Incidental Mutation 'R1962:Mical2'
ID |
216985 |
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 |
039976-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.298)
|
Stock # |
R1962 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
111825063-112012313 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 112012051 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Leucine
at position 634
(I634L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000102256
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000051308]
[ENSMUST00000106645]
|
AlphaFold |
Q8BML1 Q9D5U9 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000051308
AA Change: I634L
PolyPhen 2
Score 0.138 (Sensitivity: 0.92; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000062443 Gene: ENSMUSG00000030771 AA Change: I634L
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
34 |
N/A |
INTRINSIC |
low complexity region
|
327 |
338 |
N/A |
INTRINSIC |
low complexity region
|
349 |
366 |
N/A |
INTRINSIC |
low complexity region
|
479 |
496 |
N/A |
INTRINSIC |
low complexity region
|
500 |
515 |
N/A |
INTRINSIC |
DUF3585
|
526 |
668 |
6.86e-56 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000106645
AA Change: I634L
PolyPhen 2
Score 0.138 (Sensitivity: 0.92; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000102256 Gene: ENSMUSG00000030771 AA Change: I634L
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
34 |
N/A |
INTRINSIC |
low complexity region
|
327 |
338 |
N/A |
INTRINSIC |
low complexity region
|
349 |
366 |
N/A |
INTRINSIC |
low complexity region
|
479 |
496 |
N/A |
INTRINSIC |
low complexity region
|
500 |
515 |
N/A |
INTRINSIC |
DUF3585
|
526 |
668 |
6.86e-56 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000140202
|
Predicted Effect |
unknown
Transcript: ENSMUST00000213108
AA Change: I525L
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000215412
|
Predicted Effect |
unknown
Transcript: ENSMUST00000216652
AA Change: I846L
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.4%
|
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: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
A |
G |
7: 119,940,468 (GRCm39) |
I354M |
probably damaging |
Het |
Abca8a |
T |
C |
11: 109,917,731 (GRCm39) |
|
probably null |
Het |
Abca8b |
T |
C |
11: 109,870,724 (GRCm39) |
R143G |
probably benign |
Het |
Actn4 |
T |
C |
7: 28,594,047 (GRCm39) |
D840G |
probably damaging |
Het |
Agpat5 |
T |
C |
8: 18,928,026 (GRCm39) |
L197P |
probably damaging |
Het |
Akr1d1 |
T |
C |
6: 37,512,983 (GRCm39) |
V93A |
probably benign |
Het |
Arap2 |
T |
C |
5: 62,834,007 (GRCm39) |
K820R |
possibly damaging |
Het |
Armc9 |
T |
A |
1: 86,135,696 (GRCm39) |
C551S |
probably damaging |
Het |
Atg7 |
T |
C |
6: 114,683,191 (GRCm39) |
L418P |
probably damaging |
Het |
Awat2 |
G |
A |
X: 99,448,165 (GRCm39) |
P148S |
probably damaging |
Het |
Brms1 |
C |
T |
19: 5,096,027 (GRCm39) |
R34W |
probably damaging |
Het |
Cbx2 |
A |
G |
11: 118,919,395 (GRCm39) |
Q320R |
possibly damaging |
Het |
Ccdc106 |
G |
A |
7: 5,062,539 (GRCm39) |
D11N |
possibly damaging |
Het |
Ccdc30 |
C |
T |
4: 119,196,988 (GRCm39) |
R426Q |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,356,885 (GRCm39) |
V47E |
probably damaging |
Het |
Cep170b |
C |
T |
12: 112,704,495 (GRCm39) |
S751L |
probably damaging |
Het |
Cfap46 |
A |
T |
7: 139,246,957 (GRCm39) |
L328Q |
probably damaging |
Het |
Crtc3 |
A |
G |
7: 80,239,679 (GRCm39) |
F558L |
probably damaging |
Het |
Cyp2d34 |
A |
G |
