Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl4 |
A |
T |
3: 95,592,784 (GRCm39) |
M1K |
probably null |
Het |
Atg2a |
G |
T |
19: 6,294,460 (GRCm39) |
V59L |
probably damaging |
Het |
Atxn7 |
C |
A |
14: 14,103,316 (GRCm38) |
T888K |
possibly damaging |
Het |
Btbd9 |
T |
C |
17: 30,749,144 (GRCm39) |
R57G |
probably damaging |
Het |
Ccdc9b |
C |
A |
2: 118,587,732 (GRCm39) |
S534I |
unknown |
Het |
Crp |
T |
C |
1: 172,526,293 (GRCm39) |
V126A |
probably benign |
Het |
Csf1r |
A |
T |
18: 61,247,942 (GRCm39) |
T337S |
probably damaging |
Het |
Dcaf12 |
T |
C |
4: 41,296,439 (GRCm39) |
N299S |
probably damaging |
Het |
Dcaf17 |
T |
C |
2: 70,917,744 (GRCm39) |
|
probably null |
Het |
Dip2c |
A |
G |
13: 9,665,830 (GRCm39) |
D985G |
probably damaging |
Het |
Dtna |
A |
G |
18: 23,716,190 (GRCm39) |
T138A |
probably benign |
Het |
Emid1 |
T |
C |
11: 5,081,517 (GRCm39) |
D212G |
probably benign |
Het |
Epyc |
G |
A |
10: 97,511,525 (GRCm39) |
D173N |
probably damaging |
Het |
Fanci |
A |
G |
7: 79,052,298 (GRCm39) |
D162G |
probably benign |
Het |
Firrm |
A |
T |
1: 163,792,040 (GRCm39) |
L626Q |
probably damaging |
Het |
Fry |
T |
C |
5: 150,317,501 (GRCm39) |
V827A |
probably benign |
Het |
Ggps1 |
T |
C |
13: 14,228,505 (GRCm39) |
E226G |
probably benign |
Het |
Gopc |
G |
A |
10: 52,230,750 (GRCm39) |
R183* |
probably null |
Het |
Grik4 |
C |
T |
9: 42,453,130 (GRCm39) |
G752S |
probably damaging |
Het |
H2-D1 |
T |
A |
17: 35,482,844 (GRCm39) |
C125S |
probably damaging |
Het |
H2-Q1 |
T |
A |
17: 35,539,869 (GRCm39) |
V46D |
probably damaging |
Het |
Hsd17b3 |
T |
C |
13: 64,219,862 (GRCm39) |
N126S |
probably damaging |
Het |
Igsf10 |
G |
A |
3: 59,238,063 (GRCm39) |
T706I |
probably benign |
Het |
Kmt2e |
A |
G |
5: 23,669,864 (GRCm39) |
D117G |
probably damaging |
Het |
Kmt5a |
C |
T |
5: 124,584,074 (GRCm39) |
A18V |
probably benign |
Het |
Krtap29-1 |
C |
T |
11: 99,869,465 (GRCm39) |
G139R |
probably damaging |
Het |
Lama5 |
T |
C |
2: 179,838,100 (GRCm39) |
Y872C |
probably damaging |
Het |
Lrriq4 |
T |
A |
3: 30,704,752 (GRCm39) |
M260K |
probably benign |
Het |
Map2 |
G |
A |
1: 66,472,755 (GRCm39) |
|
probably benign |
Het |
Mrpl51 |
C |
T |
6: 125,169,340 (GRCm39) |
A8V |
probably benign |
Het |
Ndufs3 |
T |
C |
2: 90,732,778 (GRCm39) |
T103A |
probably benign |
Het |
Numa1 |
T |
G |
7: 101,647,616 (GRCm39) |
L449R |
probably benign |
Het |
Or10g3b |
C |
T |
14: 52,587,021 (GRCm39) |
A161T |
possibly damaging |
Het |
Pan3 |
C |
T |
5: 147,424,951 (GRCm39) |
P295S |
possibly damaging |
Het |
Pds5b |
T |
C |
5: 150,704,134 (GRCm39) |
S846P |
probably damaging |
Het |
Phf2 |
A |
T |
13: 48,967,219 (GRCm39) |
M712K |
unknown |
Het |
Phlda2 |
A |
T |
7: 143,056,211 (GRCm39) |
V6E |
probably benign |
Het |
Pkdrej |
C |
A |
15: 85,704,044 (GRCm39) |
A631S |
probably benign |
Het |
Plcd3 |
G |
T |
11: 102,962,569 (GRCm39) |
N627K |
probably damaging |
Het |
Prpf6 |
T |
C |
