TAMALIN-AS1

Summary

TAMALIN-AS1 (TAMALIN antisense RNA 1, HGNC:32680) is a long non-coding RNA gene on chromosome 12q13.13.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:32680
Approved symbol	TAMALIN-AS1
Name	TAMALIN antisense RNA 1
Location	12q13.13
Locus type	RNA, long non-coding
Status	Approved
Entrez	692159
RNAcentral	URS0000BC446D — lncRNA, 1436 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 0

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

None — 0 exons

Expression profiles

Top tissues by expression

0 total, by Bgee expression score (0-100, higher = more expressed):

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Canonical reviewed UniProt: None (reviewed: )

All UniProt accessions (0):

RefSeq proteins (0): (*=MANE)

Domains & families (InterPro)

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 0 (showing top):

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

0 interactions, top by confidence:

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

0 variants total. Per-class counts are floors (≥ shown; pagination cap):

Classification	Count (floor)
Pathogenic	0
Likely pathogenic	0
Uncertain significance	0
Likely benign	0
Benign	0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000525479 (12:52008168 T>C), RS1000719644 (12:52008555 TG>T), RS1001041457 (12:52008418 C>A), RS1001173134 (12:52008291 G>A), RS1002074883 (12:52009080 G>A), RS1003025775 (12:52007823 G>A), RS1003546761 (12:52008054 T>C), RS1003630700 (12:52006546 G>A), RS1003769046 (12:52006623 C>A), RS1004105673 (12:52006312 G>A,T), RS1004749246 (12:52006122 A>G), RS1006393991 (12:52007804 C>T), RS1006447911 (12:52007570 C>T), RS1007447165 (12:52008892 T>C), RS1008248416 (12:52008336 G>A)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 0 entries

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.