1. Gene
  2. KRT81 - keratin 81 Gene

KRT81 - keratin 81 Gene

Homo sapiens

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

Gene ID: 3887 | Gene type: protein coding

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
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference 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 Reference
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