IMPACT | ENSG00000154059 | NCBI 55364

Details for: IMPACT

Gene ID: 55364

Symbol: IMPACT

Ensembl ID: ENSG00000154059

Description: impact RWD domain protein

Associated with

Cellular responses to stimuli
(R-HSA-8953897)
Cellular responses to stress
(R-HSA-2262752)
Cellular response to starvation
(R-HSA-9711097)
Response of eif2ak4 (gcn2) to amino acid deficiency
(R-HSA-9633012)
Actin binding
(GO:0003779)
Biological_process
(GO:0008150)
Cellular response to amino acid starvation
(GO:0034198)
Cellular_component
(GO:0005575)
Cytoplasm
(GO:0005737)
Gcn2-mediated signaling
(GO:0140469)
Intracellular signal transduction
(GO:0035556)
Molecular_function
(GO:0003674)
Negative regulation of protein phosphorylation
(GO:0001933)
Negative regulation of transcription by rna polymerase ii
(GO:0000122)
Neuron projection extension
(GO:1990138)
Positive regulation of neuron differentiation
(GO:0045666)
Protein binding
(GO:0005515)
Protein sequestering activity
(GO:0140311)
Regulation of cytoplasmic translational initiation in response to stress
(GO:1990611)
Regulation of translational initiation
(GO:0006446)
Ribosome binding
(GO:0043022)

Other Information

Proteins

Protein IMPACT

Genular Protein ID: 2804914496

Symbol: IMPCT_HUMAN

Name: Protein IMPACT

UniProtKB Accession Codes:

Q9P2X3 A8MXG0 Q49AM0 Q9H2X4

Database IDs:

Citations:

PubMed ID: 11116084

Title: Comparative genome analysis of the mouse imprinted gene impact and its nonimprinted human homolog IMPACT: toward the structural basis for species-specific imprinting.

PubMed ID: 11116084

DOI: 10.1101/gr.139200

PubMed ID: 11244491

Title: Human homolog of the mouse imprinted gene Impact resides at the pericentric region of chromosome 18 within the critical region for bipolar affective disorder.

PubMed ID: 11244491

DOI: 10.1038/sj.mp.4000799

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 16177791

Title: DNA sequence and analysis of human chromosome 18.

PubMed ID: 16177791

DOI: 10.1038/nature03983

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: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 24275569

Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

PubMed ID: 24275569

DOI: 10.1016/j.jprot.2013.11.014

PubMed ID: 27607563

Title: Loss of the proprioception and touch sensation channel PIEZO2 in siblings with a progressive form of contractures.

PubMed ID: 27607563

DOI: 10.1111/cge.12850

Sequence Information:

Length: 320
Mass: 36476
Checksum: 75AAB91E00594212
Sequence:

MAEGDAGSDQ RQNEEIEAMA AIYGEEWCVI DDCAKIFCIR ISDDIDDPKW TLCLQVMLPN 
EYPGTAPPIY QLNAPWLKGQ ERADLSNSLE EIYIQNIGES ILYLWVEKIR DVLIQKSQMT 
EPGPDVKKKT EEEDVECEDD LILACQPESS LKALDFDISE TRTEVEVEEL PPIDHGIPIT 
DRRSTFQAHL APVVCPKQVK MVLSKLYENK KIASATHNIY AYRIYCEDKQ TFLQDCEDDG 
ETAAGGRLLH LMEILNVKNV MVVVSRWYGG ILLGPDRFKH INNCARNILV EKNYTNSPEE 
SSKALGKNKK VRKDKKRNEH

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.

Details for: IMPACT

Associated with

Other Information

Comparative genome analysis of the mouse imprinted gene impact and its nonimprinted human homolog IMPACT: toward the structural basis for species-specific imprinting. PubMed ID: 11116084

Human homolog of the mouse imprinted gene Impact resides at the pericentric region of chromosome 18 within the critical region for bipolar affective disorder. PubMed ID: 11244491

Complete sequencing and characterization of 21,243 full-length human cDNAs. PubMed ID: 14702039

DNA sequence and analysis of human chromosome 18. PubMed ID: 16177791

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). PubMed ID: 15489334

Initial characterization of the human central proteome. PubMed ID: 21269460

An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome. PubMed ID: 24275569

Loss of the proprioception and touch sensation channel PIEZO2 in siblings with a progressive form of contractures. PubMed ID: 27607563