Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700020L24Rik |
T |
A |
11: 83,331,578 (GRCm39) |
C134S |
probably damaging |
Het |
Acox3 |
T |
G |
5: 35,747,052 (GRCm39) |
F156L |
probably damaging |
Het |
Adprhl1 |
T |
C |
8: 13,272,474 (GRCm39) |
E1428G |
probably benign |
Het |
Arhgap40 |
A |
T |
2: 158,354,758 (GRCm39) |
M15L |
probably benign |
Het |
Bahcc1 |
C |
A |
11: 120,177,173 (GRCm39) |
F2020L |
probably damaging |
Het |
BC024063 |
A |
T |
10: 81,945,352 (GRCm39) |
H324L |
probably benign |
Het |
Ccdc40 |
C |
A |
11: 119,155,292 (GRCm39) |
S1177R |
probably benign |
Het |
Ccne2 |
A |
T |
4: 11,201,355 (GRCm39) |
R294S |
probably benign |
Het |
Cib1 |
A |
C |
7: 79,882,291 (GRCm39) |
S6R |
probably damaging |
Het |
Csnk2a1 |
A |
G |
2: 152,099,886 (GRCm39) |
E114G |
probably damaging |
Het |
Cxxc1 |
A |
G |
18: 74,354,128 (GRCm39) |
|
probably benign |
Het |
Decr2 |
A |
C |
17: 26,307,911 (GRCm39) |
I47M |
possibly damaging |
Het |
Dmxl2 |
A |
G |
9: 54,327,027 (GRCm39) |
|
probably null |
Het |
Dse |
G |
A |
10: 34,060,149 (GRCm39) |
|
probably benign |
Het |
Eml6 |
A |
G |
11: 29,708,981 (GRCm39) |
V1480A |
probably benign |
Het |
Erap1 |
A |
G |
13: 74,805,755 (GRCm39) |
I165M |
probably benign |
Het |
Fan1 |
G |
T |
7: 64,016,406 (GRCm39) |
Q573K |
probably damaging |
Het |
Fndc3a |
G |
A |
14: 72,793,955 (GRCm39) |
T906I |
probably benign |
Het |
Gm21915 |
A |
C |
9: 40,582,006 (GRCm39) |
H33P |
possibly damaging |
Het |
Idh1 |
CA |
CAA |
1: 65,204,347 (GRCm39) |
|
probably null |
Het |
Lama3 |
G |
T |
18: 12,624,000 (GRCm39) |
Q1384H |
probably damaging |
Het |
Ly75 |
A |
G |
2: 60,178,785 (GRCm39) |
F677L |
probably damaging |
Het |
Megf11 |
A |
G |
9: 64,588,673 (GRCm39) |
D493G |
probably benign |
Het |
Mta3 |
A |
T |
17: 84,096,369 (GRCm39) |
I348F |
possibly damaging |
Het |
Myo1d |
A |
T |
11: 80,575,205 (GRCm39) |
F170L |
probably damaging |
Het |
Nfkbia |
A |
G |
12: 55,539,083 (GRCm39) |
|
probably benign |
Het |
Nfx1 |
A |
T |
4: 41,023,727 (GRCm39) |
E1045D |
probably damaging |
Het |
Npffr2 |
T |
G |
5: 89,731,177 (GRCm39) |
V369G |
probably benign |
Het |
Or14c44 |
T |
C |
7: 86,061,854 (GRCm39) |
C95R |
probably damaging |
Het |
Or4d5 |
A |
T |
9: 40,011,985 (GRCm39) |
M267K |
possibly damaging |
Het |
Or4f59 |
A |
T |
2: 111,872,528 (GRCm39) |
I283N |
probably damaging |
Het |
Or5t18 |
A |
T |
2: 86,636,575 (GRCm39) |
M256K |
probably damaging |
Het |
Or5w13 |
G |
T |
2: 87,524,057 (GRCm39) |
H56Q |
possibly damaging |
Het |
Otoa |
G |
A |
7: 120,691,894 (GRCm39) |
E41K |
possibly damaging |
Het |
Podxl |
A |
G |
6: 31,501,400 (GRCm39) |
V385A |
probably damaging |
Het |
Ppp4r4 |
C |
T |
12: 103,567,623 (GRCm39) |
T673M |
possibly damaging |
Het |
Rbm20 |
G |
T |
19: 53,821,120 (GRCm39) |
C525F |
probably damaging |
Het |
Rnf17 |
A |
T |
14: 56,737,886 (GRCm39) |
E1222D |
probably damaging |
Het |
Ros1 |
G |
A |
10: 51,922,143 (GRCm39) |
A2331V |
probably benign |
Het |
Rrs1 |
T |
A |
1: 9,615,819 (GRCm39) |
I24N |
probably damaging |
Het |
Sec11a |
A |
G |
7: 80,584,850 (GRCm39) |
V29A |
possibly damaging |
Het |
Shisa3 |
T |
A |
5: 67,768,749 (GRCm39) |
Y216* |
probably null |
Het |
Slc22a2 |
A |
T |
17: 12,831,425 (GRCm39) |
Y405F |
probably benign |
Het |
Slc2a12 |
A |
T |
10: 22,568,105 (GRCm39) |
M511L |
possibly damaging |
Het |
Slc38a9 |
T |
A |
13: 112,840,136 (GRCm39) |
H338Q |
probably damaging |
Het |
