Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Eng ENSRNOG00000050190

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Description

endoglin [Source:RGD Symbol;Acc:1593188]

Gene Synonyms

MGC124909

Location

Primary_assembly 3: 36,326,202-36,370,933 forward strand.

GRCr8:CM070393.1

About this gene

This gene has 6 transcripts (splice variants), 157 orthologues, 2 paralogues and is associated with 52 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000148878.1	Eng-206	3854	798aa	ENSRNOP00000100476.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,
ENSRNOT00000071801.4	Eng-201	3618	763aa	ENSRNOP00000066355.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RA19	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSRNOT00000074562.5	Eng-202	3410	603aa	ENSRNOP00000066838.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6Q3E8	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2,
ENSRNOT00000114060.2	Eng-204	3377	639aa	ENSRNOP00000094124.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GL08	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSRNOT00000123411.1	Eng-205	3189	635aa	ENSRNOP00000104828.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000101522.2	Eng-203	3166	635aa	ENSRNOP00000089152.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A813	-

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Summary

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