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

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Gene: RHEBL1 ENSG00000167550

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Description

Ras homolog enriched in brain like 1 [Source:HGNC Symbol;Acc:21166]

Gene Synonyms

FLJ25797, MGC34869, RHEBL1c

Location

Chromosome 12: 49,458,468-49,463,808 reverse strand.

GRCh37:CM000674.1

About this gene

This gene has 4 transcripts (splice variants), 107 orthologues and 35 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000301068.6	RHEBL1-001	1210	183aa	ENSP00000301068.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS8778	Q8TAI7	NM_144593.1	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, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENST00000550675.1	RHEBL1-004	380	109aa	ENSP00000447428.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		F8W1T5	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000550797.1	RHEBL1-002	1261	68aa	ENSP00000446726.1	Nonsense mediated decay		Q8TAI7	-	-
ENST00000420065.1	RHEBL1-003	1063	42aa	ENSP00000409818.1	Nonsense mediated decay		C9JQQ1	-	-

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Summary

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