ENSG00000177239


Homo sapiens

Features
Gene ID: ENSG00000177239
  
Biological name :MAN1B1
  
Synonyms : MAN1B1 / mannosidase alpha class 1B member 1 / Q9UKM7
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 9
Strand: 1
Band: q34.3
Gene start: 137086927
Gene end: 137109187
  
Corresponding Affymetrix probe sets: 218636_s_at (Human Genome U133 Plus 2.0 Array)   65884_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000450147
Ensembl peptide - ENSP00000448658
Ensembl peptide - ENSP00000483132
Ensembl peptide - ENSP00000360645
Ensembl peptide - ENSP00000440314
Ensembl peptide - ENSP00000441398
Ensembl peptide - ENSP00000444189
Ensembl peptide - ENSP00000444966
NCBI entrez gene - 11253     See in Manteia.
OMIM - 604346
RefSeq - XM_017014239
RefSeq - NM_016219
RefSeq - XM_006716945
RefSeq Peptide - NP_057303
swissprot - H0YGV7
swissprot - H0YI64
swissprot - H0YIU0
swissprot - A0A087X064
swissprot - Q9UKM7
swissprot - H0YFU3
swissprot - H0YGQ1
swissprot - H0YG20
Ensembl - ENSG00000177239
  
Related genetic diseases (OMIM): 614202 - Mental retardation, autosomal recessive 15, 614202
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
 man1b1aENSDARG00000073792Danio rerio
 man1b1bENSDARG00000076592Danio rerio
 MAN1B1ENSGALG00000037375Gallus gallus
 A2AJ15ENSMUSG00000036646Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
MAN1A2 / O60476 / mannosidase alpha class 1A member 2ENSG0000019816228
MAN1A1 / P33908 / mannosidase alpha class 1A member 1ENSG0000011188528
MAN1C1 / Q9NR34 / mannosidase alpha class 1C member 1ENSG0000011764327


Protein motifs (from Interpro)
Interpro ID Name
 IPR001382  Glycoside hydrolase family 47
 IPR036026  Seven-hairpin glycosidases


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006486 protein glycosylation IEA
 biological_processGO:0006491 N-glycan processing IBA
 biological_processGO:0008152 metabolic process IEA
 biological_processGO:0009311 oligosaccharide metabolic process TAS
 biological_processGO:0030433 ubiquitin-dependent ERAD pathway IEA
 biological_processGO:0036508 protein alpha-1,2-demannosylation IDA
 biological_processGO:0036509 trimming of terminal mannose on B branch TAS
 biological_processGO:0036510 trimming of terminal mannose on C branch TAS
 biological_processGO:0036511 trimming of first mannose on A branch TAS
 biological_processGO:0036512 trimming of second mannose on A branch TAS
 biological_processGO:1904380 endoplasmic reticulum mannose trimming IMP
 biological_processGO:1904382 mannose trimming involved in glycoprotein ERAD pathway TAS
 cellular_componentGO:0000139 Golgi membrane IBA
 cellular_componentGO:0005783 endoplasmic reticulum TAS
 cellular_componentGO:0005789 endoplasmic reticulum membrane IEA
 cellular_componentGO:0005794 Golgi apparatus TAS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0044322 endoplasmic reticulum quality control compartment TAS
 cellular_componentGO:1903561 extracellular vesicle HDA
 molecular_functionGO:0003824 catalytic activity IEA
 molecular_functionGO:0004571 mannosyl-oligosaccharide 1,2-alpha-mannosidase activity IEA
 molecular_functionGO:0005509 calcium ion binding IEA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0016798 hydrolase activity, acting on glycosyl bonds IEA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
Defective MAN1B1 causes MRT15
ER Quality Control Compartment (ERQC)


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:0000219 Thin upper lip 
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 HP:0000268 Dolichocephaly 
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 HP:0000272 Malar hypoplasia "Underdeveloped midface region." [HPO:curators]
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 HP:0000276 Long face 
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 HP:0000307 Pointed chin 
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 HP:0000316 Hypertelorism 
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 HP:0000319 Flat philtrum 
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 HP:0000322 Short philtrum 
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 HP:0000431 Broad nasal bridge "Increased horizontal dimension of the upper, bony part of the nose." [HPO:curators]
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 HP:0000448 Prominent nose 
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 HP:0000494 Downward slanting palpebral fissures 
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 HP:0000718 Aggressive behavior "Aggressive behavior can denote verbal aggression, physical aggression against objects, physical aggression against people, and may also include aggression towards oneself." [HPO:curators]
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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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:0001513 Obesity "A status with BODY WEIGHT that is grossly above the acceptable or desirable weight, usually due to accumulation of excess FATS in the body. The standards may vary with age, sex, genetic or cultural background. In the BODY MASS INDEX, a BMI greater than 30.0 kg/m2 is considered obese, and a BMI greater than 40.0 kg/m2 is considered morbidly obese (MORBID OBESITY)." [MeSH:D009765]
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 HP:0002342 Mental retardation, moderate "Moderate mental retardation is defined as an intelligence quotient (IQ) in the range of 35-49." [HPO:curators]
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 HP:0004523 very long eyelashes and eyebrows 
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 HP:0011229 Broad eyebrow "Regional increase in the width (height) of the eyebrow." [pmid:19125427]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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