Incidental Mutation 'R4771:Mga'
| ID |
367468 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Mga
|
| Ensembl Gene |
ENSMUSG00000033943 |
| Gene Name |
MAX gene associated |
| Synonyms |
Mga, C130042M01Rik, Mad5, D030062C11Rik |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.953)
|
| Stock # |
R4771 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
119727709-119800062 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 119794775 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 2820
(S2820P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000106401
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000046717]
[ENSMUST00000079934]
[ENSMUST00000110773]
[ENSMUST00000110774]
[ENSMUST00000156510]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000046717
AA Change: S2781P
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000043795
Gene: ENSMUSG00000033943
AA Change: S2781P
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:TBOX
|
6 |
73 |
6e-27 |
BLAST |
|
TBOX
|
74 |
265 |
2.34e-100 |
SMART |
|
low complexity region
|
969 |
978 |
N/A |
INTRINSIC |
|
low complexity region
|
1017 |
1031 |
N/A |
INTRINSIC |
|
low complexity region
|
1112 |
1138 |
N/A |
INTRINSIC |
|
low complexity region
|
1248 |
1269 |
N/A |
INTRINSIC |
|
low complexity region
|
1301 |
1315 |
N/A |
INTRINSIC |
|
low complexity region
|
1564 |
1581 |
N/A |
INTRINSIC |
|
low complexity region
|
1634 |
1649 |
N/A |
INTRINSIC |
|
low complexity region
|
1681 |
1716 |
N/A |
INTRINSIC |
|
low complexity region
|
1796 |
1818 |
N/A |
INTRINSIC |
|
low complexity region
|
1833 |
1850 |
N/A |
INTRINSIC |
|
low complexity region
|
1977 |
1992 |
N/A |
INTRINSIC |
|
low complexity region
|
2183 |
2197 |
N/A |
INTRINSIC |
|
low complexity region
|
2241 |
2259 |
N/A |
INTRINSIC |
|
HLH
|
2368 |
2419 |
8.27e-7 |
SMART |
|
low complexity region
|
2748 |
2769 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000079934
AA Change: S2611P
PolyPhen 2
Score 0.930 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000078853
Gene: ENSMUSG00000033943
AA Change: S2611P
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:TBOX
|
6 |
73 |
5e-27 |
BLAST |
|
TBOX
|
74 |
265 |
2.34e-100 |
SMART |
|
low complexity region
|
969 |
978 |
N/A |
INTRINSIC |
|
low complexity region
|
1017 |
1031 |
N/A |
INTRINSIC |
|
low complexity region
|
1112 |
1138 |
N/A |
INTRINSIC |
|
low complexity region
|
1247 |
1268 |
N/A |
INTRINSIC |
|
low complexity region
|
1300 |
1314 |
N/A |
INTRINSIC |
|
low complexity region
|
1626 |
1648 |
N/A |
INTRINSIC |
|
low complexity region
|
1663 |
1680 |
N/A |
INTRINSIC |
|
low complexity region
|
1807 |
1822 |
N/A |
INTRINSIC |
|
low complexity region
|
2013 |
2027 |
N/A |
INTRINSIC |
|
low complexity region
|
2071 |
2089 |
N/A |
INTRINSIC |
|
HLH
|
2198 |
2249 |
8.27e-7 |
SMART |
|
low complexity region
|
2578 |
2599 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000110773
AA Change: S2702P
PolyPhen 2
Score 0.827 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000106400
Gene: ENSMUSG00000033943
AA Change: S2702P
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:TBOX
|
6 |
73 |
5e-27 |
BLAST |
|
TBOX
|
74 |
265 |
2.34e-100 |
SMART |
|
low complexity region
|
890 |
899 |
N/A |
INTRINSIC |
|
low complexity region
|
938 |
952 |
N/A |
INTRINSIC |
|
low complexity region
|
1033 |
1059 |
N/A |
INTRINSIC |
|
low complexity region
|
1169 |
1190 |
N/A |
INTRINSIC |
|
low complexity region
|
1222 |
1236 |
N/A |
INTRINSIC |
|
low complexity region
|
1485 |
1502 |
N/A |
INTRINSIC |
|
low complexity region
|
1555 |
1570 |
N/A |
INTRINSIC |
|
low complexity region
|
1602 |
