Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Gemin7 ENSRNOG00000049772

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Description

gem (nuclear organelle) associated protein 7 [Source:RGD Symbol;Acc:1597035]

Gene Synonyms

LOC499391

Location

Primary_assembly 1: 88,342,361-88,354,571 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 7 transcripts (splice variants), 186 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000128210.1	Gemin7-205	1682	145aa	ENSRNOP00000098839.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000172932.1	Gemin7-206	3698	129aa	ENSRNOP00000098934.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J8Q0	-
ENSRNOT00000102935.2	Gemin7-203	2007	129aa	ENSRNOP00000095884.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AGJ9 A6J8Q0	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,
ENSRNOT00000173706.1	Gemin7-207	1700	129aa	ENSRNOP00000104849.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J8Q0	-
ENSRNOT00000119328.2	Gemin7-204	1353	129aa	ENSRNOP00000093079.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AGJ9 A6J8Q0	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,
ENSRNOT00000100949.2	Gemin7-202	1148	129aa	ENSRNOP00000092860.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AGJ9 A6J8Q0	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,
ENSRNOT00000074418.3	Gemin7-201	1031	143aa	ENSRNOP00000064627.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J8P9 M0R5G2	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,

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Summary

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