Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700129C05Rik |
G |
T |
14: 59,379,569 (GRCm39) |
T54K |
possibly damaging |
Het |
2210408I21Rik |
A |
T |
13: 77,451,544 (GRCm39) |
E876V |
possibly damaging |
Het |
Aasdh |
A |
T |
5: 77,049,849 (GRCm39) |
L49Q |
probably damaging |
Het |
Abca8b |
T |
C |
11: 109,847,844 (GRCm39) |
|
probably null |
Het |
Ablim1 |
A |
T |
19: 57,032,302 (GRCm39) |
L556Q |
probably damaging |
Het |
Afdn |
A |
G |
17: 14,119,408 (GRCm39) |
T1700A |
probably benign |
Het |
Agl |
G |
A |
3: 116,545,720 (GRCm39) |
R1359C |
probably damaging |
Het |
Agpat3 |
T |
A |
10: 78,113,863 (GRCm39) |
H275L |
possibly damaging |
Het |
Ahcyl1 |
A |
T |
3: 107,577,586 (GRCm39) |
C180* |
probably null |
Het |
Aim2 |
A |
G |
1: 173,289,899 (GRCm39) |
|
probably benign |
Het |
Angpt1 |
T |
C |
15: 42,331,631 (GRCm39) |
N320S |
probably benign |
Het |
Ankrd52 |
T |
A |
10: 128,225,727 (GRCm39) |
|
probably null |
Het |
Ap1g1 |
C |
T |
8: 110,581,694 (GRCm39) |
S654L |
probably benign |
Het |
Bpifa1 |
T |
A |
2: 153,987,977 (GRCm39) |
S173R |
probably benign |
Het |
Brd8 |
T |
C |
18: 34,736,947 (GRCm39) |
|
probably benign |
Het |
Btbd9 |
C |
T |
17: 30,493,916 (GRCm39) |
D492N |
possibly damaging |
Het |
C1qtnf2 |
A |
G |
11: 43,381,670 (GRCm39) |
T161A |
probably benign |
Het |
Car6 |
T |
C |
4: 150,271,965 (GRCm39) |
Y228C |
probably damaging |
Het |
Ccdc149 |
A |
G |
5: 52,557,559 (GRCm39) |
L273P |
probably damaging |
Het |
Cit |
G |
A |
5: 116,122,899 (GRCm39) |
R1405Q |
probably damaging |
Het |
Cox17 |
T |
C |
16: 38,169,638 (GRCm39) |
L48P |
probably damaging |
Het |
Cttn |
A |
G |
7: 143,995,589 (GRCm39) |
|
probably benign |
Het |
Cyp4f18 |
T |
C |
8: 72,743,619 (GRCm39) |
|
probably benign |
Het |
Dtnbp1 |
A |
G |
13: 45,076,669 (GRCm39) |
L175P |
probably damaging |
Het |
Efl1 |
T |
C |
7: 82,342,219 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
C |
T |
2: 125,162,830 (GRCm39) |
R2152Q |
possibly damaging |
Het |
Fignl1 |
A |
T |
11: 11,751,061 (GRCm39) |
S665T |
probably benign |
Het |
Gm9843 |
A |
T |
16: 76,200,449 (GRCm39) |
|
noncoding transcript |
Het |
Gpr155 |
C |
T |
2: 73,197,936 (GRCm39) |
V395I |
probably benign |
Het |
Greb1l |
T |
C |
18: 10,522,076 (GRCm39) |
|
probably benign |
Het |
Hdgfl1 |
A |
T |
13: 26,953,979 (GRCm39) |
H31Q |
probably benign |
Het |
Heatr1 |
T |
C |
13: 12,425,443 (GRCm39) |
S628P |
probably damaging |
Het |
Hivep2 |
A |
G |
10: 14,005,456 (GRCm39) |
T685A |
probably benign |
Het |
Hmgcl |
T |
G |
4: 135,686,039 (GRCm39) |
V168G |
probably damaging |
Het |
Itch |
T |
C |
2: 155,041,314 (GRCm39) |
I454T |
probably benign |
Het |
Itih2 |
T |
C |
2: 10,120,110 (GRCm39) |
D309G |
possibly damaging |
Het |
Kcmf1 |
T |
C |
6: 72,819,935 (GRCm39) |
I304V |
probably benign |
Het |
Kcnh1 |
G |
A |
1: 191,959,112 (GRCm39) |
W222* |
probably null |
Het |
Kcnh1 |
G |
T |
1: 191,959,113 (GRCm39) |
