Myo7a (myosin VIIA) - Rat Genome Database

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Advanced Search (OLGA)
Gene: Myo7a (myosin VIIA) Mus musculus
Analyze
Symbol: Myo7a
Name: myosin VIIA
RGD ID: 732207
MGI Page MGI
Description: Enables protein domain specific binding activity. Involved in protein localization. Acts upstream of or within several processes, including inner ear development; phagolysosome assembly; and pigment granule transport. Located in several cellular components, including melanosome; photoreceptor connecting cilium; and stereocilium base. Is active in stereocilium. Is expressed in central nervous system; liver; sensory organ; and small intestine epithelium. Used to study Usher syndrome type 1 and autosomal recessive nonsyndromic deafness 2. Human ortholog(s) of this gene implicated in Leber congenital amaurosis; Usher syndrome (multiple); auditory system disease (multiple); and congenital nystagmus. Orthologous to human MYO7A (myosin VIIA).
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: Hdb; motor protein; Myo; Myo7; myosin-VIIa; nmf37; nmf371; p; polka; sh-1; sh1; shaker 1; unconventional myosin-VIIa; USH1; USH1B
RGD Orthologs
Human
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCm39 - Mouse Genome Assembly GRCm39
Position:
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39797,700,261 - 97,768,730 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl797,700,267 - 97,768,731 (-)EnsemblGRCm39 Ensembl
GRCm38798,051,054 - 98,119,522 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl798,051,060 - 98,119,524 (-)EnsemblGRCm38mm10GRCm38
MGSCv377105,199,570 - 105,268,003 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36797,926,593 - 97,992,926 (-)NCBIMGSCv36mm8
Celera798,371,628 - 98,440,211 (-)NCBICelera
Cytogenetic Map7E1NCBI
cM Map753.57NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Mammalian Phenotype
abnormal auditory summating potential  (IAGP)
abnormal behavior  (IEA)
abnormal cochlear basement membrane morphology  (IAGP)
abnormal cochlear hair cell inter-stereocilial links morphology  (IAGP)
abnormal cochlear hair cell morphology  (IEA)
abnormal cochlear hair cell stereociliary bundle morphology  (IAGP)
abnormal cochlear nerve compound action potential  (IAGP)
abnormal cochlear OHC efferent innervation pattern  (IAGP)
abnormal cochlear outer hair cell morphology  (IAGP)
abnormal ear physiology  (IAGP)
abnormal electroretinogram waveform feature  (IAGP)
abnormal eye electrophysiology  (IAGP)
abnormal gait  (IEA)
abnormal hair cell morphology  (IAGP)
abnormal head movements  (IEA)
abnormal hearing physiology  (IAGP)
abnormal inner ear vestibule morphology  (IAGP)
abnormal inner hair cell stereociliary bundle morphology  (IAGP)
abnormal organ of Corti morphology  (IAGP)
abnormal orientation of cochlear hair cell stereociliary bundles  (IAGP)
abnormal orientation of inner hair cell stereociliary bundles  (IAGP)
abnormal orientation of outer hair cell stereociliary bundles  (IAGP)
abnormal outer hair cell stereociliary bundle morphology  (IAGP)
abnormal parental behavior  (IEA)
abnormal retina pigment epithelium morphology  (IAGP)
abnormal retina rod cell morphology  (IAGP)
abnormal vestibular hair cell stereociliary bundle morphology  (IAGP)
absent cochlear hair bundle ankle links  (IAGP)
absent cochlear microphonics  (IAGP)
absent distortion product otoacoustic emissions  (IAGP)
absent linear vestibular evoked potential  (IAGP)
absent pinna reflex  (IAGP)
absent startle reflex  (IAGP)
circling  (IAGP)
cochlear degeneration  (IAGP)
cochlear ganglion degeneration  (IAGP)
cochlear hair cell degeneration  (IAGP)
cochlear outer hair cell degeneration  (IAGP)
deafness  (IAGP)
decreased a-wave amplitude  (IAGP)
decreased b-wave amplitude  (IAGP)
decreased body size  (IEA)
decreased cochlear outer hair cell number  (IAGP)
