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CRYGEP crystallin gamma E, pseudogene [ Homo sapiens (human) ]

Gene ID: 200575, updated on 25-Jan-2022

Summary

Official Symbol
CRYGEPprovided by HGNC
Official Full Name
crystallin gamma E, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:2412
See related
Ensembl:ENSG00000229150 AllianceGenome:HGNC:2412
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
G2; CCL; CRYG5; CRYGEP1; D2S1472
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Genomic context

See CRYGEP in Genome Data Viewer
Location:
2q33.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (208108164..208112668, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (208972888..208977392, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene ribosomal protein L12 pseudogene 17 Neighboring gene uncharacterized LOC105373854 Neighboring gene uncharacterized LOC100507443 Neighboring gene crystallin gamma D Neighboring gene replication factor C subunit 2 pseudogene Neighboring gene crystallin gamma C

Genomic regions, transcripts, and products

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_002762.5 

    Range
    101..4605
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    208108164..208112668 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 PATCHES

Genomic

  1. NW_018654710.1 Reference GRCh38.p13 PATCHES

    Range
    106458..110962 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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