W222C |
probably damaging |
Het |
Kif24 |
T |
A |
4: 41,414,939 (GRCm39) |
K287* |
probably null |
Het |
Lrig3 |
A |
G |
10: 125,807,986 (GRCm39) |
|
probably benign |
Het |
Lrp2 |
A |
T |
2: 69,367,907 (GRCm39) |
C202S |
probably null |
Het |
Lrrc37 |
A |
T |
11: 103,494,067 (GRCm39) |
F663L |
probably benign |
Het |
Lrrn2 |
A |
G |
1: 132,865,558 (GRCm39) |
N208D |
probably damaging |
Het |
Mcm5 |
C |
T |
8: 75,852,880 (GRCm39) |
T664I |
possibly damaging |
Het |
Mfsd10 |
A |
G |
5: 34,791,790 (GRCm39) |
L365S |
probably benign |
Het |
Mfsd6 |
A |
G |
1: 52,697,849 (GRCm39) |
|
probably benign |
Het |
Mllt3 |
C |
A |
4: 87,758,969 (GRCm39) |
V360L |
probably benign |
Het |
Mrm1 |
G |
A |
11: 84,709,996 (GRCm39) |
A68V |
possibly damaging |
Het |
Myo19 |
A |
G |
11: 84,788,558 (GRCm39) |
|
probably benign |
Het |
Myo3b |
A |
G |
2: 70,047,510 (GRCm39) |
T311A |
probably benign |
Het |
Myo5b |
T |
C |
18: 74,875,251 (GRCm39) |
F1552L |
probably benign |
Het |
Myo7b |
C |
T |
18: 32,105,949 (GRCm39) |
V1353I |
probably benign |
Het |
Myo9b |
T |
C |
8: 71,806,476 (GRCm39) |
S1512P |
probably damaging |
Het |
Nanos3 |
C |
T |
8: 84,902,763 (GRCm39) |
R133Q |
probably damaging |
Het |
Osbpl3 |
A |
G |
6: 50,329,988 (GRCm39) |
W63R |
probably damaging |
Het |
Pcdh17 |
T |
C |
14: 84,685,641 (GRCm39) |
S703P |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,815,237 (GRCm39) |
I1231T |
probably damaging |
Het |
Pex16 |
A |
C |
2: 92,206,032 (GRCm39) |
|
probably benign |
Het |
Pfkl |
T |
C |
10: 77,828,368 (GRCm39) |
N399S |
probably benign |
Het |
Pkhd1l1 |
G |
A |
15: 44,390,180 (GRCm39) |
R1432K |
possibly damaging |
Het |
Prdm1 |
T |
A |
10: 44,332,692 (GRCm39) |
T106S |
probably benign |
Het |
Prrc1 |
A |
G |
18: 57,496,363 (GRCm39) |
M105V |
probably benign |
Het |
Psg26 |
A |
G |
7: 18,217,883 (GRCm39) |
C12R |
possibly damaging |
Het |
Rnf43 |
A |
T |
11: 87,622,263 (GRCm39) |
S455C |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,787,442 (GRCm39) |
K977R |
probably damaging |
Het |
Sart1 |
C |
T |
19: 5,431,150 (GRCm39) |
|
probably benign |
Het |
Sec14l5 |
A |
G |
16: 4,998,167 (GRCm39) |
S509G |
probably benign |
Het |
Sin3b |
A |
T |
8: 73,471,136 (GRCm39) |
E361V |
probably benign |
Het |
Slc35e3 |
C |
T |
10: 117,576,795 (GRCm39) |
E179K |
possibly damaging |
Het |
Sntb2 |
T |
C |
8: 107,728,215 (GRCm39) |
S388P |
probably damaging |
Het |
Srms |
A |
G |
2: 180,854,175 (GRCm39) |
S131P |
probably benign |
Het |
Sting1 |
A |
T |
18: 35,872,141 (GRCm39) |
F120L |
probably benign |
Het |
Stxbp5 |
T |
C |
10: 9,742,442 (GRCm39) |
|
probably benign |
Het |
Taar2 |
T |
C |
10: 23,816,961 (GRCm39) |
V167A |
probably damaging |
Het |
Taar2 |
G |
A |
10: 23,817,393 (GRCm39) |
R311H |
probably benign |
Het |
Thsd7a |
A |
G |
6: 12,321,899 (GRCm39) |
Y1516H |
possibly damaging |
Het |
Tlk1 |
T |
A |
2: 70,544,513 (GRCm39) |
|
probably benign |
