Incidental Mutation 'R7423:Mug2'
ID |
575821 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mug2
|
Ensembl Gene |
ENSMUSG00000030131 |
Gene Name |
murinoglobulin 2 |
Synonyms |
|
MMRRC Submission |
045501-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.055)
|
Stock # |
R7423 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
6 |
Chromosomal Location |
121983720-122062924 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 122056685 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Asparagine
at position 1210
(S1210N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000080469
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081777]
|
AlphaFold |
P28666 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000081777
AA Change: S1210N
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
SMART Domains |
Protein: ENSMUSP00000080469 Gene: ENSMUSG00000030131 AA Change: S1210N
Domain | Start | End | E-Value | Type |
Pfam:A2M_N
|
128 |
221 |
3.5e-21 |
PFAM |
A2M_N_2
|
449 |
599 |
1.05e-42 |
SMART |
low complexity region
|
711 |
728 |
N/A |
INTRINSIC |
A2M
|
740 |
830 |
7.16e-36 |
SMART |
Pfam:Thiol-ester_cl
|
963 |
992 |
1e-18 |
PFAM |
low complexity region
|
994 |
1005 |
N/A |
INTRINSIC |
Pfam:A2M_comp
|
1012 |
1097 |
5.8e-34 |
PFAM |
Pfam:A2M_comp
|
1093 |
1243 |
3e-47 |
PFAM |
A2M_recep
|
1353 |
1440 |
1.85e-38 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 98.8%
|
Validation Efficiency |
96% (91/95) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg2 |
A |
T |
17: 57,175,257 (GRCm39) |
M85K |
probably benign |
Het |
Actn4 |
C |
T |
7: 28,593,680 (GRCm39) |
A905T |
probably damaging |
Het |
Aff1 |
T |
A |
5: 103,994,967 (GRCm39) |
V1055D |
probably damaging |
Het |
Aox3 |
A |
G |
1: 58,160,228 (GRCm39) |
E137G |
possibly damaging |
Het |
Apaf1 |
A |
T |
10: 90,895,468 (GRCm39) |
D443E |
probably damaging |
Het |
Arl5b |
C |
A |
2: 15,072,983 (GRCm39) |
A28E |
probably damaging |
Het |
Atg16l1 |
T |
C |
1: 87,714,023 (GRCm39) |
V478A |
probably damaging |
Het |
Atp6v1f |
G |
C |
6: 29,468,105 (GRCm39) |
E13Q |
probably null |
Het |
Atpaf1 |
A |
T |
4: 115,647,827 (GRCm39) |
K162M |
probably damaging |
Het |
C3 |
A |
T |
17: 57,521,767 (GRCm39) |
L1100Q |
probably damaging |
Het |
Ccr1 |
A |
G |
9: 123,764,422 (GRCm39) |
L36P |
probably damaging |
Het |
Cct3 |
T |
C |
3: 88,216,503 (GRCm39) |
L153S |
probably benign |
Het |
Chd4 |
A |
G |
6: 125,105,822 (GRCm39) |
D1813G |
possibly damaging |
Het |
Chrm3 |
T |
C |
13: 9,928,845 (GRCm39) |
I64V |
probably benign |
Het |
Cnot2 |
A |
T |
10: 116,328,303 (GRCm39) |
V477E |
probably damaging |
Het |
Csf2rb2 |
T |
A |
15: 78,176,760 (GRCm39) |
I211F |
possibly damaging |
Het |
Dnah8 |
T |
C |
17: 30,923,743 (GRCm39) |
L1237P |
possibly damaging |
Het |
Dnttip2 |
T |
C |
3: 122,069,175 (GRCm39) |
V130A |
probably benign |
Het |
Dock10 |
G |
A |
1: 80,501,497 (GRCm39) |
A1852V |
possibly damaging |
Het |
Dock3 |
A |
G |
9: 106,844,370 (GRCm39) |
V910A |
probably damaging |
Het |
Drgx |
A |
G |
14: 32,350,778 (GRCm39) |
S205G |
probably damaging |
Het |
Fbrs |
G |
A |
7: 127,088,633 (GRCm39) |
W738* |
probably null |
Het |
Fmnl3 |
T |
A |
15: 99,227,281 (GRCm39) |
D162V |
probably damaging |
Het |
Fosl2 |
A |
G |
5: 32,307,807 (GRCm39) |
R133G |
probably damaging |
