ACD

GENERAL INFORMATION

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Gene name

ACD

Gene description

Adrenocortical dysplasia homolog (mouse)

Protein class

Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

6
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Normal tissues showed weak to moderate nuclear staining with occasional cytoplasmic positivity. Trophoblastic cells, decidual cells, adrenal, salivary gland and chondrocytes exhibited strong nuclear immunoreactivity. Cells in glomeruli, hematopoietic cells and the CNS tissues were negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA057660
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RNA AND PROTEIN EXPRESSION SUMMARY

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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

Adrenal gland

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

ACD (HGNC Symbol)

Synonyms

Pip1, Ptop, Tint1, Tpp1

Description

Adrenocortical dysplasia homolog (mouse) (HGNC Symbol)

Entrez gene summary

This gene encodes a protein that is involved in telomere function. This protein is one of six core proteins in the telosome/shelterin telomeric complex, which functions to maintain telomere length and to protect telomere ends. Through its interaction with other components, this protein plays a key role in the assembly and stabilization of this complex, and it mediates the access of telomerase to the telomere. Multiple transcript variants encoding different isoforms have been found for this gene. This gene, which is also referred to as TPP1, is distinct from the unrelated TPP1 gene on chromosome 11, which encodes tripeptidyl-peptidase I. [provided by RefSeq, Jul 2008]

Chromosome

16

Cytoband

q22.1

Chromosome location (bp)

67657512 - 67660815

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000102977 (version 78.38)

Entrez gene

65057

UniProt

Q96AP0 (UniProt - Evidence at protein level)

neXtProt

NX_Q96AP0

Antibodypedia

ACD antibodies


PROTEIN BROWSER

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ENST00000219251
 
ENST00000393919
 
ENST00000602320
 
ENST00000602382
 
ENST00000620338
 
ENST00000620761
 
 
 
 


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)

ACD-001 ENSP00000377496
ENST00000393919
Q96AP0
Show all »
Show » Show » 544 57.7 No 0
ACD-002 ENSP00000219251
ENST00000219251
Q96AP0
Show all »
Show » Show » 541 57.4 No 0
ACD-003 ENSP00000473679
ENST00000602320
R4GNJ5
Show all »
Show » Show » 442 47.1 No 0
ACD-012 ENSP00000473313
ENST00000602382
Show » 182 18.9 No 0
ACD-014 ENSP00000478084
ENST00000620761
Q96AP0
Show all »
Show » Show » 458 49 No 0
ACD-201 ENSP00000483117
ENST00000620338
Q96AP0
Show all »
Show » Show » 544 57.7 No 0