ENSG00000108433


Homo sapiens

Features
Gene ID: ENSG00000108433
  
Biological name :GOSR2
  
Synonyms : golgi SNAP receptor complex member 2 / GOSR2 / O14653
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 17
Strand: 1
Band: q21.32
Gene start: 46923075
Gene end: 46975524
  
Corresponding Affymetrix probe sets: 210009_s_at (Human Genome U133 Plus 2.0 Array)   213144_at (Human Genome U133 Plus 2.0 Array)   213180_s_at (Human Genome U133 Plus 2.0 Array)   213206_at (Human Genome U133 Plus 2.0 Array)   213207_s_at (Human Genome U133 Plus 2.0 Array)   229255_x_at (Human Genome U133 Plus 2.0 Array)   235041_at (Human Genome U133 Plus 2.0 Array)   239159_at (Human Genome U133 Plus 2.0 Array)   243880_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000491361
Ensembl peptide - ENSP00000491283
Ensembl peptide - ENSP00000491396
Ensembl peptide - ENSP00000492830
Ensembl peptide - ENSP00000492751
Ensembl peptide - ENSP00000492736
Ensembl peptide - ENSP00000492669
Ensembl peptide - ENSP00000492607
Ensembl peptide - ENSP00000492595
Ensembl peptide - ENSP00000492565
Ensembl peptide - ENSP00000492548
Ensembl peptide - ENSP00000492544
Ensembl peptide - ENSP00000492524
Ensembl peptide - ENSP00000492396
Ensembl peptide - ENSP00000492360
Ensembl peptide - ENSP00000492278
Ensembl peptide - ENSP00000492275
Ensembl peptide - ENSP00000492206
Ensembl peptide - ENSP00000492146
Ensembl peptide - ENSP00000492139
Ensembl peptide - ENSP00000491979
Ensembl peptide - ENSP00000491961
Ensembl peptide - ENSP00000491946
Ensembl peptide - ENSP00000491863
Ensembl peptide - ENSP00000491859
Ensembl peptide - ENSP00000491785
Ensembl peptide - ENSP00000491749
Ensembl peptide - ENSP00000491709
Ensembl peptide - ENSP00000491682
Ensembl peptide - ENSP00000491432
Ensembl peptide - ENSP00000491399
Ensembl peptide - ENSP00000225567
Ensembl peptide - ENSP00000377101
Ensembl peptide - ENSP00000394559
Ensembl peptide - ENSP00000458154
Ensembl peptide - ENSP00000458911
Ensembl peptide - ENSP00000461673
Ensembl peptide - ENSP00000461784
Ensembl peptide - ENSP00000491100
Ensembl peptide - ENSP00000491135
Ensembl peptide - ENSP00000491253
Ensembl peptide - ENSP00000491266
NCBI entrez gene - 9570     See in Manteia.
OMIM - 604027
RefSeq - XM_017025395
RefSeq - NM_001012511
RefSeq - NM_001321133
RefSeq - NM_001321134
RefSeq - NM_001330252
RefSeq - NM_001353114
RefSeq - NM_001353115
RefSeq - NM_004287
RefSeq - NM_054022
RefSeq - XM_005257844
RefSeq - XM_006722190
RefSeq - XM_011525501
RefSeq - XM_011525502
RefSeq - XM_017025378
RefSeq - XM_017025379
RefSeq - XM_017025380
RefSeq - XM_017025381
RefSeq - XM_017025382
RefSeq - XM_017025383
RefSeq - XM_017025384
RefSeq - XM_017025385
RefSeq - XM_017025386
RefSeq - XM_017025387
RefSeq - XM_017025388
RefSeq - XM_017025389
RefSeq - XM_017025390
RefSeq - XM_017025391
RefSeq - XM_017025392
RefSeq - XM_017025393
RefSeq - XM_017025394
RefSeq Peptide - NP_001317181
RefSeq Peptide - NP_001012529
RefSeq Peptide - NP_001308062
RefSeq Peptide - NP_001340043
RefSeq Peptide - NP_001340044
RefSeq Peptide - NP_004278
RefSeq Peptide - NP_473363
RefSeq Peptide - NP_001308063
swissprot - A0A1W2PRV0
swissprot - A0A1W2PRP7
swissprot - A0A1W2PRL0
swissprot - A0A1W2PRH7
swissprot - A0A1W2PRE6
swissprot - A0A1W2PRD0
swissprot - A0A1W2PRC2
swissprot - A0A1W2PR23
swissprot - A0A1W2PR02
swissprot - A0A1W2PQS3
swissprot - A0A1W2PQQ4
swissprot - A0A1W2PQP2
swissprot - A0A1W2PQM3
swissprot - A0A1W2PQE0
swissprot - A0A1W2PQ77
swissprot - A0A1W2PQ38
swissprot - A0A1W2PQ12
swissprot - A0A1W2PQ06
swissprot - A0A1W2PPW8
swissprot - A0A1W2PPP5
swissprot - A0A1W2PPJ0
swissprot - A0A1W2PPG5
swissprot - A0A1W2PPG1
swissprot - A0A1W2PPE0
swissprot - A0A1W2PP28
swissprot - I3L1K7
swissprot - I3L0K1
swissprot - I3L4Z6
swissprot - I3NI02
swissprot - O14653
swissprot - A0A1W2PNV3
swissprot - A0A1X7SBU8
swissprot - A0A1W2PS81
swissprot - A0A1W2PS12
Ensembl - ENSG00000108433
  
