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

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Gene: ENSSSCG00000010359

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Description

LIM domain binding 3 [Source:VGNC Symbol;Acc:VGNC:107405]

Location

Primary_assembly 14: 87,658,943-87,690,144 forward strand.

Sscrofa11.1:CM000825.5

About this gene

This gene has 3 transcripts (splice variants), 4 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000063205.3	-	2080	466aa	ENSSSCP00000045131.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AM97 A0A4X1VGZ2	-
ENSSSCT00000011341.5	-	1294	288aa	ENSSSCP00000011047.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1VGZ7 F1SEN8	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
ENSSSCT00000038432.3	-	1279	283aa	ENSSSCP00000052902.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287B9Z6 A0A4X1VHY0	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,

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Summary

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