1637 |
N/A |
INTRINSIC |
|
low complexity region
|
1717 |
1739 |
N/A |
INTRINSIC |
|
low complexity region
|
1754 |
1771 |
N/A |
INTRINSIC |
|
low complexity region
|
1898 |
1913 |
N/A |
INTRINSIC |
|
low complexity region
|
2104 |
2118 |
N/A |
INTRINSIC |
|
low complexity region
|
2162 |
2180 |
N/A |
INTRINSIC |
|
HLH
|
2289 |
2340 |
8.27e-7 |
SMART |
|
low complexity region
|
2669 |
2690 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000110774
AA Change: S2820P
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000106401
Gene: ENSMUSG00000033943
AA Change: S2820P
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:TBOX
|
6 |
73 |
7e-27 |
BLAST |
|
TBOX
|
74 |
265 |
2.34e-100 |
SMART |
|
low complexity region
|
969 |
978 |
N/A |
INTRINSIC |
|
low complexity region
|
1017 |
1031 |
N/A |
INTRINSIC |
|
Pfam:DUF4801
|
1037 |
1085 |
1e-19 |
PFAM |
|
low complexity region
|
1112 |
1138 |
N/A |
INTRINSIC |
|
low complexity region
|
1248 |
1269 |
N/A |
INTRINSIC |
|
low complexity region
|
1301 |
1315 |
N/A |
INTRINSIC |
|
low complexity region
|
1564 |
1581 |
N/A |
INTRINSIC |
|
low complexity region
|
1634 |
1649 |
N/A |
INTRINSIC |
|
low complexity region
|
1681 |
1716 |
N/A |
INTRINSIC |
|
low complexity region
|
1835 |
1857 |
N/A |
INTRINSIC |
|
low complexity region
|
1872 |
1889 |
N/A |
INTRINSIC |
|
low complexity region
|
2016 |
2031 |
N/A |
INTRINSIC |
|
low complexity region
|
2222 |
2236 |
N/A |
INTRINSIC |
|
low complexity region
|
2280 |
2298 |
N/A |
INTRINSIC |
|
HLH
|
2407 |
2458 |
8.27e-7 |
SMART |
|
low complexity region
|
2787 |
2808 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000122889
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000131396
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000156510
|
| SMART Domains |
Protein: ENSMUSP00000119044
Gene: ENSMUSG00000033943
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:TBOX
|
6 |
73 |
4e-27 |
BLAST |
|
TBOX
|
74 |
265 |
2.34e-100 |
SMART |
|
low complexity region
|
969 |
978 |
N/A |
INTRINSIC |
|
low complexity region
|
1017 |
1031 |
N/A |
INTRINSIC |
|
low complexity region
|
1112 |
1138 |
N/A |
INTRINSIC |
|
low complexity region
|
1247 |
1268 |
N/A |
INTRINSIC |
|
low complexity region
|
1300 |
1314 |
N/A |
INTRINSIC |
|
low complexity region
|
1626 |
1648 |
N/A |
INTRINSIC |
|
low complexity region
|
1663 |
1680 |
N/A |
INTRINSIC |
|
low complexity region
|
1807 |
1822 |
N/A |
INTRINSIC |
|
low complexity region
|
2013 |
2027 |
N/A |
INTRINSIC |
|
low complexity region
|
2071 |
2089 |
N/A |
INTRINSIC |
|
HLH
|
2198 |
2249 |
8.27e-7 |
SMART |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 95.0%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Embryos homozygous for a gene trap allele die shortly after implantation due to defective development of the inner cell mass (ICM) and the epiblast. ICM derivatives fail to develop past E4.5 and show increased apoptosis but no change in cell proliferation. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(135) : Gene trapped(135)
|
| Other mutations in this stock |
Total: 111 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310022B05Rik |
T |
C |
8: 125,366,300 (GRCm39) |
T148A |
probably benign |
Het |
| Abcc4 |
G |
T |
14: 118,721,796 (GRCm39) |
N1234K |
probably benign |
Het |
| Adamts20 |
C |
T |
15: 94,249,516 (GRCm39) |
|
probably null |
Het |
| Aqp9 |
C |
T |
9: 71,030,152 (GRCm39) |
G212S |
probably damaging |
Het |
| Asb15 |
A |
T |
6: 24,570,621 (GRCm39) |
N533I |
probably damaging |
Het |
| Brwd1 |
A |
G |
16: 95,804,518 (GRCm39) |
V1884A |
probably benign |
Het |
| Ccdc106 |
G |
A |
7: 5,060,521 (GRCm39) |
