Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110018I06Rik |
A |
T |
12: 107,455,215 (GRCm39) |
K100N |
unknown |
Het |
Abi3bp |
T |
A |
16: 56,453,263 (GRCm39) |
|
probably null |
Het |
Akr1c20 |
T |
C |
13: 4,558,218 (GRCm39) |
D210G |
probably benign |
Het |
Arid5b |
C |
T |
10: 67,934,417 (GRCm39) |
G495E |
probably benign |
Het |
Ascc1 |
A |
C |
10: 59,885,629 (GRCm39) |
N227H |
probably damaging |
Het |
Atp5f1a |
G |
T |
18: 77,861,802 (GRCm39) |
A18S |
possibly damaging |
Het |
Bcl2l13 |
A |
G |
6: 120,842,558 (GRCm39) |
T84A |
possibly damaging |
Het |
Blmh |
T |
A |
11: 76,877,341 (GRCm39) |
V419D |
probably damaging |
Het |
Cacna1d |
G |
A |
14: 29,769,177 (GRCm39) |
P1918S |
probably benign |
Het |
Capza3 |
C |
A |
6: 139,987,498 (GRCm39) |
D32E |
probably benign |
Het |
Cilk1 |
G |
C |
9: 78,074,902 (GRCm39) |
V586L |
probably benign |
Het |
Cldn20 |
T |
A |
17: 3,583,133 (GRCm39) |
M102K |
possibly damaging |
Het |
Dennd1a |
T |
C |
2: 37,734,841 (GRCm39) |
Q479R |
probably benign |
Het |
Dpp10 |
A |
T |
1: 123,312,681 (GRCm39) |
I432N |
probably damaging |
Het |
Dst |
T |
A |
1: 34,295,434 (GRCm39) |
|
probably null |
Het |
Efcab3 |
T |
A |
11: 104,617,503 (GRCm39) |
D741E |
probably benign |
Het |
Fam135a |
C |
T |
1: 24,111,843 (GRCm39) |
|
probably null |
Het |
Fam47e |
C |
T |
5: 92,735,384 (GRCm39) |
L206F |
probably damaging |
Het |
Focad |
G |
A |
4: 88,221,772 (GRCm39) |
R714H |
unknown |
Het |
Hace1 |
T |
G |
10: 45,481,649 (GRCm39) |
V124G |
probably damaging |
Het |
Ifit1bl2 |
T |
A |
19: 34,596,428 (GRCm39) |
Y396F |
probably damaging |
Het |
Il22ra2 |
A |
G |
10: 19,497,826 (GRCm39) |
I13M |
probably benign |
Het |
Kif21a |
A |
G |
15: 90,865,122 (GRCm39) |
F517L |
possibly damaging |
Het |
Lrrc4 |
T |
C |
6: 28,829,762 (GRCm39) |
T618A |
probably benign |
Het |
Mdn1 |
A |
G |
4: 32,691,229 (GRCm39) |
T952A |
probably benign |
Het |
Mindy3 |
A |
T |
2: 12,402,328 (GRCm39) |
I208K |
probably damaging |
Het |
Mug1 |
C |
A |
6: 121,838,179 (GRCm39) |
H470N |
possibly damaging |
Het |
Mycbp2 |
A |
G |
14: 103,450,059 (GRCm39) |
I1744T |
probably damaging |
Het |
Nanog |
A |
T |
6: 122,690,431 (GRCm39) |
R279W |
probably damaging |
Het |
Ncoa2 |
T |
A |
1: 13,244,761 (GRCm39) |
T646S |
probably damaging |
Het |
Ndufa5 |
A |
G |
6: 24,518,724 (GRCm39) |
*117R |
probably null |
Het |
Nudt18 |
A |
T |
14: 70,817,276 (GRCm39) |
E293D |
probably benign |
Het |
Or1e22 |
A |
G |
11: 73,377,426 (GRCm39) |
S75P |
probably damaging |
Het |
Or51aa2 |
A |
T |
7: 103,187,826 (GRCm39) |
V205E |
probably damaging |
Het |
Paip1 |
C |
T |
13: 119,587,306 (GRCm39) |
T390I |
possibly damaging |
Het |
Pigg |
G |
A |
5: 108,486,485 (GRCm39) |
V713I |
probably benign |
Het |
Pih1d2 |
T |
C |
9: 50,529,558 (GRCm39) |
|
probably null |
Het |
Ppp2r3d |
A |
G |
9: 124,442,696 (GRCm38) |
F17L |
|
Het |
Ptprk |
T |
C |
10: 28,342,036 (GRCm39) |
I481T |
probably benign |
