Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc3 |
A |
T |
11: 94,252,062 (GRCm39) |
H840Q |
probably benign |
Het |
Amotl2 |
C |
T |
9: 102,605,767 (GRCm39) |
R540C |
probably damaging |
Het |
Brpf1 |
A |
G |
6: 113,294,115 (GRCm39) |
E605G |
probably damaging |
Het |
Cacna2d3 |
T |
C |
14: 28,694,199 (GRCm39) |
I865V |
probably benign |
Het |
Cdh24 |
A |
T |
14: 54,876,046 (GRCm39) |
F199I |
probably damaging |
Het |
Cdk9 |
A |
G |
2: 32,600,521 (GRCm39) |
V27A |
probably damaging |
Het |
Cfap69 |
G |
T |
5: 5,690,230 (GRCm39) |
|
probably null |
Het |
Cyp2d11 |
G |
T |
15: 82,273,498 (GRCm39) |
L458I |
probably damaging |
Het |
Dchs1 |
T |
C |
7: 105,408,138 (GRCm39) |
E1898G |
probably damaging |
Het |
Dennd4b |
G |
T |
3: 90,178,177 (GRCm39) |
L456F |
probably damaging |
Het |
Dgat1 |
T |
C |
15: 76,395,786 (GRCm39) |
T66A |
probably benign |
Het |
Dock10 |
C |
A |
1: 80,583,881 (GRCm39) |
|
probably null |
Het |
Fam110b |
A |
G |
4: 5,799,578 (GRCm39) |
D332G |
possibly damaging |
Het |
Fem1al |
A |
C |
11: 29,773,994 (GRCm39) |
Y488D |
probably benign |
Het |
Frmd4b |
G |
A |
6: 97,273,347 (GRCm39) |
P628S |
probably damaging |
Het |
Ice1 |
A |
T |
13: 70,753,529 (GRCm39) |
H852Q |
probably benign |
Het |
Il17ra |
T |
C |
6: 120,450,751 (GRCm39) |
V116A |
probably damaging |
Het |
Ints9 |
T |
C |
14: 65,232,460 (GRCm39) |
I173T |
probably benign |
Het |
Kctd14 |
A |
T |
7: 97,107,074 (GRCm39) |
M110L |
probably benign |
Het |
Krt6a |
T |
G |
15: 101,602,637 (GRCm39) |
Y16S |
probably benign |
Het |
Lamc2 |
T |
C |
1: 153,006,502 (GRCm39) |
N883S |
probably benign |
Het |
Larp4b |
C |
T |
13: 9,195,486 (GRCm39) |
T195M |
probably damaging |
Het |
Lrp1 |
A |
G |
10: 127,375,398 (GRCm39) |
L4432P |
probably damaging |
Het |
Mei4 |
T |
C |
9: 81,772,252 (GRCm39) |
S22P |
probably damaging |
Het |
Mep1a |
T |
C |
17: 43,802,527 (GRCm39) |
Q166R |
probably damaging |
Het |
Mroh2b |
C |
A |
15: 4,980,612 (GRCm39) |
|
probably null |
Het |
Myoc |
T |
G |
1: 162,476,220 (GRCm39) |
L308R |
probably damaging |
Het |
Ndn |
C |
T |
7: 61,998,256 (GRCm39) |
P34L |
probably benign |
Het |
Or1j21 |
A |
T |
2: 36,684,155 (GRCm39) |
R302S |
probably null |
Het |
Or2t6 |
T |
A |
14: 14,175,725 (GRCm38) |
Y119F |
probably damaging |
Het |
Or4c101 |
C |
G |
2: 88,389,985 (GRCm39) |
S57R |
probably damaging |
Het |
Pdilt |
T |
A |
7: 119,087,217 (GRCm39) |
T478S |
probably damaging |
Het |
Pias1 |
T |
C |
9: 62,827,769 (GRCm39) |
K222E |
probably damaging |
Het |
Prss16 |
A |
C |
13: 22,193,613 (GRCm39) |
L61V |
possibly damaging |
Het |
Pvr |
G |
A |
7: 19,644,551 (GRCm39) |
Q328* |
probably null |
Het |
Ranbp3 |
A |
G |
17: 57,017,865 (GRCm39) |
D481G |
possibly damaging |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGGCGGCGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
G |
T |
2: 112,508,435 (GRCm39) |
D3419E |
probably damaging |
Het |
Scn1a |
C |
T |
2: 66,149,806 (GRCm39) |
W946* |
probably null |
Het |
