KRT71 - keratin 71 Gene

Also Known as HYPT13; K6IRS1; KRT6IRS; KRT6IRS1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 112802

About KRT71

Cytogenetic location: 12q13.13 Genomic coordinates (GRCh38): 12:52,543,909-52,553,145 (from NCBI)

This gene has 1 transcript (splice variant), 79 orthologues, 68 paralogues and is associated with 2 phenotypes. Low expression observed in reference dataset.

Summary

Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. This gene encodes a protein that is expressed in the inner root sheath of hair follicles. The type II keratins are clustered in a region of chromosome 12q13.[provided by RefSeq, Jun 2009]

KRT71 Products (1)

mRNA Protein Name
NM_033448.3 NP_258259.1 keratin, type II cytoskeletal 71
Molecular Function GO Annotation Evidence Verweise Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in hair follicle morphogenesis IMP
IMP: Inferred from mutant phenotype
22592156 GOA
involved in intermediate filament organization IMP
IMP: Inferred from mutant phenotype
22592156 GOA
Cellular Component GO Annotation Evidence Verweise Source
located in keratin filament IDA
IDA: Inferred from direct assay
22592156 GOA
located in keratin filament IPI
IPI: Inferred from physical interaction
32296183 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

KRT71 Protein Structure

Filament

Filament: Intermediate filament protein (129 - 442)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 523 a.a.
Protein Preferred Names Protein Names

keratin, type II cytoskeletal 71

  • CK-71

KRT71 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
KRT71 Q3SY84 KRT13 Homo sapiens A1A4E9 25416956
Intra
KRT71 Q3SY84 KRT13 Homo sapiens A1A4E9 25416956
Intra
KRT71 Q3SY84 KRT40 Homo sapiens Q6A162 32296183
Intra
KRT71 Q3SY84 KRT40 Homo sapiens Q6A162 32296183
Intra
KRT71 Q3SY84 KRT40 Homo sapiens Q6A162 25416956
Intra
KRT71 Q3SY84 KRT40 Homo sapiens Q6A162 32296183
Intra
KRT71 Q3SY84 KRT37 Homo sapiens O76014 32296183
Intra
KRT71 Q3SY84 KRT37 Homo sapiens O76014 32296183
Intra
KRT71 Q3SY84 KRT34 Homo sapiens O76011 32296183
Intra
KRT71 Q3SY84 KRT34 Homo sapiens O76011 32296183
Intra
KRT71 Q3SY84 KRT38 Homo sapiens O76015 32296183
Intra
KRT71 Q3SY84 KRT38 Homo sapiens O76015 25416956
Intra
KRT71 Q3SY84 KRT38 Homo sapiens O76015 32296183
Intra
KRT71 Q3SY84 KRT33B Homo sapiens Q14525 32296183
Intra
KRT71 Q3SY84 KRT33B Homo sapiens Q14525 32296183
Intra
KRT71 Q3SY84 KRT35 Homo sapiens Q92764 32296183
Intra
KRT71 Q3SY84 KRT35 Homo sapiens Q92764 32296183
Intra
KRT71 Q3SY84 KRT35 Homo sapiens Q92764 32296183
Intra
KRT71 Q3SY84 KRT25 Homo sapiens Q7Z3Z0 32296183
Intra
KRT71 Q3SY84 KRT25 Homo sapiens Q7Z3Z0 32296183
Intra
KRT71 Q3SY84 KRT25 Homo sapiens Q7Z3Z0 32296183
Intra
KRT71 Q3SY84 KRT28 Homo sapiens Q7Z3Y7 32296183
Intra
KRT71 Q3SY84 KRT28 Homo sapiens Q7Z3Y7 32296183
Intra
KRT71 Q3SY84 KRT28 Homo sapiens Q7Z3Y7 32296183
Intra
KRT71 Q3SY84 KRT26 Homo sapiens Q7Z3Y9 32296183
Intra
KRT71 Q3SY84 KRT26 Homo sapiens Q7Z3Y9 32296183
Intra
KRT71 Q3SY84 KRT26 Homo sapiens Q7Z3Y9 32296183
Intra
KRT71 Q3SY84 KRT24 Homo sapiens Q2M2I5 32296183
Intra
KRT71 Q3SY84 KRT24 Homo sapiens Q2M2I5 32296183
Intra
KRT71 Q3SY84 KRT18 Homo sapiens P05783 32296183
Intra
KRT71 Q3SY84 KRT18 Homo sapiens P05783 32296183
Intra
KRT71 Q3SY84 KRT27 Homo sapiens Q7Z3Y8 32296183
Intra
KRT71 Q3SY84 KRT27 Homo sapiens Q7Z3Y8 32296183
Intra
KRT71 Q3SY84 KRT27 Homo sapiens Q7Z3Y8 32296183
Intra
KRT71 Q3SY84 KRT16 Homo sapiens P08779 32296183
Intra
KRT71 Q3SY84 KRT16 Homo sapiens P08779 32296183
Intra
KRT71 Q3SY84 WASHC3 Homo sapiens Q9Y3C0 32296183
Intra
KRT71 Q3SY84 WASHC3 Homo sapiens Q9Y3C0 32296183
Intra
KRT71 Q3SY84 WASHC3 Homo sapiens Q9Y3C0 32296183
Intra
KRT71 Q3SY84 KRT15 Homo sapiens P19012 32296183
Intra
KRT71 Q3SY84 KRT15 Homo sapiens P19012 32296183
Intra
KRT71 Q3SY84 USHBP1 Homo sapiens Q8N6Y0 32296183
Intra
KRT71 Q3SY84 USHBP1 Homo sapiens Q8N6Y0 32296183
Intra
KRT71 Q3SY84 USHBP1 Homo sapiens Q8N6Y0 32296183
Intra
KRT71 Q3SY84 KRT19 Homo sapiens P08727 32296183
Intra
KRT71 Q3SY84 KRT19 Homo sapiens P08727 32296183
Intra
KRT71 Q3SY84 KRT31 Homo sapiens Q15323 32296183
Intra
KRT71 Q3SY84 KRT31 Homo sapiens Q15323 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Hypotrichosis 13
  • HYPT13

