| 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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Excessive
|
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dermatomycoses; postoperative complications; precancerous conditions;
|
fingers Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term fingers in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
synostosis involving bones of the fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the synostosis involving bones of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
clubbing of fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the clubbing of fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanges of all fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanges of all fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of the hand or of fingers of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the long fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
camptodactyly of 2nd-5th fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the camptodactyly of 2nd-5th fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shortening of all proximal phalanges of the fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the shortening of all proximal phalanges of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
swan neck-like deformities of the fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the swan neck-like deformities of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shortening of all middle phalanges of the fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the shortening of all middle phalanges of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
radial deviation of the hand or of fingers of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the radial deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shortening of all distal phalanges of the fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the shortening of all distal phalanges of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ulnar deviation of the hand or of fingers of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the ulnar deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shortening of all phalanges of fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the shortening of all phalanges of fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased laxity of fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the increased laxity of fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
overlapping fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the overlapping fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
DNA polymerase lambda, fingers domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA polymerase lambda, fingers domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Clubbed Fingers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Clubbed Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ulnar Polydactyly Of Fingers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ulnar Polydactyly Of Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Overlapping Fingers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Overlapping Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Distal Phalanges Of All Fingers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Distal Phalanges Of All Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Shortening Of All Proximal Phalanges Of The Fingers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Shortening Of All Proximal Phalanges Of The Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Simple Syndactyly Of Fingers - First Web Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Simple Syndactyly Of Fingers - First Web in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Curved Fingers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Curved Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tapering Fingers (Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tapering Fingers (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Fingers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of Fingers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Laxity Of Fingers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Laxity Of Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Deviation Of The Hand Or Of Fingers Of The Hand Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deviation Of The Hand Or Of Fingers Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cutaneous Syndactyly Between Fingers 2 And 5 Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cutaneous Syndactyly Between Fingers 2 And 5 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Swan Neck-Like Deformities Of The Fingers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Swan Neck-Like Deformities Of The Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Camptodactyly Of 2Nd-5Th Fingers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Camptodactyly Of 2Nd-5Th Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Long fingers Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Long fingers 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;
|
[
|
[
|
[
|
[
|
[
|
Acute Bacterial
|
Complicated
|
|
|
|
|
|
|
Inflammatory
|
|
|
Inflammatory
|
Stiff
|
Dominant dystrophic epidermolysis bullosa with absence of
|
|
Hypotrichosis and recurrent
|
Ectodermal dysplasia
|
Peeling
|
Tight
|
|
|
Wrinkly
|
Hypotrichosis And Recurrent
|
|
|
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/
|
Peeling
|
Stiff
|
Epidermolysis Bullosa With Congenital Localized Absence Of
|
|
Peeling
|
|
|
vascular
|
|
vesiculobullous
|
|
|
vascular
|
|
verruciform xanthoma of
|
|
|
malignant
|
|
|
sarcomatoid squamous cell
|
autoimmune disease of
|
bullous
|
|
|
vesiculobullous
|
eccrine mixed tumor of
|
|
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vascular
|
|
|
|
|
chronic ulcer of
|
|
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H3K4me3_fibroblast of
|
H3K4me3_fibroblast of
|