Het |
Frmpd1 |
A |
G |
4: 45,256,948 (GRCm39) |
Q172R |
probably damaging |
Het |
Fsd1l |
A |
T |
4: 53,686,406 (GRCm39) |
D273V |
probably damaging |
Het |
Fstl4 |
T |
A |
11: 52,959,382 (GRCm39) |
M141K |
possibly damaging |
Het |
Gcfc2 |
A |
G |
6: 81,923,541 (GRCm39) |
D535G |
probably damaging |
Het |
Gm19410 |
A |
C |
8: 36,271,761 (GRCm39) |
D1277A |
probably benign |
Het |
Gnmt |
T |
A |
17: 47,037,066 (GRCm39) |
N211Y |
probably damaging |
Het |
Hic2 |
A |
G |
16: 17,075,993 (GRCm39) |
D274G |
probably damaging |
Het |
Hnrnpu |
A |
G |
1: 178,156,849 (GRCm39) |
|
probably benign |
Het |
Icam5 |
T |
C |
9: 20,948,201 (GRCm39) |
S670P |
probably benign |
Het |
Ighv5-4 |
A |
T |
12: 113,561,120 (GRCm39) |
L100Q |
probably damaging |
Het |
Il17rb |
A |
T |
14: 29,719,072 (GRCm39) |
S337T |
probably damaging |
Het |
Inf2 |
G |
T |
12: 112,576,172 (GRCm39) |
R883L |
unknown |
Het |
Inhbc |
C |
T |
10: 127,193,275 (GRCm39) |
C247Y |
probably damaging |
Het |
Ints4 |
A |
G |
7: 97,156,926 (GRCm39) |
K333E |
probably damaging |
Het |
Iyd |
A |
T |
10: 3,497,088 (GRCm39) |
I148F |
probably damaging |
Het |
Klk1b26 |
A |
T |
7: 43,664,193 (GRCm39) |
D16V |
probably damaging |
Het |
Krt15 |
A |
T |
11: 100,026,386 (GRCm39) |
V100E |
possibly damaging |
Het |
Lama2 |
A |
T |
10: 27,088,222 (GRCm39) |
S852T |
probably benign |
Het |
Mbtd1 |
A |
G |
11: 93,834,622 (GRCm39) |
E600G |
probably benign |
Het |
Mfap3 |
T |
G |
11: 57,420,329 (GRCm39) |
N103K |
probably damaging |
Het |
Mtor |
G |
A |
4: 148,640,801 (GRCm39) |
E2536K |
possibly damaging |
Het |
Nat8 |
G |
A |
6: 85,807,477 (GRCm39) |
L219F |
probably benign |
Het |
Nisch |
A |
G |
14: 30,893,658 (GRCm39) |
V1305A |
probably benign |
Het |
Nup153 |
A |
T |
13: 46,850,120 (GRCm39) |
|
probably null |
Het |
Or3a1b |
G |
A |
11: 74,012,811 (GRCm39) |
R232H |
probably benign |
Het |
Otud6b |
A |
T |
4: 14,825,858 (GRCm39) |
|
probably null |
Het |
Pbld2 |
A |
G |
10: 62,883,783 (GRCm39) |
T83A |
probably damaging |
Het |
Pcx |
A |
T |
19: 4,671,206 (GRCm39) |
M1144L |
probably benign |
Het |
Pdpk1 |
C |
A |
17: 24,329,874 (GRCm39) |
R81L |
probably benign |
Het |
Pik3cd |
A |
T |
4: 149,736,220 (GRCm39) |
|
probably null |
Het |
Plch2 |
A |
C |
4: 155,068,194 (GRCm39) |
D1477E |
probably damaging |
Het |
Plek2 |
A |
G |
12: 78,946,884 (GRCm39) |
I51T |
probably damaging |
Het |
Plekhn1 |
A |
G |
4: 156,315,142 (GRCm39) |
V505A |
probably benign |
Het |
Pofut2 |
T |
C |
10: 77,098,273 (GRCm39) |
S129P |
possibly damaging |
Het |
Prdx5 |
C |
A |
19: 6,887,370 (GRCm39) |
|
probably benign |
Het |
Proca1 |
G |
T |
11: 78,085,643 (GRCm39) |
|
probably benign |
Het |
Ptprs |
A |
C |
17: 56,721,793 (GRCm39) |
Y1752D |
probably damaging |
Het |
Pum1 |
G |
A |
4: 130,501,856 (GRCm39) |
V1127M |
probably damaging |
Het |
Ralbp1 |
T |
C |
17: 66,165,976 (GRCm39) |
R403G |
probably damaging |
Het |
Reps1 |
A |
T |
10: 17,969,635 (GRCm39) |
H246L |
possibly damaging |
Het |
Rps6kc1 |
A |
C |
1: 190,531,293 (GRCm39) |
M903R |
probably damaging |
Het |
Rubcnl |
A |
G |
14: 75,287,083 (GRCm39) |
T584A |
probably benign |
Het |
Samd9l |
A |
T |
6: 3,374,408 (GRCm39) |
V951E |
probably damaging |
Het |
Sbf2 |
A |
G |
7: 110,038,055 (GRCm39) |
F463L |
possibly damaging |
Het |
Sdr16c6 |
G |
