Human (GRCh38.p14)
Description

septin 9 [Source:HGNC Symbol;Acc:HGNC:7323]

Gene Synonyms

AF17Q25, KIAA0991, MSF, MSF1, PNUTL4, SEPT9, SEPTD1

Location

Scaffold HSCHR17_3_CTG4: 71,462-85,796 forward strand.

GRCh38:GL383566.1

View this gene on the primary assembly.

About this gene

This gene has 7 transcripts (splice variants), 1 gene allele and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000633557.1SEPTIN9-25423810aaENSP00000487985.1
 
Protein coding
A0A0J9YWJ2 -Ensembl CanonicalTSL:NACDS 3' incomplete
ENST00000634088.1SEPTIN9-2551456aaENSP00000488209.1
 
Protein coding
--TSL:NACDS 3' incomplete
ENST00000632729.1SEPTIN9-2511046aaENSP00000488820.1
 
Protein coding
--TSL:NACDS 3' incomplete
ENST00000633211.1SEPTIN9-25324844aaENSP00000488513.1
 
Nonsense mediated decay
K7EMW8 -GENCODE basicTSL:4
ENST00000632430.1SEPTIN9-250349No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000633175.1SEPTIN9-252324No protein-
 
Protein coding CDS not defined
--TSL:NA
ENST00000631417.1SEPTIN9-249135No protein-
 
Protein coding CDS not defined
--TSL:NA