Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
A |
G |
14: 118,853,800 (GRCm39) |
V444A |
possibly damaging |
Het |
Add1 |
T |
A |
5: 34,770,622 (GRCm39) |
|
probably benign |
Het |
Adgrg3 |
A |
G |
8: 95,762,891 (GRCm39) |
|
probably benign |
Het |
Adgrl3 |
A |
C |
5: 81,842,299 (GRCm39) |
Q809P |
possibly damaging |
Het |
Ankmy2 |
T |
C |
12: 36,236,806 (GRCm39) |
C205R |
probably damaging |
Het |
Atp6v1b2 |
A |
G |
8: 69,541,476 (GRCm39) |
N11S |
|
Het |
B3gnt6 |
T |
A |
7: 97,843,958 (GRCm39) |
M1L |
not run |
Het |
Bltp1 |
A |
G |
3: 37,098,907 (GRCm39) |
K1256R |
|
Het |
Ccdc88b |
T |
C |
19: 6,833,213 (GRCm39) |
E278G |
probably damaging |
Het |
Cdca8 |
T |
C |
4: 124,830,238 (GRCm39) |
T45A |
probably benign |
Het |
Ces2b |
C |
A |
8: 105,558,221 (GRCm39) |
|
probably benign |
Het |
Clip4 |
G |
A |
17: 72,117,884 (GRCm39) |
G310R |
probably damaging |
Het |
Cnot3 |
A |
G |
7: 3,661,192 (GRCm39) |
D567G |
probably benign |
Het |
Cnot6l |
T |
C |
5: 96,230,875 (GRCm39) |
D364G |
probably damaging |
Het |
Cpped1 |
A |
G |
16: 11,646,419 (GRCm39) |
V111A |
|
Het |
Cstdc4 |
T |
A |
16: 36,008,285 (GRCm39) |
M57K |
possibly damaging |
Het |
Cyp11b2 |
T |
C |
15: 74,722,995 (GRCm39) |
K468E |
probably damaging |
Het |
Dpp4 |
T |
G |
2: 62,204,733 (GRCm39) |
T245P |
possibly damaging |
Het |
Efcab15 |
T |
C |
11: 103,090,893 (GRCm39) |
T151A |
probably benign |
Het |
Fat2 |
A |
G |
11: 55,153,347 (GRCm39) |
W3622R |
probably damaging |
Het |
Fat4 |
A |
C |
3: 39,064,803 (GRCm39) |
K4920Q |
|
Het |
Frmpd2 |
A |
G |
14: 33,252,407 (GRCm39) |
I656M |
probably benign |
Het |
Gck |
A |
G |
11: 5,856,516 (GRCm39) |
Y214H |
probably damaging |
Het |
Gde1 |
C |
T |
7: 118,294,305 (GRCm39) |
R166H |
probably benign |
Het |
Gdf7 |
A |
T |
12: 8,348,652 (GRCm39) |
F215Y |
unknown |
Het |
Gdpgp1 |
A |
G |
7: 79,888,282 (GRCm39) |
I104M |
probably benign |
Het |
Gldc |
A |
G |
19: 30,077,314 (GRCm39) |
S953P |
possibly damaging |
Het |
Golga3 |
C |
T |
5: 110,337,544 (GRCm39) |
H411Y |
probably benign |
Het |
Gpn1 |
G |
T |
5: 31,655,740 (GRCm39) |
R101I |
probably damaging |
Het |
Itgb5 |
T |
A |
16: 33,740,551 (GRCm39) |
S554T |
possibly damaging |
Het |
Klhl1 |
G |
A |
14: 96,584,364 (GRCm39) |
L289F |
probably damaging |
Het |
Klhl13 |
C |
T |
X: 23,113,733 (GRCm39) |
R95Q |
probably benign |
Het |
Kmt2d |
G |
C |
15: 98,747,832 (GRCm39) |
T3164R |
unknown |
Het |
Knl1 |
T |
C |
2: 118,899,469 (GRCm39) |
V390A |
probably benign |
Het |
Krtap5-2 |
GCCACAGCCTCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACCACAGCCCCCACAGGAACTACA |
GCCACAGCCCCCACAGGAACTACA |
7: 141,728,836 (GRCm39) |
|
probably benign |
Het |
Lamtor4 |
G |
A |
5: 138,254,595 (GRCm39) |
|
probably benign |
Het |
Lonrf1 |
AGGCGGCGGCGGCGG |
AGGCGGCGGCGG |
8: 36,715,919 (GRCm39) |
|
probably benign |
Het |
Ltbp1 |
C |
T |
17: 75,622,102 (GRCm39) |
L829F |
probably benign |
Het |
Ltbp1 |
T |
A |
17: 75,622,103 (GRCm39) |
L829H |
