Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr1 |
T |
A |
1: 173,159,598 (GRCm39) |
H307L |
probably benign |
Het |
Acnat1 |
A |
T |
4: 49,450,652 (GRCm39) |
L153H |
probably damaging |
Het |
Actn4 |
A |
T |
7: 28,618,431 (GRCm39) |
D76E |
probably benign |
Het |
Afdn |
A |
C |
17: 14,066,782 (GRCm39) |
M640L |
probably benign |
Het |
Angpt1 |
A |
T |
15: 42,539,837 (GRCm39) |
F7L |
probably benign |
Het |
Ap3b2 |
A |
G |
7: 81,126,092 (GRCm39) |
F373S |
probably damaging |
Het |
Armc2 |
T |
A |
10: 41,800,457 (GRCm39) |
Y650F |
probably damaging |
Het |
Atg2b |
G |
T |
12: 105,630,197 (GRCm39) |
T398K |
possibly damaging |
Het |
Baz1a |
CCATT |
CCATTCATT |
12: 55,021,895 (GRCm39) |
|
probably null |
Het |
Capn8 |
G |
A |
1: 182,438,670 (GRCm39) |
|
probably null |
Het |
Cdr1 |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
X: 60,228,130 (GRCm39) |
|
probably benign |
Het |
Cfap54 |
T |
C |
10: 92,637,081 (GRCm39) |
N3103D |
probably benign |
Het |
Chd9 |
G |
A |
8: 91,738,063 (GRCm39) |
R1565Q |
unknown |
Het |
Cir1 |
G |
A |
2: 73,134,152 (GRCm39) |
T139I |
probably damaging |
Het |
Cmah |
T |
C |
13: 24,619,673 (GRCm39) |
|
probably null |
Het |
Cnpy1 |
T |
C |
5: 28,450,800 (GRCm39) |
D2G |
probably damaging |
Het |
Dennd4a |
A |
T |
9: 64,801,793 (GRCm39) |
T979S |
probably benign |
Het |
Dnah11 |
T |
A |
12: 117,842,311 (GRCm39) |
K4423* |
probably null |
Het |
Dnajb4 |
A |
G |
3: 151,892,320 (GRCm39) |
I171T |
possibly damaging |
Het |
Dpm1 |
A |
T |
2: 168,072,307 (GRCm39) |
|
probably null |
Het |
Dtwd1 |
A |
G |
2: 125,996,595 (GRCm39) |
T27A |
probably benign |
Het |
Ep400 |
C |
T |
5: 110,889,872 (GRCm39) |
D464N |
unknown |
Het |
Epb42 |
A |
T |
2: 120,855,091 (GRCm39) |
I498N |
probably benign |
Het |
Fhod1 |
A |
G |
8: 106,064,048 (GRCm39) |
V219A |
unknown |
Het |
Gabrb2 |
A |
T |
11: 42,517,436 (GRCm39) |
E419D |
probably benign |
Het |
Gm29106 |
T |
A |
1: 118,127,254 (GRCm39) |
H315Q |
possibly damaging |
Het |
Gprin2 |
G |
T |
14: 33,917,615 (GRCm39) |
Q52K |
probably benign |
Het |
Grm4 |
A |
T |
17: 27,657,765 (GRCm39) |
Y414N |
probably damaging |
Het |
Gulo |
C |
A |
14: 66,225,630 (GRCm39) |
|
probably null |
Het |
H2-M1 |
A |
C |
17: 36,980,997 (GRCm39) |
V313G |
possibly damaging |
Het |
Hectd3 |
T |
C |
4: 116,852,951 (GRCm39) |
W118R |
probably damaging |
Het |
Hs6st3 |
G |
A |
14: 120,106,492 (GRCm39) |
C300Y |
probably damaging |
Het |
Il1rl2 |
T |
A |
1: 40,404,519 (GRCm39) |
S547T |
possibly damaging |
Het |
Kank1 |
G |
T |
19: 25,386,872 (GRCm39) |
V182F |
probably damaging |
Het |
Kif20b |
T |
A |
19: 34,928,149 (GRCm39) |
L1137* |
probably null |
Het |
Klhl7 |
A |
G |
5: 24,331,818 (GRCm39) |
|
probably null |
Het |
Krt13 |
T |
A |
11: 100,011,987 (GRCm39) |
D112V |
possibly damaging |
Het |
Ltbr |
A |
G |
6: 125,290,064 (GRCm39) |
V71A |
probably benign |
Het |
Ly6g |
T |
C |
15: 75,030,458 (GRCm39) |
V92A |
probably benign |
Het |
Map2k3 |
G |
A |
11: 60,822,929 (GRCm39) |
|
probably benign |
Het |
Mast2 |
A |
C |
4: 116,168,927 (GRCm39) |
D842E |
probably benign |
Het |
Mpo |
T |
G |
11: 87,694,349 (GRCm39) |
M693R |
probably benign |
Het |
Myo15a |
C |
A |
11: 60,378,234 (GRCm39) |
S212* |
probably null |
Het |
Nadk2 |
C |
T |
15: 9,106,824 (GRCm39) |
R37* |
probably null |
