Version: 8.1.0
Date: Fri Apr 18 2025
1,059 results for nipa2

Nipa2

(Rattus norvegicus)
Gene
Name: NIPA magnesium transporter 2
Synonyms: SLC56A2, RGD1306051, similar to hypothetical protein MGC5466, non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human), LOC308667, magnesium transporter NIPA2, solute carrier family 56 member 2, non imprinted in Prader-Willi/Angelman syndrome 2 homolog, non imprinted in Prader-Willi/Angelman syndrome 2
Source: RGD:1306051
Biotype: protein coding gene
Symbol: Nipa2 (Rno)
Symbol: Nipa2
Gene Synopsis: Orthologous to human NIPA2 (NIPA magnesium transporter 2); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine
Automated Gene Synopsis: Orthologous to human NIPA2 (NIPA magnesium transporter 2).
Synonyms: magnesium transporter NIPA2
Strict Orthology Symbols: nipa2

nipa2

(Danio rerio)
Gene
Name: NIPA magnesium transporter 2
Synonyms: wu:fb72g02, zgc:66088, fb72g02
Source: ZFIN:ZDB-GENE-040426-2134
Biotype: protein coding gene
Symbol: nipa2 (Dre)
Symbol: nipa2
Automated Gene Synopsis: Orthologous to human NIPA2 (NIPA magnesium transporter 2).
Strict Orthology Symbols: nipa2

NIPA2

(Homo sapiens)
Gene
Name: NIPA magnesium transporter 2
Synonyms: non-imprinted in Prader-Willi/Angelman syndrome region protein 2, SLC57A2, MGC5466, magnesium transporter NIPA2, non imprinted in Prader-Willi/Angelman syndrome 2
Source: HGNC:17044
Biotype: protein coding gene
Symbol: NIPA2 (Hsa)
Symbol: NIPA2
Synonyms: magnesium transporter NIPA2
Strict Orthology Symbols: nipa2

Nipa2

(Mus musculus)
Gene
Name: non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human)
Synonyms: RGD1306051, SLC56A2, RIKEN cDNA 2600017P10 gene, 3830408P04Rik, RIKEN cDNA 3830408P04 gene, 2600017P10Rik
Source: MGI:1913918
Biotype: protein coding gene
Symbol: Nipa2 (Mmu)
Symbol: Nipa2
Automated Gene Synopsis: Orthologous to human NIPA2 (NIPA magnesium transporter 2).
Strict Orthology Symbols: nipa2
Alleles: Nipa2 (Mmu)

nipa2

(Xenopus tropicalis)
Gene
Name: NIPA magnesium transporter 2
Synonyms: NIPA magnesium transporter 2, nipa2
Source: Xenbase:XB-GENE-973321
Biotype: gene
Symbol: nipa2
Symbol: nipa2 (Xtr)
Automated Gene Synopsis: Orthologous to human NIPA2 (NIPA magnesium transporter 2).
Synonyms: nipa2...nipa2...nipa2
Strict Orthology Symbols: nipa2

nipa2.S

(Xenopus laevis)
Gene
Name: NIPA magnesium transporter 2
Synonyms: NIPA magnesium transporter 2, nipa2.S
Source: Xenbase:XB-GENE-17344002
Biotype: gene
Symbol: nipa2.S (Xla)
Automated Gene Synopsis: Orthologous to human NIPA2 (NIPA magnesium transporter 2).
Strict Orthology Symbols: nipa2
Symbol: nipa2.S

Nipa2tm1Lex

(Mus musculus)
Allele/Variant
Source: MGI:3529013
Genes: Nipa2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nipa2 (Mmu)
Genes: Nipa2 (Mmu)
Symbol: Nipa2tm1Lex

NIPA2P3

(Homo sapiens)
Gene
Name: NIPA2 pseudogene 3
Synonyms: non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 3, NIPA magnesium transporter 2 pseudogene 3
Source: HGNC:42043
Biotype: pseudogene
Symbol: NIPA2P3 (Hsa)
Symbol: NIPA2P3

NIPA2P4

(Homo sapiens)
Gene
Name: NIPA2 pseudogene 4
Synonyms: non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 4, NIPA magnesium transporter 2 pseudogene 4
Source: HGNC:42044
Biotype: pseudogene
Symbol: NIPA2P4 (Hsa)
Symbol: NIPA2P4

NIPA2P2

(Homo sapiens)
Gene
Name: NIPA2 pseudogene 2
Synonyms: non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 2, NIPA magnesium transporter 2 pseudogene 2
Source: HGNC:42042
Biotype: pseudogene
Symbol: NIPA2P2 (Hsa)
Symbol: NIPA2P2

NIPA2P5

(Homo sapiens)
Gene
Name: NIPA2 pseudogene 5
Synonyms: NIPA magnesium transporter 2 pseudogene 5, non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 5
Source: HGNC:42045
Biotype: pseudogene
Symbol: NIPA2P5 (Hsa)
Symbol: NIPA2P5

NIPA2P1

(Homo sapiens)
Gene
Name: NIPA2 pseudogene 1
Synonyms: non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 1, NIPA magnesium transporter 2 pseudogene 1
Source: HGNC:42041
Biotype: pseudogene
Symbol: NIPA2P1 (Hsa)
Symbol: NIPA2P1

nipa2uab383/+ (AB)

(Danio rerio)
Model
Id: ZFIN:ZDB-FISH-220322-33
Synonyms: Not Available
Symbol: nipa2 (AB) (Dre)
Genes: nipa2 (Dre)
Name: nipa2 (AB)

PLIN4

(Homo sapiens)
Gene
Name: perilipin 4
Synonyms: muscular dystrophy, with rimmed vacuoles, perilipin-4, MRUPAV, S3-12, NIPA2, adipocyte protein S3-12, KIAA1881, MDRV
Source: HGNC:29393
Biotype: protein coding gene
Synonyms: NIPA2...NIPA2

Nipal1

(Rattus norvegicus)
Gene
Name: NIPA-like domain containing 1
Synonyms: similar to NIPA2, Npal1, magnesium transporter NIPA3, RGD1310092, LOC289594
Source: RGD:1310092
Biotype: protein coding gene
Synonyms: similar to NIPA2

nipa-1

(Caenorhabditis elegans)
Gene
Name: NIPA1 (NonImprinted gene in Prader-Willi/Angelman syndrome region 1) homolog 1
Synonyms: CELE_Y53G8B.4, Y53G8B.4
Source: WB:WBGene00021820
Biotype: protein coding gene
Strict Orthology Symbols: nipa2

spict

(Drosophila melanogaster)
Gene
Name: spichthyin
Synonyms: CG12292, Spichthyin, spg6, Spict
Source: FB:FBgn0032451
Biotype: protein coding gene
Strict Orthology Symbols: nipa2

uab383

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-220322-36
Genes: nipa2 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: nipa2 (Dre)

magnesium ion transport

Gene Ontology
Source: GO:0015693
Synonyms:
  • magnesium transport
Branch: biological process
Genes: NIPA2 (Hsa)...Nipa2 (Mmu)...Nipa2 (Rno)...nipa2 (Dre)

la015913Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-120806-11566
Genes: nipa2 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: nipa2 (Dre)

magnesium ion transmembrane transporter activity

Gene Ontology
Source: GO:0015095
Synonyms: Not Available
Branch: molecular function
Genes: NIPA2 (Hsa)...Nipa2 (Mmu)...Nipa2 (Rno)...nipa2 (Dre)

magnesium ion transmembrane transport

Gene Ontology
Source: GO:1903830
Synonyms: Not Available
Branch: biological process
Genes: NIPA2 (Hsa)...Nipa2 (Mmu)...Nipa2 (Rno)

Hsap\NIPA2UAS.Tag:HA

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0353476
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Hsap\NIPA2
Construct Expressed Component: NIPA2 (Hsa)

hereditary spastic paraplegia

Disease
Source: DOID:2476
Definition: A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs.
Genes: NIPA2 (Hsa)...Nipa2 (Rno)...nipa2 (Xtr)...nipa2 (Dre)...Nipa2 (Mmu)

Df(chr6:cyfip1,nipa1,nipa2,tubgcp5,chst7)uab429/+ (AB)

