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Human (GRCh38.p14)
Description

mesencephalic astrocyte derived neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:15461]

Gene Synonyms

ARMET, ARP

Location

Chromosome 3: 51,385,291-51,389,397 forward strand.

GRCh38:CM000665.2

About this gene

This gene has 5 transcripts (splice variants), 209 orthologues, 1 paralogue and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000528157.7MANF-204909182aaENSP00000432799.3
 
Protein coding
CCDS46836P55145 NM_006010.6MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000446668.5MANF-20184671aaENSP00000405280.1
 
Nonsense mediated decay
H7C2D6 -TSL:3CDS 5' incomplete
ENST00000470900.1MANF-2021509No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000649711.1MANF-205992No protein-
 
Retained intron
---
ENST00000482262.1MANF-203436No protein-
 
Retained intron
--TSL:2