Incidental Mutation 'R2141:Myo10'
ID |
236291 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo10
|
Ensembl Gene |
ENSMUSG00000022272 |
Gene Name |
myosin X |
Synonyms |
myosin-X, D15Ertd600e |
MMRRC Submission |
040144-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R2141 (G1)
|
Quality Score |
199 |
Status
|
Validated
|
Chromosome |
15 |
Chromosomal Location |
25622636-25813759 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 25714194 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Glycine
at position 87
(E87G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000118280
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000110457]
[ENSMUST00000137601]
|
AlphaFold |
F8VQB6 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000110457
AA Change: E120G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000106087 Gene: ENSMUSG00000022272 AA Change: E120G
Domain | Start | End | E-Value | Type |
MYSc
|
57 |
740 |
N/A |
SMART |
IQ
|
741 |
763 |
1.27e-3 |
SMART |
IQ
|
764 |
786 |
1.06e0 |
SMART |
IQ
|
787 |
809 |
7.07e-2 |
SMART |
Pfam:MYO10_CC
|
881 |
932 |
4.2e-22 |
PFAM |
low complexity region
|
959 |
981 |
N/A |
INTRINSIC |
low complexity region
|
1090 |
1102 |
N/A |
INTRINSIC |
low complexity region
|
1147 |
1165 |
N/A |
INTRINSIC |
PH
|
1217 |
1316 |
1.39e-21 |
SMART |
PH
|
1397 |
1503 |
6.76e-11 |
SMART |
MyTH4
|
1551 |
1699 |
4.12e-37 |
SMART |
B41
|
1700 |
1962 |
1.72e-44 |
SMART |
low complexity region
|
2050 |
2062 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126076
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000130517
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000137601
AA Change: E87G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000118280 Gene: ENSMUSG00000022272 AA Change: E87G
Domain | Start | End | E-Value | Type |
MYSc
|
24 |
707 |
N/A |
SMART |
IQ
|
708 |
730 |
1.27e-3 |
SMART |
IQ
|
731 |
753 |
1.06e0 |
SMART |
IQ
|
754 |
776 |
7.07e-2 |
SMART |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.1%
|
Validation Efficiency |
97% (107/110) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-10 (MYH10). Unconventional myosins contain the basic domains of conventional myosins and are further distinguished from class members by their tail domains. This gene functions as an actin-based molecular motor and plays a role in integration of F-actin and microtubule cytoskeletons during meiosis. [provided by RefSeq, Dec 2011] PHENOTYPE: Homozygous null mutations are semi-lethal with over half of homozygous embryos exhibiting exencephaly. Surviving mutants show decreased body weight, white spotting, syndactyly, persistence of hyaloid vascular system and other eye defects. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
G |
T |
11: 58,314,752 (GRCm39) |
C150F |
probably damaging |
Het |
Aagab |
T |
A |
9: 63,523,957 (GRCm39) |
|
probably null |
Het |
Abca15 |
A |
C |
7: 120,006,697 (GRCm39) |
T1654P |
probably damaging |
Het |
Abca17 |
T |
A |
17: 24,553,240 (GRCm39) |
Y157F |
probably benign |
Het |
Aftph |
A |
T |
11: 20,648,318 (GRCm39) |
L813* |
probably null |
Het |
Agap1 |
T |
C |
1: 89,765,477 (GRCm39) |
I615T |
probably damaging |
Het |
Ak3 |
T |
G |
19: 29,000,247 (GRCm39) |
Q221H |
probably benign |
Het |
Aldoa |
A |
G |
7: 126,396,814 (GRCm39) |
|
probably null |
Het |
Anxa8 |
T |
C |
14: 33,813,873 (GRCm39) |
|
probably null |
Het |
Atpsckmt |
T |
C |
15: 31,609,718 (GRCm39) |
F146L |
probably benign |
Het |
Baz2a |
A |
G |
10: 127,959,481 (GRCm39) |
D1329G |
probably damaging |
Het |
