Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2 |
C |
T |
3: 59,932,484 (GRCm39) |
T333I |
probably damaging |
Het |
Acacb |
C |
T |
5: 114,333,798 (GRCm39) |
R574C |
probably damaging |
Het |
Actr10 |
T |
C |
12: 71,001,430 (GRCm39) |
|
probably benign |
Het |
Ankdd1a |
T |
A |
9: 65,411,472 (GRCm39) |
|
probably null |
Het |
Anks4b |
C |
T |
7: 119,781,646 (GRCm39) |
Q226* |
probably null |
Het |
AW146154 |
C |
A |
7: 41,130,801 (GRCm39) |
G105V |
probably benign |
Het |
Cdh4 |
T |
A |
2: 179,502,019 (GRCm39) |
N326K |
probably damaging |
Het |
Cnbd1 |
T |
C |
4: 18,860,517 (GRCm39) |
T410A |
possibly damaging |
Het |
Cndp2 |
A |
T |
18: 84,690,201 (GRCm39) |
M247K |
probably damaging |
Het |
Crx |
G |
A |
7: 15,602,262 (GRCm39) |
R139C |
probably damaging |
Het |
Ctrc |
A |
G |
4: 141,571,037 (GRCm39) |
Y68H |
probably damaging |
Het |
Ddx4 |
T |
C |
13: 112,757,779 (GRCm39) |
D326G |
probably damaging |
Het |
Edem1 |
C |
T |
6: 108,831,290 (GRCm39) |
R584C |
possibly damaging |
Het |
Emcn |
A |
G |
3: 137,085,638 (GRCm39) |
T79A |
probably benign |
Het |
Ext1 |
C |
A |
15: 52,939,213 (GRCm39) |
W612L |
probably damaging |
Het |
Fbrsl1 |
C |
T |
5: 110,526,307 (GRCm39) |
G437R |
probably damaging |
Het |
Fbxo7 |
A |
C |
10: 85,869,149 (GRCm39) |
Q201P |
probably benign |
Het |
Fbxo9 |
T |
C |
9: 78,008,938 (GRCm39) |
M12V |
possibly damaging |
Het |
Fcgbpl1 |
A |
T |
7: 27,854,914 (GRCm39) |
I1847F |
probably damaging |
Het |
Flii |
A |
G |
11: 60,609,688 (GRCm39) |
S640P |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,812,207 (GRCm39) |
N2842I |
possibly damaging |
Het |
Fst |
G |
T |
13: 114,592,241 (GRCm39) |
Q159K |
probably damaging |
Het |
Fuom |
A |
T |
7: 139,680,025 (GRCm39) |
*109R |
probably null |
Het |
Hhipl2 |
A |
G |
1: 183,214,055 (GRCm39) |
D377G |
probably damaging |
Het |
Hspa14 |
A |
G |
2: 3,503,560 (GRCm39) |
V116A |
possibly damaging |
Het |
Ighm |
A |
G |
12: 113,382,601 (GRCm39) |
|
probably benign |
Het |
Ighv1-85 |
T |
A |
12: 115,963,847 (GRCm39) |
Y51F |
probably benign |
Het |
Ighv2-3 |
A |
T |
12: 113,574,833 (GRCm39) |
D107E |
probably benign |
Het |
Ighv2-6-8 |
T |
A |
12: 113,760,187 (GRCm39) |
M1L |
probably benign |
Het |
Ipo5 |
T |
C |
14: 121,163,683 (GRCm39) |
V247A |
probably benign |
Het |
Itga9 |
T |
C |
9: 118,672,729 (GRCm39) |
F154L |
possibly damaging |
Het |
Itprid1 |
C |
A |
6: 55,955,380 (GRCm39) |
P996Q |
probably damaging |
Het |
Knl1 |
T |
A |
2: 118,898,829 (GRCm39) |
C177S |
possibly damaging |
Het |
Lrrc17 |
G |
A |
5: 21,780,156 (GRCm39) |
G377S |
probably damaging |
Het |
Marveld3 |
A |
T |
8: 110,675,249 (GRCm39) |
I189K |
probably benign |
Het |
Msantd2 |
G |
A |
9: 37,428,555 (GRCm39) |
G185R |
probably damaging |
Het |
Mtcl1 |
G |
A |
17: 66,691,354 (GRCm39) |
|
probably benign |
Het |
Muc21 |
T |
C |
17: 35,933,395 (GRCm39) |
|
probably benign |
Het |
Mycbpap |
A |
T |
11: 94,398,572 (GRCm39) |
|
probably null |
Het |
Nbeal1 |
A |
G |
1: 60,316,353 (GRCm39) |
D1852G |
probably benign |
Het |
Ndc80 |
A |
T |
17: 71,807,276 (GRCm39) |
V560D |
probably benign |
Het |
Nscme3l |
A |
T |
19: 5,553,463 (GRCm39) |
V106D |
probably damaging |
Het |
Or1e25 |
T |
A |
11: 73,494,030 (GRCm39) |
V208E |
possibly damaging |
Het |
Or2t48 |
A |
C |
11: 58,420,710 (GRCm39) |
V34G |
probably benign |
Het |
Or56a3 |
A |
T |
7: 104,735,565 (GRCm39) |
D214V |
probably damaging |
Het |
Or6a2 |
A |
T |
7: 106,600,286 (GRCm39) |
S260R |
probably damaging |
Het |
Or9i1b |
T |
C |
19: 13,896,411 (GRCm39) |
V9A |
probably benign |
Het |
Pcdhga4 |
A |
T |
