Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn4 |
A |
G |
7: 28,603,975 (GRCm39) |
W429R |
probably damaging |
Het |
Afg1l |
C |
T |
10: 42,236,236 (GRCm39) |
C272Y |
probably damaging |
Het |
Agrn |
T |
C |
4: 156,251,770 (GRCm39) |
T1831A |
probably damaging |
Het |
Aifm2 |
T |
C |
10: 61,561,696 (GRCm39) |
V14A |
probably damaging |
Het |
Angptl3 |
A |
T |
4: 98,920,321 (GRCm39) |
|
probably null |
Het |
Arfgap1 |
A |
T |
2: 180,615,912 (GRCm39) |
D197V |
possibly damaging |
Het |
Atp1a3 |
T |
C |
7: 24,678,294 (GRCm39) |
|
probably benign |
Het |
Brwd1 |
T |
C |
16: 95,817,350 (GRCm39) |
I1387M |
probably damaging |
Het |
Cavin4 |
A |
G |
4: 48,672,499 (GRCm39) |
T315A |
probably benign |
Het |
Cep128 |
T |
C |
12: 90,966,410 (GRCm39) |
T1066A |
probably benign |
Het |
Cln3 |
T |
C |
7: 126,171,558 (GRCm39) |
T376A |
probably benign |
Het |
Cntn4 |
A |
T |
6: 106,656,397 (GRCm39) |
|
silent |
Het |
Csmd3 |
T |
C |
15: 47,559,151 (GRCm39) |
I2371V |
possibly damaging |
Het |
Cspg4b |
A |
G |
13: 113,453,701 (GRCm39) |
S55G |
possibly damaging |
Het |
Cxcl3 |
T |
C |
5: 90,935,299 (GRCm39) |
S99P |
unknown |
Het |
Ddx60 |
A |
G |
8: 62,453,612 (GRCm39) |
R1244G |
probably benign |
Het |
Dhx38 |
T |
C |
8: 110,280,048 (GRCm39) |
D914G |
probably damaging |
Het |
Dlc1 |
T |
G |
8: 37,404,655 (GRCm39) |
|
probably benign |
Het |
Eif4a3l1 |
A |
T |
6: 136,306,393 (GRCm39) |
I264F |
probably benign |
Het |
Fam161b |
A |
G |
12: 84,403,124 (GRCm39) |
S169P |
probably damaging |
Het |
Fastkd1 |
A |
G |
2: 69,537,725 (GRCm39) |
S286P |
possibly damaging |
Het |
Fmn2 |
A |
T |
1: 174,409,603 (GRCm39) |
E612V |
unknown |
Het |
Foxb1 |
T |
A |
9: 69,667,528 (GRCm39) |
M1L |
probably damaging |
Het |
Gm14412 |
A |
T |
2: 177,007,402 (GRCm39) |
C164* |
probably null |
Het |
Gm43302 |
T |
A |
5: 105,423,678 (GRCm39) |
M432L |
probably benign |
Het |
Gm4353 |
C |
A |
7: 115,682,913 (GRCm39) |
A223S |
probably damaging |
Het |
Gpatch8 |
T |
C |
11: 102,391,693 (GRCm39) |
K143R |
unknown |
Het |
Gpr15 |
A |
G |
16: 58,538,013 (GRCm39) |
S359P |
probably damaging |
Het |
Gucy2e |
A |
G |
11: 69,119,207 (GRCm39) |
L649P |
probably damaging |
Het |
H2-M10.5 |
C |
A |
17: 37,085,473 (GRCm39) |
H211N |
probably damaging |
Het |
Hs6st1 |
T |
C |
1: 36,142,970 (GRCm39) |
Y302H |
probably damaging |
Het |
Khdrbs2 |
A |
T |
1: 32,506,851 (GRCm39) |
D165V |
probably damaging |
Het |
Klra13-ps |
T |
G |
6: 130,281,246 (GRCm39) |
|
noncoding transcript |
Het |
Lrrc37 |
T |
A |
11: 103,507,880 (GRCm39) |
|
probably benign |
Het |
Lrrc37a |
T |
A |
11: 103,391,001 (GRCm39) |
T1475S |
probably benign |
Het |
Ly75 |
A |
G |
2: 60,184,844 (GRCm39) |
S437P |
probably damaging |
Het |
Maz |
C |
T |
7: 126,624,494 (GRCm39) |
C342Y |
probably damaging |
Het |
Mcf2l |
C |
A |
8: 13,063,812 (GRCm39) |
S1008* |
