Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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Gene: Reln ENSRNOG00000021441

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Description

reelin [Source:RGD Symbol;Acc:3553]

Gene Synonyms

Rl

Location

Primary_assembly 4: 13,628,399-14,055,162 forward strand.

GRCr8:CM070394.1

About this gene

This gene has 4 transcripts (splice variants), 228 orthologues and is associated with 28 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000129632.1	Reln-203	10847	3499aa	ENSRNOP00000099957.1	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,
ENSRNOT00000061858.6	Reln-202	11731	3462aa	ENSRNOP00000058574.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LZI7	-
ENSRNOT00000166047.1	Reln-204	11478	3425aa	ENSRNOP00000101019.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000010521.10	Reln-201	11446	3472aa	ENSRNOP00000010521.9	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LM29	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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