MPLKIP - Gene browser | 3billion

MPLKIP

MPLKIP

M-phase specific PLK1 interacting protein

HCNC Approved Symbol: MPLKIP (HGNC:16002)
Genomic Coordinates: 7:40,126,027 - 40,134,622 (7p14.1)
Synonyms: ORF20, TTDN1, C7orf11
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

3Patients

In total, 3 patients were diagnosed with a variant in the MPLKIP gene.

Frequently observed phenotypes(Top 5 only)

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

03
Patient count

Alopecia: 2 (66.7%)
Patient Count: 2 (66.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (66.7%)
Mental retardation: 2 (66.7%)
Patient Count: 2 (66.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (66.7%)
Developmental delay: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Muscular weakness: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)

Last updated: 2024-06-30

MPLKIP - Gene browser | 3billion