Het |
Tnfaip3 |
T |
C |
10: 18,878,495 (GRCm39) |
K771R |
probably damaging |
Het |
Treml1 |
C |
T |
17: 48,667,486 (GRCm39) |
L124F |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,611,141 (GRCm39) |
Q9137K |
possibly damaging |
Het |
Unkl |
T |
A |
17: 25,449,685 (GRCm39) |
I469N |
probably damaging |
Het |
Vmn1r173 |
G |
T |
7: 23,402,508 (GRCm39) |
V248L |
possibly damaging |
Het |
Vps35 |
T |
C |
8: 86,000,204 (GRCm39) |
Q474R |
probably damaging |
Het |
Wdr17 |
T |
A |
8: 55,116,043 (GRCm39) |
T580S |
probably benign |
Het |
Xpnpep1 |
T |
C |
19: 52,998,583 (GRCm39) |
K222E |
probably benign |
Het |
Ylpm1 |
A |
G |
12: 85,096,511 (GRCm39) |
T1446A |
probably benign |
Het |
Zfp277 |
A |
G |
12: 40,414,161 (GRCm39) |
L228S |
possibly damaging |
Het |
Zfp941 |
T |
A |
7: 140,393,188 (GRCm39) |
K57M |
probably damaging |
Het |
Zmpste24 |
A |
T |
4: 120,938,406 (GRCm39) |
S244R |
probably benign |
Het |
|
Other mutations in Mgat4e |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01314:Mgat4e
|
APN |
1 |
134,469,187 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02863:Mgat4e
|
APN |
1 |
134,468,896 (GRCm39) |
missense |
probably benign |
|
IGL02999:Mgat4e
|
APN |
1 |
134,468,928 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4449:Mgat4e
|
UTSW |
1 |
134,468,735 (GRCm39) |
utr 3 prime |
probably benign |
|
PIT4480001:Mgat4e
|
UTSW |
1 |
134,469,103 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1396:Mgat4e
|
UTSW |
1 |
134,469,271 (GRCm39) |
missense |
probably benign |
0.18 |
R1626:Mgat4e
|
UTSW |
1 |
134,469,016 (GRCm39) |
missense |
probably benign |
0.08 |
R2020:Mgat4e
|
UTSW |
1 |
134,469,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R3011:Mgat4e
|
UTSW |
1 |
134,469,846 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4748:Mgat4e
|
UTSW |
1 |
134,469,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Mgat4e
|
UTSW |
1 |
134,469,063 (GRCm39) |
missense |
probably damaging |
0.98 |
R4859:Mgat4e
|
UTSW |
1 |
134,469,478 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4894:Mgat4e
|
UTSW |
1 |
134,468,856 (GRCm39) |
missense |
probably benign |
0.23 |
R4910:Mgat4e
|
UTSW |
1 |
134,469,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R5007:Mgat4e
|
UTSW |
1 |
134,468,890 (GRCm39) |
missense |
probably benign |
0.39 |
R5108:Mgat4e
|
UTSW |
1 |
134,468,961 (GRCm39) |
missense |
probably benign |
0.03 |
R5691:Mgat4e
|
UTSW |
1 |
134,468,729 (GRCm39) |
utr 3 prime |
probably benign |
|
R5994:Mgat4e
|
UTSW |
1 |
134,469,234 (GRCm39) |
missense |
probably benign |
0.05 |
R6467:Mgat4e
|
UTSW |
1 |
134,468,944 (GRCm39) |
missense |
probably benign |
0.01 |
R7155:Mgat4e
|
UTSW |
1 |
134,469,697 (GRCm39) |
missense |
probably damaging |
0.98 |
R7612:Mgat4e
|
UTSW |
1 |
134,469,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R9046:Mgat4e
|
UTSW |
1 |
134,474,742 (GRCm39) |
missense |
possibly damaging |
0.53 |
|