decreased inner hair cell stereocilia number  (IAGP)
decreased outer hair cell stereocilia number  (IAGP)
decreased startle reflex  (IAGP)
decreased vestibular hair cell stereocilia number  (IAGP)
fused inner hair cell stereocilia  (IAGP)
gliosis  (IEA)
head bobbing  (IAGP)
head shaking  (IEA)
head tilt  (IAGP)
head tossing  (IAGP)
hyperactivity  (IAGP)
impaired balance  (IEA)
impaired hearing  (IAGP)
impaired pupillary reflex  (IAGP)
impaired righting response  (IEA)
impaired swimming  (IAGP)
increased anxiety-related response  (IEA)
increased blood urea nitrogen level  (IEA)
increased circulating sodium level  (IEA)
increased cochlear nerve compound action potential  (IAGP)
increased fluid intake  (IEA)
increased food intake  (IEA)
increased or absent threshold for auditory brainstem response  (IAGP)
increased susceptibility to age-related hearing loss  (IAGP)
jerky movement  (IEA)
male infertility  (IEA)
persistence of hyaloid vascular system  (IEA)
reduced male fertility  (IEA)
retina rod cell degeneration  (IAGP)
retropulsion  (IEA)
sensorineural hearing loss  (IAGP)
short cochlear hair cell stereocilia  (IAGP)
short cochlear outer hair cells  (IAGP)
slow postnatal weight gain  (IEA)
spinning  (IAGP)
stereotypic behavior  (IEA)
straub tail  (IEA)
stria vascularis degeneration  (IAGP)
thin stria vascularis  (IAGP)
trunk curl  (IAGP)
vestibular ganglion hypoplasia  (IAGP)
vestibular saccular macula degeneration  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. Point mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1. Aponte JL, etal., Proc Natl Acad Sci U S A 2001 Jan 16;98(2):641-5.
2. Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7A. Ben-Salem S, etal., Mol Biol Rep. 2014 Jan;41(1):193-200. doi: 10.1007/s11033-013-2851-5. Epub 2013 Nov 6.
3. Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle. Boeda B, etal., EMBO J 2002 Dec 16;21(24):6689-99.
4. Myosin7a deficiency results in reduced retinal activity which is improved by gene therapy. Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
5. Mechanotransduction by hair cells: models, molecules, and mechanisms. Gillespie PG and Muller U, Cell. 2009 Oct 2;139(1):33-44. doi: 10.1016/j.cell.2009.09.010.
6. Sensing sound: molecules that orchestrate mechanotransduction by hair cells. Kazmierczak P and Muller U, Trends Neurosci. 2012 Apr;35(4):220-9. doi: 10.1016/j.tins.2011.10.007. Epub 2011 Dec 15.
7. Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A. Kumar A, etal., Mol Vis. 2004 Nov 24;10:910-6.
8. Mutation analysis of the mouse myosin VIIA deafness gene. Mburu P, etal., Genes Funct. 1997 Jun;1(3):191-203.
9. MGDs mouse GO annotations MGD data from the GO Consortium
10. MGD IEA MGD IEA
11. Mutations in myosin VIIA (MYO7A) and usherin (USH2A) in Spanish patients with Usher syndrome types I and II, respectively. Najera C, etal., Hum Mutat. 2002 Jul;20(1):76-7.
12. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
13. Mouse MP Annotation Import Pipeline RGD automated import pipeline
14. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
15. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
16. Identification of a rat model for usher syndrome type 1B by N-ethyl-N-nitrosourea mutagenesis-driven forward genetics. Smits BM, etal., Genetics. 2005 Aug;170(4):1887-96. Epub 2005 Jun 18.
17. Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis. Wang X, etal., Hum Mutat. 2011 Dec;32(12):1450-9. doi: 10.1002/humu.21587. Epub 2011 Sep 23.
18. Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients. Weston MD, etal., Am J Hum Genet. 1996 Nov;59(5):1074-83.
19. Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait. Wright AF, etal., Nat Rev Genet. 2010 Apr;11(4):273-84. doi: 10.1038/nrg2717.
20. Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes. Zheng QY, etal., Hum Mol Genet. 2012 Jun 1;21(11):2588-98. doi: 10.1093/hmg/dds084. Epub 2012 Feb 29.