  • Hypotrichosis With Woolly Hair

  • Hypotrichosis, Type 13

Familial Woolly Hair Syndrome
  • Wooly Hair

  • Familial Wooly Hair Syndrome

  • Hereditary Woolly Hair Syndrome

  • Hereditary Wooly Hair Syndrome

  • Woolly Hair

  • Syndrome With Woolly Hair

  • Wooly Hair Syndrome

Hypotrichosis
Woolly Hair, Autosomal Dominant
  • Autosomal Dominant Woolly Hair

  • ADWH

  • Woolly Hair Autosomal Dominant

T-Cell Immunodeficiency, Congenital Alopecia, And Nail Dystrophy
  • Winged Helix Deficiency

  • Alymphoid Cystic Thymic Dysgenesis

  • Severe T-Cell Immunodeficiency-Congenital Alopecia-Nail Dystrophy Syndrome

  • Pignata Guarino Syndrome

  • TIDAND

  • T-Cell Immunodeficiency, Congenital Alopecia And Nail Dystrophy

  • Congenital Alopecia And Nail Dystrophy Associated With Severe Functional T-Cell Immunodeficiency

  • Severe Combined Immunodeficiency Due To Foxn1 Deficiency

  • Foxn1 Deficiency

  • Nude/Scid

  • Nude/Severe Combined Immunodeficiency

  • Scid Due To Foxn1 Deficiency

  • Severe T-Cell Immunodeficiency-Congenital Alopecia-Nail Dystrophy

Hypotrichosis 3
  • HYPT3

  • Hypotrichosis Simplex Of The Scalp 2

  • Htss2

  • Hypotrichosis, Type 3

Nail Disorder, Nonsyndromic Congenital, 4
  • Anonychia Congenita

  • Anonychia

  • Hyponychia Congenita

  • NDNC4

  • Anonychia/Hyponychia Congenita

  • Nonsyndromic Congenital Nail Disorder 4

  • Isolated Congenital Anonychia

  • Anonychia Congenita Totalis

  • Anonychia Totalis

  • Autosomal Recessive Nonsyndromic Congenital Nail Disorder-4

  • Congenital Anonychia

  • Nonsyndromic Congenital Nail Disorder, 4

  • Absent Nails

  • Aplastic Nails

  • Congenital Absence Of Nails

  • Isolated Anonychia

  • Nail Disorder, Non-Syndromic Congenital, 4

  • Nail Disorder, Nonsyndromic, Congenital, Type 4

Ectodermal Dysplasia 4, Hair/Nail Type
  • Pure Hair And Nail Ectodermal Dysplasia

