Human (GRCh37.p13)
Description

family with sequence similarity 189, member B [Source:HGNC Symbol;Acc:1233]

Gene Synonyms

C1orf2, COTE1, cote1

Location

Chromosome 1: 155,216,996-155,225,274 reverse strand.

GRCh37:CM000663.1

View alleles of this gene on alternative sequences

About this gene

This gene has 9 transcripts (splice variants), 1 gene allele and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000361361.2FAM189B-0013082668aaENSP00000354958.2
 
Protein coding
CCDS1103P81408 NM_006589.2GENCODE basic
ENST00000368368.3FAM189B-0042609650aaENSP00000357352.3
 
Protein coding
CCDS58035P81408 NM_001267608.1GENCODE basic
ENST00000350210.2FAM189B-0022379572aaENSP00000307128.4
 
Protein coding
CCDS1104P81408 NM_198264.1GENCODE basic
ENST00000491082.1FAM189B-0081006325aaENSP00000427011.1
 
Protein coding
D6RD59 -CDS 3' incomplete
ENST00000487649.1FAM189B-0071499144aaENSP00000427520.1
 
Nonsense mediated decay
Q96AD8 --
ENST00000472550.1FAM189B-010948No protein-
 
Processed transcript
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ENST00000481822.1FAM189B-0062103No protein-
 
Retained intron
---
ENST00000368366.1FAM189B-0031962No protein-
 
Retained intron
---
ENST00000497941.1FAM189B-009871No protein-
 
Retained intron
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