Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
C |
G |
10: 100,603,528 (GRCm38) |
P187R |
probably damaging |
Het |
Ahnak |
T |
A |
19: 9,009,963 (GRCm38) |
H2870Q |
probably benign |
Het |
Arhgef33 |
C |
T |
17: 80,347,651 (GRCm38) |
S95F |
probably damaging |
Het |
Atp1a2 |
T |
A |
1: 172,278,954 (GRCm38) |
D827V |
probably damaging |
Het |
Bcat1 |
T |
G |
6: 145,039,628 (GRCm38) |
D96A |
probably damaging |
Het |
Birc6 |
A |
T |
17: 74,548,746 (GRCm38) |
I184L |
probably benign |
Het |
Ccdc129 |
C |
T |
6: 55,968,766 (GRCm38) |
T824I |
probably damaging |
Het |
Clca3b |
A |
T |
3: 144,837,824 (GRCm38) |
L415M |
probably damaging |
Het |
Clstn1 |
T |
C |
4: 149,643,726 (GRCm38) |
V617A |
probably benign |
Het |
Col22a1 |
G |
A |
15: 71,799,361 (GRCm38) |
A1050V |
unknown |
Het |
Col5a3 |
C |
T |
9: 20,784,668 (GRCm38) |
|
probably null |
Het |
Csmd3 |
G |
A |
15: 47,741,170 (GRCm38) |
T1059I |
probably damaging |
Het |
Dclk2 |
C |
T |
3: 86,805,639 (GRCm38) |
R503Q |
possibly damaging |
Het |
Dnm3 |
A |
G |
1: 162,010,976 (GRCm38) |
V272A |
probably benign |
Het |
Dnmt3a |
A |
G |
12: 3,873,361 (GRCm38) |
Q187R |
probably damaging |
Het |
Dpp9 |
A |
G |
17: 56,190,103 (GRCm38) |
Y710H |
probably benign |
Het |
Eef1a2 |
A |
T |
2: 181,152,941 (GRCm38) |
M155K |
possibly damaging |
Het |
Entpd8 |
G |
A |
2: 25,084,024 (GRCm38) |
C331Y |
probably damaging |
Het |
Erc1 |
A |
C |
6: 119,575,761 (GRCm38) |
L1072R |
probably damaging |
Het |
Fam160b2 |
T |
C |
14: 70,586,851 (GRCm38) |
Y482C |
probably damaging |
Het |
Gtf3c2 |
A |
G |
5: 31,173,868 (GRCm38) |
S155P |
probably damaging |
Het |
Gucy2c |
A |
G |
6: 136,722,493 (GRCm38) |
S617P |
probably damaging |
Het |
Ice1 |
T |
C |
13: 70,605,448 (GRCm38) |
R840G |
probably benign |
Het |
Il1rl2 |
T |
C |
1: 40,351,793 (GRCm38) |
Y299H |
possibly damaging |
Het |
Ints7 |
T |
G |
1: 191,621,162 (GRCm38) |
|
probably null |
Het |
Ireb2 |
C |
T |
9: 54,881,518 (GRCm38) |
T92I |
probably damaging |
Het |
Kcnj8 |
A |
T |
6: 142,570,189 (GRCm38) |
L64* |
probably null |
Het |
Mapk8ip3 |
A |
G |
17: 24,901,011 (GRCm38) |
V983A |
probably damaging |
Het |
Mertk |
A |
G |
2: 128,801,636 (GRCm38) |
D985G |
probably benign |
Het |
Mical3 |
A |
T |
6: 120,959,643 (GRCm38) |
S1307R |
probably benign |
Het |
Ncaph2 |
A |
G |
15: 89,364,622 (GRCm38) |
D222G |
probably benign |
Het |
Nf1 |
C |
A |
11: 79,550,998 (GRCm38) |
S295* |
probably null |
Het |
Nlrp12 |
T |
A |
7: 3,241,174 (GRCm38) |
D236V |
probably damaging |
Het |
Npnt |
A |
G |
3: 132,906,802 (GRCm38) |
V74A |
probably benign |
Het |
Oasl1 |
A |
G |
5: 114,935,944 (GRCm38) |
D304G |
probably damaging |
Het |
Olfr1098 |
C |
T |
2: 86,923,161 (GRCm38) |
V124I |
probably benign |
Het |
Olfr556 |
A |
G |
7: 102,670,733 (GRCm38) |
D271G |
possibly damaging |
Het |
Olfr834 |
A |
G |
9: 18,988,516 (GRCm38) |
H176R |
possibly damaging |
Het |
Olfr936 |
T |
C |
9: 39,047,000 (GRCm38) |
I140V |
probably benign |
Het |
Patz1 |
A |
G |
11: 3,307,812 (GRCm38) |
K604E |
probably damaging |
Het |
Pcsk6 |
T |
A |
7: 66,035,250 (GRCm38) |
V793E |
probably benign |
Het |
Pla2g4d |
C |
T |
2: 120,277,750 (GRCm38) |
|
probably null |
Het |
Plxnc1 |
A |
C |
10: 94,841,551 (GRCm38) |
L938R |
probably benign |
Het |
Pou4f2 |
G |
T |
8: 78,434,831 (GRCm38) |
A381D |
probably damaging |
Het |
Prdm4 |
A |
G |
10: 85,899,223 (GRCm38) |
L685P |
possibly damaging |
Het |
Pxn |
T |
A |
5: 115,552,147 (GRCm38) |
V383E |
probably damaging |
Het |
Rbl1 |
A |
G |
2: 157,174,783 (GRCm38) |
L632P |
probably damaging |
