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- NCIT_C74966 IAO_0000115 "Human ALX4 wild-type allele is located in the vicinity of 11p11.2 and is approximately 50 kb in length. This allele, which encodes homeobox protein aristaless-like 4, plays a role in transcriptional regulation. Mutation of the gene is associated with parietal foramina 2." @default.
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- NCIT_C74966 NCIT_P100 "605420" @default.
- NCIT_C74966 NCIT_P102 "AF294629" @default.
- NCIT_C74966 NCIT_P106 "Gene or Genome" @default.
- NCIT_C74966 NCIT_P108 "ALX4 wt Allele" @default.
- NCIT_C74966 NCIT_P207 "C2698717" @default.
- NCIT_C74966 NCIT_P321 "60529" @default.
- NCIT_C74966 NCIT_P366 "ALX4_wt_Allele" @default.
- NCIT_C74966 NCIT_P98 "Deletion of the chromosomal region in which the ALX4 gene resides is associated with Potocki-Shaffer syndrome. (OMIM and UniProt)" @default.
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- NCIT_C74966 normalizedInformationContent "100" @default.
- NCIT_C74966 referenceCount "1" @default.
- NCIT_C74966 hasExactSynonym "ALX4 wt Allele" @default.
- NCIT_C74966 hasExactSynonym "Aristaless-Like Homeobox 4 wt Allele" @default.
- NCIT_C74966 hasExactSynonym "FPP" @default.
- NCIT_C74966 hasExactSynonym "KIAA1788" @default.
- NCIT_C74966 hasExactSynonym "PFM" @default.
- NCIT_C74966 hasExactSynonym "PFM1" @default.
- NCIT_C74966 hasExactSynonym "PFM2" @default.
- NCIT_C74966 type Class @default.
- NCIT_C74966 isDefinedBy ncit.owl @default.
- NCIT_C74966 label "ALX4 wt Allele" @default.
- NCIT_C74966 subClassOf B1563522093186184313d481d5d1b0c19 @default.
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