Primary Identifier | MGI:1891228 | Organism | mouse, laboratory |
Chromosome | 14 | NCBI Gene Number | 64929 |
Mgi Type | protein coding gene |
description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to enable metal ion binding activity. Involved in embryo development and epidermis development. Located in cytoplasm. Is expressed in several structures, including amnion; brain; genitourinary system; and skin. Orthologous to human SCEL (sciellin). PHENOTYPE: Homozygous null mice are viable and fertile with normal hair morphology and development and normal skin morphology and barrier function. [provided by MGI curators] |