Het |
Rnf135 |
T |
A |
11: 80,196,881 (GRCm38) |
S219T |
possibly damaging |
Het |
Sdk2 |
T |
C |
11: 113,791,436 (GRCm38) |
D2039G |
possibly damaging |
Het |
Sdk2 |
C |
T |
11: 113,838,646 (GRCm38) |
|
silent |
Het |
Slc5a6 |
A |
G |
5: 31,042,644 (GRCm38) |
Y131H |
probably damaging |
Het |
Slc9a1 |
T |
C |
4: 133,418,080 (GRCm38) |
I492T |
probably damaging |
Het |
Soga3 |
A |
T |
10: 29,196,839 (GRCm38) |
Q709L |
probably damaging |
Het |
Spag5 |
A |
G |
11: 78,320,616 (GRCm38) |
K993E |
probably damaging |
Het |
Sptbn1 |
T |
G |
11: 30,159,371 (GRCm38) |
I75L |
possibly damaging |
Het |
Syngap1 |
T |
C |
17: 26,952,579 (GRCm38) |
S46P |
possibly damaging |
Het |
Tmem67 |
A |
G |
4: 12,087,840 (GRCm38) |
V102A |
probably benign |
Het |
Tomm70a |
T |
C |
16: 57,121,961 (GRCm38) |
S34P |
unknown |
Het |
Txlnb |
G |
T |
10: 17,843,233 (GRCm38) |
G604V |
probably benign |
Het |
Ube2q1 |
A |
G |
3: 89,776,176 (GRCm38) |
T143A |
probably benign |
Het |
Unc80 |
C |
T |
1: 66,503,669 (GRCm38) |
R361* |
probably null |
Het |
Vcan |
T |
C |
13: 89,703,547 (GRCm38) |
D1098G |
probably benign |
Het |
Vmn1r176 |
T |
A |
7: 23,835,381 (GRCm38) |
T116S |
probably damaging |
Het |
Wdr81 |
C |
T |
11: 75,454,423 (GRCm38) |
R6K |
probably benign |
Het |
Zan |
T |
A |
5: 137,403,050 (GRCm38) |
T4136S |
unknown |
Het |
Zbtb14 |
C |
A |
17: 69,388,502 (GRCm38) |
F398L |
probably damaging |
Het |
Zfp606 |
A |
T |
7: 12,493,971 (GRCm38) |
H615L |
probably damaging |
Het |
Zp3r |
A |
T |
1: 130,582,880 (GRCm38) |
N433K |
probably benign |
Het |
|
Other mutations in Tfcp2l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01079:Tfcp2l1
|
APN |
1 |
118,652,882 (GRCm38) |
missense |
possibly damaging |
0.70 |
IGL01725:Tfcp2l1
|
APN |
1 |
118,668,636 (GRCm38) |
missense |
possibly damaging |
0.80 |
IGL02281:Tfcp2l1
|
APN |
1 |
118,669,380 (GRCm38) |
splice site |
probably benign |
|
R1272:Tfcp2l1
|
UTSW |
1 |
118,632,313 (GRCm38) |
missense |
probably damaging |
1.00 |
R1959:Tfcp2l1
|
UTSW |
1 |
118,669,389 (GRCm38) |
missense |
probably benign |
0.40 |
R1965:Tfcp2l1
|
UTSW |
1 |
118,652,923 (GRCm38) |
nonsense |
probably null |
|
R3928:Tfcp2l1
|
UTSW |
1 |
118,669,476 (GRCm38) |
missense |
possibly damaging |
0.92 |
R4236:Tfcp2l1
|
UTSW |
1 |
118,662,065 (GRCm38) |
missense |
probably benign |
0.44 |
R4678:Tfcp2l1
|
UTSW |
1 |
118,668,648 (GRCm38) |
missense |
probably benign |
0.33 |
R4839:Tfcp2l1
|
UTSW |
1 |
118,669,464 (GRCm38) |
missense |
probably benign |
0.00 |
R4858:Tfcp2l1
|
UTSW |
1 |
118,669,509 (GRCm38) |
missense |
possibly damaging |
0.62 |
R5587:Tfcp2l1
|
UTSW |
1 |
118,664,762 (GRCm38) |
missense |
possibly damaging |
0.59 |
R5679:Tfcp2l1
|
UTSW |
1 |
118,668,647 (GRCm38) |
missense |
probably benign |
|
R6899:Tfcp2l1
|
UTSW |
1 |
118,675,575 (GRCm38) |
missense |
probably benign |
|
R7010:Tfcp2l1
|
UTSW |
1 |
118,653,727 (GRCm38) |
missense |
probably damaging |
1.00 |
R7155:Tfcp2l1
|
UTSW |
1 |
118,668,632 (GRCm38) |
missense |
probably damaging |
1.00 |
R7494:Tfcp2l1
|
UTSW |
1 |
118,664,956 (GRCm38) |
missense |
probably damaging |
1.00 |
R7849:Tfcp2l1
|
UTSW |
1 |
118,675,595 (GRCm38) |
missense |
probably damaging |
1.00 |
R8553:Tfcp2l1
|
UTSW |
1 |
118,632,352 (GRCm38) |
missense |
probably damaging |
1.00 |
R8794:Tfcp2l1
|
UTSW |
1 |
118,632,388 (GRCm38) |
missense |
probably damaging |
1.00 |
R8937:Tfcp2l1
|
UTSW |
1 |
118,668,717 (GRCm38) |
missense |
possibly damaging |
0.52 |
Z1177:Tfcp2l1
|
UTSW |
1 |
118,656,498 (GRCm38) |
missense |
probably damaging |
0.99 |
|