Calhm6 |
G |
T |
10: 34,003,691 (GRCm39) |
A72E |
probably damaging |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cep70 |
A |
G |
9: 99,178,438 (GRCm39) |
Y512C |
probably damaging |
Het |
Cfhr2 |
T |
G |
1: 139,758,893 (GRCm39) |
R52S |
probably benign |
Het |
Clcn6 |
A |
G |
4: 148,108,594 (GRCm39) |
F145S |
possibly damaging |
Het |
Cnksr1 |
A |
G |
4: 133,956,939 (GRCm39) |
Y488H |
probably damaging |
Het |
Diablo |
A |
G |
5: 123,661,424 (GRCm39) |
V24A |
probably benign |
Het |
Dnah7b |
T |
A |
1: 46,307,830 (GRCm39) |
M3048K |
probably damaging |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Efnb1 |
A |
G |
X: 98,191,123 (GRCm39) |
Y343C |
probably damaging |
Het |
Esco1 |
A |
G |
18: 10,574,873 (GRCm39) |
|
probably null |
Het |
Fancd2 |
A |
G |
6: 113,526,282 (GRCm39) |
N335S |
probably benign |
Het |
Flnc |
A |
G |
6: 29,448,674 (GRCm39) |
Y1304C |
probably damaging |
Het |
Fubp3 |
A |
G |
2: 31,490,569 (GRCm39) |
|
probably benign |
Het |
Gemin4 |
G |
C |
11: 76,101,876 (GRCm39) |
P962A |
probably damaging |
Het |
Gjc3 |
A |
C |
5: 137,955,808 (GRCm39) |
L159R |
probably damaging |
Het |
Gli1 |
A |
G |
10: 127,172,596 (GRCm39) |
L182P |
probably damaging |
Het |
Gm21957 |
G |
T |
7: 124,818,625 (GRCm39) |
|
noncoding transcript |
Het |
Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,255,059 (GRCm39) |
|
probably benign |
Het |
Gm5885 |
A |
G |
6: 133,506,238 (GRCm39) |
|
noncoding transcript |
Het |
Gon4l |
A |
T |
3: 88,794,902 (GRCm39) |
T402S |
possibly damaging |
Het |
Gprasp1 |
G |
A |
X: 134,702,791 (GRCm39) |
E995K |
possibly damaging |
Het |
Gvin-ps5 |
T |
A |
7: 105,929,163 (GRCm39) |
T245S |
probably damaging |
Het |
Helb |
A |
T |
10: 119,941,926 (GRCm39) |
M254K |
possibly damaging |
Het |
Ift20 |
G |
A |
11: 78,430,860 (GRCm39) |
E68K |
probably damaging |
Het |
Igfn1 |
AGGG |
AGG |
1: 135,902,590 (GRCm39) |
|
probably benign |
Het |
Impdh2 |
A |
G |
9: 108,442,546 (GRCm39) |
E305G |
possibly damaging |
Het |
Ints7 |
T |
A |
1: 191,336,972 (GRCm39) |
C351S |
possibly damaging |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Kcnq3 |
T |
C |
15: 65,867,700 (GRCm39) |
M648V |
probably benign |
Het |
Kctd16 |
A |
G |
18: 40,392,231 (GRCm39) |
E273G |
possibly damaging |
Het |
Kif18a |
T |
A |
2: 109,163,848 (GRCm39) |
N732K |
probably benign |
Het |
Kif21b |
C |
T |
1: 136,080,002 (GRCm39) |
R513W |
probably damaging |
Het |
Klhl36 |
T |
C |
8: 120,603,511 (GRCm39) |
C589R |
possibly damaging |
Het |
Lck |
A |
G |
4: 129,442,713 (GRCm39) |
Y481H |
probably damaging |
Het |
Lmtk2 |
A |
G |
5: 144,084,433 (GRCm39) |
Y156C |
probably damaging |
Het |
Mical3 |
A |
T |
6: 121,008,095 (GRCm39) |
|
probably null |
Het |
Mki67 |
A |
G |
7: 135,297,321 (GRCm39) |
I2571T |
possibly damaging |
Het |
Mx2 |
G |
A |
16: 97,339,903 (GRCm39) |
E20K |
probably benign |
Het |
Myo18b |
T |
C |
5: 113,021,892 (GRCm39) |
K500R |
probably benign |
Het |
N4bp2l2 |
A |
T |
5: 150,571,001 (GRCm39) |
I458N |
probably damaging |
Het |
Nat10 |
T |
C |
2: 103,561,648 (GRCm39) |
|
probably null |
Het |
Nfasc |
G |
A |
1: 132,524,383 (GRCm39) |
P932L |
probably damaging |
Het |
Nipa1 |
C |
A |
7: 55,647,259 (GRCm39) |
|
probably null |
Het |
Nkpd1 |
A |
G |
7: 19,258,162 (GRCm39) |
Q647R |
probably damaging |
Het |
Nlrc4 |
T |
A |
17: 74,754,946 (GRCm39) |
|
probably benign |
Het |
Nmbr |
C |
A |
10: 14,646,186 (GRCm39) |
Y353* |
probably null |
Het |
Nos1ap |
T |
A |
1: 170,156,735 (GRCm39) |
D241V |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or4f4b |
