Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030458C11Rik |
T |
C |
15: 12,812,068 (GRCm38) |
H270R |
probably damaging |
Het |
Abcb1a |
T |
C |
5: 8,701,628 (GRCm38) |
I336T |
probably benign |
Het |
Adam19 |
T |
A |
11: 46,112,875 (GRCm38) |
F177I |
probably benign |
Het |
Ankrd53 |
T |
C |
6: 83,768,173 (GRCm38) |
V455A |
probably damaging |
Het |
Arrdc1 |
A |
G |
2: 24,925,665 (GRCm38) |
S415P |
probably benign |
Het |
Atp10a |
T |
C |
7: 58,797,352 (GRCm38) |
L614P |
probably benign |
Het |
C130060K24Rik |
A |
T |
6: 65,456,336 (GRCm38) |
N380I |
probably benign |
Het |
Catsper1 |
G |
T |
19: 5,343,963 (GRCm38) |
V668F |
probably damaging |
Het |
Cluh |
T |
A |
11: 74,661,918 (GRCm38) |
D596E |
probably damaging |
Het |
Cnot10 |
A |
G |
9: 114,615,107 (GRCm38) |
S407P |
probably benign |
Het |
Commd6 |
T |
C |
14: 101,634,350 (GRCm38) |
T86A |
probably damaging |
Het |
D5Ertd579e |
A |
T |
5: 36,604,657 (GRCm38) |
|
probably null |
Het |
Eif3l |
A |
G |
15: 79,085,560 (GRCm38) |
D252G |
probably damaging |
Het |
Epha2 |
A |
T |
4: 141,328,468 (GRCm38) |
S962C |
probably damaging |
Het |
Fcho1 |
C |
A |
8: 71,714,425 (GRCm38) |
|
probably null |
Het |
Fgf23 |
G |
T |
6: 127,073,216 (GRCm38) |
G63C |
probably damaging |
Het |
Flnc |
A |
T |
6: 29,445,749 (GRCm38) |
Y834F |
probably damaging |
Het |
Gcn1l1 |
T |
C |
5: 115,588,110 (GRCm38) |
L608P |
probably damaging |
Het |
Hdac5 |
T |
A |
11: 102,202,276 (GRCm38) |
E545V |
probably damaging |
Het |
Hecw2 |
A |
T |
1: 53,937,132 (GRCm38) |
M166K |
probably benign |
Het |
Ikbkb |
T |
C |
8: 22,665,893 (GRCm38) |
D586G |
probably damaging |
Het |
Il1f9 |
G |
C |
2: 24,188,621 (GRCm38) |
|
probably null |
Het |
Ipo13 |
A |
T |
4: 117,904,911 (GRCm38) |
I422N |
possibly damaging |
Het |
Iqgap3 |
GGAGAG |
GGAG |
3: 88,112,771 (GRCm38) |
|
probably null |
Het |
Kat6a |
G |
A |
8: 22,932,361 (GRCm38) |
A896T |
probably benign |
Het |
Kif28 |
A |
G |
1: 179,735,994 (GRCm38) |
I139T |
probably damaging |
Het |
Klhl25 |
A |
G |
7: 75,866,342 (GRCm38) |
E332G |
probably damaging |
Het |
Krt8 |
C |
T |
15: 101,997,908 (GRCm38) |
A389T |
probably benign |
Het |
Msrb3 |
T |
C |
10: 120,784,106 (GRCm38) |
S175G |
probably benign |
Het |
Muc5ac |
C |
T |
7: 141,809,744 (GRCm38) |
|
probably benign |
Het |
Myo10 |
T |
C |
15: 25,805,659 (GRCm38) |
Y1709H |
probably benign |
Het |
Nckap5 |
A |
G |
1: 126,023,194 (GRCm38) |
S1519P |
probably benign |
Het |
Npnt |
T |
A |
3: 132,909,910 (GRCm38) |
D124V |
probably damaging |
Het |
Nr1d1 |
A |
T |
11: 98,770,836 (GRCm38) |
|
probably null |
Het |
Ogdh |
A |
G |
11: 6,340,477 (GRCm38) |
Y365C |
probably benign |
Het |
Olfr1305 |
A |
T |
2: 111,872,961 (GRCm38) |
I298N |
possibly damaging |
Het |
Phf21b |
A |
T |
15: 84,787,446 (GRCm38) |
C416S |
probably damaging |
Het |
Prpsap1 |
A |
G |
11: 116,471,438 (GRCm38) |
S373P |
probably damaging |
Het |
Rab28 |
T |
C |
5: 41,703,534 (GRCm38) |
T26A |
probably damaging |
Het |
Rbbp8nl |
A |
G |
2: 180,279,226 (GRCm38) |
I455T |
probably benign |
Het |
Rrp36 |
G |
T |
17: 46,672,371 (GRCm38) |
Q106K |
probably benign |
Het |
