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Serpinb9f Gene Detail
Summary
  • Symbol
    Serpinb9f
  • Name
    serine (or cysteine) peptidase inhibitor, clade B, member 9f
  • Synonyms
    MGC:61007, NK21, ovalbumin, Spi13
  • Feature Type
    protein coding gene
  • IDs
    MGI:894671
    NCBI Gene: 20709
  • Gene Overview
    MyGene.info: SERPINB9
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr13:33324077-33335370 bp, + strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 13, 13.86 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    30 from dbSNP Build 142
  • Strain Annotations
    12
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_894671
protein coding gene Chr13:33324077-33335370 (+)
129S1/SvImJ MGP_129S1SvImJ_G0020436
protein coding gene Chr13:31214839-31223285 (+)
A/J MGP_AJ_G0020393
protein coding gene Chr13:30674981-30692647 (+)
AKR/J MGP_AKRJ_G0020370
protein coding gene Chr13:31000183-31110036 (+)
BALB/cJ MGP_BALBcJ_G0020386
protein coding gene Chr13:30432285-30599859 (+)
C3H/HeJ no annotation
C57BL/6NJ no annotation
CAROLI/EiJ MGP_CAROLIEiJ_G0018410
protein coding gene Chr13:29000125-29011199 (+)
CAST/EiJ no annotation
CBA/J MGP_CBAJ_G0020145
protein coding gene Chr13:33657470-33778267 (+)
DBA/2J MGP_DBA2J_G0020270
protein coding gene Chr13:29911125-30175806 (+)
FVB/NJ no annotation
LP/J MGP_LPJ_G0020346
protein coding gene Chr13:31505388-31516613 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0020279
protein coding gene Chr13:33773619-33795632 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0020865
protein coding gene Chr13:30875692-30887475 (+)
PWK/PhJ no annotation
SPRET/EiJ MGP_SPRETEiJ_G0019282
protein coding gene Chr13:29599061-29800148 (+)
WSB/EiJ no annotation



Homology
more
  • Human Ortholog
    SERPINB9, serpin family B member 9
  • Vertebrate Orthologs
    6
  • Human Ortholog
    SERPINB9, serpin family B member 9
    Orthology source: HGNC
  • Synonyms
    CAP3, CAP-3, PI9, PI-9
  • Links
    NCBI Gene ID: 5272
    neXtProt AC: NX_P50453
    UniProt: P50453

  • Chr Location
    6p25.2; chr6:2887265-2903318 (-)  GRCh38.p7

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

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell death
cell differentiation
cell population proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
nucleic acid-templated transcription
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
synapse
vacuole
Click cells to view annotations.
Expression
less
  • cDNA Data
Interactions
less
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic 20709 NCBI Gene Model | MGI Sequence Detail 11294 C57BL/6J ±  kb
transcript NM_183197 RefSeq | MGI Sequence Detail 1920 Not Specified  
polypeptide NP_899020 RefSeq | MGI Sequence Detail 377 Not Specified  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 14
    Genomic 2
    cDNA 12

    Microarray probesets 1
Other
Accession IDs
less
MGI:2682310
References
more
  • Summaries
    All 24
    Gene Ontology 2
    Phenotypes 8
  • Earliest
    J:182573 Roderick TH, Producing and detecting paracentric chromosomal inversions in mice. Mutat Res. 1971 Jan;11(1):59-69
  • Latest
    J:202604 Nagamachi A, et al., Haploinsufficiency of SAMD9L, an endosome fusion facilitator, causes myeloid malignancies in mice mimicking human diseases with monosomy 7. Cancer Cell. 2013 Sep 9;24(3):305-17

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)
Citing These Resources
Funding Information
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last database update
09/10/2019
MGI 6.14
The Jackson Laboratory