Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agl |
A |
G |
3: 116,574,384 (GRCm39) |
C767R |
probably benign |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Ap3d1 |
A |
T |
10: 80,551,775 (GRCm39) |
I644N |
probably benign |
Het |
Asb16 |
A |
G |
11: 102,163,402 (GRCm39) |
I131V |
probably benign |
Het |
Atp6v0a2 |
C |
A |
5: 124,784,638 (GRCm39) |
A307D |
probably damaging |
Het |
C1qtnf1 |
C |
T |
11: 118,338,749 (GRCm39) |
H140Y |
probably benign |
Het |
Cacna1g |
T |
A |
11: 94,347,865 (GRCm39) |
D741V |
probably damaging |
Het |
Caprin2 |
T |
A |
6: 148,777,969 (GRCm39) |
T211S |
probably benign |
Het |
Carmil1 |
T |
C |
13: 24,283,037 (GRCm39) |
E89G |
possibly damaging |
Het |
Casz1 |
T |
A |
4: 149,027,357 (GRCm39) |
|
probably benign |
Het |
Catsperb |
G |
A |
12: 101,378,589 (GRCm39) |
R30Q |
probably benign |
Het |
Ccdc102a |
A |
T |
8: 95,634,341 (GRCm39) |
|
probably null |
Het |
Ccdc110 |
G |
T |
8: 46,395,362 (GRCm39) |
E418* |
probably null |
Het |
Ccdc90b |
C |
T |
7: 92,231,024 (GRCm39) |
A210V |
probably benign |
Het |
Cdadc1 |
G |
T |
14: 59,823,532 (GRCm39) |
A320E |
probably damaging |
Het |
Cdadc1 |
T |
A |
14: 59,823,541 (GRCm39) |
Q317L |
probably damaging |
Het |
Cep170 |
C |
A |
1: 176,567,498 (GRCm39) |
W1396L |
probably damaging |
Het |
Col4a6 |
T |
C |
X: 140,010,854 (GRCm39) |
T129A |
probably damaging |
Het |
Dclk1 |
T |
C |
3: 55,385,244 (GRCm39) |
S45P |
probably damaging |
Het |
Efcab3 |
T |
C |
11: 104,999,726 (GRCm39) |
I5581T |
probably benign |
Het |
Evi2 |
T |
C |
11: 79,406,412 (GRCm39) |
I388V |
probably benign |
Het |
Fbxl5 |
A |
T |
5: 43,915,978 (GRCm39) |
V435E |
possibly damaging |
Het |
Fig4 |
A |
T |
10: 41,064,582 (GRCm39) |
M887K |
possibly damaging |
Het |
Glt8d1 |
G |
A |
14: 30,733,549 (GRCm39) |
V345I |
probably benign |
Het |
Gm5709 |
T |
C |
3: 59,526,073 (GRCm39) |
|
noncoding transcript |
Het |
Hsp90b1 |
A |
G |
10: 86,529,906 (GRCm39) |
F264L |
probably damaging |
Het |
Id3 |
A |
G |
4: 135,871,250 (GRCm39) |
S21G |
possibly damaging |
Het |
Ighe |
T |
A |
12: 113,235,066 (GRCm39) |
N365Y |
unknown |
Het |
Il17rd |
T |
G |
14: 26,821,915 (GRCm39) |
M403R |
probably damaging |
Het |
Ints10 |
A |
G |
8: 69,249,365 (GRCm39) |
|
probably benign |
Het |
Kcnc4 |
T |
A |
3: 107,352,743 (GRCm39) |
|
probably null |
Het |
Kctd19 |
A |
G |
8: 106,114,511 (GRCm39) |
S517P |
probably damaging |
Het |
Lama5 |
A |
G |
2: 179,821,944 (GRCm39) |
F2964L |
probably benign |
Het |
Lin54 |
A |
T |
5: 100,628,109 (GRCm39) |
N31K |
probably damaging |
Het |
Lrrc8e |
A |
G |
8: 4,284,990 (GRCm39) |
K405R |
probably benign |
Het |
Lyst |
T |
A |
13: 13,809,686 (GRCm39) |
M452K |
possibly damaging |
Het |
Mroh7 |
A |
G |
4: 106,560,273 (GRCm39) |
L677P |
probably benign |
Het |
Mrps27 |
T |
A |
13: 99,541,558 (GRCm39) |
F221I |
probably benign |
Het |
Nhlrc1 |
C |
T |
13: 47,167,820 (GRCm39) |
V146M |
probably damaging |
Het |
Nlrp9b |
T |
A |
7: 19,782,772 (GRCm39) |
C895* |
probably null |
Het |
