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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: NUP62CL ENSG00000198088

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Description

nucleoporin 62kDa C-terminal like [Source:HGNC Symbol;Acc:25960]

Gene Synonyms

FLJ20130, NUP62L

Location

Chromosome X: 106,366,657-106,449,670 reverse strand.

GRCh37:CM000685.1

About this gene

This gene has 5 transcripts (splice variants) and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000372466.4	NUP62CL-001	1755	184aa	ENSP00000361544.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS14527	Q5JSN5 Q9H1M0	NM_017681.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000372461.3	NUP62CL-201	1608	72aa	ENSP00000361539.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q9H1M0	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000432145.1	NUP62CL-004	688	198aa	ENSP00000408612.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		-	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENST00000421752.1	NUP62CL-003	618	136aa	ENSP00000405906.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q5JSN5	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000484614.1	NUP62CL-002	1515	72aa	ENSP00000433269.1	Nonsense mediated decay		Q9H1M0	-	-

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Summary

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