Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Capn5 |
T |
A |
7: 97,780,950 (GRCm39) |
K276* |
probably null |
Het |
Cct4 |
T |
C |
11: 22,952,394 (GRCm39) |
V495A |
probably damaging |
Het |
Dapk3 |
A |
G |
10: 81,026,131 (GRCm39) |
K141E |
probably damaging |
Het |
Dnah2 |
T |
C |
11: 69,313,385 (GRCm39) |
N4264S |
probably damaging |
Het |
Dok1 |
A |
G |
6: 83,009,812 (GRCm39) |
L99P |
probably damaging |
Het |
Ebf3 |
A |
G |
7: 136,833,030 (GRCm39) |
V215A |
possibly damaging |
Het |
Efnb2 |
A |
G |
8: 8,710,488 (GRCm39) |
S43P |
probably benign |
Het |
Jhy |
G |
A |
9: 40,828,674 (GRCm39) |
Q411* |
probably null |
Het |
Krt73 |
G |
A |
15: 101,708,370 (GRCm39) |
T229I |
probably damaging |
Het |
Mroh8 |
A |
G |
2: 157,113,882 (GRCm39) |
|
probably null |
Het |
Olfm1 |
A |
G |
2: 28,112,637 (GRCm39) |
T223A |
probably damaging |
Het |
Oprk1 |
T |
A |
1: 5,672,512 (GRCm39) |
D216E |
probably damaging |
Het |
Or4b1d |
T |
A |
2: 89,969,159 (GRCm39) |
E108V |
probably damaging |
Het |
Or8g23 |
A |
G |
9: 38,971,881 (GRCm39) |
L27P |
probably damaging |
Het |
Pim1 |
T |
A |
17: 29,712,777 (GRCm39) |
I230N |
probably damaging |
Het |
Ppm1f |
A |
C |
16: 16,732,035 (GRCm39) |
T162P |
possibly damaging |
Het |
Rbbp8 |
T |
C |
18: 11,838,876 (GRCm39) |
Y186H |
probably damaging |
Het |
Sema4a |
C |
T |
3: 88,357,829 (GRCm39) |
R225H |
probably damaging |
Het |
Slc15a2 |
A |
C |
16: 36,582,743 (GRCm39) |
F215C |
probably damaging |
Het |
Slc25a1 |
A |
G |
16: 17,745,490 (GRCm39) |
C41R |
possibly damaging |
Het |
Stil |
C |
A |
4: 114,880,834 (GRCm39) |
H459Q |
probably benign |
Het |
Tbc1d32 |
A |
G |
10: 55,964,499 (GRCm39) |
I900T |
possibly damaging |
Het |
Tmem33 |
T |
C |
5: 67,443,446 (GRCm39) |
F208L |
probably damaging |
Het |
Utp25 |
T |
C |
1: 192,812,367 (GRCm39) |
H31R |
probably damaging |
Het |
Vmn2r72 |
A |
G |
7: 85,387,575 (GRCm39) |
V663A |
probably damaging |
Het |
|
Other mutations in Adam22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01325:Adam22
|
APN |
5 |
8,177,333 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01368:Adam22
|
APN |
5 |
8,177,411 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01406:Adam22
|
APN |
5 |
8,180,212 (GRCm39) |
nonsense |
probably null |
|
IGL01463:Adam22
|
APN |
5 |
8,142,790 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01691:Adam22
|
APN |
5 |
8,142,742 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01798:Adam22
|
APN |
5 |
8,282,604 (GRCm39) |
splice site |
probably null |
|
IGL01975:Adam22
|
APN |
5 |
8,217,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02170:Adam22
|
APN |
5 |
8,184,845 (GRCm39) |
missense |
probably benign |
|
IGL02189:Adam22
|
APN |
5 |
8,380,029 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02859:Adam22
|
APN |
5 |
8,217,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03189:Adam22
|
APN |
5 |
8,161,897 (GRCm39) |
nonsense |
probably null |
|
IGL03326:Adam22
|
APN |
5 |
8,177,421 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03329:Adam22
|
APN |
5 |
8,199,210 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL03354:Adam22
|
APN |
5 |
8,208,890 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03394:Adam22
|
APN |
5 |
8,217,379 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03047:Adam22
|
UTSW |
5 |
8,132,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R0445:Adam22
|
UTSW |
5 |
8,230,591 (GRCm39) |
intron |
probably benign |
|
R0486:Adam22
|
UTSW |
5 |
8,380,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R0669:Adam22
|
UTSW |
5 |
8,193,036 (GRCm39) |
splice site |
probably benign |
|
R0866:Adam22
|
UTSW |
5 |
8,132,156 (GRCm39) |
missense |
probably damaging |
0.98 |
R1510:Adam22
|
UTSW |
5 |
8,202,408 (GRCm39) |
missense |
probably benign |
0.06 |
R1562:Adam22
|
UTSW |
5 |
8,145,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R1640:Adam22
|
UTSW |
5 |
8,195,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Adam22
|
UTSW |
5 |
8,184,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R1939:Adam22
|
UTSW |
5 |
8,380,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R1998:Adam22
|
UTSW |
5 |
8,379,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R2012:Adam22
|
UTSW |
5 |
8,167,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R2214:Adam22
|
UTSW |
5 |
8,186,805 (GRCm39) |
critical splice donor site |
probably null |
|
R2270:Adam22
|
UTSW |
5 |
8,171,108 (GRCm39) |
missense |
probably damaging |
0.98 |
R2271:Adam22
|
UTSW |
5 |
8,171,108 (GRCm39) |
missense |
probably damaging |
0.98 |
R2286:Adam22
|
UTSW |
5 |
8,195,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R2304:Adam22
|
UTSW |
5 |
8,142,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R2406:Adam22
|
UTSW |
5 |
8,230,064 (GRCm39) |
intron |
probably benign |
|
R2656:Adam22
|
UTSW |
5 |
8,167,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R3106:Adam22
|
UTSW |
5 |
8,167,583 (GRCm39) |
splice site |
probably null |
|
R3870:Adam22
|
UTSW |
5 |
8,182,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Adam22
|
UTSW |
5 |
8,180,514 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4092:Adam22
|
UTSW |
5 |
8,145,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R4180:Adam22
|
UTSW |
5 |
8,199,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R4247:Adam22
|
UTSW |
5 |
8,195,626 (GRCm39) |
missense |
probably benign |
|
R4486:Adam22
|
UTSW |
5 |
8,230,227 (GRCm39) |
intron |
probably benign |
|
R4629:Adam22
|
UTSW |
5 |
8,282,663 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4744:Adam22
|
UTSW |
5 |
8,128,699 (GRCm39) |
missense |
probably damaging |
0.98 |
R4839:Adam22
|
UTSW |
5 |
8,186,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R5007:Adam22
|
UTSW |
5 |
8,217,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R5030:Adam22
|
UTSW |
5 |
8,229,645 (GRCm39) |
intron |
probably benign |
|
R5061:Adam22
|
UTSW |
5 |
8,230,238 (GRCm39) |
intron |
probably benign |
|
R5312:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5353:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5356:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5424:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5719:Adam22
|
UTSW |
5 |
8,417,217 (GRCm39) |
missense |
probably benign |
|
R5763:Adam22
|
UTSW |
5 |
8,184,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R5768:Adam22
|
UTSW |
5 |
8,177,426 (GRCm39) |
missense |
probably benign |
0.35 |
R5776:Adam22
|
UTSW |
5 |
8,177,361 (GRCm39) |
missense |
probably benign |
0.26 |
R5839:Adam22
|
UTSW |
5 |
8,186,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R6314:Adam22
|
UTSW |
5 |
8,177,365 (GRCm39) |
nonsense |
probably null |
|
R6520:Adam22
|
UTSW |
5 |
8,166,635 (GRCm39) |
missense |
probably damaging |
0.98 |
R6798:Adam22
|
UTSW |
5 |
8,210,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R6924:Adam22
|
UTSW |
5 |
8,417,322 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6938:Adam22
|
UTSW |
5 |
8,196,499 (GRCm39) |
missense |
probably benign |
0.01 |
R7317:Adam22
|
UTSW |
5 |
8,140,202 (GRCm39) |
missense |
probably benign |
|
R7402:Adam22
|
UTSW |
5 |
8,145,049 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7431:Adam22
|
UTSW |
5 |
8,142,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R7527:Adam22
|
UTSW |
5 |
8,132,239 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7571:Adam22
|
UTSW |
5 |
8,132,160 (GRCm39) |
nonsense |
probably null |
|
R7627:Adam22
|
UTSW |
5 |
8,417,933 (GRCm39) |
missense |
probably benign |
|
R7678:Adam22
|
UTSW |
5 |
8,137,750 (GRCm39) |
splice site |
probably null |
|
R7714:Adam22
|
UTSW |
5 |
8,167,587 (GRCm39) |
critical splice donor site |
probably null |
|
R7806:Adam22
|
UTSW |
5 |
8,142,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R7834:Adam22
|
UTSW |
5 |
8,180,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R7837:Adam22
|
UTSW |
5 |
8,199,284 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7979:Adam22
|
UTSW |
5 |
8,186,804 (GRCm39) |
critical splice donor site |
probably null |
|
R8123:Adam22
|
UTSW |
5 |
8,142,833 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8511:Adam22
|
UTSW |
5 |
8,184,558 (GRCm39) |
missense |
probably damaging |
0.98 |
R8722:Adam22
|
UTSW |
5 |
8,166,554 (GRCm39) |
missense |
probably benign |
|
R8730:Adam22
|
UTSW |
5 |
8,208,830 (GRCm39) |
missense |
probably benign |
0.00 |
R8956:Adam22
|
UTSW |
5 |
8,142,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R9015:Adam22
|
UTSW |
5 |
8,136,688 (GRCm39) |
intron |
probably benign |
|
R9068:Adam22
|
UTSW |
5 |
8,177,343 (GRCm39) |
missense |
probably benign |
0.01 |
R9198:Adam22
|
UTSW |
5 |
8,167,583 (GRCm39) |
splice site |
probably null |
|
R9441:Adam22
|
UTSW |
5 |
8,161,974 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9480:Adam22
|
UTSW |
5 |
8,193,077 (GRCm39) |
missense |
probably benign |
0.01 |
X0067:Adam22
|
UTSW |
5 |
8,177,329 (GRCm39) |
missense |
probably benign |
0.05 |
|