Het |
Pygo2 |
T |
C |
3: 89,338,038 (GRCm39) |
|
probably null |
Het |
Raet1d |
T |
C |
10: 22,248,156 (GRCm39) |
S225P |
possibly damaging |
Het |
Rnf24 |
T |
C |
2: 131,164,135 (GRCm39) |
|
probably benign |
Het |
Ror1 |
A |
G |
4: 100,298,687 (GRCm39) |
S687G |
probably damaging |
Het |
Rsph9 |
A |
G |
17: 46,446,013 (GRCm39) |
S186P |
probably damaging |
Het |
Sash1 |
C |
T |
10: 8,605,155 (GRCm39) |
M1078I |
probably benign |
Het |
Scd4 |
C |
A |
19: 44,327,510 (GRCm39) |
D195E |
probably benign |
Het |
Spopfm3 |
C |
T |
3: 94,105,709 (GRCm39) |
T9I |
probably damaging |
Het |
Syn3 |
A |
G |
10: 85,904,940 (GRCm39) |
C348R |
probably damaging |
Het |
Uspl1 |
T |
C |
5: 149,151,827 (GRCm39) |
F1009S |
probably benign |
Het |
Vmn1r2 |
T |
A |
4: 3,172,149 (GRCm39) |
F23I |
probably benign |
Het |
Vmn1r257 |
A |
G |
7: 22,391,229 (GRCm39) |
S172P |
probably benign |
Het |
Vmn2r-ps158 |
T |
A |
7: 42,672,582 (GRCm39) |
N72K |
probably benign |
Het |
Zfp747l1 |
A |
T |
7: 126,984,135 (GRCm39) |
C322* |
probably null |
Het |
Zfp839 |
C |
T |
12: 110,835,226 (GRCm39) |
T827I |
probably benign |
Het |
|
Other mutations in Calr4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Calr4
|
APN |
4 |
109,101,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01392:Calr4
|
APN |
4 |
109,111,071 (GRCm39) |
missense |
probably benign |
0.41 |
IGL01676:Calr4
|
APN |
4 |
109,101,447 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02587:Calr4
|
APN |
4 |
109,096,134 (GRCm39) |
missense |
possibly damaging |
0.76 |
PIT4576001:Calr4
|
UTSW |
4 |
109,093,053 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0525:Calr4
|
UTSW |
4 |
109,099,461 (GRCm39) |
splice site |
probably benign |
|
R1444:Calr4
|
UTSW |
4 |
109,103,438 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1899:Calr4
|
UTSW |
4 |
109,103,490 (GRCm39) |
critical splice donor site |
probably null |
|
R4561:Calr4
|
UTSW |
4 |
109,103,379 (GRCm39) |
missense |
probably damaging |
0.97 |
R5001:Calr4
|
UTSW |
4 |
109,096,179 (GRCm39) |
critical splice donor site |
probably null |
|
R5014:Calr4
|
UTSW |
4 |
109,092,994 (GRCm39) |
nonsense |
probably null |
|
R5088:Calr4
|
UTSW |
4 |
109,101,859 (GRCm39) |
intron |
probably benign |
|
R5267:Calr4
|
UTSW |
4 |
109,101,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Calr4
|
UTSW |
4 |
109,101,442 (GRCm39) |
missense |
probably benign |
0.03 |
R6262:Calr4
|
UTSW |
4 |
109,108,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R6795:Calr4
|
UTSW |
4 |
109,101,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R7099:Calr4
|
UTSW |
4 |
109,099,426 (GRCm39) |
missense |
probably benign |
0.01 |
R7202:Calr4
|
UTSW |
4 |
109,101,254 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7576:Calr4
|
UTSW |
4 |
109,096,161 (GRCm39) |
missense |
probably benign |
0.37 |
Z1177:Calr4
|
UTSW |
4 |
109,092,930 (GRCm39) |
missense |
probably benign |
0.02 |
|