Gm10152 Gene Detail

Summary

• Symbol
  Gm10152
• Name
  predicted gene 10152

• Feature Type
  unclassified gene
• IDs
  MGI:3641809
  NCBI Gene: 791284
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr7:144316876-144318219 bp, + strand

  From Ensembl annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 7, 88.85 cM
• Mapping Data
  1 experiment

Strain
Comparison

• SNPs within 2kb
  69 from dbSNP Build 142
• Strain Annotations
  18

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_3641809	unclassified gene	Chr7:144316876-144318219 (+)
129S1/SvImJ	MGP_129S1SvImJ_G0002258	unclassified gene	Chr7:150139179-150140522 (+)
A/J	MGP_AJ_G0002235	unclassified gene	Chr7:145771369-145772712 (+)
AKR/J	MGP_AKRJ_G0002221	unclassified gene	Chr7:149877351-149878694 (+)
BALB/cJ	MGP_BALBcJ_G0002230	unclassified gene	Chr7:145553111-145554454 (+)
C3H/HeJ	MGP_C3HHeJ_G0002206	unclassified gene	Chr7:149638336-149639679 (+)
C57BL/6NJ	MGP_C57BL6NJ_G0002355	unclassified gene	Chr7:155551589-155552932 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0001971	unclassified gene	Chr7:146928819-146930158 (+)
CAST/EiJ	MGP_CASTEiJ_G0002171	unclassified gene	Chr7:141959117-141960460 (+)
CBA/J	MGP_CBAJ_G0002200	unclassified gene	Chr7:160845696-160847039 (+)
DBA/2J	MGP_DBA2J_G0002203	unclassified gene	Chr7:143749636-143750979 (+)
FVB/NJ	MGP_FVBNJ_G0002213	unclassified gene	Chr7:143691044-143692387 (+)
LP/J	MGP_LPJ_G0002257	unclassified gene	Chr7:151669240-151670583 (+)
NOD/ShiLtJ	MGP_NODShiLtJ_G0002187	unclassified gene	Chr7:161380375-161381718 (+)
NZO/HlLtJ	MGP_NZOHlLtJ_G0002343	unclassified gene	Chr7:148842850-148844193 (+)
PWK/PhJ	MGP_PWKPhJ_G0002131	unclassified gene	Chr7:137062226-137063570 (+)
SPRET/EiJ	MGP_SPRETEiJ_G0002095	unclassified gene	Chr7:135625494-135626837 (+)
WSB/EiJ	MGP_WSBEiJ_G0002198	unclassified gene	Chr7:149835043-149836386 (+)

Homology

• Gene Tree
  Gm10152
  

Human Diseases

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  3 phenotype references
  

• All Mutations and Alleles
  1
• Spontaneous
  1
• Genomic Mutations
  1 involving Gm10152
• Incidental Mutations
  APF
• Find Mice (IMSR)
  4 strains or lines available

Gene Ontology
(GO)
Classifications

Expression

• Assay Results
  706
• cDNA Data
  1

Tissue x Stage Matrix

• Other Mouse Links
  GEO
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  21
• UniProt
  1

• Ensembl
  ENSMUSG00000103394 (Evidence)
• NCBI Gene
  791284

Representative Sequences			Length	Strain/Species
genomic	ENSMUSG00000103394	Ensembl Gene Model | MGI Sequence Detail	1344	C57BL/6J
transcript	AK051186	GenBank | ENA | DDBJ | MGI Sequence Detail	1345	C57BL/6J
polypeptide	Q8BQ98	UniProt | EBI | MGI Sequence Detail	136	Not Applicable

Protein
Information

• UniProt
  1 Sequence

Molecular
Reagents

• All nucleic 1

  cDNA 1

  
  

  Microarray probesets 1

References

• Summaries
  All 10

  Diseases 1

  Phenotypes 3
• Earliest
  J:8618 Theiler K, et al., Low set ears (Lse), a new mutation of the house mouse. Anat Embryol (Berl). 1986;175(2):241-6
• Latest
  J:338204 Luzzio A, et al., The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4. Mamm Genome. 2023 Jun 21;