|
probably null |
Het |
| Cfap46 |
A |
T |
7: 139,210,524 (GRCm39) |
L1774Q |
probably null |
Het |
| Cfap95 |
A |
G |
19: 23,536,337 (GRCm39) |
L190P |
probably damaging |
Het |
| Cibar1 |
T |
A |
4: 12,155,689 (GRCm39) |
Q311L |
probably benign |
Het |
| Clec2h |
G |
A |
6: 128,651,118 (GRCm39) |
E133K |
probably damaging |
Het |
| Cntn1 |
T |
A |
15: 92,202,972 (GRCm39) |
F751L |
possibly damaging |
Het |
| Col20a1 |
A |
T |
2: 180,630,917 (GRCm39) |
M62L |
probably benign |
Het |
| Col7a1 |
T |
C |
9: 108,800,993 (GRCm39) |
V1899A |
probably damaging |
Het |
| Cpa5 |
T |
A |
6: 30,612,684 (GRCm39) |
L28* |
probably null |
Het |
| Crb1 |
T |
A |
1: 139,255,942 (GRCm39) |
E264D |
probably damaging |
Het |
| Creb3l2 |
A |
T |
6: 37,311,512 (GRCm39) |
S426T |
probably benign |
Het |
| Cspg5 |
T |
A |
9: 110,080,195 (GRCm39) |
N373K |
probably damaging |
Het |
| Ctso |
T |
C |
3: 81,840,047 (GRCm39) |
S26P |
probably benign |
Het |
| Depdc1b |
A |
C |
13: 108,519,434 (GRCm39) |
D348A |
probably benign |
Het |
| Diaph1 |
A |
T |
18: 37,986,604 (GRCm39) |
M1127K |
probably damaging |
Het |
| Dlgap1 |
A |
T |
17: 70,900,375 (GRCm39) |
K397* |
probably null |
Het |
| Dock3 |
T |
A |
9: 106,829,557 (GRCm39) |
H1119L |
possibly damaging |
Het |
| Dok4 |
G |
T |
8: 95,591,795 (GRCm39) |
|
probably null |
Het |
| Dram2 |
A |
G |
3: 106,480,361 (GRCm39) |
T225A |
probably damaging |
Het |
| Dst |
G |
A |
1: 34,288,565 (GRCm39) |
R5603H |
probably damaging |
Het |
| Ehbp1l1 |
A |
G |
19: 5,775,996 (GRCm39) |
F18S |
probably damaging |
Het |
| Epha5 |
A |
G |
5: 84,298,278 (GRCm39) |
V427A |
probably damaging |
Het |
| Exoc4 |
A |
T |
6: 33,418,884 (GRCm39) |
|
probably null |
Het |
| Exph5 |
C |
T |
9: 53,284,965 (GRCm39) |
T682I |
possibly damaging |
Het |
| Fnbp1l |
A |
T |
3: 122,351,752 (GRCm39) |
S264T |
possibly damaging |
Het |
| Ggnbp2 |
A |
T |
11: 84,725,314 (GRCm39) |
D580E |
probably benign |
Het |
| Gm10277 |
G |
A |
11: 77,676,534 (GRCm39) |
|
probably benign |
Het |
| Golm2 |
T |
A |
2: 121,756,126 (GRCm39) |
V352E |
probably damaging |
Het |
| Gtf2a1l |
C |
A |
17: 88,997,448 (GRCm39) |
P93Q |
probably benign |
Het |
| Hydin |
A |
T |
8: 111,259,515 (GRCm39) |
I2496F |
probably benign |
Het |
| Ighv7-2 |
A |
C |
12: 113,876,087 (GRCm39) |
I6S |
probably benign |
Het |
| Irs1 |
A |
G |
1: 82,265,696 (GRCm39) |
V840A |
probably benign |
Het |
| Itgal |
A |
G |
7: 126,927,405 (GRCm39) |
E965G |
probably damaging |
Het |
| Izumo1 |
T |
G |
7: 45,272,233 (GRCm39) |
F5V |
probably benign |
Het |
| Izumo1 |
T |
A |
7: 45,272,234 (GRCm39) |
F5Y |
probably damaging |
Het |
| Kif13a |
A |
G |
13: 46,978,687 (GRCm39) |
S175P |
probably damaging |
Het |
| Klf14 |
A |
G |
6: 30,934,960 (GRCm39) |
F225L |
probably damaging |
Het |
| Kpna1 |
T |
C |
16: 35,853,773 (GRCm39) |
Y468H |
probably damaging |
Het |
| Krt5 |
T |
A |
15: 101,617,494 (GRCm39) |
Q413L |
probably damaging |
Het |
| Lbr |
T |
C |
1: 181,665,986 (GRCm39) |
Y41C |
probably damaging |
Het |
| Lmcd1 |
A |
T |
6: 112,292,834 (GRCm39) |
N229Y |
probably damaging |
Het |
| Marchf3 |
T |
A |
18: 56,916,170 (GRCm39) |
H175L |
probably benign |
Het |
| Mcmbp |
A |
G |
7: 128,300,124 (GRCm39) |
|
probably null |
Het |
| Med27 |
T |
A |
2: 29,303,515 (GRCm39) |
L16Q |
probably damaging |
Het |
| Mex3b |
A |
T |
7: 82,518,273 (GRCm39) |
Q196L |
possibly damaging |
Het |
| Mroh2a |
C |
T |
1: 88,179,087 (GRCm39) |
L1104F |
probably damaging |
Het |
| Mta3 |
A |
G |
17: 84,063,103 (GRCm39) |
E166G |
probably damaging |
Het |
| Mthfd2l |
A |
G |
5: 91,096,727 (GRCm39) |
E116G |
possibly damaging |
Het |
| Musk |