A |
T |
2: 111,313,975 (GRCm39) |
T95S |
probably benign |
Het |
Or5d43 |
A |
G |
2: 88,105,354 (GRCm39) |
V13A |
probably benign |
Het |
Or5m13 |
A |
G |
2: 85,749,171 (GRCm39) |
I301V |
probably null |
Het |
Or6c201 |
A |
G |
10: 128,968,875 (GRCm39) |
I254T |
probably benign |
Het |
Pank1 |
G |
A |
19: 34,856,380 (GRCm39) |
R33C |
possibly damaging |
Het |
Pcmtd1 |
C |
T |
1: 7,239,789 (GRCm39) |
R77C |
probably damaging |
Het |
Phkg2 |
G |
A |
7: 127,181,386 (GRCm39) |
|
probably null |
Het |
Plcb4 |
G |
A |
2: 135,818,019 (GRCm39) |
V762M |
probably damaging |
Het |
Pramel7 |
T |
A |
2: 87,320,321 (GRCm39) |
H324L |
probably damaging |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Ptgr3 |
T |
C |
18: 84,112,668 (GRCm39) |
Y115H |
probably benign |
Het |
Rai1 |
C |
A |
11: 60,080,293 (GRCm39) |
S1452R |
possibly damaging |
Het |
Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
Het |
Rev3l |
T |
C |
10: 39,724,045 (GRCm39) |
V785A |
probably benign |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Rufy2 |
G |
T |
10: 62,826,773 (GRCm39) |
R104L |
probably damaging |
Het |
Senp6 |
T |
A |
9: 80,031,102 (GRCm39) |
N8K |
probably damaging |
Het |
Septin4 |
A |
T |
11: 87,474,262 (GRCm39) |
Q60L |
probably benign |
Het |
Sipa1l2 |
G |
A |
8: 126,218,230 (GRCm39) |
P369L |
probably benign |
Het |
Slc43a1 |
T |
C |
2: 84,671,305 (GRCm39) |
L37P |
probably damaging |
Het |
Slf1 |
T |
A |
13: 77,197,338 (GRCm39) |
|
probably null |
Het |
Ssr2 |
T |
A |
3: 88,483,949 (GRCm39) |
|
probably benign |
Het |
Syt2 |
ACTCTCTCT |
ACTCTCTCTCT |
1: 134,674,479 (GRCm39) |
|
probably benign |
Het |
Tas2r115 |
T |
C |
6: 132,714,321 (GRCm39) |
K210R |
probably benign |
Het |
Tbx18 |
A |
G |
9: 87,597,706 (GRCm39) |
V276A |
probably damaging |
Het |
Tesl1 |
T |
A |
X: 23,773,549 (GRCm39) |
V350E |
probably benign |
Het |
Tie1 |
G |
A |
4: 118,330,008 (GRCm39) |
R1072* |
probably null |
Het |
Tm2d2 |
C |
A |
8: 25,512,674 (GRCm39) |
T174K |
probably damaging |
Het |
Tmem98 |
A |
G |
11: 80,705,158 (GRCm39) |
D82G |
possibly damaging |
Het |
Tmub2 |
A |
G |
11: 102,178,379 (GRCm39) |
E94G |
possibly damaging |
Het |
Tnnt2 |
TG |
TGG |
1: 135,774,499 (GRCm39) |
|
probably benign |
Het |
Tonsl |
A |
T |
15: 76,516,861 (GRCm39) |
I923N |
probably damaging |
Het |
Ttc21a |
G |
A |
9: 119,793,361 (GRCm39) |
V977M |
probably damaging |
Het |
Ube2ql1 |
T |
C |
13: 69,886,783 (GRCm39) |
D226G |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,204,518 (GRCm39) |
T4810M |
probably damaging |
Het |
Wdr87-ps |
T |
C |
7: 29,230,935 (GRCm39) |
|
noncoding transcript |
Het |
Zfp408 |
A |
G |
2: 91,478,194 (GRCm39) |
|
probably benign |
Het |
Zfp473 |
T |
C |
7: 44,382,501 (GRCm39) |
T610A |
possibly damaging |
Het |
Zfp804b |
A |
G |
5: 6,822,583 (GRCm39) |
V160A |
probably benign |
Het |
Zfp960 |
A |
G |
17: 17,308,146 (GRCm39) |
T287A |
probably benign |
Het |
|
Other mutations in Myo10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00557:Myo10
|
APN |
15 |
25,776,466 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01068:Myo10
|
APN |
15 |
25,739,395 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01352:Myo10
|
APN |
15 |
25,701,783 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01388:Myo10
|
APN |
15 |
25,736,703 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01460:Myo10
|
APN |
15 |
25,714,194 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01553:Myo10
|
APN |
15 |
25,776,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01732:Myo10
