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.

mRNA and Protein(s)

1. NM_001389307.2 → NP_001376236.2  probable ATP-dependent RNA helicase DDX49

   Status: VALIDATED

   Source sequence(s)

   JAENSK010000376

   UniProtKB/TrEMBL

   A0A8V1A7P4, Q5ZLA8

   Related

   ENSGALP00010041970.1, ENSGALT00010068227.1

   Conserved Domains (1) summary

   COG0513
   Location:1 → 466

   SrmB; Superfamily II DNA and RNA helicase [Replication, recombination and repair]

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

This section includes genomic Reference Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate assemblies. Model RNAs and proteins are also reported here.

Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly

Genomic

1. NC_052559.1 Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly

   Range

   4164396..4170066 complement

   Download

   GenBank, FASTA, Sequence Viewer (Graphics)

Alternate bGalGal1.pat.whiteleghornlayer.GRCg7w

Genomic

1. NC_052600.1 Alternate bGalGal1.pat.whiteleghornlayer.GRCg7w

   Range

   3726901..3732583 complement

   Download

   GenBank, FASTA, Sequence Viewer (Graphics)

The following Reference Sequences have been suppressed. Explain

These RefSeqs were suppressed for the cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related sequence links, or BLAST links (BLink), but may still be retrieved by clicking on their accession.version below.

1. NM_001030938.1: Suppressed sequence

   Description

   NM_001030938.1: This RefSeq was removed because currently there is insufficient support for the transcript and the protein.