2: 181,262,415 (GRCm39) |
I138T |
possibly damaging |
Het |
Psd4 |
G |
A |
2: 24,295,444 (GRCm39) |
S866N |
probably benign |
Het |
Ptprb |
A |
C |
10: 116,155,306 (GRCm39) |
T400P |
probably benign |
Het |
Rxfp1 |
T |
C |
3: 79,570,677 (GRCm39) |
|
probably null |
Het |
Sbf2 |
A |
G |
7: 110,063,793 (GRCm39) |
|
probably null |
Het |
Serpinb9h |
G |
A |
13: 33,588,204 (GRCm39) |
R263H |
probably benign |
Het |
Setd4 |
C |
T |
16: 93,390,162 (GRCm39) |
R89Q |
probably benign |
Het |
Sgpp1 |
A |
G |
12: 75,763,152 (GRCm39) |
I343T |
probably benign |
Het |
Sh2b2 |
T |
C |
5: 136,260,658 (GRCm39) |
D186G |
probably benign |
Het |
Slc12a4 |
A |
T |
8: 106,680,549 (GRCm39) |
I191N |
probably damaging |
Het |
Slc4a4 |
A |
T |
5: 89,232,549 (GRCm39) |
D251V |
probably benign |
Het |
Slc6a5 |
A |
T |
7: 49,561,843 (GRCm39) |
D125V |
possibly damaging |
Het |
Slf1 |
T |
A |
13: 77,274,806 (GRCm39) |
I16F |
possibly damaging |
Het |
Sncaip |
T |
C |
18: 53,031,334 (GRCm39) |
V521A |
probably damaging |
Het |
Spmip10 |
T |
C |
18: 56,727,568 (GRCm39) |
F89L |
probably damaging |
Het |
Stx19 |
T |
C |
16: 62,642,775 (GRCm39) |
L197P |
probably damaging |
Het |
Sucla2 |
A |
G |
14: 73,797,905 (GRCm39) |
N39D |
probably benign |
Het |
Sult1d1 |
T |
A |
5: 87,712,575 (GRCm39) |
T90S |
probably benign |
Het |
Syna |
C |
T |
5: 134,588,723 (GRCm39) |
M75I |
probably benign |
Het |
Tas2r138 |
A |
G |
6: 40,589,611 (GRCm39) |
S212P |
probably damaging |
Het |
Tdrd3 |
T |
A |
14: 87,709,637 (GRCm39) |
C106* |
probably null |
Het |
Tlk2 |
C |
T |
11: 105,172,059 (GRCm39) |
A743V |
unknown |
Het |
Tlr3 |
T |
C |
8: 45,851,286 (GRCm39) |
D537G |
possibly damaging |
Het |
Tmc1 |
A |
G |
19: 20,803,953 (GRCm39) |
Y375H |
probably damaging |
Het |
Tsen54 |
T |
A |
11: 115,711,498 (GRCm39) |
M305K |
probably damaging |
Het |
Umod |
C |
T |
7: 119,076,581 (GRCm39) |
V62M |
possibly damaging |
Het |
Vmn1r10 |
A |
G |
6: 57,091,010 (GRCm39) |
T201A |
probably benign |
Het |
Vmn1r103 |
T |
C |
7: 20,243,676 (GRCm39) |
T262A |
probably benign |
Het |
Vmn2r100 |
T |
C |
17: 19,742,838 (GRCm39) |
V404A |
probably damaging |
Het |
Vmn2r56 |
A |
G |
7: 12,449,393 (GRCm39) |
F282L |
probably damaging |
Het |
Wdr64 |
A |
T |
1: 175,636,327 (GRCm39) |
K982* |
probably null |
Het |
Xpo6 |
A |
T |
7: 125,712,127 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Catspere2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01925:Catspere2
|
APN |
1 |
177,842,687 (GRCm39) |
splice site |
probably benign |
|
IGL02345:Catspere2
|
APN |
1 |
177,842,754 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0089:Catspere2
|
UTSW |
1 |
177,874,555 (GRCm39) |
missense |
unknown |
|
R0103:Catspere2
|
UTSW |
1 |
177,943,771 (GRCm39) |
missense |
unknown |
|
R1491:Catspere2
|
UTSW |
1 |
177,843,495 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1662:Catspere2
|
UTSW |
1 |
177,874,552 (GRCm39) |
missense |
unknown |
|
R1840:Catspere2