Additional References at PubMed
PMID:621381   PMID:863237   PMID:1063212   PMID:1349573   PMID:1952626   PMID:2300582   PMID:2813427   PMID:5795329   PMID:6627025   PMID:7568224   PMID:7849737   PMID:7870171  
PMID:7870172   PMID:8111122   PMID:8307326   PMID:8307327   PMID:8422502   PMID:8622919   PMID:8661014   PMID:8690736   PMID:8842737   PMID:8884266   PMID:9027465   PMID:9171832  
PMID:9186010   PMID:9278160   PMID:9382088   PMID:9435277   PMID:9620764   PMID:9735355   PMID:9927480   PMID:10079221   PMID:10224267   PMID:10320095   PMID:10349636   PMID:10414956  
PMID:10574757   PMID:10722873   PMID:10742111   PMID:11023859   PMID:11042159   PMID:11076861   PMID:11162241   PMID:11212352   PMID:11217851   PMID:11222540   PMID:11374883   PMID:11425898  
PMID:11468276   PMID:11506947   PMID:11753415   PMID:11839794   PMID:11964381   PMID:11973280   PMID:12091321   PMID:12121736   PMID:12221080   PMID:12441305   PMID:12466851   PMID:12692478  
PMID:12717441   PMID:12743369   PMID:12768423   PMID:12833159   PMID:12966030   PMID:13336002   PMID:13853422   PMID:14198707   PMID:14487977   PMID:14534255   PMID:14578428   PMID:14609561  
PMID:14648237   PMID:14978221   PMID:15078071   PMID:15254021   PMID:15316067   PMID:15329890   PMID:15389316   PMID:15572405   PMID:15590698   PMID:15590703   PMID:15653467   PMID:15654330  
PMID:15657400   PMID:15702992   PMID:15782199   PMID:15843406   PMID:15846349   PMID:15905332   PMID:15927964   PMID:15976448   PMID:16141072   PMID:16141073   PMID:16141228   PMID:16207888  
PMID:16219682   PMID:16235133   PMID:16410827   PMID:16481439   PMID:16538679   PMID:16545802   PMID:16602821   PMID:16691564   PMID:16790479   PMID:16914494   PMID:17050716   PMID:17117437  
PMID:17247190   PMID:17268537   PMID:17329413   PMID:17331196   PMID:17352418   PMID:17376975   PMID:17567809   PMID:17604700   PMID:17615572   PMID:17663432   PMID:17666436   PMID:17823936  
PMID:17825816   PMID:18039969   PMID:18160714   PMID:18339676   PMID:18463160   PMID:18652815   PMID:18678597   PMID:18715234   PMID:18796539   PMID:19317802   PMID:19324852   PMID:19339464  
PMID:19363478   PMID:19389353   PMID:19463703   PMID:19619645   PMID:19706712   PMID:19743445   PMID:19774077   PMID:19854167   PMID:19936227   PMID:20016096   PMID:20016102   PMID:20043895  
PMID:20058045   PMID:20111592   PMID:20152827   PMID:20186345   PMID:20215345   PMID:20332152   PMID:20346939   PMID:20451170   PMID:20503364   PMID:20512592   PMID:20554841   PMID:20639393  
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PMID:38682291  


Genomics

Comparative Map Data
Myo7a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39797,700,261 - 97,768,730 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl797,700,267 - 97,768,731 (-)EnsemblGRCm39 Ensembl
GRCm38798,051,054 - 98,119,522 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl798,051,060 - 98,119,524 (-)EnsemblGRCm38mm10GRCm38
MGSCv377105,199,570 - 105,268,003 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36797,926,593 - 97,992,926 (-)NCBIMGSCv36mm8
Celera798,371,628 - 98,440,211 (-)NCBICelera
Cytogenetic Map7E1NCBI
cM Map753.57NCBI
MYO7A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381177,128,246 - 77,215,241 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1177,128,246 - 77,215,241 (+)EnsemblGRCh38hg38GRCh38
GRCh371176,839,292 - 76,926,286 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361176,516,964 - 76,603,932 (+)NCBINCBI36Build 36hg18NCBI36
Build 341176,516,957 - 76,603,931NCBI
Celera1174,146,794 - 74,233,913 (+)NCBICelera
Cytogenetic Map11q13.5NCBI
HuRef1173,136,682 - 73,224,253 (+)NCBIHuRef
CHM1_11176,722,561 - 76,809,502 (+)NCBICHM1_1
T2T-CHM13v2.01177,058,823 - 77,147,851 (+)NCBIT2T-CHM13v2.0
Myo7a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81161,755,110 - 161,825,397 (-)NCBIGRCr8
mRatBN7.21152,342,611 - 152,414,171 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1152,344,448 - 152,414,157 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1160,331,375 - 160,401,213 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01167,511,561 - 167,581,393 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01160,385,070 - 160,454,912 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01163,001,313 - 163,071,545 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1163,001,875 - 163,071,508 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01169,206,150 - 169,276,706 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41155,292,620 - 155,362,698 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11155,371,025 - 155,441,104 (-)NCBI
