Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
A |
G |
13: 119,621,016 (GRCm39) |
I572M |
possibly damaging |
Het |
4930447A16Rik |
T |
C |
15: 37,425,863 (GRCm39) |
M1T |
probably null |
Het |
4930590J08Rik |
C |
A |
6: 91,919,559 (GRCm39) |
C739* |
probably null |
Het |
Adcy1 |
T |
A |
11: 7,096,514 (GRCm39) |
V634E |
probably benign |
Het |
Ankfy1 |
T |
A |
11: 72,644,434 (GRCm39) |
H710Q |
possibly damaging |
Het |
Ankrd60 |
C |
T |
2: 173,412,859 (GRCm39) |
V90M |
probably damaging |
Het |
Asgr2 |
A |
T |
11: 69,988,703 (GRCm39) |
Q132L |
probably benign |
Het |
Cchcr1 |
T |
A |
17: 35,839,865 (GRCm39) |
|
probably null |
Het |
Clec3a |
G |
T |
8: 115,152,476 (GRCm39) |
G161C |
probably damaging |
Het |
Cracr2b |
G |
A |
7: 141,044,848 (GRCm39) |
|
probably benign |
Het |
Cyp2b10 |
A |
T |
7: 25,597,160 (GRCm39) |
L17F |
probably damaging |
Het |
Dhx29 |
T |
A |
13: 113,084,748 (GRCm39) |
N655K |
probably benign |
Het |
Dst |
C |
A |
1: 34,332,508 (GRCm39) |
L4748I |
probably damaging |
Het |
Eif2b5 |
G |
C |
16: 20,321,303 (GRCm39) |
L285F |
probably benign |
Het |
Enox1 |
T |
A |
14: 77,875,117 (GRCm39) |
D441E |
probably damaging |
Het |
Fam110a |
T |
C |
2: 151,812,404 (GRCm39) |
E122G |
probably damaging |
Het |
Fam161b |
T |
A |
12: 84,395,413 (GRCm39) |
E510V |
probably damaging |
Het |
Gabrd |
T |
C |
4: 155,469,880 (GRCm39) |
Y443C |
probably damaging |
Het |
Gcn1 |
T |
G |
5: 115,733,118 (GRCm39) |
S1052A |
probably benign |
Het |
Gnptab |
A |
G |
10: 88,264,419 (GRCm39) |
E279G |
possibly damaging |
Het |
Hoxa6 |
T |
A |
6: 52,185,163 (GRCm39) |
|
probably null |
Het |
Ibtk |
T |
A |
9: 85,590,234 (GRCm39) |
|
probably benign |
Het |
Il6ra |
A |
T |
3: 89,785,149 (GRCm39) |
|
probably null |
Het |
Iqgap3 |
C |
T |
3: 87,998,032 (GRCm39) |
|
probably benign |
Het |
Kcnk2 |
A |
C |
1: 189,071,998 (GRCm39) |
L110R |
probably damaging |
Het |
Knl1 |
T |
A |
2: 118,927,916 (GRCm39) |
V1919D |
possibly damaging |
Het |
Lrp1b |
A |
T |
2: 40,779,251 (GRCm39) |
L2597Q |
probably benign |
Het |
Magi3 |
A |
G |
3: 103,923,358 (GRCm39) |
S1120P |
probably benign |
Het |
Map3k8 |
T |
C |
18: 4,349,162 (GRCm39) |
D52G |
probably benign |
Het |
Mcat |
C |
T |
15: 83,433,449 (GRCm39) |
R198H |
probably benign |
Het |
Mnd1 |
A |
G |
3: 84,012,286 (GRCm39) |
V141A |
probably benign |
Het |
Morc1 |
T |
C |
16: 48,407,485 (GRCm39) |
L667P |
probably benign |
Het |
Mrps6 |
A |
G |
16: 91,908,808 (GRCm39) |
K125E |
possibly damaging |
Het |
Mst1 |
T |
C |
9: 107,959,500 (GRCm39) |
F262S |
probably damaging |
Het |
Or5j3 |
T |
G |
2: 86,128,941 (GRCm39) |
I260M |
probably damaging |
Het |
Or7e178 |
T |
A |
9: 20,225,875 (GRCm39) |
I114F |
probably damaging |
Het |
Pbsn |
C |
G |
X: 76,897,046 (GRCm39) |
G15A |
possibly damaging |
Het |
Pcnx1 |
T |
C |
12: 82,038,804 (GRCm39) |
I2023T |
probably benign |
Het |
Pds5a |
T |
G |
5: 65,813,744 (GRCm39) |
N247T |
probably damaging |
Het |
Peak1 |
T |
C |
9: 56,167,373 (GRCm39) |
Y185C |
probably damaging |
Het |
Phkb |
T |
A |
8: 86,744,031 (GRCm39) |
I560N |
probably damaging |
Het |
Plekhn1 |
T |
C |
4: 156,309,658 (GRCm39) |
I160V |
probably damaging |
Het |
Rabgap1 |
T |
G |
2: 37,379,729 (GRCm39) |