A |
4: 4,076,921 (GRCm39) |
|
probably benign |
Het |
Shoc1 |
A |
T |
4: 59,076,264 (GRCm39) |
S560T |
probably benign |
Het |
Slc26a8 |
A |
G |
17: 28,867,177 (GRCm39) |
I548T |
probably benign |
Het |
Slc2a13 |
T |
A |
15: 91,456,883 (GRCm39) |
I140F |
probably damaging |
Het |
Smtn |
A |
T |
11: 3,481,200 (GRCm39) |
|
probably null |
Het |
Sobp |
G |
T |
10: 42,898,564 (GRCm39) |
C340* |
probably null |
Het |
Sox6 |
A |
T |
7: 115,149,258 (GRCm39) |
V413E |
probably benign |
Het |
Spin1 |
T |
C |
13: 51,277,326 (GRCm39) |
|
probably null |
Het |
Sra1 |
T |
C |
18: 36,800,536 (GRCm39) |
T224A |
probably benign |
Het |
Sv2c |
A |
T |
13: 96,185,056 (GRCm39) |
F207Y |
probably benign |
Het |
Tcp10c |
T |
A |
17: 13,581,503 (GRCm39) |
|
probably null |
Het |
Tkt |
G |
A |
14: 30,292,992 (GRCm39) |
G490S |
possibly damaging |
Het |
Tpgs1 |
G |
T |
10: 79,511,655 (GRCm39) |
A266S |
probably damaging |
Het |
Tprg1 |
T |
G |
16: 25,241,003 (GRCm39) |
S260A |
probably damaging |
Het |
Trdv2-1 |
T |
A |
14: 54,183,935 (GRCm39) |
W56R |
probably damaging |
Het |
Trgv6 |
G |
T |
13: 19,374,814 (GRCm39) |
G40W |
possibly damaging |
Het |
Trpc4 |
T |
A |
3: 54,225,450 (GRCm39) |
V933E |
probably benign |
Het |
Ulk4 |
A |
T |
9: 120,932,687 (GRCm39) |
M1051K |
possibly damaging |
Het |
Unc119b |
A |
G |
5: 115,272,743 (GRCm39) |
L76P |
probably damaging |
Het |
Vmn2r15 |
G |
A |
5: 109,445,394 (GRCm39) |
S10F |
probably benign |
Het |
Vwce |
A |
G |
19: 10,641,704 (GRCm39) |
E810G |
probably benign |
Het |
Wdr7 |
T |
A |
18: 63,910,451 (GRCm39) |
|
probably null |
Het |
Wnk2 |
T |
A |
13: 49,191,608 (GRCm39) |
E1283V |
probably benign |
Het |
Zfp28 |
T |
C |
7: 6,396,956 (GRCm39) |
C464R |
probably damaging |
Het |
Zpld1 |
C |
T |
16: 55,054,027 (GRCm39) |
C255Y |
probably damaging |
Het |
|
Other mutations in Mug2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00708:Mug2
|
APN |
6 |
122,024,446 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL00957:Mug2
|
APN |
6 |
122,017,613 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01314:Mug2
|
APN |
6 |
122,058,238 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01338:Mug2
|
APN |
6 |
122,026,587 (GRCm39) |
splice site |
probably benign |
|
IGL01477:Mug2
|
APN |
6 |
122,058,643 (GRCm39) |
splice site |
probably benign |
|
IGL01926:Mug2
|
APN |
6 |
122,013,063 (GRCm39) |
splice site |
probably benign |
|
IGL02019:Mug2
|
APN |
6 |
122,024,394 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02305:Mug2
|
APN |
6 |
122,013,015 (GRCm39) |
missense |
probably benign |
|
IGL02310:Mug2
|
APN |
6 |
122,036,082 (GRCm39) |
splice site |
probably benign |
|
IGL02484:Mug2
|
APN |
6 |
122,049,712 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02516:Mug2
|
APN |
6 |
122,047,802 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02531:Mug2
|
APN |
6 |
122,049,730 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02666:Mug2
|
APN |
6 |
122,058,285 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02936:Mug2
|
APN |
6 |
122,058,346 (GRCm39) |
critical splice donor site |
probably null |
|
R0114:Mug2
|
UTSW |
6 |
122,017,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R0119:Mug2
|
UTSW |
6 |
122,013,022 (GRCm39) |
missense |
probably benign |
0.00 |
R0123:Mug2
|
UTSW |
6 |
