Gene
LAMB1
laminin subunit beta 1
- HGNC 6486↗(opens in a new tab)
- Ensembl gene ENSG00000091136↗(opens in a new tab)
- NCBI Gene 3912↗(opens in a new tab)
Summary
- Cytogenetic location
- 7q31.1
- Coordinates
- Chromosome 7: 107,923,799–108,003,161 (GRCh38)
- Exons
- 34 exons across 79.4 kb
- Protein
- 1,786 amino acids
- Previous symbols
- CLM
- MANE Select transcript
- ENST00000222399.11NM_002291.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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No Genome Test report reads LAMB1 yet. The test sequences your whole genome, so your data includes it all the same.
How LAMB1 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 5.7 kb of the gene's 79.4 kb; 5,361 of those bases code for the protein.
How a genome test reads LAMB1
18
positions in LAMB1 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 79.4 kb of LAMB1, introns included, not only the 5.7 kb of exons.
Traits linked to LAMB1
The Human Phenotype Ontology lists these as features of the rare conditions LAMB1 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Abnormal cerebral white matter morphology
- Anterograde memory impairment
- Balance impairment
- Bilateral tonic-clonic seizure with generalized onset
- Cerebellar hemisphere hypoplasia
- Cerebellar vermis hypoplasia
- Confusion
- Depression
Show 28 more traits
- Difficulty articulating speech
- Epilepsy
- Hyperintensity of cerebral white matter on MRI
- Impaired executive functioning
- Intellectual disability
- Intention tremor
- Lack of feeling, emotion, interest
- Lack of insight
- Migraine without aura
- Motor delay
- Numbness
- Pins and needles feeling
- Small brainstem
- Too much cerebrospinal fluid in the brain
- Type II lissencephaly
- Typical absence seizure
- Word-finding difficulty
- Abnormal myelination
- Dysgyria
- Gray matter heterotopia
- Memory impairment
- Severe global developmental delay
- Small cerebellum
- Underdevelopment of part of brain called corpus callosum
- Cavity within brain
- Global developmental delay
- Leukoencephalopathy
- Subcortical band heterotopia
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.
- 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 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). LAMB1 gene: laminin subunit beta 1. Retrieved 16 October 2026, from https://dantelabs.com/genes/lamb1
Dante Labs. LAMB1 gene: laminin subunit beta 1 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/lamb1
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