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Fam171a1 Gene Detail
Summary
  • Symbol
    Fam171a1
  • Name
    family with sequence similarity 171, member A1
  • Synonyms
    9630050M13Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:2442917
    NCBI Gene: 269233
  • Alliance
  • Transcription Start Sites
    6 TSS
Location &
Maps
more
  • Sequence Map
    Chr2:3115261-3228843 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 2, 1.73 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    2480 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2442917
protein coding gene Chr2:3115261-3228843 (+)
129S1/SvImJ ENSMUSG00200029892
protein coding gene Chr2:40599-155845 (+)
A/J ENSMUSG00195016211
protein coding gene Chr2:75674-189275 (+)
AKR/J ENSMUSG00220005563
protein coding gene Chr2:65145-178738 (+)
BALB/cJ ENSMUSG00180029200
protein coding gene Chr2:163511-277122 (+)
C3H/HeJ ENSMUSG00175015885
protein coding gene Chr2:64623-178225 (+)
C57BL/6NJ ENSMUSG00215013815
protein coding gene Chr2:189939-303543 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0023131
protein coding gene Chr2:20599-136699 (+)
CAST/EiJ ENSTCUG00005004634
protein coding gene Chr2:84381-202193 (+)
CBA/J ENSMUSG00210027003
protein coding gene Chr2:106093-219682 (+)
DBA/2J ENSMUSG00185012151
protein coding gene Chr2:65533-179130 (+)
FVB/NJ ENSMUSG00205029454
protein coding gene Chr2:69003-182795 (+)
JF1/MsJ ENSUMUG00000002021
protein coding gene Chr2:72147-189937 (+)
LP/J ENSMUSG00230003000
protein coding gene Chr2:2024530-2139776 (+)
NOD/ShiLtJ ENSMUSG00190005351
protein coding gene Chr2:65538-179138 (+)
NZO/HlLtJ ENSMUSG00225000044
protein coding gene Chr2:9728921-9846064 (+)
PWK/PhJ ENSLUMG00010026674
protein coding gene Chr2:98729-219142 (+)
SPRET/EiJ ENSMSPG00010025138
protein coding gene Chr2:74800-189540 (+)
WSB/EiJ ENSIUOG00005022549
protein coding gene Chr2:43420-158683 (+)



Homology
more
  • Human Ortholog
    FAM171A1, family with sequence similarity 171 member A1
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    FAM171A1, family with sequence similarity 171 member A1
  • Synonyms
    APCN, C10orf38
  • Links
    NCBI Gene ID: 221061
    UniProt: Q5VUB5

  • Chr Location
    10p13; chr10:15211643-15374554 (-)  GRCh38

Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    1 phenotype from 1 allele in 1 genetic background
    41 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Molecular Function

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

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
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
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
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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
  • Tissues
  • cDNA Data
  • Literature Summary
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic 269233 NCBI Gene Model | MGI Sequence Detail 113583 C57BL/6J ±  kb
transcript NM_001081161 RefSeq | MGI Sequence Detail 4149 C57BL/6  
polypeptide NP_001074630 RefSeq | MGI Sequence Detail 892 C57BL/6  
For the selected sequence
Protein
Information
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  • UniProt
    6 Sequences
  • InterPro Domains
    IPR018890 FAM171
    IPR049175 FAM171, C-terminal
    IPR048530 FAM171, N-terminal
  • GlyGen
    A2ATK9 3 sites, 1 N-linked glycan (1 site), 1 O-linked glycan (2 sites)
Molecular
Reagents
less
  • All nucleic 53
    cDNA 53

    Microarray probesets 4
Other
Accession IDs
less
MGI:2138771
References
more
  • Summaries
    All 66
    Developmental Gene Expression 1
    Diseases 1
    Gene Ontology 4
    Phenotypes 41
  • Earliest
    J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573
  • Latest
    J:375075 Knowles S, et al., In vivo investigation of STN1 downregulation in melanoma formation in adult mice following UV irradiation. PLoS One. 2025;20(11):e0326647

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
09/01/2026
MGI 6.24
The Jackson Laboratory