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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: NT5C1B-RDH14 ENSG00000250741

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Description

NT5C1B-RDH14 readthrough [Source:HGNC Symbol;Acc:38831]

Location

Chromosome 2: 18,736,811-18,770,830 reverse strand.

GRCh37:CM000664.1

About this gene

This gene has 2 transcripts (splice variants) and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000532967.1	NT5C1B-RDH14-002	2142	602aa	ENSP00000433415.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS56111	-	NM_001199104.1	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,
ENST00000444297.2	NT5C1B-RDH14-001	1695	533aa	ENSP00000412639.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		C9J2C7	NM_001199103.1	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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