KRT81 - keratin 81 Gene

Also Known as HB1; K81; Hb-1; KRTHB1; MLN137; ghHkb1; hHAKB2-1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 3887

About KRT81

Cytogenetic location: 12q13.13 Genomic coordinates (GRCh38): 12:52,285,913-52,308,624 (from NCBI)

This gene has 1 transcript (splice variant), 46 orthologues, 68 paralogues and is associated with 3 phenotypes. Biased expression in placenta (RPKM 1.1), salivary gland (RPKM 0.5) and 13 other tissues.

Summary

The protein encoded by this gene is a member of the keratin gene family. As a type II hair keratin, it is a basic protein which heterodimerizes with type I keratins to form hair and nails. The type II hair keratins are clustered in a region of chromosome 12q13 and are grouped into two distinct subfamilies based on structure similarity. One subfamily, consisting of KRTHB1, KRTHB3, and KRTHB6, is highly related. The Other less-related subfamily includes KRTHB2, KRTHB4, and KRTHB5. All hair keratins are expressed in the hair follicle; this hair keratin, as well as KRTHB3 and KRTHB6, is found primarily in the hair cortex. Mutations in this gene and KRTHB6 have been observed in patients with a rare dominant hair disease, monilethrix. [provided by RefSeq, Jul 2008]

KRT81 Products (1)

mRNA Protein Name
NM_002281.4 NP_002272.2 keratin, type II cuticular Hb1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 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

KRT81 Protein Structure

Filament

Filament: Intermediate filament protein (105 - 416)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 505 a.a.
Protein Preferred Names Protein Names

keratin, type II cuticular Hb1

  • hair keratin K2.9

KRT81 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
KRT81 Q14533 KRT40 Homo sapiens Q6A162 32296183
Intra
KRT81 Q14533 KRT40 Homo sapiens Q6A162 25416956
Intra
KRT81 Q14533 KRT40 Homo sapiens Q6A162 32296183
Intra
KRT81 Q14533 KRT40 Homo sapiens Q6A162 32296183
Intra
KRT81 Q14533 KRT40 Homo sapiens Q6A162 25416956
Intra
KRT81 Q14533 KRT37 Homo sapiens O76014 32296183
Intra
KRT81 Q14533 KRT37 Homo sapiens O76014 32296183
Intra
KRT81 Q14533 KRT34 Homo sapiens O76011 32296183
Intra
KRT81 Q14533 KRT34 Homo sapiens O76011 32296183
Intra
KRT81 Q14533 KRT38 Homo sapiens O76015 25416956
Intra
KRT81 Q14533 KRT38 Homo sapiens O76015 32296183
Intra
KRT81 Q14533 KRT38 Homo sapiens O76015 25416956
Intra
KRT81 Q14533 KRT38 Homo sapiens O76015 29892012
Intra
KRT81 Q14533 KRT38 Homo sapiens O76015 32296183
Intra
KRT81 Q14533 KRT35 Homo sapiens Q92764 32296183
Intra
KRT81 Q14533 KRT35 Homo sapiens Q92764 32296183
Intra
KRT81 Q14533 KRT35 Homo sapiens Q92764 32296183
Intra
KRT81 Q14533 ATN1 Homo sapiens Q86V38 32814053
Intra
KRT81 Q14533 ATN1 Homo sapiens Q86V38 32814053
Intra
KRT81 Q14533 ATN1 Homo sapiens Q86V38 32814053
Intra
KRT81 Q14533 KRT39 Homo sapiens Q6A163 32296183
Intra
KRT81 Q14533 KRT39 Homo sapiens Q6A163 32296183
Intra
KRT81 Q14533 KRT39 Homo sapiens Q6A163 32296183
Intra
KRT81 Q14533 KRT28 Homo sapiens Q7Z3Y7 32296183
Intra
KRT81 Q14533 KRT28 Homo sapiens Q7Z3Y7 32296183
Intra
KRT81 Q14533 KRT28 Homo sapiens Q7Z3Y7 32296183
Intra
KRT81 Q14533 KRT26 Homo sapiens Q7Z3Y9 32296183
Intra
KRT81 Q14533 KRT26 Homo sapiens Q7Z3Y9 32296183
Intra
KRT81 Q14533 KRT26 Homo sapiens Q7Z3Y9 32296183
Intra
KRT81 Q14533 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
KRT81 Q14533 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
KRT81 Q14533 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
KRT81 Q14533 KRT18 Homo sapiens P05783 32296183
Intra
KRT81 Q14533 KRT18 Homo sapiens P05783 32296183
Intra
KRT81 Q14533 KRT27 Homo sapiens Q7Z3Y8 32296183
Intra
KRT81 Q14533 KRT27 Homo sapiens Q7Z3Y8 32296183
Intra
KRT81 Q14533 KRT27 Homo sapiens Q7Z3Y8 32296183
Intra
KRT81 Q14533 KRT16 Homo sapiens P08779 32296183
Intra
KRT81 Q14533 KRT16 Homo sapiens P08779 32296183
Intra
KRT81 Q14533 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
KRT81 Q14533 CYSRT1 Homo sapiens A8MQ03 32296183
Cross
KRT81 Q14533 Hoxa1 Mus musculus P09022 23088713
Cross
KRT81 Q14533 Hoxa1 Mus musculus P09022 23088713
Intra
KRT81 Q14533 OIP5 Homo sapiens O43482 32296183
Intra
KRT81 Q14533 OIP5 Homo sapiens O43482 32296183
Intra
KRT81 Q14533 KRT14 Homo sapiens P02533 32296183
Intra
KRT81 Q14533 KRT14 Homo sapiens P02533 32296183
Intra
KRT81 Q14533 KRT15 Homo sapiens P19012 32296183
Intra
KRT81 Q14533 KRT15 Homo sapiens P19012 32296183
Intra
KRT81 Q14533 KXD1 Homo sapiens Q9BQD3 16189514
Intra
KRT81 Q14533 KXD1 Homo sapiens Q9BQD3 16189514
Intra
KRT81 Q14533 OTX1 Homo sapiens P32242 25416956
Intra
KRT81 Q14533 OTX1 Homo sapiens P32242 32296183
Intra
KRT81 Q14533 OTX1 Homo sapiens P32242 25416956
Intra
KRT81 Q14533 HOXA1 Homo sapiens P49639 32296183
Intra
KRT81 Q14533 HOXA1 Homo sapiens P49639 32296183
Intra
KRT81 Q14533 KRT19 Homo sapiens P08727 32296183
Intra
KRT81 Q14533 KRT19 Homo sapiens P08727 32296183
Intra
KRT81 Q14533 LCA5L Homo sapiens O95447 32296183
Intra
KRT81 Q14533 LCA5L Homo sapiens O95447 32296183
Intra
KRT81 Q14533 KRT31 Homo sapiens Q15323 32296183
Intra
KRT81 Q14533 KRT31 Homo sapiens Q15323 25416956
Intra
KRT81 Q14533 KRT31 Homo sapiens Q15323 32296183
Intra
KRT81 Q14533 KRT31 Homo sapiens Q15323 25416956
Intra
KRT81 Q14533 KRT31 Homo sapiens Q15323 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Monilethrix
  • Beaded Hair

