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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_001007255.3 → NP_001007256.1 kelch domain-containing protein 9 isoform b
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) uses an alternate splice site compared to variant 1, that causes a frameshift. The resulting isoform (b) is shorter and has a distinct C-terminus compared to isoform a.
- Source sequence(s)
-
AL591806, AY601914, BC066896, BG718418
- Consensus CDS
-
CCDS41425.1
- UniProtKB/Swiss-Prot
-
Q8NEP7
- Related
- ENSP00000376030.2, ENST00000392192.6
- Conserved Domains (2) summary
-
- PLN02153
Location:11 → 164
- PLN02153; epithiospecifier protein
- sd00038
Location:28 → 76
- Kelch; KELCH repeat [structural motif]
-
NM_152366.5 → NP_689579.3 kelch domain-containing protein 9 isoform a
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the longer isoform (a).
- Source sequence(s)
-
AL591806, BC022077, BC066896, BG718418
- Consensus CDS
-
CCDS30919.1
- UniProtKB/Swiss-Prot
- Q5SY56, Q6NXT9, Q6PKN4, Q8N5E1, Q8NA16, Q8NEP7
- Related
- ENSP00000356990.4, ENST00000368011.9
- Conserved Domains (3) summary
-
- sd00038
Location:28 → 76
- Kelch; KELCH repeat [structural motif]
- pfam01344
Location:78 → 118
- Kelch_1; Kelch motif
- pfam13415
Location:37 → 85
- Kelch_3; Galactose oxidase, central domain
RNA
-
NR_033385.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) contains an alternate 5' terminal exon compared to variant 1. This variant is represented as non-coding because it lacks a large portion of the coding region, including the translational start codon, found in variant 1.
- Source sequence(s)
-
BC022077, BI549017, BP379202, BQ638407, BU173744
- Related
-
ENST00000490724.6
-
NR_033386.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (4) contains an alternate 5' terminal exon and uses an alternate splice site in an internal exon, compared to variant 1. This variant is represented as non-coding because it lacks a large portion of the coding region, including the translational start codon, found in variant 1.
- Source sequence(s)
-
BC022077, BI549017, BP379202, BU173744
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 GRCh38.p14 Primary Assembly
Genomic
-
NC_000001.11 Reference GRCh38.p14 Primary Assembly
- Range
-
161098361..161100346
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060925.1 Alternate T2T-CHM13v2.0
- Range
-
160235842..160237827
- 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_001007256.1: Suppressed sequence
- Description
- NM_001007256.1: This RefSeq was permanently suppressed because currently there is insufficient support for the protein.