| Name |
|---|
LOC105375109 Gene
|
PI3 Gene
peptidase inhibitor 3, This gene encodes an elastase-specific inhibitor that functions as an antimicrobial peptide against Gram-positive and Gram-negative bacteria, and fungal pathogens. The protein contains a WAP-type four-disulfide core (WFDC) domain, and is thus a member of the WFDC domain family. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the centromeric cluster. Expression of this gene is upgulated by bacterial lipopolysaccharides and cytokines. [provided by RefSeq, Oct 2014] |
LOC105379200 Gene
|
TST2 Gene
Tuberculin |
TST1 Gene
Tuberculin |
LOC105374086 Gene
|
SHEP8 Gene
|
KWE Gene
keratolytic winter erythema (Oudtshoorn |
LOC105378948 Gene
|
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dermatomycoses; postoperative complications; precancerous conditions;
|
|
confetti-like
|
discrete 2 to 5-mm hyper- and
|
|
achromatic retinal
|
hyperpigmented/
|
enlarged peyer's
|
small peyer's
|
absent peyer's
|
|
Confetti-Like
|
Achromatic Retinal
|
Discrete 2 To 5-Mm Hyper- And
|
Obsolete
|
enlarged Peyer's
|
absent Peyer's
|
small Peyer's
|
arms Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term arms in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
absent outer dynein arms Gene SetFrom HPO Gene-Disease Associations genes associated with the absent outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent/shortened outer dynein arms Gene SetFrom HPO Gene-Disease Associations genes associated with the absent/shortened outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shortened outer dynein arms Gene SetFrom HPO Gene-Disease Associations genes associated with the shortened outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent/shortened dynein arms Gene SetFrom HPO Gene-Disease Associations genes associated with the absent/shortened dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent inner and outer dynein arms Gene SetFrom HPO Gene-Disease Associations genes associated with the absent inner and outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent inner dynein arms Gene SetFrom HPO Gene-Disease Associations genes associated with the absent inner dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ARMS-mediated activation Gene Setproteins participating in the ARMS-mediated activation pathway from the Reactome Pathways dataset. |
Absent Inner And Outer Dynein Arms Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Inner And Outer Dynein Arms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Outer Dynein Arms Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Outer Dynein Arms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Inner Dynein Arms Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Inner Dynein Arms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent/Shortened Outer Dynein Arms Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent/Shortened Outer Dynein Arms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
ARMS-mediated activation Gene Setproteins participating in the ARMS-mediated activation pathway from the Reactome Pathways 2024 dataset. |
Absent inner and outer dynein arms Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Absent inner and outer dynein arms phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary;
|
carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced;
|
carcinoma, basal cell; carcinoma, squamous cell; melanoma;
|
carcinoma, basal cell; carcinoma, squamous cell; dna damage;
|
carcinoma, basal cell;
|
carcinoma, basal cell; carcinoma, squamous cell; postoperative complications;
|
carcinoma, basal cell; carcinoma, squamous cell;
|
carcinoma, basal cell; melanoma;
|
carcinoma, basal cell; neoplasms, second primary;
|
carcinoma, basal cell; carcinoma, squamous cell; melanoma;
|
carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications;
|
[
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[
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[
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[
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[
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Acute Bacterial
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Complicated
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Inflammatory
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Inflammatory
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Stiff
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Dominant dystrophic epidermolysis bullosa with absence of
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Hypotrichosis and recurrent
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Ectodermal dysplasia
|
Peeling
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Tight
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Wrinkly
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Hypotrichosis And Recurrent
|
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|
PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset. |
|
Ectodermal dysplasia/
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Peeling
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Stiff
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Epidermolysis Bullosa With Congenital Localized Absence Of
|
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Peeling
|
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vascular
|
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vesiculobullous
|
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vascular
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verruciform xanthoma of
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malignant
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sarcomatoid squamous cell
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autoimmune disease of
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bullous
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vesiculobullous
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eccrine mixed tumor of
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vascular
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chronic ulcer of
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H3K4me3_fibroblast of
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H3K4me3_fibroblast of
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CTCF_fibroblast of
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CTCF_fibroblast of
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lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral;
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crohn disease; crohn's disease; melanoma;
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melanoma; nevus;
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melanoma; neoplasms, multiple primary; nevus;
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precancerous conditions;
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behcet syndrome; disease susceptibility;
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eye diseases; sarcoidosis;
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breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms;
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melanoma; nevus;
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chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions;
|
erythema; psoriasis;