Sh3pxd2a |
T |
C |
19: 47,266,864 (GRCm39) |
K242E |
probably damaging |
Het |
Slc34a2 |
A |
G |
5: 53,226,848 (GRCm39) |
D657G |
probably benign |
Het |
Stard9 |
T |
A |
2: 120,532,533 (GRCm39) |
I2930K |
probably benign |
Het |
Syna |
T |
C |
5: 134,588,112 (GRCm39) |
D279G |
probably benign |
Het |
Tfr2 |
T |
C |
5: 137,577,292 (GRCm39) |
F415L |
probably benign |
Het |
Tmem97 |
T |
A |
11: 78,433,586 (GRCm39) |
Y103F |
probably damaging |
Het |
Tmem97 |
A |
T |
11: 78,433,587 (GRCm39) |
Y103N |
probably damaging |
Het |
Txndc2 |
T |
A |
17: 65,945,310 (GRCm39) |
D289V |
probably damaging |
Het |
Zbtb1 |
T |
G |
12: 76,433,206 (GRCm39) |
D397E |
probably benign |
Het |
Zc3h18 |
T |
C |
8: 123,140,677 (GRCm39) |
S847P |
probably benign |
Het |
Zfp382 |
G |
A |
7: 29,833,144 (GRCm39) |
G265E |
probably damaging |
Het |
Zfp410 |
T |
C |
12: 84,369,740 (GRCm39) |
L39S |
probably damaging |
Het |
Zfp729a |
G |
T |
13: 67,767,440 (GRCm39) |
P930T |
probably benign |
Het |
|
Other mutations in Pttg1ip2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02125:Pttg1ip2
|
APN |
5 |
5,500,644 (GRCm39) |
makesense |
probably null |
|
IGL02701:Pttg1ip2
|
APN |
5 |
5,516,623 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02821:Pttg1ip2
|
APN |
5 |
5,502,039 (GRCm39) |
nonsense |
probably null |
|
R1029:Pttg1ip2
|
UTSW |
5 |
5,505,919 (GRCm39) |
missense |
probably benign |
0.21 |
R1463:Pttg1ip2
|
UTSW |
5 |
5,502,073 (GRCm39) |
splice site |
probably benign |
|
R1550:Pttg1ip2
|
UTSW |
5 |
5,502,019 (GRCm39) |
missense |
probably benign |
0.00 |
R1764:Pttg1ip2
|
UTSW |
5 |
5,528,943 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1911:Pttg1ip2
|
UTSW |
5 |
5,502,019 (GRCm39) |
missense |
probably benign |
0.00 |
R1912:Pttg1ip2
|
UTSW |
5 |
5,502,019 (GRCm39) |
missense |
probably benign |
0.00 |
R1930:Pttg1ip2
|
UTSW |
5 |
5,502,019 (GRCm39) |
missense |
probably benign |
0.00 |
R1931:Pttg1ip2
|
UTSW |
5 |
5,502,019 (GRCm39) |
missense |
probably benign |
0.00 |
R2013:Pttg1ip2
|
UTSW |
5 |
5,505,964 (GRCm39) |
missense |
probably benign |
0.00 |
R2014:Pttg1ip2
|
UTSW |
5 |
5,505,964 (GRCm39) |
missense |
probably benign |
0.00 |
R2015:Pttg1ip2
|
UTSW |
5 |
5,505,964 (GRCm39) |
missense |
probably benign |
0.00 |
R2151:Pttg1ip2
|
UTSW |
5 |
5,528,875 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2420:Pttg1ip2
|
UTSW |
5 |
5,505,912 (GRCm39) |
missense |
probably benign |
0.00 |
R2421:Pttg1ip2
|
UTSW |
5 |
5,505,912 (GRCm39) |
missense |
probably benign |
0.00 |
R3056:Pttg1ip2
|
UTSW |
5 |
5,507,283 (GRCm39) |
critical splice donor site |
probably null |
|
R4012:Pttg1ip2
|
UTSW |
5 |
5,528,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R7136:Pttg1ip2
|
UTSW |
5 |
5,516,631 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7448:Pttg1ip2
|
UTSW |
5 |
5,505,952 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Pttg1ip2
|
UTSW |
5 |
5,507,284 (GRCm39) |
critical splice donor site |
probably null |
|
|