Human (GRCh38.p14)
Description

family with sequence similarity 186 member B [Source:HGNC Symbol;Acc:HGNC:25296]

Gene Synonyms

C12ORF25, DKFZP434J0113

Location
About this transcript

This transcript has 7 exons, is annotated with 13 domains and features, is associated with 7481 variant alleles and maps to 381 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000257894.2FAM186B-2012944893aaENSP00000257894.2
 
Protein coding
CCDS8788Q8IYM0-1 NM_032130.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000551047.5FAM186B-2052173241aaENSP00000448656.1
 
Protein coding
F8VRJ5 -GENCODE basicTSL:5
ENST00000532262.5FAM186B-2021901506aaENSP00000436995.1
 
Protein coding
A0A0C4DGG0 -TSL:1CDS 5' incomplete
ENST00000548841.5FAM186B-204621117aaENSP00000448989.1
 
Protein coding
H0YIB0 -TSL:5CDS 5' incomplete
ENST00000533372.1FAM186B-203308857aaENSP00000433047.1
 
Nonsense mediated decay
E9PMM1 -TSL:2
Statistics

Exons: 7, Coding exons: 7, Transcript length: 2,944 bps, Translation length: 893 residues

MANE

This MANE Select transcript contains ENSP00000257894 and matches to NM_032130.3 and NP_115506.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8IYM0

CCDS

This transcript is a member of the Human CCDS set: CCDS8788

Transcript Support Level (TSL)

TSL:1

Version

ENST00000257894.2

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.