Bos taurus Gene: STRA6
Summary
InnateDB Gene IDBG-631877.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol STRA6
Gene Name stimulated by retinoic acid gene 6 protein homolog
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000007348
Encoded Proteins
stimulated by retinoic acid gene 6 protein homolog
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 ENSG00000137868:
The protein encoded by this gene is a membrane protein involved in the metabolism of retinol. The encoded protein acts as a receptor for retinol/retinol binding protein complexes. This protein removes the retinol from the complex and transports it across the cell membrane. Defects in this gene are a cause of syndromic microphthalmia type 9 (MCOPS9). Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 21:34878677-34901785
Strand Forward strand
Band
Transcripts
ENSBTAT00000038724 ENSBTAP00000038534
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:0004872 receptor activity
GO:0051183 vitamin transporter activity
Biological Process
GO:0001568 blood vessel development
GO:0001822 kidney development
GO:0003184 pulmonary valve morphogenesis
GO:0003281 ventricular septum development
GO:0007507 heart development
GO:0007612 learning
GO:0007631 feeding behavior
GO:0030324 lung development
GO:0030325 adrenal gland development
GO:0030540 female genitalia development
GO:0034633 retinol transport
GO:0042297 vocal learning
GO:0043583 ear development
GO:0043585 nose morphogenesis
GO:0046427 positive regulation of JAK-STAT cascade
GO:0048286 lung alveolus development
GO:0048520 positive regulation of behavior
GO:0048546 digestive tract morphogenesis
GO:0048566 embryonic digestive tract development
GO:0048589 developmental growth
GO:0048745 smooth muscle tissue development
GO:0048844 artery morphogenesis
GO:0050890 cognition
GO:0050905 neuromuscular process
GO:0051180 vitamin transport
GO:0060322 head development
GO:0060323 head morphogenesis
GO:0060325 face morphogenesis
GO:0060426 lung vasculature development
GO:0060539 diaphragm development
GO:0060900 embryonic camera-type eye formation
GO:0061029 eyelid development in camera-type eye
GO:0061038 uterus morphogenesis
GO:0061143 alveolar primary septum development
GO:0061156 pulmonary artery morphogenesis
GO:0061205 paramesonephric duct development
GO:0097070 ductus arteriosus closure
Cellular Component
GO:0043234 protein complex
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
The canonical retinoid cycle in rods (twilight vision) pathway
Retinoid cycle disease events pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
Visual phototransduction pathway
Disease pathway
Disease pathway
The canonical retinoid cycle in rods (twilight vision) pathway
Visual phototransduction pathway
Retinoid cycle disease events pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Bt.3196
RefSeq NM_001075730 XM_005221952 XM_005221953 XM_005221954 XM_005221955 XM_005221957
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas