ANKRD30BP1 ankyrin repeat domain 30B pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: ANKRD30BP1provided by HGNC
Official Full Name: ankyrin repeat domain 30B pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:19722
See related: Ensembl:ENSG00000175302 AllianceGenome:HGNC:19722
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: PRED4; ANKRD30BP; C21orf110
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Genomic context

Location:: 21q11.2

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	21	NC_000021.9 (13384241..13427775, complement)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	21	NC_060945.1 (11728581..11772122, complement)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	21	NC_000021.8 (14756562..14800096, complement)

Chromosome 21 - NC_000021.9 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

D21S215 (e-PCR)
- UniSTS:146948

G48498 (e-PCR)
- UniSTS:95558

SHGC-170076 (e-PCR)
- UniSTS:173727

D21S308 (e-PCR)
- UniSTS:147692

SHGC-51833 (e-PCR)
- UniSTS:22765

D21S369 (e-PCR)
- UniSTS:148207

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.