Human (GRCh37.p13)
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.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000218099.2F9-0012780461aa
 
Protein coding
CCDS14666P00740 Q19UG6 Q19UH6
Q19UI2 Q19UK3 Q19UK4
Q19UK5 Q19UK7 Q19UL6
Q86XR9
NM_000133.3Ensembl CanonicalGENCODE Basic
ENST00000394090.2F9-2011272423aa
 
Protein coding
P00740 Q19UG6 Q19UH6
Q19UI2 Q19UK3 Q19UK4
Q19UK5 Q19UK7 Q19UL6
Q86XR9
-GENCODE Basic
ENST00000479617.2F9-002374No protein
 
Processed transcript
---
Name

F9 (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: P00740

CCDS

This gene is a member of the Human CCDS set: CCDS14666.1

Ensembl version

ENSG00000101981.6

Other assemblies

This gene maps to 139,530,758-139,563,458 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000022536 (version 2)

Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Contigs

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