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NDE1 information


NDE1
Identifiers
AliasesNDE1, HOM-TES-87, LIS4, MHAC, NDE, NUDE, NUDE1, nudE neurodevelopment protein 1
External IDsOMIM: 609449 MGI: 1914453 HomoloGene: 32354 GeneCards: NDE1
Orthologs
SpeciesHumanMouse
Entrez

54820

67203

Ensembl

ENSG00000072864
ENSG00000275911

ENSMUSG00000022678

UniProt

Q9NXR1

Q9CZA6

RefSeq (mRNA)

NM_001143979
NM_017668

NM_001114085
NM_001285503
NM_001285504
NM_023317

RefSeq (protein)

NP_001137451
NP_060138

NP_001107557
NP_001272432
NP_001272433
NP_075806

Location (UCSC)Chr 16: 15.64 – 15.73 MbChr 16: 13.98 – 14.01 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Nuclear distribution protein nudE homolog 1 is a protein that in humans is encoded by the NDE1 gene.[5][6][7]

  1. ^ a b c ENSG00000275911 GRCh38: Ensembl release 89: ENSG00000072864, ENSG00000275911 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022678 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Kitagawa M, Umezu M, Aoki J, Koizumi H, Arai H, Inoue K (Sep 2000). "Direct association of LIS1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE". FEBS Lett. 479 (1–2): 57–62. doi:10.1016/S0014-5793(00)01856-1. PMID 10940388.
  6. ^ Meyer G, Perez-Garcia CG, Gleeson JG (Nov 2002). "Selective expression of doublecortin and LIS1 in developing human cortex suggests unique modes of neuronal movement". Cereb Cortex. 12 (12): 1225–36. doi:10.1093/cercor/12.12.1225. PMID 12427674.
  7. ^ "Entrez Gene: NDE1 nudE nuclear distribution gene E homolog 1 (A. nidulans)".

and 16 Related for: NDE1 information

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NDE1

Last Update:

homolog 1 is a protein that in humans is encoded by the NDE1 gene. Mutations in both copies of NDE1 cause microlissencephaly type 4. ENSG00000275911 GRCh38:...

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Microhydranencephaly

Last Update:

an autosomal recessive manner via a loss-of-function mutation of the gene NDE1. Jaxon Buell was born on August 27, 2014, with 80% of his brain, and most...

Word Count : 254

Cutis verticis gyrata

Last Update:

intellectual disability Hypertrophic osteoarthropathy, primary, autosomal dominant NDE1-related microhydranencephaly Necrotizing encephalomyelopathy, subacute, of...

Word Count : 1105

Exophthalmos

Last Update:

autosomal recessive Microcephaly 5, primary, autosomal recessive Muenke syndrome NDE1-related microhydranencephaly Neonatal pseudo-hydrocephalic progeroid syndrome...

Word Count : 1097

Microcephaly

Last Update:

Jan, M; Shaheen, R; Feng, Y; Walsh, CA (13 May 2011). "Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]". American Journal...

Word Count : 4199

Ciliopathy

Last Update:

syndrome 248700 PIEZO2 MASA syndrome 303350 L1CAM Microhydranencephaly 605013 NDE1 Mowat–Wilson syndrome 235730 ZEB2 NDH syndrome 610199 GLIS3 Oculoauriculofrontonasal...

Word Count : 2498

Microlissencephaly

Last Update:

inheritance. Mutation of RELN gene or CIT could cause MLIS. Human NDE1 mutations and mouse Nde1 loss lead to cortical lamination deficits, which, together with...

Word Count : 2704

NDEL1

Last Update:

neuronal function and development. Nde1 and Ndel1 were in the past referred to as NudE and NudEL respectively. The Nde1 protein is involved in nuclear migration...

Word Count : 2014

PDGFRB

Last Update:

t(5;14)(q32;q32) CCDC88C 14q32 t(5;14)(q33;q32) TP53BP1 15q22 t(5;15)q33;22) NDE1 16p13 t(5;16)(q33;p13) SPECC1 17p11 t(5;17)(q32;p11.2) NDEL1 17p13 t(5;17)(q32;p13)...

Word Count : 3403

Polymicrogyria

Last Update:

GPR56 (Bilateral frontoparietal PMG), TUBB2B (anterior predominant PMG), NDE1 (Diffuse PMG), AKT3 (Bilateral perisylvian PMG), and PIK3CA (Bilateral perisylvian...

Word Count : 3206

Radial glial cell

Last Update:

effects in the development of the nervous system. Mutations in either Lis1 or Nde1, essential proteins for radial glial differentiation and stabilization, cause...

Word Count : 2628

PITPNM3

Last Update:

in PITPNM function has not been established The LNS2 domain is the Lipin/Nde1/Smp2 domain. This domain was discovered as having sequence similarities to...

Word Count : 1094

Clonal hypereosinophilia

Last Update:

CCDC6, H4D10S170), GPIAP1, ETV6, ERC1, GIT2, NIN, TRIP11, CCDC88C TP53BP1, NDE1, SPECC1, NDEL1, MYO18A, BIN2, COL1A1, DTD1 CPSF6, RABEP1, MPRIP, SPTBN1,...

Word Count : 5760

PAFAH1B1

Last Update:

kilodaltons). PAFAH1B1 has been shown to interact with DYNC1H1, CLIP1, NDEL1, NDE1, PAFAH1B3, PAFAH1B2, NUDC, TUBA1A and Doublecortin. platelet-activating factor...

Word Count : 1514

MCRS1

Last Update:

Greene MI (Aug 2006). "p78/MCRS1 forms a complex with centrosomal protein Nde1 and is essential for cell viability". Oncogene. 25 (35): 4937–46. doi:10...

Word Count : 1199

ZNF365

Last Update:

Furuuchi K, Masuda K, Sato N, Greene MI (Oct 2006). "Centrosomal proteins Nde1 and Su48 form a complex regulated by phosphorylation". Oncogene. 25 (45):...

Word Count : 430
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