Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp8b3 |
A |
G |
10: 80,365,540 (GRCm39) |
F405L |
possibly damaging |
Het |
BC035947 |
G |
T |
1: 78,474,482 (GRCm39) |
N683K |
probably benign |
Het |
Bmper |
T |
A |
9: 23,384,727 (GRCm39) |
|
probably null |
Het |
Btnl7-ps |
A |
G |
17: 34,761,550 (GRCm39) |
|
noncoding transcript |
Het |
Cmya5 |
A |
G |
13: 93,231,140 (GRCm39) |
V1316A |
probably damaging |
Het |
Cracd |
A |
T |
5: 77,006,858 (GRCm39) |
Q1073L |
unknown |
Het |
Dgcr6 |
C |
A |
16: 17,888,077 (GRCm39) |
Y200* |
probably null |
Het |
Dsp |
A |
C |
13: 38,381,681 (GRCm39) |
I2210L |
probably benign |
Het |
Eef1e1 |
G |
A |
13: 38,840,167 (GRCm39) |
T46I |
probably damaging |
Het |
Epc2 |
A |
G |
2: 49,378,750 (GRCm39) |
K68R |
probably damaging |
Het |
F11r |
G |
T |
1: 171,288,457 (GRCm39) |
R100L |
probably damaging |
Het |
Fam83c |
C |
T |
2: 155,676,668 (GRCm39) |
R34H |
probably benign |
Het |
Fbxw25 |
A |
T |
9: 109,491,202 (GRCm39) |
Y105* |
probably null |
Het |
Ggt1 |
T |
A |
10: 75,417,219 (GRCm39) |
Y5* |
probably null |
Het |
Hipk2 |
T |
C |
6: 38,795,861 (GRCm39) |
E136G |
probably damaging |
Het |
Hsph1 |
T |
A |
5: 149,544,180 (GRCm39) |
|
probably null |
Het |
Impdh1 |
A |
G |
6: 29,202,768 (GRCm39) |
S421P |
probably damaging |
Het |
Jhy |
T |
A |
9: 40,856,142 (GRCm39) |
E115V |
probably benign |
Het |
Kmt2a |
T |
C |
9: 44,742,588 (GRCm39) |
|
probably benign |
Het |
Ldlrap1 |
T |
C |
4: 134,477,747 (GRCm39) |
T159A |
probably damaging |
Het |
Lrrc4c |
A |
G |
2: 97,460,537 (GRCm39) |
T388A |
probably damaging |
Het |
Map3k10 |
C |
A |
7: 27,357,789 (GRCm39) |
C663F |
possibly damaging |
Het |
Me3 |
A |
T |
7: 89,435,701 (GRCm39) |
N179Y |
possibly damaging |
Het |
Medag |
T |
A |
5: 149,350,888 (GRCm39) |
I121N |
probably damaging |
Het |
Mocos |
C |
T |
18: 24,809,681 (GRCm39) |
A428V |
probably damaging |
Het |
Mok |
C |
T |
12: 110,781,591 (GRCm39) |
V59M |
probably benign |
Het |
Neb |
C |
A |
2: 52,097,672 (GRCm39) |
|
probably null |
Het |
Nr2c2 |
C |
T |
6: 92,140,119 (GRCm39) |
R464W |
probably damaging |
Het |
Or52s1 |
G |
A |
7: 102,861,900 (GRCm39) |
G267R |
probably damaging |
Het |
Or6c35 |
A |
G |
10: 129,169,202 (GRCm39) |
I151V |
probably benign |
Het |
Otud1 |
G |
T |
2: 19,663,554 (GRCm39) |
E228* |
probably null |
Het |
Parp4 |
A |
T |
14: 56,825,235 (GRCm39) |
N120Y |
probably damaging |
Het |
Ptprb |
T |
C |
10: 116,182,887 (GRCm39) |
V1521A |
possibly damaging |
Het |
Rap1gap |
T |
C |
4: 137,444,758 (GRCm39) |
F182S |
probably damaging |
Het |
Rcan2 |
A |
G |
17: 44,347,870 (GRCm39) |
K193R |
probably benign |
Het |
Rdh19 |
A |
T |
10: 127,692,755 (GRCm39) |
M141L |
probably benign |
Het |
Selenok |
C |
T |
14: 29,695,337 (GRCm39) |
R72* |
probably null |
Het |
Tbpl1 |
A |
G |
10: 22,587,807 (GRCm39) |
|
probably benign |
Het |
Tnxb |
A |
G |
17: 34,917,897 (GRCm39) |
E2270G |
possibly damaging |
Het |
Tulp1 |
A |
G |
17: 28,572,689 (GRCm39) |
V489A |
probably damaging |
Het |
Utp20 |
A |
T |
10: 88,611,065 (GRCm39) |
|
probably benign |
Het |
Zfp617 |
G |
A |
8: 72,685,961 (GRCm39) |
G97E |
probably damaging |
Het |
Zfp773 |
A |
G |
7: 7,135,390 (GRCm39) |
