Mus musculus Gene: Dnahc17
Summary
InnateDB Gene IDBG-214612.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Dnahc17
Gene Name dynein, axonemal, heavy chain 17
Synonyms 2810003K23Rik; Dnahc17; Dnahcl1; Gm1178; mKIAA3028
Species Mus musculus
Ensembl Gene ENSMUSG00000033987
Encoded Proteins
dynein, axonemal, heavy chain 17
dynein, axonemal, heavy chain 17
dynein, axonemal, heavy chain 17
dynein, axonemal, heavy chain 17
dynein, axonemal, heavy chain 17
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000187775:
Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. DNAH17 is a heavy chain associated with axonemal dynein (Milisav and Affara, 1998 [PubMed 9545504]).[supplied by OMIM, Mar 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 11:118021723-118129219
Strand Reverse strand
Band E2
Transcripts
ENSMUST00000084803 ENSMUSP00000081864
ENSMUST00000018719 ENSMUSP00000018719
ENSMUST00000106308 ENSMUSP00000101915
ENSMUST00000132685 ENSMUSP00000120542
ENSMUST00000124164 ENSMUSP00000115370
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003777 microtubule motor activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016887 ATPase activity
Biological Process
GO:0006200 ATP catabolic process
GO:0007018 microtubule-based movement
GO:0007165 signal transduction
GO:0008150 biological_process
GO:0008152 metabolic process
Cellular Component
GO:0005575 cellular_component
GO:0030286 dynein complex
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
KEGG
Huntington's disease pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
KEGG
Huntington's disease pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.473893
RefSeq NM_001167746 XM_006534152
OMIM
CCDS CCDS48994
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas