- Gene Overview
- Interaction Network
- Sequence Verification
CARMIL2, capping protein regulator and myosin 1 linker 2
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This gene encodes a member of the CARMIL (capping protein, Arp2/3, myosin-I linker) family of proteins. The encoded protein interacts with and negatively regulates the heterodimeric capping protein and promotes cell migration. Reduced expression of this gene has been observed in human psoriasis patients. Mutations in this gene cause a human immunodeficiency syndrome characterized by smooth muscle tumors and impaired T-cell function. [provided by RefSeq, May 2017]
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Gene Synonyms (CARMIL2b, IMD58, LRRC16C, RLTPR, capping protein, Arp2/3 and myosin-I linker protein 2, F-actin-uncapping protein RLTPR, RGD motif, leucine rich repeats, tropomodulin domain and proline-rich containing, RGD, leucine-rich repeat, tropomodulin and proline-rich containing protein, leucine rich repeat containing 16C, leucine-rich repeat-containing protein 16C,)
- NCBI Gene ID:
146206
- Species:
Homo sapiens (Human)
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UNIPROT ID#>>Q6F5E8
- View the NCBI Database
for this Gene »
Gene products are often involved in multiple pathways and networks within a living
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capping protein regulator and myosin 1 linker 2 interacts with:
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