Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310009B15Rik |
A |
C |
1: 138,779,903 (GRCm39) |
Y116* |
probably null |
Het |
Abtb3 |
C |
T |
10: 85,223,242 (GRCm39) |
T17M |
unknown |
Het |
Acer3 |
T |
C |
7: 97,906,908 (GRCm39) |
T91A |
possibly damaging |
Het |
Acsbg3 |
A |
T |
17: 57,183,324 (GRCm39) |
I22F |
possibly damaging |
Het |
Adam12 |
T |
C |
7: 133,774,550 (GRCm39) |
K20E |
possibly damaging |
Het |
Adamtsl3 |
T |
C |
7: 82,223,822 (GRCm39) |
V275A |
possibly damaging |
Het |
Afg1l |
C |
T |
10: 42,330,374 (GRCm39) |
V98I |
probably benign |
Het |
Ajm1 |
G |
A |
2: 25,469,759 (GRCm39) |
R51C |
possibly damaging |
Het |
Alpk1 |
C |
T |
3: 127,467,124 (GRCm39) |
G1052R |
probably damaging |
Het |
Anln |
A |
T |
9: 22,291,484 (GRCm39) |
S115T |
possibly damaging |
Het |
Apob |
T |
A |
12: 8,063,099 (GRCm39) |
N3827K |
probably damaging |
Het |
Aqr |
G |
A |
2: 113,980,990 (GRCm39) |
L264F |
probably damaging |
Het |
Arhgap33 |
T |
C |
7: 30,231,617 (GRCm39) |
S123G |
probably damaging |
Het |
Arvcf |
C |
T |
16: 18,216,863 (GRCm39) |
R333* |
probably null |
Het |
Brca2 |
T |
A |
5: 150,480,402 (GRCm39) |
L2724Q |
probably damaging |
Het |
C2cd6 |
T |
A |
1: 59,133,893 (GRCm39) |
T43S |
probably benign |
Het |
Cacna1h |
A |
G |
17: 25,596,261 (GRCm39) |
V1920A |
possibly damaging |
Het |
Capsl |
A |
T |
15: 9,457,858 (GRCm39) |
I26F |
possibly damaging |
Het |
Card10 |
A |
T |
15: 78,665,724 (GRCm39) |
V673E |
possibly damaging |
Het |
Catspere2 |
A |
G |
1: 177,931,515 (GRCm39) |
Y478C |
unknown |
Het |
Ccar1 |
A |
G |
10: 62,588,997 (GRCm39) |
S829P |
unknown |
Het |
Ccdc121 |
A |
G |
5: 31,643,596 (GRCm39) |
I109V |
probably benign |
Het |
Cdc42bpa |
T |
C |
1: 179,972,200 (GRCm39) |
M1334T |
possibly damaging |
Het |
Ceacam2 |
C |
T |
7: 25,220,257 (GRCm39) |
C267Y |
probably benign |
Het |
Cep68 |
G |
A |
11: 20,189,239 (GRCm39) |
T591M |
probably benign |
Het |
Chil4 |
T |
C |
3: 106,111,460 (GRCm39) |
K218R |
probably benign |
Het |
Cldn14 |
G |
T |
16: 93,716,747 (GRCm39) |
T33K |
possibly damaging |
Het |
Copa |
T |
A |
1: 171,919,843 (GRCm39) |
C140S |
probably benign |
Het |
Coq6 |
T |
C |
12: 84,419,070 (GRCm39) |
L358P |
probably damaging |
Het |
Cyfip1 |
C |
T |
7: 55,521,816 (GRCm39) |
P40L |
probably damaging |
Het |
Dennd2a |
A |
C |
6: 39,474,093 (GRCm39) |
S414A |
probably benign |
Het |
Dpm1 |
T |
C |
2: 168,059,679 (GRCm39) |
N139S |
probably benign |
Het |
Dpp7 |
T |
A |
2: 25,242,770 (GRCm39) |
|
probably null |
Het |
Ednrb |
T |
C |
14: 104,057,447 (GRCm39) |
I372V |
possibly damaging |
Het |
Edrf1 |
G |
T |
7: 133,260,339 (GRCm39) |
M83I |
probably damaging |
Het |
Fam135a |
G |
A |
1: 24,063,334 (GRCm39) |
Q1087* |
probably null |
Het |
Fancg |
T |
C |
4: 43,006,866 (GRCm39) |
T275A |
probably benign |
Het |
Fbn1 |
T |
A |
2: 125,151,694 (GRCm39) |
H2520L |
probably damaging |
Het |
Fmn2 |
T |
C |
1: 174,409,527 (GRCm39) |
S587P |
unknown |
Het |
Foxr2 |
A |
G |
X: 151,913,312 (GRCm39) |
Q61R |
probably damaging |
Het |
Frrs1 |
A |
G |
3: 116,696,065 (GRCm39) |
*124W |
probably null |
Het |
Gm7535 |
T |
A |
17: 18,131,333 (GRCm39) |
|
probably benign |
Het |
H4c1 |
T |
C |
13: 23,944,935 (GRCm39) |
