C230037L18Rik Gene Detail

Summary

• Symbol
  C230037L18Rik
• Name
  RIKEN cDNA C230037L18 gene

• Feature Type
  lncRNA gene
• IDs
  MGI:3697701
  NCBI Gene: 100532730
• Alliance
  genome feature page

Location &
Maps

• Sequence Map
  Chr15:89360455-89369053 bp, + strand

  From NCBI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 15, 44.94 cM
• Mapping Data
  1 experiment

Strain
Comparison

• SNPs within 2kb
  246 from dbSNP Build 142
• Strain Annotations
  19

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_3697701	lncRNA gene	Chr15:89359001-89373499 (+)
129S1/SvImJ	ENSMUSG00200035731	lncRNA gene	Chr15:86512653-86521267 (+)
A/J	ENSMUSG00195020356	lncRNA gene	Chr15:86434385-86442999 (+)
AKR/J	ENSMUSG00220031619	lncRNA gene	Chr15:86464953-86473564 (+)
BALB/cJ	ENSMUSG00180015323	lncRNA gene	Chr15:86288180-86296733 (+)
C3H/HeJ	ENSMUSG00175029401	lncRNA gene	Chr15:86620990-86629601 (+)
C57BL/6NJ	ENSMUSG00215030443	lncRNA gene	Chr15:86381697-86390308 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0002931	antisense lncRNA gene	Chr15:83429287-83437959 (+)
CAST/EiJ	ENSTCUG00005031585	lncRNA gene	Chr15:85886072-85894635 (+)
CBA/J	ENSMUSG00210013176	lncRNA gene	Chr15:86390435-86399046 (+)
DBA/2J	ENSMUSG00185022413	lncRNA gene	Chr15:86402328-86410960 (+)
FVB/NJ	ENSMUSG00205038322	lncRNA gene	Chr15:86163082-86171697 (+)
JF1/MsJ	ENSUMUG00000042549	lncRNA gene	Chr15:85968964-85977682 (+)
LP/J	ENSMUSG00230046790	lncRNA gene	Chr15:89752833-89761440 (+)
NOD/ShiLtJ	ENSMUSG00190029086	lncRNA gene	Chr15:86406820-86415431 (+)
NZO/HlLtJ	ENSMUSG00225051225	lncRNA gene	Chr15:90069437-90078049 (+)
PWK/PhJ	ENSLUMG00010034119	lncRNA gene	Chr15:86121483-86130150 (+)
SPRET/EiJ	ENSMSPG00010014874	lncRNA gene	Chr15:87827269-87836036 (+)
WSB/EiJ	ENSIUOG00005011605	lncRNA gene	Chr15:86496811-86505375 (+)

Homology

• Gene Tree
  C230037L18Rik
  

Human Diseases

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  25 phenotype references
  

• All Mutations and Alleles
  10
• Chemically induced (other)
  1
• Endonuclease-mediated
  1
• Gene trapped
  6
• Radiation induced
  2
• Genomic Mutations
  3 involving C230037L18Rik
• Find Mice (IMSR)
  1 strains or lines available

Expression

• Assay Results
  597
• cDNA Data
  3

Tissue x Stage Matrix

• Other Mouse Links
  GEO
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  78
• RefSeq
  1

• Ensembl
  ENSMUSG00000084915 (Evidence)
• NCBI Gene
  100532730

Representative Sequences			Length	Strain/Species
genomic	100532730	NCBI Gene Model | MGI Sequence Detail	8599	C57BL/6J
transcript	NR_077233	RefSeq | MGI Sequence Detail	872	ZRU/MplStud

Molecular
Reagents

• All nucleic 3

  cDNA 3

  
  

  Microarray probesets 1

References

• Summaries
  All 35

  Diseases 1

  Phenotypes 25
• Earliest
  J:7688 Lane PW, et al., Association of megacolon with a new dominant spotting gene (Dom) in the mouse. J Hered. 1984 Nov-Dec;75(6):435-9
• Latest
  J:387680 Ahn B, et al., Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice. Genes (Basel). 2026 Jan 31;17(2)