Incidental Mutation 'R1676:Mdga2'
| ID |
188106 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Mdga2
|
| Ensembl Gene |
ENSMUSG00000034912 |
| Gene Name |
MAM domain containing glycosylphosphatidylinositol anchor 2 |
| Synonyms |
6720489L24Rik, Mdga2, Adp, 9330209L04Rik, Mamdc1 |
| MMRRC Submission |
039712-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R1676 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
12 |
| Chromosomal Location |
66512834-67269323 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to A
at 66615547 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glycine to Stop codon
at position 618
(G618*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000152613
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037181]
[ENSMUST00000222167]
[ENSMUST00000223141]
|
| AlphaFold |
P60755 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000037181
AA Change: G687*
|
| SMART Domains |
Protein: ENSMUSP00000046761
Gene: ENSMUSG00000034912
AA Change: G687*
| Domain | Start | End | E-Value | Type |
|---|
|
IGc2
|
122 |
186 |
1.38e-15 |
SMART |
|
IG
|
213 |
307 |
1.79e0 |
SMART |
|
IGc2
|
324 |
386 |
1.56e-14 |
SMART |
|
IGc2
|
419 |
493 |
4.43e-5 |
SMART |
|
low complexity region
|
495 |
507 |
N/A |
INTRINSIC |
|
IGc2
|
525 |
591 |
1.97e-11 |
SMART |
|
IG_like
|
621 |
687 |
2.5e0 |
SMART |
|
Blast:FN3
|
707 |
795 |
4e-40 |
BLAST |
|
MAM
|
812 |
990 |
3.4e-49 |
SMART |
|
transmembrane domain
|
999 |
1021 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000101379
|
| SMART Domains |
Protein: ENSMUSP00000098930
Gene: ENSMUSG00000034912
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
|
SCOP:d1cs6a1
|
40 |
72 |
2e-5 |
SMART |
|
Blast:IG
|
47 |
72 |
9e-11 |
BLAST |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000178814
AA Change: G677*
|
| SMART Domains |
Protein: ENSMUSP00000137608
Gene: ENSMUSG00000034912
AA Change: G677*
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
|
IGc2
|
53 |
117 |
1.38e-15 |
SMART |
|
IG
|
144 |
238 |
1.79e0 |
SMART |
|
IGc2
|
255 |
317 |
1.56e-14 |
SMART |
|
IGc2
|
350 |
424 |
4.43e-5 |
SMART |
|
low complexity region
|
426 |
438 |
N/A |
INTRINSIC |
|
IGc2
|
456 |
522 |
1.97e-11 |
SMART |
|
IG_like
|
552 |
618 |
2.5e0 |
SMART |
|
Blast:FN3
|
638 |
726 |
3e-40 |
BLAST |
|
MAM
|
736 |
914 |
1.38e-49 |
SMART |
|
transmembrane domain
|
923 |
945 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000222167
AA Change: G618*
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000223141
AA Change: G618*
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000223289
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.5%
- 20x: 93.0%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Mice that paternally inherit an allele disrupted by transgene insertion exhibit varying degrees of abnormalities in the skull, paw, and tail. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 90 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2810021J22Rik |
G |
T |
11: 58,771,819 (GRCm39) |
A434S |
possibly damaging |
Het |
| Abhd8 |
T |
A |
8: 71,914,517 (GRCm39) |
D37V |
probably damaging |
Het |
| Acvr2a |
G |
A |
2: 48,763,095 (GRCm39) |
S97N |
probably benign |
Het |
| Ampd3 |
T |
A |
7: 110,394,940 (GRCm39) |
H296Q |
probably damaging |
Het |
| Arid4a |
G |
A |
12: 71,122,112 (GRCm39) |
S509N |
probably benign |
Het |
| Cap2 |
T |
G |
13: 46,791,335 (GRCm39) |
H167Q |
probably damaging |
Het |
| Car8 |
A |
G |
4: 8,185,616 (GRCm39) |
L180S |
