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NF1P1 neurofibromin 1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100419006, updated on 17-Sep-2024

Summary

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Official Symbol
NF1P1provided by HGNC
Official Full Name
neurofibromin 1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:7772
See related
Ensembl:ENSG00000270831
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
NF1HHS
Annotation information
Note: The name of this locus was changed from NF1P2 to NF1P1 in collaboration with HGNC. [13 Sep 2011]
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Genomic context

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See NF1P1 in Genome Data Viewer
Location:
15q11.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (20916682..20935708, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (19732483..19751510)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (21122011..21141037, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene vomeronasal 1 receptor 61 pseudogene Neighboring gene zinc finger protein 519 pseudogene 2 Neighboring gene microRNA 5701-1 Neighboring gene long intergenic non-protein coding RNA 1193 Neighboring gene olfactory receptor family 11 subfamily J member 2 pseudogene

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2. Kehrer-Sawatzki H, et al. Hum Genet, 1997 Oct. PMID 9341878
  2. Detection of a neurofibromatosis type I (NF1) homologous sequence by PCR: implications for the diagnosis and screening of genetic diseases. Gasparini P, et al. Mol Cell Probes, 1993 Oct. PMID 8264676
  3. NF1-related locus on chromosome 15. Legius E, et al. Genomics, 1992 Aug. PMID 1505963
  4. Identification of neurofibromatosis 1 (NF1) homologous loci by direct sequencing, fluorescence in situ hybridization, and PCR amplification of somatic cell hybrids. Purandare SM, et al. Genomics, 1995 Dec 10. PMID 8825634

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • Albright osteodystrophy

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_025283.2 

    Range
    101..19127
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000015.10 Reference GRCh38.p14 Primary Assembly

    Range
    20916682..20935708 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_021160017.1 Reference GRCh38.p14 PATCHES

    Range
    1138190..1181006 complement
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1 Alternate T2T-CHM13v2.0

    Range
    19732483..19751510
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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