Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg5 |
G |
A |
17: 84,976,425 (GRCm39) |
H471Y |
probably damaging |
Het |
Ank2 |
T |
A |
3: 126,733,744 (GRCm39) |
D622V |
probably damaging |
Het |
Apoe |
T |
A |
7: 19,432,375 (GRCm39) |
|
probably benign |
Het |
Asz1 |
T |
C |
6: 18,054,561 (GRCm39) |
E414G |
probably benign |
Het |
Atp2a2 |
A |
T |
5: 122,604,918 (GRCm39) |
C420* |
probably null |
Het |
Cd84 |
A |
T |
1: 171,712,153 (GRCm39) |
|
probably null |
Het |
Cdca2 |
T |
A |
14: 67,917,762 (GRCm39) |
R545S |
probably benign |
Het |
Cep250 |
C |
T |
2: 155,812,042 (GRCm39) |
A446V |
unknown |
Het |
Cib1 |
T |
C |
7: 79,877,751 (GRCm39) |
D182G |
probably damaging |
Het |
Cpsf2 |
A |
G |
12: 101,963,555 (GRCm39) |
D428G |
probably damaging |
Het |
Cspg4b |
C |
T |
13: 113,505,374 (GRCm39) |
P2168S |
|
Het |
Dap3 |
T |
A |
3: 88,837,861 (GRCm39) |
T130S |
probably benign |
Het |
Ddb2 |
T |
A |
2: 91,064,593 (GRCm39) |
K106* |
probably null |
Het |
Ehd2 |
G |
A |
7: 15,684,626 (GRCm39) |
A391V |
probably damaging |
Het |
Evpl |
A |
T |
11: 116,115,008 (GRCm39) |
I894N |
possibly damaging |
Het |
Gabrb2 |
A |
G |
11: 42,482,693 (GRCm39) |
T184A |
probably damaging |
Het |
Gfpt1 |
G |
A |
6: 87,053,248 (GRCm39) |
V403I |
probably benign |
Het |
Gli1 |
A |
G |
10: 127,167,202 (GRCm39) |
S684P |
possibly damaging |
Het |
Gm7276 |
A |
G |
18: 77,273,147 (GRCm39) |
S196P |
unknown |
Het |
Hoxc10 |
C |
T |
15: 102,875,810 (GRCm39) |
P173L |
probably benign |
Het |
Hrnr |
A |
G |
3: 93,238,863 (GRCm39) |
N3034D |
unknown |
Het |
Kif2c |
A |
T |
4: 117,024,291 (GRCm39) |
S359T |
probably benign |
Het |
Lmln |
T |
G |
16: 32,930,202 (GRCm39) |
L553R |
probably benign |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Mettl1 |
T |
A |
10: 126,880,911 (GRCm39) |
V191D |
possibly damaging |
Het |
Mical2 |
A |
C |
7: 111,870,589 (GRCm39) |
K26T |
possibly damaging |
Het |
Myl1 |
A |
T |
1: 66,973,675 (GRCm39) |
|
probably null |
Het |
Nfat5 |
A |
G |
8: 108,078,141 (GRCm39) |
T427A |
probably damaging |
Het |
Or5d14 |
C |
T |
2: 87,880,294 (GRCm39) |
V225M |
probably damaging |
Het |
Or8b49 |
T |
A |
9: 38,506,108 (GRCm39) |
I197K |
probably damaging |
Het |
Piezo2 |
A |
G |
18: 63,178,589 (GRCm39) |
I1776T |
probably benign |
Het |
Ppp1r7 |
A |
G |
1: 93,285,497 (GRCm39) |
I246V |
probably benign |
Het |
Ppp4c |
T |
A |
7: 126,386,739 (GRCm39) |
E116V |
probably damaging |
Het |
Psme2 |
T |
A |
14: 55,828,302 (GRCm39) |
K15N |
possibly damaging |
Het |
Retreg1 |
C |
T |
15: 25,968,618 (GRCm39) |
R125C |
probably damaging |
Het |
Rnf145 |
G |
T |
11: 44,450,819 (GRCm39) |
R381L |
probably damaging |
Het |
Rsf1 |
G |
GACGGCGGCA |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Ryr1 |
G |
A |
7: 28,771,229 (GRCm39) |
T2604I |
probably damaging |
Het |
Sag |
T |
C |
1: 87,751,043 (GRCm39) |
S170P |
probably damaging |
Het |
Sema3b |
T |
A |
9: 107,478,173 (GRCm39) |
N404I |
possibly damaging |
Het |
Serpina1b |
A |
T |
12: 103,696,566 (GRCm39) |
L281Q |
probably damaging |
Het |
Slc22a1 |
T |
A |
17: 12,878,598 (GRCm39) |
T372S |
probably benign |
Het |
Slco6d1 |
A |
T |
1: 98,423,919 (GRCm39) |
N524Y |
probably damaging |