Het |
Ncapd3 |
G |
A |
9: 26,974,655 (GRCm39) |
R709H |
probably benign |
Het |
Nck2 |
T |
A |
1: 43,572,892 (GRCm39) |
Y55* |
probably null |
Het |
Neurl4 |
A |
G |
11: 69,798,301 (GRCm39) |
D777G |
probably damaging |
Het |
Npr2 |
G |
A |
4: 43,633,527 (GRCm39) |
V224M |
possibly damaging |
Het |
Nptx2 |
T |
A |
5: 144,484,950 (GRCm39) |
S148T |
probably benign |
Het |
Nr1d1 |
T |
C |
11: 98,661,160 (GRCm39) |
T369A |
probably benign |
Het |
Nub1 |
T |
G |
5: 24,908,483 (GRCm39) |
F411V |
probably damaging |
Het |
Nup188 |
T |
A |
2: 30,194,300 (GRCm39) |
Y158N |
probably damaging |
Het |
Or2d36 |
A |
T |
7: 106,746,660 (GRCm39) |
I46F |
probably benign |
Het |
Or5e1 |
A |
G |
7: 108,354,639 (GRCm39) |
N192S |
probably benign |
Het |
Or5m8 |
A |
G |
2: 85,823,091 (GRCm39) |
Y310C |
probably benign |
Het |
Or6c6c |
A |
T |
10: 129,541,208 (GRCm39) |
I154F |
probably damaging |
Het |
Or8c19-ps1 |
T |
A |
9: 38,220,928 (GRCm39) |
I279K |
unknown |
Het |
Orc2 |
C |
T |
1: 58,536,610 (GRCm39) |
G85S |
probably damaging |
Het |
Pak1ip1 |
T |
A |
13: 41,162,743 (GRCm39) |
V182D |
probably damaging |
Het |
Parvg |
T |
G |
15: 84,210,424 (GRCm39) |
C30W |
probably benign |
Het |
Pcdha1 |
T |
A |
18: 37,065,713 (GRCm39) |
D792E |
probably benign |
Het |
Ppp1r13b |
G |
T |
12: 111,800,242 (GRCm39) |
Q635K |
probably benign |
Het |
Pramel26 |
T |
C |
4: 143,536,886 (GRCm39) |
T482A |
probably benign |
Het |
Psg16 |
A |
G |
7: 16,832,086 (GRCm39) |
I341V |
probably benign |
Het |
Psme4 |
C |
T |
11: 30,826,868 (GRCm39) |
Q1796* |
probably null |
Het |
Ptn |
T |
G |
6: 36,692,699 (GRCm39) |
|
probably null |
Het |
Rapsn |
C |
T |
2: 90,875,823 (GRCm39) |
P400L |
probably damaging |
Het |
Rasal1 |
G |
A |
5: 120,800,358 (GRCm39) |
G207D |
probably damaging |
Het |
Rdx |
A |
G |
9: 51,974,878 (GRCm39) |
I5V |
probably benign |
Het |
Rpf1 |
A |
G |
3: 146,223,533 (GRCm39) |
I105T |
probably damaging |
Het |
Rps15a |
A |
T |
7: 117,709,220 (GRCm39) |
F79I |
possibly damaging |
Het |
Rwdd2b |
G |
A |
16: 87,233,641 (GRCm39) |
P153L |
probably benign |
Het |
Scaf11 |
G |
A |
15: 96,318,298 (GRCm39) |
S422L |
probably damaging |
Het |
Serpinb3b |
T |
A |
1: 107,082,403 (GRCm39) |
E287V |
possibly damaging |
Het |
Sgta |
T |
C |
10: 80,887,118 (GRCm39) |
D49G |
possibly damaging |
Het |
Sin3a |
T |
A |
9: 57,025,358 (GRCm39) |
M1068K |
probably benign |
Het |
Slc12a9 |
G |
A |
5: 137,319,671 (GRCm39) |
R615W |
probably damaging |
Het |
Slc26a3 |
T |
A |
12: 31,499,145 (GRCm39) |
S151T |
probably benign |
Het |
Slc4a8 |
C |
A |
15: 100,681,721 (GRCm39) |
H111N |
probably damaging |
Het |
Syngr1 |
G |
A |
15: 79,975,659 (GRCm39) |
R22K |
probably benign |
Het |
Tars2 |
A |
T |
3: 95,662,077 (GRCm39) |
V25E |
probably benign |
Het |
Tbx15 |
A |
G |
3: 99,259,647 (GRCm39) |
Y506C |
probably damaging |
Het |
Tgm4 |
A |
T |
9: 122,875,634 (GRCm39) |
K162N |
possibly damaging |
Het |
Tmem253 |
A |
G |
14: 52,255,439 (GRCm39) |
E83G |
probably damaging |
Het |
Trp73 |
G |
A |
4: 154,165,859 (GRCm39) |
T118I |
probably damaging |
Het |
Trpm7 |
A |
G |
2: 126,664,578 (GRCm39) |
S934P |
possibly damaging |
Het |
Ttc23l |
G |
A |
15: 10,523,729 (GRCm39) |
S330L |
probably benign |
Het |
Tub |
A |
C |
7: 108,624,845 (GRCm39) |
D199A |
probably benign |
