Description: | sprouty RTK signaling antagonist 4 [Source:HGNC Symbol;Acc:HGNC:15533] |
Synonyms: | HH17 |
Other ID(s): | HGNC:15533, ENSG00000187678 |
Protein Accession Numbers: | ENST00000511815, ENST00000344120, NP_001280218, ENST00000434127, NP_112226, NP_001120968, ENST00000344120.4, NP_001280219 |
Statistics: | ClinVar(16) COSMIC(122) |
∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000344120 You are here now!
ENST00000434127
ENST00000511815
NP_001120968
NP_001280218
NP_001280219
NP_112226 You are here now!
Pfam Domain filter_list | Domain Name filter_list | Description filter_list | Positions filter_list | Clan filter_list | Clan Name filter_list | Organism filter_list |
---|---|---|---|---|---|---|
NO RESULT FOUND | ||||||
PF05210 | Sprouty | Sprouty protein (Spry) | 187-299 | Homo sapiens |
Disease Name filter_list | Disease Category filter_list | DSI* filter_list | DPI** filter_list | ||
---|---|---|---|---|---|
Leukemia, Myelocytic, Acute | Neoplasms ; | 0.602 | 0.552 | ||
Acute Myeloid Leukemia, M1 | Neoplasms ; | 0.602 | 0.552 | ||
Kallmann Syndrome | Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Endocrine System Diseases ; | 0.602 | 0.552 | ||
Idiopathic hypogonadotropic hypogonadism | Endocrine System Diseases ; | 0.602 | 0.552 | ||
Acute Myeloid Leukemia (AML-M2) | Neoplasms ; | 0.602 | 0.552 | ||
HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA | N/A | 0.602 | 0.552 | ||
NO RESULT FOUND |