Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl9 |
A |
G |
17: 33,652,738 (GRCm39) |
K266R |
probably benign |
Het |
Cebpd |
T |
C |
16: 15,705,327 (GRCm39) |
S47P |
possibly damaging |
Het |
Celf4 |
A |
G |
18: 25,670,811 (GRCm39) |
M124T |
probably benign |
Het |
Ckap4 |
C |
T |
10: 84,364,028 (GRCm39) |
R345H |
probably benign |
Het |
Clasp1 |
T |
C |
1: 118,395,611 (GRCm39) |
V183A |
probably damaging |
Het |
Cyp2s1 |
C |
T |
7: 25,503,379 (GRCm39) |
R424Q |
probably null |
Het |
Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
Etl4 |
A |
G |
2: 20,344,854 (GRCm39) |
T53A |
probably benign |
Het |
Glyat |
A |
T |
19: 12,617,197 (GRCm39) |
K16N |
probably benign |
Het |
Gm6522 |
T |
C |
3: 106,206,120 (GRCm39) |
|
noncoding transcript |
Het |
Grin1 |
G |
A |
2: 25,203,465 (GRCm39) |
T182M |
probably damaging |
Het |
Hmgcs2 |
T |
C |
3: 98,204,793 (GRCm39) |
F317S |
possibly damaging |
Het |
Hoxd8 |
C |
T |
2: 74,536,884 (GRCm39) |
Q18* |
probably null |
Het |
Itpr2 |
C |
T |
6: 146,327,008 (GRCm39) |
V120I |
probably damaging |
Het |
Kmt2d |
G |
A |
15: 98,753,430 (GRCm39) |
T141M |
possibly damaging |
Het |
Lrp1 |
A |
G |
10: 127,407,827 (GRCm39) |
S1821P |
probably benign |
Het |
Neb |
T |
C |
2: 52,153,641 (GRCm39) |
E2428G |
probably damaging |
Het |
Nepn |
T |
C |
10: 52,276,804 (GRCm39) |
V119A |
probably benign |
Het |
Or4k41 |
G |
T |
2: 111,280,230 (GRCm39) |
L248F |
possibly damaging |
Het |
Otogl |
T |
C |
10: 107,657,786 (GRCm39) |
D1048G |
probably damaging |
Het |
Panx1 |
GTTCTTCT |
GTTCT |
9: 14,917,467 (GRCm39) |
|
probably benign |
Het |
Ppp6r3 |
A |
T |
19: 3,546,583 (GRCm39) |
V305D |
probably damaging |
Het |
Prkg2 |
G |
T |
5: 99,145,354 (GRCm39) |
T160K |
possibly damaging |
Het |
Prmt8 |
G |
A |
6: 127,709,707 (GRCm39) |
T51I |
probably benign |
Het |
Rgl3 |
T |
C |
9: 21,886,885 (GRCm39) |
|
probably benign |
Het |
Sec23ip |
C |
G |
7: 128,378,574 (GRCm39) |
T796S |
probably benign |
Het |
Selp |
T |
C |
1: 163,953,855 (GRCm39) |
S52P |
probably benign |
Het |
Slc44a2 |
T |
C |
9: 21,259,837 (GRCm39) |
I615T |
probably damaging |
Het |
Snap91 |
T |
C |
9: 86,720,183 (GRCm39) |
Y118C |
probably damaging |
Het |
Tmem106b |
A |
T |
6: 13,081,587 (GRCm39) |
N165Y |
probably damaging |
Het |
Ucp3 |
A |
G |
7: 100,131,946 (GRCm39) |
T266A |
probably benign |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Utrn |
T |
C |
10: 12,625,852 (GRCm39) |
I110V |
probably damaging |
Het |
|
Other mutations in Hcn4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00486:Hcn4
|
APN |
9 |
58,767,336 (GRCm39) |
missense |
unknown |
|
IGL00939:Hcn4
|
APN |
9 |
58,751,210 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01154:Hcn4
|
APN |
9 |
58,766,362 (GRCm39) |
missense |
unknown |
|
IGL01408:Hcn4
|
APN |
9 |
58,767,169 (GRCm39) |
missense |
unknown |
|
IGL02658:Hcn4
|
APN |
9 |
58,766,748 (GRCm39) |
missense |
unknown |
|
IGL02877:Hcn4
|
APN |
9 |
58,766,450 (GRCm39) |
missense |
unknown |
|
IGL03211:Hcn4
|
APN |
9 |
58,765,434 (GRCm39) |
missense |
unknown |
|
PIT1430001:Hcn4
|
UTSW |
9 |
58,766,833 (GRCm39) |
missense |
unknown |
|
R0049:Hcn4
|
UTSW |
9 |
58,767,582 (GRCm39) |
missense |
probably damaging |
0.98 |
R0268:Hcn4
|
UTSW |
9 |
58,767,445 (GRCm39) |
missense |
unknown |
|
R0812:Hcn4
|
UTSW |
9 |
58,730,795 (GRCm39) |
start codon destroyed |
probably null |
|
R2121:Hcn4
|
UTSW |
9 |
58,731,341 (GRCm39) |
missense |
unknown |
|
R3035:Hcn4
|
