Gene Gene information from NCBI Gene database.
Entrez ID 1953
Gene name Multiple EGF like domains 6
Gene symbol MEGF6
Synonyms (NCBI Gene)
EGFL3
Chromosome 1
Chromosome location 1p36.32
miRNA miRNA information provided by mirtarbase database.
159
miRTarBase ID miRNA Experiments Reference
MIRT1142437 hsa-miR-1248 CLIP-seq
MIRT1142438 hsa-miR-1257 CLIP-seq
MIRT1142439 hsa-miR-1273f CLIP-seq
MIRT1142440 hsa-miR-1292 CLIP-seq
MIRT1142441 hsa-miR-143 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005509 Function Calcium ion binding IEA
GO:0005515 Function Protein binding IPI 21078624
GO:0005576 Component Extracellular region IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604266 3232 ENSG00000162591
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O75095
Protein name Multiple epidermal growth factor-like domains protein 6 (Multiple EGF-like domains protein 6) (Epidermal growth factor-like protein 3) (EGF-like protein 3)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14670 FXa_inhibition 165 200 Domain
PF07645 EGF_CA 285 324 Calcium-binding EGF domain Domain
PF14670 FXa_inhibition 416 451 Domain
PF12661 hEGF 527 546 Human growth factor-like EGF Domain
PF00053 Laminin_EGF 568 613 Laminin EGF domain Domain
PF00053 Laminin_EGF 873 919 Laminin EGF domain Domain
PF12661 hEGF 919 938 Human growth factor-like EGF Domain
PF12661 hEGF 1005 1024 Human growth factor-like EGF Domain
PF12661 hEGF 1048 1067 Human growth factor-like EGF Domain
PF12661 hEGF 1091 1110 Human growth factor-like EGF Domain
PF00053 Laminin_EGF 1128 1174 Laminin EGF domain Domain
PF00053 Laminin_EGF 1175 1221 Laminin EGF domain Domain
PF00053 Laminin_EGF 1344 1391 Laminin EGF domain Domain
Sequence
MSFLEEARAAGRAVVLALVLLLLPAVPVGASVPPRPLLPLQPGMPHVCAEQELTLVGRRQ
PCVQALSHTVPVWKAGCGWQAWCVGHERRTVYYMGYRQVYTTEARTVLRCCRGWMQQPDE
EGCLSAECSASLCFHGGRCVPGSAQPCHCPPGFQGPRCQYDVDECRTHNGGCQHRCVNTP
GSYLCECKPGFRLHTDSRTC
LAINSCALGNGGCQHHCVQLTITRHRCQCRPGFQLQEDGR
HCVRRSPCANRNGSCMHRCQVVRGLARCECHVGYQLAADGKACEDVDECAAGLAQCAHGC
LNTQGSFKCVCHAGYELGADGRQC
YRIEMEIVNSCEANNGGCSHGCSHTSAGPLCTCPRG
YELDTDQRTCIDVDDCADSPCCQQVCTNNPGGYECGCYAGYRLSADGCGCEDVDECASSR
GGCEHHCTNLAGSFQCSCEAGYRLHEDRRGC
SPLEEPMVDLDGELPFVRPLPHIAVLQDE
LPQLFQDDDVGADEEEAELRGEHTLTEKFVCLDDSFGHDCSLTCDDCRNGGTCLLGLDGC
DCPEGW
TGLICNETCPPDTFGKNCSFSCSCQNGGTCDSVTGACRCPPGVSGTNCEDGCPK
GYYGKHCRKKCNC
ANRGRCHRLYGACLCDPGLYGRFCHLTCPPWAFGPGCSEECQCVQPH
TQSCDKRDGSCSCKAGFRGERCQAECELGYFGPGCWQACTCPVGVACDSVSGECGKRCPA
GFQGEDCGQECPVGTFGVNCSSSCSCGGAPCHGVTGQCRCPPGRTGEDCEADCPEGRWGL
GCQEICPACQHAARCDPETGACLCLPGFVGSRCQDVCPAGWYGPSCQTRCSCANDGHCHP
ATGHCSCAPGWTGFSCQRACDTGHWGPDCSHPCNCSAGHGSCDAISGLCLCEAGYVGPRC
EQQCPQGHFGPGCEQRCQ
CQHGAACDHVSGACTCPAGWRGTFCEHACPAGFFGLDCRSAC
NCTAGAACDAVNGSCLCPAGRRGPRCAETCPAHTYGHNCSQACACFNGASCDPVHGQCHC
APGW
MGPSCLQACPAGLYGDNCRHSCLCQNGGTCDPVSGHCACPEGWAGLACEKECLPRD
VRAGCRHSGGCLNGGLCDPHTGRCLCPAGWTGDKCQSPCLRGWFGEACAQRCSCPPGAAC
HHVTGACRCPPGFTGSGCEQACPPGSFGEDCAQM
CQCPGENPACHPATGTCSCAAGYHGP
SCQQRCPPGRYGPGCEQLCGC
LNGGSCDAATGACRCPTGFLGTDCNLTCPQGRFGPNCTH
VCGCGQGAACDPVTGTCLCPPGRAGVRCERGCPQNRFGVGCEHTCSCRNGGLCHASNGSC
SCGLGWTGRHCELACPPGRYGAACHLECSCHNNSTCEPATGTCRCGPGFYGQACEHPCPP
GFHGAGCQGLC
WCQHGAPCDPISGRCLCPAGFHGHFCERGCEPGSFGEGCHQRCDCDGGA
PCDPVTGLCLCPPGRSGATCNLDCRRGQFGPSCTLHCDCGGGADCDPVSGQCHCVDGYMG
PTCREGGPLRLPENPSLAQGSAGTLPASSRPTSRSGGPARH
Sequence length 1541
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
14
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Acute myeloid leukemia Uncertain significance; Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BLADDER EXSTROPHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BREAST CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BREAST CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations