Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
A |
G |
2: 151,315,489 (GRCm39) |
L63P |
possibly damaging |
Het |
Abca13 |
A |
T |
11: 9,479,010 (GRCm39) |
Y4286F |
probably benign |
Het |
Aldh5a1 |
A |
C |
13: 25,095,572 (GRCm39) |
V515G |
possibly damaging |
Het |
Ankrd42 |
T |
C |
7: 92,241,141 (GRCm39) |
E406G |
possibly damaging |
Het |
Arfgef2 |
T |
A |
2: 166,707,733 (GRCm39) |
M1043K |
probably benign |
Het |
Arhgef11 |
T |
A |
3: 87,616,879 (GRCm39) |
Y383* |
probably null |
Het |
Aste1 |
C |
T |
9: 105,282,335 (GRCm39) |
P614L |
probably damaging |
Het |
B3galt5 |
T |
A |
16: 96,117,005 (GRCm39) |
S213T |
probably damaging |
Het |
Bak1 |
A |
G |
17: 27,241,434 (GRCm39) |
L108P |
possibly damaging |
Het |
Bcl6 |
G |
A |
16: 23,784,976 (GRCm39) |
R675* |
probably null |
Het |
Bdp1 |
T |
G |
13: 100,197,659 (GRCm39) |
T909P |
possibly damaging |
Het |
Cacna1i |
A |
G |
15: 80,279,439 (GRCm39) |
H2060R |
probably benign |
Het |
Cdhr3 |
G |
T |
12: 33,111,772 (GRCm39) |
P246Q |
probably damaging |
Het |
Colgalt1 |
T |
C |
8: 72,076,354 (GRCm39) |
S602P |
probably damaging |
Het |
Csde1 |
T |
C |
3: 102,947,269 (GRCm39) |
S74P |
probably damaging |
Het |
Cyp51 |
A |
T |
5: 4,137,846 (GRCm39) |
C366S |
possibly damaging |
Het |
Dcaf7 |
A |
G |
11: 105,928,016 (GRCm39) |
N23D |
probably damaging |
Het |
Ddx10 |
G |
A |
9: 53,028,588 (GRCm39) |
A772V |
probably benign |
Het |
Ddx4 |
A |
G |
13: 112,750,319 (GRCm39) |
F404S |
probably benign |
Het |
Dlg4 |
T |
A |
11: 69,908,042 (GRCm39) |
M1K |
probably null |
Het |
Dnajc6 |
T |
C |
4: 101,470,142 (GRCm39) |
V293A |
probably damaging |
Het |
Etl4 |
G |
T |
2: 20,811,742 (GRCm39) |
R1643L |
probably damaging |
Het |
F13b |
G |
A |
1: 139,435,895 (GRCm39) |
E234K |
probably damaging |
Het |
Fam171a1 |
T |
C |
2: 3,226,766 (GRCm39) |
I633T |
probably benign |
Het |
Frem3 |
A |
G |
8: 81,342,668 (GRCm39) |
I1654V |
probably benign |
Het |
Galr2 |
A |
G |
11: 116,174,408 (GRCm39) |
E346G |
possibly damaging |
Het |
Gck |
G |
A |
11: 5,899,705 (GRCm39) |
|
probably benign |
Het |
Gen1 |
G |
T |
12: 11,291,833 (GRCm39) |
T717K |
probably benign |
Het |
Gpatch8 |
TTCCTCCTCCTCCTCTTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTCTTCCTCCTCCTC |
11: 102,371,014 (GRCm39) |
|
probably benign |
Het |
Hat1 |
A |
G |
2: 71,251,595 (GRCm39) |
T215A |
possibly damaging |
Het |
Hmbox1 |
A |
T |
14: 65,134,486 (GRCm39) |
M38K |
probably damaging |
Het |
Ifi47 |
A |
G |
11: 48,987,369 (GRCm39) |
K379E |
probably benign |
Het |
Ift81 |
T |
C |
5: 122,707,062 (GRCm39) |
Y460C |
probably damaging |
Het |
Jarid2 |
T |
A |
13: 45,055,938 (GRCm39) |
S381R |
probably damaging |
Het |
Kmt2b |
A |
T |
7: 30,279,388 (GRCm39) |
V1458E |
probably damaging |
Het |
Kpna4 |
G |
T |
3: 68,997,266 (GRCm39) |
P336Q |
probably damaging |
Het |
Krt84 |
T |
C |
15: 101,440,689 (GRCm39) |
R168G |
probably damaging |
Het |
Lhx8 |
T |
A |
3: 154,030,221 (GRCm39) |
Y137F |
possibly damaging |
