Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
G |
T |
11: 58,314,752 (GRCm39) |
C150F |
probably damaging |
Het |
Aagab |
T |
A |
9: 63,523,957 (GRCm39) |
|
probably null |
Het |
Abca15 |
A |
C |
7: 120,006,697 (GRCm39) |
T1654P |
probably damaging |
Het |
Abca17 |
T |
A |
17: 24,553,240 (GRCm39) |
Y157F |
probably benign |
Het |
Aftph |
A |
T |
11: 20,648,318 (GRCm39) |
L813* |
probably null |
Het |
Agap1 |
T |
C |
1: 89,765,477 (GRCm39) |
I615T |
probably damaging |
Het |
Ak3 |
T |
G |
19: 29,000,247 (GRCm39) |
Q221H |
probably benign |
Het |
Aldoa |
A |
G |
7: 126,396,814 (GRCm39) |
|
probably null |
Het |
Anxa8 |
T |
C |
14: 33,813,873 (GRCm39) |
|
probably null |
Het |
Atpsckmt |
T |
C |
15: 31,609,718 (GRCm39) |
F146L |
probably benign |
Het |
Baz2a |
A |
G |
10: 127,959,481 (GRCm39) |
D1329G |
probably damaging |
Het |
Calhm6 |
G |
T |
10: 34,003,691 (GRCm39) |
A72E |
probably damaging |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cep70 |
A |
G |
9: 99,178,438 (GRCm39) |
Y512C |
probably damaging |
Het |
Cfhr2 |
T |
G |
1: 139,758,893 (GRCm39) |
R52S |
probably benign |
Het |
Clcn6 |
A |
G |
4: 148,108,594 (GRCm39) |
F145S |
possibly damaging |
Het |
Cnksr1 |
A |
G |
4: 133,956,939 (GRCm39) |
Y488H |
probably damaging |
Het |
Diablo |
A |
G |
5: 123,661,424 (GRCm39) |
V24A |
probably benign |
Het |
Dnah7b |
T |
A |
1: 46,307,830 (GRCm39) |
M3048K |
probably damaging |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Efnb1 |
A |
G |
X: 98,191,123 (GRCm39) |
Y343C |
probably damaging |
Het |
Esco1 |
A |
G |
18: 10,574,873 (GRCm39) |
|
probably null |
Het |
Fancd2 |
A |
G |
6: 113,526,282 (GRCm39) |
N335S |
probably benign |
Het |
Flnc |
A |
G |
6: 29,448,674 (GRCm39) |
Y1304C |
probably damaging |
Het |
Fubp3 |
A |
G |
2: 31,490,569 (GRCm39) |
|
probably benign |
Het |
Gemin4 |
G |
C |
11: 76,101,876 (GRCm39) |
P962A |
probably damaging |
Het |
Gjc3 |
A |
C |
5: 137,955,808 (GRCm39) |
L159R |
probably damaging |
Het |
Gli1 |
A |
G |
10: 127,172,596 (GRCm39) |
L182P |
probably damaging |
Het |
Gm21957 |
G |
T |
7: 124,818,625 (GRCm39) |
|
noncoding transcript |
Het |
Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,255,059 (GRCm39) |
|
probably benign |
Het |
Gm5885 |
A |
G |
6: 133,506,238 (GRCm39) |
|
noncoding transcript |
Het |
Gon4l |
A |
T |
3: 88,794,902 (GRCm39) |
T402S |
possibly damaging |
Het |
Gprasp1 |
G |
A |
X: 134,702,791 (GRCm39) |
E995K |
possibly damaging |
Het |
Gvin-ps5 |
T |
A |
7: 105,929,163 (GRCm39) |
T245S |
probably damaging |
Het |
Helb |
A |
T |
10: 119,941,926 (GRCm39) |
M254K |
possibly damaging |
Het |
Ift20 |
G |
A |
11: 78,430,860 (GRCm39) |
E68K |
probably damaging |
Het |
Igfn1 |
AGGG |
AGG |
1: 135,902,590 (GRCm39) |
|
probably benign |
Het |
Impdh2 |
A |
G |
9: 108,442,546 (GRCm39) |
E305G |
possibly damaging |
Het |
Ints7 |
T |
A |
1: 191,336,972 (GRCm39) |
C351S |
possibly damaging |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Kcnq3 |
T |
C |
15: 65,867,700 (GRCm39) |
M648V |
probably benign |
Het |
Kctd16 |
A |
G |
18: 40,392,231 (GRCm39) |
E273G |
possibly damaging |
Het |
Kif18a |
T |
A |
2: 109,163,848 (GRCm39) |
N732K |
probably benign |
Het |
Kif21b |
C |
T |
1: 136,080,002 (GRCm39) |
R513W |
probably damaging |
Het |
Klhl36 |
T |
C |
8: 120,603,511 (GRCm39) |
C589R |
possibly damaging |
Het |
Lck |
A |
G |
4: 129,442,713 (GRCm39) |
Y481H |
probably damaging |
Het |
Lmtk2 |
A |
G |
5: 144,084,433 (GRCm39) |
Y156C |
probably damaging |
Het |
Mical3 |
A |
T |
6: 121,008,095 (GRCm39) |
|
probably null |
Het |
Mki67 |
A |
G |
7: 135,297,321 (GRCm39) |
I2571T |
possibly damaging |
Het |
Mx2 |
G |
A |
16: 97,339,903 (GRCm39) |
E20K |
probably benign |
Het |
Myo10 |
A |
G |
15: 25,714,194 (GRCm39) |
E87G |
probably benign |
Het |
Myo18b |
T |
C |
5: 113,021,892 (GRCm39) |
K500R |
probably benign |
Het |
N4bp2l2 |
A |
T |
5: 150,571,001 (GRCm39) |
I458N |
probably damaging |
Het |
Nat10 |
T |
C |
2: 103,561,648 (GRCm39) |
|
probably null |
Het |
Nfasc |
G |
A |
1: 132,524,383 (GRCm39) |
P932L |
probably damaging |
Het |
Nipa1 |
C |
A |
7: 55,647,259 (GRCm39) |
|
probably null |
Het |
Nkpd1 |
A |
G |
7: 19,258,162 (GRCm39) |
Q647R |
probably damaging |
Het |
Nlrc4 |
T |
A |
17: 74,754,946 (GRCm39) |
|
probably benign |
Het |
Nmbr |
C |
A |
10: 14,646,186 (GRCm39) |
Y353* |
probably null |
Het |
Nos1ap |
T |
A |
1: 170,156,735 (GRCm39) |
D241V |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or4f4b |
A |
T |
2: 111,313,975 (GRCm39) |
T95S |
probably benign |
Het |
Or5d43 |
A |
G |
2: 88,105,354 (GRCm39) |
V13A |
probably benign |
Het |
Or5m13 |
A |
G |
2: 85,749,171 (GRCm39) |
I301V |
probably null |
Het |
Or6c201 |
A |
G |
10: 128,968,875 (GRCm39) |
I254T |
probably benign |
Het |
Pank1 |
G |
A |
19: 34,856,380 (GRCm39) |
R33C |
possibly damaging |
Het |
Pcmtd1 |
C |
T |
1: 7,239,789 (GRCm39) |
R77C |
probably damaging |
Het |
Phkg2 |
G |
A |
7: 127,181,386 (GRCm39) |
|
probably null |
Het |
Plcb4 |
G |
A |
2: 135,818,019 (GRCm39) |
V762M |
probably damaging |
Het |
Pramel7 |
T |
A |
2: 87,320,321 (GRCm39) |
H324L |
probably damaging |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Ptgr3 |
T |
C |
18: 84,112,668 (GRCm39) |
Y115H |
probably benign |
Het |
Rai1 |
C |
A |
11: 60,080,293 (GRCm39) |
S1452R |
possibly damaging |
Het |
Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
Het |
Rev3l |
T |
C |
10: 39,724,045 (GRCm39) |
V785A |
probably benign |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Rufy2 |
G |
T |
10: 62,826,773 (GRCm39) |
R104L |
probably damaging |
Het |
Senp6 |
T |
A |
9: 80,031,102 (GRCm39) |
N8K |
probably damaging |
Het |
Septin4 |
A |
T |
11: 87,474,262 (GRCm39) |
Q60L |
probably benign |
Het |
Sipa1l2 |
G |
A |
8: 126,218,230 (GRCm39) |
P369L |
probably benign |
Het |
Slc43a1 |
T |
C |
2: 84,671,305 (GRCm39) |
L37P |
probably damaging |
Het |
Slf1 |
T |
A |
13: 77,197,338 (GRCm39) |
|
probably null |
Het |
Ssr2 |
T |
A |
3: 88,483,949 (GRCm39) |
|
probably benign |
Het |
Tas2r115 |
T |
C |
6: 132,714,321 (GRCm39) |
K210R |
probably benign |
Het |
Tbx18 |
A |
G |
9: 87,597,706 (GRCm39) |
V276A |
probably damaging |
Het |
Tesl1 |
T |
A |
X: 23,773,549 (GRCm39) |
V350E |
probably benign |
Het |
Tie1 |
G |
A |
4: 118,330,008 (GRCm39) |
R1072* |
probably null |
Het |
Tm2d2 |
C |
A |
8: 25,512,674 (GRCm39) |
T174K |
probably damaging |
Het |
Tmem98 |
A |
G |
11: 80,705,158 (GRCm39) |
D82G |
possibly damaging |
Het |
Tmub2 |
A |
G |
11: 102,178,379 (GRCm39) |
E94G |
possibly damaging |
Het |
Tnnt2 |
TG |
TGG |
1: 135,774,499 (GRCm39) |
|
probably benign |
Het |
Tonsl |
A |
T |
15: 76,516,861 (GRCm39) |
I923N |
probably damaging |
Het |
Ttc21a |
G |
A |
9: 119,793,361 (GRCm39) |
V977M |
probably damaging |
Het |
Ube2ql1 |
T |
C |
13: 69,886,783 (GRCm39) |
D226G |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,204,518 (GRCm39) |
T4810M |
probably damaging |
Het |
Wdr87-ps |
T |
C |
7: 29,230,935 (GRCm39) |
|
noncoding transcript |
Het |
Zfp408 |
A |
G |
2: 91,478,194 (GRCm39) |
|
probably benign |
Het |
Zfp473 |
T |
C |
7: 44,382,501 (GRCm39) |
T610A |
possibly damaging |
Het |
Zfp804b |
A |
G |
5: 6,822,583 (GRCm39) |
V160A |
probably benign |
Het |
Zfp960 |
A |
G |
17: 17,308,146 (GRCm39) |
T287A |
probably benign |
Het |
|
Other mutations in Syt2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02385:Syt2
|
APN |
1 |
134,673,553 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02476:Syt2
|
APN |
1 |
134,675,369 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02487:Syt2
|
APN |
1 |
134,668,603 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02524:Syt2
|
APN |
1 |
134,669,703 (GRCm39) |
missense |
probably benign |
|
IGL02611:Syt2
|
APN |
1 |
134,669,620 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03173:Syt2
|
APN |
1 |
134,671,317 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03303:Syt2
|
APN |
1 |
134,669,649 (GRCm39) |
missense |
probably benign |
0.44 |
kringle
|
UTSW |
1 |
134,675,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R1661:Syt2
|
UTSW |
1 |
134,675,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R1665:Syt2
|
UTSW |
1 |
134,675,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R2049:Syt2
|
UTSW |
1 |
134,674,479 (GRCm39) |
splice site |
probably benign |
|
R2130:Syt2
|
UTSW |
1 |
134,674,479 (GRCm39) |
splice site |
probably benign |
|
R3154:Syt2
|
UTSW |
1 |
134,669,599 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5392:Syt2
|
UTSW |
1 |
134,671,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R5431:Syt2
|
UTSW |
1 |
134,668,695 (GRCm39) |
missense |
probably benign |
0.03 |
R6065:Syt2
|
UTSW |
1 |
134,675,295 (GRCm39) |
missense |
probably benign |
0.00 |
R6381:Syt2
|
UTSW |
1 |
134,674,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R6816:Syt2
|
UTSW |
1 |
134,673,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R6923:Syt2
|
UTSW |
1 |
134,674,501 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7002:Syt2
|
UTSW |
1 |
134,671,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R7973:Syt2
|
UTSW |
1 |
134,668,570 (GRCm39) |
splice site |
probably null |
|
R7994:Syt2
|
UTSW |
1 |
134,675,330 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8410:Syt2
|
UTSW |
1 |
134,674,602 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8902:Syt2
|
UTSW |
1 |
134,675,391 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9592:Syt2
|
UTSW |
1 |
134,671,773 (GRCm39) |
missense |
possibly damaging |
0.60 |
|