CTCF_fibroblast of
|
CTCF_fibroblast of
|
lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral;
|
crohn disease; crohn's disease; melanoma;
|
|
melanoma; nevus;
|
melanoma; neoplasms, multiple primary; nevus;
|
precancerous conditions;
|
behcet syndrome; disease susceptibility;
|
eye diseases; sarcoidosis;
|
breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms;
|
melanoma; nevus;
|
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions;
|
erythema; psoriasis;
|
carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma;
|
melanoma, amelanotic;
|
lymphoma, t-cell, cutaneous; parapsoriasis;
|
|
lung cancer;
|
|
colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases;
|
dna damage; melanoma;
|
|
melanoma;
|
|
psoriasis;
|
carcinoma, basal cell; carcinoma, squamous cell; melanoma;
|
papillomavirus infections;
|
melanoma; neoplasm invasiveness;
|
erythema; rare diseases;
|
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neoplasms, basal cell;
|
carcinoma, squamous cell;
|
|
carcinoma, basal cell;
|
|
dna damage; neoplasms;
|
bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism;
|
carcinoma, basal cell; melanoma;
|
carcinoma, basal cell; melanoma; neoplasm metastasis;
|
carcinoma, squamous cell;
|
|
cell transformation, neoplastic; epidermodysplasia verruciformis; papillomavirus infections;
|
cell transformation, neoplastic; melanoma;
|
lupus erythematosus, cutaneous; lupus erythematosus, discoid; photosensitivity disorders;
|
abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome;
|
edema; hypertension;
|
keratosis; melanoma;
|
carcinoma, squamous cell; papillomavirus infections;
|
autoimmune diseases;
|
carcinoma, basal cell; carcinoma, squamous cell;
|
chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions;
|
breast neoplasms; dna damage; lung neoplasms; mammary neoplasms; neoplasm of lung ;
|
arsenic poisoning;
|
melanoma; neoplasms, multiple primary;
|
keratosis;
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facial neoplasms; horse diseases; melanoma;
|
hypersensitivity;
|
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autoimmune diseases;
|
connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth;
|
arthritis; sarcoidosis;
|
hyperpigmentation; melanoma;
|
|
melanoma; neoplasm metastasis;
|
breast neoplasms; melanoma;
|
melanoma;
|
brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ;
|
scleroderma, systemic;
|
|
carcinoma, basal cell;
|
scleroderma, systemic;
|
dysplastic nevus syndrome; melanoma;
|
carcinoma, basal cell; carcinoma, squamous cell; head and neck neoplasms; lip neoplasms;
|
melanoma
|
cocarcinogenesis;
|
|
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;
|
mycobacterium infections, atypical;
|
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
|
establishment of
|
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Non-melanoma
|
|
|
|
bullous
|
|
inflammatory abnormality of the
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neoplasm of the
|
localized
|
abnormality of
|
abnormality of
|
abnormality of the
|
vascular
|
atypical scarring of
|
|
abnormality of
|
generalized abnormality of
|
abnormality of
|
|
|
dry
|
thin
|
reticulated
|
telangiectases in sun-exposed and nonexposed
|
aplasia/hypoplasia of the
|
generalized abnormality of
|
hypopigmentation of the
|
abnormal delayed hypersensitivity
|
inflammatory abnormality of the
|
|
fine, reticulate
|
punctate vasculitis
|
profuse pigmented
|
congenital localized absence of
|
excessive wrinkling of palmar
|
abnormality of the
|
abnormality of
|
postauricular
|
blotching pigmentation of the
|
abnormality of the plantar
|
diffuse
|
|
|
vascular
|
abnormal elasticity of
|
localized
|
hypopigmented
|
stiff
|
|
periauricular
|
atypical scarring of
|
desquamation of
|
|
excessive wrinkled
|
midline
|
neonatal wrinkled
|
vasculitis in the
|
hyperextensible
|
preauricular
|
squamous cell carcinoma of the
|
abnormality of
|
thickened nuchal
|
premature
|
abnormal blistering of the
|
pigmentation anomalies of sun-exposed
|
hyperpigmentation of the
|
neoplasm of the
|
preauricular
|
soft
|
hypertrophy of
|
hypopigmented
|
warfarin-induced
|
|
abnormality of
|
recurrent
|
|
yellow subcutaneous tissue covered by thin, scaly
|
lack of
|
fragile
|
|
depigmentation/hyperpigmentation of
|
abnormality of
|
mixed hypo- and hyperpigmentation of the
|
soft, doughy
|
regional abnormality of
|
recurrent bacterial
|
|
teleangiectasia of the
|
abnormally lax or hyperextensible
|
asymmetric, linear
|
thickened
|
absent
|
|
|
|
|
|
|
Galvanic
|
|
|
|
|
Staphylococcal
|
|
|
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dry
|
thin
|
abnormal
|
reddish
|
decreased
|
abnormal
|
decreased
|
scaly
|
blotchy
|
|
wrinkled
|
calcified
|
|
abnormal
|
tight
|
delayed
|
flaky
|
abnormal
|
shiny
|
loose
|
|
spontaneous
|
abnormal
|
increased sensitivity to
|
abnormal
|
impaired
|
translucent
|
abnormal
|
increased
|
abnormal
|
decreased sensitivity to
|
decreased
|
|
abnormal
|
abnormal
|
|
increased
|
oily
|
abnormal
|
|
abnormal
|
thick
|
|
abnormal
|
absent
|
increased
|
abnormal
|
|
[
|
[tuberculin
|
[
|
[
|
[
|
[
|
[
|
[
|
[
|
stiff
|
[
|
?hypotrichosis and recurrent
|
[tuberculin
|
?inflammatory
|
?inflammatory
|
[
|
palmoplantar hyperkeratosis with squamous cell carcinoma of
|
ectodermal dysplasia/
|
[
|
{uv-induced
|
[
|
wrinkly
|
[
|
peeling
|
peeling
|
|
|
|
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melanoma
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Lymphoproliferative Disorder Of The
|
Melanocytic Nevus Of
|
|
|
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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
|
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
|
|
Hypopigmented
|
Pricking Of
|
|
Desquamation Of
|
Fragile
|
Soft, Doughy
|
Petechiae Of
|
Recurrent
|
|
|
Severe Dry
|
Hypopigmented
|
|
|
|
|
Preauricular
|
Abnormality Of
|
Aplasia/Hypoplasia Of The
|
Abnormal Blistering Of The
|
|
|
Neonatal Wrinkled
|
|
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
|