Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
C |
10: 79,067,396 (GRCm38) |
E362G |
probably damaging |
Het |
Abcc5 |
T |
C |
16: 20,338,887 (GRCm38) |
M1307V |
probably benign |
Het |
Adamts9 |
A |
G |
6: 92,863,376 (GRCm38) |
V1142A |
probably benign |
Het |
Ano10 |
T |
C |
9: 122,253,030 (GRCm38) |
N525S |
probably damaging |
Het |
Bpifa2 |
T |
C |
2: 154,011,504 (GRCm38) |
|
probably null |
Het |
C7 |
C |
T |
15: 5,012,021 (GRCm38) |
V468I |
possibly damaging |
Het |
Carf |
A |
T |
1: 60,141,505 (GRCm38) |
H362L |
possibly damaging |
Het |
Ccdc171 |
A |
C |
4: 83,546,895 (GRCm38) |
I37L |
probably benign |
Het |
Ccdc182 |
T |
C |
11: 88,294,190 (GRCm38) |
L32P |
possibly damaging |
Het |
Celsr3 |
A |
T |
9: 108,834,626 (GRCm38) |
D1678V |
possibly damaging |
Het |
Col7a1 |
A |
T |
9: 108,960,997 (GRCm38) |
Y920F |
unknown |
Het |
Cpsf3 |
T |
C |
12: 21,313,790 (GRCm38) |
V627A |
probably benign |
Het |
D7Ertd443e |
A |
G |
7: 134,270,212 (GRCm38) |
M640T |
probably damaging |
Het |
Ddi2 |
T |
C |
4: 141,683,972 (GRCm38) |
D543G |
probably damaging |
Het |
Dnah9 |
T |
C |
11: 65,955,297 (GRCm38) |
N2972D |
probably damaging |
Het |
Dnajc18 |
T |
C |
18: 35,680,804 (GRCm38) |
D304G |
probably damaging |
Het |
Epg5 |
T |
C |
18: 77,983,490 (GRCm38) |
V1232A |
possibly damaging |
Het |
Ezr |
T |
C |
17: 6,742,372 (GRCm38) |
T358A |
possibly damaging |
Het |
Filip1 |
A |
G |
9: 79,815,846 (GRCm38) |
S1164P |
probably damaging |
Het |
Gm14085 |
C |
T |
2: 122,521,652 (GRCm38) |
R324C |
possibly damaging |
Het |
Gm5346 |
A |
T |
8: 43,625,917 (GRCm38) |
C423* |
probably null |
Het |
Gmip |
T |
C |
8: 69,814,477 (GRCm38) |
V341A |
probably benign |
Het |
Gnb3 |
A |
C |
6: 124,835,636 (GRCm38) |
F286V |
probably benign |
Het |
Gpatch2 |
T |
A |
1: 187,225,831 (GRCm38) |
S128T |
probably benign |
Het |
Gpr87 |
T |
C |
3: 59,179,392 (GRCm38) |
R231G |
possibly damaging |
Het |
Hip1r |
G |
A |
5: 123,998,808 (GRCm38) |
R613Q |
probably benign |
Het |
Hsd3b7 |
T |
C |
7: 127,803,034 (GRCm38) |
Y284H |
possibly damaging |
Het |
Il1rap |
A |
T |
16: 26,698,875 (GRCm38) |
D275V |
probably damaging |
Het |
Il4 |
G |
T |
11: 53,618,538 (GRCm38) |
H23Q |
possibly damaging |
Het |
Kit |
A |
G |
5: 75,648,393 (GRCm38) |
Y749C |
probably damaging |
Het |
Klb |
A |
G |
5: 65,349,235 (GRCm38) |
K275R |
probably null |
Het |
Klhl12 |
G |
T |
1: 134,489,070 (GRCm38) |
R510L |
probably damaging |
Het |
Lrrc8b |
A |
G |
5: 105,480,823 (GRCm38) |
Y345C |
probably damaging |
Het |
Med15 |
T |
C |
16: 17,680,735 (GRCm38) |
T98A |
possibly damaging |
Het |
Mmp1a |
T |
A |
9: 7,475,390 (GRCm38) |
Y387N |
probably damaging |
Het |
Myrf |
C |
A |
19: 10,214,191 (GRCm38) |
V928L |
probably benign |
Het |
Nr1d1 |
T |
C |
11: 98,771,499 (GRCm38) |
K134E |
probably damaging |
Het |
Nrxn3 |
A |
T |
12: 90,283,582 (GRCm38) |
D305V |
probably damaging |
Het |
Obscn |
A |
C |
11: 58,998,321 (GRCm38) |
S7542A |
unknown |
Het |
Olfr1197 |
T |
A |
