Incidental Mutation 'R9789:Mical2'
ID |
734527 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mical2
|
Ensembl Gene |
ENSMUSG00000038244 |
Gene Name |
microtubule associated monooxygenase, calponin and LIM domain containing 2 |
Synonyms |
4921517J23Rik, Ebitein1, 5330438E18Rik, Micalcl |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.242)
|
Stock # |
R9789 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
111825063-112012313 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 111945996 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Histidine
at position 986
(R986H)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000047639
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037991]
[ENSMUST00000050149]
|
AlphaFold |
Q8BML1 Q9D5U9 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000037991
AA Change: R986H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000047639 Gene: ENSMUSG00000038244 AA Change: R986H
Domain | Start | End | E-Value | Type |
Pfam:FAD_binding_3
|
86 |
143 |
1e-8 |
PFAM |
Pfam:FAD_binding_2
|
88 |
127 |
3.2e-6 |
PFAM |
low complexity region
|
175 |
188 |
N/A |
INTRINSIC |
low complexity region
|
500 |
515 |
N/A |
INTRINSIC |
CH
|
518 |
617 |
4.14e-17 |
SMART |
low complexity region
|
691 |
700 |
N/A |
INTRINSIC |
low complexity region
|
894 |
925 |
N/A |
INTRINSIC |
LIM
|
979 |
1033 |
9.91e-10 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000050149
AA Change: R759H
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000051163 Gene: ENSMUSG00000038244 AA Change: R759H
Domain | Start | End | E-Value | Type |
Pfam:FAD_binding_3
|
86 |
143 |
1.1e-8 |
PFAM |
Pfam:FAD_binding_2
|
88 |
127 |
1.5e-6 |
PFAM |
Pfam:Pyr_redox_2
|
88 |
259 |
1.3e-6 |
PFAM |
low complexity region
|
500 |
515 |
N/A |
INTRINSIC |
CH
|
518 |
617 |
4.14e-17 |
SMART |
low complexity region
|
691 |
700 |
N/A |
INTRINSIC |
LIM
|
752 |
806 |
9.91e-10 |
SMART |
low complexity region
|
918 |
926 |
N/A |
INTRINSIC |
|
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000123341 Gene: ENSMUSG00000038244 AA Change: R20H
Domain | Start | End | E-Value | Type |
LIM
|
14 |
68 |
9.91e-10 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000215412
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000216652
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.8%
- 10x: 99.5%
- 20x: 98.9%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a monooxygenase that enhances depolymerization of F-actin and is therefore involved in cytoskeletal dynamics. The encoded protein is a regulator of the SRF signaling pathway. Increased expression of this gene has been associated with cancer progression and metastasis. [provided by RefSeq, Oct 2016]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,231,357 (GRCm39) |
S1038R |
probably benign |
Het |
Aar2 |
T |
C |
2: 156,392,745 (GRCm39) |
F45L |
probably damaging |
Het |
Abcg2 |
A |
G |
6: 58,641,533 (GRCm39) |
Y122C |
probably damaging |
Het |
Arfgef1 |
A |
T |
1: 10,243,427 (GRCm39) |
W1041R |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,873,373 (GRCm39) |
N52S |
probably benign |
Het |
Asrgl1 |
T |
