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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_001395720.2 → NP_001382649.1 tumor necrosis factor receptor superfamily member 10B precursor
Status: VALIDATED
- Source sequence(s)
-
JAXUCZ010000015
- UniProtKB/TrEMBL
- A0A0G2JZE1, B8YBG7
- Related
- ENSRNOP00000063335.6, ENSRNOT00000066128.6
- Conserved Domains (2) summary
-
- cd08315
Location:243 → 329
- Death_TRAILR_DR4_DR5; Death domain of Tumor necrosis factor-Related Apoptosis-Inducing Ligand Receptors
- cd10580
Location:34 → 133
- TNFRSF10; Tumor necrosis factor receptor superfamily member 10 (TNFRSF10), includes TNFRSF10A (DR4), TNFRSF10B (DR5), TNFRSF10C (DcR1) and TNFRSF10D (DcR2)
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 GRCr8
Genomic
-
NC_086033.1 Reference GRCr8
- Range
-
51249883..51278091
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_063274494.1 → XP_063130564.1 tumor necrosis factor receptor superfamily member 10B isoform X1
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_001108873.1: Suppressed sequence
- Description
- NM_001108873.1: This RefSeq was removed because currently there is insufficient support for the transcript and the protein.