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

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Gene: SLFN14 ENSG00000236320

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Description

schlafen family member 14 [Source:HGNC Symbol;Acc:32689]

Location

Chromosome 17: 33,875,144-33,885,117 reverse strand.

GRCh37:CM000679.1

About this gene

This gene has 1 transcript (splice variant), 5 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000415846.3	SLFN14-001	2889	912aa	ENSP00000391101.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS45650	P0C7P3	NM_001129820.1	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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