Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd2 |
A |
G |
15: 91,033,184 (GRCm39) |
|
probably benign |
Het |
Abcg5 |
C |
T |
17: 84,977,827 (GRCm39) |
R143Q |
probably damaging |
Het |
Arap3 |
G |
A |
18: 38,129,711 (GRCm39) |
T150I |
probably benign |
Het |
Arhgap32 |
T |
C |
9: 32,158,490 (GRCm39) |
V175A |
probably damaging |
Het |
Bpifb3 |
A |
G |
2: 153,766,721 (GRCm39) |
E208G |
probably benign |
Het |
C2 |
T |
A |
17: 35,083,325 (GRCm39) |
D518V |
possibly damaging |
Het |
C6 |
T |
A |
15: 4,820,646 (GRCm39) |
C552* |
probably null |
Het |
Ccdc38 |
A |
T |
10: 93,415,685 (GRCm39) |
D447V |
probably damaging |
Het |
Cept1 |
C |
T |
3: 106,411,035 (GRCm39) |
R386H |
probably benign |
Het |
Comt |
A |
G |
16: 18,230,454 (GRCm39) |
V85A |
probably damaging |
Het |
Ddx24 |
G |
T |
12: 103,383,571 (GRCm39) |
L627I |
probably damaging |
Het |
Efemp1 |
T |
C |
11: 28,866,971 (GRCm39) |
|
probably null |
Het |
Etf1 |
T |
C |
18: 35,046,714 (GRCm39) |
T99A |
possibly damaging |
Het |
Fhad1 |
T |
C |
4: 141,660,105 (GRCm39) |
E68G |
probably null |
Het |
Fzd3 |
C |
A |
14: 65,473,389 (GRCm39) |
|
probably benign |
Het |
Gins3 |
T |
C |
8: 96,364,606 (GRCm39) |
F119L |
probably benign |
Het |
Golga5 |
G |
T |
12: 102,438,338 (GRCm39) |
V18L |
probably benign |
Het |
Il16 |
C |
A |
7: 83,310,484 (GRCm39) |
R474M |
probably damaging |
Het |
Itpr1 |
C |
A |
6: 108,316,515 (GRCm39) |
Q71K |
possibly damaging |
Het |
Kif21b |
T |
G |
1: 136,100,605 (GRCm39) |
L1562R |
probably damaging |
Het |
Lamc2 |
T |
C |
1: 153,042,008 (GRCm39) |
E42G |
possibly damaging |
Het |
Mmp3 |
T |
G |
9: 7,446,001 (GRCm39) |
L35R |
probably benign |
Het |
Naip6 |
C |
A |
13: 100,452,780 (GRCm39) |
G94W |
probably damaging |
Het |
Nccrp1 |
G |
A |
7: 28,243,905 (GRCm39) |
A226V |
probably damaging |
Het |
Nckap5l |
A |
G |
15: 99,323,564 (GRCm39) |
Y980H |
probably damaging |
Het |
Ncoa3 |
T |
C |
2: 165,911,277 (GRCm39) |
S1345P |
probably damaging |
Het |
Nop2 |
T |
C |
6: 125,117,813 (GRCm39) |
S455P |
probably damaging |
Het |
Nup93 |
T |
C |
8: 95,036,263 (GRCm39) |
F689S |
probably damaging |
Het |
Or5b112 |
T |
C |
19: 13,319,583 (GRCm39) |
F154L |
probably benign |
Het |
Plekhm1 |
T |
A |
11: 103,285,876 (GRCm39) |
E186D |
probably damaging |
Het |
Plxdc1 |
T |
C |
11: 97,869,390 (GRCm39) |
Q66R |
probably damaging |
Het |
Prkdc |
T |
G |
16: 15,544,406 (GRCm39) |
Y1799D |
probably damaging |
Het |
Rasa2 |
A |
G |
9: 96,462,563 (GRCm39) |
F220L |
probably damaging |
Het |
Rftn1 |
T |
C |
17: 50,344,027 (GRCm39) |
D87G |
probably damaging |
Het |
Rgs6 |
C |
T |
12: 83,117,376 (GRCm39) |
T266M |
probably benign |
Het |
Sec16a |
A |
G |
2: 26,326,054 (GRCm39) |
Y1208H |
probably damaging |
Het |
Slc12a1 |
G |
T |
2: 125,026,648 (GRCm39) |
V428L |
probably damaging |
Het |
Svep1 |
T |
A |
4: 58,135,441 (GRCm39) |
T556S |
probably benign |
Het |
Tanc2 |
T |
A |
11: 105,667,777 (GRCm39) |
N119K |
probably benign |
Het |
Tpgs1 |
T |
A |
10: 79,505,238 (GRCm39) |
|
probably benign |
Het |
Tpm3-rs7 |
A |
G |
14: 113,552,370 (GRCm39) |
E88G |
probably damaging |
Het |
Tsr1 |
T |
C |
11: 74,791,204 (GRCm39) |
V261A |
probably benign |
Het |
Usp18 |
C |
T |
6: 121,238,050 (GRCm39) |
T143I |
probably benign |
Het |
Vmn2r24 |
T |
C |
6: 123,792,812 (GRCm39) |
I713T |
probably benign |
Het |
Zfp518a |
G |
A |
19: 40,903,061 (GRCm39) |
G997R |
probably 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 |
|
IGL02073: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 |
|
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 |
|
|