A |
19: 9,093,974 (GRCm39) |
T185S |
probably damaging |
Het |
Astl |
T |
A |
2: 127,192,146 (GRCm39) |
S234T |
probably damaging |
Het |
Atp5mf |
T |
C |
5: 145,120,656 (GRCm39) |
Y87C |
probably damaging |
Het |
Atxn7l1 |
A |
T |
12: 33,396,062 (GRCm39) |
R264W |
probably damaging |
Het |
Axin2 |
T |
C |
11: 108,840,180 (GRCm39) |
Y828H |
probably damaging |
Het |
Bnipl |
T |
C |
3: 95,153,140 (GRCm39) |
D145G |
possibly damaging |
Het |
C8b |
A |
T |
4: 104,640,191 (GRCm39) |
M165L |
probably benign |
Het |
Cd109 |
T |
C |
9: 78,541,944 (GRCm39) |
L87P |
possibly damaging |
Het |
Cdk17 |
C |
T |
10: 93,060,891 (GRCm39) |
P232S |
probably damaging |
Het |
Cnot1 |
T |
C |
8: 96,455,772 (GRCm39) |
E1995G |
probably damaging |
Het |
Csf2rb2 |
G |
A |
15: 78,169,196 (GRCm39) |
A653V |
probably benign |
Het |
Cutc |
A |
G |
19: 43,756,699 (GRCm39) |
N264D |
probably benign |
Het |
Cxcr4 |
C |
T |
1: 128,516,884 (GRCm39) |
W259* |
probably null |
Het |
Dnah8 |
T |
C |
17: 30,980,104 (GRCm39) |
|
probably null |
Het |
Dsp |
T |
C |
13: 38,367,937 (GRCm39) |
I652T |
probably benign |
Het |
Dstyk |
A |
T |
1: 132,381,859 (GRCm39) |
M538L |
probably benign |
Het |
Eppk1 |
T |
A |
15: 75,993,219 (GRCm39) |
I1221F |
probably benign |
Het |
Ern2 |
T |
A |
7: 121,769,485 (GRCm39) |
Y847F |
probably damaging |
Het |
Exosc7 |
T |
A |
9: 122,959,990 (GRCm39) |
V197D |
probably damaging |
Het |
Gabra1 |
T |
C |
11: 42,024,352 (GRCm39) |
Y441C |
probably damaging |
Het |
Garem1 |
G |
A |
18: 21,262,985 (GRCm39) |
P610S |
possibly damaging |
Het |
Garem2 |
T |
A |
5: 30,319,330 (GRCm39) |
V264E |
probably damaging |
Het |
Gata2 |
G |
A |
6: 88,177,272 (GRCm39) |
G101S |
probably benign |
Het |
Gcnt4 |
A |
G |
13: 97,083,429 (GRCm39) |
T242A |
probably benign |
Het |
Ghitm |
A |
C |
14: 36,852,719 (GRCm39) |
Y120* |
probably null |
Het |
Gimap7 |
A |
G |
6: 48,700,470 (GRCm39) |
S19G |
probably damaging |
Het |
Gm5475 |
G |
A |
15: 100,324,881 (GRCm39) |
G103E |
unknown |
Het |
Gstcd |
A |
T |
3: 132,790,357 (GRCm39) |
C137S |
probably damaging |
Het |
Gtf2b |
AATCATC |
AATC |
3: 142,477,178 (GRCm39) |
|
probably benign |
Het |
Hfm1 |
T |
C |
5: 107,065,346 (GRCm39) |
D111G |
probably benign |
Het |
Ighg2b |
A |
G |
12: 113,270,304 (GRCm39) |
I238T |
|
Het |
Il2ra |
A |
C |
2: 11,685,161 (GRCm39) |
M166L |
probably benign |
Het |
Itga1 |
A |
T |
13: 115,171,820 (GRCm39) |
L95* |
probably null |
Het |
Itpr3 |
A |
G |
17: 27,308,915 (GRCm39) |
T373A |
probably benign |
Het |
Klhl28 |
A |
G |
12: 64,996,871 (GRCm39) |
V490A |
probably damaging |
Het |
Kntc1 |
A |
T |
5: 123,898,706 (GRCm39) |
N200I |
possibly damaging |
Het |
L3mbtl4 |
A |
G |
17: 68,766,794 (GRCm39) |
K167R |
probably benign |
Het |
Lgals1 |
A |
T |
15: 78,813,930 (GRCm39) |
T63S |
probably benign |
Het |
Lnpep |
C |
A |
17: 17,795,596 (GRCm39) |
C305F |
probably damaging |
Het |
Mcm5 |
C |
T |
8: 75,844,168 (GRCm39) |
S313F |
probably benign |
Het |
Mcmbp |
A |
G |
7: 128,311,583 (GRCm39) |
I310T |
possibly damaging |
Het |
Muc5b |
A |
T |
7: 141,415,330 (GRCm39) |
S2759C |
possibly damaging |
Het |
Myh7 |
A |
G |
