LAMB2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 3[14]
- Cytogenetic location
- 3p21.31[18]
- Encodes
- Laminin subunit beta 2, Laminin subunit beta-2[11][12]
- Expressed in
- apex of heart, right lobe of thyroid gland, stromal cell of endometrium, right ovary, left ovary, right adrenal cortex, left lobe of thyroid gland, ascending aorta, Descending thoracic aorta, canal of the cervix[19][20][21][22][23][24][25][26][27][28]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- Pierson syndrome, LAMB2-related infantile-onset nephrotic syndrome[15][16]
- HomoloGene ID
- 1723[3]
- Strand orientation
- reverse strand[17]
🏷️ Also known as
en LAMB2
en Laminin, beta 2
en laminin subunit beta 2
en LAMS
en NPHS5
en PIERS
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000172037
- Ensembl transcript ID
- ENST00000542580, ENST00000305544, ENST00000418109, ENST00000462930, ENST00000464891, ENST00000467506, ENST00000469665, ENST00000477225, ENST00000477701, ENST00000480640, ENST00000483057, ENST00000483321, ENST00000484713, ENST00000486298, ENST00000488638, ENST00000493571, ENST00000494831, ENST00000498377, ENST00000538659
- Entrez Gene ID
- 3913
- Exact match
- identifiers.org
- Freebase ID
- /m/02kg7v8
- HGNC ID
- 6487
- HGNC gene symbol
- LAMB2
- OMIM ID
- 150325
- RefSeq RNA ID
- XM_005265127, NM_002292
- UMLS CUI
- C1416781
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