|
probably benign |
Het |
Rdh10 |
T |
G |
1: 16,199,517 (GRCm39) |
V241G |
probably damaging |
Het |
Selenow |
A |
T |
7: 15,654,042 (GRCm39) |
C37S |
probably benign |
Het |
Sema6a |
A |
T |
18: 47,403,872 (GRCm39) |
|
probably null |
Het |
Slc12a3 |
T |
C |
8: 95,057,153 (GRCm39) |
|
probably null |
Het |
Slc22a21 |
T |
G |
11: 53,842,636 (GRCm39) |
M498L |
probably benign |
Het |
Spink5 |
A |
T |
18: 44,122,486 (GRCm39) |
N317I |
probably damaging |
Het |
Srek1 |
A |
G |
13: 103,885,370 (GRCm39) |
|
probably benign |
Het |
Syt11 |
A |
G |
3: 88,655,230 (GRCm39) |
V357A |
probably benign |
Het |
Tcof1 |
T |
A |
18: 60,962,107 (GRCm39) |
K707N |
possibly damaging |
Het |
Tfip11 |
C |
T |
5: 112,475,960 (GRCm39) |
R42C |
probably damaging |
Het |
Trim39 |
T |
C |
17: 36,574,623 (GRCm39) |
K260E |
probably benign |
Het |
Ttn |
T |
C |
2: 76,553,663 (GRCm39) |
T22658A |
possibly damaging |
Het |
Unc45b |
C |
T |
11: 82,827,638 (GRCm39) |
|
probably benign |
Het |
Vmn1r236 |
A |
G |
17: 21,507,172 (GRCm39) |
I97V |
probably benign |
Het |
Vps13c |
T |
C |
9: 67,881,001 (GRCm39) |
V657A |
probably damaging |
Het |
Zkscan2 |
A |
G |
7: 123,097,898 (GRCm39) |
V166A |
probably benign |
Het |
|
Other mutations in Ces1h |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00160:Ces1h
|
APN |
8 |
94,084,091 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00227:Ces1h
|
APN |
8 |
94,079,098 (GRCm39) |
missense |
unknown |
|
IGL02343:Ces1h
|
APN |
8 |
94,078,654 (GRCm39) |
makesense |
probably null |
|
IGL02490:Ces1h
|
APN |
8 |
94,083,627 (GRCm39) |
critical splice donor site |
probably null |
|
H8786:Ces1h
|
UTSW |
8 |
94,089,550 (GRCm39) |
missense |
probably damaging |
0.99 |
P0012:Ces1h
|
UTSW |
8 |
94,080,138 (GRCm39) |
missense |
unknown |
|
R0395:Ces1h
|
UTSW |
8 |
94,083,706 (GRCm39) |
missense |
unknown |
|
R0538:Ces1h
|
UTSW |
8 |
94,083,628 (GRCm39) |
critical splice donor site |
probably null |
|
R0562:Ces1h
|
UTSW |
8 |
94,083,771 (GRCm39) |
missense |
unknown |
|
R1854:Ces1h
|
UTSW |
8 |
94,085,450 (GRCm39) |
missense |
probably benign |
0.13 |
R5945:Ces1h
|
UTSW |
8 |
94,090,254 (GRCm39) |
missense |
probably benign |
0.04 |
R5950:Ces1h
|
UTSW |
8 |
94,089,587 (GRCm39) |
missense |
probably benign |
|
R6015:Ces1h
|
UTSW |
8 |
94,083,691 (GRCm39) |
missense |
unknown |
|
R6275:Ces1h
|
UTSW |
8 |
94,099,274 (GRCm39) |
missense |
probably benign |
0.23 |
R6317:Ces1h
|
UTSW |
8 |
94,084,046 (GRCm39) |
missense |
unknown |
|
R6647:Ces1h
|
UTSW |
8 |
94,078,654 (GRCm39) |
makesense |
probably null |
|
R6981:Ces1h
|
UTSW |
8 |
94,080,123 (GRCm39) |
missense |
unknown |
|
R7800:Ces1h
|
UTSW |
8 |
94,106,322 (GRCm39) |
missense |
|
|
R7861:Ces1h
|
UTSW |
8 |
94,084,053 (GRCm39) |
missense |
unknown |
|
R8121:Ces1h
|
UTSW |
8 |
94,080,104 (GRCm39) |
missense |
unknown |
|
R8897:Ces1h
|
UTSW |
8 |
94,080,093 (GRCm39) |
missense |
unknown |
|
R9355:Ces1h
|
UTSW |
8 |
94,101,149 (GRCm39) |
missense |
|
|
X0027:Ces1h
|
UTSW |
8 |
94,089,506 (GRCm39) |
missense |
probably benign |
0.00 |
X0066:Ces1h
|
UTSW |
8 |
94,078,662 (GRCm39) |
missense |
unknown |
|
Z1177:Ces1h
|
UTSW |
8 |
94,093,468 (GRCm39) |
critical splice acceptor site |
probably null |
|
|