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: LIN7B ENSPTRG00000011278

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Description

lin-7 homolog B, crumbs cell polarity complex component [Source:VGNC Symbol;Acc:VGNC:7789]

Location

Chromosome 19: 51,335,295-51,339,446 forward strand.

Pan_tro_3.0:CM000333.3

About this gene

This gene has 2 transcripts (splice variants), 179 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000020952.5	LIN7B-202	779	207aa	ENSPTRP00000019344.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WAU6 K7D105	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, 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,
ENSPTRT00000092410.1	LIN7B-201	574	137aa	ENSPTRP00000088316.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TGE4 A0A6D2VUP2	-

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Summary

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