|
APN |
15 |
25,732,149 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01992:Myo10
|
APN |
15 |
25,799,634 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02000:Myo10
|
APN |
15 |
25,808,152 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02045:Myo10
|
APN |
15 |
25,726,574 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02307:Myo10
|
APN |
15 |
25,776,401 (GRCm39) |
splice site |
probably benign |
|
IGL02511:Myo10
|
APN |
15 |
25,723,975 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03240:Myo10
|
APN |
15 |
25,701,688 (GRCm39) |
missense |
probably damaging |
1.00 |
least
|
UTSW |
15 |
25,726,561 (GRCm39) |
nonsense |
probably null |
|
R0037:Myo10
|
UTSW |
15 |
25,666,618 (GRCm39) |
intron |
probably benign |
|
R0153:Myo10
|
UTSW |
15 |
25,781,324 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0282:Myo10
|
UTSW |
15 |
25,793,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Myo10
|
UTSW |
15 |
25,804,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R0585:Myo10
|
UTSW |
15 |
25,736,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Myo10
|
UTSW |
15 |
25,738,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Myo10
|
UTSW |
15 |
25,722,243 (GRCm39) |
splice site |
probably benign |
|
R0771:Myo10
|
UTSW |
15 |
25,778,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R0960:Myo10
|
UTSW |
15 |
25,801,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R1562:Myo10
|
UTSW |
15 |
25,780,497 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1651:Myo10
|
UTSW |
15 |
25,742,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R1789:Myo10
|
UTSW |
15 |
25,726,611 (GRCm39) |
critical splice donor site |
probably null |
|
R1816:Myo10
|
UTSW |
15 |
25,800,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Myo10
|
UTSW |
15 |
25,805,673 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1908:Myo10
|
UTSW |
15 |
25,801,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R2082:Myo10
|
UTSW |
15 |
25,786,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:Myo10
|
UTSW |
15 |
25,722,345 (GRCm39) |
missense |
probably benign |
0.26 |
R2129:Myo10
|
UTSW |
15 |
25,781,885 (GRCm39) |
missense |
probably benign |
0.09 |
R2142:Myo10
|
UTSW |
15 |
25,714,194 (GRCm39) |
missense |
probably benign |
|
R2920:Myo10
|
UTSW |
15 |
25,801,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R2938:Myo10
|
UTSW |
15 |
25,795,803 (GRCm39) |
missense |
probably damaging |
0.99 |
R3723:Myo10
|
UTSW |
15 |
25,803,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R3852:Myo10
|
UTSW |
15 |
25,779,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R4162:Myo10
|
UTSW |
15 |
25,726,501 (GRCm39) |
splice site |
probably null |
|
R4163:Myo10
|
UTSW |
15 |
25,726,501 (GRCm39) |
splice site |
probably null |
|
R4164:Myo10
|
UTSW |
15 |
25,726,501 (GRCm39) |
splice site |
probably null |
|
R4177:Myo10
|
UTSW |
15 |
25,734,137 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4409:Myo10
|
UTSW |
15 |
25,807,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:Myo10
|
UTSW |
15 |
25,793,239 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4905:Myo10
|
UTSW |
15 |
25,800,298 (GRCm39) |
missense |
probably damaging |
0.99 |
R4933:Myo10
|
UTSW |
15 |
25,781,204 (GRCm39) |
missense |
probably damaging |
0.96 |
R4968:Myo10
|
UTSW |
15 |
25,808,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R5081:Myo10
|
UTSW |
15 |
25,786,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R5123:Myo10
|
UTSW |
15 |
