Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930566N20Rik |
C |
A |
3: 156,914,039 (GRCm39) |
|
probably benign |
Het |
6330409D20Rik |
T |
G |
2: 32,630,698 (GRCm39) |
|
probably benign |
Het |
Als2cl |
A |
G |
9: 110,723,407 (GRCm39) |
K659E |
probably benign |
Het |
Bbx |
G |
A |
16: 50,022,854 (GRCm39) |
T702I |
probably damaging |
Het |
Bcas3 |
A |
G |
11: 85,448,263 (GRCm39) |
D405G |
probably damaging |
Het |
Brpf3 |
A |
G |
17: 29,026,370 (GRCm39) |
Y481C |
probably benign |
Het |
Csnk1g1 |
T |
A |
9: 65,909,533 (GRCm39) |
Y217N |
probably damaging |
Het |
Cyp4f37 |
G |
T |
17: 32,846,825 (GRCm39) |
V171L |
possibly damaging |
Het |
Dock8 |
G |
A |
19: 25,178,350 (GRCm39) |
|
probably null |
Het |
Extl3 |
C |
A |
14: 65,313,788 (GRCm39) |
G465W |
probably damaging |
Het |
Fbxo10 |
A |
G |
4: 45,046,349 (GRCm39) |
I587T |
possibly damaging |
Het |
Fstl5 |
A |
C |
3: 76,566,959 (GRCm39) |
|
probably benign |
Het |
Gabbr2 |
T |
C |
4: 46,667,547 (GRCm39) |
N866S |
probably benign |
Het |
Gm4871 |
T |
A |
5: 144,969,388 (GRCm39) |
K44* |
probably null |
Het |
Hnrnpul1 |
T |
C |
7: 25,421,766 (GRCm39) |
|
probably benign |
Het |
Jup |
A |
G |
11: 100,274,215 (GRCm39) |
|
probably benign |
Het |
Mccc2 |
A |
T |
13: 100,136,783 (GRCm39) |
H57Q |
probably benign |
Het |
Myo1a |
A |
T |
10: 127,546,094 (GRCm39) |
D239V |
probably damaging |
Het |
Ncapd3 |
T |
A |
9: 26,974,612 (GRCm39) |
S695T |
probably benign |
Het |
Ncor1 |
A |
T |
11: 62,249,743 (GRCm39) |
S1052T |
probably damaging |
Het |
Or5k8 |
A |
G |
16: 58,644,169 (GRCm39) |
I301T |
probably benign |
Het |
Or7g12 |
T |
A |
9: 18,899,621 (GRCm39) |
N112K |
possibly damaging |
Het |
Or8c10 |
C |
T |
9: 38,279,603 (GRCm39) |
H244Y |
probably damaging |
Het |
Pcnx3 |
A |
T |
19: 5,729,414 (GRCm39) |
I526K |
probably damaging |
Het |
Pcnx4 |
A |
G |
12: 72,621,102 (GRCm39) |
D974G |
possibly damaging |
Het |
Peg3 |
T |
C |
7: 6,714,001 (GRCm39) |
E407G |
probably damaging |
Het |
Polk |
A |
G |
13: 96,641,059 (GRCm39) |
V166A |
probably damaging |
Het |
Prkar2a |
A |
G |
9: 108,610,322 (GRCm39) |
I184V |
probably damaging |
Het |
Ptpra |
T |
C |
2: 30,333,362 (GRCm39) |
S64P |
probably damaging |
Het |
Rbsn |
A |
G |
6: 92,166,340 (GRCm39) |
L768P |
probably damaging |
Het |
Ripk3 |
C |
T |
14: 56,023,482 (GRCm39) |
|
probably null |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Sar1b |
T |
C |
11: 51,680,020 (GRCm39) |
|
probably benign |
Het |
Slx |
A |
T |
X: 26,489,755 (GRCm39) |
W89R |
probably benign |
Het |
Svep1 |
T |
C |
4: 58,070,104 (GRCm39) |
I2561V |
probably benign |
Het |
Tasor2 |
T |
C |
13: 3,624,721 (GRCm39) |
D1743G |
probably benign |
Het |
Tm7sf3 |
A |
G |
6: 146,525,208 (GRCm39) |
L79P |
possibly damaging |
Het |
Trub1 |
A |
T |
19: 57,441,379 (GRCm39) |
M1L |
probably benign |
Het |
Unc80 |
A |
G |
1: 66,651,386 (GRCm39) |
D1577G |
possibly damaging |
Het |
Vat1 |
A |
T |
11: 101,351,405 (GRCm39) |
M312K |
possibly damaging |
Het |
Vmn1r17 |
T |
C |
6: 57,337,787 (GRCm39) |
I193V |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,875,732 (GRCm39) |
I2706V |
possibly damaging |
Het |
Wls |
T |
C |
3: 159,612,890 (GRCm39) |
|
probably null |
Het |
Zfp955b |
A |
G |
17: 33,519,564 (GRCm39) |
T11A |
possibly damaging |
Het |
|
Other mutations in Srrm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02063:Srrm1
|
APN |
4 |
135,074,518 (GRCm39) |
splice site |
probably null |
|
IGL02070:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02193:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02232:Srrm1
|
APN |
4 |
135,080,427 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
IGL02377:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02379:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02380:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02382:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02386:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02387:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02393:Srrm1
|
APN |
4 |
135,048,725 (GRCm39) |
unclassified |
probably benign |
|