|
UTSW |
1 |
177,830,581 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2168:Catspere2
|
UTSW |
1 |
177,843,477 (GRCm39) |
splice site |
probably benign |
|
R3764:Catspere2
|
UTSW |
1 |
177,940,698 (GRCm39) |
missense |
unknown |
|
R4586:Catspere2
|
UTSW |
1 |
177,950,351 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4887:Catspere2
|
UTSW |
1 |
177,931,515 (GRCm39) |
missense |
unknown |
|
R4990:Catspere2
|
UTSW |
1 |
177,925,987 (GRCm39) |
missense |
probably benign |
0.14 |
R4991:Catspere2
|
UTSW |
1 |
177,925,987 (GRCm39) |
missense |
probably benign |
0.14 |
R5225:Catspere2
|
UTSW |
1 |
177,976,474 (GRCm39) |
utr 3 prime |
probably benign |
|
R5285:Catspere2
|
UTSW |
1 |
177,931,454 (GRCm39) |
missense |
unknown |
|
R5569:Catspere2
|
UTSW |
1 |
177,939,162 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5743:Catspere2
|
UTSW |
1 |
177,950,328 (GRCm39) |
splice site |
silent |
|
R5756:Catspere2
|
UTSW |
1 |
177,943,793 (GRCm39) |
missense |
unknown |
|
R6050:Catspere2
|
UTSW |
1 |
177,931,490 (GRCm39) |
missense |
unknown |
|
R6166:Catspere2
|
UTSW |
1 |
177,931,403 (GRCm39) |
missense |
unknown |
|
R6200:Catspere2
|
UTSW |
1 |
177,939,124 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6322:Catspere2
|
UTSW |
1 |
177,845,296 (GRCm39) |
nonsense |
probably null |
|
R6438:Catspere2
|
UTSW |
1 |
177,938,869 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6736:Catspere2
|
UTSW |
1 |
177,845,278 (GRCm39) |
nonsense |
probably null |
|
R6879:Catspere2
|
UTSW |
1 |
177,926,338 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6897:Catspere2
|
UTSW |
1 |
177,939,139 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7030:Catspere2
|
UTSW |
1 |
177,845,280 (GRCm39) |
missense |
probably damaging |
0.97 |
R7335:Catspere2
|
UTSW |
1 |
177,926,074 (GRCm39) |
missense |
probably benign |
0.05 |
R7509:Catspere2
|
UTSW |
1 |
177,905,078 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7896:Catspere2
|
UTSW |
1 |
177,938,740 (GRCm39) |
missense |
probably benign |
0.01 |
R7980:Catspere2
|
UTSW |
1 |
177,830,610 (GRCm39) |
critical splice donor site |
probably null |
|
R8079:Catspere2
|
UTSW |
1 |
177,874,525 (GRCm39) |
missense |
probably benign |
0.16 |
R8355:Catspere2
|
UTSW |
1 |
177,845,276 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8360:Catspere2
|
UTSW |
1 |
177,842,724 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8786:Catspere2
|
UTSW |
1 |
177,843,362 (GRCm39) |
intron |
probably benign |
|
R8810:Catspere2
|
UTSW |
1 |
177,905,048 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9170:Catspere2
|
UTSW |
1 |
177,967,949 (GRCm39) |
missense |
probably benign |
0.07 |
R9252:Catspere2
|
UTSW |
1 |
177,938,996 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9442:Catspere2
|
UTSW |
1 |
177,931,275 (GRCm39) |
missense |
unknown |
|
Z1177:Catspere2
|
UTSW |
1 |
177,984,368 (GRCm39) |
critical splice donor site |
probably benign |
|
|