MYO10 (myosin X) - Rat Genome Database

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Gene: MYO10 (myosin X) Homo sapiens
Analyze
Symbol: MYO10
Name: myosin X
RGD ID: 1316238
HGNC Page HGNC:7593
Description: Enables spectrin binding activity. Involved in regulation of cell shape and regulation of filopodium assembly. Located in cytosol; nucleolus; and plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FLJ10639; FLJ21066; FLJ22268; FLJ43256; KIAA0799; MGC131988; myosin-X; MyoX; unconventional myosin-10; unconventional myosin-X; unconventionnal myosin-X
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38516,661,907 - 16,936,288 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl516,661,907 - 16,936,288 (-)EnsemblGRCh38hg38GRCh38
GRCh37516,662,016 - 16,936,397 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36516,715,016 - 16,989,385 (-)NCBINCBI36Build 36hg18NCBI36
Build 34516,718,412 - 16,989,139NCBI
Celera516,686,791 - 16,961,521 (-)NCBICelera
Cytogenetic Map5p15.1NCBI
HuRef516,634,005 - 16,909,126 (-)NCBIHuRef
CHM1_1516,661,893 - 16,936,226 (-)NCBICHM1_1
T2T-CHM13v2.0516,601,148 - 16,875,413 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
(-)-epigallocatechin 3-gallate  (EXP)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (EXP,ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,6-dinitrotoluene  (ISO)
2-palmitoylglycerol  (EXP)
3,4-dichloroaniline  (EXP)
4,4'-diaminodiphenylmethane  (ISO)
acetamide  (ISO)
acrolein  (EXP)
aflatoxin B1  (EXP)
Aflatoxin B2 alpha  (EXP)
all-trans-retinoic acid  (EXP)
alpha-pinene  (EXP)
amphetamine  (ISO)
antirheumatic drug  (EXP)
arsenite(3-)  (EXP)
atrazine  (ISO)
azoxystrobin  (ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
bisphenol A  (EXP,ISO)
C60 fullerene  (ISO)
CGP 52608  (EXP)
chloroprene  (ISO)
chlorpyrifos  (ISO)
cisplatin  (EXP)
cobalt dichloride  (EXP)
copper(II) sulfate  (EXP)
dibutyl phthalate  (ISO)
diuron  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP,ISO)
entinostat  (EXP)
epoxiconazole  (ISO)
ethanol  (ISO)
folic acid  (EXP)
FR900359  (EXP)
gentamycin  (ISO)
glycidyl methacrylate  (EXP)
glyphosate  (ISO)
imidacloprid  (ISO)
inulin  (ISO)
Lasiocarpine  (EXP)
leflunomide  (EXP)
lipopolysaccharide  (EXP)
menadione  (EXP)
mercury dibromide  (EXP)
methoxyacetic acid  (EXP)
methylmercury chloride  (EXP)
methylseleninic acid  (EXP)
mitomycin C  (EXP)
nickel sulfate  (EXP)
ozone  (EXP)
p-chloromercuribenzoic acid  (EXP)
paracetamol  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
phenol red  (EXP)
phenylmercury acetate  (EXP)
pirinixic acid  (ISO)
potassium chromate  (EXP)
promegestone  (EXP)
raloxifene  (EXP)
rotenone  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
Salinomycin  (EXP)
SB 431542  (EXP)
silicon dioxide  (ISO)
sodium arsenite  (EXP)
sotorasib  (EXP)
sunitinib  (EXP)
tebufenpyrad  (EXP)
tert-butyl hydroperoxide  (EXP)
tetrachloromethane  (ISO)
thiabendazole  (ISO)
thioacetamide  (ISO)
trametinib  (EXP)
trichostatin A  (EXP)
triptonide  (ISO)
troglitazone  (EXP,ISO)
urethane  (EXP)
valproic acid  (EXP)
vorinostat  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8884266   PMID:9872452   PMID:10610710   PMID:10984435   PMID:11278607   PMID:12055636   PMID:12477932   PMID:14676191   PMID:14702039   PMID:14760703   PMID:15156152   PMID:15158464  
PMID:16169070   PMID:16344560   PMID:16371656   PMID:16894163   PMID:17081983   PMID:18029348   PMID:18295593   PMID:18570893   PMID:18599451   PMID:18818677   PMID:19204726   PMID:19615732  
PMID:20123970   PMID:20379614   PMID:20682791   PMID:20811636   PMID:20930142   PMID:21145461   PMID:21321230   PMID:21642953   PMID:21873635   PMID:23083060   PMID:23251661   PMID:23377640  
PMID:23398456   PMID:23400010   PMID:23704327   PMID:23912628   PMID:23943878   PMID:24379415   PMID:24487586   PMID:24921915   PMID:25416956   PMID:25605337   PMID:25749519   PMID:25819274  
PMID:25900982   PMID:26235048   PMID:26496610   PMID:26573744   PMID:26673895   PMID:28378594   PMID:28514442   PMID:29117863   PMID:29507755   PMID:29738550   PMID:29864913   PMID:29934580  
PMID:30021884   PMID:30652415   PMID:30979931   PMID:31586073   PMID:31665067   PMID:32329857   PMID:32618228   PMID:32694731   PMID:32707033   PMID:33306668   PMID:33961781   PMID:34133714  
PMID:34299191   PMID:34525374   PMID:34674267   PMID:35470858   PMID:35563538   PMID:35676659   PMID:35748872   PMID:35912545   PMID:36114006   PMID:36215168   PMID:36283390   PMID:36574265  
PMID:36861887   PMID:37200188  


Genomics

Comparative Map Data
MYO10
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38516,661,907 - 16,936,288 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl516,661,907 - 16,936,288 (-)EnsemblGRCh38hg38GRCh38
GRCh37516,662,016 - 16,936,397 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36516,715,016 - 16,989,385 (-)NCBINCBI36Build 36hg18NCBI36
Build 34516,718,412 - 16,989,139NCBI
Celera516,686,791 - 16,961,521 (-)NCBICelera
Cytogenetic Map5p15.1NCBI
HuRef516,634,005 - 16,909,126 (-)NCBIHuRef
CHM1_1516,661,893 - 16,936,226 (-)NCBICHM1_1
T2T-CHM13v2.0516,601,148 - 16,875,413 (-)NCBIT2T-CHM13v2.0
Myo10
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391525,622,636 - 25,813,759 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1525,622,611 - 25,813,759 (+)EnsemblGRCm39 Ensembl
GRCm381525,622,550 - 25,813,673 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1525,622,525 - 25,813,673 (+)EnsemblGRCm38mm10GRCm38
MGSCv371525,552,305 - 25,743,426 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361525,567,651 - 25,756,950 (+)NCBIMGSCv36mm8
Celera1526,396,055 - 26,587,057 (+)NCBICelera
Cytogenetic Map15B1NCBI
cM Map159.36NCBI
Myo10
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8277,831,532 - 78,036,137 (+)NCBIGRCr8
mRatBN7.2276,100,989 - 76,305,619 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl276,100,987 - 76,303,030 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx283,221,335 - 83,423,563 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0281,343,060 - 81,545,291 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0276,347,046 - 76,550,445 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0277,868,398 - 78,072,443 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl277,868,412 - 78,071,309 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0297,588,995 - 97,790,396 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4277,183,028 - 77,385,896 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1277,111,353 - 77,314,838 (+)NCBI
Celera271,812,056 - 72,011,101 (+)NCBICelera
Cytogenetic Map2q22NCBI
Myo10
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554265,727,042 - 5,885,302 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554265,725,766 - 5,885,316 (-)NCBIChiLan1.0ChiLan1.0
MYO10
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2416,899,283 - 17,169,889 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1515,052,893 - 15,323,471 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0516,969,146 - 17,239,732 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1516,805,022 - 17,075,001 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl516,804,216 - 17,074,534 (-)Ensemblpanpan1.1panPan2
MYO10
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1486,701,907 - 86,792,432 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl486,596,225 - 86,792,257 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha486,115,654 - 86,310,421 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0487,234,383 - 87,429,285 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl487,233,833 - 87,429,284 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1486,757,648 - 86,953,127 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0487,010,925 - 87,189,505 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0487,850,904 - 88,046,417 (+)NCBIUU_Cfam_GSD_1.0
Myo10
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213210,344,226 - 210,506,772 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648019,282,085 - 19,443,271 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648019,280,723 - 19,443,267 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MYO10
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl165,907,116 - 6,094,845 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1165,907,111 - 6,145,485 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2166,353,453 - 6,590,952 (-)NCBISscrofa10.2Sscrofa10.2susScr3
MYO10
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1416,337,933 - 16,608,115 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl416,334,559 - 16,451,166 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366606411,870,730 - 12,140,712 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Myo10