probably damaging |
Het |
| Casp8 |
T |
A |
1: 58,883,575 (GRCm39) |
I314N |
probably damaging |
Het |
| Cavin2 |
T |
A |
1: 51,340,330 (GRCm39) |
S336T |
probably benign |
Het |
| Cdc14b |
A |
T |
13: 64,373,416 (GRCm39) |
I119N |
possibly damaging |
Het |
| Cemip |
T |
A |
7: 83,613,246 (GRCm39) |
I651F |
possibly damaging |
Het |
| Cfap57 |
T |
A |
4: 118,453,137 (GRCm39) |
D522V |
probably damaging |
Het |
| Clrn3 |
A |
T |
7: 135,120,307 (GRCm39) |
V93D |
probably damaging |
Het |
| Crppa |
T |
C |
12: 36,526,720 (GRCm39) |
C170R |
probably benign |
Het |
| Cyp4f39 |
A |
G |
17: 32,701,176 (GRCm39) |
D222G |
probably benign |
Het |
| D5Ertd579e |
A |
G |
5: 36,773,453 (GRCm39) |
V314A |
probably benign |
Het |
| Dchs1 |
C |
T |
7: 105,404,128 (GRCm39) |
V2805I |
probably benign |
Het |
| Dsp |
A |
T |
13: 38,377,350 (GRCm39) |
K1712* |
probably null |
Het |
| Emilin2 |
T |
C |
17: 71,581,085 (GRCm39) |
D547G |
probably benign |
Het |
| Erbb3 |
T |
C |
10: 128,419,117 (GRCm39) |
H248R |
probably benign |
Het |
| Erich3 |
A |
G |
3: 154,468,260 (GRCm39) |
|
probably benign |
Het |
| Fbn1 |
T |
C |
2: 125,151,701 (GRCm39) |
T2518A |
probably damaging |
Het |
| Fzd2 |
G |
A |
11: 102,496,707 (GRCm39) |
V384M |
probably damaging |
Het |
| Gpc5 |
T |
A |
14: 115,607,510 (GRCm39) |
S371T |
probably damaging |
Het |
| Hbb-bh2 |
T |
C |
7: 103,488,362 (GRCm39) |
K145R |
probably null |
Het |
| Hectd1 |
G |
T |
12: 51,791,571 (GRCm39) |
P2558Q |
probably damaging |
Het |
| Hgsnat |
C |
T |
8: 26,444,633 (GRCm39) |
|
probably null |
Het |
| Hirip3 |
T |
C |
7: 126,462,647 (GRCm39) |
|
probably null |
Het |
| Itpkc |
T |
C |
7: 26,907,706 (GRCm39) |
D666G |
probably damaging |
Het |
| Jmjd1c |
T |
A |
10: 67,060,588 (GRCm39) |
D693E |
probably benign |
Het |
| Katnbl1 |
T |
C |
2: 112,236,454 (GRCm39) |
L60P |
probably damaging |
Het |
| Kcna1 |
T |
A |
6: 126,619,645 (GRCm39) |
E225V |
probably damaging |
Het |
| Kcnj6 |
T |
A |
16: 94,633,443 (GRCm39) |
M223L |
probably damaging |
Het |
| Kcnk7 |
G |
T |
19: 5,757,006 (GRCm39) |
V332F |
probably benign |
Het |
| Kmt5a |
GAA |
GA |
5: 124,597,948 (GRCm39) |
|
probably null |
Het |
| Morc2b |
T |
C |
17: 33,354,955 (GRCm39) |
E939G |
possibly damaging |
Het |
| Mstn |
T |
A |
1: 53,101,224 (GRCm39) |
D100E |
probably benign |
Het |
| Mthfd1l |
G |
A |
10: 4,033,877 (GRCm39) |
|
probably null |
Het |
| Muc20 |
T |
A |
16: 32,614,649 (GRCm39) |
T243S |
probably damaging |
Het |
| Myo1d |
A |
T |
11: 80,575,247 (GRCm39) |
N156K |
probably damaging |
Het |
| Myo7a |
A |
G |
7: 97,748,679 (GRCm39) |
|
probably null |
Het |
| Naa35 |
A |
T |
13: 59,760,490 (GRCm39) |
Q274L |
probably damaging |
Het |
| Ncam1 |
G |
A |
9: 49,468,472 (GRCm39) |
T329I |
probably damaging |
Het |
| Nisch |
T |
C |
14: 30,902,859 (GRCm39) |
|
probably benign |
Het |
| Nlrp1b |
A |
T |
11: 71,073,637 (GRCm39) |
W69R |
probably benign |
Het |
| Nrap |
T |
A |
19: 56,323,687 (GRCm39) |
H1294L |
probably damaging |
Het |
| Nsun6 |
T |
A |
2: 15,052,024 (GRCm39) |
R56* |
probably null |
Het |
| Nudt1 |
A |
G |
5: 140,320,378 (GRCm39) |
|
probably null |
Het |
| Nxph4 |
T |
G |
10: 127,362,077 (GRCm39) |
K271N |
probably damaging |
Het |
| Or1af1 |
A |
T |
2: 37,109,653 (GRCm39) |
R51* |
probably null |
Het |
| Or4a66 |
T |
G |
2: 88,531,661 (GRCm39) |
H4P |
probably benign |
Het |
| Or51e2 |
T |
A |
7: 102,391,605 (GRCm39) |
I202F |
probably damaging |
Het |
| Or52a20 |
T |
C |
7: 103,366,319 (GRCm39) |