  • MNLIX

  • Nodose Hair

  • Moniliform Hair Syndrome

Hair Disease
  • Hair Diseases

  • Hair Anomaly

  • Hair Disorder

  • Hair Problems

Pilomatrixoma
  • Pilomatricoma

  • PTR

  • Epithelioma Calcificans Of Malherbe

  • Benign Pilomatricoma

  • Calcifying Epithelioma Of Malherbe

  • Pilomatricoma, Somatic

  • Benign Pilomatrixoma

  • Malherbe Calcifying Epithelioma

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

Epidermolytic Hyperkeratosis
  • Bullous Congenital Ichthyosiform Erythroderma

  • Bullous Ichthyosiform Erythroderma

  • EHK

  • Bullous Erythroderma Ichthyosiformis Congenita Of Brocq

  • Bcie

  • Bie

  • Epidermolytic Ichthyosis

  • Ichthyosis Bullosa Of Siemens

  • Superficial Epidermolytic Ichthyosis

  • Hyperkeratosis, Epidermolytic

  • Congenital Bullous Ichthyosiform Erythroderma

  • Bullous Type Ichthyosis

  • Epidermolytic Palmoplantar Hyperkeratosis

  • Bullous Ichthyosiform Erythroderma Congenita

  • Bullous Erythroderma Ichthyosiforme

  • Sei

  • Epidermolytic Hyperkeratosis Late-Onset

  • Epidermolytic Hyperkeratosis, Late-Onset

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

Nonsyndromic Congenital Nail Disorder
  • Nail Disorder, Nonsyndromic Congenital

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

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
Mus musculus KRT81 MGD MGI:1928858
Rattus norvegicus KRT81 RGD RGD:1303316
Others KRT81 NCBI