Het |
Lin7b |
T |
C |
7: 45,019,651 (GRCm39) |
E19G |
probably damaging |
Het |
Lrmda |
A |
T |
14: 22,634,608 (GRCm39) |
R131S |
probably damaging |
Het |
Lrrc75b |
C |
T |
10: 75,389,512 (GRCm39) |
A280T |
possibly damaging |
Het |
Megf11 |
G |
A |
9: 64,555,233 (GRCm39) |
R268K |
probably null |
Het |
Mgat4e |
G |
T |
1: 134,469,697 (GRCm39) |
Q116K |
probably damaging |
Het |
Mlkl |
A |
G |
8: 112,046,035 (GRCm39) |
L325P |
probably damaging |
Het |
Mup2 |
A |
G |
4: 60,137,641 (GRCm39) |
L134P |
probably damaging |
Het |
Myo19 |
A |
G |
11: 84,791,412 (GRCm39) |
E489G |
probably damaging |
Het |
Ncbp3 |
C |
A |
11: 72,938,835 (GRCm39) |
P37Q |
probably damaging |
Het |
Nf2 |
A |
G |
11: 4,749,964 (GRCm39) |
V236A |
probably damaging |
Het |
Nlrp1a |
A |
T |
11: 71,014,905 (GRCm39) |
M115K |
possibly damaging |
Het |
Nsf |
T |
A |
11: 103,719,356 (GRCm39) |
K649* |
probably null |
Het |
Olfml2b |
A |
T |
1: 170,494,354 (GRCm39) |
I313L |
probably benign |
Het |
Or2ak4 |
T |
A |
11: 58,649,109 (GRCm39) |
I206N |
probably damaging |
Het |
Or52u1 |
T |
A |
7: 104,237,764 (GRCm39) |
V251D |
possibly damaging |
Het |
Papln |
T |
A |
12: 83,823,295 (GRCm39) |
L444Q |
probably damaging |
Het |
Phc3 |
T |
C |
3: 30,968,346 (GRCm39) |
I897V |
probably benign |
Het |
Plcg1 |
T |
C |
2: 160,596,300 (GRCm39) |
L632P |
probably damaging |
Het |
Pramel21 |
A |
T |
4: 143,342,735 (GRCm39) |
I281F |
probably benign |
Het |
Prkg1 |
T |
C |
19: 31,279,701 (GRCm39) |
T178A |
probably damaging |
Het |
Ptges |
T |
A |
2: 30,782,816 (GRCm39) |
T79S |
probably benign |
Het |
Rab26 |
T |
C |
17: 24,751,263 (GRCm39) |
T81A |
probably damaging |
Het |
Rai14 |
T |
A |
15: 10,595,089 (GRCm39) |
I145L |
possibly damaging |
Het |
Rasgrf1 |
A |
G |
9: 89,884,414 (GRCm39) |
T960A |
possibly damaging |
Het |
Rfx1 |
A |
T |
8: 84,821,455 (GRCm39) |
I755F |
probably damaging |
Het |
Rims1 |
T |
G |
1: 22,503,174 (GRCm39) |
L670F |
probably damaging |
Het |
Rtkn |
G |
A |
6: 83,126,692 (GRCm39) |
C297Y |
probably damaging |
Het |
Sec23a |
A |
T |
12: 59,036,229 (GRCm39) |
N378K |
probably benign |
Het |
Slc1a2 |
T |
C |
2: 102,597,340 (GRCm39) |
M449T |
probably damaging |
Het |
Slc22a3 |
G |
A |
17: 12,652,518 (GRCm39) |
L369F |
possibly damaging |
Het |
Slc34a1 |
A |
G |
13: 24,006,390 (GRCm39) |
E472G |
probably benign |
Het |
Smad6 |
G |
T |
9: 63,929,069 (GRCm39) |
D82E |
unknown |
Het |
Smgc |
A |
T |
15: 91,736,811 (GRCm39) |
I463F |
possibly damaging |
Het |
Strada |
C |
A |
11: 106,061,865 (GRCm39) |
G166C |
probably damaging |
Het |
Tcaf3 |
A |
G |
6: 42,570,825 (GRCm39) |
V309A |
probably benign |
Het |
Tet2 |
C |
T |
3: 133,175,352 (GRCm39) |
E1332K |
possibly damaging |
Het |
Tfcp2l1 |
A |
G |
1: 118,596,362 (GRCm39) |
N366D |
probably damaging |
Het |
Tll2 |
G |
A |
19: 41,105,723 (GRCm39) |
P369L |
possibly damaging |
Het |
Tox4 |
T |
C |
14: 52,529,554 (GRCm39) |
V505A |
probably benign |
Het |
Trbv4 |
A |
G |