Rsf1 |
CG |
CGACGGCGGAG |
7: 97,579,908 (GRCm38) |
|
probably benign |
Het |
Runx2 |
G |
A |
17: 44,814,192 (GRCm38) |
P80L |
probably damaging |
Het |
Scn5a |
A |
G |
9: 119,486,644 (GRCm38) |
L1666P |
probably damaging |
Het |
Siglecf |
A |
C |
7: 43,355,200 (GRCm38) |
T318P |
probably benign |
Het |
Slc22a1 |
C |
T |
17: 12,667,305 (GRCm38) |
W147* |
probably null |
Het |
Smchd1 |
T |
C |
17: 71,353,506 (GRCm38) |
I1868V |
probably damaging |
Het |
Snx21 |
A |
G |
2: 164,791,902 (GRCm38) |
S203G |
probably damaging |
Het |
Srl |
T |
C |
16: 4,482,831 (GRCm38) |
K792R |
probably benign |
Het |
Srrt |
A |
G |
5: 137,298,673 (GRCm38) |
F100S |
probably benign |
Het |
Stard9 |
G |
T |
2: 120,697,436 (GRCm38) |
M1391I |
probably benign |
Het |
Syne2 |
A |
G |
12: 76,035,630 (GRCm38) |
E119G |
probably damaging |
Het |
Syt11 |
G |
T |
3: 88,762,155 (GRCm38) |
S143R |
possibly damaging |
Het |
Tiparp |
T |
A |
3: 65,531,642 (GRCm38) |
H126Q |
probably benign |
Het |
Tulp2 |
C |
A |
7: 45,518,614 (GRCm38) |
T150K |
probably benign |
Het |
Ugt2b37 |
T |
A |
5: 87,242,429 (GRCm38) |
Y386F |
probably benign |
Het |
Usp31 |
C |
T |
7: 121,649,640 (GRCm38) |
W860* |
probably null |
Het |
Zfp317 |
A |
G |
9: 19,643,665 (GRCm38) |
R30G |
probably damaging |
Het |
Zfp709 |
C |
A |
8: 71,889,007 (GRCm38) |
N93K |
possibly damaging |
Het |
|
Other mutations in Rnft2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00913:Rnft2
|
APN |
5 |
118,201,215 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02063:Rnft2
|
APN |
5 |
118,242,522 (GRCm38) |
splice site |
probably benign |
|
R0201:Rnft2
|
UTSW |
5 |
118,194,680 (GRCm38) |
splice site |
probably benign |
|
R0349:Rnft2
|
UTSW |
5 |
118,201,385 (GRCm38) |
missense |
possibly damaging |
0.92 |
R1167:Rnft2
|
UTSW |
5 |
118,228,882 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1865:Rnft2
|
UTSW |
5 |
118,232,475 (GRCm38) |
missense |
probably damaging |
1.00 |
R2518:Rnft2
|
UTSW |
5 |
118,194,605 (GRCm38) |
intron |
probably benign |
|
R2876:Rnft2
|
UTSW |
5 |
118,193,621 (GRCm38) |
missense |
probably damaging |
0.99 |
R4622:Rnft2
|
UTSW |
5 |
118,232,406 (GRCm38) |
missense |
probably damaging |
1.00 |
R4623:Rnft2
|
UTSW |
5 |
118,232,406 (GRCm38) |
missense |
probably damaging |
1.00 |
R4705:Rnft2
|
UTSW |
5 |
118,228,863 (GRCm38) |
missense |
probably damaging |
1.00 |
R4796:Rnft2
|
UTSW |
5 |
118,201,246 (GRCm38) |
missense |
probably damaging |
1.00 |
R4898:Rnft2
|
UTSW |
5 |
118,237,442 (GRCm38) |
missense |
probably benign |
0.02 |
R5407:Rnft2
|
UTSW |
5 |
118,242,502 (GRCm38) |
missense |
probably damaging |
1.00 |
R5860:Rnft2
|
UTSW |
5 |
118,228,803 (GRCm38) |
missense |
possibly damaging |
0.92 |
R6971:Rnft2
|
UTSW |
5 |
118,194,570 (GRCm38) |
intron |
probably benign |
|
R8266:Rnft2
|
UTSW |
5 |
118,237,558 (GRCm38) |
missense |
possibly damaging |
0.79 |
R8690:Rnft2
|
UTSW |
5 |
118,228,870 (GRCm38) |
missense |
probably benign |
0.01 |
R9371:Rnft2
|
UTSW |
5 |
118,202,917 (GRCm38) |
missense |
probably damaging |
1.00 |
R9574:Rnft2
|
UTSW |
5 |
118,237,265 (GRCm38) |
missense |
probably benign |
|
|