Transcript: ENST00000309602.5 LRFN4-201

Description

leucine rich repeat and fibronectin type III domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28456]

Gene Synonyms

FIGLER6, MGC3103, SALM3.

Location

Chromosome 11: 66,857,064-66,860,475 forward strand.

About this transcript

This transcript has 2 exons, is annotated with 35 domains and features, is associated with 2344 variant alleles and maps to 477 oligo probes.

Gene

This transcript is a product of gene ENSG00000173621.9 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000309602.5	LRFN4-201	2869	635aa	ENSP00000312535.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS8153	A0A024R5I6 Q6PJG9	NM_024036.5	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, 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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENST00000393952.3	LRFN4-202	1550	418aa	ENSP00000377524.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E7ENX6	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5,
ENST00000531590.1	LRFN4-203	274	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-	TSL 3: A transcript where the only support is from a single EST The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:3,

Transcript: ENST00000309602.5 LRFN4-201

Protein summary

Protein domains for ENSP00000312535.4

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Transcript: ENST00000309602.5 LRFN4-201

Protein summary

Protein domains for ENSP00000312535.4

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