MLXIPL

GENERAL INFORMATION

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Gene name

MLXIPL

Gene description

MLX interacting protein-like

Protein class

Disease related genes
Plasma proteins
Predicted intracellular proteins
Predicted secreted proteins
Transcription factors

Predicted localization

Intracellular,Secreted

Number of transcripts

7
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (adipose tissue, adrenal gland, duodenum, kidney, liver, small intestine, testis)
GTEx:Tissue enhanced (liver)

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Group enriched (adipose tissue, adrenal gland, duodenum, kidney, liver, small intestine, testis)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (liver)

Organ

Expression



GENE INFORMATION

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Gene name

MLXIPL (HGNC Symbol)

Synonyms

bHLHd14, CHREBP, MIO, MONDOB, WBSCR14, WS-bHLH

Description

MLX interacting protein-like (HGNC Symbol)

Entrez gene summary

This gene encodes a basic helix-loop-helix leucine zipper transcription factor of the Myc/Max/Mad superfamily. This protein forms a heterodimeric complex and binds and activates, in a glucose-dependent manner, carbohydrate response element (ChoRE) motifs in the promoters of triglyceride synthesis genes. The gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. [provided by RefSeq, Jul 2008]

Chromosome

7

Cytoband

q11.23

Chromosome location (bp)

73593194 - 73624543

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000009950 (version 78.38)

Entrez gene

51085

UniProt

Q9NP71 (UniProt - Evidence at protein level)

neXtProt

NX_Q9NP71

Antibodypedia

MLXIPL antibodies


PROTEIN BROWSER

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ENST00000313375
 
ENST00000354613
 
ENST00000414749
 
ENST00000429400
 
ENST00000434326
 
ENST00000453275
 
ENST00000456640
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

MLXIPL-001 ENSP00000320886
ENST00000313375
Q9NP71
Show all »
Show » Show » 852 93.1 Yes 0
MLXIPL-002 ENSP00000346629
ENST00000354613
Q9NP71
Show all »
Show » Show » 831 90.7 Yes 0
MLXIPL-003 ENSP00000392636
ENST00000434326
Q9NP71
Show all »
Show » Show » 721 78.2 Yes 0
MLXIPL-006 ENSP00000395172
ENST00000453275
C9JDF5
Show all »
Show » 213 23.1 Yes 0
MLXIPL-007 ENSP00000402615
ENST00000456640
H7C1V3
Show all »
Show » 235 26.7 No 0
MLXIPL-010 ENSP00000412330
ENST00000414749
Q9NP71
Show all »
Show » Show » 850 92.8 Yes 0
MLXIPL-011 ENSP00000406296
ENST00000429400
Q9NP71
Show all »
Show » Show » 833 90.9 Yes 0