Incidental Mutation 'R9500:Mical2'
| ID |
717502 |
| 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? |
Possibly non essential
(E-score: 0.298)
|
| Stock # |
R9500 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
111825063-112012313 bp(+) (GRCm39) |
| Type of Mutation |
critical splice acceptor site |
| DNA Base Change (assembly) |
A to T
at 111936054 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000047639
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037991]
[ENSMUST00000050149]
|
| AlphaFold |
Q8BML1
Q9D5U9 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000037991
|
| SMART Domains |
Protein: ENSMUSP00000047639
Gene: ENSMUSG00000038244
| 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 benign
Transcript: ENSMUST00000050149
|
| SMART Domains |
Protein: ENSMUSP00000051163
Gene: ENSMUSG00000038244
| 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 |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
| 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: 75 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310022A10Rik |
C |
T |
7: 27,265,091 (GRCm39) |
T107I |
possibly damaging |
Het |
| Acyp1 |
T |
A |
12: 85,325,786 (GRCm39) |
Y71F |
unknown |
Het |
| Akap11 |
A |
T |
14: 78,748,543 (GRCm39) |
H1281Q |
|
Het |
| Amz1 |
T |
C |
5: 140,737,975 (GRCm39) |
Y412H |
probably benign |
Het |
| Anxa10 |
C |
T |
8: 62,545,545 (GRCm39) |
M62I |
probably benign |
Het |
| Arhgap25 |
T |
C |
6: 87,469,184 (GRCm39) |
K109E |
probably damaging |
Het |
| Arhgap31 |
T |
A |
16: 38,460,683 (GRCm39) |
E43D |
probably damaging |
Het |
| Atf6 |
T |
C |
1: 170,574,708 (GRCm39) |
M577V |
probably damaging |
Het |
| Auts2 |
C |
A |
5: 131,505,620 (GRCm39) |
A82S |
unknown |
Het |
| Bcl3 |
T |
C |
7: 19,556,602 (GRCm39) |
M1V |
probably null |
Het |
| Cblb |
T |
C |
16: 51,959,993 (GRCm39) |
|
probably null |
Het |
| Cc2d2b |
T |
C |
19: 40,797,840 (GRCm39) |
V820A |
unknown |
Het |
| Clint1 |
T |
G |
11: 45,797,194 (GRCm39) |
M425R |
possibly damaging |
Het |
| Clvs1 |
A |
G |
4: 9,429,834 (GRCm39) |
D279G |
probably damaging |
Het |
| Colec11 |
A |
C |
12: 28,645,302 (GRCm39) |
I123S |
probably damaging |
Het |
| Crebbp |
C |
T |
16: 3,911,355 (GRCm39) |
E1460K |
probably damaging |
Het |
| Cyp2t4 |
G |
A |
7: 26,854,717 (GRCm39) |
V66M |
possibly damaging |
Het |
| Dcaf8 |
C |
G |
1: 171,999,909 (GRCm39) |
S22R |
possibly damaging |
Het |
| Dmxl1 |
T |
C |
18: 50,011,271 (GRCm39) |
S1143P |
probably damaging |
Het |
| Dnhd1 |
T |
C |
7: 105,353,709 (GRCm39) |
I2954T |
probably benign |
Het |
| Dop1b |
C |
T |
16: 93,607,171 (GRCm39) |
P2275L |
probably benign |
Het |
| Drc3 |
A |
G |
11: 60,261,334 (GRCm39) |
S162G |
probably benign |
Het |
| Ehd2 |
T |
C |
7: 15,686,077 (GRCm39) |
I332V |
possibly damaging |
Het |
| Eml1 |
T |
A |
12: 108,493,958 (GRCm39) |
D584E |
probably damaging |
Het |
| Eogt |
T |
C |
6: 97,096,992 (GRCm39) |
T339A |
probably benign |
Het |
| Gbf1 |
A |
G |
19: 46,258,389 (GRCm39) |
T949A |
probably benign |
Het |
| Gm11568 |
GCTGCTGCCAGCCCTGCTGCCAGCCC |
GCTGCTGCCAGCCCTGCTGCCAGCCCTGCTGCCAGCCC |
11: 99,749,044 (GRCm39) |
|
probably benign |
Het |
| Gm11568 |
AGCCC |
AGCCCTGCTGCCTGCCC |
11: 99,749,065 (GRCm39) |
|
probably benign |
Het |
| Gtpbp10 |
A |
T |
5: 5,606,120 (GRCm39) |
C88* |
probably null |
Het |
| Ifit1bl2 |
A |
T |
19: 34,596,508 (GRCm39) |
Y369* |
probably null |
Het |
| Igsf6 |
A |
G |
7: 120,673,697 (GRCm39) |
L11P |
probably benign |
Het |
| Lars1 |
A |
T |
18: 42,361,726 (GRCm39) |
I627N |
probably damaging |
Het |
| Lmo3 |
G |
T |
6: 138,393,621 (GRCm39) |
Q11K |
|
Het |
| Mmp23 |
A |
G |
4: 155,736,567 (GRCm39) |