Celera1150,435,342 - 150,505,024 (-)NCBICelera
Cytogenetic Map1q32NCBI
Myo7a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541414,576,356 - 14,647,500 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541414,576,356 - 14,647,500 (-)NCBIChiLan1.0ChiLan1.0
MYO7A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2978,045,811 - 78,134,539 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11179,093,985 - 79,182,922 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01172,187,024 - 72,265,931 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11175,834,409 - 75,908,297 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1175,834,185 - 75,907,752 (+)Ensemblpanpan1.1panPan2
MYO7A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12121,539,735 - 21,624,063 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2121,539,785 - 21,624,279 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2121,371,283 - 21,451,548 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02121,739,388 - 21,823,670 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2121,739,387 - 21,823,979 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12121,514,983 - 21,599,193 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02121,731,135 - 21,815,380 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02121,654,692 - 21,739,052 (-)NCBIUU_Cfam_GSD_1.0
Myo7a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494764,150,067 - 64,224,924 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364985,751,779 - 5,824,378 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364985,758,572 - 5,824,526 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MYO7A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl911,249,075 - 11,666,296 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1911,251,187 - 11,337,618 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2912,345,556 - 12,430,950 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MYO7A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1168,334,781 - 68,423,215 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl168,350,598 - 68,425,625 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604357,352,101 - 57,439,357 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Myo7a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624863205,478 - 283,839 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_004624863205,468 - 283,840 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in Myo7a
2538 total Variants
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2171
Count of miRNA genes:637
Interacting mature miRNAs:811
Transcripts:ENSMUST00000084979, ENSMUST00000107122, ENSMUST00000107127, ENSMUST00000107128, ENSMUST00000124787, ENSMUST00000131632, ENSMUST00000138627, ENSMUST00000149079, ENSMUST00000152975, ENSMUST00000153657, ENSMUST00000155637, ENSMUST00000156992
Prediction methods: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.


QTLs in Region (GRCm39)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
25314307Mlh1fc2_mMLH1 foci count 2 (mouse)76502999133501729Mouse
27226781Tibl3_mtibia length 3, 5 week (mouse)774849748122199223Mouse
25314305Vmm6_mvariable multisystem mineralization 6, eye (mouse)761849748102749207Mouse
27226778Femd11_mfemur midshaft diameter 11, 16 week (mouse)756949748134001729Mouse
1301781Capsq3_mcapsaicin sensitivity related QTL 3 (mouse)Not determined787143137119485380Mouse
1301784Ses2_msalmonella enteritidis susceptibility 2 (mouse)Not determined767290094101290240Mouse
14746989Manh62_mmandible shape 62 (mouse)775742528109742528Mouse
27226769Tibl12_mtibia length 12, 10 week (mouse)787249208126499172Mouse
10043926Bw1n_mbody weight 1 in NSY (mouse)Not determined745161966118693530Mouse
27226765Tibl18_mtibia length 18, 16 week (mouse)781849748126499172Mouse
1301383Aem2_manti-erythrocyte autoantibody modifier 2 (mouse)Not determined76413542498135653Mouse
27226763Feml20_mfemur length 20, 16 week (mouse)785049208124199223Mouse
4142500Morq1_mmodifier of Rs1 QTL 1 (mouse)Not determined80551681114551791Mouse
27095937Ulnl7_mulna length 7, 10 week (mouse)76644974898349207Mouse
1301647Elpt_melevated leptin (mouse)Not determined786500186120500329Mouse
1300620Pgia21_mproteoglycan induced arthritis 21 (mouse)Not determined767290094101290240Mouse
