SEMA4A Polyclonal Antibody, 20ul Recombinant Ab Production Defects in TMEM237 are a

Defects in TMEM237 are a cause of Joubert syndrome-14

The 5' untranslated region of this gene is alternatively spliced

The estrogen receptor 1 localizes to the nucleus where it may form a homodimer or a heterodimer with estrogen receptor 2

Midline-1 encoded by this MID1 is a member of the tripartite motif (TRIM) family

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SEMA4A Polyclonal Antibody, 20ul Recombinant Ab Production Defects in TMEM237 are aSEMA4A encodes a member of the semaphorin family of soluble and transmembrane proteins. Semaphorins are involved in numerous functions, including axon guidance, morphogenesis, carcinogenesis, and immunomodulation. The encoded protein is a single pass type I membrane protein containing an immunoglobulin like C2 type domain, a PSI domain and a sema domain. It inhibits axonal extension by providing local signals to specify territories inaccessible for