Pidd1 | ENSMUSG00000025507 | NCBI 57913

Details for: Pidd1

Gene ID: 57913

Symbol: Pidd1

Ensembl ID: ENSMUSG00000025507

Description: p53 induced death domain protein 1

Associated with

Gene expression (transcription)
(R-MMU-74160)
Generic transcription pathway
(R-MMU-212436)
Rna polymerase ii transcription
(R-MMU-73857)
Tp53 regulates transcription of caspase activators and caspases
(R-MMU-6803207)
Tp53 regulates transcription of cell death genes
(R-MMU-5633008)
Transcriptional regulation by tp53
(R-MMU-3700989)
Activation of cysteine-type endopeptidase activity involved in apoptotic process
(GO:0006919)
Apoptotic process
(GO:0006915)
Apoptotic signaling pathway
(GO:0097190)
Cytoplasm
(GO:0005737)
Cytosol
(GO:0005829)
Dna damage response
(GO:0006974)
Dna damage response, signal transduction by p53 class mediator resulting in cell cycle arrest
(GO:0006977)
Endopeptidase activity
(GO:0004175)
Endopeptidase complex
(GO:1905369)
Extrinsic apoptotic signaling pathway
(GO:0097191)
Extrinsic apoptotic signaling pathway via death domain receptors
(GO:0008625)
Golgi apparatus
(GO:0005794)
Hydrolase activity
(GO:0016787)
Negative regulation of apoptotic process
(GO:0043066)
Nucleolus
(GO:0005730)
Nucleus
(GO:0005634)
Positive regulation of apoptotic process
(GO:0043065)
Protein autoprocessing
(GO:0016540)
Protein binding
(GO:0005515)
Regulation of canonical nf-kappab signal transduction
(GO:0043122)
Signal transduction
(GO:0007165)

Other Information

Proteins

Leucine-rich repeat and death domain-containing protein

Genular Protein ID: 3712434097

Symbol: PIDD1_MOUSE

Name: Leucine-rich repeat and death domain-containing protein

UniProtKB Accession Codes:

Q9ERV7 A6H6F4

Database IDs:

Citations:

PubMed ID: 10973264

Title: Pidd, a new death-domain-containing protein, is induced by p53 and promotes apoptosis.

PubMed ID: 10973264

DOI: 10.1038/79102

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 22279524

Title: Genetic mapping and exome sequencing identify variants associated with five novel diseases.

PubMed ID: 22279524

DOI: 10.1371/journal.pone.0028936

Sequence Information:

Length: 915
Mass: 101141
Checksum: 49FAA7B91D08E135
Sequence:

MAAVLEGQEP EETAAAAEDA ATSTLEAVDA GPGAPFLPAG NQLNLDLRPG GCHRLQYLCS 
QQPPQLLQVE FLRLSTHEDP QLLDDTLAKV PWSLLRLRSL VLKGGQSRGA LGACLHGTLT 
TLPAGLSDLA CLAHLDLSFN RLETLPTCVP ELHGLDALLL SHNHLSELPE ALGALPALTF 
LTVTHNRLER LPLTLGSLST LQRLDLSENL LDTIPSEIGN LRSLSELNLA SNRLQSLPAS 
LAGLRSLRLL VLHSNLLTSV PTGLVHLPLI TRLDLRDNRL RDLPAELLDA PFVRLQGNPL 
GEASPAPPSP PDISQVPEMP RLLLTSDLDS FLVTPHGCSV TLACGVRLQF PAGATTTPVT 
IHYRLWLPEP GLVSLGPHDF LLSSVLELQP HGVAFQQDVS LWLLFVPPRV RRCREVVVRT 
RSNNTWNDLE TQLEEEAPKR LWARCQVPHF SWFLVVLRPV SNTCLLPPEG ALLCSSGHPG 
VRVTFPPGVT EEPRQVSMQV VHMAGLELRT LLEESEASVS PLLCLSQSGP PSFLQPVTVQ 
LPLPPGVTGF SLDRSHLHLL YRTPLTTTWD DITTQVALEF THLYARFQVT HFSWYWLWYT 
TKTCVGGLAR KAWERLRLHR VNLIALQRRR DPEQVLLQCL PRNKVDATLS RLLVRYRGPE 
PSETVEMFEG EKFFAAFERG IDVDADRPDC VDGRICFVFY SHLKNVKEVY ITTALDREAQ 
DVRGQVSFYR GSLPVEVPAE AEAARQRKGT DALWMATLPI KLPRLRGAQG SGQGTDFSLM 
PLNLGDAETG FLTQSNLLSV ASRLGPDWPA VALHLGMPYH KLQRIRHEFR DDLDGQVRHM 
LFSWAERQTG QPGAVGHLVQ ALEQSDRRDV AEEVRAILEL GRHKYQDSIR RTGLAPEDST 
LPGTSASQTP ESAQA

The gene details are incomplete or unavailable at the moment.

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.