W173R |
probably benign |
Het |
| Otud6b |
T |
A |
4: 14,825,617 (GRCm39) |
N71I |
probably damaging |
Het |
| Parp8 |
T |
A |
13: 117,014,064 (GRCm39) |
D623V |
probably damaging |
Het |
| Pcdhb5 |
T |
C |
18: 37,453,805 (GRCm39) |
S62P |
probably benign |
Het |
| Ppp1r12b |
A |
G |
1: 134,705,190 (GRCm39) |
S833P |
probably damaging |
Het |
| Ppp1r1a |
T |
G |
15: 103,441,915 (GRCm39) |
D51A |
probably damaging |
Het |
| Prag1 |
C |
A |
8: 36,570,052 (GRCm39) |
P212T |
probably damaging |
Het |
| Prxl2b |
C |
T |
4: 154,981,520 (GRCm39) |
V186I |
probably benign |
Het |
| Ptdss1 |
A |
G |
13: 67,081,701 (GRCm39) |
T44A |
probably damaging |
Het |
| Rab14 |
T |
C |
2: 35,076,735 (GRCm39) |
H83R |
possibly damaging |
Het |
| Rapgef3 |
C |
T |
15: 97,659,063 (GRCm39) |
G101E |
probably benign |
Het |
| Rimbp3 |
T |
A |
16: 17,028,977 (GRCm39) |
D800E |
probably benign |
Het |
| Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
| Selenbp1 |
A |
G |
3: 94,851,854 (GRCm39) |
D465G |
probably damaging |
Het |
| Slc28a2b |
T |
C |
2: 122,352,340 (GRCm39) |
S366P |
probably damaging |
Het |
| Slc29a1 |
T |
C |
17: 45,899,936 (GRCm39) |
D251G |
probably damaging |
Het |
| Slc6a11 |
G |
T |
6: 114,224,627 (GRCm39) |
V604F |
probably benign |
Het |
| Sltm |
T |
A |
9: 70,480,929 (GRCm39) |
D260E |
probably damaging |
Het |
| Spta1 |
G |
A |
1: 174,007,405 (GRCm39) |
V212M |
probably damaging |
Het |
| St6gal2 |
T |
C |
17: 55,803,396 (GRCm39) |
|
probably null |
Het |
| Tc2n |
A |
G |
12: 101,655,251 (GRCm39) |
S235P |
probably damaging |
Het |
| Tenm3 |
T |
A |
8: 48,870,154 (GRCm39) |
N213I |
possibly damaging |
Het |
| Ticam2 |
T |
C |
18: 46,693,677 (GRCm39) |
T137A |
probably damaging |
Het |
| Ttn |
TCCC |
TCCCC |
2: 76,573,251 (GRCm39) |
|
probably null |
Het |
| Tyk2 |
G |
A |
9: 21,026,545 (GRCm39) |
Q684* |
probably null |
Het |
| Ubqln1 |
A |
G |
13: 58,327,205 (GRCm39) |
F478S |
possibly damaging |
Het |
| Uckl1 |
G |
A |
2: 181,216,711 (GRCm39) |
T78I |
probably damaging |
Het |
| Uhmk1 |
A |
G |
1: 170,027,581 (GRCm39) |
V372A |
probably damaging |
Het |
| Unc5c |
G |
A |
3: 141,463,598 (GRCm39) |
V240I |
possibly damaging |
Het |
| Ush2a |
T |
C |
1: 188,460,782 (GRCm39) |
L2681P |
probably damaging |
Het |
| Vmn2r1 |
C |
T |
3: 63,997,603 (GRCm39) |
Q420* |
probably null |
Het |
| Vmn2r101 |
A |
T |
17: 19,832,184 (GRCm39) |
T727S |
probably benign |
Het |
| Vmn2r79 |
A |
G |
7: 86,651,839 (GRCm39) |
T413A |
probably benign |
Het |
| Vps13c |
T |
C |
9: 67,834,244 (GRCm39) |
V1637A |
probably benign |
Het |
| Xpc |
A |
G |
6: 91,469,929 (GRCm39) |
V765A |
possibly damaging |
Het |
| Zbtb18 |
T |
G |
1: 177,274,913 (GRCm39) |
|
probably null |
Het |
| Zfp712 |
A |
T |
13: 67,200,400 (GRCm39) |
D28E |
probably benign |
Het |
| Zfp735 |
A |
G |
11: 73,602,301 (GRCm39) |
N415S |
possibly damaging |
Het |
|
| Other mutations in Mdga2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01343:Mdga2
|
APN |
12 |
66,769,883 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL01632:Mdga2
|
APN |
12 |
66,676,672 (GRCm39) |
splice site |
probably benign |
|
|
IGL01843:Mdga2
|
APN |
12 |
66,769,905 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL02230:Mdga2
|
APN |
12 |
66,702,197 (GRCm39) |
nonsense |
probably null |
|
|
IGL02348:Mdga2
|
APN |
12 |
66,597,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02473:Mdga2
|
APN |
12 |
66,597,385 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