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462475113,518,258 - 13,678,148 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462475113,517,132 - 13,719,953 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MYO10
124 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5p15.33-13.2(chr5:54839-35680845)x3 copy number gain See cases [RCV000051811] Chr5:54839..35680845 [GRCh38]
Chr5:54954..35680947 [GRCh37]
Chr5:107954..35716704 [NCBI36]
Chr5:5p15.33-13.2		 pathogenic
GRCh38/hg38 5p15.33-12(chr5:54839-45649861)x3 copy number gain See cases [RCV000051810] Chr5:54839..45649861 [GRCh38]
Chr5:54954..45649963 [GRCh37]
Chr5:107954..45685720 [NCBI36]
Chr5:5p15.33-12		 pathogenic
GRCh38/hg38 5p15.33-14.3(chr5:22149-23132046)x1 copy number loss See cases [RCV000053398] Chr5:22149..23132046 [GRCh38]
Chr5:22149..23132155 [GRCh37]
Chr5:75149..23167912 [NCBI36]
Chr5:5p15.33-14.3		 pathogenic
GRCh38/hg38 5p15.33-15.1(chr5:22149-17425613)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053401]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053401]|See cases [RCV000053401] Chr5:22149..17425613 [GRCh38]
Chr5:22149..17425722 [GRCh37]
Chr5:75149..17478722 [NCBI36]
Chr5:5p15.33-15.1		 pathogenic
GRCh38/hg38 5p15.33-14.3(chr5:22419-19280892)x1 copy number loss See cases [RCV000053419] Chr5:22419..19280892 [GRCh38]
Chr5:22419..19281001 [GRCh37]
Chr5:75419..19316758 [NCBI36]
Chr5:5p15.33-14.3		 pathogenic
GRCh38/hg38 5p15.33-15.1(chr5:49778-16908798)x1 copy number loss See cases [RCV000053422] Chr5:49778..16908798 [GRCh38]
Chr5:49893..16908907 [GRCh37]
Chr5:102893..16961907 [NCBI36]
Chr5:5p15.33-15.1		 pathogenic
GRCh38/hg38 5p15.33-14.3(chr5:49778-19125522)x1 copy number loss See cases [RCV000053424] Chr5:49778..19125522 [GRCh38]
Chr5:49893..19125631 [GRCh37]
Chr5:102893..19161388 [NCBI36]
Chr5:5p15.33-14.3		 pathogenic
GRCh38/hg38 5p15.33-14.1(chr5:547757-26541238)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053445]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053445]|See cases [RCV000053445] Chr5:547757..26541238 [GRCh38]
Chr5:547872..26541347 [GRCh37]
Chr5:600872..26577104 [NCBI36]
Chr5:5p15.33-14.1		 pathogenic
GRCh38/hg38 5p15.33-15.1(chr5:2180761-17602433)x1 copy number loss See cases [RCV000053446] Chr5:2180761..17602433 [GRCh38]
Chr5:2180875..17602542 [GRCh37]
Chr5:2233875..17645646 [NCBI36]
Chr5:5p15.33-15.1		 pathogenic
GRCh38/hg38 5p15.2-14.3(chr5:13609772-21930280)x1 copy number loss See cases [RCV000053447] Chr5:13609772..21930280 [GRCh38]
Chr5:13609881..21930389 [GRCh37]
Chr5:13662881..21966146 [NCBI36]
Chr5:5p15.2-14.3		 pathogenic
NM_012334.2(MYO10):c.121-12303A>G single nucleotide variant Lung cancer [RCV000095551] Chr5:16830470 [GRCh38]
Chr5:16830579 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh38/hg38 5p15.33-13.3(chr5:22149-33418188)x3 copy number gain See cases [RCV000133788] Chr5:22149..33418188 [GRCh38]
Chr5:22149..33418294 [GRCh37]
Chr5:75149..33454051 [NCBI36]
Chr5:5p15.33-13.3		 pathogenic
GRCh37/hg19 5p15.33-13.3(chr5:22149-29048823)x1 copy number loss See cases [RCV001310287] Chr5:22149..29048823 [GRCh37]
Chr5:5p15.33-13.3		 pathogenic
GRCh38/hg38 5p15.33-14.1(chr5:22149-25699605)x1 copy number loss See cases [RCV000133768] Chr5:22149..25699605 [GRCh38]
Chr5:22149..25699714 [GRCh37]
Chr5:75149..25735471 [NCBI36]
Chr5:5p15.33-14.1		 pathogenic
GRCh38/hg38 5p15.33-14.1(chr5:22149-27788616)x1 copy number loss See cases [RCV000134873] Chr5:22149..27788616 [GRCh38]
Chr5:22149..27788723 [GRCh37]
Chr5:75149..27824480 [NCBI36]
Chr5:5p15.33-14.1		 pathogenic
GRCh38/hg38 5p15.33-13.3(chr5:22149-32248010)x1 copy number loss See cases [RCV000135668] Chr5:22149..32248010 [GRCh38]
Chr5:22149..32248116 [GRCh37]
Chr5:75149..32283873 [NCBI36]
Chr5:5p15.33-13.3		 pathogenic
GRCh38/hg38 5p15.33-13.3(chr5:49978-30112535)x1 copy number loss See cases [RCV000135878] Chr5:49978..30112535 [GRCh38]
Chr5:50093..30112642 [GRCh37]
Chr5:103093..30148399 [NCBI36]
Chr5:5p15.33-13.3		 pathogenic
GRCh38/hg38 5p15.33-11(chr5:49978-46114984)x3 copy number gain See cases [RCV000135453] Chr5:49978..46114984 [GRCh38]
Chr5:50093..46115086 [GRCh37]
Chr5:103093..46150843 [NCBI36]
Chr5:5p15.33-11		 pathogenic
GRCh38/hg38 5p15.2-15.1(chr5:12572563-17965988)x1 copy number loss See cases [RCV000136041] Chr5:12572563..17965988 [GRCh38]
Chr5:12572675..17966097 [GRCh37]
Chr5:12625675..18001854 [NCBI36]
Chr5:5p15.2-15.1		 pathogenic
GRCh38/hg38 5p15.2-15.1(chr5:10212880-16770474)x3 copy number gain See cases [RCV000136902] Chr5:10212880..16770474 [GRCh38]
Chr5:10212992..16770583 [GRCh37]
Chr5:10265992..16823583 [NCBI36]
Chr5:5p15.2-15.1		 pathogenic
GRCh38/hg38 5p15.33-14.1(chr5:22149-27485619)x1 copy number loss See cases [RCV000137072] Chr5:22149..27485619 [GRCh38]
Chr5:22149..27485726 [GRCh37]
Chr5:75149..27521483 [NCBI36]
Chr5:5p15.33-14.1		 pathogenic
GRCh38/hg38 5p15.33-14.1(chr5:22149-28075106)x3 copy number gain See cases [RCV000137682] Chr5:22149..28075106 [GRCh38]
Chr5:22149..28075213 [GRCh37]
Chr5:75149..28110970 [NCBI36]
Chr5:5p15.33-14.1		 pathogenic|uncertain significance
GRCh38/hg38 5p15.33-14.1(chr5:22149-28429241)x1 copy number loss See cases [RCV000137165] Chr5:22149..28429241 [GRCh38]
Chr5:22149..28429348 [GRCh37]
Chr5:75149..28465105 [NCBI36]
Chr5:5p15.33-14.1		 pathogenic
GRCh38/hg38 5p15.33-14.3(chr5:22149-22775295)x1 copy number loss See cases [RCV000138116] Chr5:22149..22775295 [GRCh38]
Chr5:22149..22775404 [GRCh37]
Chr5:75149..22811161 [NCBI36]
Chr5:5p15.33-14.3		 pathogenic
GRCh38/hg38 5p15.1-14.3(chr5:16823926-19476603)x1 copy number loss See cases [RCV000138043] Chr5:16823926..19476603 [GRCh38]
Chr5:16824035..19476712 [GRCh37]
Chr5:16877035..19512469 [NCBI36]
Chr5:5p15.1-14.3		 likely pathogenic
GRCh38/hg38 5p15.33-14.1(chr5:22149-27187950)x1 copy number loss See cases [RCV000138099] Chr5:22149..27187950 [GRCh38]
Chr5:22149..27188057 [GRCh37]
Chr5:75149..27223814 [NCBI36]
Chr5:5p15.33-14.1		 pathogenic
GRCh38/hg38 5p15.33-14.2(chr5:22149-23607053)x3 copy number gain See cases [RCV000137806] Chr5:22149..23607053 [GRCh38]
Chr5:22149..23607162 [GRCh37]
Chr5:75149..23642919 [NCBI36]
Chr5:5p15.33-14.2		 pathogenic
GRCh38/hg38 5p15.33-13.2(chr5:22149-35831538)x1 copy number loss See cases [RCV000138888] Chr5:22149..35831538 [GRCh38]
Chr5:22149..35831640 [GRCh37]
Chr5:75149..35867397 [NCBI36]
Chr5:5p15.33-13.2		 pathogenic
GRCh38/hg38 5p15.33-q13.3(chr5:22149-74412725)x3 copy number gain See cases [RCV000138780] Chr5:22149..74412725 [GRCh38]
Chr5:22149..73708550 [GRCh37]
Chr5:75149..73744306 [NCBI36]
Chr5:5p15.33-q13.3		 pathogenic
GRCh38/hg38 5p15.33-14.3(chr5:22149-21217120)x1 copy number loss See cases [RCV000138553] Chr5:22149..21217120 [GRCh38]
Chr5:22149..21217229 [GRCh37]
Chr5:75149..21252986 [NCBI36]
Chr5:5p15.33-14.3		 pathogenic
GRCh38/hg38 5p15.33-15.1(chr5:22149-17788697)x1 copy number loss See cases [RCV000138288] Chr5:22149..17788697 [GRCh38]
Chr5:22149..17788806 [GRCh37]
Chr5:75149..17824563 [NCBI36]
Chr5:5p15.33-15.1		 likely benign
GRCh38/hg38 5p15.1(chr5:16687561-16803648)x3 copy number gain See cases [RCV000141388] Chr5:16687561..16803648 [GRCh38]
Chr5:16687670..16803757 [GRCh37]
Chr5:16740670..16856757 [NCBI36]
Chr5:5p15.1		 uncertain significance
GRCh38/hg38 5p15.33-14.1(chr5:22149-28589192)x1 copy number loss See cases [RCV000141225] Chr5:22149..28589192 [GRCh38]
Chr5:22149..28589299 [GRCh37]
Chr5:75149..28625056 [NCBI36]
Chr5:5p15.33-14.1		 pathogenic
GRCh38/hg38 5p15.32-13.2(chr5:4849498-36818719)x3 copy number gain See cases [RCV000141246] Chr5:4849498..36818719 [GRCh38]
Chr5:4849611..36818821 [GRCh37]
Chr5:4902611..36854578 [NCBI36]
Chr5:5p15.32-13.2		 pathogenic
GRCh38/hg38 5p15.33-15.1(chr5:22149-16930016)x1 copy number loss See cases [RCV000140964] Chr5:22149..16930016 [GRCh38]
Chr5:22149..16930125 [GRCh37]
Chr5:75149..16983125 [NCBI36]
Chr5:5p15.33-15.1		 pathogenic
GRCh38/hg38 5p15.33-13.2(chr5:113461-33998289)x1 copy number loss See cases [RCV000141844] Chr5:113461..33998289 [GRCh38]
Chr5:113576..33998394 [GRCh37]
Chr5:166576..34034151 [NCBI36]
Chr5:5p15.33-13.2		 pathogenic
GRCh38/hg38 5p15.32-14.3(chr5:4932707-18465361)x1 copy number loss See cases [RCV000141795] Chr5:4932707..18465361 [GRCh38]
Chr5:4932820..18465470 [GRCh37]
Chr5:4985820..18501227 [NCBI36]
Chr5:5p15.32-14.3		 pathogenic
GRCh38/hg38 5p15.33-14.3(chr5:22149-21726360)x1 copy number loss See cases [RCV000143022] Chr5:22149..21726360 [GRCh38]
Chr5:22149..21726469 [GRCh37]
Chr5:75149..21762226 [NCBI36]
Chr5:5p15.33-14.3		 pathogenic
GRCh38/hg38 5p15.33-14.1(chr5:22149-27611163)x1 copy number loss See cases [RCV000142934] Chr5:22149..27611163 [GRCh38]
Chr5:22149..27611270 [GRCh37]
Chr5:75149..27647027 [NCBI36]
Chr5:5p15.33-14.1		 pathogenic
