Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Fmnl1 ENSRNOG00000003207

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Description

formin-like 1 [Source:RGD Symbol;Acc:1311042]

Gene Synonyms

LOC287746

Location

Primary_assembly 10: 88,615,869-88,643,411 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 5 transcripts (splice variants), 286 orthologues, 15 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000118615.2	Fmnl1-204	4050	1097aa	ENSRNOP00000083255.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZYX6	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,
ENSRNOT00000110316.2	Fmnl1-203	4032	1091aa	ENSRNOP00000084134.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A0N3	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,
ENSRNOT00000087218.3	Fmnl1-202	3891	1095aa	ENSRNOP00000070794.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JYU6	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,
ENSRNOT00000122620.1	Fmnl1-205	3660	1053aa	ENSRNOP00000107106.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000065373.4	Fmnl1-201	3659	1034aa	ENSRNOP00000062888.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HJQ4 D3ZAZ1	-

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Summary

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