Het |
Smarca2 |
T |
A |
19: 26,693,583 (GRCm39) |
D1262E |
possibly damaging |
Het |
Syne2 |
A |
T |
12: 76,040,838 (GRCm39) |
H3832L |
probably damaging |
Het |
Tarbp1 |
G |
T |
8: 127,174,202 (GRCm39) |
T868K |
possibly damaging |
Het |
Trp63 |
C |
T |
16: 25,639,247 (GRCm39) |
A145V |
probably damaging |
Het |
Tsc2 |
C |
T |
17: 24,823,802 (GRCm39) |
R1001K |
probably null |
Het |
Ttc39b |
T |
C |
4: 83,189,444 (GRCm39) |
D30G |
probably damaging |
Het |
Usf3 |
A |
G |
16: 44,041,030 (GRCm39) |
T1837A |
probably benign |
Het |
Usp25 |
T |
A |
16: 76,911,969 (GRCm39) |
|
probably null |
Het |
Vmn1r27 |
G |
A |
6: 58,192,416 (GRCm39) |
T196I |
probably benign |
Het |
Vrk3 |
C |
T |
7: 44,407,254 (GRCm39) |
S75F |
possibly damaging |
Het |
Washc5 |
T |
C |
15: 59,209,134 (GRCm39) |
Y1030C |
probably damaging |
Het |
Wdr47 |
T |
C |
3: 108,526,106 (GRCm39) |
F210L |
probably damaging |
Het |
Zfp853 |
G |
A |
5: 143,274,496 (GRCm39) |
Q390* |
probably null |
Het |
Zfyve9 |
A |
T |
4: 108,575,760 (GRCm39) |
D440E |
probably benign |
Het |
|
Other mutations in Noa1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02119:Noa1
|
APN |
5 |
77,455,426 (GRCm39) |
missense |
probably benign |
|
IGL02850:Noa1
|
APN |
5 |
77,442,338 (GRCm39) |
missense |
probably benign |
0.14 |
R0149:Noa1
|
UTSW |
5 |
77,445,020 (GRCm39) |
nonsense |
probably null |
|
R0361:Noa1
|
UTSW |
5 |
77,445,020 (GRCm39) |
nonsense |
probably null |
|
R0645:Noa1
|
UTSW |
5 |
77,457,722 (GRCm39) |
missense |
probably benign |
0.00 |
R1226:Noa1
|
UTSW |
5 |
77,455,402 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1710:Noa1
|
UTSW |
5 |
77,457,572 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1721:Noa1
|
UTSW |
5 |
77,455,428 (GRCm39) |
missense |
probably benign |
0.00 |
R1732:Noa1
|
UTSW |
5 |
77,454,221 (GRCm39) |
missense |
probably benign |
0.01 |
R2061:Noa1
|
UTSW |
5 |
77,452,034 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2262:Noa1
|
UTSW |
5 |
77,457,651 (GRCm39) |
nonsense |
probably null |
|
R2965:Noa1
|
UTSW |
5 |
77,454,191 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2966:Noa1
|
UTSW |
5 |
77,454,191 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4405:Noa1
|
UTSW |
5 |
77,454,219 (GRCm39) |
missense |
probably benign |
0.00 |
R4664:Noa1
|
UTSW |
5 |
77,447,600 (GRCm39) |
missense |
probably benign |
0.31 |
R4849:Noa1
|
UTSW |
5 |
77,454,179 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4920:Noa1
|
UTSW |
5 |
77,454,334 (GRCm39) |
splice site |
probably null |
|
R5005:Noa1
|
UTSW |
5 |
77,456,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R5325:Noa1
|
UTSW |
5 |
77,452,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R6112:Noa1
|
UTSW |
5 |
77,457,593 (GRCm39) |
missense |
probably benign |
0.01 |
R6254:Noa1
|
UTSW |
5 |
77,457,516 (GRCm39) |
missense |
probably benign |
0.12 |
R7659:Noa1
|
UTSW |
5 |
77,457,237 (GRCm39) |
missense |
not run |
|
R7810:Noa1
|
UTSW |
5 |
77,457,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R7879:Noa1
|
UTSW |
5 |
77,445,044 (GRCm39) |
missense |
probably benign |
0.01 |
R7911:Noa1
|
UTSW |
5 |
77,457,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|