IGL02795:Mdga2
|
APN |
12 |
66,736,206 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02901:Mdga2
|
APN |
12 |
66,844,583 (GRCm39) |
splice site |
probably benign |
|
|
IGL03373:Mdga2
|
APN |
12 |
66,763,496 (GRCm39) |
missense |
probably damaging |
0.99 |
|
PIT4362001:Mdga2
|
UTSW |
12 |
66,844,542 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
PIT4377001:Mdga2
|
UTSW |
12 |
66,763,469 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0106:Mdga2
|
UTSW |
12 |
66,763,480 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0106:Mdga2
|
UTSW |
12 |
66,763,480 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0110:Mdga2
|
UTSW |
12 |
66,517,700 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R0218:Mdga2
|
UTSW |
12 |
66,701,894 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0450:Mdga2
|
UTSW |
12 |
66,517,700 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R0801:Mdga2
|
UTSW |
12 |
66,533,507 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0847:Mdga2
|
UTSW |
12 |
66,769,854 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1056:Mdga2
|
UTSW |
12 |
66,769,894 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1086:Mdga2
|
UTSW |
12 |
66,552,876 (GRCm39) |
splice site |
probably benign |
|
|
R1335:Mdga2
|
UTSW |
12 |
66,763,516 (GRCm39) |
splice site |
probably null |
|
|
R1382:Mdga2
|
UTSW |
12 |
66,517,690 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R1490:Mdga2
|
UTSW |
12 |
66,844,530 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1521:Mdga2
|
UTSW |
12 |
66,615,700 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1556:Mdga2
|
UTSW |
12 |
66,597,367 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1676:Mdga2
|
UTSW |
12 |
66,615,546 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1698:Mdga2
|
UTSW |
12 |
66,736,109 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1954:Mdga2
|
UTSW |
12 |
66,533,482 (GRCm39) |
splice site |
probably benign |
|
|
R2069:Mdga2
|
UTSW |
12 |
66,615,691 (GRCm39) |
nonsense |
probably null |
|
|
R2077:Mdga2
|
UTSW |
12 |
66,702,136 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2118:Mdga2
|
UTSW |
12 |
66,915,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2146:Mdga2
|
UTSW |
12 |
66,915,515 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2158:Mdga2
|
UTSW |
12 |
66,736,155 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R2189:Mdga2
|
UTSW |
12 |
66,519,970 (GRCm39) |
splice site |
probably null |
|
|
R2293:Mdga2
|
UTSW |
12 |
66,615,759 (GRCm39) |
nonsense |
probably null |
|
|
R2886:Mdga2
|
UTSW |
12 |
66,553,044 (GRCm39) |
splice site |
probably benign |
|
|
R2960:Mdga2
|
UTSW |
12 |
66,676,752 (GRCm39) |
nonsense |
probably null |
|
|
R3937:Mdga2
|
UTSW |
12 |
67,267,980 (GRCm39) |
unclassified |
probably benign |
|
|
R4437:Mdga2
|
UTSW |
12 |
66,519,972 (GRCm39) |
splice site |
probably null |
|
|
R4514:Mdga2
|
UTSW |
12 |
66,763,496 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4693:Mdga2
|
UTSW |
12 |
66,844,407 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R4719:Mdga2
|
UTSW |
12 |
66,517,775 (GRCm39) |
unclassified |
probably benign |
|
|
R4744:Mdga2
|
UTSW |
12 |
66,844,501 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4756:Mdga2
|
UTSW |
12 |
66,844,427 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4781:Mdga2
|
UTSW |
12 |
66,844,396 (GRCm39) |
splice site |
probably null |
|
|
R5022:Mdga2
|
UTSW |
12 |
66,517,534 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R5108:Mdga2
