Human (GRCh38.p14)
Description

myosin XVIIIB [Source:HGNC Symbol;Acc:HGNC:18150]

Gene Synonyms

BK125H2.1

Location

Chromosome 22: 25,742,144-26,031,045 forward strand.

GRCh38:CM000684.2

About this gene

This gene has 10 transcripts (splice variants), 191 orthologues, 43 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000335473.12MYO18B-20185342567aaENSP00000334563.8
 
Protein coding
CCDS54507Q8IUG5-1 NM_032608.7MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT2TSL:1
ENST00000407587.6MYO18B-20280902568aaENSP00000386096.2
 
Protein coding
CCDS82703Q8IUG5-3 -GENCODE basicAPPRIS P5TSL:1
ENST00000536101.5MYO18B-20580512567aaENSP00000441229.1
 
Protein coding
CCDS54507Q8IUG5-1 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000543971.1MYO18B-2101768517aaENSP00000444262.1
 
Protein coding
H0YGQ4 -TSL:2CDS 5' incomplete
ENST00000539302.5MYO18B-2077774798aaENSP00000437587.1
 
Nonsense mediated decay
F5H6I8 -TSL:1
ENST00000540454.1MYO18B-2091099209aaENSP00000441301.1
 
Nonsense mediated decay
A0A2Q2TCQ6 -TSL:1CDS 5' incomplete
ENST00000536204.1MYO18B-206615No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000534908.5MYO18B-204607No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000539544.1MYO18B-208552No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000418374.6MYO18B-2036363No protein-
 
Retained intron
--TSL:1