Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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374393
|
Gene name
Gene Name - the full gene name approved by the HGNC.
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FAM111 trypsin like peptidase B |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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FAM111B |
Synonyms (NCBI Gene)
Gene synonyms aliases
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CANP, POIKTMP |
Disease Acronyms (UniProt)
Disease acronyms from UniProt database
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POIKTMP |
Chromosome
Chromosome number
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11 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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11q12.1 |
Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a protein with a trypsin-like cysteine/serine peptidase domain in the C-terminus. Mutations in this gene are associated with an autosomal dominant form of hereditary fibrosing poikiloderma (HFP). Affected individuals display mottled pigm |
Causal |
Disease term |
Disease name |
dbSNP ID |
References |
Papillary renal carcinoma |
Papillary Renal Cell Carcinoma |
rs5030823, rs2137087134, rs121913668, rs121913669, rs121913670, rs121913671, rs121913673, rs121913243, rs786202724 |
22138691 |
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis |
POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS |
rs587777236, rs587777237, rs587777238 |
26495788, 24268661, 26471370 |
Pulmonary fibrosis |
Pulmonary Fibrosis |
rs121918666, rs199422300, rs121917834, rs199422294, rs201159197, rs199422297, rs199422305, rs751381953, rs876661305, rs878853260, rs1555811762, rs1060502990, rs1555903332, rs1554038539, rs1554042899, rs938938578 View all (1 more) |
|
Renal carcinoma |
Renal Cell Carcinoma, Conventional (Clear Cell) Renal Cell Carcinoma, Sarcomatoid Renal Cell Carcinoma, Collecting Duct Carcinoma of the Kidney |
rs121913668, rs121913670, rs121913243, rs786202724 |
22138691 |
|
Unknown |
Disease term |
Disease name |
Evidence |
References |
Source |
Chromophobe carcinoma |
Chromophobe Renal Cell Carcinoma |
|
22138691 |
ClinVar |
Poikiloderma |
hereditary sclerosing poikiloderma with tendon and pulmonary involvement |
|
|
GenCC |
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Associations from Text Mining |
Disease Name |
Relationship Type |
References |
Adenocarcinoma of Lung |
Associate
|
31514295, 32418298, 35406786, 39337462 |
Adenocarcinoma Papillary |
Stimulate
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32418298 |
Carcinogenesis |
Associate
|
34071532 |
Contracture |
Associate
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24268661, 26471370, 30375432, 36875114 |
Fatty Liver |
Associate
|
26495788 |
Fibrosarcoma |
Associate
|
36610347 |
Fibrosis |
Associate
|
24268661, 26471370, 36610347 |
Hereditary pancreatitis |
Associate
|
26495788 |
Infections |
Associate
|
34071532 |
Maturity Onset Diabetes of the Young Type 8 with Exocrine Dysfunction |
Associate
|
26495788 |
Multiple System Atrophy |
Associate
|
26471370, 32776417 |
Muscular Atrophy |
Associate
|
26471370 |
Muscular Diseases |
Associate
|
24268661, 26471370, 30375432, 36875114 |
Neoplasm Metastasis |
Associate
|
28639897, 35864964 |
Neoplasms |
Associate
|
32418298, 34841291, 36610347, 36761753, 39337462, 40243892 |
Neoplasms |
Stimulate
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35406786 |
Neoplastic Syndromes Hereditary |
Associate
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24268661, 26471370, 30375432, 32776417 |
Pancreatic Neoplasms |
Associate
|
35077391 |
Pancreatic Neoplasms |
Stimulate
|
36408702 |
Pathological Conditions Anatomical |
Associate
|
30375432 |
Pneumonia |
Associate
|
36875114 |
Poikiloderma Hereditary Sclerosing |
Associate
|
26471370 |
Polyendocrinopathies Autoimmune |
Associate
|
36875114 |
Pulmonary Fibrosis |
Associate
|
24268661, 26471370, 30375432, 36875114 |
Rothmund Thomson Syndrome |
Associate
|
24268661, 36875114 |
Scleroderma Systemic |
Associate
|
30375432 |
Tertiary Lymphoid Structures |
Associate
|
36408702 |
Thyroid Cancer Papillary |
Associate
|
35864964 |
Uterine Cervical Neoplasms |
Associate
|
28639897 |
|