Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam3 |
T |
C |
8: 25,201,400 (GRCm39) |
D251G |
probably damaging |
Het |
Aqp3 |
T |
C |
4: 41,093,836 (GRCm39) |
D219G |
probably damaging |
Het |
Arhgef15 |
C |
A |
11: 68,842,517 (GRCm39) |
W404C |
probably damaging |
Het |
Bdp1 |
T |
A |
13: 100,197,847 (GRCm39) |
E846V |
probably damaging |
Het |
Bdp1 |
C |
A |
13: 100,197,838 (GRCm39) |
S849I |
probably benign |
Het |
Bmp5 |
T |
A |
9: 75,683,830 (GRCm39) |
N152K |
possibly damaging |
Het |
Bpifb2 |
C |
T |
2: 153,720,399 (GRCm39) |
Q53* |
probably null |
Het |
Cep250 |
G |
A |
2: 155,834,552 (GRCm39) |
R2159K |
probably damaging |
Het |
Chd9 |
C |
T |
8: 91,760,615 (GRCm39) |
P2120L |
probably benign |
Het |
Clca3a1 |
A |
G |
3: 144,463,785 (GRCm39) |
V164A |
probably damaging |
Het |
Dnajc28 |
G |
A |
16: 91,413,755 (GRCm39) |
T187M |
probably damaging |
Het |
Gcn1 |
T |
C |
5: 115,749,234 (GRCm39) |
I1922T |
probably damaging |
Het |
Gnpat |
A |
G |
8: 125,603,659 (GRCm39) |
D179G |
probably benign |
Het |
Hook1 |
A |
G |
4: 95,886,957 (GRCm39) |
Q188R |
probably benign |
Het |
Hsf4 |
G |
A |
8: 105,996,628 (GRCm39) |
D18N |
probably null |
Het |
Ifi44 |
T |
C |
3: 151,438,025 (GRCm39) |
N421D |
probably benign |
Het |
Igdcc4 |
C |
T |
9: 65,038,025 (GRCm39) |
T801I |
probably damaging |
Het |
Itgad |
T |
C |
7: 127,804,342 (GRCm39) |
S107P |
possibly damaging |
Het |
Kank2 |
C |
A |
9: 21,681,080 (GRCm39) |
M816I |
probably damaging |
Het |
Kcnma1 |
T |
A |
14: 23,593,151 (GRCm39) |
R120* |
probably null |
Het |
Lgi4 |
T |
G |
7: 30,760,037 (GRCm39) |
L78V |
probably damaging |
Het |
Lypla1 |
T |
G |
1: 4,911,321 (GRCm39) |
|
probably null |
Het |
Mknk1 |
C |
T |
4: 115,732,690 (GRCm39) |
A306V |
probably damaging |
Het |
Ncoa6 |
A |
T |
2: 155,249,570 (GRCm39) |
S1245T |
possibly damaging |
Het |
Npas3 |
T |
A |
12: 53,687,285 (GRCm39) |
V122E |
possibly damaging |
Het |
Nrxn2 |
G |
C |
19: 6,531,883 (GRCm39) |
Q789H |
probably damaging |
Het |
Or2h1b |
A |
T |
17: 37,462,145 (GRCm39) |
C239* |
probably null |
Het |
Or3a1 |
T |
C |
11: 74,225,991 (GRCm39) |
E22G |
probably benign |
Het |
Or5p69 |
T |
C |
7: 107,967,288 (GRCm39) |
V197A |
probably benign |
Het |
Or5w12 |
A |
G |
2: 87,502,289 (GRCm39) |
C141R |
possibly damaging |
Het |
Otog |
G |
A |
7: 45,949,468 (GRCm39) |
V2369M |
probably damaging |
Het |
Pfkp |
T |
C |
13: 6,669,245 (GRCm39) |
|
probably null |
Het |
Pja2 |
T |
C |
17: 64,599,865 (GRCm39) |
S478G |
probably damaging |
Het |
Prune2 |
A |
G |
19: 17,095,919 (GRCm39) |
I474M |
possibly damaging |
Het |
Psg22 |
C |
A |
7: 18,460,762 (GRCm39) |
Q464K |
possibly damaging |
Het |
Rp1 |
C |
T |
1: 4,418,250 (GRCm39) |
S954N |
possibly damaging |
Het |
Rps27l |
T |
A |
9: 66,854,208 (GRCm39) |
D34E |
probably benign |
Het |
Sae1 |
A |
C |
7: 16,104,291 (GRCm39) |
L106R |
probably damaging |
Het |
Siglec1 |
T |
A |
2: 130,913,257 (GRCm39) |
Q1553L |
probably benign |
Het |
Slc11a2 |
A |
G |
15: 100,307,962 (GRCm39) |
|
probably null |
Het |
Slc14a2 |
A |
T |
18: 78,203,159 (GRCm39) |
M556K |
probably benign |
Het |
Slk |
T |
G |
19: 47,608,188 (GRCm39) |
I380M |
probably damaging |
Het |
Spink5 |
A |
G |
18: 44,119,396 (GRCm39) |
N236D |
probably benign |
Het |
Syne2 |
A |
G |
12: 75,974,240 (GRCm39) |
E1146G |
possibly damaging |
Het |
Tiam2 |
G |
A |
17: 3,477,495 (GRCm39) |
V573M |
probably damaging |
Het |
Tmem170 |
C |
A |
8: 112,596,349 (GRCm39) |
V59L |
probably benign |
Het |
Tmem255b |
C |
T |
8: 13,501,081 (GRCm39) |
A106V |
probably damaging |
Het |
Ttc23l |
A |
G |
15: 10,523,678 (GRCm39) |
I347T |
possibly damaging |
Het |
Vps13c |
A |
G |
9: 67,846,354 (GRCm39) |
M2141V |
probably benign |
Het |
Vwa5a |
T |
C |
9: 38,634,503 (GRCm39) |
Y143H |
probably damaging |
Het |
Zfp280d |
T |
A |
9: 72,246,055 (GRCm39) |
C707* |
probably null |
Het |
Zfp668 |
A |
T |
7: 127,465,998 (GRCm39) |
N395K |
probably benign |
Het |
Znhit6 |
G |
T |
3: 145,281,991 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Kcnk18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00339:Kcnk18
|
APN |
19 |
59,223,502 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01460:Kcnk18
|
APN |
19 |
59,208,289 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02054:Kcnk18
|
APN |
19 |
59,224,045 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02304:Kcnk18
|
APN |
19 |
59,223,295 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02499:Kcnk18
|
APN |
19 |
59,223,614 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02527:Kcnk18
|
APN |
19 |
59,223,707 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03033:Kcnk18
|
APN |
19 |
59,223,616 (GRCm39) |
missense |
probably benign |
0.21 |
cedar
|
UTSW |
19 |
59,223,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R1552:Kcnk18
|
UTSW |
19 |
59,223,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R1775:Kcnk18
|
UTSW |
19 |
59,223,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R1913:Kcnk18
|
UTSW |
19 |
59,223,490 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3036:Kcnk18
|
UTSW |
19 |
59,223,494 (GRCm39) |
missense |
probably benign |
0.38 |
R4478:Kcnk18
|
UTSW |
19 |
59,223,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R4494:Kcnk18
|
UTSW |
19 |
59,223,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R4827:Kcnk18
|
UTSW |
19 |
59,208,362 (GRCm39) |
missense |
probably damaging |
0.97 |
R5393:Kcnk18
|
UTSW |
19 |
59,208,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R6077:Kcnk18
|
UTSW |
19 |
59,223,746 (GRCm39) |
missense |
probably damaging |
0.98 |
R6145:Kcnk18
|
UTSW |
19 |
59,224,039 (GRCm39) |
makesense |
probably null |
|
R6881:Kcnk18
|
UTSW |
19 |
59,208,390 (GRCm39) |
missense |
probably benign |
|
R9641:Kcnk18
|
UTSW |
19 |
59,223,266 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kcnk18
|
UTSW |
19 |
59,223,391 (GRCm39) |
missense |
probably benign |
0.39 |
Z1177:Kcnk18
|
UTSW |
19 |
59,213,911 (GRCm39) |
frame shift |
probably null |
|
|