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Krtap19-9b Gene Detail
Summary
  • Symbol
    Krtap19-9b
  • Name
    keratin associated protein 19-9B
  • Synonyms
    AY026312, Krtap16-10b
  • Feature Type
    protein coding gene
  • IDs
    MGI:2181750
    NCBI Gene: 170939
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr16:88728692-88729152 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 16, 51.42 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    187 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2181750
protein coding gene Chr16:88728692-88729153 (-)
129S1/SvImJ MGP_129S1SvImJ_G0023003
protein coding gene Chr16:89752308-89752768 (-)
A/J MGP_AJ_G0022971
protein coding gene Chr16:85591258-85591718 (-)
AKR/J MGP_AKRJ_G0022941
protein coding gene Chr16:88197479-88197939 (-)
BALB/cJ MGP_BALBcJ_G0022973
protein coding gene Chr16:86123071-86123531 (-)
C3H/HeJ MGP_C3HHeJ_G0022734
protein coding gene Chr16:88760967-88761427 (-)
C57BL/6NJ MGP_C57BL6NJ_G0023420
protein coding gene Chr16:92637201-92637661 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0020924
protein coding gene Chr16:83406853-83407323 (-)
CAST/EiJ MGP_CASTEiJ_G0022255
protein coding gene Chr16:89208014-89208468 (-)
CBA/J MGP_CBAJ_G0022703
protein coding gene Chr16:96603132-96603592 (-)
DBA/2J MGP_DBA2J_G0022837
protein coding gene Chr16:85526335-85526795 (-)
FVB/NJ MGP_FVBNJ_G0022812
protein coding gene Chr16:84620311-84620771 (-)
LP/J MGP_LPJ_G0022907
protein coding gene Chr16:89444300-89444760 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0022832
protein coding gene Chr16:101184407-101184867 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0023438
protein coding gene Chr16:88691069-88691529 (-)
PWK/PhJ MGP_PWKPhJ_G0022000
protein coding gene Chr16:85679518-85679972 (-)
SPRET/EiJ MGP_SPRETEiJ_G0021830
protein coding gene Chr16:88251216-88251676 (-)
WSB/EiJ MGP_WSBEiJ_G0022305
protein coding gene Chr16:88927562-88928022 (-)



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    7 phenotype references
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Molecular Function

No experimental evidence to support Molecular Function annotation, following literature review. See J:73796.
Biological Process

No experimental evidence to support Biological Process annotation, following literature review. See J:73796.
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
  • cDNA Data
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic 170939 NCBI Gene Model | MGI Sequence Detail 461 C57BL/6J ±  kb
transcript NM_133359 RefSeq | MGI Sequence Detail 461 C3H/HeN  
polypeptide Q99NG9 UniProt | EBI | MGI Sequence Detail 58 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 13
    cDNA 13

    Microarray probesets 2
References
more
  • Summaries
    All 30
    Gene Ontology 2
    Phenotypes 7
  • Earliest
    J:68213 Tkatchenko AV, et al., Overexpression of Hoxc13 in differentiating keratinocytes results in downregulation of a novel hair keratin gene cluster and alopecia. Development. 2001 May;128(9):1547-58
  • Latest
    J:335294 Redhead Y, et al., Craniofacial dysmorphology in Down syndrome is caused by increased dosage of Dyrk1a and at least three other genes. Development. 2023 Apr 15;150(8):dev201077

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Funding Information
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory