Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
T |
C |
5: 8,903,468 (GRCm39) |
F1040L |
probably damaging |
Het |
Adamts7 |
A |
G |
9: 90,075,745 (GRCm39) |
N1201S |
probably benign |
Het |
Ahnak |
C |
T |
19: 8,983,089 (GRCm39) |
P1458S |
probably damaging |
Het |
Akap6 |
T |
C |
12: 53,187,707 (GRCm39) |
V1707A |
probably benign |
Het |
Arap2 |
A |
C |
5: 62,833,361 (GRCm39) |
C894G |
probably damaging |
Het |
Atp2a2 |
T |
C |
5: 122,604,901 (GRCm39) |
D426G |
possibly damaging |
Het |
Azi2 |
A |
T |
9: 117,884,909 (GRCm39) |
Q132L |
possibly damaging |
Het |
Carmil1 |
C |
T |
13: 24,283,032 (GRCm39) |
D91N |
probably damaging |
Het |
Cnot7 |
A |
T |
8: 40,960,494 (GRCm39) |
|
probably null |
Het |
Cntnap5b |
A |
G |
1: 100,202,086 (GRCm39) |
E311G |
probably benign |
Het |
Csmd1 |
A |
G |
8: 16,283,036 (GRCm39) |
V640A |
probably benign |
Het |
Cst7 |
T |
C |
2: 150,417,647 (GRCm39) |
S31P |
probably benign |
Het |
Cyp7b1 |
T |
A |
3: 18,151,530 (GRCm39) |
I228L |
probably benign |
Het |
Ddx28 |
G |
A |
8: 106,736,921 (GRCm39) |
T379I |
probably benign |
Het |
Drd1 |
T |
A |
13: 54,207,600 (GRCm39) |
I205F |
probably damaging |
Het |
Flnb |
T |
A |
14: 7,896,115 (GRCm38) |
V837D |
probably damaging |
Het |
Fsd1l |
A |
G |
4: 53,647,664 (GRCm39) |
|
probably null |
Het |
Fubp1 |
T |
A |
3: 151,925,841 (GRCm39) |
Y264* |
probably null |
Het |
Gbp5 |
T |
A |
3: 142,212,680 (GRCm39) |
|
probably null |
Het |
Gm7094 |
A |
G |
1: 21,342,958 (GRCm39) |
|
noncoding transcript |
Het |
Gpr55 |
A |
G |
1: 85,868,858 (GRCm39) |
V241A |
probably benign |
Het |
Impa1 |
C |
T |
3: 10,394,020 (GRCm39) |
A16T |
probably damaging |
Het |
Llgl2 |
T |
C |
11: 115,735,680 (GRCm39) |
L92P |
probably damaging |
Het |
Ltbp2 |
T |
A |
12: 84,833,132 (GRCm39) |
Q1472L |
probably benign |
Het |
Lyplal1 |
A |
T |
1: 185,820,943 (GRCm39) |
M168K |
probably benign |
Het |
Macc1 |
A |
T |
12: 119,410,815 (GRCm39) |
R528* |
probably null |
Het |
Mdm1 |
T |
A |
10: 118,002,585 (GRCm39) |
D635E |
probably damaging |
Het |
Miox |
C |
T |
15: 89,220,477 (GRCm39) |
L189F |
possibly damaging |
Het |
Mrpl23 |
C |
T |
7: 142,088,851 (GRCm39) |
R69W |
probably damaging |
Het |
Ncoa6 |
TGC |
TGCGC |
2: 155,250,211 (GRCm39) |
|
probably null |
Het |
Nr0b2 |
A |
G |
4: 133,281,049 (GRCm39) |
Q105R |
probably damaging |
Het |
Or8b53 |
T |
A |
9: 38,667,484 (GRCm39) |
S167T |
probably benign |
Het |
Otog |
G |
A |
7: 45,953,655 (GRCm39) |
V2638M |
probably damaging |
Het |
Pcdhb14 |
A |
T |
18: 37,581,542 (GRCm39) |
|
probably null |
Het |
Plxna1 |
A |
G |
6: 89,310,001 (GRCm39) |
W1055R |
probably damaging |
Het |
Pramel22 |
T |
A |
4: 143,381,081 (GRCm39) |
H314L |
probably benign |
Het |
Prdm1 |
C |
T |
10: 44,316,087 (GRCm39) |
R716Q |
probably damaging |
Het |
Proser1 |
C |
A |
3: 53,388,038 (GRCm39) |
Q909K |
possibly damaging |
Het |
Pus10 |
T |
A |
11: 23,617,358 (GRCm39) |
C24S |
probably damaging |
Het |
Rpl27 |
T |
A |
11: 101,336,146 (GRCm39) |
F69I |
possibly damaging |
Het |
Sctr |
A |
T |
1: 119,983,124 (GRCm39) |
I325F |
probably damaging |
Het |
Slc49a4 |
G |
A |
16: 35,539,684 (GRCm39) |
T379I |
possibly damaging |
Het |
Slc5a3 |
G |
A |
16: 91,874,581 (GRCm39) |
V213I |
possibly damaging |
Het |
Spib |
G |
T |
7: 44,179,324 (GRCm39) |
D28E |
