Entity Details
Primary name |
LIPH_HUMAN |
Entity type |
UniProt |
Source |
Source Link |
Details
Accession | Q8WWY8 |
EntryName | LIPH_HUMAN |
FullName | Lipase member H |
TaxID | 9606 |
Evidence | evidence at protein level |
Length | 451 |
SequenceStatus | complete |
DateCreated | 2007-01-23 |
DateModified | 2021-06-02 |
Subcellular Location
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Subcellular Location |
Cell membrane |
Secreted |
Domains
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Domain | Name | Category | Type |
IPR000734 | Triacylglycerol lipase family | Family | Family |
IPR013818 | Lipase/vitellogenin | Domain | Domain |
IPR016272 | Lipase, LIPH-type | Family | Family |
IPR029058 | Alpha/Beta hydrolase fold | Family | Homologous superfamily |
IPR033906 | Lipase, N-terminal | Domain | Domain |
Diseases
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Disease ID | Source | Name | Description |
604379 | OMIM | Hypotrichosis 7 (HYPT7) | A condition characterized by the presence of less than the normal amount of hair. Affected individuals have sparse or absent scalp, axillary and body hair and sparse eyebrows and eyelashes. HYPT7 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry. |
604379 | OMIM | Hypotrichosis 7 (HYPT7) | A condition characterized by the presence of less than the normal amount of hair. Affected individuals have sparse or absent scalp, axillary and body hair and sparse eyebrows and eyelashes. HYPT7 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
0 interactions
Interactor | Partner | Sources | Publications | Link |