A |
G |
4: 58,301,706 (GRCm39) |
I155V |
probably benign |
Het |
| Myh7b |
G |
A |
2: 155,468,314 (GRCm39) |
W834* |
probably null |
Het |
| Myo18b |
T |
A |
5: 112,840,093 (GRCm39) |
R2567* |
probably null |
Het |
| Nars2 |
A |
T |
7: 96,684,452 (GRCm39) |
E325V |
probably damaging |
Het |
| Nploc4 |
A |
G |
11: 120,312,260 (GRCm39) |
V106A |
possibly damaging |
Het |
| Nudcd1 |
A |
T |
15: 44,268,878 (GRCm39) |
S167R |
probably damaging |
Het |
| Nup133 |
T |
A |
8: 124,656,137 (GRCm39) |
D448V |
probably damaging |
Het |
| Or5al1 |
G |
T |
2: 85,990,417 (GRCm39) |
T99N |
probably benign |
Het |
| Or5p70 |
A |
T |
7: 107,995,229 (GRCm39) |
K301* |
probably null |
Het |
| Pax6 |
C |
A |
2: 105,526,847 (GRCm39) |
P251Q |
probably benign |
Het |
| Pcdh8 |
C |
T |
14: 80,005,710 (GRCm39) |
A893T |
possibly damaging |
Het |
| Per3 |
A |
T |
4: 151,093,716 (GRCm39) |
V1033E |
probably damaging |
Het |
| Polr1e |
T |
C |
4: 45,019,282 (GRCm39) |
S44P |
probably damaging |
Het |
| Pou4f2 |
T |
A |
8: 79,161,865 (GRCm39) |
H246L |
possibly damaging |
Het |
| Psmd2 |
G |
A |
16: 20,481,429 (GRCm39) |
R828Q |
probably damaging |
Het |
| Ptprq |
A |
G |
10: 107,524,288 (GRCm39) |
S482P |
probably benign |
Het |
| Rbm14 |
G |
T |
19: 4,852,671 (GRCm39) |
|
probably benign |
Het |
| Reln |
T |
C |
5: 22,254,698 (GRCm39) |
D557G |
probably damaging |
Het |
| Rhobtb2 |
A |
G |
14: 70,034,499 (GRCm39) |
I242T |
probably benign |
Het |
| Runx1 |
C |
A |
16: 92,492,629 (GRCm39) |
V5L |
possibly damaging |
Het |
| Shld2 |
G |
A |
14: 33,990,663 (GRCm39) |
T81M |
probably damaging |
Het |
| Slc13a1 |
A |
T |
6: 24,100,339 (GRCm39) |
Y381* |
probably null |
Het |
| Smyd3 |
A |
T |
1: 178,921,961 (GRCm39) |
C180S |
probably damaging |
Het |
| Sntg2 |
T |
A |
12: 30,326,658 (GRCm39) |
|
probably null |
Het |
| Snx19 |
G |
A |
9: 30,344,934 (GRCm39) |
V678I |
probably damaging |
Het |
| Spag5 |
G |
A |
11: 78,195,592 (GRCm39) |
A300T |
probably damaging |
Het |
| Spdl1 |
T |
A |
11: 34,704,154 (GRCm39) |
R560W |
probably damaging |
Het |
| Spen |
T |
C |
4: 141,199,907 (GRCm39) |
T2884A |
probably benign |
Het |
| Spg11 |
G |
A |
2: 121,895,963 (GRCm39) |
Q1752* |
probably null |
Het |
| Srrm4 |
C |
A |
5: 116,613,234 (GRCm39) |
|
probably null |
Het |
| Ssc4d |
A |
G |
5: 135,999,074 (GRCm39) |
L43P |
probably damaging |
Het |
| Sspo |
A |
G |
6: 48,437,813 (GRCm39) |
D1324G |
probably damaging |
Het |
| Tkt |
T |
G |
14: 30,288,982 (GRCm39) |
I238S |
probably damaging |
Het |
| Tmem184b |
A |
T |
15: 79,261,377 (GRCm39) |
N76K |
probably benign |
Het |
| Trpm6 |
A |
G |
19: 18,790,857 (GRCm39) |
M631V |
probably damaging |
Het |
| Ttll6 |
A |
C |
11: 96,024,655 (GRCm39) |
E15A |
possibly damaging |
Het |
| Ttn |
T |
C |
2: 76,569,296 (GRCm39) |
D27199G |
probably damaging |
Het |
| Ubn2 |
A |
T |
6: 38,464,088 (GRCm39) |
|
probably null |
Het |
| Ubr5 |
A |
C |
15: 38,018,541 (GRCm39) |
I866M |
possibly damaging |
Het |
| Urb1 |
T |
C |
16: 90,550,406 (GRCm39) |
T2149A |
probably benign |
Het |
| Ush2a |
G |
T |
1: 188,529,966 (GRCm39) |
V3252L |
possibly damaging |
Het |
| Usp24 |
A |
G |
4: 106,219,377 (GRCm39) |
|
probably null |
Het |
| Vill |
T |
A |
9: 118,897,502 (GRCm39) |
M259K |
probably damaging |
Het |
| Vldlr |
T |
C |
19: 27,217,290 (GRCm39) |
I411T |
probably damaging |
Het |
| Vmn2r120 |
A |
T |
17: 57,831,887 (GRCm39) |
W301R |
probably damaging |
Het |
| Vps13b |
G |
A |
15: 35,910,946 (GRCm39) |
S3570N |
probably damaging |
Het |
| Vps13c |
T |
C |
9: 67,836,821 (GRCm39) |
V1773A |
probably benign |
Het |
| Vtn |
A |
G |
11: 78,392,400 (GRCm39) |
D326G |
