Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
A |
G |
16: 4,680,980 (GRCm39) |
I106V |
possibly damaging |
Het |
Aars1 |
C |
A |
8: 111,763,615 (GRCm39) |
F18L |
probably damaging |
Het |
Abca7 |
C |
T |
10: 79,837,535 (GRCm39) |
T473I |
probably damaging |
Het |
Ap1m2 |
A |
T |
9: 21,209,524 (GRCm39) |
I384N |
probably damaging |
Het |
Atg16l2 |
G |
A |
7: 100,948,248 (GRCm39) |
Q99* |
probably null |
Het |
Bptf |
A |
T |
11: 106,964,954 (GRCm39) |
Y1413* |
probably null |
Het |
Cat |
T |
C |
2: 103,307,250 (GRCm39) |
T28A |
probably damaging |
Het |
Ccdc65 |
T |
A |
15: 98,620,759 (GRCm39) |
V418D |
probably benign |
Het |
Cd226 |
A |
C |
18: 89,265,444 (GRCm39) |
I241L |
probably benign |
Het |
Crybg1 |
A |
G |
10: 43,873,428 (GRCm39) |
S1227P |
probably benign |
Het |
Csn2 |
C |
T |
5: 87,842,794 (GRCm39) |
A78T |
probably benign |
Het |
Cyp21a1 |
T |
A |
17: 35,021,652 (GRCm39) |
H305L |
possibly damaging |
Het |
Ddx55 |
A |
G |
5: 124,706,707 (GRCm39) |
E572G |
possibly damaging |
Het |
Dguok |
A |
G |
6: 83,467,548 (GRCm39) |
Y100H |
probably damaging |
Het |
Dync1h1 |
T |
A |
12: 110,615,533 (GRCm39) |
S2955R |
probably damaging |
Het |
Etfbkmt |
A |
T |
6: 149,045,640 (GRCm39) |
|
probably benign |
Het |
Fam222a |
T |
A |
5: 114,749,347 (GRCm39) |
I181N |
probably damaging |
Het |
Fam24b |
T |
C |
7: 130,927,877 (GRCm39) |
D104G |
probably benign |
Het |
Fbn2 |
A |
T |
18: 58,181,611 (GRCm39) |
C1883* |
probably null |
Het |
Fchsd2 |
T |
G |
7: 100,920,778 (GRCm39) |
L461R |
probably benign |
Het |
Hdgfl1 |
C |
T |
13: 26,953,239 (GRCm39) |
G278E |
probably damaging |
Het |
Hectd4 |
G |
A |
5: 121,472,532 (GRCm39) |
R2756Q |
possibly damaging |
Het |
Mapkapk5 |
C |
T |
5: 121,672,490 (GRCm39) |
A163T |
probably benign |
Het |
Micu3 |
A |
T |
8: 40,835,156 (GRCm39) |
K504* |
probably null |
Het |
Myh1 |
C |
G |
11: 67,108,618 (GRCm39) |
H1345D |
possibly damaging |
Het |
Myh7 |
C |
A |
14: 55,216,146 (GRCm39) |
R1289L |
probably damaging |
Het |
Neb |
G |
T |
2: 52,132,068 (GRCm39) |
H280Q |
|
Het |
Nrbp1 |
T |
A |
5: 31,404,771 (GRCm39) |
|
probably null |
Het |
Oacyl |
T |
A |
18: 65,831,414 (GRCm39) |
V17D |
possibly damaging |
Het |
Obsl1 |
C |
A |
1: 75,480,157 (GRCm39) |
R463L |
possibly damaging |
Het |
Or1f19 |
T |
A |
16: 3,410,725 (GRCm39) |
L155Q |
probably damaging |
Het |
Or8b40 |
G |
A |
9: 38,028,010 (GRCm39) |
S311N |
probably benign |
Het |
Pcnt |
A |
T |
10: 76,217,128 (GRCm39) |
C2184* |
probably null |
Het |
Pfpl |
G |
C |
19: 12,406,297 (GRCm39) |
E183Q |
probably damaging |
Het |
Phrf1 |
T |
G |
7: 140,834,815 (GRCm39) |
S198A |
unknown |
Het |
Plekhg2 |
C |
G |
7: 28,064,249 (GRCm39) |
A431P |
probably damaging |
Het |
Ppp1r13b |
C |
T |
12: 111,810,077 (GRCm39) |
D244N |
probably damaging |
Het |
Raph1 |
T |
C |
1: 60,564,887 (GRCm39) |
E200G |
possibly damaging |
Het |
Rnf6 |
A |
G |
5: 146,147,936 (GRCm39) |
S361P |
probably benign |
Het |
Scgb2b19 |
G |
A |
7: 32,978,039 (GRCm39) |
A86V |
probably benign |
Het |
Sec23b |
T |
A |
2: 144,408,728 (GRCm39) |
C138S |
possibly damaging |
Het |
Slco1c1 |
T |
C |
6: 141,505,606 (GRCm39) |
S511P |
possibly damaging |
Het |
Tas2r130 |
A |
G |
6: 131,607,175 (GRCm39) |
S207P |
probably damaging |
Het |
Tdpoz1 |
A |
T |
3: 93,578,540 (GRCm39) |
H81Q |
probably benign |
Het |
Usp8 |
A |
G |
2: 126,578,414 (GRCm39) |
K289E |
probably damaging |
Het |
Vmn1r18 |
A |
C |
6: 57,367,202 (GRCm39) |
N117K |
probably benign |
Het |
Vps13c |
G |
T |
9: 67,872,794 (GRCm39) |
G3270V |
probably damaging |
Het |
Wdr20 |
A |
G |
12: 110,760,187 (GRCm39) |
T358A |
probably benign |
Het |
Wwc1 |
A |
C |
11: 35,870,796 (GRCm39) |
|
probably null |
Het |
Yars2 |
G |
T |
16: 16,127,242 (GRCm39) |
V436L |
possibly damaging |
Het |
Zfp609 |
G |
A |
9: 65,604,512 (GRCm39) |
Q1324* |
probably null |
Het |
Zfp81 |
T |
C |
17: 33,553,774 (GRCm39) |
T347A |
probably benign |
Het |
Zgpat |
T |
C |
2: 181,021,366 (GRCm39) |
V292A |
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 |
R5067:Ints14
|
UTSW |
9 |
64,871,694 (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 |
R9700:Ints14
|
UTSW |
9 |
64,880,007 (GRCm39) |
nonsense |
probably null |
|
|