RecName: Full=Magnesium transporter NIPA4; AltName: Full=Ichthyin; Alt - Protein

Analyze this sequence

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Identify Conserved Domains
View conserved domains detected in this protein sequence using CD-search.

Articles about the NIPAL4 gene

Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital Ichthyosis. [PLoS One. 2021]
Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital Ichthyosis.
Charfeddine C, Laroussi N, Mkaouar R, Jouini R, Khayat O, Redissi A, Mosbah A, Dallali H, Chedly Debbiche A, Zaouak A, et al. PLoS One. 2021; 16(10):e0258777. Epub 2021 Oct 20.
Identification of a novel missense mutation in NIPAL4 gene: First 3D model construction predicted its pathogenicity. [Mol Genet Genomic Med. 2020]
Identification of a novel missense mutation in NIPAL4 gene: First 3D model construction predicted its pathogenicity.
Laadhar S, Ben Mansour R, Marrakchi S, Miled N, Ennouri M, Fischer J, Kaddechi MA, Turki H, Fakhfakh F. Mol Genet Genomic Med. 2020 Mar; 8(3):e1104. Epub 2019 Dec 26.
Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4. [Hum Mutat. 2019]
Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4.
Ballin N, Hotz A, Bourrat E, Küsel J, Oji V, Bouadjar B, Brognoli D, Hickman G, Heinz L, Vabres P, et al. Hum Mutat. 2019 Dec; 40(12):2318-2333. Epub 2019 Sep 6.

See all...

Reference sequence information

RefSeq genomic sequence
See the genomic reference sequence for the NIPAL4 gene (NG_016626.1).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the NIPAL4 gene.

More about the NIPAL4 gene

This gene likely encodes a membrane receptor. Mutations in this gene have been associated with autosomal recessive congenital ichthyosis. [p...
Also Known As: ARCI6, ICHTHYIN, ICHYN,...

LinkOut to external resources

Q0D2K0 [Domain Mapping of Disease Mut...]
Q0D2K0
Domain Mapping of Disease Mutations
Reactome [Reactome]
Reactome

Recent activity

Clear Turn Off Turn On

7461[uid] (1)
Taxonomy
MULTISPECIES: multidrug efflux transporter transcriptional repressor AcrR [Enter...
MULTISPECIES: multidrug efflux transporter transcriptional repressor AcrR [Enterobacteriaceae]
gi|446023882|ref|WP_000101737.1|

Protein
cytosolic phospholipase A2 zeta isoform X4 [Ailuropoda melanoleuca]
cytosolic phospholipase A2 zeta isoform X4 [Ailuropoda melanoleuca]
gi|1126232585|ref|XP_019657522.1|

Protein
cytochrome oxidase subunit 1, partial (mitochondrion) [Ceratinopsis labradorensi...
cytochrome oxidase subunit 1, partial (mitochondrion) [Ceratinopsis labradorensis]
gi|1509152935|gb|AYQ20968.1|

Protein
cytochrome oxidase subunit 1, partial (mitochondrion) [Agape arctioides]
cytochrome oxidase subunit 1, partial (mitochondrion) [Agape arctioides]
gi|460841891|gb|AGH15274.1|

Protein

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Protein

Result Filters

Send to:

RecName: Full=Magnesium transporter NIPA4; AltName: Full=Ichthyin; AltName: Full=NIPA-like protein 4; AltName: Full=Non-imprinted in Prader-Willi/Angelman syndrome region protein 4

Supplemental Content

Analyze this sequence

Articles about the NIPAL4 gene

Reference sequence information

More about the NIPAL4 gene

LinkOut to external resources

Recent activity