Nod1 |
T |
C |
6: 54,920,960 (GRCm39) |
T453A |
probably benign |
Het |
Nodal |
T |
C |
10: 61,258,764 (GRCm39) |
V67A |
probably damaging |
Het |
Ntsr1 |
T |
C |
2: 180,184,440 (GRCm39) |
L381P |
probably damaging |
Het |
Or13c25 |
T |
C |
4: 52,910,996 (GRCm39) |
D266G |
probably benign |
Het |
Or2b2b |
T |
A |
13: 21,858,700 (GRCm39) |
Q138L |
probably benign |
Het |
Or9e1 |
T |
A |
11: 58,732,477 (GRCm39) |
M179K |
probably benign |
Het |
P2ry14 |
T |
A |
3: 59,022,686 (GRCm39) |
K267M |
probably benign |
Het |
Pcdh1 |
T |
C |
18: 38,322,779 (GRCm39) |
N1018S |
probably benign |
Het |
Pkn3 |
G |
A |
2: 29,974,703 (GRCm39) |
V406I |
probably damaging |
Het |
Prkcb |
C |
T |
7: 122,226,916 (GRCm39) |
T634I |
probably damaging |
Het |
Psme2b |
T |
A |
11: 48,836,209 (GRCm39) |
|
probably null |
Het |
Ptgfrn |
A |
G |
3: 100,967,970 (GRCm39) |
I541T |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Ralgapb |
T |
C |
2: 158,307,746 (GRCm39) |
V684A |
probably benign |
Het |
Rbbp5 |
C |
T |
1: 132,422,020 (GRCm39) |
R307* |
probably null |
Het |
Rcor1 |
T |
A |
12: 111,070,037 (GRCm39) |
|
probably benign |
Het |
Rlbp1 |
C |
T |
7: 79,029,808 (GRCm39) |
A142T |
probably damaging |
Het |
Rps6ka2 |
A |
G |
17: 7,560,305 (GRCm39) |
E581G |
probably null |
Het |
Sars1 |
A |
T |
3: 108,340,461 (GRCm39) |
V155E |
probably benign |
Het |
Sec31a |
G |
C |
5: 100,523,178 (GRCm39) |
P569A |
probably damaging |
Het |
Selenof |
A |
T |
3: 144,300,685 (GRCm39) |
K111* |
probably null |
Het |
Serpinb7 |
C |
T |
1: 107,355,998 (GRCm39) |
A7V |
possibly damaging |
Het |
Smc4 |
T |
A |
3: 68,924,105 (GRCm39) |
Y298N |
probably damaging |
Het |
Snrpa1 |
T |
A |
7: 65,720,409 (GRCm39) |
I204N |
probably damaging |
Het |
Spry4 |
T |
G |
18: 38,734,740 (GRCm39) |
|
probably benign |
Het |
Tcea2 |
A |
G |
2: 181,328,751 (GRCm39) |
N261S |
possibly damaging |
Het |
Tmem59l |
A |
G |
8: 70,937,804 (GRCm39) |
F192S |
probably benign |
Het |
Tnr |
T |
A |
1: 159,677,675 (GRCm39) |
I20N |
probably damaging |
Het |
Ttll5 |
C |
T |
12: 85,938,982 (GRCm39) |
Q427* |
probably null |
Het |
Vps45 |
C |
T |
3: 95,955,658 (GRCm39) |
A111T |
probably damaging |
Het |
Zfp395 |
T |
C |
14: 65,630,523 (GRCm39) |
S358P |
probably benign |
Het |
Zfp438 |
A |
G |
18: 5,210,740 (GRCm39) |
V766A |
probably benign |
Het |
|
Other mutations in Ctcfl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01344:Ctcfl
|
APN |
2 |
172,936,527 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01418:Ctcfl
|
APN |
2 |
172,960,124 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01524:Ctcfl
|
APN |
2 |
172,959,177 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02610:Ctcfl
|
APN |
2 |
172,947,819 (GRCm39) |
splice site |
probably benign |
|
IGL02961:Ctcfl
|
APN |
2 |
172,943,712 (GRCm39) |
missense |
possibly damaging |
0.70 |
BB001:Ctcfl
|
UTSW |
2 |
172,955,449 (GRCm39) |
missense |
possibly damaging |
0.71 |
BB011:Ctcfl
|
UTSW |
2 |
172,955,449 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0147:Ctcfl