probably null |
Het |
Mcmbp |
T |
C |
7: 128,314,478 (GRCm39) |
D246G |
probably benign |
Het |
Mipol1 |
G |
A |
12: 57,372,346 (GRCm39) |
R135H |
possibly damaging |
Het |
Mycbp2 |
T |
A |
14: 103,357,955 (GRCm39) |
Y4613F |
possibly damaging |
Het |
Nup188 |
G |
A |
2: 30,226,336 (GRCm39) |
A1118T |
probably damaging |
Het |
Or10g6 |
A |
T |
9: 39,933,964 (GRCm39) |
I92F |
probably damaging |
Het |
Or2k2 |
T |
A |
4: 58,785,489 (GRCm39) |
I78F |
probably benign |
Het |
Or4a76 |
G |
A |
2: 89,460,688 (GRCm39) |
L185F |
probably damaging |
Het |
Or4c121 |
A |
T |
2: 89,024,170 (GRCm39) |
D69E |
possibly damaging |
Het |
Or4z4 |
A |
G |
19: 12,076,290 (GRCm39) |
S238P |
probably damaging |
Het |
Or51f1e |
A |
T |
7: 102,747,103 (GRCm39) |
S52C |
probably benign |
Het |
Or51h7 |
T |
C |
7: 102,591,128 (GRCm39) |
K219E |
probably benign |
Het |
P3h1 |
T |
A |
4: 119,101,243 (GRCm39) |
I460N |
possibly damaging |
Het |
Pcnt |
T |
C |
10: 76,245,334 (GRCm39) |
D1101G |
probably benign |
Het |
Phlpp2 |
C |
A |
8: 110,655,205 (GRCm39) |
Q667K |
possibly damaging |
Het |
Plec |
A |
G |
15: 76,074,666 (GRCm39) |
F434L |
possibly damaging |
Het |
Ppp6r2 |
T |
A |
15: 89,164,602 (GRCm39) |
I602N |
probably damaging |
Het |
Rdh8 |
A |
C |
9: 20,736,475 (GRCm39) |
I181L |
probably benign |
Het |
Rnf181 |
A |
G |
6: 72,338,505 (GRCm39) |
M1T |
probably null |
Het |
Rpl29-ps2 |
A |
G |
13: 4,664,221 (GRCm39) |
|
noncoding transcript |
Het |
Sart3 |
A |
G |
5: 113,883,217 (GRCm39) |
|
probably null |
Het |
Sec14l2 |
A |
C |
11: 4,059,189 (GRCm39) |
L160R |
probably damaging |
Het |
Senp1 |
C |
T |
15: 97,946,236 (GRCm39) |
R503H |
probably damaging |
Het |
Shoc1 |
A |
G |
4: 59,047,399 (GRCm39) |
S1407P |
probably benign |
Het |
Slc22a2 |
T |
C |
17: 12,827,296 (GRCm39) |
V316A |
probably benign |
Het |
Slc34a1 |
A |
T |
13: 55,556,898 (GRCm39) |
I365F |
possibly damaging |
Het |
Spag5 |
T |
C |
11: 78,195,542 (GRCm39) |
V283A |
possibly damaging |
Het |
Srebf2 |
C |
T |
15: 82,076,456 (GRCm39) |
T702I |
probably benign |
Het |
Sun3 |
A |
G |
11: 8,981,433 (GRCm39) |
|
probably null |
Het |
Syt6 |
A |
G |
3: 103,528,217 (GRCm39) |
Y312C |
probably damaging |
Het |
Tas2r121 |
T |
A |
6: 132,677,756 (GRCm39) |
Y72F |
possibly damaging |
Het |
Tfrc |
A |
G |
16: 32,442,194 (GRCm39) |
Y473C |
probably damaging |
Het |
Trp63 |
C |
T |
16: 25,684,935 (GRCm39) |
A274V |
possibly damaging |
Het |
Trpm5 |
T |
C |
7: 142,626,966 (GRCm39) |
D1085G |
probably benign |
Het |
Ttn |
A |
G |
2: 76,745,008 (GRCm39) |
V5347A |
probably benign |
Het |
Uqcc4 |
G |
A |
17: 25,403,963 (GRCm39) |
S101N |
probably damaging |
Het |
Vma21-ps |
T |
A |
4: 52,496,946 (GRCm39) |
Q100L |
possibly damaging |
Het |
Vmn2r22 |
T |
C |
6: 123,614,873 (GRCm39) |
N239S |
probably benign |
Het |
Wfdc8 |
T |
C |
2: 164,439,339 (GRCm39) |
|
probably benign |
Het |
Xkr4 |
T |
A |
1: 3,741,258 (GRCm39) |
Y105F |
probably damaging |
Het |
Xpo7 |
C |
T |
14: 70,920,286 (GRCm39) |
V627I |
possibly damaging |
Het |
Zfp606 |
T |
C |
7: 12,226,479 (GRCm39) |
V200A |
probably benign |
Het |
Zfp936 |
A |
T |
7: 42,839,858 (GRCm39) |
S441C |
possibly damaging |
Het |
|
Other mutations in Colec12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01099:Colec12
|
APN |
18 |
9,848,826 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02477:Colec12
|
APN |
18 |
9,859,858 (GRCm39) |
missense |
unknown |
|
R0128:Colec12
|
UTSW |
18 |
9,858,921 (GRCm39) |
missense |
unknown |
|
R0130:Colec12
|
UTSW |
18 |
9,858,921 (GRCm39) |
missense |
unknown |
|
R0178:Colec12
|
UTSW |
18 |
9,858,921 (GRCm39) |
missense |
unknown |
|
R0179:Colec12
|
UTSW |
18 |
9,858,921 (GRCm39) |
missense |
unknown |
|
R0180:Colec12
|
UTSW |
18 |
9,858,921 (GRCm39) |
missense |
unknown |
|
R0180:Colec12
|
UTSW |
18 |
9,848,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R0318:Colec12
|
UTSW |
18 |
9,848,446 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0344:Colec12
|
UTSW |
18 |
9,858,921 (GRCm39) |
missense |
unknown |
|
R0573:Colec12
|
UTSW |
18 |
9,858,650 (GRCm39) |
missense |
probably damaging |
0.97 |
R1028:Colec12
|
UTSW |
18 |
9,866,837 (GRCm39) |
missense |
unknown |
|
R1693:Colec12
|
UTSW |
18 |
9,866,765 (GRCm39) |
missense |
unknown |
|
R1951:Colec12
|
UTSW |
18 |
9,859,975 (GRCm39) |
critical splice donor site |
probably null |
|
R2008:Colec12
|
UTSW |
18 |
9,874,813 (GRCm39) |
missense |
probably benign |
0.03 |
R2181:Colec12
|
UTSW |
18 |
9,846,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R4258:Colec12
|
UTSW |
18 |
9,720,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R4794:Colec12
|
UTSW |
18 |
9,848,984 (GRCm39) |
missense |
probably damaging |
0.99 |
R5269:Colec12
|
UTSW |
18 |
9,846,825 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5369:Colec12
|
UTSW |
18 |
9,866,750 (GRCm39) |
missense |
unknown |
|
R5421:Colec12
|
UTSW |
18 |
9,858,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R5608:Colec12
|
UTSW |
18 |
9,848,267 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5684:Colec12
|
UTSW |
18 |
9,849,009 (GRCm39) |
missense |
probably damaging |
0.99 |
R6547:Colec12
|
UTSW |
18 |
9,840,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R7194:Colec12
|
UTSW |
18 |
9,848,248 (GRCm39) |
missense |
probably benign |
0.08 |
R7253:Colec12
|
UTSW |
18 |
9,848,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Colec12
|
UTSW |
18 |
9,876,980 (GRCm39) |
splice site |
probably null |
|
R9365:Colec12
|
UTSW |
18 |
9,848,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R9649:Colec12
|
UTSW |
18 |
9,877,000 (GRCm39) |
missense |
unknown |
|
Z1088:Colec12
|
UTSW |
18 |
9,848,727 (GRCm39) |
missense |
probably benign |
0.31 |
|