Het |
Uri1 |
A |
C |
7: 37,696,110 (GRCm39) |
|
probably null |
Het |
Usp16 |
C |
T |
16: 87,276,120 (GRCm39) |
A486V |
probably benign |
Het |
Vmn1r12 |
A |
G |
6: 57,136,526 (GRCm39) |
I208V |
probably benign |
Het |
Vmn2r116 |
A |
T |
17: 23,620,797 (GRCm39) |
M844L |
probably benign |
Het |
Vmn2r13 |
C |
T |
5: 109,339,773 (GRCm39) |
|
probably null |
Het |
Xpnpep1 |
T |
C |
19: 53,001,892 (GRCm39) |
D118G |
probably damaging |
Het |
Zfp111 |
G |
A |
7: 23,898,067 (GRCm39) |
P516S |
possibly damaging |
Het |
|
Other mutations in Galnt18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00584:Galnt18
|
APN |
7 |
111,071,202 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03110:Galnt18
|
APN |
7 |
111,147,920 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03263:Galnt18
|
APN |
7 |
111,119,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Galnt18
|
UTSW |
7 |
111,153,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Galnt18
|
UTSW |
7 |
111,153,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R0141:Galnt18
|
UTSW |
7 |
111,198,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R0471:Galnt18
|
UTSW |
7 |
111,378,506 (GRCm39) |
splice site |
probably benign |
|
R0494:Galnt18
|
UTSW |
7 |
111,153,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Galnt18
|
UTSW |
7 |
111,107,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R0682:Galnt18
|
UTSW |
7 |
111,119,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R0938:Galnt18
|
UTSW |
7 |
111,119,206 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1321:Galnt18
|
UTSW |
7 |
111,378,639 (GRCm39) |
missense |
probably benign |
0.19 |
R1457:Galnt18
|
UTSW |
7 |
111,378,635 (GRCm39) |
nonsense |
probably null |
|
R1656:Galnt18
|
UTSW |
7 |
111,215,699 (GRCm39) |
splice site |
probably benign |
|
R2077:Galnt18
|
UTSW |
7 |
111,153,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Galnt18
|
UTSW |
7 |
111,153,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R3788:Galnt18
|
UTSW |
7 |
111,119,322 (GRCm39) |
nonsense |
probably null |
|
R4835:Galnt18
|
UTSW |
7 |
111,378,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R4962:Galnt18
|
UTSW |
7 |
111,071,271 (GRCm39) |
missense |
probably benign |
0.10 |
R6125:Galnt18
|
UTSW |
7 |
111,084,400 (GRCm39) |
missense |
probably damaging |
0.96 |
R6216:Galnt18
|
UTSW |
7 |
111,112,757 (GRCm39) |
missense |
probably benign |
0.39 |
R7075:Galnt18
|
UTSW |
7 |
111,155,595 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7831:Galnt18
|
UTSW |
7 |
111,155,665 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8728:Galnt18
|
UTSW |
7 |
111,119,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R8729:Galnt18
|
UTSW |
7 |
111,119,198 (GRCm39) |
missense |
probably null |
0.90 |
R8888:Galnt18
|
UTSW |
7 |
111,378,709 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8895:Galnt18
|
UTSW |
7 |
111,378,709 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9330:Galnt18
|
UTSW |
7 |
111,071,271 (GRCm39) |
missense |
probably benign |
0.10 |
R9448:Galnt18
|
UTSW |
7 |
111,153,649 (GRCm39) |
missense |
probably damaging |
1.00 |
RF017:Galnt18
|
UTSW |
7 |
111,198,221 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Galnt18
|
UTSW |
7 |
111,084,358 (GRCm39) |
missense |
probably damaging |
1.00 |
|