Fanconi Anemia, Complementation Group P (FANCP)

Alias:
Fanconi Anemia Complementation Group P
Fancp
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Fanconi Anemia, Complementation Group P, also known as fanconi anemia complementation group p, is related to fanconi anemia, complementation group a and deficiency anemia. An important gene associated with Fanconi Anemia, Complementation Group P is SLX4 (SLX4 Structure-Specific Endonuclease Subunit). Affiliated tissues include bone marrow and bone, and related phenotypes are cryptorchidism and vitiligo
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
2
18
3

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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