Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1955
Gene name Gene Name - the full gene name approved by the HGNC.
Multiple EGF like domains 9
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MEGF9
Synonyms (NCBI Gene) Gene synonyms aliases
EGFL5
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q33.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019118 hsa-miR-335-5p Microarray 18185580
MIRT019512 hsa-miR-151a-3p Sequencing 20371350
MIRT031063 hsa-miR-21-5p Microarray 18591254
MIRT048112 hsa-miR-197-3p CLASH 23622248
MIRT037264 hsa-miR-877-5p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005575 Component Cellular_component ND
GO:0005604 Component Basement membrane IBA 21873635
GO:0008150 Process Biological_process ND
GO:0009887 Process Animal organ morphogenesis IBA 21873635
GO:0009888 Process Tissue development IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604268 3234 ENSG00000106780
Protein
UniProt ID Q9H1U4
Protein name Multiple epidermal growth factor-like domains protein 9 (Multiple EGF-like domains protein 9) (Epidermal growth factor-like protein 5) (EGF-like protein 5)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00053 Laminin_EGF 204 251 Laminin EGF domain Domain
PF00053 Laminin_EGF 254 298 Laminin EGF domain Domain
PF00053 Laminin_EGF 301 346 Laminin EGF domain Domain
PF00053 Laminin_EGF 349 399 Laminin EGF domain Domain
PF00053 Laminin_EGF 400 449 Laminin EGF domain Domain
Sequence
MNGGAERAMRSLPSLGGLALLCCAAAAAAAAVASAASAGNVTGGGGAAGQVDASPGPGLR
GEPSHPFPRATAPTAQAPRTGPPRATVHRPLAATSPAQSPETTPLWATAGPSSTTFQAPL
GPSPTTPPAAERTSTTSQAPTRPAPTTLSTTTGPAPTTPVATTVPAPTTPRTPTPDLPSS
SNSSVLPTPPATEAPSSPPPEYVCNCSVVGSLNVNRCNQTTGQCECRPGYQGLHCETCKE
GFYLNYTSGLC
QPCDCSPHGALSIPCNSSGKCQCKVGVIGSICDRCQDGYYGFSKNGCLP
CQCNNRSASCDALTGACLNCQENSKGNHCEECKEGFYQSPDATKECLRCPCSAVTSTGSC
SIKSSELEPECDQCKDGYIGPNCNKCENGYYNFDSICRK
CQCHGHVDPVKTPKICKPESG
ECINCLHNTTGFWCENCLEGYVHDLEGNC
IKKEVILPTPEGSTILVSNASLTTSVPTPVI
NSTFTPTTLQTIFSVSTSENSTSALADVSWTQFNIIILTVIIIVVVLLMGFVGAVYMYRE
YQNRKLNAPFWTIELKEDNISFSSYHDSIPNADVSGLLEDDGNEVAPNGQLTLTTPIHNY
KA
Sequence length 602
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Anxiety Disorder Anxiety Disorder GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 24098452
Fibrosis Associate 39208548
Hereditary Breast and Ovarian Cancer Syndrome Associate 24098452
Multiple Myeloma Associate 24816239
Neoplasms Stimulate 24098452
Neutropenia Associate 39208548
Paraproteinemias Associate 24816239
Scleroderma Systemic Associate 39208548