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MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.

Term:abnormal hair follicle morphology
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Accession:MP:0000377 term browser browse the term
Definition:any structural anomaly of the invagination of the epidermis from which the hair shaft develops
Synonyms:exact_synonym: abnormal hair follicle structure;   abnormal hair follicles;   hair follicle dysplasia;   hair follicle structure abnormalities;   hair follicles abnormalities
 alt_id: MP:0000375



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abnormal piliary canal morphology term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Hr HR, lysine demethylase and nuclear receptor corepressor IMP RGD PMID:21325752 RGD:150520024 NCBI chr15:45,626,835...45,646,313
Ensembl chr15:45,626,835...45,646,313
JBrowse link
decreased hair follicle number term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Edaradd EDAR associated via death domain IAGP compared to heterozygous animals RGD PMID:15829729 RGD:2304219 NCBI chr17:85,866,629...85,910,612
Ensembl chr17:85,656,905...85,910,447
JBrowse link
G EdaraddswhKyo EDAR-associated death domain;swh Kyo mutant IAGP compared to heterozygous animals RGD PMID:15829729 RGD:2304219
dilated hair follicle term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Hr HR, lysine demethylase and nuclear receptor corepressor IMP RGD PMID:21325752 RGD:150520024 NCBI chr15:45,626,835...45,646,313
Ensembl chr15:45,626,835...45,646,313
JBrowse link
G Krt71 keratin 71 IAGP DNA:deletion:cds:intron 1, p.Val149_Gln154 del RGD PMID:20179389 RGD:11570415 NCBI chr 7:132,873,532...132,898,975
Ensembl chr 7:132,873,540...132,882,325
JBrowse link
G Krt71Rex keratin 71; autosomal dominant Rex IAGP DNA:deletion:cds:intron 1, p.Val149_Gln154 del RGD PMID:20179389 RGD:11570415
small hair follicles term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Edaradd EDAR associated via death domain IAGP compared to heterozygous animals RGD PMID:15829729 RGD:2304219 NCBI chr17:85,866,629...85,910,612
Ensembl chr17:85,656,905...85,910,447
JBrowse link
G EdaraddswhKyo EDAR-associated death domain;swh Kyo mutant IAGP compared to heterozygous animals RGD PMID:15829729 RGD:2304219

Term paths to the root
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Term Annotations click to browse term
  mammalian phenotype 5415
    integument phenotype 171
      abnormal skin adnexa morphology 169
        abnormal pilosebaceous unit morphology 11
          abnormal hair follicle morphology 8
            abnormal hair follicle bulb morphology + 0
            abnormal hair follicle development + 0
            abnormal hair follicle infundibulum morphology + 0
            abnormal hair follicle inner root sheath morphology + 0
            abnormal hair follicle isthmus morphology 0
            abnormal hair follicle melanin granule morphology + 0
            abnormal hair follicle orientation 0
            abnormal hair follicle ostium morphology 0
            abnormal hair follicle outer root sheath morphology + 0
            abnormal piliary canal morphology + 2
            absent hair follicles 0
            decreased hair follicle number 3
            dilated hair follicle + 5
            distorted hair follicle pattern 0
            enlarged hair follicles 0
            folliculitis 0
            hair follicle comedo 0
            hair follicle degeneration 0
            increased hair follicle number 0
            small hair follicles 3
paths to the root