Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak2 |
T |
C |
12: 112,748,936 (GRCm39) |
N304D |
probably benign |
Het |
Akr7a5 |
T |
C |
4: 139,038,333 (GRCm39) |
S90P |
probably damaging |
Het |
Aplnr |
T |
A |
2: 84,967,128 (GRCm39) |
V51E |
probably damaging |
Het |
Arhgap21 |
A |
T |
2: 20,884,848 (GRCm39) |
H776Q |
probably damaging |
Het |
Asxl3 |
C |
G |
18: 22,658,356 (GRCm39) |
A2122G |
possibly damaging |
Het |
Bsn |
T |
A |
9: 107,989,152 (GRCm39) |
Y2200F |
probably damaging |
Het |
Btbd10 |
A |
T |
7: 112,925,043 (GRCm39) |
D268E |
probably damaging |
Het |
Cacna1h |
T |
C |
17: 25,616,782 (GRCm39) |
N113D |
probably damaging |
Het |
Cfap54 |
T |
C |
10: 92,902,628 (GRCm39) |
N175D |
probably benign |
Het |
Cfap61 |
A |
G |
2: 145,943,956 (GRCm39) |
D134G |
probably damaging |
Het |
Clybl |
A |
T |
14: 122,616,701 (GRCm39) |
I239L |
possibly damaging |
Het |
Defb11 |
A |
T |
8: 22,396,352 (GRCm39) |
F15Y |
probably damaging |
Het |
Dlc1 |
A |
G |
8: 37,051,647 (GRCm39) |
S695P |
probably benign |
Het |
Fbxl5 |
T |
C |
5: 43,916,114 (GRCm39) |
K432E |
probably benign |
Het |
Fryl |
T |
C |
5: 73,215,098 (GRCm39) |
E2226G |
probably benign |
Het |
Gm10337 |
T |
A |
15: 102,412,306 (GRCm39) |
|
probably null |
Het |
Gm5828 |
A |
G |
1: 16,839,516 (GRCm39) |
|
noncoding transcript |
Het |
Gm8674 |
A |
T |
13: 50,053,870 (GRCm39) |
|
noncoding transcript |
Het |
Ighv6-5 |
T |
C |
12: 114,380,191 (GRCm39) |
|
probably null |
Het |
Insyn2a |
A |
T |
7: 134,520,284 (GRCm39) |
V82E |
probably benign |
Het |
Kcp |
G |
A |
6: 29,492,107 (GRCm39) |
P153L |
probably benign |
Het |
Lrrk2 |
A |
C |
15: 91,649,993 (GRCm39) |
N1710T |
probably benign |
Het |
Marchf10 |
T |
A |
11: 105,280,933 (GRCm39) |
T451S |
possibly damaging |
Het |
Mcf2l |
T |
G |
8: 12,965,959 (GRCm39) |
|
probably benign |
Het |
Mfng |
C |
T |
15: 78,648,588 (GRCm39) |
R163H |
probably benign |
Het |
Neurod2 |
T |
A |
11: 98,218,063 (GRCm39) |
H367L |
possibly damaging |
Het |
Nfatc4 |
A |
T |
14: 56,069,875 (GRCm39) |
Q681L |
probably damaging |
Het |
Nkx3-2 |
T |
C |
5: 41,919,220 (GRCm39) |
N256S |
probably damaging |
Het |
Ntng1 |
G |
A |
3: 110,042,661 (GRCm39) |
T55M |
possibly damaging |
Het |
Snd1 |
C |
A |
6: 28,888,239 (GRCm39) |
N891K |
probably damaging |
Het |
Syt7 |
T |
C |
19: 10,420,222 (GRCm39) |
V382A |
possibly damaging |
Het |
Trim72 |
T |
C |
7: 127,609,139 (GRCm39) |
S314P |
possibly damaging |
Het |
Ttc41 |
T |
C |
10: 86,580,408 (GRCm39) |
S785P |
probably damaging |
Het |
Ube2z |
C |
T |
11: 95,953,835 (GRCm39) |
V128I |
probably benign |
Het |
Vps26c |
T |
A |
16: 94,327,263 (GRCm39) |
|
probably benign |
Het |
Wdr43 |
T |
C |
17: 71,933,849 (GRCm39) |
Y149H |
probably benign |
Het |
Wnk4 |
T |
A |
11: 101,153,682 (GRCm39) |
V248E |
probably damaging |
Het |
Zcchc2 |
A |
T |
1: 105,958,694 (GRCm39) |
N1055I |
probably damaging |
Het |
Zdhhc23 |
T |
C |
16: 43,794,134 (GRCm39) |
Y180C |
probably benign |
Het |
|
Other mutations in Ints14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00546:Ints14
|
APN |
9 |
64,880,074 (GRCm39) |
missense |
probably benign |
0.30 |
R0376:Ints14
|
UTSW |
9 |
64,891,272 (GRCm39) |
missense |
probably damaging |
0.98 |
R0589:Ints14
|
UTSW |
9 |
64,887,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Ints14
|
UTSW |
9 |
64,871,715 (GRCm39) |
missense |
probably benign |
|
R0708:Ints14
|
UTSW |
9 |
64,891,266 (GRCm39) |
missense |
probably benign |
0.29 |
R1192:Ints14
|
UTSW |
9 |
64,874,045 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2114:Ints14
|
UTSW |
9 |
64,887,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2115:Ints14
|
UTSW |
9 |
64,887,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Ints14
|
UTSW |
9 |
64,887,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2484:Ints14
|
UTSW |
9 |
64,893,366 (GRCm39) |
missense |
probably benign |
|
R4811:Ints14
|
UTSW |
9 |
64,871,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4953:Ints14
|
UTSW |
9 |
64,889,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R6080:Ints14
|
UTSW |
9 |
64,874,044 (GRCm39) |
missense |
probably benign |
0.02 |
R6326:Ints14
|
UTSW |
9 |
64,871,719 (GRCm39) |
missense |
probably benign |
0.08 |
R6395:Ints14
|
UTSW |
9 |
64,885,406 (GRCm39) |
splice site |
probably null |
|
R7036:Ints14
|
UTSW |
9 |
64,871,827 (GRCm39) |
missense |
probably benign |
|
R7147:Ints14
|
UTSW |
9 |
64,891,267 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7203:Ints14
|
UTSW |
9 |
64,871,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Ints14
|
UTSW |
9 |
64,880,532 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9390:Ints14
|
UTSW |
9 |
64,891,314 (GRCm39) |
missense |
probably benign |
0.08 |
R9561:Ints14
|
UTSW |
9 |
64,882,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R9700:Ints14
|
UTSW |
9 |
64,880,007 (GRCm39) |
nonsense |
probably null |
|
|