Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam39 |
A |
G |
8: 41,279,610 (GRCm39) |
N667S |
probably benign |
Het |
Ap4e1 |
T |
A |
2: 126,908,508 (GRCm39) |
C1085* |
probably null |
Het |
BC035044 |
A |
T |
6: 128,861,997 (GRCm39) |
|
probably benign |
Het |
Bltp2 |
A |
G |
11: 78,164,084 (GRCm39) |
M1142V |
possibly damaging |
Het |
Capn11 |
T |
C |
17: 45,941,692 (GRCm39) |
D693G |
probably damaging |
Het |
Cavin4 |
A |
T |
4: 48,663,917 (GRCm39) |
H99L |
possibly damaging |
Het |
Ccdc86 |
T |
C |
19: 10,925,945 (GRCm39) |
K218R |
possibly damaging |
Het |
Ccno |
T |
C |
13: 113,126,379 (GRCm39) |
S283P |
probably damaging |
Het |
Ccser2 |
A |
T |
14: 36,662,276 (GRCm39) |
S303T |
probably benign |
Het |
Cd53 |
T |
A |
3: 106,674,680 (GRCm39) |
N129I |
probably damaging |
Het |
Cd63 |
G |
A |
10: 128,747,933 (GRCm39) |
|
probably null |
Het |
Cyp2j6 |
G |
C |
4: 96,424,323 (GRCm39) |
L145V |
probably damaging |
Het |
Daam2 |
A |
G |
17: 49,776,694 (GRCm39) |
M797T |
probably damaging |
Het |
Dennd2b |
A |
C |
7: 109,156,095 (GRCm39) |
D218E |
probably benign |
Het |
Dmgdh |
G |
A |
13: 93,888,794 (GRCm39) |
V811I |
possibly damaging |
Het |
Dpysl4 |
A |
T |
7: 138,670,250 (GRCm39) |
T123S |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,814,345 (GRCm39) |
E428G |
possibly damaging |
Het |
Fam124b |
T |
A |
1: 80,177,902 (GRCm39) |
T366S |
possibly damaging |
Het |
Fbxw22 |
T |
C |
9: 109,215,747 (GRCm39) |
D167G |
probably damaging |
Het |
Flrt2 |
C |
T |
12: 95,746,012 (GRCm39) |
Q117* |
probably null |
Het |
Ftsj3 |
A |
T |
11: 106,144,166 (GRCm39) |
|
probably null |
Het |
Ggn |
A |
G |
7: 28,872,474 (GRCm39) |
Y618C |
probably damaging |
Het |
Glis1 |
T |
A |
4: 107,484,710 (GRCm39) |
S402T |
probably benign |
Het |
Gm4781 |
T |
A |
10: 100,232,349 (GRCm39) |
|
noncoding transcript |
Het |
Gm7168 |
T |
A |
17: 14,168,858 (GRCm39) |
I75K |
probably damaging |
Het |
Gm7298 |
C |
T |
6: 121,737,782 (GRCm39) |
H348Y |
probably benign |
Het |
Gria1 |
G |
T |
11: 57,133,618 (GRCm39) |
R499L |
probably damaging |
Het |
Gtf2ird2 |
C |
T |
5: 134,245,389 (GRCm39) |
T549M |
probably damaging |
Het |
H2-M10.6 |
T |
A |
17: 37,125,178 (GRCm39) |
V323E |
probably damaging |
Het |
Hoxb3 |
G |
A |
11: 96,236,929 (GRCm39) |
V336I |
probably benign |
Het |
Il12b |
G |
A |
11: 44,303,453 (GRCm39) |
A327T |
probably benign |
Het |
Inpp4a |
C |
A |
1: 37,419,183 (GRCm39) |
P588T |
probably benign |
Het |
Kctd12 |
C |
A |
14: 103,219,027 (GRCm39) |
D284Y |
probably damaging |
Het |
Kif28 |
C |
A |
1: 179,525,337 (GRCm39) |
|
probably null |
Het |
Krt1c |
T |
C |
15: 101,723,479 (GRCm39) |
N332S |
probably benign |
Het |
Lama2 |
G |
A |
10: 26,857,495 (GRCm39) |
T3118I |
probably benign |
Het |
Lgi1 |
T |
C |
19: 38,253,404 (GRCm39) |
L25P |
probably damaging |
Het |
Lhx3 |
T |
A |
2: 26,091,503 (GRCm39) |
M269L |
probably benign |
Het |
Lmtk2 |
A |
T |
5: 144,112,160 (GRCm39) |
E960V |
probably damaging |
Het |
Loxl4 |
A |
T |
19: 42,596,791 (GRCm39) |
D60E |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,333,868 (GRCm39) |
N1458Y |
possibly damaging |
Het |
Ltn1 |
A |
T |
16: 87,224,677 (GRCm39) |
S16T |
probably damaging |
Het |
Mllt6 |
G |
A |
11: 97,569,362 (GRCm39) |
A875T |
possibly damaging |
Het |
Mrgprb4 |
A |
T |
7: 47,848,574 (GRCm39) |
I118N |
probably damaging |
Het |
Mrps7 |
A |
G |
11: 115,495,707 (GRCm39) |
T82A |
possibly damaging |
Het |
Mug2 |
A |
G |
6: 122,056,565 (GRCm39) |
E1170G |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,107,915 (GRCm39) |