UTSW |
9 |
58,730,963 (GRCm39) |
missense |
unknown |
|
R3715:Hcn4
|
UTSW |
9 |
58,751,319 (GRCm39) |
missense |
unknown |
|
R3737:Hcn4
|
UTSW |
9 |
58,751,172 (GRCm39) |
missense |
probably benign |
0.39 |
R4035:Hcn4
|
UTSW |
9 |
58,751,172 (GRCm39) |
missense |
probably benign |
0.39 |
R4393:Hcn4
|
UTSW |
9 |
58,751,583 (GRCm39) |
missense |
unknown |
|
R4418:Hcn4
|
UTSW |
9 |
58,751,178 (GRCm39) |
missense |
probably benign |
0.39 |
R4532:Hcn4
|
UTSW |
9 |
58,765,081 (GRCm39) |
missense |
unknown |
|
R4765:Hcn4
|
UTSW |
9 |
58,765,260 (GRCm39) |
missense |
unknown |
|
R4857:Hcn4
|
UTSW |
9 |
58,766,853 (GRCm39) |
missense |
unknown |
|
R4967:Hcn4
|
UTSW |
9 |
58,767,111 (GRCm39) |
missense |
unknown |
|
R5068:Hcn4
|
UTSW |
9 |
58,767,304 (GRCm39) |
missense |
unknown |
|
R5253:Hcn4
|
UTSW |
9 |
58,731,558 (GRCm39) |
missense |
unknown |
|
R5304:Hcn4
|
UTSW |
9 |
58,751,215 (GRCm39) |
missense |
probably benign |
0.39 |
R5600:Hcn4
|
UTSW |
9 |
58,766,576 (GRCm39) |
splice site |
probably null |
|
R6346:Hcn4
|
UTSW |
9 |
58,766,327 (GRCm39) |
missense |
unknown |
|
R6575:Hcn4
|
UTSW |
9 |
58,731,435 (GRCm39) |
missense |
unknown |
|
R6622:Hcn4
|
UTSW |
9 |
58,765,010 (GRCm39) |
missense |
unknown |
|
R6967:Hcn4
|
UTSW |
9 |
58,731,228 (GRCm39) |
missense |
unknown |
|
R7038:Hcn4
|
UTSW |
9 |
58,730,867 (GRCm39) |
missense |
unknown |
|
R7054:Hcn4
|
UTSW |
9 |
58,763,000 (GRCm39) |
missense |
unknown |
|
R7229:Hcn4
|
UTSW |
9 |
58,760,682 (GRCm39) |
missense |
unknown |
|
R7407:Hcn4
|
UTSW |
9 |
58,766,653 (GRCm39) |
missense |
unknown |
|
R7448:Hcn4
|
UTSW |
9 |
58,751,582 (GRCm39) |
missense |
unknown |
|
R7531:Hcn4
|
UTSW |
9 |
58,767,420 (GRCm39) |
missense |
unknown |
|
R7572:Hcn4
|
UTSW |
9 |
58,731,063 (GRCm39) |
missense |
unknown |
|
R7680:Hcn4
|
UTSW |
9 |
58,767,954 (GRCm39) |
missense |
probably benign |
0.08 |
R7915:Hcn4
|
UTSW |
9 |
58,731,218 (GRCm39) |
missense |
unknown |
|
R7956:Hcn4
|
UTSW |
9 |
58,751,456 (GRCm39) |
missense |
unknown |
|
R8146:Hcn4
|
UTSW |
9 |
58,731,027 (GRCm39) |
missense |
unknown |
|
R8234:Hcn4
|
UTSW |
9 |
58,751,433 (GRCm39) |
missense |
unknown |
|
R8421:Hcn4
|
UTSW |
9 |
58,765,379 (GRCm39) |
missense |
unknown |
|
R8690:Hcn4
|
UTSW |
9 |
58,751,193 (GRCm39) |
missense |
probably benign |
0.39 |
R8855:Hcn4
|
UTSW |
9 |
58,765,387 (GRCm39) |
missense |
unknown |
|
R8884:Hcn4
|
UTSW |
9 |
58,760,705 (GRCm39) |
missense |
unknown |
|
R9017:Hcn4
|
UTSW |
9 |
58,731,482 (GRCm39) |
missense |
unknown |
|
R9151:Hcn4
|
UTSW |
9 |
58,767,880 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9331:Hcn4
|
UTSW |
9 |
58,767,705 (GRCm39) |
missense |
probably damaging |
0.97 |
R9433:Hcn4
|
UTSW |
9 |
58,731,222 (GRCm39) |
missense |
unknown |
|
R9523:Hcn4
|
UTSW |
9 |
58,766,809 (GRCm39) |
missense |
unknown |
|
R9541:Hcn4
|
UTSW |
9 |
58,767,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R9730:Hcn4
|
UTSW |
9 |
58,731,493 (GRCm39) |
missense |
unknown |
|
R9748:Hcn4
|
UTSW |
9 |
58,730,996 (GRCm39) |
missense |
unknown |
|
R9753:Hcn4
|
UTSW |
9 |
58,751,319 (GRCm39) |
missense |
unknown |
|
R9795:Hcn4
|
UTSW |
9 |
58,760,762 (GRCm39) |
nonsense |
probably null |
|
RF011:Hcn4
|
UTSW |
9 |
58,767,198 (GRCm39) |
missense |
unknown |
|
X0009:Hcn4
|
UTSW |
9 |
58,768,042 (GRCm39) |
nonsense |
probably null |
|
X0057:Hcn4
|
UTSW |
9 |
58,766,651 (GRCm39) |
missense |
unknown |
|
Z1176:Hcn4
|
UTSW |
9 |
58,765,431 (GRCm39) |
missense |
unknown |
|
|