V158A |
probably benign |
Het |
| Mmp24 |
T |
C |
2: 155,654,195 (GRCm39) |
I391T |
probably damaging |
Het |
| Mrgpra3 |
A |
T |
7: 47,239,400 (GRCm39) |
Y175* |
probably null |
Het |
| Mrpl23 |
G |
A |
7: 142,089,859 (GRCm39) |
V65M |
probably damaging |
Het |
| Mup1 |
A |
G |
4: 60,456,488 (GRCm39) |
L85S |
possibly damaging |
Het |
| Myo15b |
T |
C |
11: 115,777,466 (GRCm39) |
L747S |
probably damaging |
Het |
| Nanog |
G |
T |
6: 122,690,219 (GRCm39) |
W208L |
probably damaging |
Het |
| Nkg7 |
A |
G |
7: 43,087,229 (GRCm39) |
Y112C |
probably damaging |
Het |
| Nup155 |
A |
G |
15: 8,141,800 (GRCm39) |
D64G |
probably damaging |
Het |
| Or13p4 |
A |
G |
4: 118,546,930 (GRCm39) |
S240P |
possibly damaging |
Het |
| Palm3 |
T |
C |
8: 84,753,636 (GRCm39) |
S108P |
probably damaging |
Het |
| Pam |
T |
C |
1: 97,772,325 (GRCm39) |
N579D |
probably benign |
Het |
| Pclo |
A |
G |
5: 14,725,648 (GRCm39) |
E1502G |
unknown |
Het |
| Pde4dip |
A |
G |
3: 97,795,896 (GRCm39) |
S31P |
unknown |
Het |
| Peg10 |
A |
T |
6: 4,756,871 (GRCm39) |
K482N |
unknown |
Het |
| Phf19 |
A |
T |
2: 34,801,708 (GRCm39) |
L34* |
probably null |
Het |
| Pla2g2c |
A |
T |
4: 138,461,689 (GRCm39) |
K53* |
probably null |
Het |
| Pla2g4f |
T |
A |
2: 120,142,713 (GRCm39) |
|
probably null |
Het |
| Polk |
G |
T |
13: 96,630,349 (GRCm39) |
T404K |
probably damaging |
Het |
| Prkdc |
T |
A |
16: 15,657,079 (GRCm39) |
V4058D |
possibly damaging |
Het |
| Prox2 |
T |
A |
12: 85,134,851 (GRCm39) |
I477F |
probably damaging |
Het |
| Ptk6 |
A |
G |
2: 180,837,566 (GRCm39) |
V451A |
probably benign |
Het |
| Ptpn3 |
C |
T |
4: 57,205,914 (GRCm39) |
E693K |
possibly damaging |
Het |
| Rag2 |
G |
A |
2: 101,461,217 (GRCm39) |
G509D |
probably damaging |
Het |
| Rapgef2 |
A |
G |
3: 78,974,093 (GRCm39) |
C1418R |
probably benign |
Het |
| Rev1 |
A |
T |
1: 38,102,214 (GRCm39) |
Y716* |
probably null |
Het |
| Rsl1d1 |
T |
A |
16: 11,011,385 (GRCm39) |
T440S |
possibly damaging |
Het |
| Samd14 |
T |
A |
11: 94,914,372 (GRCm39) |
Y343* |
probably null |
Het |
| Sema3a |
A |
T |
5: 13,615,854 (GRCm39) |
D426V |
possibly damaging |
Het |
| Slc7a11 |
G |
A |
3: 50,382,201 (GRCm39) |
T182M |
probably benign |
Het |
| Slitrk5 |
A |
G |
14: 111,916,726 (GRCm39) |
I117V |
possibly damaging |
Het |
| Son |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,457,222 (GRCm39) |
|
probably benign |
Het |
| Stil |
A |
T |
4: 114,878,716 (GRCm39) |
H384L |
possibly damaging |
Het |
| Suclg2 |
C |
A |
6: 95,546,666 (GRCm39) |
R270L |
probably damaging |
Het |
| Taf5 |
A |
G |
19: 47,065,771 (GRCm39) |
D492G |
probably damaging |
Het |
| Tes3-ps |
T |
A |
13: 49,647,815 (GRCm39) |
Y230* |
probably null |
Het |
| Ttc41 |
G |
T |
10: 86,565,726 (GRCm39) |
A427S |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,553,994 (GRCm39) |
D30903G |
probably damaging |
Het |
| Txndc16 |
A |
T |
14: 45,406,798 (GRCm39) |
L219Q |
probably null |
Het |
| Usp34 |
T |
A |
11: 23,331,337 (GRCm39) |
H1098Q |
probably damaging |
Het |
| Vmn2r52 |
T |
A |
7: 9,905,281 (GRCm39) |
Y186F |
probably damaging |
Het |
| Zbtb41 |
T |
C |
1: 139,359,806 (GRCm39) |
F512S |
probably 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 |
|
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 |
|
R9789:Mical2
|
UTSW |
7 |
111,945,996 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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'- AAGCACAGTATAGTCCAGCC -3'
(R):5'- AGCCTGGCTCCAGATGTTTG -3'
Sequencing Primer
(F):5'- CAGGAGCTACATAATCCCACTTGG -3'
(R):5'- GATGGAGCCCGAGAACAACTC -3'
|
| Posted On |
2022-07-18 |
Incidental Mutation