AA914427 Gene Detail

Summary

• Symbol
  AA914427
• Name
  EST AA914427

• Feature Type
  unclassified gene
• IDs
  MGI:1858439
  NCBI Gene: 53959
• Alliance
  genome feature page
• Transcription Start Sites
  1 TSS

Location &
Maps

• Sequence Map
  Chr16:17739907-17741083 bp, + strand

  From Ensembl annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 16, Syntenic
• Mapping Data
  1 experiment

Strain
Comparison

• Strain Annotations
  19

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_1858439	unclassified gene	Chr16:17739907-17741083 (+)
129S1/SvImJ	ENSMUSG00200046511	unclassified gene	Chr16:14736476-14737652 (+)
A/J	ENSMUSG00195035719	unclassified gene	Chr16:14293770-14294946 (+)
AKR/J	ENSMUSG00220046555	unclassified gene	Chr16:14610023-14611199 (+)
BALB/cJ	ENSMUSG00180042630	unclassified gene	Chr16:14535007-14536183 (+)
C3H/HeJ	ENSMUSG00175050061	unclassified gene	Chr16:14680012-14681188 (+)
C57BL/6NJ	ENSMUSG00215043333	unclassified gene	Chr16:14401132-14402308 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0000726	unclassified gene	Chr16:14415703-14416889 (+)
CAST/EiJ	ENSTCUG00005045556	unclassified gene	Chr16:14618467-14619639 (+)
CBA/J	ENSMUSG00210047089	unclassified gene	Chr16:14696337-14697513 (+)
DBA/2J	ENSMUSG00185036426	unclassified gene	Chr16:14642486-14643662 (+)
FVB/NJ	ENSMUSG00205048313	unclassified gene	Chr16:14650108-14651284 (+)
JF1/MsJ	ENSUMUG00000054854	unclassified gene	Chr16:14732852-14734027 (+)
LP/J	ENSMUSG00230045950	unclassified gene	Chr16:17220350-17221526 (+)
NOD/ShiLtJ	ENSMUSG00190051451	unclassified gene	Chr16:14782391-14783567 (+)
NZO/HlLtJ	ENSMUSG00225038153	unclassified gene	Chr16:20466190-20467366 (+)
PWK/PhJ	ENSLUMG00010049084	unclassified gene	Chr16:14606663-14607838 (+)
SPRET/EiJ	ENSMSPG00010048480	unclassified gene	Chr16:14624289-14625459 (+)
WSB/EiJ	ENSIUOG00005045474	unclassified gene	Chr16:14776460-14777636 (+)

Homology

• Gene Tree
  AA914427
  

Human Diseases

• References
  5 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  146 phenotype references
  

• All Mutations and Alleles
  11
• Endonuclease-mediated
  2
• Targeted
  9
• Genomic Mutations
  11 involving AA914427
• Find Mice (IMSR)
  0 strains or lines available

Expression

• Assay Results
  597
• cDNA Data
  2

Tissue x Stage Matrix

• Other Mouse Links
  GEO
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  25
• RefSeq
  1

• Ensembl
  ENSMUSG00000103149 (Evidence)
• NCBI Gene
  53959

Representative Sequences			Length	Strain/Species
genomic	ENSMUSG00000103149	Ensembl Gene Model | MGI Sequence Detail	1177	C57BL/6J
transcript	NR_188871	RefSeq | MGI Sequence Detail	1170	C57BL/6

Molecular
Reagents

• All nucleic 3

  Genomic 1

  cDNA 2

  
  

  Microarray probesets 1

References

• Summaries
  All 154

  Diseases 5

  Phenotypes 146
• Earliest
  J:57757 Lindsay EA, et al., Congenital heart disease in mice deficient for the DiGeorge syndrome region [see comments]. Nature. 1999 Sep 23;401(6751):379-83
• Latest
  J:390319 Son GY, et al., Dysregulated calcium signaling underlies hyposalivation and microbial dysbiosis in Down syndrome. Cell Rep. 2026 Jul 1;:117619

TSS for AA914427:

(View these features in JBrowse)

Transcription Start Site	Location	Distance from Gene 5'-end
Tssr137346	Chr16:17739905-17739940 (+)	16 bp