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

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Gene: Nabp2 ENSRNOG00000023480

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Description

nucleic acid binding protein 2 [Source:RGD Symbol;Acc:1308158]

Gene Synonyms

LOC362813, MGC125161, Obfc2b, RGD1308158

Location

Primary_assembly 7: 1,415,492-1,422,682 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 4 transcripts (splice variants), 147 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000086656.3	Nabp2-202	1392	255aa	ENSRNOP00000074864.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K954	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,
ENSRNOT00000111806.2	Nabp2-204	1356	243aa	ENSRNOP00000090943.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q3SWT1	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSRNOT00000031362.8	Nabp2-201	1287	254aa	ENSRNOP00000036341.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QI91	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2,
ENSRNOT00000098497.2	Nabp2-203	1206	227aa	ENSRNOP00000088017.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A9W9	-

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Summary

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