probably damaging |
Het |
Spic |
T |
C |
10: 88,511,579 (GRCm39) |
S226G |
possibly damaging |
Het |
Tet1 |
T |
A |
10: 62,676,058 (GRCm39) |
T673S |
probably benign |
Het |
Tph1 |
A |
G |
7: 46,297,020 (GRCm39) |
F392L |
probably damaging |
Het |
Ttc28 |
T |
C |
5: 111,373,500 (GRCm39) |
S979P |
probably benign |
Het |
Unc79 |
T |
C |
12: 103,122,812 (GRCm39) |
L2110P |
probably damaging |
Het |
Vmn1r28 |
G |
A |
6: 58,242,702 (GRCm39) |
A182T |
probably benign |
Het |
Zfp467 |
T |
C |
6: 48,415,615 (GRCm39) |
T346A |
probably benign |
Het |
|
Other mutations in Akr1c21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00645:Akr1c21
|
APN |
13 |
4,626,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01093:Akr1c21
|
APN |
13 |
4,631,139 (GRCm39) |
splice site |
probably benign |
|
IGL01408:Akr1c21
|
APN |
13 |
4,627,431 (GRCm39) |
missense |
probably benign |
|
IGL02470:Akr1c21
|
APN |
13 |
4,627,406 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02683:Akr1c21
|
APN |
13 |
4,626,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02738:Akr1c21
|
APN |
13 |
4,630,300 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03126:Akr1c21
|
APN |
13 |
4,627,457 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03365:Akr1c21
|
APN |
13 |
4,633,851 (GRCm39) |
missense |
probably benign |
0.00 |
R0391:Akr1c21
|
UTSW |
13 |
4,631,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R0505:Akr1c21
|
UTSW |
13 |
4,626,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R1069:Akr1c21
|
UTSW |
13 |
4,625,333 (GRCm39) |
splice site |
probably benign |
|
R1168:Akr1c21
|
UTSW |
13 |
4,633,836 (GRCm39) |
missense |
probably benign |
0.04 |
R1617:Akr1c21
|
UTSW |
13 |
4,626,351 (GRCm39) |
splice site |
probably null |
|
R1686:Akr1c21
|
UTSW |
13 |
4,627,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Akr1c21
|
UTSW |
13 |
4,625,177 (GRCm39) |
missense |
probably damaging |
0.98 |
R1753:Akr1c21
|
UTSW |
13 |
4,627,134 (GRCm39) |
nonsense |
probably null |
|
R1977:Akr1c21
|
UTSW |
13 |
4,624,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R2005:Akr1c21
|
UTSW |
13 |
4,624,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R2036:Akr1c21
|
UTSW |
13 |
4,626,305 (GRCm39) |
missense |
probably damaging |
0.98 |
R2198:Akr1c21
|
UTSW |
13 |
4,627,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R2925:Akr1c21
|
UTSW |
13 |
4,626,349 (GRCm39) |
splice site |
probably null |
|
R4965:Akr1c21
|
UTSW |
13 |
4,630,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R6245:Akr1c21
|
UTSW |
13 |
4,625,231 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6381:Akr1c21
|
UTSW |
13 |
4,624,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R6711:Akr1c21
|
UTSW |
13 |
4,627,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R6843:Akr1c21
|
UTSW |
13 |
4,625,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R6998:Akr1c21
|
UTSW |
13 |
4,633,850 (GRCm39) |
missense |
probably benign |
0.05 |
R7253:Akr1c21
|
UTSW |
13 |
4,627,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Akr1c21
|
UTSW |
13 |
4,626,318 (GRCm39) |
missense |
probably benign |
0.09 |
R8389:Akr1c21
|
UTSW |
13 |
4,626,278 (GRCm39) |
missense |
probably damaging |
0.96 |
R8391:Akr1c21
|
UTSW |
13 |
4,626,278 (GRCm39) |
missense |
probably damaging |
0.96 |
|