ZNF733P zinc finger protein 733, pseudogene [Homo sapiens (human)] - Gene

Summary

Official Symbol: ZNF733Pprovided by HGNC
Official Full Name: zinc finger protein 733, pseudogeneprovided by HGNC
Primary source: HGNC:HGNC:32473
See related: Ensembl:ENSG00000290558 AllianceGenome:HGNC:32473
Gene type: pseudo
RefSeq status: VALIDATED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: ZNF733
Expression: Restricted expression toward testis (RPKM 1.3) See more
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Genomic context

Location:: 7q11.21

Exon count:: 3

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	7	NC_000007.14 (63291287..63304056, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	7	NC_060931.1 (64490006..64502775, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	7	NC_000007.13 (62751665..62764434, complement)

Chromosome 7 - NC_000007.14 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?

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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

SHGC-83805 (e-PCR)
- UniSTS:101788

SHGC-144883 (e-PCR)
- UniSTS:172475

D7S1945 (e-PCR)
- UniSTS:12486

RH121583 (e-PCR)
- UniSTS:134355

GDB:1317750 (e-PCR)
- UniSTS:42483

Other Names

Putative zinc finger protein ENSP00000353728
zinc finger protein 479 pseudogene

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.