D69G |
probably damaging |
Het |
Herc3 |
T |
C |
6: 58,864,484 (GRCm39) |
V706A |
probably damaging |
Het |
Hivep3 |
A |
G |
4: 119,980,131 (GRCm39) |
E1723G |
probably damaging |
Het |
Igsf9b |
A |
G |
9: 27,233,946 (GRCm39) |
I382V |
probably benign |
Het |
Ints1 |
G |
T |
5: 139,756,911 (GRCm39) |
T467N |
possibly damaging |
Het |
Iqca1 |
G |
A |
1: 89,973,423 (GRCm39) |
T783M |
probably damaging |
Het |
Kng1 |
A |
G |
16: 22,886,448 (GRCm39) |
K131R |
possibly damaging |
Het |
Krt35 |
T |
C |
11: 99,983,956 (GRCm39) |
Y348C |
probably damaging |
Het |
Ldlrad3 |
A |
G |
2: 101,943,881 (GRCm39) |
C64R |
probably damaging |
Het |
Lilrb4b |
C |
T |
10: 51,360,616 (GRCm39) |
A272V |
possibly damaging |
Het |
Lrrc37 |
T |
C |
11: 103,505,698 (GRCm39) |
H2090R |
probably benign |
Het |
Ltn1 |
A |
T |
16: 87,195,697 (GRCm39) |
C1276* |
probably null |
Het |
Matn1 |
G |
A |
4: 130,679,425 (GRCm39) |
A360T |
probably benign |
Het |
Minpp1 |
G |
A |
19: 32,475,784 (GRCm39) |
V306I |
probably benign |
Het |
Mkx |
G |
A |
18: 6,992,904 (GRCm39) |
R127W |
probably damaging |
Het |
Mrpl48 |
G |
T |
7: 100,195,616 (GRCm39) |
|
probably benign |
Het |
Ms4a2 |
A |
G |
19: 11,595,793 (GRCm39) |
L166S |
possibly damaging |
Het |
Mtus2 |
T |
A |
5: 148,013,913 (GRCm39) |
Y235* |
probably null |
Het |
Myh4 |
G |
T |
11: 67,131,880 (GRCm39) |
W113C |
probably damaging |
Het |
Nav2 |
T |
A |
7: 49,198,182 (GRCm39) |
C1270* |
probably null |
Het |
Ncoa5 |
A |
G |
2: 164,844,070 (GRCm39) |
L111P |
probably damaging |
Het |
Nup107 |
T |
C |
10: 117,606,383 (GRCm39) |
Y453C |
probably damaging |
Het |
Oca2 |
C |
T |
7: 55,980,106 (GRCm39) |
Q604* |
probably null |
Het |
Or13a19 |
T |
C |
7: 139,903,014 (GRCm39) |
M134T |
probably benign |
Het |
Or13p5 |
A |
C |
4: 118,591,885 (GRCm39) |
H53P |
probably benign |
Het |
Or14j10 |
A |
T |
17: 37,934,782 (GRCm39) |
V248D |
probably damaging |
Het |
Or5p58 |
T |
A |
7: 107,694,303 (GRCm39) |
N158I |
probably benign |
Het |
Or8g33 |
T |
C |
9: 39,337,531 (GRCm39) |
T279A |
possibly damaging |
Het |
Pde3a |
G |
T |
6: 141,416,668 (GRCm39) |
G514V |
possibly damaging |
Het |
Pik3cb |
A |
T |
9: 98,983,381 (GRCm39) |
C76S |
probably damaging |
Het |
Plk1 |
T |
C |
7: 121,767,828 (GRCm39) |
V411A |
probably damaging |
Het |
Pole |
C |
T |
5: 110,472,619 (GRCm39) |
P1600L |
probably damaging |
Het |
Prr36 |
T |
C |
8: 4,260,881 (GRCm39) |
T979A |
probably benign |
Het |
Rdh7 |
T |
A |
10: 127,721,590 (GRCm39) |
T229S |
probably benign |
Het |
Rnpepl1 |
A |
T |
1: 92,842,835 (GRCm39) |
T140S |
probably damaging |
Het |
Rps6kc1 |
A |
T |
1: 190,530,891 (GRCm39) |
S947T |
probably benign |
Het |
Rtl1 |
A |
G |
12: 109,558,138 (GRCm39) |
F1234L |
probably damaging |
Het |
Sdc1 |
G |
A |
12: 8,841,708 (GRCm39) |
M279I |
probably damaging |
Het |
Siae |
T |
C |
9: 37,539,096 (GRCm39) |
L169P |
possibly damaging |
Het |
Slc22a22 |
C |
T |
15: 57,113,148 (GRCm39) |
V364I |
probably benign |
Het |
Sltm |
G |
T |
9: 70,496,260 (GRCm39) |
V932F |
probably damaging |
Het |
Smad1 |
A |
G |
8: 80,076,381 (GRCm39) |
L279P |
probably damaging |
Het |
Spag17 |
G |
T |
3: 99,958,147 (GRCm39) |
G935V |
probably damaging |