GRCh38/hg38 5p15.33-14.1(chr5:22149-26593891)x1 copy number loss See cases [RCV000142645] Chr5:22149..26593891 [GRCh38]
Chr5:22149..26594000 [GRCh37]
Chr5:75149..26629757 [NCBI36]
Chr5:5p15.33-14.1		 pathogenic
GRCh38/hg38 5p15.1-14.3(chr5:16456444-18561765)x1 copy number loss See cases [RCV000143153] Chr5:16456444..18561765 [GRCh38]
Chr5:16456553..18561874 [GRCh37]
Chr5:16509553..18597631 [NCBI36]
Chr5:5p15.1-14.3		 uncertain significance
GRCh37/hg19 5p15.2-12(chr5:13461664-46098927)x3 copy number gain See cases [RCV000239779] Chr5:13461664..46098927 [GRCh37]
Chr5:5p15.2-12		 pathogenic
GRCh37/hg19 5p15.33-13.3(chr5:113576-33493797)x1 copy number loss See cases [RCV000449075] Chr5:113576..33493797 [GRCh37]
Chr5:5p15.33-13.3		 pathogenic
GRCh37/hg19 5p15.33-13.3(chr5:25328-30672798)x1 copy number loss See cases [RCV000515550] Chr5:25328..30672798 [GRCh37]
Chr5:5p15.33-13.3		 pathogenic
GRCh37/hg19 5p15.33-14.3(chr5:25328-19661628)x3 copy number gain not provided [RCV000234904] Chr5:25328..19661628 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.33-14.1(chr5:140474-26906925) copy number loss 5p partial monosomy syndrome [RCV000767709] Chr5:140474..26906925 [GRCh37]
Chr5:5p15.33-14.1		 pathogenic
GRCh37/hg19 5p15.33-13.2(chr5:22149-34041255)x3 copy number gain See cases [RCV000240016] Chr5:22149..34041255 [GRCh37]
Chr5:5p15.33-13.2		 pathogenic
NM_012334.3(MYO10):c.3404G>A (p.Arg1135Gln) single nucleotide variant Inborn genetic diseases [RCV003245717] Chr5:16700991 [GRCh38]
Chr5:16701100 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.1(chr5:16875518-17014287)x3 copy number gain not provided [RCV000415981] Chr5:16875518..17014287 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-15.1(chr5:113576-16854340)x1 copy number loss See cases [RCV000449097] Chr5:113576..16854340 [GRCh37]
Chr5:5p15.33-15.1		 pathogenic
GRCh37/hg19 5p15.33-13.3(chr5:3159498-30585683)x3 copy number gain See cases [RCV000449100] Chr5:3159498..30585683 [GRCh37]
Chr5:5p15.33-13.3		 pathogenic
GRCh37/hg19 5p15.33-13.3(chr5:113576-30279389)x3 copy number gain See cases [RCV000446077] Chr5:113576..30279389 [GRCh37]
Chr5:5p15.33-13.3		 pathogenic
GRCh37/hg19 5p15.33-14.1(chr5:22149-24835567)x1 copy number loss See cases [RCV000447672] Chr5:22149..24835567 [GRCh37]
Chr5:5p15.33-14.1		 pathogenic
GRCh37/hg19 5p15.33-13.2(chr5:113576-34372083)x1 copy number loss See cases [RCV000446974] Chr5:113576..34372083 [GRCh37]
Chr5:5p15.33-13.2		 pathogenic
GRCh37/hg19 5p15.1(chr5:16384928-16969392)x1 copy number loss See cases [RCV000446370] Chr5:16384928..16969392 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-15.1(chr5:113576-17334977)x1 copy number loss See cases [RCV000446645] Chr5:113576..17334977 [GRCh37]
Chr5:5p15.33-15.1		 pathogenic
GRCh37/hg19 5p15.33-14.1(chr5:113576-27338567)x1 copy number loss See cases [RCV000446054] Chr5:113576..27338567 [GRCh37]
Chr5:5p15.33-14.1		 pathogenic
GRCh37/hg19 5p15.33-14.1(chr5:113576-25948451)x1 copy number loss See cases [RCV000447462] Chr5:113576..25948451 [GRCh37]
Chr5:5p15.33-14.1		 pathogenic
GRCh37/hg19 5p15.31-13.3(chr5:7806183-31019599)x1 copy number loss See cases [RCV000445859] Chr5:7806183..31019599 [GRCh37]
Chr5:5p15.31-13.3		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-13.2(chr5:22149-34041196)x1 copy number loss See cases [RCV000448019] Chr5:22149..34041196 [GRCh37]
Chr5:5p15.33-13.2		 pathogenic
GRCh37/hg19 5p15.33-14.3(chr5:113576-21786246)x1 copy number loss See cases [RCV000448521] Chr5:113576..21786246 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.1(chr5:16652934-16771046) copy number gain Abnormal esophagus morphology [RCV000416785] Chr5:16652934..16771046 [GRCh37]
Chr5:5p15.1		 likely benign
GRCh37/hg19 5p15.33-14.3(chr5:113576-23147737)x1 copy number loss See cases [RCV000448408] Chr5:113576..23147737 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.31-14.2(chr5:9120813-24274030)x1 copy number loss See cases [RCV000448421] Chr5:9120813..24274030 [GRCh37]
Chr5:5p15.31-14.2		 pathogenic
GRCh37/hg19 5p15.33-14.3(chr5:79146-22152284)x1 copy number loss See cases [RCV000447737] Chr5:79146..22152284 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.33-14.1(chr5:113576-25091472)x1 copy number loss See cases [RCV000512066] Chr5:113576..25091472 [GRCh37]
Chr5:5p15.33-14.1		 pathogenic
GRCh37/hg19 5p15.33-14.1(chr5:113576-26234903)x1 copy number loss See cases [RCV000510193] Chr5:113576..26234903 [GRCh37]
Chr5:5p15.33-14.1		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-14.1(chr5:113576-26948599)x1 copy number loss See cases [RCV000510921] Chr5:113576..26948599 [GRCh37]
Chr5:5p15.33-14.1		 pathogenic
GRCh37/hg19 5p15.33-14.3(chr5:113576-23047959)x1 copy number loss See cases [RCV000510786] Chr5:113576..23047959 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
NM_012334.3(MYO10):c.1439T>C (p.Val480Ala) single nucleotide variant Inborn genetic diseases [RCV003239479] Chr5:16763536 [GRCh38]
Chr5:16763645 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3319G>A (p.Val1107Met) single nucleotide variant Inborn genetic diseases [RCV003286512] Chr5:16701076 [GRCh38]
Chr5:16701185 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.1817A>G (p.His606Arg) single nucleotide variant Inborn genetic diseases [RCV003252722] Chr5:16758149 [GRCh38]
Chr5:16758258 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2674C>T (p.Arg892Cys) single nucleotide variant Inborn genetic diseases [RCV003297916] Chr5:16701721 [GRCh38]
Chr5:16701830 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.1780C>T (p.Arg594Cys) single nucleotide variant Inborn genetic diseases [RCV003255153] Chr5:16758186 [GRCh38]
Chr5:16758295 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-14.3(chr5:113576-20240392)x3 copy number gain See cases [RCV000512567] Chr5:113576..20240392 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.33-14.3(chr5:113576-19167699)x1 copy number loss not provided [RCV000682515] Chr5:113576..19167699 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.33-13.2(chr5:113576-35739404)x3 copy number gain not provided [RCV000682516] Chr5:113576..35739404 [GRCh37]
Chr5:5p15.33-13.2		 pathogenic
GRCh37/hg19 5p15.32-14.3(chr5:5830053-19490899)x1 copy number loss not provided [RCV000682520] Chr5:5830053..19490899 [GRCh37]
Chr5:5p15.32-14.3		 pathogenic
GRCh37/hg19 5p15.2-15.1(chr5:10515035-17607385)x1 copy number loss not provided [RCV000682524] Chr5:10515035..17607385 [GRCh37]
Chr5:5p15.2-15.1		 pathogenic
GRCh37/hg19 5p15.1(chr5:16609762-16999804)x3 copy number gain not provided [RCV000682530] Chr5:16609762..16999804 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-14.3(chr5:25328-18662625)x1 copy number loss not provided [RCV000744320] Chr5:25328..18662625 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.33-14.3(chr5:25328-18698028)x3 copy number gain not provided [RCV000744321] Chr5:25328..18698028 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.33-13.3(chr5:25328-31343671)x1 copy number loss not provided [RCV000744322] Chr5:25328..31343671 [GRCh37]
Chr5:5p15.33-13.3		 pathogenic
GRCh37/hg19 5p15.1(chr5:16870083-16878237)x1 copy number loss not provided [RCV000744513] Chr5:16870083..16878237 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.3207C>T (p.Gly1069=) single nucleotide variant not provided [RCV000893630] Chr5:16701188 [GRCh38]
Chr5:16701297 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.4482C>T (p.Asn1494=) single nucleotide variant not provided [RCV000896165] Chr5:16680007 [GRCh38]
Chr5:16680116 [GRCh37]
Chr5:5p15.1		 likely benign
NM_012334.3(MYO10):c.2129A>G (p.Tyr710Cys) single nucleotide variant Inborn genetic diseases [RCV003244577] Chr5:16710948 [GRCh38]
Chr5:16711057 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.4593G>A (p.Pro1531=) single nucleotide variant not provided [RCV000898385] Chr5:16676104 [GRCh38]
Chr5:16676213 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.3207C>A (p.Gly1069=) single nucleotide variant not provided [RCV000898386] Chr5:16701188 [GRCh38]
Chr5:16701297 [GRCh37]
Chr5:5p15.1		 likely benign
NM_012334.3(MYO10):c.4554G>A (p.Leu1518=) single nucleotide variant not provided [RCV000972735] Chr5:16676143 [GRCh38]
Chr5:16676252 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.4818G>A (p.Leu1606=) single nucleotide variant not provided [RCV000881245] Chr5:16674999 [GRCh38]
Chr5:16675108 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.3990G>A (p.Val1330=) single nucleotide variant not provided [RCV000881246] Chr5:16685738 [GRCh38]
Chr5:16685847 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.925G>A (p.Val309Ile) single nucleotide variant not provided [RCV000923063] Chr5:16779550 [GRCh38]
Chr5:16779659 [GRCh37]
Chr5:5p15.1		 likely benign
