Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013G24Rik |
A |
G |
4: 137,182,666 (GRCm39) |
N274D |
possibly damaging |
Het |
6430571L13Rik |
T |
A |
9: 107,219,689 (GRCm39) |
N47K |
probably damaging |
Het |
Aasdh |
C |
T |
5: 77,034,136 (GRCm39) |
A472T |
probably benign |
Het |
Abca13 |
A |
G |
11: 9,248,580 (GRCm39) |
T2776A |
probably damaging |
Het |
Adamts10 |
T |
A |
17: 33,764,613 (GRCm39) |
V711D |
probably damaging |
Het |
Adrb3 |
G |
A |
8: 27,717,415 (GRCm39) |
R345C |
probably damaging |
Het |
Ak7 |
T |
C |
12: 105,708,520 (GRCm39) |
V325A |
possibly damaging |
Het |
Armc6 |
G |
A |
8: 70,677,943 (GRCm39) |
L129F |
probably benign |
Het |
Bend6 |
T |
C |
1: 33,917,424 (GRCm39) |
N10S |
probably benign |
Het |
Bmpr1b |
T |
C |
3: 141,577,134 (GRCm39) |
E59G |
possibly damaging |
Het |
Brd3 |
A |
G |
2: 27,340,263 (GRCm39) |
|
probably null |
Het |
Brd3 |
A |
G |
2: 27,347,028 (GRCm39) |
Y369H |
probably damaging |
Het |
Cacna1e |
C |
T |
1: 154,361,408 (GRCm39) |
|
probably null |
Het |
Camk4 |
A |
G |
18: 33,072,528 (GRCm39) |
D27G |
probably damaging |
Het |
Camkk1 |
T |
G |
11: 72,924,710 (GRCm39) |
S308A |
probably damaging |
Het |
Catsperb |
A |
G |
12: 101,554,456 (GRCm39) |
T717A |
probably benign |
Het |
Cdh23 |
A |
T |
10: 60,212,730 (GRCm39) |
S1563R |
probably damaging |
Het |
Cep44 |
A |
T |
8: 56,993,985 (GRCm39) |
S197R |
probably benign |
Het |
Col3a1 |
T |
A |
1: 45,360,771 (GRCm39) |
I67N |
unknown |
Het |
Dcaf12l1 |
T |
C |
X: 43,878,304 (GRCm39) |
T165A |
probably benign |
Het |
Dicer1 |
T |
C |
12: 104,695,502 (GRCm39) |
Y143C |
possibly damaging |
Het |
Dlg5 |
A |
G |
14: 24,185,711 (GRCm39) |
I1898T |
possibly damaging |
Het |
Dnah1 |
T |
C |
14: 30,985,908 (GRCm39) |
N3762D |
probably damaging |
Het |
Dscaml1 |
A |
T |
9: 45,653,521 (GRCm39) |
T1382S |
possibly damaging |
Het |
Entpd3 |
A |
T |
9: 120,395,555 (GRCm39) |
R513W |
probably damaging |
Het |
Foxred1 |
A |
G |
9: 35,120,738 (GRCm39) |
S132P |
probably damaging |
Het |
Ftsj3 |
T |
C |
11: 106,143,826 (GRCm39) |
I273V |
probably benign |
Het |
Hsd17b7 |
C |
T |
1: 169,787,251 (GRCm39) |
|
probably null |
Het |
Iars1 |
T |
A |
13: 49,887,186 (GRCm39) |
V1253D |
probably damaging |
Het |
Iqsec1 |
T |
A |
6: 90,667,790 (GRCm39) |
K216* |
probably null |
Het |
Itga7 |
A |
G |
10: 128,789,370 (GRCm39) |
D971G |
probably benign |
Het |
Kcnk2 |
G |
A |
1: 189,072,223 (GRCm39) |
S35L |
probably benign |
Het |
Kif13a |
T |
C |
13: 46,966,212 (GRCm39) |
Y402C |
probably damaging |
Het |
Lamc1 |
A |
G |
1: 153,126,241 (GRCm39) |
S484P |
probably benign |
Het |
Lap3 |
T |
C |
5: 45,666,861 (GRCm39) |
|
probably null |
Het |
Lhx8 |
G |
T |
3: 154,033,742 (GRCm39) |
S46* |
probably null |
Het |
Lin7a |
T |
C |
10: 107,159,813 (GRCm39) |
S42P |
probably damaging |
Het |
Lrba |
G |
A |
3: 86,261,585 (GRCm39) |
R1513Q |
probably damaging |
Het |
Maml2 |
C |
A |
9: 13,531,980 (GRCm39) |
P398Q |
possibly damaging |
Het |
Mast2 |
T |
C |
4: 116,166,210 (GRCm39) |
I1201V |
probably damaging |
Het |
Mmp20 |
A |
T |
9: 7,642,769 (GRCm39) |
D201V |
probably damaging |
Het |
Morn5 |
T |
A |
2: 35,947,092 (GRCm39) |
C123* |
probably null |
Het |
Mrpl4 |
A |
G |
9: 20,918,807 (GRCm39) |
K175E |
possibly damaging |
Het |
Nav3 |
A |
T |
10: 109,689,372 (GRCm39) |
S302T |
probably benign |
Het |
Ndrg2 |
T |
C |
14: 52,145,591 (GRCm39) |
Y217C |
probably damaging |
Het |
Nfx1 |
A |
G |
4: 40,976,803 (GRCm39) |
D159G |
probably damaging |
Het |
Nlrp9b |
A |
T |
7: 19,757,089 (GRCm39) |
T109S |
possibly damaging |
Het |
Npepps |
A |
G |
11: 97,097,980 (GRCm39) |
Y909H |
probably benign |
Het |
Or10g1 |
A |
G |
14: 52,648,024 (GRCm39) |
C102R |
probably damaging |
Het |
Or11g7 |
A |
G |
14: 50,691,378 (GRCm39) |
N290D |
probably damaging |
