Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Dnah12 ENSMUSG00000021879

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Description

dynein, axonemal, heavy chain 12 [Source:MGI Symbol;Acc:MGI:107720]

Gene Synonyms

4921531P07Rik, DHC3, DLP12, Dnahc12, Dnahc7l, HL-19, HL19, Hdhc3, LOC380889

Location

Chromosome 14: 26,414,429-26,613,660 forward strand.

GRCm39:CM001007.3

About this gene

This gene has 2 transcripts (splice variants), 276 orthologues and 17 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000022433.12	Dnah12-201	12009	3960aa	ENSMUSP00000022433.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9QPU2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1, TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5,
ENSMUST00000073309.5	Dnah12-202	611	203aa	ENSMUSP00000073035.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding		F7D0D4	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,

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Summary

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