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Index / GenWay / Wolf-Hirschhorn syndrome candidate 2 protein variant - / Product Detail : 10-288-22230F Wolf-Hirschhorn syndrome candidate 2 protein variant -
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#10-288-22230F Wolf-Hirschhorn syndrome candidate 2 protein variant -
| Price : | 494 | EUR |
| 561 | USD | |
| 383 | GBP | |
| 2076 | Zloty | |
| 66130 | JPY | |
| 3811 | NOK | |
| 4084 | SEK | |
| 559 | CHF |
Product name : Wolf-Hirschhorn syndrome candidate 2 protein variant -
Catalog number : 10-288-22230F
Quantity: 0.1 mg
Availability: Yes
Supplier name : GenWay
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Related products : Wolf-Hirschhorn syndrome candidate 2 protein variant -
Gentaurpub
WP1049: G Protein Signaling Pathways
WP1165: G Protein Signaling Pathways
WP1371: G Protein Signaling Pathways
WP1438: Influenza A virus infection
WP1493: Carbon assimilation C4 pathway
WP1502: Mitochondrial biogenesis
WP1531: Vitamin D synthesis
WP1566: Citrate cycle (TCA cycle)
WP1613: 1,4-Dichlorobenzene degradation
WP1616: ABC transporters
WP1624: Bacterial secretion system
WP1625: Base excision repair
WP1644: DNA replication
WP1650: Fluorobenzoate degradation
WP1654: gamma-Hexachlorocyclohexane degradation
WP1657: Glycerolipid metabolism
WP1659: Glycine, serine and threonine metabolism
WP1661: Glyoxylate and dicarboxylate metabolism
WP1663: Homologous recombination
WP1665: Limonene and pinene degradation
WP1672: Mismatch repair
WP1673: Naphthalene and anthracene degradation
WP1675: Nitrogen metabolism
WP1676: Non-homologous end-joining
WP1678: Nucleotide excision repair
Related Genes :
[NSD2 KIAA1090 MMSET TRX5 WHSC1] Histone-lysine N-methyltransferase NSD2 (EC 2.1.1.43) (Multiple myeloma SET domain-containing protein) (MMSET) (Nuclear SET domain-containing protein 2) (Protein trithorax-5) (Wolf-Hirschhorn syndrome candidate 1 protein)
[Nsd2 Kiaa1090 Whsc1] Histone-lysine N-methyltransferase NSD2 (EC 2.1.1.43) (Multiple myeloma SET domain-containing protein) (MMSET) (Nuclear SET domain-containing protein 2) (Wolf-Hirschhorn syndrome candidate 1 protein homolog)
[NSD3 WHSC1L1 DC28] Histone-lysine N-methyltransferase NSD3 (EC 2.1.1.43) (Nuclear SET domain-containing protein 3) (Protein whistle) (WHSC1-like 1 isoform 9 with methyltransferase activity to lysine) (Wolf-Hirschhorn syndrome candidate 1-like protein 1) (WHSC1-like protein 1)
[NELFA WHSC2 P/OKcl.15] Negative elongation factor A (NELF-A) (Wolf-Hirschhorn syndrome candidate 2 protein)
[Nsd3 Whsc1l1] Histone-lysine N-methyltransferase NSD3 (EC 2.1.1.43) (Nuclear SET domain-containing protein 3) (Wolf-Hirschhorn syndrome candidate 1-like protein 1 homolog) (WHSC1-like protein 1)
[GAA] Lysosomal alpha-glucosidase (EC 3.2.1.20) (Acid maltase) (Aglucosidase alfa) [Cleaved into: 76 kDa lysosomal alpha-glucosidase; 70 kDa lysosomal alpha-glucosidase]
[Nelfa Whsc2 Whsc2h] Negative elongation factor A (NELF-A) (Wolf-Hirschhorn syndrome candidate 2 homolog) (mWHSC2)
[ADA ADA1] Adenosine deaminase (EC 3.5.4.4) (Adenosine aminohydrolase)
[TP53 P53] Cellular tumor antigen p53 (Antigen NY-CO-13) (Phosphoprotein p53) (Tumor suppressor p53)
