Mus musculus Gene: Stra6
Summary
InnateDB Gene IDBG-171524.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Stra6
Gene Name stimulated by retinoic acid gene 6
Synonyms AI891933
Species Mus musculus
Ensembl Gene ENSMUSG00000032327
Encoded Proteins
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
stimulated by retinoic acid gene 6
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 9:58063788-58153996
Strand Forward strand
Band B
Transcripts
ENSMUST00000085677 ENSMUSP00000082820
ENSMUST00000034880 ENSMUSP00000034880
ENSMUST00000145886
ENSMUST00000136154 ENSMUSP00000119062
ENSMUST00000128021 ENSMUSP00000117832
ENSMUST00000133287 ENSMUSP00000114346
ENSMUST00000136338 ENSMUSP00000115314
ENSMUST00000134955 ENSMUSP00000117280
ENSMUST00000147134 ENSMUSP00000115315
ENSMUST00000128378 ENSMUSP00000115511
ENSMUST00000150820 ENSMUSP00000122373
ENSMUST00000134450 ENSMUSP00000118242
ENSMUST00000170397 ENSMUSP00000130232
ENSMUST00000167479 ENSMUSP00000128417
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
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:0042573 retinoic acid metabolic process
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: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:0071939 vitamin A import
GO:0097070 ductus arteriosus closure
Cellular Component
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
GO:0043234 protein complex
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
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
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
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.10801
RefSeq NM_001162475 NM_001162476 NM_001162479 NM_009291 XM_006510941 XM_006510942 XM_006510943 XM_006510944 XM_006510945 XM_006510946
OMIM
CCDS CCDS23236
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas