Gene: Ccl19 ENSRNOG00000015668

Description

C-C motif chemokine ligand 19 [Source:RGD Symbol;Acc:1310336]

Gene Synonyms

LOC362506

Location

Primary_assembly 5: 61,759,220-61,772,022 reverse strand.

GRCr8:CM070395.1

About this gene

This gene has 6 transcripts (splice variants), 100 orthologues, 13 paralogues and is associated with 17 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000140435.1	Ccl19-203	1044	212aa	ENSRNOP00000106570.1	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,
ENSRNOT00000153957.1	Ccl19-205	996	161aa	ENSRNOP00000110206.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000020982.7	Ccl19-201	872	153aa	ENSRNOP00000020982.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZI84	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,
ENSRNOT00000146177.1	Ccl19-204	789	110aa	ENSRNOP00000104179.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000167842.1	Ccl19-206	566	109aa	ENSRNOP00000099773.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000101776.2	Ccl19-202	527	114aa	ENSRNOP00000086421.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A271	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,