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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: F9 ENSG00000101981

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Description

coagulation factor IX [Source:HGNC Symbol;Acc:3551]

Gene Synonyms

FIX, HEMB, P19, PTC, THPH8

Location

Chromosome X: 138,612,917-138,645,617 forward strand.

GRCh37:CM000685.1

About this gene

This gene has 3 transcripts (splice variants), 12 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000218099.2	F9-001	2780	461aa	ENSP00000218099.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS14666	P00740 Q19UG6 Q19UH6 Q19UI2 Q19UK3 Q19UK4 Q19UK5 Q19UK7 Q19UL6 Q86XR9	NM_000133.3	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000394090.2	F9-201	1272	423aa	ENSP00000377650.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		P00740 Q19UG6 Q19UH6 Q19UI2 Q19UK3 Q19UK4 Q19UK5 Q19UK7 Q19UL6 Q86XR9	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000479617.2	F9-002	374	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-

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Summary

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