Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430110L20Rik |
A |
G |
1: 181,055,384 (GRCm39) |
|
noncoding transcript |
Het |
Acp2 |
A |
T |
2: 91,041,068 (GRCm39) |
R419W |
probably benign |
Het |
Actr5 |
A |
G |
2: 158,469,991 (GRCm39) |
N207S |
probably damaging |
Het |
Afap1 |
G |
A |
5: 36,119,126 (GRCm39) |
V254M |
probably benign |
Het |
Arfgef1 |
A |
T |
1: 10,259,836 (GRCm39) |
M544K |
possibly damaging |
Het |
Arhgap5 |
A |
T |
12: 52,565,860 (GRCm39) |
M944L |
probably benign |
Het |
Bnip3l-ps |
G |
A |
12: 18,266,773 (GRCm39) |
|
noncoding transcript |
Het |
Carf |
A |
G |
1: 60,148,477 (GRCm39) |
T58A |
probably benign |
Het |
Carns1 |
A |
G |
19: 4,220,927 (GRCm39) |
|
probably benign |
Het |
Ccp110 |
T |
A |
7: 118,323,771 (GRCm39) |
I670K |
possibly damaging |
Het |
Cftr |
T |
A |
6: 18,299,882 (GRCm39) |
D1218E |
probably benign |
Het |
Chrna9 |
A |
T |
5: 66,125,214 (GRCm39) |
T52S |
probably damaging |
Het |
Chst9 |
T |
C |
18: 15,585,834 (GRCm39) |
Y243C |
probably damaging |
Het |
Ciao3 |
A |
T |
17: 26,000,283 (GRCm39) |
H322L |
probably damaging |
Het |
Cilk1 |
A |
G |
9: 78,057,936 (GRCm39) |
T162A |
probably damaging |
Het |
Clk2 |
A |
T |
3: 89,076,016 (GRCm39) |
H62L |
probably benign |
Het |
Cntnap2 |
A |
T |
6: 45,037,251 (GRCm39) |
R10W |
possibly damaging |
Het |
Cpt1b |
C |
T |
15: 89,305,609 (GRCm39) |
D369N |
probably benign |
Het |
Crhr2 |
G |
T |
6: 55,068,290 (GRCm39) |
H423Q |
probably damaging |
Het |
D8Ertd738e |
T |
A |
8: 84,976,150 (GRCm39) |
I33F |
probably damaging |
Het |
Dbt |
T |
C |
3: 116,332,781 (GRCm39) |
I200T |
probably damaging |
Het |
Ddhd1 |
A |
T |
14: 45,866,278 (GRCm39) |
|
probably benign |
Het |
Ddx27 |
A |
G |
2: 166,871,219 (GRCm39) |
I480V |
probably benign |
Het |
Dpp9 |
A |
C |
17: 56,505,970 (GRCm39) |
|
probably null |
Het |
Dpy19l3 |
A |
T |
7: 35,402,926 (GRCm39) |
M562K |
probably damaging |
Het |
Dus3l |
T |
C |
17: 57,074,868 (GRCm39) |
L330P |
probably damaging |
Het |
Egfr |
T |
C |
11: 16,819,231 (GRCm39) |
F254L |
probably damaging |
Het |
Eml5 |
C |
T |
12: 98,765,111 (GRCm39) |
V1566M |
probably damaging |
Het |
Entpd7 |
T |
A |
19: 43,679,634 (GRCm39) |
Y62* |
probably null |
Het |
Erbb4 |
T |
C |
1: 68,383,059 (GRCm39) |
M313V |
probably damaging |
Het |
Gm5528 |
A |
G |
1: 72,043,711 (GRCm39) |
|
noncoding transcript |
Het |
H2-M9 |
G |
T |
17: 36,951,631 (GRCm39) |
Y281* |
probably null |
Het |
Hmcn1 |
T |
G |
1: 150,565,346 (GRCm39) |
K2260N |
possibly damaging |
Het |
Hnf4a |
A |
G |
2: 163,406,139 (GRCm39) |
I259V |
probably benign |
Het |
Insm1 |
A |
T |
2: 146,064,822 (GRCm39) |
T213S |
probably benign |
Het |
Iqca1 |
T |
C |
1: 90,005,544 (GRCm39) |
D488G |
probably damaging |
Het |
Kdm5a |
T |
A |
6: 120,382,976 (GRCm39) |
|
probably benign |
Het |
Kdm7a |
G |
C |
6: 39,129,773 (GRCm39) |
L468V |
possibly damaging |
Het |
Lck |
G |
A |
4: 129,449,777 (GRCm39) |
T229I |
possibly damaging |
Het |
Lig3 |
T |
C |
11: 82,678,553 (GRCm39) |
L265P |
probably damaging |
Het |
Lipa |
T |
A |
19: 34,479,034 (GRCm39) |
K229* |
probably null |
Het |
Lrrk1 |
C |
T |
7: 65,956,621 (GRCm39) |
S418N |
probably benign |
Het |
Mark2 |
A |
G |
19: 7,258,597 (GRCm39) |
V126A |
probably damaging |
Het |
Met |
T |
C |
6: 17,491,540 (GRCm39) |
C101R |
probably damaging |
Het |
Mkln1 |
A |
T |
