 |
4,130,995 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8700:Akr1c14
|
UTSW |
13 |
4,131,157 (GRCm39) |
critical splice donor site |
probably benign |
|
R9135:Akr1c14
|
UTSW |
13 |
4,128,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Akr1c14
|
UTSW |
13 |
4,130,695 (GRCm39) |
missense |
possibly damaging |
0.51 |
|