Publication for KRT81 and KRT86

Species	Symbol	Function*	Entrez Gene ID*	Other ID	Gene coexpression	CoexViewer
hsa	KRT81	keratin 81	3887			[link]
hsa	KRT86	keratin 86	3892

Pubmed ID	Priority	Text
25287022	0.98	K81, K85 and K86), we found differences in the rate of evolution, suggesting that these cetacean hair-type keratin genes may be under reduced selective constraints (P < 0.01, for all genes).
	0.96	K81, K86, K83, K85, K84 and K82) and 21 other type II keratin genes (Figure 1).
	0.96	K81, K86 and K83 hair-type keratin genes were responsible for the hairless phenotype of the Hirosaki hairless rat.
	0.95	K81, K83 and K86 genes (Figure 3).
28785294	0.98	K81, K83, K87 and K86 in the type II (Figs. 2 and 3).
	0.97	K81-K86) expressed in hair follicle and hair which could directly affect hair growth.
26317522	0.98	K81, K83, K85, and K86 (Fig 1).
29371649	0.97	K81, K82, K83, K84, K85, and K86; and type I K31, K33a, K33b, K34, K35, K32, K36, K37, and K38 (Supplementary Fig. S3a,b).
	0.94	K81, K83, and K86) and group C (K82, K84, and K85).
	0.84	K81-K86).
	0.54	K81-87), and interestingly, deamidation was observed in keratin type I belonging to the families K33A, K33B, K34, and K35; type II belonging to families K82-K86; and several KAPs.
31847069	0.97	K81-K86 (type II), K31-K40 (type I)), located both in the cortex and in the cuticle, representing the most important cells within the hair follicle involved in hair growth.
	0.93	K81-K86 (former designation hHb1-hHb4), as reported in the experimental section.
	0.86	K81, K83, K85, and K86 (all types II hair keratin isoforms), increased cellular content was already detectable after 48 h of treatment.
	0.82	K81-K86) hair keratins expressed by hair follicular keratinocytes.
22393391	0.97	keratin81 (NM_002281), keratin86 (NM_002284), Serpina3 (NM_001085), collagen type VIII alpha1 (NM_001850) (f.c.>5) and STAT1 (IFN-gamma signalling pathway) (NM_139266) (f.c.>2).
26610607	0.97	KRT81, KRT83 and KRT86) is upregulated in all resistant cells and its putative SE belongs to cluster 1 (Fig. 3b).
21188018	0.96	K81, K83, K86.
24361867	0.96	KRT86, KRT81 and KRT83 loci.
28839397	0.96	KRT81, KRT83, and KRT86 lead to autosomal dominant monilethrix whereas mutations in the desmoglein 4 gene cause an autosomal recessive form.
30050820	0.96	KRT81, KRT83, or KRT86, whereas in autosomal recessive form, mutation in the desmoglein-4 gene (DSG4) has been reported.
31113963	0.96	K81 - K86) with high-sulfur content.
16831889	0.95	K81-K86, led to last digit matching between the old (Table IV, column 1) and the new nomenclature (Table IV, column 4), so that this kind of "aide-memoire" exists for both types of human hair keratins.
29784039	0.94	K81, K83, and K86)..
22628999	0.93	KRT86 gene were identified in large families from Turkey and India as well as in the KRT81 gene in a family of Indian origin.
32030317	0.92	K81, K83 and K86 (spot 7)) compared to the Chinese and three keratins that were differently altered (K33b and two K86 (spots 7 and 8)) compared to the Malays.
27284572	0.87	KRT86, KRT83, and KRT81.
23554671	0.82	KRT81, KRT83 and KRT86.
	0.76	KRT86 and KRT81 is thought to be a possible mutation hot spot in monilethrix.
	0.73	KRT86, KRT83 and KRT81 gene led to the detection of a heterozygous G to A point mutation in the KRT86 gene in the family (Fig. 4A).
	0.57	KRT86, as well as an HTM E413K mutation in hair keratin KRT81, have been reported.
	0.55	KRT81 and KRT83 and exon 1 of KRT86 among the patients.
32257198	0.82	KRT81-KRT86) in each group of samples (Fig. 4).
21176769	0.81	K81 (Hb1) and K86 (Hb6) in the mid-cortex and shares an almost identical rod domain sequence, only one mutation in the 2B region (p.Glu407Lys) has been identified so far in a single monilethrix family with co-dominant manner.
	0.63	KRT86 (previously KRTHB6), and HTM mutation in K86 (Hb6; 90%) as well as HTM mutation in K81 (Hb1;100%) have been identified.
30814526	0.76	KRT81, and KRT86), intercellular junction associated proteins (DSG3, GJB2, JPH1, JPH2, PKP2, UPK2) and genes related to keratinocyte differentiation (IVL, EPPK).
22716242	0.71	K81, K83, K85 and K86, are expressed only in the hair shaft and follicles, and are responsible for keratodermas of the hair and nails (see www.interfil.org).
24778539	0.65	KRT86, KRT 81 and KRT 83 gene in autosomal dominant trait and mutation in desmoglein 4 was associated with autosomal recessive type of monilethrix.