15: 82,502,809 (GRCm39) |
V139A |
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,413,408 (GRCm39) |
Y1136H |
probably damaging |
Het |
Dhrs4 |
T |
C |
14: 55,725,060 (GRCm39) |
V185A |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,281,263 (GRCm39) |
K2775E |
possibly damaging |
Het |
Dst |
C |
A |
1: 34,230,097 (GRCm39) |
S2238R |
possibly damaging |
Het |
Duox2 |
T |
C |
2: 122,127,853 (GRCm39) |
|
probably null |
Het |
Dusp16 |
G |
T |
6: 134,695,099 (GRCm39) |
Y577* |
probably null |
Het |
Dync1h1 |
G |
A |
12: 110,602,943 (GRCm39) |
E2195K |
probably benign |
Het |
Eml5 |
A |
G |
12: 98,842,570 (GRCm39) |
F176S |
probably damaging |
Het |
Esco2 |
C |
A |
14: 66,068,982 (GRCm39) |
R109S |
probably damaging |
Het |
Galnt7 |
C |
T |
8: 57,985,748 (GRCm39) |
E541K |
probably benign |
Het |
Gbf1 |
C |
T |
19: 46,255,658 (GRCm39) |
T707I |
probably damaging |
Het |
Gdf5 |
A |
G |
2: 155,783,672 (GRCm39) |
C427R |
probably damaging |
Het |
Glyctk |
T |
C |
9: 106,035,064 (GRCm39) |
M1V |
probably null |
Het |
Gm5478 |
T |
C |
15: 101,552,830 (GRCm39) |
E367G |
probably damaging |
Het |
Golga7b |
G |
A |
19: 42,251,768 (GRCm39) |
V5I |
probably benign |
Het |
Gpt2 |
T |
C |
8: 86,219,764 (GRCm39) |
L70P |
probably damaging |
Het |
Gsdmc3 |
C |
A |
15: 63,730,315 (GRCm39) |
Q416H |
probably damaging |
Het |
Hoxb5 |
A |
G |
11: 96,194,918 (GRCm39) |
E160G |
probably benign |
Het |
Ift81 |
A |
T |
5: 122,698,772 (GRCm39) |
Y532N |
probably benign |
Het |
Igf1 |
G |
A |
10: 87,700,726 (GRCm39) |
C66Y |
probably damaging |
Het |
Igf1r |
T |
C |
7: 67,857,023 (GRCm39) |
V995A |
probably damaging |
Het |
Ip6k1 |
T |
C |
9: 107,918,287 (GRCm39) |
|
probably null |
Het |
Jaml |
T |
C |
9: 45,015,495 (GRCm39) |
I333T |
possibly damaging |
Het |
Kdm4c |
T |
C |
4: 74,225,253 (GRCm39) |
|
probably benign |
Het |
Kdm6b |
T |
C |
11: 69,292,191 (GRCm39) |
|
probably benign |
Het |
Krt6a |
C |
T |
15: 101,599,900 (GRCm39) |
R404H |
probably damaging |
Het |
Larp4b |
C |
A |
13: 9,186,878 (GRCm39) |
H69N |
probably benign |
Het |
Lcat |
A |
T |
8: 106,668,355 (GRCm39) |
W222R |
probably damaging |
Het |
Lrrc40 |
T |
A |
3: 157,746,086 (GRCm39) |
C54S |
probably benign |
Het |
Mcpt9 |
T |
A |
14: 56,265,024 (GRCm39) |
H159L |
probably benign |
Het |
Megf8 |
T |
C |
7: 25,062,976 (GRCm39) |
V2444A |
probably damaging |
Het |
Memo1 |
T |
C |
17: 74,552,003 (GRCm39) |
T98A |
possibly damaging |
Het |
Mov10 |
C |
T |
3: 104,704,293 (GRCm39) |
R835Q |
probably damaging |
Het |
Mybpc1 |
A |
T |
10: 88,384,688 (GRCm39) |
L546Q |
probably damaging |
Het |
Myo6 |
T |
C |
9: 80,168,117 (GRCm39) |
V427A |
probably damaging |
Het |
Myom2 |
T |
A |
8: 15,182,599 (GRCm39) |
|
probably null |
Het |
Mzt2 |
G |
A |
16: 15,666,543 (GRCm39) |
R125C |
probably damaging |
Het |
Neb |
T |
A |
2: 52,162,949 (GRCm39) |
R2031* |
probably null |
Het |
Nphp3 |
T |
C |
9: 103,898,537 (GRCm39) |
S447P |
probably benign |
Het |
Nrp2 |
T |
A |
1: 62,758,090 (GRCm39) |
D25E |
probably benign |
Het |
Nts |
A |
G |
10: 102,320,918 (GRCm39) |
L57S |
probably damaging |
Het |
Nudt9 |
G |
A |
5: 104,212,971 (GRCm39) |
R348H |
probably benign |
Het |
Or10d5j |
T |
C |
9: 39,867,979 (GRCm39) |
Y84C |
probably benign |
Het |
Or13a1 |
C |
T |
6: 116,470,725 (GRCm39) |
P52S |
probably benign |
Het |
Or3a1b |
C |
A |
11: 74,012,650 (GRCm39) |
D178E |
probably benign |
Het |
Or4k49 |
T |
C |
2: 111,495,234 (GRCm39) |
I221T |
probably damaging |
Het |
Or5ac16 |
T |
A |
16: 59,022,271 (GRCm39) |