|
UTSW |
2 |
172,960,340 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0148:Ctcfl
|
UTSW |
2 |
172,960,340 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0362:Ctcfl
|
UTSW |
2 |
172,960,236 (GRCm39) |
missense |
probably damaging |
0.99 |
R1099:Ctcfl
|
UTSW |
2 |
172,954,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1892:Ctcfl
|
UTSW |
2 |
172,960,478 (GRCm39) |
missense |
probably benign |
0.24 |
R2036:Ctcfl
|
UTSW |
2 |
172,943,778 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2060:Ctcfl
|
UTSW |
2 |
172,960,299 (GRCm39) |
missense |
probably benign |
0.00 |
R2925:Ctcfl
|
UTSW |
2 |
172,936,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4327:Ctcfl
|
UTSW |
2 |
172,955,299 (GRCm39) |
intron |
probably benign |
|
R4837:Ctcfl
|
UTSW |
2 |
172,955,449 (GRCm39) |
missense |
probably benign |
0.00 |
R4894:Ctcfl
|
UTSW |
2 |
172,959,196 (GRCm39) |
missense |
probably benign |
0.19 |
R4909:Ctcfl
|
UTSW |
2 |
172,937,191 (GRCm39) |
missense |
probably benign |
0.42 |
R5128:Ctcfl
|
UTSW |
2 |
172,959,189 (GRCm39) |
missense |
probably benign |
0.00 |
R5247:Ctcfl
|
UTSW |
2 |
172,955,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R6263:Ctcfl
|
UTSW |
2 |
172,937,130 (GRCm39) |
missense |
probably benign |
0.00 |
R6768:Ctcfl
|
UTSW |
2 |
172,959,084 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7045:Ctcfl
|
UTSW |
2 |
172,954,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R7180:Ctcfl
|
UTSW |
2 |
172,947,770 (GRCm39) |
splice site |
probably null |
|
R7256:Ctcfl
|
UTSW |
2 |
172,960,268 (GRCm39) |
missense |
probably benign |
0.01 |
R7268:Ctcfl
|
UTSW |
2 |
172,949,588 (GRCm39) |
missense |
probably benign |
0.26 |
R7378:Ctcfl
|
UTSW |
2 |
172,954,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R7560:Ctcfl
|
UTSW |
2 |
172,960,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R7657:Ctcfl
|
UTSW |
2 |
172,955,449 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7733:Ctcfl
|
UTSW |
2 |
172,958,985 (GRCm39) |
missense |
probably benign |
|
R7924:Ctcfl
|
UTSW |
2 |
172,955,449 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7945:Ctcfl
|
UTSW |
2 |
172,960,451 (GRCm39) |
missense |
probably benign |
|
R8022:Ctcfl
|
UTSW |
2 |
172,960,559 (GRCm39) |
missense |
probably benign |
0.15 |
R8038:Ctcfl
|
UTSW |
2 |
172,943,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R8911:Ctcfl
|
UTSW |
2 |
172,937,121 (GRCm39) |
critical splice donor site |
probably null |
|
R9031:Ctcfl
|
UTSW |
2 |
172,959,044 (GRCm39) |
missense |
probably benign |
0.07 |
R9358:Ctcfl
|
UTSW |
2 |
172,960,581 (GRCm39) |
start codon destroyed |
possibly damaging |
0.81 |
R9401:Ctcfl
|
UTSW |
2 |
172,947,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R9490:Ctcfl
|
UTSW |
2 |
172,960,548 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Ctcfl
|
UTSW |
2 |
172,960,137 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Ctcfl
|
UTSW |
2 |
172,943,829 (GRCm39) |
missense |
probably benign |
0.00 |
|