V402A |
possibly damaging |
Het |
|
Other mutations in 4921524L21Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01286:4921524L21Rik
|
APN |
18 |
6,629,578 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01402:4921524L21Rik
|
APN |
18 |
6,638,653 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01404:4921524L21Rik
|
APN |
18 |
6,638,653 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02680:4921524L21Rik
|
APN |
18 |
6,635,949 (GRCm39) |
splice site |
probably benign |
|
PIT4812001:4921524L21Rik
|
UTSW |
18 |
6,630,053 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0532:4921524L21Rik
|
UTSW |
18 |
6,638,618 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1069:4921524L21Rik
|
UTSW |
18 |
6,624,037 (GRCm39) |
missense |
probably benign |
0.01 |
R1706:4921524L21Rik
|
UTSW |
18 |
6,624,059 (GRCm39) |
splice site |
probably benign |
|
R1768:4921524L21Rik
|
UTSW |
18 |
6,623,470 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1912:4921524L21Rik
|
UTSW |
18 |
6,620,205 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3820:4921524L21Rik
|
UTSW |
18 |
6,630,166 (GRCm39) |
critical splice donor site |
probably null |
|
R3840:4921524L21Rik
|
UTSW |
18 |
6,620,104 (GRCm39) |
missense |
probably benign |
0.44 |
R4201:4921524L21Rik
|
UTSW |
18 |
6,623,952 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4852:4921524L21Rik
|
UTSW |
18 |
6,623,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R4852:4921524L21Rik
|
UTSW |
18 |
6,623,487 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5218:4921524L21Rik
|
UTSW |
18 |
6,629,628 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5389:4921524L21Rik
|
UTSW |
18 |
6,638,795 (GRCm39) |
missense |
probably benign |
0.14 |
R5428:4921524L21Rik
|
UTSW |
18 |
6,635,918 (GRCm39) |
missense |
probably benign |
0.04 |
R5873:4921524L21Rik
|
UTSW |
18 |
6,630,167 (GRCm39) |
critical splice donor site |
probably null |
|
R6120:4921524L21Rik
|
UTSW |
18 |
6,638,795 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6345:4921524L21Rik
|
UTSW |
18 |
6,626,399 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7246:4921524L21Rik
|
UTSW |
18 |
6,635,902 (GRCm39) |
missense |
probably damaging |
0.98 |
R7296:4921524L21Rik
|
UTSW |
18 |
6,626,385 (GRCm39) |
missense |
probably damaging |
0.99 |
R8796:4921524L21Rik
|
UTSW |
18 |
6,629,482 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8897:4921524L21Rik
|
UTSW |
18 |
6,635,934 (GRCm39) |
missense |
probably damaging |
0.98 |
R8930:4921524L21Rik
|
UTSW |
18 |
6,629,693 (GRCm39) |
critical splice donor site |
probably null |
|
R8932:4921524L21Rik
|
UTSW |
18 |
6,629,693 (GRCm39) |
critical splice donor site |
probably null |
|
R8991:4921524L21Rik
|
UTSW |
18 |
6,620,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R9108:4921524L21Rik
|
UTSW |
18 |
6,638,794 (GRCm39) |
missense |
probably benign |
0.04 |
R9235:4921524L21Rik
|
UTSW |
18 |
6,623,518 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9642:4921524L21Rik
|
UTSW |
18 |
6,619,412 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:4921524L21Rik
|
UTSW |
18 |
6,635,865 (GRCm39) |
missense |
probably benign |
0.00 |
|