Human (GRCh37.p13) ▼
Description

family with sequence similarity 132, member B [Source:HGNC Symbol;Acc:26727]

Gene Synonyms

C1QTNF15, CTRP15, FLJ37034

Location

Chromosome 2: 239,067,623-239,077,541 forward strand.

GRCh37:CM000664.1

About this gene

This gene has 7 transcripts (splice variants), 105 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000546354.1FAM132B-0081065354aaENSP00000442304.1
 
Protein coding
Q4G0M1 -Ensembl CanonicalGENCODE Basic
ENST00000357303.3FAM132B-004201263aaENSP00000349855.3
 
Protein coding
--CDS 5' incomplete
ENST00000344233.6FAM132B-00761274aaENSP00000343261.6
 
Protein coding
--CDS 5' incomplete
ENST00000473274.1FAM132B-0012307No protein-
 
Retained intron
---
ENST00000479091.1FAM132B-0021416No protein-
 
Retained intron
---
ENST00000486834.1FAM132B-0051279No protein-
 
Retained intron
---
ENST00000481917.1FAM132B-006756No protein-
 
Retained intron
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As of the latest update in March 2020 we are not supporting data for species other than human on this GRCh37 site and the view you wish to use is disabled.

You can read more about why we have done this on our blog.

You can still view this page on the following archive resources:

1. The Ensembl 75 archive represents a code and data freeze taken in February 2014.

2. The GRCh37 archive represents a code and data freeze taken in January 2019.