I173F |
possibly damaging |
Het |
Pafah1b1 |
T |
C |
11: 74,590,177 (GRCm39) |
|
probably benign |
Het |
Piezo2 |
C |
A |
18: 63,211,911 (GRCm39) |
M1291I |
probably damaging |
Het |
Pik3ca |
T |
C |
3: 32,498,016 (GRCm39) |
F486S |
probably benign |
Het |
Podnl1 |
C |
T |
8: 84,853,926 (GRCm39) |
H99Y |
probably benign |
Het |
Prdm6 |
A |
T |
18: 53,701,233 (GRCm39) |
Y341F |
probably damaging |
Het |
Prr5l |
C |
T |
2: 101,588,854 (GRCm39) |
|
probably null |
Het |
Psmd4 |
G |
T |
3: 94,944,012 (GRCm39) |
T24N |
possibly damaging |
Het |
Rbbp8nl |
G |
A |
2: 179,922,667 (GRCm39) |
T242M |
probably benign |
Het |
Rsf1 |
GCG |
GCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
GGCGGCGGCGGCGGCGGCGGCGGCGGCGGC |
GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Scfd1 |
T |
C |
12: 51,469,769 (GRCm39) |
V438A |
probably benign |
Het |
Scn9a |
A |
G |
2: 66,314,655 (GRCm39) |
C1677R |
probably damaging |
Het |
Sgsm2 |
T |
A |
11: 74,782,854 (GRCm39) |
H34L |
probably damaging |
Het |
Shank1 |
T |
A |
7: 43,993,747 (GRCm39) |
|
probably null |
Het |
Smarca2 |
G |
T |
19: 26,650,124 (GRCm39) |
E24* |
probably null |
Het |
Sncaip |
C |
T |
18: 53,004,434 (GRCm39) |
H354Y |
probably damaging |
Het |
St8sia2 |
T |
A |
7: 73,593,057 (GRCm39) |
D333V |
probably damaging |
Het |
Stxbp2 |
C |
A |
8: 3,692,672 (GRCm39) |
R575S |
probably benign |
Het |
Syt9 |
T |
A |
7: 107,024,314 (GRCm39) |
V69D |
probably damaging |
Het |
Tanc2 |
A |
G |
11: 105,689,558 (GRCm39) |
N240S |
probably benign |
Het |
Tcl1b1 |
T |
C |
12: 105,130,727 (GRCm39) |
L70S |
probably benign |
Het |
Tmem44 |
C |
T |
16: 30,362,219 (GRCm39) |
|
probably null |
Het |
Tor1b |
A |
G |
2: 30,846,931 (GRCm39) |
R293G |
probably benign |
Het |
Trim29 |
T |
C |
9: 43,222,615 (GRCm39) |
V148A |
probably benign |
Het |
Trmt10b |
C |
A |
4: 45,314,378 (GRCm39) |
Y271* |
probably null |
Het |
Ubqln5 |
A |
T |
7: 103,778,095 (GRCm39) |
V243E |
possibly damaging |
Het |
Ubqln5 |
T |
C |
7: 103,778,134 (GRCm39) |
D230G |
probably damaging |
Het |
Ugt2b37 |
A |
G |
5: 87,402,193 (GRCm39) |
F146S |
probably damaging |
Het |
Vmn1r160 |
T |
A |
7: 22,570,827 (GRCm39) |
V60E |
probably damaging |
Het |
Vmn2r109 |
T |
A |
17: 20,774,185 (GRCm39) |
D390V |
probably damaging |
Het |
Vmn2r27 |
C |
T |
6: 124,200,793 (GRCm39) |
R388Q |
possibly damaging |
Het |
Vmn2r72 |
A |
T |
7: 85,398,369 (GRCm39) |
V537D |
probably benign |
Het |
Vmn2r84 |
A |
G |
10: 130,226,591 (GRCm39) |
S416P |
probably damaging |
Het |
Vmn2r98 |
C |
A |
17: 19,285,595 (GRCm39) |
Y138* |
probably null |
Het |
Vmn2r-ps158 |
T |
C |
7: 42,696,824 (GRCm39) |
V620A |
probably benign |
Het |
Xrra1 |
A |
C |
7: 99,560,227 (GRCm39) |
E401A |
probably damaging |
Het |
Zfp280d |
T |
A |
9: 72,242,362 (GRCm39) |
C688* |
probably null |
Het |
Zfp3 |
T |
A |
11: 70,662,954 (GRCm39) |
Y304* |
probably null |
Het |
Zfp407 |
A |
T |
18: 84,577,461 (GRCm39) |
D1217E |
probably benign |
Het |
Zfp658 |
T |
C |
7: 43,223,245 (GRCm39) |
Y507H |
possibly damaging |
Het |
Zfyve16 |
T |
C |
13: 92,659,252 (GRCm39) |
T220A |
possibly damaging |
Het |
Zmym4 |
C |
G |
4: 126,796,463 (GRCm39) |
K820N |
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 |
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 |
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'- GAGCTGACTCCCTCACAAAG -3'
(R):5'- AAATTCAGTGCCTGGGTGGG -3'
Sequencing Primer
(F):5'- AGCTCCTTGGTGTTAGATTCAC -3'
(R):5'- AAAGTGTGGTGTTCTTGGCTCTC -3'
|
Posted On |
2014-08-01 |