NM_012334.3(MYO10):c.4559C>T (p.Ser1520Leu) single nucleotide variant not provided [RCV000950129] Chr5:16676138 [GRCh38]
Chr5:16676247 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.4143G>A (p.Arg1381=) single nucleotide variant not provided [RCV000950676] Chr5:16681917 [GRCh38]
Chr5:16682026 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.2708T>C (p.Met903Thr) single nucleotide variant not provided [RCV000879263] Chr5:16701687 [GRCh38]
Chr5:16701796 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.819A>C (p.Glu273Asp) single nucleotide variant not provided [RCV000959590] Chr5:16780531 [GRCh38]
Chr5:16780640 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.4782G>A (p.Gln1594=) single nucleotide variant not provided [RCV000966938] Chr5:16675035 [GRCh38]
Chr5:16675144 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.2871C>T (p.Ile957=) single nucleotide variant not provided [RCV000966939] Chr5:16701524 [GRCh38]
Chr5:16701633 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.6071G>C (p.Ser2024Thr) single nucleotide variant not provided [RCV000971506] Chr5:16668281 [GRCh38]
Chr5:16668390 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.179C>T (p.Thr60Met) single nucleotide variant not provided [RCV000880069] Chr5:16818109 [GRCh38]
Chr5:16818218 [GRCh37]
Chr5:5p15.1		 likely benign
NM_012334.3(MYO10):c.4107G>A (p.Pro1369=) single nucleotide variant not provided [RCV000958771] Chr5:16681953 [GRCh38]
Chr5:16682062 [GRCh37]
Chr5:5p15.1		 benign
GRCh37/hg19 5p15.2-14.3(chr5:11182916-18624750)x3 copy number gain not provided [RCV000849007] Chr5:11182916..18624750 [GRCh37]
Chr5:5p15.2-14.3		 uncertain significance
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32		 uncertain significance
NM_012334.3(MYO10):c.4629G>A (p.Pro1543=) single nucleotide variant not provided [RCV000960251] Chr5:16676068 [GRCh38]
Chr5:16676177 [GRCh37]
Chr5:5p15.1		 benign
GRCh37/hg19 5p15.1(chr5:16526710-16743952)x3 copy number gain not provided [RCV000847625] Chr5:16526710..16743952 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-14.2(chr5:113576-23364376)x1 copy number loss not provided [RCV001005642] Chr5:113576..23364376 [GRCh37]
Chr5:5p15.33-14.2		 pathogenic
NM_012334.3(MYO10):c.3710G>A (p.Arg1237His) single nucleotide variant Inborn genetic diseases [RCV003288588] Chr5:16694461 [GRCh38]
Chr5:16694570 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.1408G>C (p.Glu470Gln) single nucleotide variant Inborn genetic diseases [RCV003245572] Chr5:16763674 [GRCh38]
Chr5:16763783 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3794C>T (p.Thr1265Met) single nucleotide variant Inborn genetic diseases [RCV003269756] Chr5:16694377 [GRCh38]
Chr5:16694486 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.146T>A (p.Ile49Asn) single nucleotide variant Inborn genetic diseases [RCV003290333] Chr5:16818142 [GRCh38]
Chr5:16818251 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3271T>C (p.Tyr1091His) single nucleotide variant Inborn genetic diseases [RCV003293035] Chr5:16701124 [GRCh38]
Chr5:16701233 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2449G>A (p.Glu817Lys) single nucleotide variant Inborn genetic diseases [RCV003242229] Chr5:16702986 [GRCh38]
Chr5:16703095 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5004C>T (p.Tyr1668=) single nucleotide variant not provided [RCV000974611] Chr5:16673850 [GRCh38]
Chr5:16673959 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.5370C>T (p.Cys1790=) single nucleotide variant not provided [RCV000885760] Chr5:16671482 [GRCh38]
Chr5:16671591 [GRCh37]
Chr5:5p15.1		 benign|likely benign
NM_012334.3(MYO10):c.1889A>G (p.Asn630Ser) single nucleotide variant not provided [RCV000888589] Chr5:16754868 [GRCh38]
Chr5:16754977 [GRCh37]
Chr5:5p15.1		 benign
NM_012334.3(MYO10):c.976G>C (p.Val326Leu) single nucleotide variant not provided [RCV000891350] Chr5:16769158 [GRCh38]
Chr5:16769267 [GRCh37]
Chr5:5p15.1		 likely benign
NM_012334.3(MYO10):c.5549C>T (p.Pro1850Leu) single nucleotide variant Inborn genetic diseases [RCV002836504] Chr5:16670860 [GRCh38]
Chr5:16670969 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.352A>G (p.Met118Val) single nucleotide variant Inborn genetic diseases [RCV003276617] Chr5:16794761 [GRCh38]
Chr5:16794870 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.31-14.3(chr5:8081005-22210970)x1 copy number loss not provided [RCV002472646] Chr5:8081005..22210970 [GRCh37]
Chr5:5p15.31-14.3		 pathogenic
GRCh37/hg19 5p15.1(chr5:15093064-16669298)x3 copy number gain not provided [RCV001005656] Chr5:15093064..16669298 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-14.3(chr5:71904-22078969) copy number loss 5p partial monosomy syndrome [RCV001195139] Chr5:71904..22078969 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.1(chr5:16670513-17011470)x1 copy number loss not provided [RCV001258688] Chr5:16670513..17011470 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-13.3(chr5:113576-29310520) copy number gain 5p partial monosomy syndrome [RCV002280773] Chr5:113576..29310520 [GRCh37]
Chr5:5p15.33-13.3		 pathogenic
GRCh37/hg19 5p15.33-13.3(chr5:113576-30712376)x1 copy number loss See cases [RCV002285039] Chr5:113576..30712376 [GRCh37]
Chr5:5p15.33-13.3		 pathogenic
GRCh37/hg19 5p15.1-14.2(chr5:16741484-23963898)x3 copy number gain not provided [RCV001258689] Chr5:16741484..23963898 [GRCh37]
Chr5:5p15.1-14.2		 uncertain significance
NM_012334.3(MYO10):c.5467C>G (p.Pro1823Ala) single nucleotide variant Inborn genetic diseases [RCV003253988] Chr5:16670942 [GRCh38]
Chr5:16671051 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-15.1(chr5:113577-16952167)x1 copy number loss not provided [RCV001827855] Chr5:113577..16952167 [GRCh37]
Chr5:5p15.33-15.1		 pathogenic
GRCh37/hg19 5p15.1(chr5:16384928-16969392) copy number loss not specified [RCV002053482] Chr5:16384928..16969392 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.1(chr5:16341722-16701378) copy number gain not specified [RCV002053481] Chr5:16341722..16701378 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-13.3(chr5:1-32091038)x1 copy number loss not provided [RCV002472712] Chr5:1..32091038 [GRCh37]
Chr5:5p15.33-13.3		 pathogenic
GRCh37/hg19 5p15.33-15.1(chr5:113577-17654787)x1 copy number loss not provided [RCV002473919] Chr5:113577..17654787 [GRCh37]
Chr5:5p15.33-15.1		 pathogenic
GRCh37/hg19 5p15.1(chr5:16920463-17134432)x3 copy number gain not provided [RCV002474938] Chr5:16920463..17134432 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2847G>C (p.Glu949Asp) single nucleotide variant Inborn genetic diseases [RCV003013012] Chr5:16701548 [GRCh38]
Chr5:16701657 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3612C>G (p.Phe1204Leu) single nucleotide variant Inborn genetic diseases [RCV002771783] Chr5:16694559 [GRCh38]
Chr5:16694668 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5014A>G (p.Thr1672Ala) single nucleotide variant Inborn genetic diseases [RCV002990928] Chr5:16673840 [GRCh38]
Chr5:16673949 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.1036G>T (p.Gly346Trp) single nucleotide variant Inborn genetic diseases [RCV002817541] Chr5:16769098 [GRCh38]
Chr5:16769207 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3895A>G (p.Ser1299Gly) single nucleotide variant Inborn genetic diseases [RCV002860023] Chr5:16689825 [GRCh38]
Chr5:16689934 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3190C>T (p.His1064Tyr) single nucleotide variant Inborn genetic diseases [RCV002865564] Chr5:16701205 [GRCh38]
Chr5:16701314 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.4448A>G (p.Asn1483Ser) single nucleotide variant Inborn genetic diseases [RCV002794034] Chr5:16680041 [GRCh38]
Chr5:16680150 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3358G>A (p.Asp1120Asn) single nucleotide variant Inborn genetic diseases [RCV002689673] Chr5:16701037 [GRCh38]
Chr5:16701146 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5551C>T (p.Leu1851Phe) single nucleotide variant Inborn genetic diseases [RCV002865219] Chr5:16670858 [GRCh38]
Chr5:16670967 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.113A>G (p.Tyr38Cys) single nucleotide variant Inborn genetic diseases [RCV002689316] Chr5:16877616 [GRCh38]
Chr5:16877725 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.4103C>T (p.Thr1368Met) single nucleotide variant Inborn genetic diseases [RCV002733468] Chr5:16681957 [GRCh38]
Chr5:16682066 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2795A>G (p.Glu932Gly) single nucleotide variant Inborn genetic diseases [RCV002749885] Chr5:16701600 [GRCh38]
Chr5:16701709 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.370C>T (p.Arg124Cys) single nucleotide variant Inborn genetic diseases [RCV002945874] Chr5:16794743 [GRCh38]