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carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma;
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melanoma, amelanotic;
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lymphoma, t-cell, cutaneous; parapsoriasis;
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lung cancer;
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colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases;
|
dna damage; melanoma;
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melanoma;
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psoriasis;
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carcinoma, basal cell; carcinoma, squamous cell; melanoma;
|
papillomavirus infections;
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melanoma; neoplasm invasiveness;
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erythema; rare diseases;
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neoplasms, basal cell;
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carcinoma, squamous cell;
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carcinoma, basal cell;
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dna damage; neoplasms;
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bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism;
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carcinoma, basal cell; melanoma;
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carcinoma, basal cell; melanoma; neoplasm metastasis;
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carcinoma, squamous cell;
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cell transformation, neoplastic; epidermodysplasia verruciformis; papillomavirus infections;
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cell transformation, neoplastic; melanoma;
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lupus erythematosus, cutaneous; lupus erythematosus, discoid; photosensitivity disorders;
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abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome;
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edema; hypertension;
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keratosis; melanoma;
|
carcinoma, squamous cell; papillomavirus infections;
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autoimmune diseases;
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carcinoma, basal cell; carcinoma, squamous cell;
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chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions;
|
breast neoplasms; dna damage; lung neoplasms; mammary neoplasms; neoplasm of lung ;
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arsenic poisoning;
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melanoma; neoplasms, multiple primary;
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keratosis;
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facial neoplasms; horse diseases; melanoma;
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hypersensitivity;
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autoimmune diseases;
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connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth;
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arthritis; sarcoidosis;
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hyperpigmentation; melanoma;
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melanoma; neoplasm metastasis;
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breast neoplasms; melanoma;
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melanoma;
|
brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ;
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scleroderma, systemic;
|
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carcinoma, basal cell;
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scleroderma, systemic;
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dysplastic nevus syndrome; melanoma;
|
carcinoma, basal cell; carcinoma, squamous cell; head and neck neoplasms; lip neoplasms;
|
melanoma
|
cocarcinogenesis;
|
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carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced;
|
bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia;
|
microsatellite instability; nevus, pigmented;
|
behcet syndrome;
|
cutaneous melanoma which is largely independent of
|
melanoma; nevus; precancerous conditions;
|
hypertension, pulmonary; raynaud disease; scleroderma, systemic;
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mycobacterium infections, atypical;
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carcinoma, squamous cell; cell transformation, neoplastic;
|
brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced;
|
severe photoaging of facial
|
|
Get-1_Deficiency_GDS2629_161_mouse_embryonic
|
regulation of water loss via
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establishment of
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Non-melanoma
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bullous
|
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inflammatory abnormality of the
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neoplasm of the
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localized
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abnormality of
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abnormality of
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abnormality of the
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vascular
|
atypical scarring of
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abnormality of
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generalized abnormality of
|
abnormality of
|
|
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dry
|
thin
|
reticulated
|
telangiectases in sun-exposed and nonexposed
|
aplasia/hypoplasia of the
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generalized abnormality of
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hypopigmentation of the
|
abnormal delayed hypersensitivity
|
inflammatory abnormality of the
|
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fine, reticulate
|
punctate vasculitis
|
profuse pigmented
|
congenital localized absence of
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excessive wrinkling of palmar
|
abnormality of the
|
abnormality of
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postauricular
|
blotching pigmentation of the
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abnormality of the plantar
|
diffuse
|
|
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vascular
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abnormal elasticity of
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localized
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stiff
|
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periauricular
|
redundant
|
atypical scarring of
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desquamation of
|
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excessive wrinkled
|
midline
|
neonatal wrinkled
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vasculitis in the
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redundant
|
hyperextensible
|
redundant neck
|
preauricular
|