probably benign |
Het |
| Wdr93 |
A |
T |
7: 79,426,511 (GRCm39) |
H592L |
probably damaging |
Het |
| Zdhhc19 |
A |
G |
16: 32,317,953 (GRCm39) |
D94G |
probably damaging |
Het |
| Zfand4 |
A |
T |
6: 116,291,311 (GRCm39) |
E188V |
probably damaging |
Het |
| Zfp523 |
C |
A |
17: 28,420,312 (GRCm39) |
|
probably null |
Het |
| Zfp536 |
T |
C |
7: 37,268,309 (GRCm39) |
D369G |
probably damaging |
Het |
| Zfp608 |
T |
A |
18: 55,121,372 (GRCm39) |
T72S |
probably benign |
Het |
| Zfp804a |
T |
A |
2: 82,088,286 (GRCm39) |
V705E |
probably benign |
Het |
| Zfp974 |
T |
C |
7: 27,625,733 (GRCm39) |
T46A |
probably damaging |
Het |
| Zkscan4 |
C |
T |
13: 21,663,416 (GRCm39) |
Q52* |
probably null |
Het |
|
| Other mutations in Mga |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00551:Mga
|
APN |
2 |
119,750,295 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
IGL00719:Mga
|
APN |
2 |
119,777,934 (GRCm39) |
nonsense |
probably null |
|
|
IGL01619:Mga
|
APN |
2 |
119,762,309 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
IGL01721:Mga
|
APN |
2 |
119,765,720 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01759:Mga
|
APN |
2 |
119,781,676 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL01785:Mga
|
APN |
2 |
119,733,393 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01786:Mga
|
APN |
2 |
119,733,393 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01950:Mga
|
APN |
2 |
119,772,135 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
IGL01960:Mga
|
APN |
2 |
119,769,138 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02086:Mga
|
APN |
2 |
119,754,517 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02364:Mga
|
APN |
2 |
119,794,535 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
IGL02602:Mga
|
APN |
2 |
119,762,365 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
IGL02751:Mga
|
APN |
2 |
119,778,251 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
IGL02794:Mga
|
APN |
2 |
119,776,770 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
IGL03247:Mga
|
APN |
2 |
119,765,994 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
IGL03303:Mga
|
APN |
2 |
119,733,933 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4515001:Mga
|
UTSW |
2 |
119,746,985 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0060:Mga
|
UTSW |
2 |
119,791,442 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0060:Mga
|
UTSW |
2 |
119,791,442 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0417:Mga
|
UTSW |
2 |
119,733,271 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0449:Mga
|
UTSW |
2 |
119,771,862 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0457:Mga
|
UTSW |
2 |
119,746,969 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0538:Mga
|
UTSW |
2 |
119,750,187 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0568:Mga
|
UTSW |
2 |
119,765,903 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0614:Mga
|
UTSW |
2 |
119,794,947 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0671:Mga
|
UTSW |
2 |
119,750,391 (GRCm39) |
splice site |
probably null |
|
|
R0811:Mga
|
UTSW |
2 |
119,778,442 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0812:Mga
|
UTSW |
2 |
119,778,442 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0948:Mga
|
UTSW |
2 |
119,772,140 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R1177:Mga
|
UTSW |
2 |
119,756,927 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1445:Mga
|
UTSW |
2 |
119,733,179 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1476:Mga
|
UTSW |
2 |
119,772,156 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1527:Mga
|
UTSW |
2 |