Slco1c1 |
T |
G |
6: 141,505,531 (GRCm39) |
S486A |
probably benign |
Het |
Slit2 |
T |
C |
5: 48,461,524 (GRCm39) |
S1524P |
possibly damaging |
Het |
Spata31d1c |
T |
C |
13: 65,184,140 (GRCm39) |
S561P |
possibly damaging |
Het |
Stac3 |
T |
A |
10: 127,340,781 (GRCm39) |
M182K |
probably damaging |
Het |
Stt3b |
T |
C |
9: 115,077,685 (GRCm39) |
E689G |
probably damaging |
Het |
Suclg1 |
A |
G |
6: 73,248,091 (GRCm39) |
K271E |
probably benign |
Het |
Tas1r1 |
A |
G |
4: 152,116,708 (GRCm39) |
Y309H |
probably benign |
Het |
Tbc1d5 |
TGC |
TGCCGC |
17: 51,106,969 (GRCm39) |
|
probably benign |
Het |
Tbc1d5 |
TG |
TGCGG |
17: 51,106,978 (GRCm39) |
|
probably benign |
Het |
Tbc1d5 |
TTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTGCTGCTG |
17: 51,106,962 (GRCm39) |
|
probably benign |
Het |
Tbc1d5 |
TGC |
TGCGGC |
17: 51,106,963 (GRCm39) |
|
probably benign |
Het |
Tmem101 |
A |
G |
11: 102,044,336 (GRCm39) |
F184L |
probably benign |
Het |
Zfp474 |
A |
G |
18: 52,772,166 (GRCm39) |
Q273R |
probably benign |
Het |
Zfyve28 |
A |
G |
5: 34,390,670 (GRCm39) |
L197P |
probably damaging |
Het |
|
Other mutations in Lrrc34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02502:Lrrc34
|
APN |
3 |
30,699,394 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02738:Lrrc34
|
APN |
3 |
30,685,441 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02985:Lrrc34
|
APN |
3 |
30,690,444 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02999:Lrrc34
|
APN |
3 |
30,688,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R0367:Lrrc34
|
UTSW |
3 |
30,684,142 (GRCm39) |
missense |
probably benign |
0.08 |
R0761:Lrrc34
|
UTSW |
3 |
30,685,425 (GRCm39) |
splice site |
probably null |
|
R1426:Lrrc34
|
UTSW |
3 |
30,697,728 (GRCm39) |
unclassified |
probably benign |
|
R1980:Lrrc34
|
UTSW |
3 |
30,696,890 (GRCm39) |
missense |
probably benign |
0.33 |
R2215:Lrrc34
|
UTSW |
3 |
30,697,678 (GRCm39) |
missense |
probably benign |
0.03 |
R2414:Lrrc34
|
UTSW |
3 |
30,688,711 (GRCm39) |
missense |
probably benign |
0.00 |
R4379:Lrrc34
|
UTSW |
3 |
30,685,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Lrrc34
|
UTSW |
3 |
30,690,397 (GRCm39) |
nonsense |
probably null |
|
R5418:Lrrc34
|
UTSW |
3 |
30,696,923 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5662:Lrrc34
|
UTSW |
3 |
30,685,473 (GRCm39) |
missense |
probably benign |
0.03 |
R6736:Lrrc34
|
UTSW |
3 |
30,679,008 (GRCm39) |
missense |
probably benign |
0.03 |
R6809:Lrrc34
|
UTSW |
3 |
30,688,749 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6941:Lrrc34
|
UTSW |
3 |
30,678,969 (GRCm39) |
missense |
probably benign |
0.01 |
R7017:Lrrc34
|
UTSW |
3 |
30,699,465 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7080:Lrrc34
|
UTSW |
3 |
30,688,705 (GRCm39) |
missense |
probably damaging |
0.96 |
R7139:Lrrc34
|
UTSW |
3 |
30,679,036 (GRCm39) |
missense |
probably benign |
0.22 |
R7191:Lrrc34
|
UTSW |
3 |
30,679,027 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7398:Lrrc34
|
UTSW |
3 |
30,697,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7662:Lrrc34
|
UTSW |
3 |
30,697,452 (GRCm39) |
missense |
probably benign |
0.16 |
R7707:Lrrc34
|
UTSW |
3 |
30,679,041 (GRCm39) |
missense |
probably benign |
0.00 |
R7945:Lrrc34
|
UTSW |
3 |
30,696,886 (GRCm39) |
critical splice donor site |
probably null |
|
R9764:Lrrc34
|
UTSW |
3 |
30,697,467 (GRCm39) |
missense |
probably damaging |
1.00 |
|