ENSG00000115525


Homo sapiens

Features
Gene ID: ENSG00000115525
  
Biological name :ST3GAL5
  
Synonyms : Q9UNP4 / ST3 beta-galactoside alpha-2,3-sialyltransferase 5 / ST3GAL5
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 2
Strand: -1
Band: p11.2
Gene start: 85837120
Gene end: 85905199
  
Corresponding Affymetrix probe sets: 203217_s_at (Human Genome U133 Plus 2.0 Array)   239755_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000491356
Ensembl peptide - ENSP00000491316
Ensembl peptide - ENSP00000491395
Ensembl peptide - ENSP00000492866
Ensembl peptide - ENSP00000492847
Ensembl peptide - ENSP00000492753
Ensembl peptide - ENSP00000492710
Ensembl peptide - ENSP00000492635
Ensembl peptide - ENSP00000492602
Ensembl peptide - ENSP00000492473
Ensembl peptide - ENSP00000492468
Ensembl peptide - ENSP00000492459
Ensembl peptide - ENSP00000492305
Ensembl peptide - ENSP00000492299
Ensembl peptide - ENSP00000492280
Ensembl peptide - ENSP00000492244
Ensembl peptide - ENSP00000492209
Ensembl peptide - ENSP00000492103
Ensembl peptide - ENSP00000492098
Ensembl peptide - ENSP00000492097
Ensembl peptide - ENSP00000492089
Ensembl peptide - ENSP00000492045
Ensembl peptide - ENSP00000492035
Ensembl peptide - ENSP00000492030
Ensembl peptide - ENSP00000491917
Ensembl peptide - ENSP00000491880
Ensembl peptide - ENSP00000491857
Ensembl peptide - ENSP00000491853
Ensembl peptide - ENSP00000491828
Ensembl peptide - ENSP00000491802
Ensembl peptide - ENSP00000491701
Ensembl peptide - ENSP00000491699
Ensembl peptide - ENSP00000491664
Ensembl peptide - ENSP00000491564
Ensembl peptide - ENSP00000491495
Ensembl peptide - ENSP00000491443
Ensembl peptide - ENSP00000491398
Ensembl peptide - ENSP00000306247
Ensembl peptide - ENSP00000366549
Ensembl peptide - ENSP00000377394
Ensembl peptide - ENSP00000377397
Ensembl peptide - ENSP00000401375
Ensembl peptide - ENSP00000408635
Ensembl peptide - ENSP00000490979
Ensembl peptide - ENSP00000491027
Ensembl peptide - ENSP00000491029
Ensembl peptide - ENSP00000491038
Ensembl peptide - ENSP00000491084
Ensembl peptide - ENSP00000491126
Ensembl peptide - ENSP00000491172
Ensembl peptide - ENSP00000491238
Ensembl peptide - ENSP00000491314
Ensembl peptide - ENSP00000491315
NCBI entrez gene - 8869     See in Manteia.
OMIM - 604402
RefSeq - XM_017005215
RefSeq - NM_001042437
RefSeq - NM_001354223
RefSeq - NM_001354224
RefSeq - NM_001354226
RefSeq - NM_001354227
RefSeq - NM_001354229
RefSeq - NM_001354233
RefSeq - NM_001354234
RefSeq - NM_001354238
RefSeq - NM_003896
RefSeq - XM_005264630
RefSeq - XM_011533143
RefSeq - XM_017005199
RefSeq - XM_017005200
RefSeq - XM_017005201
RefSeq - XM_017005202
RefSeq - XM_017005203
RefSeq - XM_017005204
RefSeq - XM_017005205
RefSeq - XM_017005206
RefSeq - XM_017005207
RefSeq - XM_017005208
RefSeq - XM_017005209
RefSeq - XM_017005210
RefSeq - XM_017005211
RefSeq - XM_017005212
RefSeq - XM_017005213
RefSeq - XM_017005214
RefSeq Peptide - NP_001035902
RefSeq Peptide - NP_001341152
RefSeq Peptide - NP_001341156
RefSeq Peptide - NP_001341158
RefSeq Peptide - NP_001341162
RefSeq Peptide - NP_001341163
RefSeq Peptide - NP_001341167
RefSeq Peptide - NP_003887
RefSeq Peptide - NP_001341153
RefSeq Peptide - NP_001341155
swissprot - C9JYS9
swissprot - A0A1X7SBT2
swissprot - A0A1W2PRY1
swissprot - A0A1W2PRT0
swissprot - A0A1W2PRP8
swissprot - A0A1W2PRD9
swissprot - A0A1W2PRC6
swissprot - A0A1W2PR69
swissprot - A0A1W2PR45
swissprot - A0A1W2PR43
swissprot - A0A1W2PR24
swissprot - A0A1W2PQT6
swissprot - A0A1W2PQR0
swissprot - A0A1W2PQQ6
swissprot - A0A1W2PQM6
swissprot - A0A1W2PQH5
swissprot - A0A1W2PQB4
swissprot - A0A1W2PQ40
swissprot - A0A1W2PQ22
swissprot - A0A1W2PQ08
swissprot - A0A1W2PQ01
swissprot - A0A1W2PPT1
swissprot - A0A1W2PPQ6
swissprot - A0A1W2PPG4
swissprot - A0A1W2PPF6
swissprot - A0A1W2PPB0
swissprot - A0A1W2PP82
swissprot - A0A1W2PP90
swissprot - A0A1W2PP52
swissprot - A0A1W2PNZ0
swissprot - A0A1W2PNV2
swissprot - A0A1W2PNR4
swissprot - A0A0S2Z4S6
swissprot - F8WEA8
swissprot - Q9UNP4
swissprot - A0A0S2Z4Q7
swissprot - E7EPY0
Ensembl - ENSG00000115525
  