6: 31,403,734 (GRCm39) |
K85M |
probably damaging |
Het |
Mst1 |
A |
G |
9: 107,957,720 (GRCm39) |
R15G |
probably benign |
Het |
Muc6 |
T |
G |
7: 141,226,426 (GRCm39) |
|
probably benign |
Het |
Muc6 |
G |
T |
7: 141,218,685 (GRCm39) |
T1996N |
possibly damaging |
Het |
Myo7b |
T |
C |
18: 32,131,655 (GRCm39) |
S514G |
probably damaging |
Het |
Nars1 |
T |
C |
18: 64,649,498 (GRCm39) |
E11G |
probably benign |
Het |
Ogdh |
T |
A |
11: 6,247,044 (GRCm39) |
F23I |
probably benign |
Het |
Or10g9 |
A |
T |
9: 39,911,718 (GRCm39) |
D268E |
probably damaging |
Het |
Or12e9 |
T |
C |
2: 87,202,665 (GRCm39) |
I263T |
probably damaging |
Het |
Or4a39 |
C |
T |
2: 89,236,830 (GRCm39) |
V198I |
probably benign |
Het |
Or4b1b |
A |
G |
2: 90,112,725 (GRCm39) |
S65P |
probably damaging |
Het |
Or4c100 |
C |
T |
2: 88,356,569 (GRCm39) |
S214F |
probably damaging |
Het |
Or52r1c |
C |
T |
7: 102,735,121 (GRCm39) |
A127V |
probably damaging |
Het |
Or9k2 |
T |
A |
10: 129,998,707 (GRCm39) |
T163S |
probably benign |
Het |
Otub2 |
T |
A |
12: 103,359,103 (GRCm39) |
L64Q |
probably benign |
Het |
Pappa2 |
T |
C |
1: 158,784,582 (GRCm39) |
R143G |
probably benign |
Het |
Patl2 |
T |
A |
2: 121,955,787 (GRCm39) |
T250S |
probably damaging |
Het |
Pcdhac2 |
C |
T |
18: 37,278,952 (GRCm39) |
T644I |
possibly damaging |
Het |
Pi4kb |
C |
T |
3: 94,911,649 (GRCm39) |
T690I |
probably damaging |
Het |
Pla2g4d |
T |
C |
2: 120,097,271 (GRCm39) |
Y776C |
probably benign |
Het |
Plekhh2 |
C |
T |
17: 84,871,387 (GRCm39) |
S215L |
probably benign |
Het |
Psmd2 |
T |
G |
16: 20,478,565 (GRCm39) |
|
probably benign |
Het |
Ptpn21 |
T |
C |
12: 98,675,103 (GRCm39) |
E183G |
probably benign |
Het |
Ptprg |
T |
A |
14: 12,226,314 (GRCm38) |
D527E |
probably damaging |
Het |
Rhobtb1 |
T |
A |
10: 69,115,327 (GRCm39) |
|
probably null |
Het |
Scel |
T |
A |
14: 103,809,473 (GRCm39) |
M271K |
possibly damaging |
Het |
Senp3 |
A |
T |
11: 69,569,655 (GRCm39) |
C310* |
probably null |
Het |
Slc25a3 |
T |
C |
10: 90,958,050 (GRCm39) |
T97A |
possibly damaging |
Het |
Srsf11 |
A |
T |
3: 157,732,369 (GRCm39) |
Y82* |
probably null |
Het |
Tbc1d8 |
G |
A |
1: 39,441,959 (GRCm39) |
T211I |
possibly damaging |
Het |
Tbkbp1 |
T |
C |
11: 97,039,474 (GRCm39) |
E145G |
probably damaging |
Het |
Tln1 |
T |
C |
4: 43,540,588 (GRCm39) |
N1471S |
probably benign |
Het |
Tnn |
T |
G |
1: 159,973,659 (GRCm39) |
D236A |
probably damaging |
Het |
Trmt2a |
C |
T |
16: 18,069,150 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Ubxn10 |
G |
A |
4: 138,463,259 (GRCm39) |
|
probably benign |
Het |
Ulk4 |
G |
A |
9: 120,902,938 (GRCm39) |
Q1180* |
probably null |
Het |
Usp43 |
T |
A |
11: 67,746,331 (GRCm39) |
K1120N |
probably damaging |
Het |
Uspl1 |
T |
A |
5: 149,131,149 (GRCm39) |
L244Q |
possibly damaging |
Het |
Vmn1r32 |
T |
C |
6: 66,530,629 (GRCm39) |
H49R |
probably damaging |
Het |
Vmn2r4 |
T |
C |
3: 64,317,384 (GRCm39) |
D118G |
probably damaging |
Het |
Vwce |
A |
G |
19: 10,627,943 (GRCm39) |
I468V |
probably benign |
Het |
Zbtb7c |
G |
T |
18: 76,279,225 (GRCm39) |
R561L |
probably benign |
Het |
Zfp956 |
T |
C |
6: 47,939,476 (GRCm39) |
S175P |
probably damaging |
Het |
|
Other mutations in Efcab7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00492:Efcab7
|
APN |
4 |
99,719,700 (GRCm39) |