25,726,569 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5310:Myo10
|
UTSW |
15 |
25,778,164 (GRCm39) |
splice site |
probably null |
|
R6073:Myo10
|
UTSW |
15 |
25,736,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6117:Myo10
|
UTSW |
15 |
25,805,745 (GRCm39) |
missense |
probably benign |
0.00 |
R6185:Myo10
|
UTSW |
15 |
25,726,596 (GRCm39) |
missense |
probably damaging |
0.99 |
R6749:Myo10
|
UTSW |
15 |
25,714,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R6819:Myo10
|
UTSW |
15 |
25,781,496 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6875:Myo10
|
UTSW |
15 |
25,805,745 (GRCm39) |
missense |
probably benign |
0.00 |
R6908:Myo10
|
UTSW |
15 |
25,804,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R6963:Myo10
|
UTSW |
15 |
25,734,149 (GRCm39) |
missense |
probably benign |
0.31 |
R7144:Myo10
|
UTSW |
15 |
25,724,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R7266:Myo10
|
UTSW |
15 |
25,783,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R7380:Myo10
|
UTSW |
15 |
25,779,706 (GRCm39) |
missense |
probably benign |
0.01 |
R7460:Myo10
|
UTSW |
15 |
25,807,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R7614:Myo10
|
UTSW |
15 |
25,701,709 (GRCm39) |
missense |
probably benign |
0.00 |
R7618:Myo10
|
UTSW |
15 |
25,726,561 (GRCm39) |
nonsense |
probably null |
|
R7717:Myo10
|
UTSW |
15 |
25,732,056 (GRCm39) |
missense |
probably benign |
0.01 |
R7811:Myo10
|
UTSW |
15 |
25,804,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R7830:Myo10
|
UTSW |
15 |
25,738,057 (GRCm39) |
nonsense |
probably null |
|
R7862:Myo10
|
UTSW |
15 |
25,666,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R8232:Myo10
|
UTSW |
15 |
25,804,400 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8264:Myo10
|
UTSW |
15 |
25,800,195 (GRCm39) |
missense |
probably damaging |
0.99 |
R8377:Myo10
|
UTSW |
15 |
25,804,481 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8385:Myo10
|
UTSW |
15 |
25,804,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R8426:Myo10
|
UTSW |
15 |
25,799,576 (GRCm39) |
missense |
probably damaging |
0.99 |
R8439:Myo10
|
UTSW |
15 |
25,725,158 (GRCm39) |
missense |
probably benign |
0.00 |
R8696:Myo10
|
UTSW |
15 |
25,799,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R8775:Myo10
|
UTSW |
15 |
25,800,145 (GRCm39) |
missense |
probably damaging |
0.97 |
R8775-TAIL:Myo10
|
UTSW |
15 |
25,800,145 (GRCm39) |
missense |
probably damaging |
0.97 |
R8970:Myo10
|
UTSW |
15 |
25,803,467 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9024:Myo10
|
UTSW |
15 |
25,793,295 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9196:Myo10
|
UTSW |
15 |
25,805,716 (GRCm39) |
missense |
probably damaging |
0.96 |
R9224:Myo10
|
UTSW |
15 |
25,808,081 (GRCm39) |
missense |
probably benign |
0.33 |
R9308:Myo10
|
UTSW |
15 |
25,781,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R9358:Myo10
|
UTSW |
15 |
25,781,520 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9606:Myo10
|
UTSW |
15 |
25,776,401 (GRCm39) |
frame shift |
probably null |
|
R9722:Myo10
|
UTSW |
15 |
25,801,227 (GRCm39) |
missense |
probably damaging |
1.00 |
RF013:Myo10
|
UTSW |
15 |
25,799,565 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Myo10
|
UTSW |
15 |
25,799,640 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Myo10
|
UTSW |
15 |
25,781,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GATCATTTCGCTGGATCGCTC -3'
(R):5'- ATCTGTCTGCAACTGAGCG -3'
Sequencing Primer
(F):5'- CTGGATCGCTCCCGCCC -3'
(R):5'- AGCGCTCTCCAGTGAATG -3'
|
Posted On |
2014-10-01 |