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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
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: NMI ENSG00000123609

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Description

N-myc (and STAT) interactor [Source:HGNC Symbol;Acc:7854]

Location

Chromosome 2: 152,126,979-152,146,571 reverse strand.

GRCh37:CM000664.1

About this gene

This gene has 4 transcripts (splice variants), 192 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000243346.5	NMI-001	1623	307aa	ENSP00000243346.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS2192	C9JW17 Q13287	NM_004688.2	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, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENST00000414946.1	NMI-003	581	28aa	ENSP00000387373.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		C9JW17	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000491771.1	NMI-002	2094	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-
ENST00000477072.1	NMI-004	455	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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