missense |
probably benign |
0.12 |
3-1:Efcab7
|
UTSW |
4 |
99,758,966 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0023:Efcab7
|
UTSW |
4 |
99,758,834 (GRCm39) |
splice site |
probably benign |
|
R0085:Efcab7
|
UTSW |
4 |
99,761,877 (GRCm39) |
unclassified |
probably benign |
|
R0122:Efcab7
|
UTSW |
4 |
99,749,560 (GRCm39) |
splice site |
probably benign |
|
R0326:Efcab7
|
UTSW |
4 |
99,719,631 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0382:Efcab7
|
UTSW |
4 |
99,758,966 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0410:Efcab7
|
UTSW |
4 |
99,735,487 (GRCm39) |
critical splice donor site |
probably null |
|
R0413:Efcab7
|
UTSW |
4 |
99,766,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R0611:Efcab7
|
UTSW |
4 |
99,758,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R0689:Efcab7
|
UTSW |
4 |
99,761,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R1114:Efcab7
|
UTSW |
4 |
99,735,452 (GRCm39) |
nonsense |
probably null |
|
R1459:Efcab7
|
UTSW |
4 |
99,769,744 (GRCm39) |
missense |
probably null |
1.00 |
R1722:Efcab7
|
UTSW |
4 |
99,757,815 (GRCm39) |
missense |
probably benign |
0.36 |
R1932:Efcab7
|
UTSW |
4 |
99,768,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Efcab7
|
UTSW |
4 |
99,757,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R2305:Efcab7
|
UTSW |
4 |
99,719,718 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2358:Efcab7
|
UTSW |
4 |
99,719,823 (GRCm39) |
unclassified |
probably benign |
|
R2845:Efcab7
|
UTSW |
4 |
99,766,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R3915:Efcab7
|
UTSW |
4 |
99,735,375 (GRCm39) |
missense |
probably damaging |
0.98 |
R4469:Efcab7
|
UTSW |
4 |
99,766,901 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4686:Efcab7
|
UTSW |
4 |
99,735,318 (GRCm39) |
missense |
probably benign |
0.29 |
R4970:Efcab7
|
UTSW |
4 |
99,719,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R5120:Efcab7
|
UTSW |
4 |
99,754,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R5264:Efcab7
|
UTSW |
4 |
99,735,372 (GRCm39) |
missense |
probably benign |
0.27 |
R5366:Efcab7
|
UTSW |
4 |
99,761,931 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5901:Efcab7
|
UTSW |
4 |
99,766,941 (GRCm39) |
missense |
probably damaging |
0.99 |
R6255:Efcab7
|
UTSW |
4 |
99,717,627 (GRCm39) |
unclassified |
probably benign |
|
R6438:Efcab7
|
UTSW |
4 |
99,766,969 (GRCm39) |
missense |
probably benign |
0.39 |
R6451:Efcab7
|
UTSW |
4 |
99,719,738 (GRCm39) |
nonsense |
probably null |
|
R6717:Efcab7
|
UTSW |
4 |
99,761,931 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6766:Efcab7
|
UTSW |
4 |
99,735,161 (GRCm39) |
frame shift |
probably null |
|
R6855:Efcab7
|
UTSW |
4 |
99,757,777 (GRCm39) |
nonsense |
probably null |
|
R6865:Efcab7
|
UTSW |
4 |
99,769,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R7868:Efcab7
|
UTSW |
4 |
99,746,154 (GRCm39) |
missense |
probably benign |
0.01 |
R7893:Efcab7
|
UTSW |
4 |
99,746,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R8069:Efcab7
|
UTSW |
4 |
99,717,615 (GRCm39) |
missense |
unknown |
|
R8787:Efcab7
|
UTSW |
4 |
99,757,791 (GRCm39) |
missense |
probably null |
0.99 |
R9214:Efcab7
|
UTSW |
4 |
99,735,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R9649:Efcab7
|
UTSW |
4 |
99,761,902 (GRCm39) |
missense |
probably damaging |
0.99 |
|