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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_012277.1 RefSeqGene
- Range
-
5073..14286
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_001160124.2 → NP_001153596.1 Krueppel-like factor 6 isoform B
See identical proteins and their annotated locations for NP_001153596.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (B), also known as sv2, uses an alternate splice site in the central coding region that results in a frameshift, compared to variant A. The resulting isoform (B) has a shorter and distinct C-terminus, compared to isoform A.
- Source sequence(s)
-
AL450322, BC000311, BP357332, BQ017028
- UniProtKB/TrEMBL
-
D3GC14
- Conserved Domains (3) summary
-
- sd00017
Location:190 → 212
- ZF_C2H2; C2H2 Zn finger [structural motif]
- pfam00096
Location:218 → 240
- zf-C2H2; Zinc finger, C2H2 type
- pfam13465
Location:204 → 229
- zf-H2C2_2; Zinc-finger double domain
-
NM_001160125.2 → NP_001153597.1 Krueppel-like factor 6 isoform C
See identical proteins and their annotated locations for NP_001153597.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (C), also known as sv3, lacks an alternate exon in the 3' coding region that results in a frameshift, compared to variant A. The resulting isoform (C) has a shorter and distinct C-terminus, compared to isoform A.
- Source sequence(s)
-
AL450322, BC000311, BM695496, BP357332, BQ017028
- Consensus CDS
-
CCDS53490.1
- UniProtKB/Swiss-Prot
-
Q99612
- Related
- ENSP00000445301.1, ENST00000542957.1
- Conserved Domains (2) summary
-
- sd00017
Location:202 → 224
- ZF_C2H2; C2H2 Zn finger [structural motif]
- pfam00096
Location:200 → 224
- zf-C2H2; Zinc finger, C2H2 type
-
NM_001300.6 → NP_001291.3 Krueppel-like factor 6 isoform A
See identical proteins and their annotated locations for NP_001291.3
Status: REVIEWED
- Description
- Transcript Variant: This variant (A) represents the longest transcript and encodes the longest isoform (A).
- Source sequence(s)
-
AL450322, BC000311, BP357332, BQ017028
- Consensus CDS
-
CCDS7060.1
- UniProtKB/Swiss-Prot
- B2RE86, B4DDN0, D3DRR1, F5H3M5, Q5VUT7, Q5VUT8, Q99612, Q9BT79
- Related
- ENSP00000419923.1, ENST00000497571.6
- Conserved Domains (3) summary
-
- COG5048
Location:177 → 265
- COG5048; FOG: Zn-finger [General function prediction only]
- sd00017
Location:205 → 224
- ZF_C2H2; C2H2 Zn finger [structural motif]
- pfam00096
Location:260 → 282
- zf-C2H2; Zinc finger, C2H2 type
RNA
-
NR_027653.2 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (D), also known as sv1, uses an alternate splice site, compared to variant A. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant A, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AL450322, AL513303, BC000311, BP357332, BQ017028
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_000010.11 Reference GRCh38.p14 Primary Assembly
- Range
-
3775996..3785209 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060934.1 Alternate T2T-CHM13v2.0
- Range
-
3779895..3789103 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_001008490.1: Suppressed sequence
- Description
- NM_001008490.1: This RefSeq was suppressed because the 3'UTR structure is not strongly supported and it renders the transcript a candidate for nonsense-mediated decay (NMD).