Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: NHSL2 ENSOCUG00000014345

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Description

NHS like 2 [Source:HGNC Symbol;Acc:HGNC:33737]

Location

Chromosome X: 50,556,869-50,854,838 forward strand.

OryCun2.0:CM000811.1

About this gene

This gene has 4 transcripts (splice variants), 214 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000039503.1	NHSL2-201	3666	1221aa	ENSOCUP00000042505.1	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,
ENSOCUT00000014338.4	NHSL2-203	3429	1142aa	ENSOCUP00000012325.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1T774	-
ENSOCUT00000036826.1	NHSL2-204	3297	1098aa	ENSOCUP00000037705.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSOCUT00000057785.1	NHSL2-202	2841	946aa	ENSOCUP00000032535.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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