probably damaging |
Het |
Mrgpra1 |
C |
T |
7: 46,984,732 (GRCm39) |
E316K |
probably damaging |
Het |
Muc16 |
T |
A |
9: 18,556,966 (GRCm39) |
H3109L |
unknown |
Het |
Nck1 |
T |
C |
9: 100,377,561 (GRCm39) |
E368G |
probably damaging |
Het |
Nox4 |
G |
A |
7: 87,025,448 (GRCm39) |
R525Q |
probably benign |
Het |
Nus1 |
A |
T |
10: 52,305,287 (GRCm39) |
|
probably null |
Het |
Nxph2 |
T |
C |
2: 23,289,780 (GRCm39) |
V44A |
probably benign |
Het |
Or1e30 |
A |
G |
11: 73,678,687 (GRCm39) |
K308E |
probably benign |
Het |
Or4f56 |
A |
G |
2: 111,703,606 (GRCm39) |
M198T |
possibly damaging |
Het |
Or4k35 |
A |
G |
2: 111,100,094 (GRCm39) |
L206P |
probably benign |
Het |
Or4z4 |
G |
T |
19: 12,076,254 (GRCm39) |
H250N |
probably benign |
Het |
Or5d35 |
T |
C |
2: 87,855,330 (GRCm39) |
I88T |
probably benign |
Het |
Or5m11b |
A |
G |
2: 85,806,096 (GRCm39) |
K170E |
probably benign |
Het |
Or6d13 |
A |
T |
6: 116,517,990 (GRCm39) |
N192I |
possibly damaging |
Het |
Otof |
T |
C |
5: 30,539,696 (GRCm39) |
D1039G |
possibly damaging |
Het |
Parpbp |
T |
A |
10: 87,968,969 (GRCm39) |
Q159L |
possibly damaging |
Het |
Per2 |
A |
T |
1: 91,351,464 (GRCm39) |
L1014Q |
possibly damaging |
Het |
Pik3ap1 |
C |
G |
19: 41,312,924 (GRCm39) |
|
silent |
Het |
Pik3ca |
A |
G |
3: 32,514,168 (GRCm39) |
N885D |
probably damaging |
Het |
Pip5k1c |
T |
C |
10: 81,145,056 (GRCm39) |
V299A |
probably benign |
Het |
Polr3h |
A |
T |
15: 81,806,717 (GRCm39) |
|
probably benign |
Het |
Pramel11 |
T |
A |
4: 143,623,646 (GRCm39) |
N176I |
probably benign |
Het |
Pramel23 |
T |
G |
4: 143,425,727 (GRCm39) |
N72T |
probably benign |
Het |
Pus3 |
C |
A |
9: 35,476,946 (GRCm39) |
Q248K |
probably benign |
Het |
Sectm1a |
T |
A |
11: 120,960,569 (GRCm39) |
Q82L |
possibly damaging |
Het |
Sema3e |
A |
G |
5: 14,282,208 (GRCm39) |
Y448C |
probably damaging |
Het |
Slc12a4 |
A |
T |
8: 106,675,774 (GRCm39) |
S584T |
probably benign |
Het |
Slc25a40 |
T |
C |
5: 8,499,613 (GRCm39) |
F249L |
probably benign |
Het |
St3gal6 |
T |
A |
16: 58,306,793 (GRCm39) |
N79I |
|
Het |
Stxbp4 |
A |
T |
11: 90,426,320 (GRCm39) |
I496K |
possibly damaging |
Het |
Sulf1 |
A |
G |
1: 12,878,118 (GRCm39) |
Y202C |
probably damaging |
Het |
Swt1 |
A |
G |
1: 151,299,256 (GRCm39) |
|
probably null |
Het |
Tdrd6 |
T |
C |
17: 43,936,305 (GRCm39) |
Y1581C |
possibly damaging |
Het |
Tenm4 |
G |
C |
7: 96,495,061 (GRCm39) |
G1163A |
probably damaging |
Het |
Tlr4 |
A |
G |
4: 66,758,518 (GRCm39) |
E437G |
probably benign |
Het |
Txnrd2 |
A |
T |
16: 18,256,315 (GRCm39) |
H101L |
probably damaging |
Het |
Uba3 |
A |
T |
6: 97,163,671 (GRCm39) |
V306E |
probably damaging |
Het |
Unc5b |
T |
C |
10: 60,604,152 (GRCm39) |
Q814R |
probably damaging |
Het |
Vamp5 |
T |
G |
6: 72,347,304 (GRCm39) |
E5A |
possibly damaging |
Het |
Vmn1r69 |
T |
A |
7: 10,314,064 (GRCm39) |
R222S |
probably damaging |
Het |
Zfp507 |
G |
A |
7: 35,494,446 (GRCm39) |
T199I |
