SLC31A1P1 solute carrier family 31 member 1 pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: SLC31A1P1provided by HGNC
Official Full Name: solute carrier family 31 member 1 pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:17124
See related: AllianceGenome:HGNC:17124
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: CTR1P; CTR1psi; SLC31A1P
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Genomic context

Location:: 3q26.31

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	3	NC_000003.12 (172599386..172604174, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	3	NC_060927.1 (175384442..175389237, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	3	NC_000003.11 (172317176..172321964, complement)

Chromosome 3 - NC_000003.12 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

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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Markers

D9S262 (e-PCR), detects polymorphism
- UniSTS:63922

RH65620 (e-PCR)
- UniSTS:90106

Other Names

CRT1 pseudogene
solute carrier family 31 (copper transporter), member 1 pseudogene 1
solute carrier family 31 (copper transporters), member 1 pseudogene 1

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.