Chr5:16794852 [GRCh37]
Chr5:5p15.1		 likely benign
NM_012334.3(MYO10):c.853A>C (p.Asn285His) single nucleotide variant Inborn genetic diseases [RCV002858735] Chr5:16779622 [GRCh38]
Chr5:16779731 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5362C>G (p.Leu1788Val) single nucleotide variant Inborn genetic diseases [RCV002778743] Chr5:16671490 [GRCh38]
Chr5:16671599 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.637G>A (p.Val213Met) single nucleotide variant Inborn genetic diseases [RCV002989895] Chr5:16781795 [GRCh38]
Chr5:16781904 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-13.3(chr5:113577-31448527)x1 copy number loss not provided [RCV002475666] Chr5:113577..31448527 [GRCh37]
Chr5:5p15.33-13.3		 pathogenic
GRCh37/hg19 5p15.33-14.1(chr5:113577-26164852)x1 copy number loss not provided [RCV002475573] Chr5:113577..26164852 [GRCh37]
Chr5:5p15.33-14.1		 pathogenic
NM_012334.3(MYO10):c.2459A>G (p.Glu820Gly) single nucleotide variant Inborn genetic diseases [RCV002794608] Chr5:16702976 [GRCh38]
Chr5:16703085 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.425G>A (p.Arg142His) single nucleotide variant Inborn genetic diseases [RCV002694394] Chr5:16794688 [GRCh38]
Chr5:16794797 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.142A>C (p.Thr48Pro) single nucleotide variant Inborn genetic diseases [RCV002693320] Chr5:16818146 [GRCh38]
Chr5:16818255 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.1822C>T (p.Arg608Trp) single nucleotide variant Inborn genetic diseases [RCV002845990] Chr5:16758144 [GRCh38]
Chr5:16758253 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3853G>A (p.Asp1285Asn) single nucleotide variant Inborn genetic diseases [RCV002869364] Chr5:16689867 [GRCh38]
Chr5:16689976 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3007G>A (p.Ala1003Thr) single nucleotide variant Inborn genetic diseases [RCV002660731] Chr5:16701388 [GRCh38]
Chr5:16701497 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.1451T>C (p.Ile484Thr) single nucleotide variant Inborn genetic diseases [RCV002884443] Chr5:16763524 [GRCh38]
Chr5:16763633 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5281G>A (p.Val1761Ile) single nucleotide variant Inborn genetic diseases [RCV002844998] Chr5:16672717 [GRCh38]
Chr5:16672826 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2477A>G (p.Glu826Gly) single nucleotide variant Inborn genetic diseases [RCV002869531] Chr5:16702958 [GRCh38]
Chr5:16703067 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.4426C>T (p.Arg1476Trp) single nucleotide variant Inborn genetic diseases [RCV002692420] Chr5:16680063 [GRCh38]
Chr5:16680172 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5146A>G (p.Ile1716Val) single nucleotide variant Inborn genetic diseases [RCV002869653] Chr5:16673708 [GRCh38]
Chr5:16673817 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.1169A>G (p.Asn390Ser) single nucleotide variant Inborn genetic diseases [RCV002694724] Chr5:16766090 [GRCh38]
Chr5:16766199 [GRCh37]
Chr5:5p15.1		 likely benign
NM_012334.3(MYO10):c.5564A>T (p.Tyr1855Phe) single nucleotide variant Inborn genetic diseases [RCV002984167] Chr5:16670845 [GRCh38]
Chr5:16670954 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5528C>T (p.Thr1843Ile) single nucleotide variant Inborn genetic diseases [RCV002768622] Chr5:16670881 [GRCh38]
Chr5:16670990 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.190G>A (p.Gly64Ser) single nucleotide variant Inborn genetic diseases [RCV002701874] Chr5:16818098 [GRCh38]
Chr5:16818207 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.932C>T (p.Thr311Met) single nucleotide variant Inborn genetic diseases [RCV002956715] Chr5:16769202 [GRCh38]
Chr5:16769311 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5698C>T (p.Arg1900Trp) single nucleotide variant Inborn genetic diseases [RCV002743204] Chr5:16670711 [GRCh38]
Chr5:16670820 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.629C>T (p.Ala210Val) single nucleotide variant Inborn genetic diseases [RCV002641760] Chr5:16781803 [GRCh38]
Chr5:16781912 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.4592C>T (p.Pro1531Leu) single nucleotide variant Inborn genetic diseases [RCV002916490] Chr5:16676105 [GRCh38]
Chr5:16676214 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.4234C>A (p.Leu1412Met) single nucleotide variant Inborn genetic diseases [RCV002854020] Chr5:16681459 [GRCh38]
Chr5:16681568 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.1112A>C (p.Asp371Ala) single nucleotide variant Inborn genetic diseases [RCV003003568] Chr5:16766147 [GRCh38]
Chr5:16766256 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3000C>A (p.Asp1000Glu) single nucleotide variant Inborn genetic diseases [RCV002919313] Chr5:16701395 [GRCh38]
Chr5:16701504 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.976G>A (p.Val326Met) single nucleotide variant Inborn genetic diseases [RCV002986083] Chr5:16769158 [GRCh38]
Chr5:16769267 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3426G>T (p.Gln1142His) single nucleotide variant Inborn genetic diseases [RCV002768112] Chr5:16700969 [GRCh38]
Chr5:16701078 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.23G>T (p.Gly8Val) single nucleotide variant Inborn genetic diseases [RCV002891571] Chr5:16877706 [GRCh38]
Chr5:16877815 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.1758T>A (p.Asp586Glu) single nucleotide variant Inborn genetic diseases [RCV002673986] Chr5:16758208 [GRCh38]
Chr5:16758317 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2650A>G (p.Asn884Asp) single nucleotide variant Inborn genetic diseases [RCV002921285] Chr5:16701745 [GRCh38]
Chr5:16701854 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.632A>T (p.Lys211Met) single nucleotide variant Inborn genetic diseases [RCV002792740] Chr5:16781800 [GRCh38]
Chr5:16781909 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3181G>A (p.Gly1061Arg) single nucleotide variant Inborn genetic diseases [RCV002878793] Chr5:16701214 [GRCh38]
Chr5:16701323 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3668G>C (p.Gly1223Ala) single nucleotide variant Inborn genetic diseases [RCV002668950] Chr5:16694503 [GRCh38]
Chr5:16694612 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3686T>C (p.Leu1229Pro) single nucleotide variant Inborn genetic diseases [RCV002747268] Chr5:16694485 [GRCh38]
Chr5:16694594 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3857G>C (p.Arg1286Thr) single nucleotide variant Inborn genetic diseases [RCV002855795] Chr5:16689863 [GRCh38]
Chr5:16689972 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.931A>G (p.Thr311Ala) single nucleotide variant Inborn genetic diseases [RCV002835986] Chr5:16769203 [GRCh38]
Chr5:16769312 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.301G>A (p.Ala101Thr) single nucleotide variant Inborn genetic diseases [RCV002898444] Chr5:16794812 [GRCh38]
Chr5:16794921 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2678T>C (p.Leu893Pro) single nucleotide variant Inborn genetic diseases [RCV002652789] Chr5:16701717 [GRCh38]
Chr5:16701826 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2772C>G (p.Asp924Glu) single nucleotide variant Inborn genetic diseases [RCV002680021] Chr5:16701623 [GRCh38]
Chr5:16701732 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.6146G>A (p.Arg2049His) single nucleotide variant Inborn genetic diseases [RCV002657402] Chr5:16666723 [GRCh38]
Chr5:16666832 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.4970G>A (p.Arg1657Gln) single nucleotide variant Inborn genetic diseases [RCV003202679] Chr5:16673884 [GRCh38]
Chr5:16673993 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.4460G>T (p.Arg1487Leu) single nucleotide variant Inborn genetic diseases [RCV003195501] Chr5:16680029 [GRCh38]
Chr5:16680138 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3431C>T (p.Ser1144Leu) single nucleotide variant Inborn genetic diseases [RCV003220209] Chr5:16700964 [GRCh38]
Chr5:16701073 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5387A>G (p.Asn1796Ser) single nucleotide variant Inborn genetic diseases [RCV003204032] Chr5:16671465 [GRCh38]
Chr5:16671574 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.6092A>G (p.Lys2031Arg) single nucleotide variant Inborn genetic diseases [RCV003190945] Chr5:16666777 [GRCh38]
Chr5:16666886 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5824A>C (p.Lys1942Gln) single nucleotide variant Inborn genetic diseases [RCV003217124] Chr5:16670585 [GRCh38]
Chr5:16670694 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.580G>C (p.Glu194Gln) single nucleotide variant Inborn genetic diseases [RCV003174360] Chr5:16783357 [GRCh38]
