DYSF
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 2[13]
- Cytogenetic location
- 2p13.2[16]
- Expressed in
- blood, muscle of thigh, Skeletal muscle tissue of rectus abdominis, triceps brachii muscle, apex of heart, vastus lateralis muscle, external globus pallidus, gastrocnemius muscle, Skeletal muscle tissue of biceps brachii, glutes[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- autosomal recessive limb-girdle muscular dystrophy[14]
- HomoloGene ID
- 20748[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en DYSF
en dysferlin
en FER1L1
en LGMD2B
en LGMDR2
en MMD1
zh Dysferlin蛋白
zh DYSF基因
zh 戴斯弗林蛋白
🔖 Identifiers · 14
- OpenAlex ID
- C37113945
- Image (Wikimedia Commons)
- 4ihb pdb.png ↗
- DeCS ID
- 57102
- Ensembl gene ID
- ENSG00000135636
- Ensembl transcript ID
- ENST00000494501, ENST00000258104, ENST00000394120, ENST00000409366, ENST00000409582, ENST00000409651, ENST00000409744, ENST00000409762, ENST00000410020, ENST00000410041, ENST00000413539, ENST00000429174, ENST00000461565, ENST00000468173, ENST00000472873, ENST00000475076, ENST00000479049, ENST00000487180, ENST00000493767
- Entrez Gene ID
- 8291
- Exact match
- identifiers.org
- Freebase ID
- /m/09p2m0
- HGNC ID
- 3097
- HGNC gene symbol
- DYSF
- Microsoft Academic ID (discontinued)
- 37113945
- OMIM ID
- 603009
Show all 14 identifiers +2
- RefSeq RNA ID
- XM_005264585, NM_001130455, NM_001130976, NM_001130977, NM_001130978, NM_001130979, NM_001130980, NM_001130981, NM_001130982, NM_001130983, NM_001130984, NM_001130985, NM_001130986, NM_001130987, NM_003494, XM_005264584
- UMLS CUI
- C1414209
🔗 Connections
Expressed in 5
Chromosome 1
Found in taxon 1
Instance of 1
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