18: 37,819,651 (GRCm39) |
Y400F |
probably damaging |
Het |
Pkd2 |
A |
G |
5: 104,634,515 (GRCm39) |
|
silent |
Het |
Plxna4 |
T |
A |
6: 32,183,165 (GRCm39) |
I913F |
probably damaging |
Het |
Psmc1 |
T |
C |
12: 100,086,399 (GRCm39) |
|
probably null |
Het |
Robo2 |
G |
A |
16: 73,695,853 (GRCm39) |
T1430I |
probably benign |
Het |
Safb2 |
G |
A |
17: 56,882,647 (GRCm39) |
R329C |
probably damaging |
Het |
Septin14 |
T |
C |
5: 129,774,926 (GRCm39) |
H83R |
probably damaging |
Het |
Slc16a10 |
A |
G |
10: 39,952,784 (GRCm39) |
F237L |
probably benign |
Het |
Slc37a1 |
A |
T |
17: 31,559,236 (GRCm39) |
T439S |
probably damaging |
Het |
Slc6a6 |
T |
C |
6: 91,712,170 (GRCm39) |
F233S |
probably damaging |
Het |
Smyd3 |
A |
T |
1: 179,238,024 (GRCm39) |
D114E |
probably benign |
Het |
Sned1 |
T |
C |
1: 93,199,324 (GRCm39) |
I468T |
probably benign |
Het |
Tdrd7 |
T |
C |
4: 46,029,757 (GRCm39) |
V1030A |
probably benign |
Het |
Trip12 |
A |
T |
1: 84,727,065 (GRCm39) |
D1135E |
probably damaging |
Het |
Tsga10 |
T |
A |
1: 37,800,598 (GRCm39) |
D542V |
probably damaging |
Het |
Ubqlnl |
G |
A |
7: 103,798,904 (GRCm39) |
Q198* |
probably null |
Het |
Unc93a2 |
A |
T |
17: 7,637,187 (GRCm39) |
C334S |
probably benign |
Het |
Usp46 |
A |
T |
5: 74,189,902 (GRCm39) |
M43K |
probably benign |
Het |
Vmn1r175 |
A |
T |
7: 23,508,531 (GRCm39) |
I32N |
possibly damaging |
Het |
Vmn1r29 |
C |
T |
6: 58,285,108 (GRCm39) |
T276I |
probably benign |
Het |
Vmn1r81 |
A |
T |
7: 11,994,034 (GRCm39) |
D191E |
probably damaging |
Het |
Zbtb5 |
C |
A |
4: 44,995,052 (GRCm39) |
V111F |
probably damaging |
Het |
Zfp12 |
C |
T |
5: 143,230,240 (GRCm39) |
P189L |
possibly damaging |
Het |
Zfp729b |
A |
G |
13: 67,739,140 (GRCm39) |
F1042L |
probably benign |
Het |
|
Other mutations in Speer4a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01783:Speer4a1
|
APN |
5 |
26,240,045 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01959:Speer4a1
|
APN |
5 |
26,240,902 (GRCm39) |
nonsense |
probably null |
|
IGL02294:Speer4a1
|
APN |
5 |
26,243,240 (GRCm39) |
missense |
probably benign |
0.21 |
FR4340:Speer4a1
|
UTSW |
5 |
26,241,746 (GRCm39) |
nonsense |
probably null |
|
FR4342:Speer4a1
|
UTSW |
5 |
26,241,746 (GRCm39) |
nonsense |
probably null |
|
FR4589:Speer4a1
|
UTSW |
5 |
26,241,746 (GRCm39) |
nonsense |
probably null |
|
R0137:Speer4a1
|
UTSW |
5 |
26,240,982 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1068:Speer4a1
|
UTSW |
5 |
26,241,024 (GRCm39) |
missense |
probably null |
0.84 |
R1209:Speer4a1
|
UTSW |
5 |
26,240,123 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3805:Speer4a1
|
UTSW |
5 |
26,240,082 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4525:Speer4a1
|
UTSW |
5 |
26,244,341 (GRCm39) |
critical splice donor site |
probably null |
|
R4851:Speer4a1
|
UTSW |
5 |
26,243,210 (GRCm39) |
missense |
probably damaging |
0.99 |
R5326:Speer4a1
|
UTSW |
5 |
26,241,736 (GRCm39) |
missense |
probably damaging |
0.99 |
R6081:Speer4a1
|
UTSW |
5 |
26,239,960 (GRCm39) |
nonsense |
probably null |
|
R6742:Speer4a1
|
UTSW |
5 |
26,241,054 (GRCm39) |
splice site |
probably null |
|
R7521:Speer4a1
|
UTSW |
5 |
26,241,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R8669:Speer4a1
|
UTSW |
5 |
26,243,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R8782:Speer4a1
|
UTSW |
5 |
26,241,754 (GRCm39) |
missense |
probably benign |
0.39 |
R8830:Speer4a1
|
UTSW |
5 |
26,241,793 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1177:Speer4a1
|
UTSW |
5 |
26,240,036 (GRCm39) |
missense |
probably damaging |
1.00 |
|