14: 55,229,384 (GRCm39) |
V138A |
possibly damaging |
Het |
Ncr1 |
T |
G |
7: 4,344,300 (GRCm39) |
|
probably null |
Het |
Ndufa10 |
A |
T |
1: 92,397,610 (GRCm39) |
D145E |
possibly damaging |
Het |
Neo1 |
T |
A |
9: 58,801,307 (GRCm39) |
|
probably null |
Het |
Ninl |
A |
T |
2: 150,791,701 (GRCm39) |
S941T |
probably benign |
Het |
Nrm |
T |
A |
17: 36,172,411 (GRCm39) |
|
probably null |
Het |
Nup214 |
T |
C |
2: 31,907,227 (GRCm39) |
V1018A |
possibly damaging |
Het |
Odf1 |
A |
G |
15: 38,219,716 (GRCm39) |
I15V |
probably benign |
Het |
Or10al2 |
T |
A |
17: 37,983,059 (GRCm39) |
N48K |
probably damaging |
Het |
Or10j7 |
C |
T |
1: 173,011,458 (GRCm39) |
R181H |
probably benign |
Het |
Or1e1c |
A |
T |
11: 73,265,710 (GRCm39) |
N48I |
probably damaging |
Het |
Or4b1d |
T |
A |
2: 89,969,004 (GRCm39) |
T160S |
probably benign |
Het |
Or52e18 |
A |
T |
7: 104,609,657 (GRCm39) |
I94N |
probably damaging |
Het |
Or5m10 |
C |
T |
2: 85,717,338 (GRCm39) |
H65Y |
probably damaging |
Het |
Or5p66 |
A |
T |
7: 107,885,898 (GRCm39) |
V145D |
probably benign |
Het |
Or7g32 |
C |
A |
9: 19,389,382 (GRCm39) |
D55Y |
probably benign |
Het |
Osgin2 |
A |
T |
4: 15,998,957 (GRCm39) |
Y222N |
probably damaging |
Het |
Pcdhga10 |
T |
C |
18: 37,882,363 (GRCm39) |
V708A |
probably benign |
Het |
Pfn3 |
T |
C |
13: 55,562,900 (GRCm39) |
D27G |
possibly damaging |
Het |
Plch2 |
A |
G |
4: 155,095,322 (GRCm39) |
|
probably null |
Het |
Plin2 |
C |
A |
4: 86,576,914 (GRCm39) |
Q270H |
probably damaging |
Het |
Polk |
A |
G |
13: 96,630,403 (GRCm39) |
F386S |
probably damaging |
Het |
Prkar1a |
G |
A |
11: 109,556,778 (GRCm39) |
G286E |
probably damaging |
Het |
Prodh |
A |
T |
16: 17,898,049 (GRCm39) |
L276Q |
probably damaging |
Het |
Ranbp10 |
T |
C |
8: 106,513,306 (GRCm39) |
N202S |
probably damaging |
Het |
Rapgef6 |
C |
A |
11: 54,540,097 (GRCm39) |
T724K |
probably benign |
Het |
Rnf144a |
T |
A |
12: 26,377,574 (GRCm39) |
K56N |
probably benign |
Het |
Rpa1 |
T |
A |
11: 75,203,938 (GRCm39) |
K303I |
probably damaging |
Het |
Slc16a9 |
A |
C |
10: 70,118,340 (GRCm39) |
N220H |
possibly damaging |
Het |
Slc28a3 |
T |
C |
13: 58,724,664 (GRCm39) |
I197V |
probably benign |
Het |
Slc35d1 |
A |
T |
4: 103,071,946 (GRCm39) |
F19I |
|
Het |
Sohlh2 |
A |
T |
3: 55,099,721 (GRCm39) |
E164D |
probably damaging |
Het |
Sord |
A |
T |
2: 122,093,765 (GRCm39) |
K295* |
probably null |
Het |
Spata31d1b |
A |
G |
13: 59,860,196 (GRCm39) |
Y23C |
probably benign |
Het |
Stard9 |
T |
A |
2: 120,510,417 (GRCm39) |
Y333N |
probably damaging |
Het |
Tas2r107 |
A |
G |
6: 131,636,753 (GRCm39) |
F99L |
probably damaging |
Het |
Thap12 |
C |
T |
7: 98,352,592 (GRCm39) |
|
probably benign |
Het |
Tmprss9 |
A |
T |
10: 80,730,993 (GRCm39) |
T840S |
probably benign |
Het |
Trim16 |
T |
A |
11: 62,720,026 (GRCm39) |
|
probably null |
Het |
Ttc16 |
C |
T |
2: 32,664,805 (GRCm39) |
|
probably null |
Het |
Ttn |
C |
T |
2: 76,715,357 (GRCm39) |
E7912K |
unknown |
Het |
Unc80 |
A |
T |
1: 66,651,371 (GRCm39) |
Y1572F |
possibly damaging |
Het |
Usp42 |
G |
T |
5: 143,706,060 (GRCm39) |
A320D |
