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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)
-
NM_001398143.1 → NP_001385072.1 somatostatin receptor type 4
Status: VALIDATED
- Source sequence(s)
-
BU328445, CD214700, DQ069274, HAEK01129201, KF527718
- UniProtKB/TrEMBL
- A0A3S5ZP53, F1NVL8, Q4PLA6
- Related
- ENSGALP00010025982.1, ENSGALT00010043666.1
- Conserved Domains (1) summary
-
- cd15973
Location:42 → 317
- 7tmA_SSTR4; somatostatin receptor type 4, member of the class A family of seven-transmembrane G protein-coupled receptors
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
-
NC_052534.1 Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly
- Range
-
3518339..3520480 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate bGalGal1.pat.whiteleghornlayer.GRCg7w
Genomic
-
NC_052575.1 Alternate bGalGal1.pat.whiteleghornlayer.GRCg7w
- Range
-
3442188..3444329 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.
-
NM_001031518.1: Suppressed sequence
- Description
- NM_001031518.1: This RefSeq was removed because currently there is insufficient support for the transcript.