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KRT81

KRT81

Protein-coding gene in the species Homo sapiens

Keratin, type II cuticular Hb1 is a protein that in humans is encoded by the KRT81 gene. The protein encoded by this gene is a member of the keratin gene family

KRT81

Hair keratin

Type of keratin found in hair and nails

hair keratin 8, KRT38 basic type II hair keratin type II hair keratin 1, KRT81 type II hair keratin 2, KRT82 type II hair keratin 3, KRT83 type II hair

Hair keratin

Hair_keratin

Keratin

Structural fibrous protein

KRT71, KRT72, KRT73, KRT74, KRT75, KRT76, KRT77, KRT78, KRT79, KRT80, KRT81, KRT82, KRT83, KRT84, KRT85 and KRT86 have been used to describe keratins

Keratin

KRT86

Protein-coding gene in the species Homo sapiens

this hair keratin, as well as KRT81 and KRT83, is found primarily in the hair cortex. Mutations in this gene and KRT81 have been observed in patients

KRT86

Monilethrix

Medical condition

completely. Monilethrix is caused by mutations affecting the genes KRTHB1 (KRT81), KRTHB3 (KRT83), or KRTHB6 (KRT86) which code for type II hair cortex keratins

Monilethrix

List of genes mutated in cutaneous conditions

Pachyonychia congenita type II Steatocystoma multiplex Vellus hair cyst KRT81 Monilethrix KRT83 Monilethrix KRT85 Pure hair–nail type of ectodermal dysplasia

List of genes mutated in cutaneous conditions

List_of_genes_mutated_in_cutaneous_conditions

Keratin disease

Medical condition

nevus skin KRT4, KRT13 Steatocystoma multiplex skin KRT17 Monilethrix hair KRT81, KRT83, KRT86 Meesman juvenile epithelial corneal dystrophy cornea KRT3

Keratin disease

Keratin_disease

List of keratins

Protein name Gene name Other protein name Other gene name K81 KRT81 Kb21, Hb1, K2.9 KRTHB1 K82 KRT82 Kb22, Hb2 KRTHB2 K83 KRT83 Kb23, Hb3, K2.10 KRTHB3

List of keratins

List_of_keratins

KRT83

Protein-coding gene in Homo sapiens

subfamilies based on structure similarity. One subfamily, consisting of KRTHB1 (KRT81), KRTHB3 (KRT83, this protein), and KRTHB6 (KRT86), is highly related. The

KRT83

List of human protein-coding genes 4

Q8N1N4 8395 KRT79 HGNC:28930; Q5XKE5 8396 KRT80 HGNC:27056; Q6KB66 8397 KRT81 HGNC:6458; Q14533 8398 KRT82 HGNC:6459; Q9NSB4 8399 KRT83 HGNC:6460; P78385

List of human protein-coding genes 4

List_of_human_protein-coding_genes_4

List of OMIM disorder codes

Molybdenum cofactor deficiency, type C; 252150; GPHN Monilethrix; 158000; KRT81 Monilethrix; 158000; KRT83 Monilethrix; 158000; KRT86 Mononeuropathy of

List of OMIM disorder codes

List_of_OMIM_disorder_codes

Online names & meanings

NEASSA

Female

Irish

NEASSA

Feminine form of English Neas, NEASSA means "excellent valor." In Irish mythology, this is the name of the mother of Conchobhar.Â

Hain

Surname or Lastname

English

Hain

English : habitational name from any of various places named with Middle English heghen, a weak plural of hegh, from Old English (ge)hÃ¦g â€˜enclosureâ€™. See also Haynes.English : from the Middle English personal name Hain, Heyne. This is derived from the Germanic personal name Hagano, originally a byname meaning â€˜hawthornâ€™. It is found in England before the Conquest, but was popularized by the Normans. In the Danelaw, it may be derived from Old Norse Hagni, HÇ«gni (see Hagan), a Scandinavianized version of the same name.English : nickname for a wretched individual, from Middle English hain(e), heyne â€˜wretchâ€™, â€˜niggardâ€™.German : topographic name for someone who lived by a patch of enclosed pastureland, Middle High German hage(n) (see Hagen 1), hain, or a habitational name from a place named Hain, from this word.German : from the Germanic personal name Hagin, originally a byname from the same element as in 2 above.Jewish (eastern Ashkenazic) : metronymic from the Yiddish personal name Khaye â€˜lifeâ€™ + the Slavic possessive suffix -in.