Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: BLMH ENSBTAG00000021370

.

Description

bleomycin hydrolase [Source:VGNC Symbol;Acc:VGNC:26505]

Location

Primary_assembly 19: 21,333,634-21,375,948 reverse strand.

ARS-UCD1.3:CM008186.2

About this gene

This gene has 5 transcripts (splice variants) and 207 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000122776.1	BLMH-203	2421	468aa	ENSBTAP00000079916.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSBTAT00000028490.6	BLMH-202	2389	459aa	ENSBTAP00000028490.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BL29	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2,
ENSBTAT00000135393.1	BLMH-201	2259	414aa	ENSBTAP00000096968.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000103128.1	BLMH-204	1948	418aa	ENSBTAP00000078047.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000107759.1	BLMH-205	1528	258aa	ENSBTAP00000086288.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

.

Breeds

.

Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

.

Personal Data