Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130008F23Rik |
T |
C |
17: 41,190,962 (GRCm39) |
T156A |
probably benign |
Het |
9230106D20Rik |
A |
T |
10: 19,536,065 (GRCm39) |
|
noncoding transcript |
Het |
Abca3 |
A |
G |
17: 24,585,171 (GRCm39) |
D144G |
probably benign |
Het |
Anxa2 |
T |
A |
9: 69,390,260 (GRCm39) |
L121Q |
probably damaging |
Het |
Anxa7 |
A |
T |
14: 20,512,732 (GRCm39) |
I267N |
probably damaging |
Het |
Asb14 |
A |
T |
14: 26,633,797 (GRCm39) |
D334V |
possibly damaging |
Het |
Batf3 |
A |
G |
1: 190,830,714 (GRCm39) |
N20S |
probably benign |
Het |
Bub1b |
A |
G |
2: 118,468,920 (GRCm39) |
H895R |
probably benign |
Het |
C1qtnf12 |
G |
A |
4: 156,050,160 (GRCm39) |
|
probably null |
Het |
Cars1 |
T |
C |
7: 143,130,385 (GRCm39) |
I294V |
probably damaging |
Het |
Ccdc142 |
G |
A |
6: 83,084,462 (GRCm39) |
A527T |
probably damaging |
Het |
Ccdc168 |
A |
T |
1: 44,096,234 (GRCm39) |
N1621K |
possibly damaging |
Het |
Ccdc92 |
T |
C |
5: 124,913,242 (GRCm39) |
N96D |
probably benign |
Het |
Ceacam18 |
T |
A |
7: 43,288,880 (GRCm39) |
D210E |
probably benign |
Het |
Cenpe |
A |
G |
3: 134,952,257 (GRCm39) |
T1373A |
probably damaging |
Het |
Cfap161 |
T |
G |
7: 83,440,932 (GRCm39) |
|
probably null |
Het |
Cimip4 |
T |
C |
15: 78,270,588 (GRCm39) |
Y60C |
possibly damaging |
Het |
Cldn19 |
A |
G |
4: 119,112,990 (GRCm39) |
D74G |
probably benign |
Het |
Cox7a2l |
T |
A |
17: 83,811,397 (GRCm39) |
Q78L |
probably benign |
Het |
Crot |
T |
C |
5: 9,019,080 (GRCm39) |
N491S |
probably benign |
Het |
Cspg4b |
T |
A |
13: 113,505,342 (GRCm39) |
L2157Q |
probably damaging |
Het |
Ctr9 |
A |
G |
7: 110,643,165 (GRCm39) |
|
probably null |
Het |
Cyp4f14 |
T |
G |
17: 33,130,209 (GRCm39) |
D190A |
probably damaging |
Het |
D630039A03Rik |
C |
T |
4: 57,910,240 (GRCm39) |
V191I |
probably benign |
Het |
Dnah10 |
A |
T |
5: 124,838,343 (GRCm39) |
N1124I |
probably benign |
Het |
Duox1 |
T |
A |
2: 122,177,861 (GRCm39) |
Y1548* |
probably null |
Het |
Epdr1 |
G |
A |
13: 19,778,773 (GRCm39) |
Q6* |
probably null |
Het |
Erbin |
A |
G |
13: 103,996,577 (GRCm39) |
|
probably null |
Het |
Ero1a |
A |
T |
14: 45,525,217 (GRCm39) |
I436K |
probably damaging |
Het |
Exph5 |
A |
T |
9: 53,287,941 (GRCm39) |
Q1674L |
possibly damaging |
Het |
Fat4 |
A |
T |
3: 39,037,607 (GRCm39) |
Y3753F |
probably damaging |
Het |
Gaa |
T |
C |
11: 119,174,098 (GRCm39) |
V763A |
probably damaging |
Het |
Golim4 |
G |
A |
3: 75,809,745 (GRCm39) |
T216I |
probably damaging |
Het |
Gpr83 |
G |
T |
9: 14,779,629 (GRCm39) |
C269F |
possibly damaging |
Het |
Gtf2f2 |
A |
G |
14: 76,245,143 (GRCm39) |
|
probably null |
Het |
Gtf3c5 |
T |
C |
2: 28,469,694 (GRCm39) |
Y70C |
probably damaging |
Het |
Hao1 |
T |
A |
2: 134,372,584 (GRCm39) |
R141S |
probably benign |
Het |
Hecw2 |
T |
C |
1: 53,965,182 (GRCm39) |
D548G |
probably benign |
Het |
Hr |
G |
A |
14: 70,809,477 (GRCm39) |
|
probably null |
Het |
Hrg |
A |
C |
16: 22,774,853 (GRCm39) |
E161A |
probably damaging |
Het |
Hydin |
A |
T |
8: 111,237,526 (GRCm39) |
N1933I |
probably benign |
Het |
Itpr2 |
A |
G |
6: 146,229,830 (GRCm39) |
L1255P |
probably damaging |
Het |
Kcnma1 |
C |
A |
14: 23,380,997 (GRCm39) |
D903Y |
probably damaging |
Het |
Kif5c |
T |
C |
2: 49,570,252 (GRCm39) |
|
probably null |
Het |
Mgat5b |
C |
A |
11: 116,868,614 (GRCm39) |
H512Q |
probably damaging |
Het |
Mtmr4 |
T |
C |
11: 87,502,943 (GRCm39) |
V999A |
probably benign |
Het |
Mttp |
G |
T |
3: 137,813,041 (GRCm39) |
Q545K |
probably damaging |
Het |
Ncstn |
CAGCTCCACGAAG |
CAG |
1: 171,899,038 (GRCm39) |
|
probably null |
Het |
Nexn |
A |
G |
3: 151,948,405 (GRCm39) |
I386T |
probably damaging |
Het |
Nrip3 |
A |
G |
7: 109,365,763 (GRCm39) |
S85P |
probably benign |
Het |
Nxpe2 |
T |
C |
9: 48,237,914 (GRCm39) |