Related genetic diseases (OMIM): 609056 - Salt and pepper developmental regression syndrome, 609056
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
 st3gal5ENSDARG00000037556Danio rerio
 ST3GAL5ENSGALG00000033260Gallus gallus
 O88829ENSMUSG00000056091Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q11203 / ST3GAL3 / ST3 beta-galactoside alpha-2,3-sialyltransferase 3ENSG0000012609131
Q11206 / ST3GAL4 / ST3 beta-galactoside alpha-2,3-sialyltransferase 4ENSG0000011008025
Q9Y274 / ST3GAL6 / ST3 beta-galactoside alpha-2,3-sialyltransferase 6ENSG0000006422524
Q11201 / ST3GAL1 / ST3 beta-galactoside alpha-2,3-sialyltransferase 1ENSG0000000851318
Q9NSC7 / ST6GALNAC1 / ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1ENSG0000007052617
Q16842 / ST3GAL2 / ST3 beta-galactoside alpha-2,3-sialyltransferase 2ENSG0000015735016
Q9UJ37 / ST6GALNAC2 / ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2ENSG0000007073115


Protein motifs (from Interpro)
Interpro ID Name
 IPR001675  Glycosyl transferase family 29
 IPR012163  Sialyltransferase


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001574 ganglioside biosynthetic process NAS
 biological_processGO:0005975 carbohydrate metabolic process TAS
 biological_processGO:0006486 protein glycosylation IEA
 biological_processGO:0006688 glycosphingolipid biosynthetic process TAS
 biological_processGO:0009311 oligosaccharide metabolic process IBA
 biological_processGO:0018279 protein N-linked glycosylation via asparagine IBA
 biological_processGO:0097503 sialylation IEA
 cellular_componentGO:0000139 Golgi membrane IBA
 cellular_componentGO:0005794 Golgi apparatus IEA
 cellular_componentGO:0005887 integral component of plasma membrane TAS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0003836 beta-galactoside (CMP) alpha-2,3-sialyltransferase activity TAS
 molecular_functionGO:0004513 neolactotetraosylceramide alpha-2,3-sialyltransferase activity TAS
 molecular_functionGO:0008373 sialyltransferase activity TAS
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0016757 transferase activity, transferring glycosyl groups IEA
 molecular_functionGO:0047291 lactosylceramide alpha-2,3-sialyltransferase activity IEA


Pathways (from Reactome)
Pathway description
Sialic acid metabolism


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:0000252 Microcephaly "Microcephaly is a neurodevelopmental disorder in which the circumference of the head is more than two standard deviations smaller than the age- and gender-dependent norm." [HPO:curators]
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 HP:0000365 Hearing loss 
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 HP:0000572 Visual loss 
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 HP:0000648 Optic atrophy 
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 HP:0000737 Irritability 
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 HP:0001034 Hyperpigmented macules 
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 HP:0001252 Muscular hypotonia "Muscular hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is characterized by a diminished resistance to passive stretching." [HPO:curators]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001266 Choreoathetosis 
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 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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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:0001344 Absent speech development 
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 HP:0001508 Failure to thrive 
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 HP:0002013 Vomiting 
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 HP:0002069 Generalized tonic-clonic seizures "Generalized tonic-clonic seizures are `generalized seizures` (HP:0002197) in which the patient suddenly loses conciousness, the eyes roll back, and the entire body musculature undergoes tonic contractions. In the clonic phase of the seizure, there are rhythmic contractions of the musculature alternating with relaxation of all muscle groups. Loss of sphincter control during the seizure is common. This form of seizure was formerly commonly called grand mal seizure." [HPO:curators]
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 HP:0002133 Status epilepticus 
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 HP:0002283 Diffuse brain atrophy 
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 HP:0002376 Developmental regression 
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 HP:0002395 Lower limb hyperreflexia 
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 HP:0006834 Developmental stagnation at onset of seizures 
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 HP:0008872 Feeding problems in infancy 
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 HP:0012391 Hyporeflexia of upper limbs "Reduced intensity of muscle tendon reflexes in the upper limbs. Reflexes are elicited by stretching the tendon of a muscle, e.g., by tapping." [HPO:probinson]
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 HP:0100704 Cortical visual impairment "A form of loss of vision caused by damage to the visual cortex rather than a defect in the eye." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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