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- NCIT_C119650 IAO_0000115 "Human SH3PXD2B wild-type allele is located in the vicinity of 5q35.1 and is approximately 129 kb in length. This allele, which encodes SH3 and PX domain-containing protein 2B, plays a role in podosome assembly. Mutation of the gene is associated with Frank-Ter Haar syndrome." @default.
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- NCIT_C119650 NCIT_P106 "Gene or Genome" @default.
- NCIT_C119650 NCIT_P108 "SH3PXD2B wt Allele" @default.
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- NCIT_C119650 hasExactSynonym "FAD49" @default.
- NCIT_C119650 hasExactSynonym "FLJ20831" @default.
- NCIT_C119650 hasExactSynonym "FTHS" @default.
- NCIT_C119650 hasExactSynonym "HOFI" @default.
- NCIT_C119650 hasExactSynonym "KIAA1295" @default.
- NCIT_C119650 hasExactSynonym "SH3 and PX Domains 2B wt Allele" @default.
- NCIT_C119650 hasExactSynonym "SH3PXD2B wt Allele" @default.
- NCIT_C119650 hasExactSynonym "TKS4" @default.
- NCIT_C119650 hasExactSynonym "TSK4" @default.
- NCIT_C119650 type Class @default.
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- NCIT_C119650 label "SH3PXD2B wt Allele" @default.
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