T114A |
probably damaging |
Het |
Olr1 |
T |
C |
6: 129,465,895 (GRCm39) |
N37S |
possibly damaging |
Het |
Or14j5 |
C |
T |
17: 38,161,966 (GRCm39) |
A161V |
probably benign |
Het |
Or4b1d |
A |
G |
2: 89,968,931 (GRCm39) |
L184S |
probably damaging |
Het |
Or4c105 |
A |
T |
2: 88,648,402 (GRCm39) |
I296F |
probably benign |
Het |
Or55b3 |
A |
G |
7: 102,126,720 (GRCm39) |
L119P |
probably damaging |
Het |
Or5p80 |
G |
T |
7: 108,229,855 (GRCm39) |
V219F |
possibly damaging |
Het |
Pax4 |
T |
C |
6: 28,443,446 (GRCm39) |
Y290C |
probably benign |
Het |
Pcdhb2 |
T |
A |
18: 37,429,038 (GRCm39) |
V337D |
probably damaging |
Het |
Pglyrp4 |
T |
C |
3: 90,640,310 (GRCm39) |
Y187H |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,098,614 (GRCm39) |
M2017T |
probably benign |
Het |
Pkdrej |
T |
C |
15: 85,703,483 (GRCm39) |
T818A |
possibly damaging |
Het |
Pxk |
C |
T |
14: 8,151,507 (GRCm38) |
R441* |
probably null |
Het |
Pygm |
T |
C |
19: 6,447,637 (GRCm39) |
I648T |
possibly damaging |
Het |
Rab4a |
A |
T |
8: 124,550,565 (GRCm39) |
K15I |
probably damaging |
Het |
Rasa3 |
T |
C |
8: 13,635,035 (GRCm39) |
E428G |
probably benign |
Het |
Rnf182 |
G |
A |
13: 43,822,010 (GRCm39) |
W187* |
probably null |
Het |
Rpl3 |
C |
T |
15: 79,964,591 (GRCm39) |
V222M |
possibly damaging |
Het |
Rtl9 |
C |
T |
X: 141,886,011 (GRCm39) |
S1141F |
possibly damaging |
Het |
S100a11 |
A |
T |
3: 93,433,428 (GRCm39) |
I91F |
probably benign |
Het |
Sfswap |
C |
T |
5: 129,590,148 (GRCm39) |
T215I |
probably damaging |
Het |
Slit2 |
A |
G |
5: 48,461,372 (GRCm39) |
D1456G |
probably damaging |
Het |
Tex19.2 |
C |
T |
11: 121,008,317 (GRCm39) |
V44I |
probably benign |
Het |
Tmem127 |
G |
A |
2: 127,098,094 (GRCm39) |
|
probably null |
Het |
Tpd52 |
G |
T |
3: 9,012,579 (GRCm39) |
N59K |
probably damaging |
Het |
Trpc3 |
G |
A |
3: 36,692,695 (GRCm39) |
P766S |
possibly damaging |
Het |
Usp17la |
T |
A |
7: 104,510,331 (GRCm39) |
V312D |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,345,582 (GRCm39) |
N2608D |
possibly damaging |
Het |
Zfp764l1 |
T |
A |
7: 126,991,081 (GRCm39) |
H302L |
probably damaging |
Het |
Zscan25 |
C |
A |
5: 145,227,858 (GRCm39) |
H507Q |
possibly damaging |
Het |
|
Other mutations in Clec12a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02370:Clec12a
|
APN |
6 |
129,331,539 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0491:Clec12a
|
UTSW |
6 |
129,341,016 (GRCm39) |
missense |
probably benign |
0.01 |
R1551:Clec12a
|
UTSW |
6 |
129,327,384 (GRCm39) |
start codon destroyed |
probably damaging |
1.00 |
R1827:Clec12a
|
UTSW |
6 |
129,330,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Clec12a
|
UTSW |
6 |
129,327,444 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1961:Clec12a
|
UTSW |
6 |
129,327,444 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4280:Clec12a
|
UTSW |
6 |
129,340,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R4392:Clec12a
|
UTSW |
6 |
129,330,427 (GRCm39) |
splice site |
probably benign |
|
R4658:Clec12a
|
UTSW |
6 |
129,331,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R4922:Clec12a
|
UTSW |
6 |
129,336,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R4959:Clec12a
|
UTSW |
6 |
129,330,628 (GRCm39) |
missense |
probably benign |
0.10 |
R4973:Clec12a
|
UTSW |
6 |
129,330,628 (GRCm39) |
missense |
probably benign |
0.10 |
R6246:Clec12a
|
UTSW |
6 |
129,330,733 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6450:Clec12a
|
UTSW |
6 |
129,330,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R7494:Clec12a
|
UTSW |
6 |
129,330,362 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8946:Clec12a
|
UTSW |
6 |
129,340,949 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9678:Clec12a
|
UTSW |
6 |
129,330,628 (GRCm39) |
missense |
probably benign |
0.10 |
|