119,747,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1583:Mga
|
UTSW |
2 |
119,794,441 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R1592:Mga
|
UTSW |
2 |
119,795,147 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1627:Mga
|
UTSW |
2 |
119,795,043 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1658:Mga
|
UTSW |
2 |
119,772,170 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R1677:Mga
|
UTSW |
2 |
119,791,333 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1887:Mga
|
UTSW |
2 |
119,754,098 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1908:Mga
|
UTSW |
2 |
119,757,075 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R1909:Mga
|
UTSW |
2 |
119,757,075 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R2061:Mga
|
UTSW |
2 |
119,795,461 (GRCm39) |
unclassified |
probably benign |
|
|
R2145:Mga
|
UTSW |
2 |
119,794,638 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R2159:Mga
|
UTSW |
2 |
119,750,124 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2179:Mga
|
UTSW |
2 |
119,790,923 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2281:Mga
|
UTSW |
2 |
119,734,204 (GRCm39) |
missense |
probably benign |
|
|
R2423:Mga
|
UTSW |
2 |
119,795,274 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3620:Mga
|
UTSW |
2 |
119,747,149 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3622:Mga
|
UTSW |
2 |
119,772,245 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3624:Mga
|
UTSW |
2 |
119,772,245 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3802:Mga
|
UTSW |
2 |
119,777,820 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4011:Mga
|
UTSW |
2 |
119,762,261 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4065:Mga
|
UTSW |
2 |
119,777,483 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4520:Mga
|
UTSW |
2 |
119,778,579 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R4649:Mga
|
UTSW |
2 |
119,771,974 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R4660:Mga
|
UTSW |
2 |
119,769,104 (GRCm39) |
intron |
probably benign |
|
|
R4757:Mga
|
UTSW |
2 |
119,734,120 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R4784:Mga
|
UTSW |
2 |
119,733,538 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4866:Mga
|
UTSW |
2 |
119,794,535 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R4900:Mga
|
UTSW |
2 |
119,794,535 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R4952:Mga
|
UTSW |
2 |
119,733,782 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4995:Mga
|
UTSW |
2 |
119,763,063 (GRCm39) |
nonsense |
probably null |
|
|
R5020:Mga
|
UTSW |
2 |
119,781,654 (GRCm39) |
nonsense |
probably null |
|
|
R5082:Mga
|
UTSW |
2 |
119,733,825 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5208:Mga
|
UTSW |
2 |
119,778,462 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R5454:Mga
|
UTSW |
2 |
119,733,810 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5466:Mga
|
UTSW |
2 |
119,733,178 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5484:Mga
|
UTSW |
2 |
119,747,107 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R5669:Mga
|
UTSW |
2 |
119,733,907 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5819:Mga
|
UTSW |
2 |
119,771,744 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R5916:Mga
|
UTSW |
2 |
119,794,793 (GRCm39) |
missense |
probably benign |
0.27 |
|
R5942:Mga
|
UTSW |
2 |
119,777,440 (GRCm39) |
missense |
probably benign |
0.41 |
|
R6305:Mga
|
UTSW |
2 |
119,778,179 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6434:Mga
|
UTSW |
2 |
119,754,419 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6467:Mga
|
UTSW |
2 |