Chr5:16783466 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2875C>T (p.Arg959Trp) single nucleotide variant Inborn genetic diseases [RCV003204734] Chr5:16701520 [GRCh38]
Chr5:16701629 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5465C>T (p.Ala1822Val) single nucleotide variant Inborn genetic diseases [RCV003185908] Chr5:16670944 [GRCh38]
Chr5:16671053 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2371G>A (p.Ala791Thr) single nucleotide variant Inborn genetic diseases [RCV003196178] Chr5:16703064 [GRCh38]
Chr5:16703173 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.2-15.1(chr5:10165922-18156739)x3 copy number gain Intellectual developmental disorder, autosomal dominant 63, with macrocephaly [RCV003159551] Chr5:10165922..18156739 [GRCh37]
Chr5:5p15.2-15.1		 pathogenic|likely pathogenic
NM_012334.3(MYO10):c.3845T>A (p.Ile1282Asn) single nucleotide variant Inborn genetic diseases [RCV003216186] Chr5:16689875 [GRCh38]
Chr5:16689984 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.4097C>T (p.Ala1366Val) single nucleotide variant Inborn genetic diseases [RCV003198403] Chr5:16681963 [GRCh38]
Chr5:16682072 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3088T>G (p.Ser1030Ala) single nucleotide variant Inborn genetic diseases [RCV003266106] Chr5:16701307 [GRCh38]
Chr5:16701416 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.4511C>G (p.Thr1504Ser) single nucleotide variant Inborn genetic diseases [RCV003308610] Chr5:16679978 [GRCh38]
Chr5:16680087 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.707A>G (p.Gln236Arg) single nucleotide variant Inborn genetic diseases [RCV003265756] Chr5:16781725 [GRCh38]
Chr5:16781834 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2764C>T (p.Arg922Trp) single nucleotide variant Inborn genetic diseases [RCV003265819] Chr5:16701631 [GRCh38]
Chr5:16701740 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.563A>G (p.Glu188Gly) single nucleotide variant Inborn genetic diseases [RCV003339421] Chr5:16783374 [GRCh38]
Chr5:16783483 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5321C>T (p.Thr1774Ile) single nucleotide variant Inborn genetic diseases [RCV003344732] Chr5:16671531 [GRCh38]
Chr5:16671640 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5479C>T (p.Leu1827Phe) single nucleotide variant Inborn genetic diseases [RCV003371972] Chr5:16670930 [GRCh38]
Chr5:16671039 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.1586C>T (p.Ala529Val) single nucleotide variant Inborn genetic diseases [RCV003351246] Chr5:16762546 [GRCh38]
Chr5:16762655 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.2729C>T (p.Ser910Leu) single nucleotide variant Inborn genetic diseases [RCV003363652] Chr5:16701666 [GRCh38]
Chr5:16701775 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.5753C>T (p.Ser1918Phe) single nucleotide variant Inborn genetic diseases [RCV003364063] Chr5:16670656 [GRCh38]
Chr5:16670765 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.3938A>G (p.Asp1313Gly) single nucleotide variant Inborn genetic diseases [RCV003347261] Chr5:16685790 [GRCh38]
Chr5:16685899 [GRCh37]
Chr5:5p15.1		 uncertain significance
NM_012334.3(MYO10):c.1873A>G (p.Thr625Ala) single nucleotide variant Inborn genetic diseases [RCV003371696] Chr5:16754884 [GRCh38]
Chr5:16754993 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-13.2(chr5:113577-35613146)x1 copy number loss not provided [RCV003485447] Chr5:113577..35613146 [GRCh37]
Chr5:5p15.33-13.2		 pathogenic
GRCh37/hg19 5p15.33-13.3(chr5:113577-30529044)x1 copy number loss not provided [RCV003485449] Chr5:113577..30529044 [GRCh37]
Chr5:5p15.33-13.3		 pathogenic
GRCh37/hg19 5p15.33-14.3(chr5:113577-21529653)x1 copy number loss not provided [RCV003485450] Chr5:113577..21529653 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.33-14.3(chr5:862398-18927500)x1 copy number loss not provided [RCV003485453] Chr5:862398..18927500 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.33-14.1(chr5:113577-27800913)x3 copy number gain not provided [RCV003484599] Chr5:113577..27800913 [GRCh37]
Chr5:5p15.33-14.1		 pathogenic
NM_012334.3(MYO10):c.1620A>T (p.Ala540=) single nucleotide variant not provided [RCV003436423] Chr5:16762081 [GRCh38]
Chr5:16762190 [GRCh37]
Chr5:5p15.1		 likely benign
NM_012334.3(MYO10):c.88G>A (p.Gly30Ser) single nucleotide variant not provided [RCV003456591] Chr5:16877641 [GRCh38]
Chr5:16877750 [GRCh37]
Chr5:5p15.1		 uncertain significance
GRCh37/hg19 5p15.33-14.1(chr5:113576-28300709)x1 copy number loss not specified [RCV003986544] Chr5:113576..28300709 [GRCh37]
Chr5:5p15.33-14.1		 pathogenic
GRCh37/hg19 5p15.33-14.3(chr5:113576-19388145)x1 copy number loss not specified [RCV003986593] Chr5:113576..19388145 [GRCh37]
Chr5:5p15.33-14.3		 pathogenic
GRCh37/hg19 5p15.33-15.1(chr5:113576-17511896)x1 copy number loss not specified [RCV003986589] Chr5:113576..17511896 [GRCh37]
Chr5:5p15.33-15.1		 pathogenic
GRCh37/hg19 5p15.33-15.1(chr5:3272715-17317051)x1 copy number loss not specified [RCV003986598] Chr5:3272715..17317051 [GRCh37]
Chr5:5p15.33-15.1		 pathogenic
GRCh37/hg19 5p15.33-14.1(chr5:113576-26534253)x1 copy number loss not specified [RCV003986560] Chr5:113576..26534253 [GRCh37]
Chr5:5p15.33-14.1		 pathogenic
GRCh37/hg19 5p15.32-13.3(chr5:5259461-29748394)x1 copy number loss not specified [RCV003986556] Chr5:5259461..29748394 [GRCh37]
Chr5:5p15.32-13.3		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3184
Count of miRNA genes:1052
Interacting mature miRNAs:1260
Transcripts:ENST00000274203, ENST00000427430, ENST00000502436, ENST00000505695, ENST00000506343, ENST00000507288, ENST00000508318, ENST00000510401, ENST00000511972, ENST00000512061, ENST00000513610, ENST00000513882, ENST00000515803
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
D5S416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,720,134 - 16,720,345UniSTSGRCh37
GRCh37516,720,058 - 16,720,341UniSTSGRCh37
Build 36516,773,058 - 16,773,341RGDNCBI36
Celera516,745,121 - 16,745,404RGD
Celera516,745,197 - 16,745,408UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,692,421 - 16,692,632UniSTS
HuRef516,692,345 - 16,692,628UniSTS
Marshfield Genetic Map528.76UniSTS
Marshfield Genetic Map528.76RGD
Genethon Genetic Map527.9UniSTS
TNG Radiation Hybrid Map59127.0UniSTS
GeneMap99-GB4 RH Map560.1UniSTS
Whitehead-YAC Contig Map5 UniSTS
NCBI RH Map553.1UniSTS
D5S2114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,895,727 - 16,896,005UniSTSGRCh37
Build 36516,948,727 - 16,949,005RGDNCBI36
Celera516,920,860 - 16,921,138RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,868,322 - 16,868,600UniSTS
Marshfield Genetic Map529.52RGD
Marshfield Genetic Map529.52UniSTS
Genethon Genetic Map528.7UniSTS
A009W42  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,776,539 - 16,776,673UniSTSGRCh37
Build 36516,829,539 - 16,829,673RGDNCBI36
Celera516,801,593 - 16,801,727RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,748,825 - 16,748,959UniSTS
GeneMap99-GB4 RH Map565.24UniSTS
NCBI RH Map553.1UniSTS
RH11757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,665,468 - 16,665,634UniSTSGRCh37
Build 36516,718,468 - 16,718,634RGDNCBI36
Celera516,690,230 - 16,690,396RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,637,444 - 16,637,610UniSTS
GeneMap99-GB4 RH Map558.69UniSTS
NCBI RH Map553.1UniSTS
RH123841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,916,921 - 16,917,197UniSTSGRCh37
Build 36516,969,921 - 16,970,197RGDNCBI36
Celera516,942,045 - 16,942,321RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,889,509 - 16,889,785UniSTS
TNG Radiation Hybrid Map59247.0UniSTS
RH119176  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,741,755 - 16,742,086UniSTSGRCh37
Build 36516,794,755 - 16,795,086RGDNCBI36
Celera516,766,817 - 16,767,148RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,714,047 - 16,714,378UniSTS
TNG Radiation Hybrid Map59138.0UniSTS
D5S257  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,845,028 - 16,845,106UniSTSGRCh37
Build 36516,898,028 - 16,898,106RGDNCBI36
Celera516,870,109 - 16,870,191RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,817,623 - 16,817,699UniSTS
SHGC-112200  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,915,212 - 16,915,494UniSTSGRCh37
Build 36516,968,212 - 16,968,494RGDNCBI36
Celera516,940,338 - 16,940,620RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,887,800 - 16,888,082UniSTS
TNG Radiation Hybrid Map59254.0UniSTS
SHGC-142278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,844,474 - 16,844,804UniSTSGRCh37
Build 36516,897,474 - 16,897,804RGDNCBI36
Celera516,869,555 - 16,869,885RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,817,069 - 16,817,399UniSTS
TNG Radiation Hybrid Map59210.0UniSTS
SHGC-173063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,758,405 - 16,758,723UniSTSGRCh37