122,051,673 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0144:Mug2
|
UTSW |
6 |
122,047,970 (GRCm39) |
splice site |
probably benign |
|
R0225:Mug2
|
UTSW |
6 |
122,051,673 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0514:Mug2
|
UTSW |
6 |
122,058,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R0763:Mug2
|
UTSW |
6 |
122,052,253 (GRCm39) |
missense |
probably benign |
|
R0959:Mug2
|
UTSW |
6 |
122,062,454 (GRCm39) |
missense |
probably benign |
0.33 |
R1104:Mug2
|
UTSW |
6 |
122,036,014 (GRCm39) |
missense |
probably benign |
|
R1239:Mug2
|
UTSW |
6 |
122,058,637 (GRCm39) |
splice site |
probably benign |
|
R1318:Mug2
|
UTSW |
6 |
122,054,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R1460:Mug2
|
UTSW |
6 |
122,017,492 (GRCm39) |
splice site |
probably benign |
|
R1706:Mug2
|
UTSW |
6 |
122,013,191 (GRCm39) |
splice site |
probably benign |
|
R1761:Mug2
|
UTSW |
6 |
122,051,664 (GRCm39) |
missense |
probably benign |
0.20 |
R1901:Mug2
|
UTSW |
6 |
122,048,801 (GRCm39) |
missense |
probably benign |
0.02 |
R1913:Mug2
|
UTSW |
6 |
122,047,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R1943:Mug2
|
UTSW |
6 |
122,056,598 (GRCm39) |
missense |
probably benign |
|
R2054:Mug2
|
UTSW |
6 |
122,054,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Mug2
|
UTSW |
6 |
122,056,571 (GRCm39) |
missense |
probably benign |
|
R2420:Mug2
|
UTSW |
6 |
122,060,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R2432:Mug2
|
UTSW |
6 |
122,061,335 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2916:Mug2
|
UTSW |
6 |
122,051,683 (GRCm39) |
splice site |
probably null |
|
R2918:Mug2
|
UTSW |
6 |
122,051,683 (GRCm39) |
splice site |
probably null |
|
R3423:Mug2
|
UTSW |
6 |
122,024,465 (GRCm39) |
splice site |
probably benign |
|
R3834:Mug2
|
UTSW |
6 |
122,026,746 (GRCm39) |
critical splice donor site |
probably null |
|
R3902:Mug2
|
UTSW |
6 |
122,052,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R3941:Mug2
|
UTSW |
6 |
122,040,522 (GRCm39) |
missense |
probably benign |
|
R4227:Mug2
|
UTSW |
6 |
122,017,691 (GRCm39) |
missense |
probably benign |
0.10 |
R4284:Mug2
|
UTSW |
6 |
122,040,632 (GRCm39) |
missense |
probably benign |
0.00 |
R4287:Mug2
|
UTSW |
6 |
122,040,632 (GRCm39) |
missense |
probably benign |
0.00 |
R4377:Mug2
|
UTSW |
6 |
122,047,966 (GRCm39) |
critical splice donor site |
probably null |
|
R4419:Mug2
|
UTSW |
6 |
122,056,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R4498:Mug2
|
UTSW |
6 |
122,059,711 (GRCm39) |
missense |
probably damaging |
0.99 |
R4566:Mug2
|
UTSW |
6 |
122,056,597 (GRCm39) |
missense |
probably benign |
0.00 |
R4690:Mug2
|
UTSW |
6 |
122,013,255 (GRCm39) |
missense |
probably benign |
|
R4732:Mug2
|
UTSW |
6 |
122,048,831 (GRCm39) |
missense |
probably damaging |
0.99 |
R4733:Mug2
|
UTSW |
6 |
122,048,831 (GRCm39) |
missense |
probably damaging |
0.99 |
R4741:Mug2
|
UTSW |
6 |
122,056,572 (GRCm39) |
missense |
probably benign |
|
R4888:Mug2
|
UTSW |
6 |
122,058,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R5199:Mug2
|
UTSW |
6 |
122,017,619 (GRCm39) |
missense |
probably benign |
|
R5347:Mug2
|
UTSW |
6 |
122,058,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R5457:Mug2
|
UTSW |
6 |
122,026,688 (GRCm39) |
nonsense |
probably null |
|