possibly damaging |
Het |
Vmn2r94 |
T |
C |
17: 18,464,038 (GRCm39) |
T751A |
probably damaging |
Het |
Zbtb41 |
C |
T |
1: 139,368,084 (GRCm39) |
L591F |
probably damaging |
Het |
Zdhhc5 |
T |
A |
2: 84,524,662 (GRCm39) |
E219D |
probably damaging |
Het |
Zfp248 |
A |
T |
6: 118,406,012 (GRCm39) |
F526I |
probably damaging |
Het |
Zfp322a |
T |
C |
13: 23,540,558 (GRCm39) |
K395E |
possibly damaging |
Het |
Zfp423 |
G |
A |
8: 88,506,877 (GRCm39) |
P1156S |
probably benign |
Het |
Zfp644 |
T |
C |
5: 106,786,131 (GRCm39) |
T139A |
possibly damaging |
Het |
|
Other mutations in Mical2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00504:Mical2
|
APN |
7 |
111,981,352 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00886:Mical2
|
APN |
7 |
111,914,279 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00934:Mical2
|
APN |
7 |
111,948,610 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00941:Mical2
|
APN |
7 |
111,920,652 (GRCm39) |
splice site |
probably benign |
|
IGL01020:Mical2
|
APN |
7 |
111,914,283 (GRCm39) |
splice site |
probably benign |
|
IGL01395:Mical2
|
APN |
7 |
111,922,792 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01658:Mical2
|
APN |
7 |
111,914,205 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01775:Mical2
|
APN |
7 |
111,981,269 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02040:Mical2
|
APN |
7 |
111,910,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02051:Mical2
|
APN |
7 |
111,980,597 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02388:Mical2
|
APN |
7 |
111,934,620 (GRCm39) |
missense |
probably benign |
|
IGL02551:Mical2
|
APN |
7 |
111,923,197 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02578:Mical2
|
APN |
7 |
111,950,580 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02751:Mical2
|
APN |
7 |
111,931,243 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03114:Mical2
|
APN |
7 |
111,996,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R0091:Mical2
|
UTSW |
7 |
111,980,503 (GRCm39) |
missense |
probably benign |
0.05 |
R0101:Mical2
|
UTSW |
7 |
111,936,074 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0415:Mical2
|
UTSW |
7 |
111,980,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Mical2
|
UTSW |
7 |
111,870,524 (GRCm39) |
missense |
probably benign |
0.00 |
R0594:Mical2
|
UTSW |
7 |
111,917,657 (GRCm39) |
missense |
probably damaging |
0.97 |
R0609:Mical2
|
UTSW |
7 |
111,920,647 (GRCm39) |
splice site |
probably null |
|
R0962:Mical2
|
UTSW |
7 |
111,979,624 (GRCm39) |
missense |
probably damaging |
0.99 |
R1521:Mical2
|
UTSW |
7 |
111,980,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R1542:Mical2
|
UTSW |
7 |
111,908,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R1611:Mical2
|
UTSW |
7 |
111,980,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R1740:Mical2
|
UTSW |
7 |
111,933,043 (GRCm39) |
missense |
probably benign |
|
R1815:Mical2
|
UTSW |
7 |
112,012,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R1855:Mical2
|
UTSW |
7 |
111,944,489 (GRCm39) |
missense |
probably benign |
0.21 |
R1958:Mical2
|
UTSW |
7 |
111,980,311 (GRCm39) |
missense |
probably benign |
0.00 |
R1962:Mical2
|
UTSW |
7 |
112,012,051 (GRCm39) |
missense |
probably benign |
0.14 |
R2086:Mical2
|
UTSW |
7 |
111,917,810 (GRCm39) |
missense |
probably benign |
0.31 |
R2136:Mical2
|
UTSW |
7 |
111,870,722 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2418:Mical2
|
UTSW |
7 |
111,919,941 (GRCm39) |
critical splice donor site |
probably null |
|
R2439:Mical2
|
UTSW |
7 |
111,994,002 (GRCm39) |
missense |
probably damaging |
0.99 |
R3053:Mical2
|
UTSW |
7 |
111,910,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R3979:Mical2
|
UTSW |
7 |
112,006,885 (GRCm39) |
splice site |
probably null |
|
R4308:Mical2
|
UTSW |
7 |
111,931,199 (GRCm39) |
missense |
probably benign |
0.27 |
R4551:Mical2
|
UTSW |
7 |
111,981,123 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4583:Mical2
|
UTSW |
7 |
112,012,154 (GRCm39) |
missense |
probably benign |
0.02 |
R4663:Mical2
|
UTSW |
7 |
111,927,884 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4868:Mical2
|
UTSW |
7 |
111,917,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R4902:Mical2
|
UTSW |
7 |
111,936,107 (GRCm39) |
missense |
probably benign |
|
R5112:Mical2
|
UTSW |
7 |
111,919,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R5459:Mical2
|
UTSW |
7 |
111,981,444 (GRCm39) |
missense |
probably benign |
0.00 |
R5487:Mical2
|
UTSW |
7 |
111,919,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R5563:Mical2
|
UTSW |
7 |
111,914,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R5763:Mical2
|
UTSW |
7 |
111,973,861 (GRCm39) |
critical splice donor site |
probably null |
|
R5817:Mical2
|
UTSW |
7 |
111,922,866 (GRCm39) |
missense |
probably benign |
|
R5987:Mical2
|
UTSW |
7 |
111,934,155 (GRCm39) |
missense |
probably benign |
0.00 |
R6042:Mical2
|
UTSW |
7 |
111,979,619 (GRCm39) |
missense |
probably benign |
0.40 |
R6087:Mical2
|
UTSW |
7 |
111,917,692 (GRCm39) |
nonsense |
probably null |
|
R6189:Mical2
|
UTSW |
7 |
112,012,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R6209:Mical2
|
UTSW |
7 |
111,923,293 (GRCm39) |
splice site |
probably null |
|
R6311:Mical2
|
UTSW |
7 |
111,922,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R6319:Mical2
|
UTSW |
7 |
111,927,884 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6578:Mical2
|
UTSW |
7 |
111,910,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Mical2
|
UTSW |
7 |
111,981,046 (GRCm39) |
missense |
probably damaging |
0.98 |
R6782:Mical2
|
UTSW |
7 |
111,945,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Mical2
|
UTSW |
7 |
111,975,266 (GRCm39) |
utr 3 prime |
probably benign |
|
R7061:Mical2
|
UTSW |
7 |
111,946,008 (GRCm39) |
missense |
probably benign |
0.10 |
R7147:Mical2
|
UTSW |
7 |
111,922,810 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7260:Mical2
|
UTSW |
7 |
111,919,001 (GRCm39) |
missense |
probably benign |
0.10 |
R7266:Mical2
|
UTSW |
7 |
111,902,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R7347:Mical2
|
UTSW |
7 |
111,981,358 (GRCm39) |
missense |
probably benign |
0.01 |
R7391:Mical2
|
UTSW |
7 |
111,919,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R7724:Mical2