probably benign |
Het |
Zfyve19 |
T |
G |
2: 119,041,718 (GRCm39) |
L95R |
probably benign |
Het |
|
Other mutations in Cmklr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01447:Cmklr1
|
APN |
5 |
113,752,282 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02246:Cmklr1
|
APN |
5 |
113,752,461 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02997:Cmklr1
|
APN |
5 |
113,752,701 (GRCm39) |
missense |
probably benign |
0.15 |
R0098:Cmklr1
|
UTSW |
5 |
113,752,531 (GRCm39) |
missense |
probably benign |
0.00 |
R0360:Cmklr1
|
UTSW |
5 |
113,752,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R0364:Cmklr1
|
UTSW |
5 |
113,752,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R1217:Cmklr1
|
UTSW |
5 |
113,752,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R1702:Cmklr1
|
UTSW |
5 |
113,751,903 (GRCm39) |
missense |
probably benign |
0.20 |
R1862:Cmklr1
|
UTSW |
5 |
113,752,468 (GRCm39) |
missense |
probably damaging |
0.96 |
R4131:Cmklr1
|
UTSW |
5 |
113,752,545 (GRCm39) |
missense |
probably damaging |
0.97 |
R4132:Cmklr1
|
UTSW |
5 |
113,752,545 (GRCm39) |
missense |
probably damaging |
0.97 |
R4611:Cmklr1
|
UTSW |
5 |
113,752,930 (GRCm39) |
missense |
probably benign |
0.05 |
R4647:Cmklr1
|
UTSW |
5 |
113,752,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R5217:Cmklr1
|
UTSW |
5 |
113,752,710 (GRCm39) |
missense |
probably damaging |
0.98 |
R5484:Cmklr1
|
UTSW |
5 |
113,752,990 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5486:Cmklr1
|
UTSW |
5 |
113,752,990 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5487:Cmklr1
|
UTSW |
5 |
113,752,990 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5504:Cmklr1
|
UTSW |
5 |
113,752,990 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5505:Cmklr1
|
UTSW |
5 |
113,752,990 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6301:Cmklr1
|
UTSW |
5 |
113,752,999 (GRCm39) |
start codon destroyed |
possibly damaging |
0.72 |
R6994:Cmklr1
|
UTSW |
5 |
113,752,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7342:Cmklr1
|
UTSW |
5 |
113,752,354 (GRCm39) |
missense |
probably benign |
0.00 |
R9034:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9041:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9101:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9109:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9110:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9111:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9137:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9250:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9298:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9299:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9516:Cmklr1
|
UTSW |
5 |
113,752,341 (GRCm39) |
missense |
probably benign |
0.17 |
R9521:Cmklr1
|
UTSW |
5 |
113,752,480 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Cmklr1
|
UTSW |
5 |
113,751,952 (GRCm39) |
missense |
probably damaging |
1.00 |
|