Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503L19Rik |
T |
C |
18: 70,601,264 (GRCm39) |
N206S |
probably damaging |
Het |
Abcf2 |
A |
T |
5: 24,774,156 (GRCm39) |
Y315* |
probably null |
Het |
Adck1 |
T |
G |
12: 88,368,921 (GRCm39) |
V133G |
probably damaging |
Het |
Aoc2 |
T |
C |
11: 101,216,292 (GRCm39) |
F125S |
probably damaging |
Het |
As3mt |
A |
G |
19: 46,713,410 (GRCm39) |
D319G |
probably benign |
Het |
Atp1a2 |
C |
G |
1: 172,116,903 (GRCm39) |
R238P |
probably damaging |
Het |
Baz1a |
T |
C |
12: 55,001,585 (GRCm39) |
Q145R |
possibly damaging |
Het |
Bhlhe22 |
A |
G |
3: 18,109,778 (GRCm39) |
E276G |
probably damaging |
Het |
Cdo1 |
C |
A |
18: 46,861,104 (GRCm39) |
V36L |
probably benign |
Het |
Col6a5 |
T |
A |
9: 105,766,266 (GRCm39) |
N1885Y |
probably damaging |
Het |
Corin |
A |
T |
5: 72,496,388 (GRCm39) |
C522S |
probably damaging |
Het |
Csmd1 |
G |
T |
8: 16,760,658 (GRCm39) |
T159K |
possibly damaging |
Het |
Cspg4b |
T |
A |
13: 113,504,802 (GRCm39) |
L1977H |
probably benign |
Het |
Cwc27 |
T |
A |
13: 104,940,769 (GRCm39) |
K197* |
probably null |
Het |
Cyp20a1 |
T |
C |
1: 60,391,283 (GRCm39) |
S26P |
probably damaging |
Het |
Daxx |
T |
A |
17: 34,130,949 (GRCm39) |
D321E |
probably damaging |
Het |
Gria2 |
A |
C |
3: 80,648,311 (GRCm39) |
Y142D |
possibly damaging |
Het |
Gspt1 |
T |
C |
16: 11,041,072 (GRCm39) |
|
probably null |
Het |
Ighv1-80 |
A |
T |
12: 115,876,265 (GRCm39) |
V17D |
probably damaging |
Het |
Ints4 |
T |
A |
7: 97,178,425 (GRCm39) |
L675* |
probably null |
Het |
Kif13a |
C |
T |
13: 46,980,233 (GRCm39) |
R173Q |
probably damaging |
Het |
Map3k2 |
T |
C |
18: 32,336,086 (GRCm39) |
I91T |
probably damaging |
Het |
Map3k8 |
A |
G |
18: 4,348,979 (GRCm39) |
|
probably null |
Het |
Mcemp1 |
G |
A |
8: 3,717,284 (GRCm39) |
W101* |
probably null |
Het |
Naca |
T |
C |
10: 127,879,993 (GRCm39) |
I1675T |
probably benign |
Het |
Nol9 |
T |
C |
4: 152,125,514 (GRCm39) |
F155S |
probably damaging |
Het |
Obscn |
C |
A |
11: 58,960,721 (GRCm39) |
D3406Y |
probably damaging |
Het |
Obsl1 |
A |
G |
1: 75,466,273 (GRCm39) |
V1485A |
possibly damaging |
Het |
Oga |
A |
T |
19: 45,760,119 (GRCm39) |
|
probably null |
Het |
Or8a1 |
T |
C |
9: 37,641,725 (GRCm39) |
K185E |
possibly damaging |
Het |
Otog |
C |
A |
7: 45,950,639 (GRCm39) |
P337H |
probably damaging |
Het |
Patl1 |
T |
C |
19: 11,898,242 (GRCm39) |
L140P |
probably damaging |
Het |
Pcca |
G |
A |
14: 122,820,035 (GRCm39) |
V60M |
probably damaging |
Het |
Pex11g |
G |
T |
8: 3,514,092 (GRCm39) |
D23E |
probably damaging |
Het |
Phactr2 |
A |
T |
10: 13,137,626 (GRCm39) |
M172K |
probably damaging |
Het |
Plce1 |
G |
A |
19: 38,512,974 (GRCm39) |
W91* |
probably null |
Het |
Plch1 |
C |
T |
3: 63,688,811 (GRCm39) |
W131* |
probably null |
Het |
Podn |
A |
G |
4: 107,884,357 (GRCm39) |
F44S |
probably damaging |
Het |
Polr3e |
A |
G |
7: 120,527,205 (GRCm39) |
D87G |
possibly damaging |
Het |
Prmt2 |
T |
A |
10: 76,058,351 (GRCm39) |
I153F |
probably benign |
Het |
Prpf6 |
T |
C |
2: 181,273,229 (GRCm39) |
V258A |
probably benign |
Het |
Ptpn21 |
G |
T |
12: 98,655,521 (GRCm39) |
A482E |
probably damaging |
Het |
Qrich1 |
A |
T |
9: 108,411,491 (GRCm39) |
N339Y |
probably damaging |
Het |
Rabgap1 |
T |
A |
2: 37,432,659 (GRCm39) |
V750D |
possibly damaging |
Het |
Reg3d |
G |
A |
6: 78,354,428 (GRCm39) |
P58S |
probably damaging |
Het |
Rp1 |
A |
G |
1: 4,112,212 (GRCm39) |
L1213P |
unknown |
Het |
Sema6b |
A |
G |
17: 56,431,047 (GRCm39) |
L872S |
probably benign |
Het |
Serpinb7 |
T |
C |
1: 107,379,436 (GRCm39) |
I281T |
probably damaging |
Het |
Shank2 |
T |
C |
7: 143,838,821 (GRCm39) |
V685A |
possibly damaging |
Het |
Slc28a2 |
A |
G |
2: 122,284,980 (GRCm39) |
I323V |
possibly damaging |
Het |
Slc7a6 |
A |
T |
8: 106,919,099 (GRCm39) |
I228F |
probably damaging |
Het |
Slc9a9 |
A |
G |
9: 94,821,512 (GRCm39) |
T300A |
possibly damaging |
Het |
Spta1 |
A |
G |
1: 174,068,653 (GRCm39) |
N2151S |
probably damaging |
Het |
Sult2a1 |
T |
A |
7: 13,569,945 (GRCm39) |
I96L |
probably benign |
Het |
Tgm2 |
T |
C |
2: 157,966,070 (GRCm39) |
D528G |
probably benign |
Het |
Ubl7 |
T |
C |
9: 57,818,456 (GRCm39) |
|
probably null |
Het |
Vcan |
T |
A |
13: 89,839,716 (GRCm39) |
I983L |
probably benign |
Het |
Vmn1r172 |
T |
C |
7: 23,359,742 (GRCm39) |
L209P |
probably damaging |
Het |
Vmn1r181 |
G |
A |
7: 23,684,183 (GRCm39) |
R216Q |
probably benign |
Het |
Vmn1r3 |
T |
C |
4: 3,184,993 (GRCm39) |
S105G |
probably benign |
Het |
Zfp644 |
A |
T |
5: 106,783,711 (GRCm39) |
H945Q |
probably damaging |
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 |
|
R0569:Ces1h
|
UTSW |
8 |
94,078,774 (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 |
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 |
|
|