H647R |
probably benign |
Het |
Nbeal2 |
T |
C |
9: 110,454,215 (GRCm39) |
Y2710C |
probably damaging |
Het |
Ndc1 |
A |
T |
4: 107,268,395 (GRCm39) |
I644L |
possibly damaging |
Het |
Or4c108 |
T |
G |
2: 88,804,226 (GRCm39) |
N3T |
probably damaging |
Het |
Or8g33 |
A |
T |
9: 39,338,008 (GRCm39) |
Y120N |
probably damaging |
Het |
Padi4 |
A |
G |
4: 140,483,784 (GRCm39) |
M352T |
possibly damaging |
Het |
Pals1 |
C |
T |
12: 78,864,084 (GRCm39) |
H216Y |
probably benign |
Het |
Pcdhgc3 |
C |
A |
18: 37,939,990 (GRCm39) |
D130E |
probably damaging |
Het |
Pde6a |
A |
T |
18: 61,417,163 (GRCm39) |
|
probably null |
Het |
Pdpn |
C |
T |
4: 143,025,792 (GRCm39) |
G12R |
probably damaging |
Het |
Pot1a |
A |
T |
6: 25,771,620 (GRCm39) |
D200E |
probably benign |
Het |
Ppa1 |
A |
T |
10: 61,503,431 (GRCm39) |
D236V |
probably benign |
Het |
Ptprn2 |
T |
A |
12: 116,822,739 (GRCm39) |
S273T |
probably benign |
Het |
Rasgrf2 |
T |
C |
13: 92,165,609 (GRCm39) |
E297G |
probably damaging |
Het |
Rgl1 |
T |
C |
1: 152,394,923 (GRCm39) |
N750S |
probably damaging |
Het |
Rinl |
A |
G |
7: 28,496,365 (GRCm39) |
N449D |
probably benign |
Het |
Samd8 |
T |
A |
14: 21,825,093 (GRCm39) |
H79Q |
probably benign |
Het |
Scn11a |
T |
C |
9: 119,583,933 (GRCm39) |
I1561V |
probably benign |
Het |
Slc7a12 |
A |
T |
3: 14,546,200 (GRCm39) |
|
probably null |
Het |
Slco1a4 |
A |
G |
6: 141,763,546 (GRCm39) |
I390T |
possibly damaging |
Het |
Snta1 |
T |
C |
2: 154,219,102 (GRCm39) |
N411S |
probably benign |
Het |
Srgap2 |
T |
C |
1: 131,277,279 (GRCm39) |
T323A |
probably benign |
Het |
Ssh2 |
G |
T |
11: 77,344,291 (GRCm39) |
V759L |
probably benign |
Het |
Swap70 |
G |
T |
7: 109,869,188 (GRCm39) |
R327L |
probably damaging |
Het |
Tbc1d4 |
C |
A |
14: 101,696,206 (GRCm39) |
C914F |
probably benign |
Het |
Tbx3 |
A |
G |
5: 119,812,132 (GRCm39) |
D144G |
probably damaging |
Het |
Tgfbr2 |
T |
C |
9: 115,939,212 (GRCm39) |
K205R |
possibly damaging |
Het |
Tmem94 |
A |
T |
11: 115,681,857 (GRCm39) |
|
probably null |
Het |
Usf3 |
T |
A |
16: 44,041,468 (GRCm39) |
F1983I |
probably damaging |
Het |
Ush2a |
T |
A |
1: 188,132,068 (GRCm39) |
C763* |
probably null |
Het |
Vmn1r115 |
A |
C |
7: 20,578,640 (GRCm39) |
L91V |
probably damaging |
Het |
Vmn1r201 |
A |
T |
13: 22,659,499 (GRCm39) |
I238F |
possibly damaging |
Het |
Vmn1r28 |
T |
A |
6: 58,242,476 (GRCm39) |
S106R |
probably damaging |
Het |
Vmn1r82 |
T |
C |
7: 12,039,012 (GRCm39) |
V95A |
probably damaging |
Het |
Vrk3 |
A |
T |
7: 44,419,035 (GRCm39) |
N371I |
possibly damaging |
Het |
Wnt8b |
C |
A |
19: 44,500,082 (GRCm39) |
A223E |
probably benign |
Het |
Xirp2 |
T |
C |
2: 67,335,921 (GRCm39) |
|
probably null |
Het |
Xpo7 |
T |
C |
14: 70,920,243 (GRCm39) |
N642S |
probably benign |
Het |
Ythdc1 |
G |
A |
5: 86,975,953 (GRCm39) |
R520H |
possibly damaging |
Het |
Zfp367 |
T |
C |
13: 64,283,204 (GRCm39) |
E316G |
probably damaging |
Het |
Zfp488 |
T |
A |
14: 33,692,751 (GRCm39) |
R137S |
possibly damaging |
Het |
Zfp532 |
G |
T |
18: 65,789,542 (GRCm39) |
V994L |
probably benign |
Het |
|
Other mutations in Slc39a12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00536:Slc39a12
|
APN |
2 |
14,400,879 (GRCm39) |
splice site |
probably benign |
|
IGL01597:Slc39a12
|
APN |
2 |
14,439,120 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02516:Slc39a12
|
APN |
2 |
14,405,146 (GRCm39) |
missense |
probably damaging |
1.00 |
greenshoot
|
UTSW |
2 |
14,425,029 (GRCm39) |
missense |
