Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
G |
7: 119,846,076 (GRCm39) |
T576A |
probably damaging |
Het |
As3mt |
A |
G |
19: 46,708,864 (GRCm39) |
E286G |
probably benign |
Het |
Baiap3 |
G |
T |
17: 25,467,351 (GRCm39) |
|
probably benign |
Het |
C1qc |
T |
C |
4: 136,617,445 (GRCm39) |
E217G |
probably damaging |
Het |
Ccser2 |
A |
G |
14: 36,662,021 (GRCm39) |
Y388H |
probably damaging |
Het |
Clcn7 |
C |
A |
17: 25,370,097 (GRCm39) |
A328D |
probably damaging |
Het |
Clstn1 |
G |
A |
4: 149,719,700 (GRCm39) |
R415Q |
probably damaging |
Het |
Heph |
A |
T |
X: 95,571,284 (GRCm39) |
D748V |
probably damaging |
Het |
Herc1 |
C |
T |
9: 66,383,402 (GRCm39) |
T3691I |
probably benign |
Het |
Hsd17b14 |
A |
G |
7: 45,216,137 (GRCm39) |
T236A |
possibly damaging |
Het |
Kif28 |
C |
A |
1: 179,530,081 (GRCm39) |
L693F |
probably damaging |
Het |
Mnd1 |
T |
C |
3: 84,045,505 (GRCm39) |
E33G |
possibly damaging |
Het |
Nbas |
T |
G |
12: 13,503,076 (GRCm39) |
D1520E |
probably benign |
Het |
Poli |
C |
T |
18: 70,658,561 (GRCm39) |
G81R |
probably damaging |
Het |
Pou6f2 |
G |
A |
13: 18,314,170 (GRCm39) |
S401F |
probably damaging |
Het |
Ppp1r3c |
G |
A |
19: 36,711,324 (GRCm39) |
R149W |
probably damaging |
Het |
Ptprc |
C |
A |
1: 138,043,359 (GRCm39) |
C64F |
probably damaging |
Het |
Ptprz1 |
T |
C |
6: 22,973,053 (GRCm39) |
Y274H |
probably damaging |
Het |
Ranbp2 |
T |
A |
10: 58,313,434 (GRCm39) |
L1385I |
probably benign |
Het |
Sgms1 |
A |
T |
19: 32,137,025 (GRCm39) |
F180L |
probably damaging |
Het |
Slc7a9 |
T |
A |
7: 35,160,312 (GRCm39) |
M396K |
probably damaging |
Het |
Syt17 |
T |
C |
7: 118,033,513 (GRCm39) |
D165G |
probably damaging |
Het |
Tnxb |
T |
C |
17: 34,911,356 (GRCm39) |
L1553P |
probably damaging |
Het |
Trim31 |
C |
A |
17: 37,220,133 (GRCm39) |
Q350K |
probably benign |
Het |
Wnk3 |
A |
G |
X: 150,016,025 (GRCm39) |
R494G |
probably damaging |
Het |
Zmym6 |
A |
G |
4: 127,017,978 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Hcn4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
R3958:Hcn4
|
UTSW |
9 |
58,751,331 (GRCm39) |
missense |
unknown |
|
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 |
|
|