Build 36516,811,405 - 16,811,723RGDNCBI36
Celera516,783,465 - 16,783,783RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,730,694 - 16,731,012UniSTS
TNG Radiation Hybrid Map59167.0UniSTS
RH12641  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,740,262 - 16,740,382UniSTSGRCh37
Build 36516,793,262 - 16,793,382RGDNCBI36
Celera516,765,324 - 16,765,444RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,712,554 - 16,712,674UniSTS
GeneMap99-GB4 RH Map560.2UniSTS
NCBI RH Map553.1UniSTS
A001Y40  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,665,563 - 16,665,670UniSTSGRCh37
Build 36516,718,563 - 16,718,670RGDNCBI36
Celera516,690,325 - 16,690,432RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,637,539 - 16,637,646UniSTS
GeneMap99-GB4 RH Map563.89UniSTS
NCBI RH Map553.1UniSTS
G19798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,665,563 - 16,665,670UniSTSGRCh37
Build 36516,718,563 - 16,718,670RGDNCBI36
Celera516,690,325 - 16,690,432RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,637,539 - 16,637,646UniSTS
STS-N35986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371289,763,216 - 89,763,365UniSTSGRCh37
GRCh37516,666,144 - 16,666,301UniSTSGRCh37
Build 36516,719,144 - 16,719,301RGDNCBI36
Celera1289,434,910 - 89,435,059UniSTS
Celera516,690,906 - 16,691,063RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,638,120 - 16,638,277UniSTS
GeneMap99-GB4 RH Map560.1UniSTS
NCBI RH Map553.1UniSTS
STS-N23153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,662,031 - 16,662,182UniSTSGRCh37
Build 36516,715,031 - 16,715,182RGDNCBI36
Celera516,686,806 - 16,686,957RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,634,020 - 16,634,171UniSTS
GeneMap99-GB4 RH Map563.94UniSTS
NCBI RH Map553.1UniSTS
RH12416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,740,125 - 16,740,382UniSTSGRCh37
Build 36516,793,125 - 16,793,382RGDNCBI36
Celera516,765,187 - 16,765,444RGD
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,712,417 - 16,712,674UniSTS
GeneMap99-GB4 RH Map560.1UniSTS
NCBI RH Map553.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
G32927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,776,539 - 16,776,673UniSTSGRCh37
Celera516,801,593 - 16,801,727UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,748,825 - 16,748,959UniSTS
SHGC-152276  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,895,867 - 16,895,974UniSTSGRCh37
GRCh37516,895,863 - 16,895,974UniSTSGRCh37
GRCh37516,895,875 - 16,895,974UniSTSGRCh37
Celera516,921,008 - 16,921,107UniSTS
Celera516,920,996 - 16,921,107UniSTS
Celera516,921,000 - 16,921,107UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
HuRef516,868,470 - 16,868,569UniSTS
HuRef516,868,458 - 16,868,569UniSTS
HuRef516,868,462 - 16,868,569UniSTS
TNG Radiation Hybrid Map1222549.0UniSTS
D5S416  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5p15.1-p14.3UniSTS
TNG Radiation Hybrid Map59127.0UniSTS
GeneMap99-GB4 RH Map560.1UniSTS
NCBI RH Map553.1UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High
Medium 786 676 937 74 194 49 2658 100 2192 233 900 1536 38 529 1482 3
Low 1644 1812 773 538 851 405 1697 2070 1534 184 547 66 133 675 1305 1
Below cutoff 2 488 16 10 743 10 1 23 7 1 3 8 2 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_012334 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005248306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005248307 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006714475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011514046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054352663 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054352664 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054352665 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054352666 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB018342 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC010310 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC010607 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC024588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF132021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF132022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF184153 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF234532 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF247457 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI086647 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK024719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK025921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074717 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK125246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295630 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295736 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316138 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC014956 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC032669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC041694 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC050682 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC071965 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC094838 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC108736 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC137168 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC150285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA488271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA504301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC876937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000274203   ⟹   ENSP00000274203
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,661,914 - 16,936,276 (-)Ensembl
RefSeq Acc Id: ENST00000502436   ⟹   ENSP00000426783
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,780,734 - 16,935,938 (-)Ensembl
RefSeq Acc Id: ENST00000505695   ⟹   ENSP00000421170
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,666,562 - 16,742,228 (-)Ensembl
RefSeq Acc Id: ENST00000506343
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,702,999 - 16,741,910 (-)Ensembl
RefSeq Acc Id: ENST00000507288   ⟹   ENSP00000426664
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,814,517 - 16,936,259 (-)Ensembl
RefSeq Acc Id: ENST00000508318
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,710,672 - 16,741,909 (-)Ensembl
RefSeq Acc Id: ENST00000510401
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,704,579 - 16,758,226 (-)Ensembl
RefSeq Acc Id: ENST00000511972
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,710,704 - 16,713,468 (-)Ensembl
RefSeq Acc Id: ENST00000512061
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,703,000 - 16,741,880 (-)Ensembl
RefSeq Acc Id: ENST00000513610   ⟹   ENSP00000421280
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,661,907 - 16,936,288 (-)Ensembl
RefSeq Acc Id: ENST00000513882   ⟹   ENSP00000421309
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,702,977 - 16,916,527 (-)Ensembl
RefSeq Acc Id: ENST00000515803   ⟹   ENSP00000425051
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl516,666,380 - 16,738,414 (-)Ensembl
RefSeq Acc Id: NM_012334   ⟹   NP_036466
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38516,661,907 - 16,936,288 (-)NCBI
GRCh37516,662,016 - 16,936,385 (-)ENTREZGENE
GRCh37516,662,016 - 16,936,385 (-)NCBI
Build 36516,715,016 - 16,989,385 (-)NCBI Archive
HuRef516,634,005 - 16,909,126 (-)ENTREZGENE
CHM1_1516,661,893 - 16,936,226 (-)NCBI
T2T-CHM13v2.0516,601,148 - 16,875,413 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005248306   ⟹   XP_005248363
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38516,661,907 - 16,713,445 (-)NCBI
GRCh37516,662,016 - 16,936,385 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005248307   ⟹   XP_005248364
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38516,661,907 - 16,741,909 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006714475   ⟹   XP_006714538
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38516,661,907 - 16,936,288 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011514046   ⟹   XP_011512348
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38516,661,907 - 16,738,188 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054352663   ⟹   XP_054208638
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0516,601,148 - 16,875,413 (-)NCBI
RefSeq Acc Id: XM_054352664   ⟹   XP_054208639
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0516,601,148 - 16,662,107 (-)NCBI
RefSeq Acc Id: XM_054352665   ⟹   XP_054208640
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0516,601,148 - 16,680,969 (-)NCBI
RefSeq Acc Id: XM_054352666   ⟹   XP_054208641
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0516,601,148 - 16,686,823 (-)NCBI
Protein Sequences
Protein RefSeqs NP_036466 (Get FASTA)   NCBI Sequence Viewer  
  XP_005248363 (Get FASTA)   NCBI Sequence Viewer  
  XP_005248364 (Get FASTA)   NCBI Sequence Viewer  
  XP_006714538 (Get FASTA)   NCBI Sequence Viewer  
  XP_011512348 (Get FASTA)   NCBI Sequence Viewer  
  XP_054208638 (Get FASTA)   NCBI Sequence Viewer  
  XP_054208639 (Get FASTA)   NCBI Sequence Viewer  
  XP_054208640 (Get FASTA)   NCBI Sequence Viewer  
  XP_054208641 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF17363 (Get FASTA)   NCBI Sequence Viewer  
  AAF36524 (Get FASTA)   NCBI Sequence Viewer  
  AAF36525 (Get FASTA)   NCBI Sequence Viewer  
  AAF37875 (Get FASTA)   NCBI Sequence Viewer  
  AAF68025 (Get FASTA)   NCBI Sequence Viewer  
  AAH41694 (Get FASTA)   NCBI Sequence Viewer  
  AAH50682 (Get FASTA)   NCBI Sequence Viewer  
  AAH71965 (Get FASTA)   NCBI Sequence Viewer  
  AAH94838 (Get FASTA)   NCBI Sequence Viewer  
  AAI08737 (Get FASTA)   NCBI Sequence Viewer  
  AAI37169 (Get FASTA)   NCBI Sequence Viewer  
  AAI50286 (Get FASTA)   NCBI Sequence Viewer  
  BAA34519 (Get FASTA)   NCBI Sequence Viewer  
  BAC11158 (Get FASTA)   NCBI Sequence Viewer  
  BAG58507 (Get FASTA)   NCBI Sequence Viewer  
  BAG64502 (Get FASTA)   NCBI Sequence Viewer  
  BAH12170 (Get FASTA)   NCBI Sequence Viewer  
  BAH14509 (Get FASTA)   NCBI Sequence Viewer  
  CAH10611 (Get FASTA)   NCBI Sequence Viewer  
  EAX08016 (Get FASTA)   NCBI Sequence Viewer  
  EAX08017 (Get FASTA)   NCBI Sequence Viewer  
  EAX08018 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000274203.10
  ENSP00000421170
  ENSP00000421170.1
  ENSP00000421280
  ENSP00000421280.1
  ENSP00000421309.1
  ENSP00000425051
  ENSP00000425051.1
  ENSP00000426664.1
  ENSP00000426783.2
GenBank Protein Q9HD67 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_036466   ⟸   NM_012334
- UniProtKB: Q9P111 (UniProtKB/Swiss-Prot),   Q9P110 (UniProtKB/Swiss-Prot),   Q9NYM7 (UniProtKB/Swiss-Prot),   Q8IVX5 (UniProtKB/Swiss-Prot),   O94893 (UniProtKB/Swiss-Prot),   A7E2D1 (UniProtKB/Swiss-Prot),   Q9UHF6 (UniProtKB/Swiss-Prot),   Q9HD67 (UniProtKB/Swiss-Prot),   A0A0A0MQX1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005248364   ⟸   XM_005248307
- Peptide Label: isoform X3
- UniProtKB: B7ZA23 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005248363   ⟸   XM_005248306
- Peptide Label: isoform X2
- UniProtKB: B7ZA23 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006714538   ⟸   XM_006714475
- Peptide Label: isoform X1
- UniProtKB: A0A0A0MQX1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011512348   ⟸   XM_011514046
- Peptide Label: isoform X3
- UniProtKB: B7ZA23 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000426783   ⟸   ENST00000502436
RefSeq Acc Id: ENSP00000421170   ⟸   ENST00000505695
RefSeq Acc Id: ENSP00000426664   ⟸   ENST00000507288
RefSeq Acc Id: ENSP00000274203   ⟸   ENST00000274203
RefSeq Acc Id: ENSP00000421309   ⟸   ENST00000513882
RefSeq Acc Id: ENSP00000421280   ⟸   ENST00000513610
RefSeq Acc Id: ENSP00000425051   ⟸   ENST00000515803
RefSeq Acc Id: XP_054208638   ⟸   XM_054352663
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054208641   ⟸   XM_054352666
- Peptide Label: isoform X3
- UniProtKB: B7Z3D4 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054208640   ⟸   XM_054352665
- Peptide Label: isoform X3
- UniProtKB: B7Z3D4 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054208639   ⟸   XM_054352664
- Peptide Label: isoform X2
Protein Domains
FERM   IQ   Myosin motor   MyTH4   PH   Ras-associating

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9HD67-F1-model_v2 AlphaFold Q9HD67 1-2058 view protein structure

Promoters
RGD ID:6869286
Promoter ID:EPDNEW_H7807
Type:initiation region
Name:MYO10_1
Description:myosin X
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H7808  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38516,936,265 - 16,936,325EPDNEW
RGD ID:6869288
Promoter ID:EPDNEW_H7808
Type:initiation region
Name:MYO10_2
Description:myosin X
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H7807  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38516,936,374 - 16,936,434EPDNEW
RGD ID:6803384
Promoter ID:HG_KWN:49829
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid,   NB4
Transcripts:NM_012334,   UC003JFU.2,   UC003JFV.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36516,989,119 - 16,989,619 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7593 AgrOrtholog
COSMIC MYO10 COSMIC
Ensembl Genes ENSG00000145555 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000274203.13 UniProtKB/TrEMBL
  ENST00000502436.5 UniProtKB/TrEMBL
  ENST00000505695 ENTREZGENE
  ENST00000505695.5 UniProtKB/TrEMBL
  ENST00000507288.1 UniProtKB/Swiss-Prot
  ENST00000513610 ENTREZGENE
  ENST00000513610.6 UniProtKB/Swiss-Prot
  ENST00000513882.5 UniProtKB/TrEMBL
  ENST00000515803 ENTREZGENE
  ENST00000515803.5 UniProtKB/TrEMBL
Gene3D-CATH 1.10.10.820 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.20.5.170 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.20.5.190 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.20.58.530 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.20.80.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.25.40.530 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.30.29.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.850.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  6.20.240.20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Myosin VI head, motor domain, U50 subdomain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000145555 GTEx
HGNC ID HGNC:7593 ENTREZGENE
Human Proteome Map MYO10 Human Proteome Map
InterPro Band_41_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM/acyl-CoA-bd_prot_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_central UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  IQ_motif_EF-hand-BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Kinesin_motor_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MYO10_CC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Myosin_head_motor_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MyoX_FERM_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MyoX_N_SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MYSc_Myo10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MyTH4_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MyTH4_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RA_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:4651 UniProtKB/Swiss-Prot
NCBI Gene 4651 ENTREZGENE
OMIM 601481 OMIM
PANTHER AGAP003327-PA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UNCONVENTIONAL MYOSIN-X UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam FERM_M UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MYO10_CC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Myosin_head UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MyTH4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PF00169 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PF00612 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PF00788 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3_19 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31394 PharmGKB
PRINTS MYOSINHEAVY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE FERM_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MYOSIN_MOTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MYTH4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH_DOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PS50096 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PS50200 UniProtKB/TrEMBL
SMART B41 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MYSc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MyTH4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00015 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00233 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP PH domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF47031 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0A0MQX1 ENTREZGENE, UniProtKB/TrEMBL
  A7E2D1 ENTREZGENE
  B7Z3D4 ENTREZGENE, UniProtKB/TrEMBL
  B7ZA23 ENTREZGENE, UniProtKB/TrEMBL
  D6RGD1_HUMAN UniProtKB/TrEMBL
  E9PCN3_HUMAN UniProtKB/TrEMBL
  E9PEW5_HUMAN UniProtKB/TrEMBL
  MYO10_HUMAN UniProtKB/Swiss-Prot
  O94893 ENTREZGENE
  Q6IPD7_HUMAN UniProtKB/TrEMBL
  Q8IVX5 ENTREZGENE
  Q9HD67 ENTREZGENE
  Q9NYM7 ENTREZGENE
  Q9P110 ENTREZGENE
  Q9P111 ENTREZGENE
  Q9UHF6 ENTREZGENE
UniProt Secondary A7E2D1 UniProtKB/Swiss-Prot
  O94893 UniProtKB/Swiss-Prot
  Q8IVX5 UniProtKB/Swiss-Prot
  Q9NYM7 UniProtKB/Swiss-Prot
  Q9P110 UniProtKB/Swiss-Prot
  Q9P111 UniProtKB/Swiss-Prot
  Q9UHF6 UniProtKB/Swiss-Prot