MAN1B1

GENERAL INFORMATION

? »

Gene name

MAN1B1

Gene description

Mannosidase, alpha, class 1B, member 1

Protein class

Disease related genes
Enzymes
Plasma proteins
Potential drug targets
Predicted intracellular proteins
Predicted membrane proteins

Predicted localization

Intracellular,Membrane

Number of transcripts

5
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Most normal tissues displayed moderate to strong cytoplasmic positivity often with a granular or distinct dot-like pattern. Additional nuclear staining was exhibited in hepatocytes, prostate and urothelial cells. Pneumocytes, bile ducts, renal glomeruli, glial cells, white pulp of spleen and smooth muscle cells were generally negative.

ANTIBODY RELIABILITY

? »

Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA051516
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

? »

Gene name

MAN1B1 (HGNC Symbol)

Synonyms

MANA-ER, MRT15

Description

Mannosidase, alpha, class 1B, member 1 (HGNC Symbol)

Entrez gene summary

This gene encodes an enzyme belonging to the glycosyl hydrolase 47 family. This enzyme functions in N-glycan biosynthesis, and is a class I alpha-1,2-mannosidase that specifically converts Man9GlcNAc to Man8GlcNAc isomer B. It is required for N-glycan trimming to Man5-6GlcNAc2 in the endoplasmic-reticulum-associated degradation pathway. Mutations in this gene cause autosomal-recessive intellectual disability. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 11. [provided by RefSeq, Dec 2011]

Chromosome

9

Cytoband

q34.3

Chromosome location (bp)

137086927 - 137109187

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000177239 (version 78.38)

Entrez gene

11253

UniProt

Q9UKM7 (UniProt - Evidence at protein level)

neXtProt

NX_Q9UKM7

Antibodypedia

MAN1B1 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000371589
 
ENST00000475449
 
ENST00000535144
 
ENST00000542372
 
ENST00000550113
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

MAN1B1-003 ENSP00000448658
ENST00000475449
Show » Show » 270 29.5 No 0
MAN1B1-004 ENSP00000360645
ENST00000371589
Q9UKM7
Show all »
Show » Show » 699 79.6 No 1
MAN1B1-008 ENSP00000441398
ENST00000535144
H0YG20
Show all »
Show » Show » 695 79 No 1
MAN1B1-015 ENSP00000444189
ENST00000542372
Show » 182 20.8 No 1
MAN1B1-017 ENSP00000450147
ENST00000550113
Show » Show » 124 14.6 No 0