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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.
Genomic
-
NG_027679.1 RefSeqGene
- Range
-
4993..86880
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_001370402.1 → NP_001357331.1 tyrosine-protein kinase BAZ1B
Status: REVIEWED
- Source sequence(s)
-
AC005074, AC005089
- Consensus CDS
-
CCDS5549.1
- UniProtKB/Swiss-Prot
- B9EGK3, D3DXE9, O95039, O95247, O95277, Q6P1K4, Q86UJ6, Q9UIG0
- Related
- ENSP00000385442.1, ENST00000404251.1
- Conserved Domains (7) summary
-
- cd05505
Location:1344 → 1440
- Bromo_WSTF_like; Bromodomain; Williams syndrome transcription factor-like subfamily (WSTF-like). The Williams-Beuren syndrome deletion transcript 9 is a putative transcriptional regulator. WSTF was found to play a role in vitamin D-mediated transcription as part of two ...
- smart00571
Location:604 → 668
- DDT; domain in different transcription and chromosome remodeling factors
- cd15628
Location:1186 → 1231
- PHD_BAZ1B; PHD finger found in bromodomain adjacent to zinc finger domain protein 1B (BAZ1B)
- pfam15613
Location:898 → 1025
- WSD; Williams-Beuren syndrome DDT (WSD), D-TOX E motif
- pfam10537
Location:21 → 120
- WAC_Acf1_DNA_bd; ATP-utilising chromatin assembly and remodelling N-terminal
- pfam15612
Location:727 → 767
- WHIM1; WSTF, HB1, Itc1p, MBD9 motif 1
- pfam17380
Location:664 → 877
- DUF5401; Family of unknown function (DUF5401)
-
NM_032408.4 → NP_115784.1 tyrosine-protein kinase BAZ1B
See identical proteins and their annotated locations for NP_115784.1
Status: REVIEWED
- Source sequence(s)
-
AC005089, AF084479, BC136520, DA739467
- Consensus CDS
-
CCDS5549.1
- UniProtKB/Swiss-Prot
- B9EGK3, D3DXE9, O95039, O95247, O95277, Q6P1K4, Q86UJ6, Q9UIG0
- Related
- ENSP00000342434.4, ENST00000339594.9
- Conserved Domains (7) summary
-
- cd05505
Location:1344 → 1440
- Bromo_WSTF_like; Bromodomain; Williams syndrome transcription factor-like subfamily (WSTF-like). The Williams-Beuren syndrome deletion transcript 9 is a putative transcriptional regulator. WSTF was found to play a role in vitamin D-mediated transcription as part of two ...
- smart00571
Location:604 → 668
- DDT; domain in different transcription and chromosome remodeling factors
- cd15628
Location:1186 → 1231
- PHD_BAZ1B; PHD finger found in bromodomain adjacent to zinc finger domain protein 1B (BAZ1B)
- pfam15613
Location:898 → 1025
- WSD; Williams-Beuren syndrome DDT (WSD), D-TOX E motif
- pfam10537
Location:21 → 120
- WAC_Acf1_DNA_bd; ATP-utilising chromatin assembly and remodelling N-terminal
- pfam15612
Location:727 → 767
- WHIM1; WSTF, HB1, Itc1p, MBD9 motif 1
- pfam17380
Location:664 → 877
- DUF5401; Family of unknown function (DUF5401)
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_000007.14 Reference GRCh38.p14 Primary Assembly
- Range
-
73440406..73522293 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_047421016.1 → XP_047276972.1 tyrosine-protein kinase BAZ1B isoform X1
Alternate T2T-CHM13v2.0
Genomic
-
NC_060931.1 Alternate T2T-CHM13v2.0
- Range
-
74640900..74722781 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_054359303.1 → XP_054215278.1 tyrosine-protein kinase BAZ1B 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_023005.2: Suppressed sequence
- Description
- NM_023005.2: This RefSeq was permanently suppressed because currently there is an insufficient support for the 3' UTR of this transcript, and it is a nonsense-mediated decay (NMD) candidate.