119,776,776 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6488:Mga
|
UTSW |
2 |
119,791,388 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6630:Mga
|
UTSW |
2 |
119,754,140 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6790:Mga
|
UTSW |
2 |
119,754,235 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7029:Mga
|
UTSW |
2 |
119,754,031 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7039:Mga
|
UTSW |
2 |
119,763,159 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7088:Mga
|
UTSW |
2 |
119,792,417 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7195:Mga
|
UTSW |
2 |
119,747,809 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7273:Mga
|
UTSW |
2 |
119,765,695 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7286:Mga
|
UTSW |
2 |
119,795,269 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7346:Mga
|
UTSW |
2 |
119,766,008 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R7383:Mga
|
UTSW |
2 |
119,790,821 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7469:Mga
|
UTSW |
2 |
119,733,527 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7484:Mga
|
UTSW |
2 |
119,776,710 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7537:Mga
|
UTSW |
2 |
119,766,032 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7781:Mga
|
UTSW |
2 |
119,747,838 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7921:Mga
|
UTSW |
2 |
119,750,159 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8165:Mga
|
UTSW |
2 |
119,777,719 (GRCm39) |
missense |
probably benign |
0.12 |
|
R8226:Mga
|
UTSW |
2 |
119,790,866 (GRCm39) |
missense |
probably benign |
0.33 |
|
R8305:Mga
|
UTSW |
2 |
119,776,800 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R8309:Mga
|
UTSW |
2 |
119,791,411 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8363:Mga
|
UTSW |
2 |
119,794,407 (GRCm39) |
missense |
probably benign |
0.43 |
|
R8388:Mga
|
UTSW |
2 |
119,794,562 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8524:Mga
|
UTSW |
2 |
119,771,997 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8693:Mga
|
UTSW |
2 |
119,794,407 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R8837:Mga
|
UTSW |
2 |
119,769,272 (GRCm39) |
splice site |
probably benign |
|
|
R8916:Mga
|
UTSW |
2 |
119,788,819 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R8936:Mga
|
UTSW |
2 |
119,794,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9028:Mga
|
UTSW |
2 |
119,778,070 (GRCm39) |
missense |
probably benign |
|
|
R9145:Mga
|
UTSW |
2 |
119,794,493 (GRCm39) |
missense |
probably benign |
|
|
R9155:Mga
|
UTSW |
2 |
119,757,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9308:Mga
|
UTSW |
2 |
119,754,369 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R9342:Mga
|
UTSW |
2 |
119,778,656 (GRCm39) |
missense |
probably benign |
|
|
R9347:Mga
|
UTSW |
2 |
119,733,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9390:Mga
|
UTSW |
2 |
119,794,332 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9408:Mga
|
UTSW |
2 |
119,765,999 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R9488:Mga
|
UTSW |
2 |
119,795,304 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9495:Mga
|
UTSW |
2 |
119,781,676 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R9521:Mga
|
UTSW |
2 |
119,794,979 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9780:Mga
|
UTSW |
2 |
119,747,253 (GRCm39) |
missense |
probably benign |
0.26 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCTGAAGGACTCAAGCATAGAGATG -3'
(R):5'- AAGGACATCTGGCTCAGAGG -3'
Sequencing Primer
(F):5'- ACTCAAGCATAGAGATGGAACTG -3'
(R):5'- GTCATCATCTTCCAAGTGCAAGAGG -3'
|
| Posted On |
2015-12-29 |
Incidental Mutation