6: 41,036,787 (GRCm39) |
D104G |
probably damaging |
Het |
Ugdh |
T |
C |
5: 65,574,380 (GRCm39) |
E416G |
probably damaging |
Het |
Usp47 |
T |
A |
7: 111,686,220 (GRCm39) |
C613S |
probably damaging |
Het |
Vmn1r11 |
T |
A |
6: 57,115,147 (GRCm39) |
N270K |
probably benign |
Het |
Wsb2 |
T |
A |
5: 117,509,160 (GRCm39) |
L147Q |
probably damaging |
Het |
Xrn1 |
G |
A |
9: 95,861,198 (GRCm39) |
A453T |
possibly damaging |
Het |
Zan |
A |
G |
5: 137,460,106 (GRCm39) |
S1262P |
unknown |
Het |
Zswim4 |
A |
G |
8: 84,946,556 (GRCm39) |
L700P |
probably damaging |
Het |
|
Other mutations in Slc49a4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02505:Slc49a4
|
APN |
16 |
35,555,928 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02990:Slc49a4
|
APN |
16 |
35,555,861 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0166:Slc49a4
|
UTSW |
16 |
35,539,684 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0319:Slc49a4
|
UTSW |
16 |
35,570,884 (GRCm39) |
missense |
probably benign |
0.01 |
R0323:Slc49a4
|
UTSW |
16 |
35,539,730 (GRCm39) |
frame shift |
probably null |
|
R0497:Slc49a4
|
UTSW |
16 |
35,555,974 (GRCm39) |
missense |
probably benign |
0.40 |
R1240:Slc49a4
|
UTSW |
16 |
35,518,379 (GRCm39) |
missense |
probably benign |
0.00 |
R1460:Slc49a4
|
UTSW |
16 |
35,539,736 (GRCm39) |
missense |
probably benign |
0.25 |
R2115:Slc49a4
|
UTSW |
16 |
35,518,309 (GRCm39) |
missense |
probably benign |
0.17 |
R4502:Slc49a4
|
UTSW |
16 |
35,539,787 (GRCm39) |
missense |
probably benign |
0.00 |
R4503:Slc49a4
|
UTSW |
16 |
35,539,787 (GRCm39) |
missense |
probably benign |
0.00 |
R4563:Slc49a4
|
UTSW |
16 |
35,518,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Slc49a4
|
UTSW |
16 |
35,555,945 (GRCm39) |
missense |
probably benign |
0.08 |
R5278:Slc49a4
|
UTSW |
16 |
35,518,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R5651:Slc49a4
|
UTSW |
16 |
35,555,986 (GRCm39) |
missense |
probably benign |
0.25 |
R5717:Slc49a4
|
UTSW |
16 |
35,539,799 (GRCm39) |
missense |
probably benign |
0.00 |
R5947:Slc49a4
|
UTSW |
16 |
35,550,676 (GRCm39) |
missense |
probably benign |
0.14 |
R6176:Slc49a4
|
UTSW |
16 |
35,525,167 (GRCm39) |
missense |
probably benign |
|
R7450:Slc49a4
|
UTSW |
16 |
35,589,344 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7645:Slc49a4
|
UTSW |
16 |
35,554,438 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7905:Slc49a4
|
UTSW |
16 |
35,589,320 (GRCm39) |
missense |
probably benign |
0.33 |
R8425:Slc49a4
|
UTSW |
16 |
35,555,967 (GRCm39) |
missense |
probably benign |
0.01 |
R8670:Slc49a4
|
UTSW |
16 |
35,556,005 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8827:Slc49a4
|
UTSW |
16 |
35,554,320 (GRCm39) |
missense |
probably benign |
0.01 |
R9022:Slc49a4
|
UTSW |
16 |
35,570,912 (GRCm39) |
missense |
probably benign |
0.00 |
R9421:Slc49a4
|
UTSW |
16 |
35,518,372 (GRCm39) |
missense |
|
|
R9779:Slc49a4
|
UTSW |
16 |
35,543,186 (GRCm39) |
missense |
probably benign |
0.30 |
|