|
UTSW |
7 |
111,922,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R7747:Mical2
|
UTSW |
7 |
111,933,046 (GRCm39) |
missense |
probably benign |
0.02 |
R7783:Mical2
|
UTSW |
7 |
112,012,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R7818:Mical2
|
UTSW |
7 |
111,944,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R7824:Mical2
|
UTSW |
7 |
112,006,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R7995:Mical2
|
UTSW |
7 |
111,980,975 (GRCm39) |
missense |
probably benign |
0.31 |
R8022:Mical2
|
UTSW |
7 |
111,902,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R8429:Mical2
|
UTSW |
7 |
111,944,460 (GRCm39) |
missense |
probably benign |
0.01 |
R8505:Mical2
|
UTSW |
7 |
111,919,007 (GRCm39) |
missense |
probably benign |
0.02 |
R8532:Mical2
|
UTSW |
7 |
111,917,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R8830:Mical2
|
UTSW |
7 |
111,980,403 (GRCm39) |
missense |
probably benign |
0.01 |
R8862:Mical2
|
UTSW |
7 |
111,910,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Mical2
|
UTSW |
7 |
111,980,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R8988:Mical2
|
UTSW |
7 |
111,910,661 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9006:Mical2
|
UTSW |
7 |
111,981,323 (GRCm39) |
missense |
probably benign |
0.13 |
R9123:Mical2
|
UTSW |
7 |
111,870,589 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9127:Mical2
|
UTSW |
7 |
111,870,589 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9128:Mical2
|
UTSW |
7 |
111,870,589 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9129:Mical2
|
UTSW |
7 |
111,870,589 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9140:Mical2
|
UTSW |
7 |
112,006,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R9187:Mical2
|
UTSW |
7 |
111,902,797 (GRCm39) |
nonsense |
probably null |
|
R9233:Mical2
|
UTSW |
7 |
111,981,399 (GRCm39) |
missense |
probably benign |
0.05 |
R9304:Mical2
|
UTSW |
7 |
111,980,974 (GRCm39) |
missense |
probably damaging |
0.97 |
R9310:Mical2
|
UTSW |
7 |
111,950,920 (GRCm39) |
missense |
probably benign |
0.45 |
R9377:Mical2
|
UTSW |
7 |
111,981,246 (GRCm39) |
missense |
probably benign |
0.10 |
R9399:Mical2
|
UTSW |
7 |
111,946,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R9457:Mical2
|
UTSW |
7 |
112,010,665 (GRCm39) |
missense |
probably damaging |
0.96 |
R9500:Mical2
|
UTSW |
7 |
111,936,054 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9620:Mical2
|
UTSW |
7 |
111,980,403 (GRCm39) |
missense |
probably benign |
0.01 |
R9652:Mical2
|
UTSW |
7 |
111,945,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R9657:Mical2
|
UTSW |
7 |
111,921,806 (GRCm39) |
missense |
probably benign |
0.37 |
R9756:Mical2
|
UTSW |
7 |
111,902,928 (GRCm39) |
missense |
probably damaging |
0.99 |
RF008:Mical2
|
UTSW |
7 |
111,922,833 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Mical2
|
UTSW |
7 |
111,946,050 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- ACATAAGCTGCAGCCAAGAG -3'
(R):5'- AAGTGTTGGGTGTCCTAGAGCC -3'
Sequencing Primer
(F):5'- AAGAGCCCAGAAGTCCCTGTG -3'
(R):5'- TTAGGACCCCAGAGTGAGGTCAC -3'
|
Posted On |
2022-11-14 |