|
UTSW |
12 |
66,533,515 (GRCm39) |
missense |
probably benign |
0.43 |
|
R5479:Mdga2
|
UTSW |
12 |
66,701,950 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5710:Mdga2
|
UTSW |
12 |
66,553,556 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5816:Mdga2
|
UTSW |
12 |
66,701,956 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5822:Mdga2
|
UTSW |
12 |
66,702,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5996:Mdga2
|
UTSW |
12 |
66,844,537 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6038:Mdga2
|
UTSW |
12 |
66,676,827 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6038:Mdga2
|
UTSW |
12 |
66,676,827 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6297:Mdga2
|
UTSW |
12 |
66,553,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6484:Mdga2
|
UTSW |
12 |
66,676,843 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R6830:Mdga2
|
UTSW |
12 |
66,769,775 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6912:Mdga2
|
UTSW |
12 |
66,552,889 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6971:Mdga2
|
UTSW |
12 |
66,597,335 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7053:Mdga2
|
UTSW |
12 |
66,736,158 (GRCm39) |
missense |
probably benign |
0.41 |
|
R7069:Mdga2
|
UTSW |
12 |
66,533,526 (GRCm39) |
missense |
probably benign |
0.31 |
|
R7381:Mdga2
|
UTSW |
12 |
66,615,670 (GRCm39) |
missense |
probably benign |
0.44 |
|
R7474:Mdga2
|
UTSW |
12 |
66,533,535 (GRCm39) |
nonsense |
probably null |
|
|
R7559:Mdga2
|
UTSW |
12 |
66,520,003 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7581:Mdga2
|
UTSW |
12 |
66,553,029 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7596:Mdga2
|
UTSW |
12 |
66,552,897 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7745:Mdga2
|
UTSW |
12 |
66,736,125 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R7745:Mdga2
|
UTSW |
12 |
66,736,124 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7852:Mdga2
|
UTSW |
12 |
66,517,724 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R8144:Mdga2
|
UTSW |
12 |
66,702,037 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8319:Mdga2
|
UTSW |
12 |
67,267,803 (GRCm39) |
missense |
unknown |
|
|
R8715:Mdga2
|
UTSW |
12 |
66,915,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8977:Mdga2
|
UTSW |
12 |
66,844,409 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9138:Mdga2
|
UTSW |
12 |
66,615,663 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R9177:Mdga2
|
UTSW |
12 |
66,517,481 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R9223:Mdga2
|
UTSW |
12 |
66,615,634 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R9248:Mdga2
|
UTSW |
12 |
66,736,226 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R9264:Mdga2
|
UTSW |
12 |
66,560,057 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9381:Mdga2
|
UTSW |
12 |
66,597,304 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R9456:Mdga2
|
UTSW |
12 |
66,615,532 (GRCm39) |
missense |
probably benign |
0.44 |
|
R9633:Mdga2
|
UTSW |
12 |
66,736,206 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1176:Mdga2
|
UTSW |
12 |
66,736,217 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:Mdga2
|
UTSW |
12 |
66,615,727 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGTGCTGCCACTGAAATGAACAAAC -3'
(R):5'- GCCTATCCAATACGAGTGCTGACC -3'
Sequencing Primer
(F):5'- GATTTGCCCTGACATCAATCAAGG -3'
(R):5'- CCAATACGAGTGCTGACCTATGAG -3'
|
| Posted On |
2014-05-09 |
Incidental Mutation