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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_001394901.1 → NP_001381830.1 LIM and senescent cell antigen-like-containing domain protein 3 isoform b
Status: VALIDATED
- Source sequence(s)
-
AC013271
- Consensus CDS
-
CCDS92835.1
- UniProtKB/TrEMBL
-
A0A0J9YXC7
- Related
- ENSP00000488486.1, ENST00000480744.3
- Conserved Domains (5) summary
-
- cd09331
Location:72 → 130
- LIM1_PINCH; The first LIM domain of protein PINCH
- cd09332
Location:133 → 184
- LIM2_PINCH; The second LIM domain of protein PINCH
- cd09333
Location:197 → 247
- LIM3_PINCH; The third LIM domain of protein PINCH
- cd09334
Location:253 → 306
- LIM4_PINCH; The fourth LIM domain of protein PINCH
- cd09335
Location:314 → 367
- LIM5_PINCH; The fifth LIM domain of protein PINCH
-
NM_001426397.1 → NP_001413326.1 LIM and senescent cell antigen-like-containing domain protein 3 isoform c
Status: VALIDATED
- Source sequence(s)
-
CP068276
- UniProtKB/TrEMBL
-
B2R5G4
-
NM_033514.5 → NP_277049.1 LIM and senescent cell antigen-like-containing domain protein 3 isoform a
See identical proteins and their annotated locations for NP_277049.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the shorter isoform (a).
- Source sequence(s)
-
AF288404, BQ013290, BX108353, CF994716
- Consensus CDS
-
CCDS2084.1
- UniProtKB/Swiss-Prot
- A0A0A6YYD2, B4DPH6, C9K0W2, P0CW19, P0CW20, Q9HB10
- UniProtKB/TrEMBL
-
B2R5G4
- Related
- ENSP00000405165.2, ENST00000437679.3
- Conserved Domains (1) summary
-
- cl02475
Location:72 → 114
- LIM; LIM is a small protein-protein interaction domain, containing two zinc fingers
RNA
-
NR_027467.3 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) includes multiple additional 3' exons, compared to variant 1. This variant is represented as non-coding because the use of the supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AC013271, AI887629, BC171890, CF994716
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_000002.12 Reference GRCh38.p14 Primary Assembly
- Range
-
109898688..109925625
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060926.1 Alternate T2T-CHM13v2.0
- Range
-
110360332..110368101
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)