  • ECTD4

  • Ectodermal Dysplasia, Pure Hair-Nail Type

  • Ectodermal Dysplasia, 'Pure' Hair/Nail Type

  • Hned

  • Hair-Nail Ectodermal Dysplasia

  • Phned

  • Ectodermal Dysplasia Pure Hair-Nail Type

  • Ectodermal Dysplasia, 'Pure' Hair-Nail Type

  • Dysplasia, Ectodermal, Type 4, Hair/Nail

Hypotrichosis 6
  • HYPT6

  • Lah1

  • Hypotrichosis, Localized, Autosomal Recessive

  • Monilethrix-Like Hypotrichosis

  • Hypotrichosis, Localized, Autosomal Recessive 1

  • Lah

  • Htl

  • Autosomal Recessive Localized Hypotrichosis

  • Hypotrichosis Localized Autosomal Recessive

  • Hypotrichosis Localized Autosomal Recessive 1

  • Hypotrichosis, Type 6

Nonsyndromic Congenital Nail Disorder
  • Nail Disorder, Nonsyndromic Congenital

Mucinoses
Hypotrichosis 4
  • HYPT4

  • Marie Unna Hereditary Hypotrichosis 1

  • Muhh1

  • Hypotrichosis, Marie Unna Type, 1

  • Hypotrichosis Marie Unna 1

  • Marie Unna Hereditary Hypotrichosis Type 1

  • Hypotrichosis, Hereditary, Marie Unna Type, 1

  • Hypotrichosis, Type 4

Monilethrix
  • Beaded Hair

  • MNLIX

  • Nodose Hair

  • Moniliform Hair Syndrome

Waardenburg Syndrome, Type 4c
  • Waardenburg Syndrome Type 4c

  • WS4C

  • Waardenburg Syndrome Type Ivc

  • Waardenburg Syndrome With Hirschsprung Disease Type 4c

  • Waardenburg Syndrome With Hirschsprung Disease, Type 4c

  • Waardenburg Syndrome, Type Ivc

  • Waardenburg Syndrome 4c

  • Hirschsprung Disease With Pigmentary Anomaly

  • Shah-Waardenburg Syndrome

  • Waardenburg-Shah Syndrome

  • Waardenburg Syndrome, Type 4a

Hair Disease
  • Hair Diseases

  • Hair Anomaly

  • Hair Disorder

  • Hair Problems

T-Cell Immunodeficiency With Thymic Aplasia
  • Nezelof Syndrome

  • T-Lymphocyte Deficiency

  • TIDTA

  • Immune Defect Due To Absence Of Thymus

  • Thymic Aplasia

  • Nezelof'S Syndrome

  • Thymic Dysplasia With Normal Immunoglobulins

  • Thymic Aplasia Syndrome

  • T-Lymphocyte Immunodeficiency

Hypotrichosis 8
  • HYPT8

  • Lah3

  • Hypotrichosis, Localized, Autosomal Recessive 3

  • Woolly Hair, Autosomal Recessive 1, With Or Without Hypotrichosis

  • Autosomal Recessive Woolly Hair 1, With Or Without Hypotrichosis

  • Hypotrichosis Localized Autosomal Recessive 3

  • Woolly Hair Autosomal Recessive 1 With Or Without Hypotrichosis

  • ARWH1

  • Hypotrichosis, Type 8

Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive
  • Hypohidrotic Ectodermal Dysplasia

  • Hed

  • Anhidrotic Ectodermal Dysplasia

  • Ectodermal Dysplasia, Hypohidrotic

  • Eda

  • Christ-Siemens-Touraine Syndrome

  • ECTD10B

  • Ectodermal Dysplasia Anhidrotic

  • Ectodermal Dysplasia, Anhidrotic

  • Cst Syndrome

  • Ectodermal Dysplasia Hypohidrotic Autosomal Recessive

  • Dysplasia, Ectodermal, Type 10b, Hypohidrotic/Hair/Tooth, Autosomal Recessive

  • Dysplasia, Ectodermal, Hypohidrotic

  • Ectodermal Dysplasia 11b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive

  • Ectodermal Dysplasia 3, Anhidrotic

  • Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus KRT71 RGD RGD:1584538
Bos taurus KRT71 VGNC VGNC:30735
Macaca mulatta KRT71 VGNC VGNC:74147
Mus musculus KRT71 MGD MGI:1861586
Felis catus KRT71 VGNC VGNC:63171
Others KRT71 NCBI