squamous cell carcinoma of the
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abnormality of
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thickened nuchal
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premature
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abnormal blistering of the
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pigmentation anomalies of sun-exposed
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hyperpigmentation of the
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neoplasm of the
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preauricular
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soft
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hypertrophy of
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warfarin-induced
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abnormality of
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recurrent
|
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yellow subcutaneous tissue covered by thin, scaly
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lack of
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fragile
|
|
depigmentation/hyperpigmentation of
|
abnormality of
|
mixed hypo- and hyperpigmentation of the
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soft, doughy
|
regional abnormality of
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recurrent bacterial
|
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teleangiectasia of the
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abnormally lax or hyperextensible
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asymmetric, linear
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thickened
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absent
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Galvanic
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Staphylococcal
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dry
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thin
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abnormal
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reddish
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decreased
|
abnormal
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decreased
|
scaly
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blotchy
|
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wrinkled
|
calcified
|
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abnormal
|
tight
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delayed
|
flaky
|
abnormal
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shiny
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loose
|
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spontaneous
|
abnormal
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increased sensitivity to
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abnormal
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impaired
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translucent
|
abnormal
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increased
|
abnormal
|
decreased sensitivity to
|
decreased
|
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abnormal
|
abnormal
|
|
increased
|
oily
|
abnormal
|
|
abnormal
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thick
|
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abnormal
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absent
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increased
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abnormal
|
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[
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[tuberculin
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[
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[
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[
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[
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[
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[
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[
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stiff
|
[
|
?hypotrichosis and recurrent
|
[tuberculin
|
?inflammatory
|
?inflammatory
|
[
|
palmoplantar hyperkeratosis with squamous cell carcinoma of
|
ectodermal dysplasia/
|
[
|
{uv-induced
|
[
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wrinkly
|
[
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peeling
|
peeling
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melanoma
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Lymphoproliferative Disorder Of The
|
Melanocytic Nevus Of
|
|
|
|
|
Strawberry Nevus Of
|
|
Squamous Cell Carcinoma Of
|
Vasculitis Of The
|
|
|
Atypical Fibroxanthoma Of
|
Stage Iv
|
Inflammatory Dry
|
Neonatal Inflammatory
|
Epithelial Hyperplasia Of
|
Carcinoma Metastatic To The
|
Collagen Nevus Of
|
Depigmentation/Hyperpigmentation Of
|
Fibrous
|
|
Superficial Spreading Malignant Melanoma Of
|
Compound Nevus Of
|
Photodamaged
|
|
Cyst Of
|
Dermatoglyphs -
|
Langerhans Cell Histiocytosis Of
|
Secondary Malignant Neoplasm Of
|
Granulomatous Slack
|
Peeling
|
Wrinkly
|
Periauricular
|
Malignant Blue Nevus Of
|
|
Congenital Localized Absence Of
|
Amelanotic
|
Desmoplastic Spindle And Epithelioid Cell Melanocytic Nevus Of
|
Pyogenic Granuloma Of
|
|
|
Stage 0
|
Chronic
|
|
Locally Advanced Squamous Cell Carcinoma Of The
|
Verruciform Xanthoma Of
|
Familial Malignant Melanoma Of
|
Peeling
|
Eccrine Mixed Tumor Of
|
Autoimmune
|
Generalized Abnormality Of
|
Linear
|
|
Lumpy
|
Staphylococcal Scalded
|
|
|
Digital Papillary Eccrine Carcinoma Of
|
Body
|
|
Stiff
|
Diffuse
|
Molluscum Contagiosum
|
Graft Versus Host Disease In
|
Epithelioid Hemangioma Of
|
Lethal Tight
|
Breast Carcinoma Metastatic In The
|
Tuberculin (
|
Tufted Angioma Of
|
Regional Abnormality Of
|
|
Pilomatrix Carcinoma Of
|
|
|
Loss Of
|
Redundant
|
Sarcoma Of
|
Streptococcal Infection Of
|
Acroangiodermatitis Of
|
Palmoplantar Hyperkeratosis With Squamous Cell Carcinoma Of
|
Congenital Accessory
|
Other Specified Congenital Malformations Of
|
|
Neoplasm Of
|
Occupational Cancer Of
|
Thickened Nuchal
|
Dry
|
Dry
|
Lack Of
|
Scaly
|
Atypical Scarring Of
|
Spots On
|
Photosensitivity Of
|
Abnormally Lax Or Hyperextensible
|
Excessive Wrinkled
|
Hyperextensible
|
Thick
|
Soft
|
Thin
|
Anal
|
|
Pricking Of
|
|
Desquamation Of
|
Fragile
|
Redundant
|
Soft, Doughy
|
Petechiae Of
|
Recurrent
|
|
|
Severe Dry
|
|
|
|
|
Preauricular
|
Abnormality Of
|
Aplasia/Hypoplasia Of The
|
Abnormal Blistering Of The
|
|
|
Excessive
|
Neonatal Wrinkled
|
Redundant Neck
|
|
Pain Of
|
Peeling Of
|
White Scaling
|
|
|
Asymmetric, Linear
|
Excessive Wrinkling Of Palmar
|
Recurrent Bacterial
|
Postauricular
|
Reticulated
|
Blotching Pigmentation Of The
|
|
Pigmentation Anomalies Of Sun-Exposed
|
Stiff
|
|
Preauricular
|
Hyperextensible
|
Localized
|
Achromia Of
|
|
Abnormality Of
|
Increased Number Of
|
Blanching Of
|
Abscess Of
|
Recurrent Viral
|
Profuse Pigmented
|
|
Fissure In
|
Uv-Induced
|
Yellow Subcutaneous Tissue Covered By Thin, Scaly
|
Warfarin-Induced
|
Macerated
|
|
Palmoplantar Scaling
|
Fine, Reticulate
|
Red, Cracking, Peeling
|
Punctate Vasculitis
|
Abnormal Elasticity Of
|
Stinging Of
|
Absent
|
Midline
|
Abnormal Delayed Hypersensitivity
|
|
establishment of
|
|
|
thin
|