IGL02436:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02438:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02439:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02440:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02500:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02561:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02562:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02566:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02567:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02568:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02569:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02570:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02572:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02583:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02584:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02585:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02586:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02587:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02588:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02589:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02596:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02597:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02601:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02602:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02609:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02614:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02631:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02632:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02657:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02658:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02659:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02660:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02677:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02683:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02686:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02690:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02713:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02723:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02724:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02725:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02730:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02731:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02732:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02733:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02734:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02743:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02744:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
IGL02752:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
Serious
|
UTSW |
4 |
135,068,237 (GRCm39) |
nonsense |
probably null |
|
R0131:Srrm1
|
UTSW |
4 |
135,067,884 (GRCm39) |
nonsense |
probably null |
|
R0131:Srrm1
|
UTSW |
4 |
135,067,884 (GRCm39) |
nonsense |
probably null |
|
R0132:Srrm1
|
UTSW |
4 |
135,067,884 (GRCm39) |
nonsense |
probably null |
|
R0510:Srrm1
|
UTSW |
4 |
135,065,854 (GRCm39) |
intron |
probably benign |
|
R0691:Srrm1
|
UTSW |
4 |
135,052,302 (GRCm39) |
nonsense |
probably null |
|
R1337:Srrm1
|
UTSW |
4 |
135,074,044 (GRCm39) |
critical splice donor site |
probably null |
|
R1397:Srrm1
|
UTSW |
4 |
135,048,742 (GRCm39) |
unclassified |
probably benign |
|
R2883:Srrm1
|
UTSW |
4 |
135,048,722 (GRCm39) |
unclassified |
probably benign |
|
R4043:Srrm1
|
UTSW |
4 |
135,068,242 (GRCm39) |
unclassified |
probably benign |
|
R4772:Srrm1
|
UTSW |
4 |
135,069,690 (GRCm39) |
unclassified |
probably benign |
|
R4837:Srrm1
|
UTSW |
4 |
135,072,823 (GRCm39) |
intron |
probably benign |
|
R4975:Srrm1
|
UTSW |
4 |
135,074,031 (GRCm39) |
splice site |
probably benign |
|
R5401:Srrm1
|
UTSW |
4 |
135,051,380 (GRCm39) |
splice site |
probably benign |
|
R6144:Srrm1
|
UTSW |
4 |
135,065,184 (GRCm39) |
unclassified |
probably benign |
|
R6542:Srrm1
|
UTSW |
4 |
135,068,237 (GRCm39) |
nonsense |
probably null |
|
R7147:Srrm1
|
UTSW |
4 |
135,074,137 (GRCm39) |
missense |
probably damaging |
0.98 |
R8054:Srrm1
|
UTSW |
4 |
135,052,326 (GRCm39) |
missense |
unknown |
|
R8371:Srrm1
|
UTSW |
4 |
135,052,532 (GRCm39) |
missense |
unknown |
|
R8523:Srrm1
|
UTSW |
4 |
135,051,313 (GRCm39) |
missense |
unknown |
|
R8767:Srrm1
|
UTSW |
4 |
135,059,532 (GRCm39) |
missense |
unknown |
|
Z1177:Srrm1
|
UTSW |
4 |
135,059,052 (GRCm39) |
missense |
unknown |
|
Z1177:Srrm1
|
UTSW |
4 |
135,051,309 (GRCm39) |
missense |
unknown |
|
|