1. Gene
  2. MEGF11 - multiple EGF like domains 11 Gene

MEGF11 - multiple EGF like domains 11 Gene

Homo sapiens
Gene ID: 84465 | Gene type: protein coding

About MEGF11

Cytogenetic location: 15q22.31 Genomic coordinates (GRCh38): 15:65,895,299-66,253,750 (from NCBI)

This gene has 15 transcripts (splice variants), 1 gene allele, 198 orthologues and 3 paralogues. Biased expression in brain (RPKM 3.0), testis (RPKM 0.5) and 2 other tissues.

Summary

Predicted to be involved in homotypic cell-cell adhesion and retina layer formation. Predicted to be located in basolateral plasma membrane. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

MEGF11 Products(9)

mRNA Protein Name
NM_001385028.1 NP_001371957.1 multiple epidermal growth factor-like domains protein 11 isoform 1 precursor
NM_001385029.1 NP_001371958.1 multiple epidermal growth factor-like domains protein 11 isoform 3 precursor
NM_001385030.1 NP_001371959.1 multiple epidermal growth factor-like domains protein 11 isoform 4
NM_001385031.1 NP_001371960.1 multiple epidermal growth factor-like domains protein 11 isoform 5
NM_001385032.1 NP_001371961.1 multiple epidermal growth factor-like domains protein 11 isoform 6
NM_001385033.1 NP_001371962.1 multiple epidermal growth factor-like domains protein 11 isoform 7 precursor
NM_001387150.1 NP_001374079.1 multiple epidermal growth factor-like domains protein 11 isoform 2 precursor
NM_001387151.1 NP_001374080.1 multiple epidermal growth factor-like domains protein 11 isoform 8 precursor
NM_032445.3 NP_115821.2 multiple epidermal growth factor-like domains protein 11 isoform 2 precursor

MEGF11 Protein Structure

hEGF

hEGF: Human growth factor-like EGF (203 - 215)

hEGF

hEGF: Human growth factor-like EGF (247 - 258)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (275 - 320)

hEGF

hEGF: Human growth factor-like EGF (333 - 344)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (362 - 407)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (450 - 493)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (579 - 619)

hEGF

hEGF: Human growth factor-like EGF (639 - 650)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (667 - 703)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (753 - 790)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (796 - 824)

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  • 1044 a.a.
Protein Preferred Names Protein Names

multiple epidermal growth factor-like domains protein 11

multiple EGF-like domains protein 11

Related Diseases

Diseases Alias
Myopathy, Areflexia, Respiratory Distress, And Dysphagia, Early-Onset

EMARDD

Myopathy, Areflexia, Respiratory Distress, And Dysphagia, Early-Onset, Mild Variant

Early-Onset Myopathy-Areflexia-Respiratory Distress-Dysphagia Syndrome

Early-Onset Myopathy, Areflexia, Respiratory Distress And Dysphagia

Myopathy, Early-Onset, Areflexia, Respiratory Distress, And Dysphagia

Folic Acid Deficiency Anemia

Folate Deficiency Anaemia

Folic Acid Deficiency Anaemia

Folate Deficiency Anemia

Folate-Deficiency Anaemia

Folate-Deficiency Anemia

Folate-Deficient Megaloblastic Anaemia

Megaloblastic Anemia Due To Folate Deficiency

Anaemia Of Folate Deficiency

Folate Or Folic Acid Deficiency Anaemia Nos

Folic Acid Deficiency Anaemia Nos

Acquired Megaloblastic Anaemia Due To Nutritional Folate Deficiency

Dietary Folic Acid Deficiency Anaemia

Dietary Folate Deficiency Anaemia

Folate Deficiency Anaemia Due To Dietary Causes

Goat'S Milk Anaemia

Acquired Megaloblastic Anaemia Due To Folate Deficiency Secondary To Increased Requirement

Megaloblastic Anaemia Due To Increased Requirements Of Folate

Acquired Megaloblastic Anaemia Due To Folate Deficiency Secondary To Intestinal Disorders

Acquired Megaloblastic Anaemia Due To Decreased Intestinal Absorption Of Folate

Megaloblastic Anaemia Due To Decreased Intestinal Absorption Of Folate

Carpenter Syndrome 1

Carpenter Syndrome

Acrocephalopolysyndactyly Type Ii

Acps Ii

CRPT1

Acrocephalopolysyndactyly Type 2

Acrocephalosyndactyly, Type Ii

Acrocephalopolysyndactyly 2

Acps2

Acps 2

Type Ii Acrocephalosyndactyly

Carpenter Syndrome, Type 1

Apert-Crouzon Disease

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus MEGF11 MGD MGI:1920951
Felis catus MEGF11 VGNC VGNC:80915
Macaca mulatta MEGF11 VGNC VGNC:84376
Bos taurus MEGF11 VGNC VGNC:55123
Rattus norvegicus MEGF11 RGD RGD:1582797
Canis familiaris MEGF11 VGNC VGNC:59120