13208555Lgth10_mbody length 10 (mouse)751649748125599172Mouse
26884408Bzwq13_mbi-zygomatic width QTL 13, 16 week (mouse)761749748121399223Mouse
1301937Skull10_mskull morphology 10 (mouse)Not determined791482996125483156Mouse
1300528Ssial3_msusceptibility to sialadenitis 3 (mouse)Not determined793391848127392041Mouse
1300791Abbp3_mA/J and C57BL/6 blood pressure 3 (mouse)Not determined739673887103510010Mouse
1301566Adip3_madiposity 3 (mouse)Not determined775394215109394346Mouse
26884404Huml1_mhumerus length 1, 5 week (mouse)730199425108999207Mouse
1301155Bpq7_mblood pressure QTL 7 (mouse)Not determined770143137104143379Mouse
26884398Humsd6_mhumerus midshaft diameter 6, 16 week (mouse)778649748136901729Mouse
1301158Eae4_msusceptibility to experimental allergic encephalomyelitis 4 (mouse)Not determined719147398141919804Mouse
27226792Feml7_mfemur length 7, 5 week (mouse)78614920898949207Mouse
10412199Sst2_msusceptibility to tuberculosis 2 (mouse)Not determined718728794119485380Mouse
27226790Feml15_mfemur length 15, 10 week (mouse)787249208126499172Mouse
1300654Bomd1_mbone mineral density 1 (mouse)Not determined768365595102365702Mouse
1302062Stheal6_msoft tissue heal 6 (mouse)Not determined787043932121044066Mouse
26884440Sklq4_mskull length QTL 4, 5 week (mouse)765249748126499172Mouse
27095903Scvln10_msacral vertebrae length 2, 10 week (mouse)781449748126499172Mouse
27226715Metcl3_mmetatarsal-calcaneal length 3, 5 week (mouse)767849748119499223Mouse
26884444Sklq8_mskull length QTL 8, 10 week (mouse)767849748124199223Mouse
25823170Hrsq7_mhost response to SARS QTL 7, log titer (mouse)754819589116822815Mouse
1301082Bbaa16_mB.burgdorferi-associated arthritis 16 (mouse)Not determined736280015116416877Mouse
10412110Cctq1_mcentral corneal thickness QTL 1 (mouse)Not determined780551681114551791Mouse
12792978Fbmd3_mfemoral bone mineral density 3, females only (mouse)77050288142367832Mouse
1301826Pgia3_mproteoglycan induced arthritis 3 (mouse)Not determined767290094101290240Mouse
1301188Heal6_mwound healing/regeneration 6 (mouse)Not determined787043932121044066Mouse
26884418Bzwq7_mbi-zygomatic width QTL 7, 10 week (mouse)767849748105449207Mouse
10043973Obq29_mobesity QTL 29 (mouse)Not determined772263372106263372Mouse
27226751Femd5_mfemur midshaft diameter 5, 10 week (mouse)753249748143153737Mouse
27095933Ulnl3_mulna length 3, 5 week (mouse)773149748143153737Mouse
27095929Pglq8_mpelvic girdle length QTL 8, 10 week (mouse)787849208108099207Mouse
27226745Metcl9_mmetatarsal-calcaneal length 9, 10 week (mouse)774849748122199223Mouse
27095930Ulnl10_mulna length 10, 16 week (mouse)780849748126699172Mouse
27095923Pglq3_mpelvic girdle length QTL 3, 5 week (mouse)781249748124199223Mouse
27095916Scvln15_msacral vertebrae length 2, 16 week (mouse)761749748123699223Mouse
13464255Ifvrq2_minfluenza virus resistance QTL 2 (mouse)792500698106455693Mouse
1357664Nba3_mNew Zealand Black autoimmunity 3 (mouse)Not determined791482996125483156Mouse
11553865Stmm1c_mskin tumor modifier of MSM 1c (mouse)76578898699788986Mouse
26884451Sklq14_mskull length QTL 14, 16 week (mouse)767849748124999172Mouse
11553866Stmm1d_mskin tumor modifier of MSM 1d (mouse)76578898699788986Mouse
27095910Pglq13_mpelvic girdle length QTL 13, 16 week (mouse)773049748125699172Mouse
13463473Hbbcq4_mhemoglobin concentration QTL 4 (mouse)787043932121044066Mouse
11553869Stmm2b_mskin tumor modifier of MSM 2a (mouse)773725965107725965Mouse
27095907Scvln4_msacral vertebrae length 2, 5 week (mouse)769949748120499223Mouse
1301997Cia7_mcollagen induced arthritis QTL 7 (mouse)Not determined785365595112533819Mouse

Markers in Region
Myo7a  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map7E2UniSTS
cM Map753.57UniSTS
D7Smh12  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38798,082,901 - 98,083,125UniSTSGRCm38
MGSCv377105,231,411 - 105,231,635UniSTSGRCm37
Cytogenetic Map7E2UniSTS
cM Map748.0UniSTS


Expression

RNA-SEQ Expression


Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001256081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001256082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001256083 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_008663 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006507427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006507428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006507429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011241688 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011241689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011241690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011241691 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC115022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC157792 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF384559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK052607 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK177446 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK192042 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK200719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK201784 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK202530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY821853 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY821854 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH466531 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U81453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENSMUST00000084979   ⟹   ENSMUSP00000082046
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,700,608 - 97,758,455 (-)Ensembl
GRCm38.p6 Ensembl798,051,401 - 98,109,248 (-)Ensembl
Ensembl Acc Id: ENSMUST00000107122   ⟹   ENSMUSP00000102739
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,700,608 - 97,758,455 (-)Ensembl
GRCm38.p6 Ensembl798,051,401 - 98,109,248 (-)Ensembl
Ensembl Acc Id: ENSMUST00000107127   ⟹   ENSMUSP00000102744
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,700,832 - 97,768,710 (-)Ensembl
GRCm38.p6 Ensembl798,051,625 - 98,119,503 (-)Ensembl
Ensembl Acc Id: ENSMUST00000107128   ⟹   ENSMUSP00000102745
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,700,267 - 97,768,731 (-)Ensembl
GRCm38.p6 Ensembl798,051,060 - 98,119,524 (-)Ensembl
Ensembl Acc Id: ENSMUST00000124787
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,711,850 - 97,714,409 (-)Ensembl
GRCm38.p6 Ensembl798,062,643 - 98,065,202 (-)Ensembl
Ensembl Acc Id: ENSMUST00000131632
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,757,939 - 97,768,699 (-)Ensembl
GRCm38.p6 Ensembl798,108,732 - 98,119,492 (-)Ensembl
Ensembl Acc Id: ENSMUST00000138627   ⟹   ENSMUSP00000114944
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,747,463 - 97,768,700 (-)Ensembl
GRCm38.p6 Ensembl798,098,256 - 98,119,493 (-)Ensembl
Ensembl Acc Id: ENSMUST00000149079
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,747,454 - 97,752,564 (-)Ensembl
GRCm38.p6 Ensembl798,098,247 - 98,103,357 (-)Ensembl
Ensembl Acc Id: ENSMUST00000152975
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,730,377 - 97,733,926 (-)Ensembl
GRCm38.p6 Ensembl798,081,170 - 98,084,719 (-)Ensembl
Ensembl Acc Id: ENSMUST00000153657
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,746,839 - 97,761,869 (-)Ensembl
GRCm38.p6 Ensembl798,097,632 - 98,112,662 (-)Ensembl
Ensembl Acc Id: ENSMUST00000155637
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,747,414 - 97,752,568 (-)Ensembl
GRCm38.p6 Ensembl798,098,207 - 98,103,361 (-)Ensembl
Ensembl Acc Id: ENSMUST00000156992   ⟹   ENSMUSP00000146114
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,700,270 - 97,718,584 (-)Ensembl
GRCm38.p6 Ensembl798,051,063 - 98,069,377 (-)Ensembl
Ensembl Acc Id: ENSMUST00000205746   ⟹   ENSMUSP00000146165
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,700,697 - 97,756,354 (-)Ensembl
GRCm38.p6 Ensembl798,051,490 - 98,107,147 (-)Ensembl
Ensembl Acc Id: ENSMUST00000238309   ⟹   ENSMUSP00000158850
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,756,199 - 97,760,770 (-)Ensembl
GRCm38.p6 Ensembl798,106,992 - 98,111,563 (-)Ensembl
Ensembl Acc Id: ENSMUST00000238540   ⟹   ENSMUSP00000158620
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl797,734,591 - 97,740,335 (-)Ensembl
GRCm38.p6 Ensembl798,085,384 - 98,091,128 (-)Ensembl
RefSeq Acc Id: NM_001256081   ⟹   NP_001243010
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39797,700,261 - 97,768,700 (-)NCBI
GRCm38798,051,054 - 98,119,493 (-)NCBI
Celera798,371,622 - 98,440,211 (-)ENTREZGENE
cM Map7 ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001256082   ⟹   NP_001243011
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39797,700,261 - 97,758,455 (-)NCBI
GRCm38798,051,054 - 98,109,248 (-)NCBI
Celera798,371,622 - 98,440,211 (-)ENTREZGENE
cM Map7 ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001256083   ⟹   NP_001243012
