Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- 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: Fibcd1 ENSRNOG00000009735

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Description

fibrinogen C domain containing 1 [Source:RGD Symbol;Acc:1309097]

Gene Synonyms

LOC100909722, LOC311861, RGD1309097

Location

Primary_assembly 3: 35,490,459-35,524,142 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 1 transcript (splice variant), 228 orthologues and 23 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000012927.8	Fibcd1-201	4666	459aa	ENSRNOP00000012928.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JU32 D4ADA1	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, 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,

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Summary

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