BCL6 corepressor like 1
OMIM: 300688, Gene2Phenotype
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BCORL1 in Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic
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1 review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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BCORL1 in Mendeliome
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1 review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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BCORL1 in Intellectual disability syndromic and non-syndromic
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2 reviews | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) |
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Phenotypes
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BCORL1 in Fetal anomalies
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1 review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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BCORL1 in Infertility and Recurrent Pregnancy Loss
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1 review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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