(Danio rerio)
Model
Id: ZFIN:ZDB-FISH-221116-9
Synonyms: Not Available
Name: Df(chr6:cyfip1,nipa1,nipa2,tubgcp5,chst7)uab429/+ (AB)

early endosome

Gene Ontology
Source: GO:0005769
Synonyms: Not Available
Branch: cellular component
Genes: NIPA2 (Hsa)...Nipa2 (Rno)...Nipa2 (Mmu)

monoatomic ion transport

Gene Ontology
Source: GO:0006811
Synonyms:
  • ion transport
Branch: biological process
Genes: NIPA2 (Hsa)

(GRCh38)19:4510467G>T

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.4510467G>T
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4510467G>T
Gene Synonyms: NIPA2

(GRCh38)19:4511404T>G

(Homo sapiens)
Allele/Variant
Source: rs777879018
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4511404T>G
Gene Synonyms: NIPA2

(GRCh38)19:4511124C>T

(Homo sapiens)
Allele/Variant
Source: rs762943924
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4511124C>T
Gene Synonyms: NIPA2

(GRCh38)19:4511145C>T

(Homo sapiens)
Allele/Variant
Source: rs150943101
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4511145C>T
Gene Synonyms: NIPA2

(GRCh38)19:4511190G>A

(Homo sapiens)
Allele/Variant
Source: rs752898669
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4511190G>A
Gene Synonyms: NIPA2

(GRCh38)19:4504656G>A

(Homo sapiens)
Allele/Variant
Source: rs1976032459
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4504656G>A
Gene Synonyms: NIPA2

(GRCh38)19:4510517C>T

(Homo sapiens)
Allele/Variant
Source: rs199694958
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4510517C>T
Gene Synonyms: NIPA2

(GRCh38)19:4513295G>A

(Homo sapiens)
Allele/Variant
Source: rs373878422
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4513295G>A
Gene Synonyms: NIPA2

(GRCh38)19:4504944C>T

(Homo sapiens)
Allele/Variant
Source: rs755865538
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4504944C>T
Gene Synonyms: NIPA2

(GRCh38)19:4510956T>A

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.4510956T>A
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4510956T>A
Gene Synonyms: NIPA2

(GRCh38)19:4504547C>G

(Homo sapiens)
Allele/Variant
Source: rs567719914
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4504547C>G
Gene Synonyms: NIPA2

(GRCh38)19:4504569C>T

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.4504569C>T
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4504569C>T
Gene Synonyms: NIPA2

(GRCh38)19:4504697C>T

(Homo sapiens)
Allele/Variant
Source: rs778167684
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4504697C>T
Gene Synonyms: NIPA2

(GRCh38)19:4511501G>A

(Homo sapiens)
Allele/Variant
Source: rs544718313
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4511501G>A
Gene Synonyms: NIPA2

(GRCh38)19:4511601T>G

(Homo sapiens)
Allele/Variant
Source: rs768830418
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4511601T>G
Gene Synonyms: NIPA2

(GRCh38)19:4510887C>T

(Homo sapiens)
Allele/Variant
Source: rs370647633
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4510887C>T
Gene Synonyms: NIPA2

(GRCh38)19:4511204G>T

(Homo sapiens)
Allele/Variant
Source: rs746541245
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4511204G>T
Gene Synonyms: NIPA2

(GRCh38)19:4511701G>C

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.4511701G>C
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4511701G>C
Gene Synonyms: NIPA2

(GRCh38)19:4510843G>C

(Homo sapiens)
Allele/Variant
Source: rs200831658
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4510843G>C
Gene Synonyms: NIPA2

(GRCh38)19:4511886C>T

(Homo sapiens)
Allele/Variant
Source: rs779510597
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4511886C>T
Gene Synonyms: NIPA2

(GRCh38)19:4510764C>T

(Homo sapiens)
Allele/Variant
Source: rs1328177809
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4510764C>T
Gene Synonyms: NIPA2

(GRCh38)19:4511185G>A

(Homo sapiens)
Allele/Variant
Source: rs199625614
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4511185G>A
Gene Synonyms: NIPA2

(GRCh38)19:4511559T>G

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.4511559T>G
Genes: PLIN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)19:4511559T>G
Gene Synonyms: NIPA2