probably damaging |
1.00 |
sapling
|
UTSW |
2 |
14,440,489 (GRCm39) |
missense |
probably benign |
|
Seedling
|
UTSW |
2 |
14,439,174 (GRCm39) |
splice site |
probably benign |
|
stripling
|
UTSW |
2 |
14,405,142 (GRCm39) |
missense |
probably benign |
0.00 |
R0068:Slc39a12
|
UTSW |
2 |
14,440,489 (GRCm39) |
missense |
probably benign |
|
R0068:Slc39a12
|
UTSW |
2 |
14,440,489 (GRCm39) |
missense |
probably benign |
|
R0453:Slc39a12
|
UTSW |
2 |
14,440,492 (GRCm39) |
missense |
probably benign |
0.04 |
R0533:Slc39a12
|
UTSW |
2 |
14,405,142 (GRCm39) |
missense |
probably benign |
0.00 |
R0718:Slc39a12
|
UTSW |
2 |
14,412,237 (GRCm39) |
splice site |
probably benign |
|
R1647:Slc39a12
|
UTSW |
2 |
14,456,803 (GRCm39) |
missense |
probably benign |
0.24 |
R1648:Slc39a12
|
UTSW |
2 |
14,456,803 (GRCm39) |
missense |
probably benign |
0.24 |
R1879:Slc39a12
|
UTSW |
2 |
14,448,868 (GRCm39) |
missense |
probably benign |
|
R1993:Slc39a12
|
UTSW |
2 |
14,439,030 (GRCm39) |
missense |
probably damaging |
0.98 |
R2429:Slc39a12
|
UTSW |
2 |
14,409,897 (GRCm39) |
missense |
probably benign |
0.06 |
R3746:Slc39a12
|
UTSW |
2 |
14,400,878 (GRCm39) |
splice site |
probably benign |
|
R3934:Slc39a12
|
UTSW |
2 |
14,439,174 (GRCm39) |
splice site |
probably benign |
|
R3941:Slc39a12
|
UTSW |
2 |
14,400,992 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4008:Slc39a12
|
UTSW |
2 |
14,456,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R4478:Slc39a12
|
UTSW |
2 |
14,424,990 (GRCm39) |
nonsense |
probably null |
|
R4622:Slc39a12
|
UTSW |
2 |
14,405,136 (GRCm39) |
missense |
probably benign |
0.11 |
R4760:Slc39a12
|
UTSW |
2 |
14,405,134 (GRCm39) |
missense |
probably benign |
0.14 |
R5477:Slc39a12
|
UTSW |
2 |
14,394,193 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5566:Slc39a12
|
UTSW |
2 |
14,412,414 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5725:Slc39a12
|
UTSW |
2 |
14,394,075 (GRCm39) |
start gained |
probably benign |
|
R5798:Slc39a12
|
UTSW |
2 |
14,454,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R6074:Slc39a12
|
UTSW |
2 |
14,412,290 (GRCm39) |
nonsense |
probably null |
|
R6169:Slc39a12
|
UTSW |
2 |
14,405,044 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6802:Slc39a12
|
UTSW |
2 |
14,424,896 (GRCm39) |
missense |
probably benign |
0.28 |
R6847:Slc39a12
|
UTSW |
2 |
14,454,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6899:Slc39a12
|
UTSW |
2 |
14,394,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R6931:Slc39a12
|
UTSW |
2 |
14,394,186 (GRCm39) |
missense |
probably benign |
0.04 |
R7131:Slc39a12
|
UTSW |
2 |
14,454,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Slc39a12
|
UTSW |
2 |
14,456,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R7525:Slc39a12
|
UTSW |
2 |
14,499,272 (GRCm39) |
missense |
probably benign |
0.01 |
R7568:Slc39a12
|
UTSW |
2 |
14,404,939 (GRCm39) |
splice site |
probably null |
|
R7684:Slc39a12
|
UTSW |
2 |
14,454,670 (GRCm39) |
missense |
probably damaging |
0.99 |
R7761:Slc39a12
|
UTSW |
2 |
14,439,141 (GRCm39) |
missense |
probably benign |
0.01 |
R7785:Slc39a12
|
UTSW |
2 |
14,425,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Slc39a12
|
UTSW |
2 |
14,454,670 (GRCm39) |
missense |
probably damaging |
0.99 |
R9199:Slc39a12
|
UTSW |
2 |
14,394,321 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9280:Slc39a12
|
UTSW |
2 |
14,401,003 (GRCm39) |
missense |
probably benign |
0.04 |
R9571:Slc39a12
|
UTSW |
2 |
14,412,380 (GRCm39) |
missense |
probably benign |
|
|