Het |
Srgap3 |
A |
G |
6: 112,723,895 (GRCm39) |
S546P |
probably damaging |
Het |
Stxbp5 |
T |
C |
10: 9,684,844 (GRCm39) |
I519V |
probably benign |
Het |
Trim43b |
C |
G |
9: 88,973,365 (GRCm39) |
G123R |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 69,843,475 (GRCm39) |
Y1572H |
probably damaging |
Het |
Umodl1 |
G |
A |
17: 31,227,639 (GRCm39) |
R1324H |
probably benign |
Het |
Vmn2r44 |
A |
T |
7: 8,380,985 (GRCm39) |
W303R |
probably benign |
Het |
Wdr93 |
T |
C |
7: 79,435,522 (GRCm39) |
Y684H |
probably damaging |
Het |
Wnk2 |
G |
A |
13: 49,224,478 (GRCm39) |
R268C |
probably damaging |
Het |
Zfp438 |
C |
T |
18: 5,213,776 (GRCm39) |
C394Y |
possibly damaging |
Het |
|
Other mutations in Syt16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00984:Syt16
|
APN |
12 |
74,269,604 (GRCm39) |
nonsense |
probably null |
|
IGL01287:Syt16
|
APN |
12 |
74,313,513 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01401:Syt16
|
APN |
12 |
74,269,437 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01780:Syt16
|
APN |
12 |
74,313,616 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02350:Syt16
|
APN |
12 |
74,313,616 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02353:Syt16
|
APN |
12 |
74,176,245 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02357:Syt16
|
APN |
12 |
74,313,616 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02360:Syt16
|
APN |
12 |
74,176,245 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02558:Syt16
|
APN |
12 |
74,281,832 (GRCm39) |
nonsense |
probably null |
|
IGL02696:Syt16
|
APN |
12 |
74,176,185 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0701:Syt16
|
UTSW |
12 |
74,281,886 (GRCm39) |
missense |
probably benign |
0.01 |
R1103:Syt16
|
UTSW |
12 |
74,313,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R2002:Syt16
|
UTSW |
12 |
74,281,977 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2079:Syt16
|
UTSW |
12 |
74,285,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R2124:Syt16
|
UTSW |
12 |
74,285,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R3806:Syt16
|
UTSW |
12 |
74,276,172 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3807:Syt16
|
UTSW |
12 |
74,276,172 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4889:Syt16
|
UTSW |
12 |
74,176,269 (GRCm39) |
missense |
probably damaging |
0.98 |
R5153:Syt16
|
UTSW |
12 |
74,269,542 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6038:Syt16
|
UTSW |
12 |
74,269,309 (GRCm39) |
splice site |
probably null |
|
R6042:Syt16
|
UTSW |
12 |
74,313,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R6328:Syt16
|
UTSW |
12 |
74,313,467 (GRCm39) |
nonsense |
probably null |
|
R6752:Syt16
|
UTSW |
12 |
74,275,987 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7248:Syt16
|
UTSW |
12 |
74,313,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R7275:Syt16
|
UTSW |
12 |
74,313,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R7276:Syt16
|
UTSW |
12 |
74,313,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R9058:Syt16
|
UTSW |
12 |
74,282,019 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Syt16
|
UTSW |
12 |
74,269,563 (GRCm39) |
missense |
possibly damaging |
0.92 |
|