Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: CFH ENSPTRG00000001799

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Description

complement factor H [Source:VGNC Symbol;Acc:VGNC:1214]

Location

Chromosome 1: 175,468,248-175,563,613 forward strand.

Pan_tro_3.0:CM000314.3

About this gene

This gene has 3 transcripts (splice variants), 15 orthologues and 39 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000003264.4	CFH-201	4245	1231aa	ENSPTRP00000003002.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2Q0T8	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,
ENSPTRT00000093695.1	CFH-202	1350	449aa	ENSPTRP00000079505.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SSI8 A0A6D2Y152	-
ENSPTRT00000081006.1	CFH-203	1158	385aa	ENSPTRP00000088245.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TG49 A0A6D2WDG9	-

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Summary

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