Gene
ANLN
anillin, actin binding protein
- HGNC 14082↗(opens in a new tab)
- Ensembl gene ENSG00000011426↗(opens in a new tab)
- NCBI Gene 54443↗(opens in a new tab)
Summary
- Cytogenetic location
- 7p14.2
- Coordinates
- Chromosome 7: 36,389,862–36,453,791 (GRCh38)
- Exons
- 24 exons across 63.9 kb
- Protein
- 1,124 amino acids
- Also known as
- ANILLIN, Scraps, scra
- MANE Select transcript
- ENST00000265748.7NM_018685.5
- Locus type
- Protein-coding
- Very high
- Confident
- Low
- Very low
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/genes/anln.json"
page <- fromJSON(url)
page$gene$nameRead ANLN, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated reports relevant to this gene
Focal Segmental Glomerulosclerosis
A renal disorder characterized by sclerotic lesions in the glomeruli. Causes include drugs, viruses, and malignancies (lymphomas), or it may be idiopathic. It presents with asymptomatic proteinuria or nephritic syndrome and it may lead to renal failure.
- 1 GenCC submitter rates it definitive or strong
Glomerulosclerosis
A hardening of the kidney glomerulus caused by scarring of the blood vessels.
- 1 GenCC submitter rates it definitive or strong
How ANLN is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 4.7 kb of the gene's 63.9 kb; 3,375 of those bases code for the protein.
Sequencing ANLN
2
positions in ANLN where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 63.9 kb of ANLN, introns included, not only the 4.7 kb of exons.
Genes linked to the same conditions
- ACTN4actinin alpha 4Shares 2 conditions
- CRB2crumbs cell polarity complex component 2Shares 2 conditions
- FAT1FAT atypical cadherin 1Shares 2 conditions
- INF2inverted formin 2Shares 2 conditions
- MYO1Emyosin IEShares 2 conditions
- PAX2paired box 2Shares 2 conditions
- TRPC6transient receptor potential cation channel subfamily C member 6Shares 2 conditions
Traits linked to ANLN
The Human Phenotype Ontology lists these as features of the rare conditions ANLN can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-17: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.17-8666dff2.
Cite this page
Dante Labs. (n.d.). ANLN gene: anillin, actin binding protein. Retrieved 17 October 2026, from https://dantelabs.com/genes/anln
Dante Labs. ANLN gene: anillin, actin binding protein [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/anln
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks