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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_001163391.2 → NP_001156863.1 zinc finger and SCAN domain-containing protein 12
See identical proteins and their annotated locations for NP_001156863.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (1), as well as variant 10, encodes the functional protein.
- Source sequence(s)
-
Z98745
- Consensus CDS
-
CCDS93876.1
- UniProtKB/Swiss-Prot
- A0A024RCI2, A8K187, O43309, O43724
- UniProtKB/TrEMBL
-
A0A804HJ42
- Related
- ENSP00000507347.1, ENST00000684592.1
- Conserved Domains (4) summary
-
- smart00431
Location:42 → 152
- SCAN; leucine rich region
- COG5048
Location:299 → 579
- COG5048; FOG: Zn-finger [General function prediction only]
- sd00017
Location:499 → 519
- ZF_C2H2; C2H2 Zn finger [structural motif]
- pfam00096
Location:581 → 603
- zf-C2H2; Zinc finger, C2H2 type
-
NM_001368124.1 → NP_001355053.1 zinc finger and SCAN domain-containing protein 12
Status: VALIDATED
- Description
- Transcript Variant: This variant (10), as well as variant 1, encodes the functional protein.
- Source sequence(s)
-
Z98745
- Consensus CDS
-
CCDS93876.1
- UniProtKB/Swiss-Prot
- A0A024RCI2, A8K187, O43309, O43724
- UniProtKB/TrEMBL
-
A0A804HJ42
- Conserved Domains (4) summary
-
- smart00431
Location:42 → 152
- SCAN; leucine rich region
- COG5048
Location:299 → 579
- COG5048; FOG: Zn-finger [General function prediction only]
- sd00017
Location:499 → 519
- ZF_C2H2; C2H2 Zn finger [structural motif]
- pfam00096
Location:581 → 603
- zf-C2H2; Zinc finger, C2H2 type
RNA
-
NR_028077.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) contains alternate 3' exon structure, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AL358785, AL602228, BC041661, CX868415
-
NR_133668.1 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) does not share exon structure with the protein-coding variant (1). This variant (3) shares 3' exons with variant (2) but uses an alternate 5' exon. This variant is represented as non-coding because it lacks all of the coding region, including the translational start codon, found in variant 1.
- Source sequence(s)
-
AL358785, CX868415, DB014565, Z98745
-
NR_133669.1 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (4) does not share exon structure with the protein-coding variant (1). This variant (4) shares 3' exons with variant (2) but uses an alternate 5' exon. This variant is represented as non-coding because it lacks all of the coding region, including the translational start codon, found in variant 1.
- Source sequence(s)
-
AL358785, BI829158, CX868415, DA301736, Z98745
-
NR_136509.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (5) contains alternate 3' exon structure, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AL358785, AL602228, BC041661, CX868415, Z98745
-
NR_136510.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (6) uses an alternate splice site in an internal exon and contains alternate 3' exon structure, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AL358785, AL602228, BC041661, BF091581, BF091593, CX868415, Z98745
-
NR_136511.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (7) contains alternate 3' exon structure, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AL358785, AL602228, BC041661, CX868415
-
NR_136512.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (8) uses an alternate splice site in an internal exon and contains alternate 3' exon structure, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AL358785, AL602228, BC041661, CX868415, Z98745
-
NR_136513.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (9) lacks three exons and contains alternate 3' exon structure, compared to variant 1. This variant is represented as non-coding because it lacks the entire ORF found in variant 1.
- Source sequence(s)
-
AL358785, AL602228, BC041661, CX868415
-
NR_160526.1 RNA Sequence
Status: VALIDATED
- Source sequence(s)
-
AL358785, Z98745
-
NR_160527.1 RNA Sequence
Status: VALIDATED
- Source sequence(s)
-
AL358785, Z98745
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_000006.12 Reference GRCh38.p14 Primary Assembly
- Range
-
28378821..28399747 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_047419596.1 → XP_047275552.1 zinc finger and SCAN domain-containing protein 12 isoform X3
- Related
- ENSP00000380039.3, ENST00000396827.3
-
XM_047419597.1 → XP_047275553.1 zinc finger and SCAN domain-containing protein 12 isoform X4
-
XM_047419599.1 → XP_047275555.1 zinc finger and SCAN domain-containing protein 12 isoform X5
-
XM_047419595.1 → XP_047275551.1 zinc finger and SCAN domain-containing protein 12 isoform X1
- UniProtKB/Swiss-Prot
- A0A024RCI2, A8K187, O43309, O43724
- UniProtKB/TrEMBL
-
A0A804HJ42
-
XM_047419594.1 → XP_047275550.1 zinc finger and SCAN domain-containing protein 12 isoform X1
- UniProtKB/Swiss-Prot
- A0A024RCI2, A8K187, O43309, O43724
- UniProtKB/TrEMBL
-
A0A804HJ42
-
XM_047419598.1 → XP_047275554.1 zinc finger and SCAN domain-containing protein 12 isoform X2
Alternate T2T-CHM13v2.0
Genomic
-
NC_060930.1 Alternate T2T-CHM13v2.0
- Range
-
28250381..28271202 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_054356893.1 → XP_054212868.1 zinc finger and SCAN domain-containing protein 12 isoform X1
-
XM_054356894.1 → XP_054212869.1 zinc finger and SCAN domain-containing protein 12 isoform X2
RNA
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XR_008487513.1 RNA Sequence
-
XR_008487514.1 RNA Sequence
-
XR_008487515.1 RNA Sequence
-
XR_008487512.1 RNA Sequence
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_014724.2: Suppressed sequence
- Description
- NM_014724.2: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.