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39797,700,261 - 97,758,455 (-)NCBI
GRCm38798,051,054 - 98,109,248 (-)NCBI
Celera798,371,622 - 98,440,211 (-)ENTREZGENE
cM Map7 ENTREZGENE
Sequence:
RefSeq Acc Id: NM_008663   ⟹   NP_032689
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39797,700,267 - 97,768,700 (-)NCBI
GRCm38798,051,060 - 98,119,493 (-)NCBI
MGSCv377105,199,570 - 105,268,003 (-)RGD
Celera798,371,622 - 98,440,211 (-)ENTREZGENE
cM Map7 ENTREZGENE
Sequence:
RefSeq Acc Id: XM_006507427   ⟹   XP_006507490
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39797,700,262 - 97,768,730 (-)NCBI
GRCm38798,051,054 - 98,119,522 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006507428   ⟹   XP_006507491
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39797,700,262 - 97,752,571 (-)NCBI
GRCm38798,051,054 - 98,103,364 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006507429   ⟹   XP_006507492
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39797,700,262 - 97,752,581 (-)NCBI
GRCm38798,051,054 - 98,103,374 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011241688   ⟹   XP_011239990
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39797,700,262 - 97,761,490 (-)NCBI
GRCm38798,051,054 - 98,112,287 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011241689   ⟹   XP_011239991
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39797,700,262 - 97,761,389 (-)NCBI
GRCm38798,051,054 - 98,112,182 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011241690   ⟹   XP_011239992
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39797,700,262 - 97,761,389 (-)NCBI
GRCm38798,051,054 - 98,112,182 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011241691   ⟹   XP_011239993
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39797,700,262 - 97,761,389 (-)NCBI
GRCm38798,051,054 - 98,112,182 (-)NCBI
Sequence:
RefSeq Acc Id: NP_032689   ⟸   NM_008663
- Peptide Label: isoform 2
- UniProtKB: A0A0U1RPX7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001243010   ⟸   NM_001256081
- Peptide Label: isoform 1
- UniProtKB: E9QLP7 (UniProtKB/Swiss-Prot),   Q5MJ57 (UniProtKB/Swiss-Prot),   P97479 (UniProtKB/Swiss-Prot),   A0A0U1RPX7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001243012   ⟸   NM_001256083
- Peptide Label: isoform 4
- UniProtKB: A0A0R4J113 (UniProtKB/TrEMBL),   A0A0U1RPX7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001243011   ⟸   NM_001256082
- Peptide Label: isoform 3
- UniProtKB: Q5MJ56 (UniProtKB/TrEMBL),   A0A0U1RPX7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006507490   ⟸   XM_006507427
- Peptide Label: isoform X5
- UniProtKB: A0A0U1RPX7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006507492   ⟸   XM_006507429
- Peptide Label: isoform X7
- UniProtKB: A0A0U1RPX7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006507491   ⟸   XM_006507428
- Peptide Label: isoform X6
- UniProtKB: A0A0U1RPX7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011239990   ⟸   XM_011241688
- Peptide Label: isoform X1
- UniProtKB: A0A0U1RPX7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011239993   ⟸   XM_011241691
- Peptide Label: isoform X4
- UniProtKB: A0A0R4J113 (UniProtKB/TrEMBL),   A0A0U1RPX7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011239991   ⟸   XM_011241689
- Peptide Label: isoform X2
- UniProtKB: A0A0U1RPX7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011239992   ⟸   XM_011241690
- Peptide Label: isoform X3
- UniProtKB: Q5MJ56 (UniProtKB/TrEMBL),   A0A0U1RPX7 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSMUSP00000114944   ⟸   ENSMUST00000138627
Ensembl Acc Id: ENSMUSP00000082046   ⟸   ENSMUST00000084979
Ensembl Acc Id: ENSMUSP00000146165   ⟸   ENSMUST00000205746
Ensembl Acc Id: ENSMUSP00000102739   ⟸   ENSMUST00000107122
Ensembl Acc Id: ENSMUSP00000102744   ⟸   ENSMUST00000107127
Ensembl Acc Id: ENSMUSP00000102745   ⟸   ENSMUST00000107128
Ensembl Acc Id: ENSMUSP00000158850   ⟸   ENSMUST00000238309
Ensembl Acc Id: ENSMUSP00000158620   ⟸   ENSMUST00000238540
Ensembl Acc Id: ENSMUSP00000146114   ⟸   ENSMUST00000156992
Protein Domains
FERM   IQ   Myosin motor   MyTH4   SH3

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P97479-F1-model_v2 AlphaFold P97479 1-2215 view protein structure

Promoters
RGD ID:8664831
Promoter ID:EPDNEW_M10447
Type:multiple initiation site
Name:Myo7a_1
Description:Mus musculus myosin VIIA , transcript variant 4, mRNA.