Related genetic diseases (OMIM): 614018 - Epilepsy, progressive myoclonic 6, 614018
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 gosr2ENSDARG00000053070Danio rerio
 GOSR2ENSGALG00000001107Gallus gallus
 Gosr2ENSMUSG00000020946Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
AC005670.2ENSG0000026263392


Protein motifs (from Interpro)
Interpro ID Name
 IPR010989  SNARE
 IPR027027  GOSR2/Membrin/Bos1


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006623 protein targeting to vacuole IBA
 biological_processGO:0006888 ER to Golgi vesicle-mediated transport TAS
 biological_processGO:0006891 intra-Golgi vesicle-mediated transport IBA
 biological_processGO:0006896 Golgi to vacuole transport IBA
 biological_processGO:0015031 protein transport IEA
 biological_processGO:0016192 vesicle-mediated transport IEA
 biological_processGO:0036498 IRE1-mediated unfolded protein response TAS
 biological_processGO:0042147 retrograde transport, endosome to Golgi IBA
 biological_processGO:0048208 COPII vesicle coating TAS
 biological_processGO:0048280 vesicle fusion with Golgi apparatus IBA
 biological_processGO:0061025 membrane fusion IEA
 cellular_componentGO:0000139 Golgi membrane TAS
 cellular_componentGO:0005783 endoplasmic reticulum IEA
 cellular_componentGO:0005789 endoplasmic reticulum membrane IBA
 cellular_componentGO:0005794 Golgi apparatus IEA
 cellular_componentGO:0005829 cytosol IEA
 cellular_componentGO:0012507 ER to Golgi transport vesicle membrane TAS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0031201 SNARE complex ISS
 cellular_componentGO:0031902 late endosome membrane IBA
 cellular_componentGO:0033116 endoplasmic reticulum-Golgi intermediate compartment membrane TAS
 molecular_functionGO:0000149 SNARE binding IBA
 molecular_functionGO:0005484 SNAP receptor activity IEA
 molecular_functionGO:0005515 protein binding IPI


Pathways (from Reactome)
Pathway description
COPII-mediated vesicle transport
XBP1(S) activates chaperone genes
Cargo concentration in the ER
COPI-mediated anterograde transport
Intra-Golgi traffic


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0001251 Ataxia "Ataxia is a nonspecific neurological sign and symptom consisting of gross lack of coordination of muscle movements. Ataxia is caused by dysfunction of one or more parts of the nervous system including the cerebellum, the sensory nervous system, the vestibular system, or the cerebral cortex." [HPO:curators]
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 HP:0001260 Dysarthria "Dysarthric speech is a general description referring to a neurological speech disorder characterized by poor articulation. Depending on the involved neurological structures, dysarthria may be further classified as spastic, flaccid, ataxic, hyperkinetic and hypokinetic, or mixed." [HPO:curators]
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 HP:0001284 Areflexia 
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 HP:0001336 Myoclonus "Very brief, involuntary random muscular contractions occurring at rest, in response to sensory stimuli, or accompanying voluntary movements." [HPO:curators]
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 HP:0001337 Tremor "An unintentional, oscillating to-and-fro muscle movement." [HPO:curators]
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 HP:0002121 Absence seizures "Recurrent absence seizures are `generalized seizures` (HP:0002197) that are characterized by a sudden cessation of motor activity and by a blank facial expression with flickering of the eyelids. There is no convulsive muscular activity or loss of postural control." [HPO:probinson]
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 HP:0002355 Difficulty walking 
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 HP:0002650 Scoliosis "The presence of an abnormal lateral curvature of the spine." [HPO:curators]
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 HP:0003236 Elevated serum creatine phosphokinase 
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 HP:0003676 Progressive disorder 
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 HP:0010819 Atonic seizures "A type of `seizure` (HP:0001250) characterized by a suddenloss of musle tone. Usually, consciousness is retained. In an atonic seizure, the eyelids may droop, the head may nod, and the person may drop things and fall to the ground." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000108587 GOSR1 / O95249 / golgi SNAP receptor complex member 1  / complex
 ENSG00000150961 O94855 / SEC24D / SEC24 homolog D, COPII coat complex component  / complex / reaction
 ENSG00000105829 BET1 / O15155 / Bet1 golgi vesicular membrane trafficking protein  / complex
 ENSG00000138768 USO1 / O60763 / USO1 vesicle transport factor  / reaction
 ENSG00000162236 STX5 / Q13190 / syntaxin 5  / complex
 ENSG00000265808 O75396 / SEC22B / SEC22 homolog B, vesicle trafficking protein (gene/pseudogene)  / reaction / complex
 ENSG00000106636 YKT6 / O15498 / YKT6 v-SNARE homolog  / complex
 ENSG00000100934 Q15436 / SEC23A / Sec23 homolog A, coat complex II component  / complex / reaction
 ENSG00000176986 P53992 / SEC24C / SEC24 homolog C, COPII coat complex component  / complex / reaction
 ENSG00000167110 GOLGA2 / Q08379 / golgin A2  / reaction
 ENSG00000114745 Q9BQQ3 / GORASP1 / golgi reassembly stacking protein 1  / reaction
 ENSG00000105402 NAPA / P54920 / NSF attachment protein alpha  / complex / reaction
 ENSG00000092108 SCFD1 / Q8WVM8 / sec1 family domain containing 1  / complex
 ENSG00000073969 NSF / P46459 / N-ethylmaleimide sensitive factor, vesicle fusing ATPase  / reaction / complex






 

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