2: 88,729,264 (GRCm38) |
I112F |
probably damaging |
Het |
Pak4 |
G |
A |
7: 28,565,190 (GRCm38) |
R96C |
probably damaging |
Het |
Papd5 |
T |
G |
8: 88,250,788 (GRCm38) |
V406G |
probably benign |
Het |
Pde6b |
A |
T |
5: 108,427,847 (GRCm38) |
D691V |
possibly damaging |
Het |
Pdss2 |
A |
G |
10: 43,345,605 (GRCm38) |
E171G |
probably benign |
Het |
Pdzd2 |
C |
T |
15: 12,387,654 (GRCm38) |
V873I |
possibly damaging |
Het |
Plb1 |
A |
T |
5: 32,293,243 (GRCm38) |
D376V |
probably damaging |
Het |
Plekhg1 |
T |
C |
10: 3,963,904 (GRCm38) |
Y1209H |
probably damaging |
Het |
Prickle2 |
A |
G |
6: 92,416,904 (GRCm38) |
C263R |
probably damaging |
Het |
Psma2 |
A |
T |
13: 14,623,605 (GRCm38) |
Y104F |
probably benign |
Het |
Ptger4 |
T |
A |
15: 5,242,800 (GRCm38) |
M113L |
possibly damaging |
Het |
Rgs10 |
T |
G |
7: 128,404,477 (GRCm38) |
D17A |
possibly damaging |
Het |
Rpap3 |
A |
G |
15: 97,694,209 (GRCm38) |
S189P |
possibly damaging |
Het |
Rsbn1 |
T |
C |
3: 103,914,872 (GRCm38) |
L102P |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,595,281 (GRCm38) |
S655G |
probably benign |
Het |
Sema4a |
C |
T |
3: 88,436,749 (GRCm38) |
D732N |
probably benign |
Het |
Sh3bp5l |
A |
G |
11: 58,346,351 (GRCm38) |
D378G |
probably benign |
Het |
Sh3gl3 |
C |
T |
7: 82,284,119 (GRCm38) |
T230I |
possibly damaging |
Het |
Slc5a1 |
A |
T |
5: 33,146,953 (GRCm38) |
Q299L |
probably damaging |
Het |
Ssc5d |
C |
A |
7: 4,936,607 (GRCm38) |
H681N |
probably benign |
Het |
Sugp2 |
T |
C |
8: 70,236,710 (GRCm38) |
S10P |
possibly damaging |
Het |
Supt5 |
A |
G |
7: 28,317,214 (GRCm38) |
|
probably null |
Het |
Syna |
A |
G |
5: 134,560,089 (GRCm38) |
V2A |
probably benign |
Het |
Tcp1 |
T |
A |
17: 12,922,202 (GRCm38) |
Y299* |
probably null |
Het |
Tenm3 |
C |
A |
8: 48,276,256 (GRCm38) |
V1572L |
probably benign |
Het |
Trp53rka |
A |
G |
2: 165,491,613 (GRCm38) |
S119P |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,452,563 (GRCm38) |
|
probably null |
Het |
Uchl4 |
T |
A |
9: 64,235,475 (GRCm38) |
D79E |
probably benign |
Het |
Vmn2r17 |
C |
A |
5: 109,428,478 (GRCm38) |
T405K |
probably damaging |
Het |
Xpnpep1 |
A |
G |
19: 53,010,133 (GRCm38) |
L228P |
probably damaging |
Het |
Xrcc4 |
T |
G |
13: 89,992,579 (GRCm38) |
E170D |
probably damaging |
Het |
Zfp945 |
T |
C |
17: 22,851,762 (GRCm38) |
T388A |
probably damaging |
Het |
Zfp947 |
G |
A |
17: 22,146,462 (GRCm38) |
A77V |
probably benign |
Het |
Zkscan5 |
G |
A |
5: 145,220,205 (GRCm38) |
G433R |
probably damaging |
Het |
|
Other mutations in Samd4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00743:Samd4b
|
APN |
7 |
28,401,877 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00979:Samd4b
|
APN |
7 |
28,414,213 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01336:Samd4b
|
APN |
7 |
28,413,963 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01432:Samd4b
|
APN |
7 |
28,414,066 (GRCm38) |
missense |
possibly damaging |
0.60 |
IGL01895:Samd4b
|
APN |
7 |
28,401,909 (GRCm38) |
critical splice acceptor site |
probably null |
|
IGL02827:Samd4b
|
APN |
7 |
28,414,121 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03077:Samd4b
|
APN |
7 |
28,406,443 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03055:Samd4b
|
UTSW |
7 |
28,405,546 (GRCm38) |
missense |
possibly damaging |
0.89 |
R0367:Samd4b
|
UTSW |
7 |
28,423,448 (GRCm38) |
missense |
probably damaging |
1.00 |
R0390:Samd4b
|
UTSW |
7 |
28,403,977 (GRCm38) |
missense |
probably benign |
0.13 |
R0440:Samd4b
|
UTSW |
7 |
28,408,160 (GRCm38) |
missense |
probably benign |
0.45 |
R0488:Samd4b
|
UTSW |
7 |
28,414,237 (GRCm38) |
missense |
probably damaging |
1.00 |
R0798:Samd4b
|
UTSW |
7 |
28,401,623 (GRCm38) |
splice site |
probably benign |
|
R1233:Samd4b
|
UTSW |
7 |
28,414,010 (GRCm38) |
missense |
probably damaging |
0.98 |
R1234:Samd4b
|
UTSW |
7 |
28,414,010 (GRCm38) |
missense |
probably damaging |
0.98 |
R1481:Samd4b
|
UTSW |
7 |
28,414,010 (GRCm38) |
missense |
probably damaging |
0.98 |
R1643:Samd4b
|
UTSW |
7 |
28,423,616 (GRCm38) |
missense |
probably damaging |
1.00 |
R1675:Samd4b
|
UTSW |
7 |
28,414,010 (GRCm38) |
missense |
probably damaging |
0.98 |
R1768:Samd4b
|
UTSW |
7 |
28,413,892 (GRCm38) |
missense |
probably benign |
0.36 |
R2831:Samd4b
|
UTSW |
7 |
28,403,913 (GRCm38) |
missense |
probably damaging |
0.99 |
R4505:Samd4b
|
UTSW |
7 |
28,407,500 (GRCm38) |
missense |
probably benign |
0.15 |
R4507:Samd4b
|
UTSW |
7 |
28,407,500 (GRCm38) |
missense |
probably benign |
0.15 |
R4731:Samd4b
|
UTSW |
7 |
28,406,663 (GRCm38) |
missense |
probably benign |
0.00 |
R5811:Samd4b
|
UTSW |
7 |
28,408,020 (GRCm38) |
missense |
probably damaging |
1.00 |
R6063:Samd4b
|
UTSW |
7 |
28,423,631 (GRCm38) |
start codon destroyed |
possibly damaging |
0.71 |
R6114:Samd4b
|
UTSW |
7 |
28,522,792 (GRCm38) |
splice site |
probably null |
|
R6356:Samd4b
|
UTSW |
7 |
28,401,593 (GRCm38) |
missense |
probably damaging |
1.00 |
R6467:Samd4b
|
UTSW |
7 |
28,401,860 (GRCm38) |
missense |
probably damaging |
1.00 |
R7055:Samd4b
|
UTSW |
7 |
28,404,033 (GRCm38) |
missense |
probably benign |
0.01 |
R7191:Samd4b
|
UTSW |
7 |
28,414,261 (GRCm38) |
missense |
probably benign |
0.18 |
R7371:Samd4b
|
UTSW |
7 |
28,423,501 (GRCm38) |
missense |
probably benign |
0.33 |
R7445:Samd4b
|
UTSW |
7 |
28,406,456 (GRCm38) |
missense |
probably benign |
0.00 |
R7543:Samd4b
|
UTSW |
7 |
28,414,286 (GRCm38) |
missense |
probably benign |
0.02 |
R7663:Samd4b
|
UTSW |
7 |
28,423,500 (GRCm38) |
nonsense |
probably null |
|
R7746:Samd4b
|
UTSW |
7 |
28,403,903 (GRCm38) |
missense |
probably damaging |
1.00 |
R7991:Samd4b
|
UTSW |
7 |
28,404,033 (GRCm38) |
missense |
probably benign |
0.01 |
R8235:Samd4b
|
UTSW |
7 |
28,406,606 (GRCm38) |
missense |
probably benign |
|
R9423:Samd4b
|
UTSW |
7 |
28,414,208 (GRCm38) |
missense |
probably benign |
0.00 |
R9615:Samd4b
|
UTSW |
7 |
28,407,289 (GRCm38) |
missense |
probably damaging |
1.00 |
|