Het |
Or51a25 |
A |
T |
7: 102,373,397 (GRCm39) |
F100Y |
probably damaging |
Het |
Or6c211 |
T |
A |
10: 129,506,238 (GRCm39) |
D50V |
probably damaging |
Het |
Or6c69b |
A |
C |
10: 129,626,723 (GRCm39) |
V245G |
probably damaging |
Het |
Pcdh1 |
T |
C |
18: 38,322,929 (GRCm39) |
H968R |
probably damaging |
Het |
Pde1b |
T |
A |
15: 103,433,470 (GRCm39) |
I296N |
probably damaging |
Het |
Phldb1 |
T |
A |
9: 44,627,930 (GRCm39) |
T172S |
probably benign |
Het |
Plxdc2 |
T |
C |
2: 16,665,592 (GRCm39) |
V215A |
possibly damaging |
Het |
Poln |
A |
G |
5: 34,171,682 (GRCm39) |
I695T |
probably damaging |
Het |
Pou6f2 |
G |
T |
13: 18,347,000 (GRCm39) |
Q31K |
probably damaging |
Het |
Psd |
T |
A |
19: 46,313,250 (GRCm39) |
Y40F |
probably damaging |
Het |
Rnf126 |
T |
C |
10: 79,597,448 (GRCm39) |
N155D |
probably benign |
Het |
Rpl36-ps3 |
C |
A |
12: 12,962,032 (GRCm39) |
|
noncoding transcript |
Het |
Rrp15 |
C |
A |
1: 186,468,465 (GRCm39) |
V184F |
possibly damaging |
Het |
Rslcan18 |
G |
T |
13: 67,250,164 (GRCm39) |
L24M |
possibly damaging |
Het |
Sall1 |
A |
G |
8: 89,759,111 (GRCm39) |
I331T |
probably benign |
Het |
Slamf7 |
A |
T |
1: 171,468,606 (GRCm39) |
N95K |
possibly damaging |
Het |
Slc1a6 |
T |
C |
10: 78,635,951 (GRCm39) |
Y339H |
probably damaging |
Het |
Slc39a8 |
A |
G |
3: 135,532,446 (GRCm39) |
N72D |
probably benign |
Het |
Slf1 |
A |
G |
13: 77,231,568 (GRCm39) |
S604P |
probably damaging |
Het |
Slfn4 |
C |
T |
11: 83,079,819 (GRCm39) |
T110M |
probably benign |
Het |
Tnpo1 |
T |
C |
13: 99,015,220 (GRCm39) |
T116A |
probably damaging |
Het |
Tor1b |
T |
C |
2: 30,845,893 (GRCm39) |
I190T |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,800,138 (GRCm39) |
E357* |
probably null |
Het |
Tubg2 |
G |
T |
11: 101,047,699 (GRCm39) |
E95* |
probably null |
Het |
Ube2i |
T |
C |
17: 25,487,538 (GRCm39) |
D67G |
possibly damaging |
Het |
Ubxn11 |
A |
G |
4: 133,852,203 (GRCm39) |
E50G |
probably damaging |
Het |
Wnk1 |
A |
G |
6: 119,929,779 (GRCm39) |
V1246A |
probably damaging |
Het |
Zcchc7 |
A |
G |
4: 44,929,124 (GRCm39) |
T38A |
possibly damaging |
Het |
Zfp236 |
A |
G |
18: 82,664,130 (GRCm39) |
S552P |
probably damaging |
Het |
|
Other mutations in Ubap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01011:Ubap2
|
APN |
4 |
41,195,328 (GRCm39) |
splice site |
probably benign |
|
IGL01109:Ubap2
|
APN |
4 |
41,195,155 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01354:Ubap2
|
APN |
4 |
41,207,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01563:Ubap2
|
APN |
4 |
41,195,998 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01602:Ubap2
|
APN |
4 |
41,227,237 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01605:Ubap2
|
APN |
4 |
41,227,237 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01688:Ubap2
|
APN |
4 |
41,226,308 (GRCm39) |
missense |
probably benign |
|
IGL01733:Ubap2
|
APN |
4 |
41,195,862 (GRCm39) |
unclassified |
probably benign |
|
IGL01896:Ubap2
|
APN |
4 |
41,202,362 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01942:Ubap2
|
APN |
4 |
41,251,608 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02095:Ubap2
|
APN |
4 |
41,229,709 (GRCm39) |
missense |
probably benign |
|
R0608:Ubap2
|
UTSW |
4 |
41,218,319 (GRCm39) |
missense |
probably benign |
0.10 |
R0938:Ubap2
|
UTSW |
4 |
41,202,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Ubap2
|
UTSW |
4 |
41,235,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R1548:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R1549:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R1604:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R1607:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R1739:Ubap2
|
UTSW |
4 |
41,206,849 (GRCm39) |
missense |
probably benign |
0.00 |
R1772:Ubap2
|
UTSW |
4 |
41,202,380 (GRCm39) |
missense |
probably benign |
0.02 |
R1862:Ubap2
|
UTSW |
4 |
41,221,607 (GRCm39) |
missense |
probably benign |
|
R1869:Ubap2
|
UTSW |
4 |
41,233,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R1886:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R1887:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R2063:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R2064:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R2065:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R2066:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R2095:Ubap2
|
UTSW |
4 |
41,206,901 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2214:Ubap2
|
UTSW |
4 |
41,199,714 (GRCm39) |
critical splice donor site |
probably null |
|
R2215:Ubap2
|
UTSW |
4 |
41,196,483 (GRCm39) |
splice site |
probably null |
|
R2318:Ubap2
|
UTSW |
4 |
41,251,542 (GRCm39) |
missense |
probably damaging |
0.99 |
R3755:Ubap2
|
UTSW |
4 |
41,195,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R4620:Ubap2
|
UTSW |
4 |
41,233,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R4717:Ubap2
|
UTSW |
4 |
41,218,333 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4756:Ubap2
|
UTSW |
4 |
41,211,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R4942:Ubap2
|
UTSW |
4 |
41,245,461 (GRCm39) |
intron |
probably benign |
|
R5344:Ubap2
|
UTSW |
4 |
41,251,578 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5763:Ubap2
|
UTSW |
4 |
41,195,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R5851:Ubap2
|
UTSW |
4 |
41,206,268 (GRCm39) |
nonsense |
probably null |
|
R5951:Ubap2
|
UTSW |
4 |
41,205,753 (GRCm39) |
splice site |
probably null |
|
R6178:Ubap2
|
UTSW |
4 |
41,206,981 (GRCm39) |
missense |
probably benign |
|
R6489:Ubap2
|
UTSW |
4 |
41,203,574 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6520:Ubap2
|
UTSW |
4 |
41,195,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6652:Ubap2
|
UTSW |
4 |
41,196,743 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6702:Ubap2
|
UTSW |
4 |
41,227,210 (GRCm39) |
small insertion |
probably benign |
|
R6736:Ubap2
|
UTSW |
4 |
41,227,224 (GRCm39) |
small insertion |
probably benign |
|
R6736:Ubap2
|
UTSW |
4 |
41,227,210 (GRCm39) |
small insertion |
probably benign |
|
R6860:Ubap2
|
UTSW |
4 |
41,233,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R7007:Ubap2
|
UTSW |
4 |
41,206,221 (GRCm39) |
missense |
probably damaging |
0.97 |
R7048:Ubap2
|
UTSW |
4 |
41,196,033 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7121:Ubap2
|
UTSW |
4 |
41,205,550 (GRCm39) |
missense |
probably benign |
0.00 |
R7371:Ubap2
|
UTSW |
4 |
41,195,779 (GRCm39) |
missense |
probably benign |
0.16 |
R7378:Ubap2
|
UTSW |
4 |
41,235,515 (GRCm39) |
critical splice donor site |
probably null |
|
R7695:Ubap2
|
UTSW |
4 |
41,211,740 (GRCm39) |
missense |
probably damaging |
0.98 |
R7811:Ubap2
|
UTSW |
4 |
41,211,710 (GRCm39) |
missense |
probably benign |
0.22 |
R7828:Ubap2
|
UTSW |
4 |
41,221,615 (GRCm39) |
missense |
probably benign |
0.00 |
R7838:Ubap2
|
UTSW |
4 |
41,233,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R8016:Ubap2
|
UTSW |
4 |
41,195,201 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8790:Ubap2
|
UTSW |
4 |
41,209,351 (GRCm39) |
critical splice donor site |
probably null |
|
R8817:Ubap2
|
UTSW |
4 |
41,223,425 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9379:Ubap2
|
UTSW |
4 |
41,216,630 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9470:Ubap2
|
UTSW |
4 |
41,195,434 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9536:Ubap2
|
UTSW |
4 |
41,195,661 (GRCm39) |
missense |
probably benign |
0.01 |
X0061:Ubap2
|
UTSW |
4 |
41,196,507 (GRCm39) |
missense |
probably damaging |
1.00 |
|