[MSX1 HOX7] Homeobox protein MSX-1 (Homeobox protein Hox-7) (Msh homeobox 1-like protein)
[Nelfa Whsc2 rCG_35875] Negative elongation factor complex member A (Wolf-Hirschhorn syndrome candidate 2 (Human))
[ABCA1 ABC1 CERP] ATP-binding cassette sub-family A member 1 (ATP-binding cassette transporter 1) (ABC-1) (ATP-binding cassette 1) (Cholesterol efflux regulatory protein)
[whsc1 RP71-77D7.3-001] Novel protein similar to vertebrate Wolf-Hirschhorn syndrome candidate 1 (WHSC1) (Fragment)
[whsc1] Wolf-Hirschhorn syndrome candidate 1 protein (Fragment)
[LETM1] LETM1 and EF-hand domain-containing protein 1, mitochondrial (Leucine zipper-EF-hand-containing transmembrane protein 1)
[] Cytochrome c oxidase subunit 1 (EC 1.9.3.1) (Fragment)
[HMGA2 HMGIC] High mobility group protein HMGI-C (High mobility group AT-hook protein 2)
[whsc1] Wolf-Hirschhorn syndrome candidate 1 (Fragment)
[whsc1 RP71-77D7.2-001] Novel protein similar to vertebrate Wolf-Hirschhorn syndrome candidate 1 (WHSC1) (Fragment)
[SCN1A NAC1 SCN1] Sodium channel protein type 1 subunit alpha (Sodium channel protein brain I subunit alpha) (Sodium channel protein type I subunit alpha) (Voltage-gated sodium channel subunit alpha Nav1.1)
[NR5A1 AD4BP FTZF1 SF1] Steroidogenic factor 1 (SF-1) (STF-1) (hSF-1) (Adrenal 4-binding protein) (Fushi tarazu factor homolog 1) (Nuclear receptor subfamily 5 group A member 1) (Steroid hormone receptor Ad4BP)
[whsc1l1] Wolf-Hirschhorn syndrome candidate 1-like 1 (Fragment)
[C9JY66] Wolf-Hirschhorn syndrome candidate 1-like 1 (Fragment)
[WHSC1L1] Wolf-Hirschhorn syndrome candidate 1-like 1 (Fragment)
[WHSC1L1] Wolf-Hirschhorn syndrome candidate 1-like 1 (Fragment)
[NELFA WHSC2] Wolf-Hirschhorn syndrome candidate 2
[MDM38 YOL027C] Mitochondrial distribution and morphology protein 38
[AR DHTR NR3C4] Androgen receptor (Dihydrotestosterone receptor) (Nuclear receptor subfamily 3 group C member 4)
[] M-lycotoxin-Hc1a (M-LCTX-Hc1a) (Lycotoxin I) (Lycotoxin-1)
[] Wolf-Hirschhorn syndrome candidate 1-like 1 (Fragment)
Bibliography :
[28538178] Wolf-Hirschhorn Syndrome Candidate 1 Is Necessary for Correct Hematopoietic and B Cell Development.
[28444681] [Wolf-Hirschhorn syndrome. Description of a Spanish cohort of 51 cases and a literature review].
[28407363] De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome.
[28397211] [Application of chromosomal microarray analysis for the diagnosis of children with intellectual disability/developmental delay and a normal karytype].
[28377151] Treatment of intractable seizure in Wolf-Hirschhorn syndrome with bromide.
[28281478] Single port laparoscopic splenectomy for wandering spleen with splenomegaly in a patient with Wolf-Hirschhorn syndrome.
[28266898] Hepatic Malignancy in an Infant with Wolf-Hirschhorn Syndrome.
[28260054] Epigenetic activation of WHSC1 functions as an oncogene and is associated with poor prognosis in cervical cancer.
[28228401] Wolf-Hirschhorn syndrome candidate 1-like 1 epigenetically regulates nephrin gene expression.
[28186593] [Prenatal diagnosis of a case with 46,XX,del(4),dup(21)].
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