R5495:Mug2
|
UTSW |
6 |
122,056,609 (GRCm39) |
missense |
probably damaging |
0.96 |
R5509:Mug2
|
UTSW |
6 |
122,061,340 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6006:Mug2
|
UTSW |
6 |
122,060,459 (GRCm39) |
missense |
probably null |
0.98 |
R6180:Mug2
|
UTSW |
6 |
122,056,565 (GRCm39) |
missense |
probably benign |
0.01 |
R6184:Mug2
|
UTSW |
6 |
122,014,005 (GRCm39) |
missense |
probably benign |
|
R6199:Mug2
|
UTSW |
6 |
122,024,398 (GRCm39) |
missense |
probably benign |
0.05 |
R6262:Mug2
|
UTSW |
6 |
122,052,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R6416:Mug2
|
UTSW |
6 |
122,059,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R6548:Mug2
|
UTSW |
6 |
122,024,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R6703:Mug2
|
UTSW |
6 |
122,055,653 (GRCm39) |
missense |
probably benign |
0.25 |
R7106:Mug2
|
UTSW |
6 |
122,059,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R7131:Mug2
|
UTSW |
6 |
122,052,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R7372:Mug2
|
UTSW |
6 |
122,060,425 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7379:Mug2
|
UTSW |
6 |
122,024,446 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7419:Mug2
|
UTSW |
6 |
122,017,529 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7581:Mug2
|
UTSW |
6 |
122,040,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R7582:Mug2
|
UTSW |
6 |
122,056,603 (GRCm39) |
missense |
probably damaging |
0.99 |
R7672:Mug2
|
UTSW |
6 |
122,017,678 (GRCm39) |
missense |
probably benign |
0.37 |
R7713:Mug2
|
UTSW |
6 |
122,055,754 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7759:Mug2
|
UTSW |
6 |
122,058,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R7834:Mug2
|
UTSW |
6 |
122,013,241 (GRCm39) |
missense |
probably benign |
|
R7850:Mug2
|
UTSW |
6 |
122,052,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R8029:Mug2
|
UTSW |
6 |
122,058,504 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8127:Mug2
|
UTSW |
6 |
122,052,567 (GRCm39) |
missense |
probably benign |
0.01 |
R8335:Mug2
|
UTSW |
6 |
122,017,543 (GRCm39) |
missense |
probably benign |
|
R8348:Mug2
|
UTSW |
6 |
122,049,192 (GRCm39) |
nonsense |
probably null |
|
R8557:Mug2
|
UTSW |
6 |
122,040,660 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:Mug2
|
UTSW |
6 |
122,058,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R8823:Mug2
|
UTSW |
6 |
122,040,648 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9029:Mug2
|
UTSW |
6 |
122,061,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R9153:Mug2
|
UTSW |
6 |
122,017,627 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9185:Mug2
|
UTSW |
6 |
122,054,442 (GRCm39) |
missense |
probably benign |
0.06 |
R9186:Mug2
|
UTSW |
6 |
122,052,248 (GRCm39) |
missense |
probably damaging |
0.99 |
R9418:Mug2
|
UTSW |
6 |
122,017,700 (GRCm39) |
missense |
probably benign |
0.00 |
R9464:Mug2
|
UTSW |
6 |
122,028,690 (GRCm39) |
missense |
probably benign |
0.01 |
R9622:Mug2
|
UTSW |
6 |
122,028,751 (GRCm39) |
missense |
probably benign |
0.29 |
Z1177:Mug2
|
UTSW |
6 |
122,014,080 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGAAGTCATGGACCACTCAGAC -3'
(R):5'- CCTACTGACAGAAAATATCCTTGAC -3'
Sequencing Primer
(F):5'- AGGCTTCCTCTGTTGAAG -3'
(R):5'- ATCTCATAACCCCATGGGG -3'
|
Posted On |
2019-10-07 |