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 growth
Accession: MP:0002073
browse the term
Definition: any anomaly in the amount of hair or abnormal onset of hair growth cycle or development, or abnormal hair pattern
Synonyms: exact_synonym: coat: hair growth defects; hair growth abnormalities
narrow_synonym: Thick hair
alt_id: MP:0000409
xref: HP:0100874; MGI:2173539
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Foxn1
forkhead box N1
IAGP
RGD
PMID:8790387
RGD:1300512
NCBI chr10:63,749,461...63,778,468
Ensembl chr10:63,251,400...63,273,710
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Krt83
keratin 83
IAGP
DNA:deletion
RGD
PMID:18420582
RGD:2316553
NCBI chr 7:132,604,180...132,610,869
Ensembl chr 7:132,604,128...132,610,799
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Krt87
keratin 87
IAGP
DNA:deletion
RGD
PMID:18420582
RGD:2316553
NCBI chr 7:132,547,388...132,555,005
Ensembl chr 7:132,548,141...132,554,978
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Aire
autoimmune regulator
IMP
RGD
PMID:29959280
RGD:38599145
NCBI chr20:10,635,775...10,650,709
Ensembl chr20:10,636,123...10,651,060
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Aireem1Ang
autoimmune regulator; ZFN induced mutant1, Ang
IMP
RGD
PMID:29959280
RGD:38599145
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Dsg4
desmoglein 4
IMP
RGD
PMID:15606503
RGD:150521560
NCBI chr18:11,720,844...11,757,927
Ensembl chr18:11,720,975...11,756,234
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Dsg4hr
desmoglein 4; hairless mutant
IMP
RGD
PMID:15606503
RGD:150521560
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Gla
galactosidase, alpha
IMP
RGD
PMID:29979634
RGD:401976416
NCBI chr X:102,062,497...102,073,915
Ensembl chr X:97,768,996...97,780,664
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Glaem2Mcwi
galactosidase, alpha; CRISPR/Cas9 system induced mutant 2, Medical College of Wisconsin
IMP
RGD
PMID:29979634
RGD:401976416
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Vdr
vitamin D receptor
IMP
RGD
PMID:32231239
RGD:32716373
NCBI chr 7:130,864,764...130,916,757
Ensembl chr 7:128,987,981...129,037,677
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Vdrem2Thka
vitamin D receptor; CRISPR/Cas9 induced mutant 2, Thka
IMP
RGD
PMID:32231239
RGD:32716373
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Hr
HR, lysine demethylase and nuclear receptor corepressor
IMP
RGD
PMID:21325752
RGD:150520024
NCBI chr15:52,036,540...52,056,019
Ensembl chr15:45,626,835...45,646,313
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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
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Krt71Rex
keratin 71; autosomal dominant Rex
IAGP
DNA:deletion:cds:intron 1, p.Val149_Gln154 del
RGD
PMID:20179389
RGD:11570415
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Mecp2
methyl CpG binding protein 2
IMP
compared to SD wild-type
RGD
PMID:27329765
RGD:40924662
NCBI chr X:156,932,481...156,995,981
Ensembl chr X:151,789,930...151,844,689
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Mecp2em1Sage
methyl CpG binding protein 2; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs
IMP
compared to SD wild-type
RGD
PMID:27329765
RGD:40924662
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Dsg4
desmoglein 4
IAGP
DNA:missense mutation:exon 8 (rat)
RGD
PMID:15617564
RGD:150521562
NCBI chr18:11,720,844...11,757,927
Ensembl chr18:11,720,975...11,756,234
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Edaradd
EDAR associated via death domain
IAGP
compared to heterozygous animals
RGD
PMID:15829729
RGD:2304219
NCBI chr17:92,850,791...92,894,808
Ensembl chr17:85,656,905...85,910,447
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EdaraddswhKyo
EDAR-associated death domain;swh Kyo mutant
IAGP
compared to heterozygous animals
RGD
PMID:15829729
RGD:2304219
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