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm38798,119,493 - 98,119,553EPDNEW
RGD ID:6841609
Promoter ID:MM_KWN:51617
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Spleen
Transcripts:OTTMUST00000042828
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv367105,214,161 - 105,214,661 (-)MPROMDB
RGD ID:6841608
Promoter ID:MM_KWN:51620
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:BoneMarrow_0Hour,   BoneMarrow_2Hour,   BoneMarrow_4Hour,   Lung
Transcripts:OTTMUST00000042827
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv367105,233,231 - 105,234,017 (-)MPROMDB
RGD ID:6841607
Promoter ID:MM_KWN:51622
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Kidney
Transcripts:ENSMUST00000033031
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv367105,256,741 - 105,257,241 (-)MPROMDB
RGD ID:6841605
Promoter ID:MM_KWN:51625
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Kidney,   MEF_B4,   MEF_B6
Transcripts:ENSMUST00000107126,   ENSMUST00000107127,   ENSMUST00000107128,   OTTMUST00000042822,   OTTMUST00000042823
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv367105,267,631 - 105,268,131 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene MGI:104510 AgrOrtholog
Ensembl Genes ENSMUSG00000030761 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENSMUST00000084979 ENTREZGENE
  ENSMUST00000084979.11 UniProtKB/TrEMBL
  ENSMUST00000107122 ENTREZGENE
  ENSMUST00000107122.8 UniProtKB/TrEMBL
  ENSMUST00000107127 ENTREZGENE
  ENSMUST00000107127.8 UniProtKB/Swiss-Prot
  ENSMUST00000107128 ENTREZGENE
  ENSMUST00000107128.8 UniProtKB/Swiss-Prot
  ENSMUST00000138627.2 UniProtKB/TrEMBL
  ENSMUST00000156992.8 UniProtKB/TrEMBL
  ENSMUST00000205746 ENTREZGENE
  ENSMUST00000205746.2 UniProtKB/TrEMBL
  ENSMUST00000238309.2 UniProtKB/TrEMBL
  ENSMUST00000238540.2 UniProtKB/TrEMBL
Gene3D-CATH 1.10.10.820 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
  SH3 Domains UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
InterPro Actin_motor_Myosin UniProtKB/TrEMBL
  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
  Myosin_head_motor_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MyoVII_FERM_C1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MyoVII_FERM_C2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MYSc_Myo7 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
  SH3-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ubiquitin-like_domsf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Unconventional_Myosin_ATPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report mmu:17921 UniProtKB/Swiss-Prot
MGD MGI:104510 ENTREZGENE
NCBI Gene 17921 ENTREZGENE
PANTHER AGAP003327-PA UniProtKB/TrEMBL
  MYOSIN VII, XV UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MYOSIN VIIA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PLECKSTRIN HOMOLOGY DOMAIN-CONTAINING FAMILY H MEMBER 3 UniProtKB/TrEMBL
Pfam FERM_M UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Myosin_head UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MyTH4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PF00612 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PhenoGen Myo7a PhenoGen
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
  PS50096 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART B41 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MYSc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MyTH4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00015 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP PH domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF47031 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF50044 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF54236 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0R4J113 ENTREZGENE, UniProtKB/TrEMBL
  A0A0U1RPT3_MOUSE UniProtKB/TrEMBL
  A0A0U1RPX7 ENTREZGENE, UniProtKB/TrEMBL
  A0A571BE72_MOUSE UniProtKB/TrEMBL
  A0A571BEN3_MOUSE UniProtKB/TrEMBL
  D3YUT5_MOUSE UniProtKB/TrEMBL
  E9QLP7 ENTREZGENE
  MYO7A_MOUSE UniProtKB/Swiss-Prot, ENTREZGENE
  Q5MJ56 ENTREZGENE, UniProtKB/TrEMBL
  Q5MJ57 ENTREZGENE
UniProt Secondary E9QLP7 UniProtKB/Swiss-Prot
  Q5MJ57 UniProtKB/Swiss-Prot