Varaico: Literature-Extracted Genetic Variants

Gene:NR0B1
Variant:p.Q395*
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NR0B1

NM_000475.5:p.Q395*

Associated Papers

Can fetal ultrasound predict adrenal hypoplasia congenita caused by Xp21 deletion?

Yokohama Y et al.

The Journal of Obstetrics and Gynaecology Research, 2025

Four Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by DAX-1 gene mutations: mutant DAX-1 failed to repress steroidogenic acute regulatory protein (StAR) and luteinizing hormone beta-subunit gene promoter activity.

Okuhara K et al.

Endocrine Journal, 2008

Genetic disorders involving adrenal development.

Lin L et al.

Endocrine Development, 2007

Analysis of DAX1 (NR0B1) and steroidogenic factor-1 (NR5A1) in children and adults with primary adrenal failure: ten years' experience.

Lin L et al.

The Journal of Clinical Endocrinology and Metabolism, 2006

[Functional analysis of mutated DAX-1 gene in patients with X linked adrenal hypoplasia congenita complicated with hypogonadotropic hypogonadism using luteinizing hormone beta-subunit gene promotor].

Okuhara K

[hokkaido Igaku Zasshi] the Hokkaido Journal of Medical Science, 2004

Identification of a novel missense mutation that is as damaging to DAX-1 repressor function as a nonsense mutation.

Brown P et al.

The Journal of Clinical Endocrinology and Metabolism, 2003

Mutations in NR0B1 (DAX1) and NR5A1 (SF1) responsible for adrenal hypoplasia congenita.

Phelan JK et al.

Human Mutation, 2001

A microdeletion within DAX-1 in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism.

Wang J et al.

Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research, 1999

Novel DAX1 mutations in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism.

Bassett JH et al.

Clinical Endocrinology, 1999

DAX1 mutations map to putative structural domains in a deduced three-dimensional model.

Zhang YH et al.

American Journal of Human Genetics, 1998

Three novel mutations and a de novo deletion mutation of the DAX-1 gene in patients with X-linked adrenal hypoplasia congenita.

Nakae J et al.

The Journal of Clinical Endocrinology and Metabolism, 1997

Truncation at the C-terminus of the DAX-1 protein impairs its biological actions in patients with X-linked adrenal hypoplasia congenita.

Nakae J et al.

The Journal of Clinical Endocrinology and Metabolism, 1996

Variable presentation of X-linked adrenal hypoplasia congenita.

Wiltshire E et al.

Journal of Pediatric Endocrinology & Metabolism : Jpem, 0

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