Incidental Mutation 'IGL01564:Homer2'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Homer2
Ensembl Gene ENSMUSG00000025813
Gene Namehomer scaffolding protein 2
Synonyms9330120H11Rik, Cupidin, Vesl-2, CPD
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.204) question?
Stock #IGL01564
Quality Score
Chromosomal Location81600481-81707527 bp(-) (GRCm38)
Type of Mutationsplice site (4 bp from exon)
DNA Base Change (assembly) T to C at 81618572 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000146521 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026922] [ENSMUST00000098326] [ENSMUST00000207371] [ENSMUST00000207983] [ENSMUST00000208937]
Predicted Effect probably null
Transcript: ENSMUST00000026922
SMART Domains Protein: ENSMUSP00000026922
Gene: ENSMUSG00000025813

WH1 1 107 1.86e-37 SMART
coiled coil region 162 320 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000098326
SMART Domains Protein: ENSMUSP00000095931
Gene: ENSMUSG00000025813

Pfam:WH1 1 43 4.6e-11 PFAM
coiled coil region 98 256 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207039
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207289
Predicted Effect probably benign
Transcript: ENSMUST00000207371
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207526
Predicted Effect probably null
Transcript: ENSMUST00000207983
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207991
Predicted Effect probably null
Transcript: ENSMUST00000208937
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the homer family of dendritic proteins. Members of this family regulate group 1 metabotrophic glutamate receptor function. The encoded protein is a postsynaptic density scaffolding protein. Alternative splicing results in multiple transcript variants. Two related pseudogenes have been identified on chromosome 14. [provided by RefSeq, Jun 2011]
PHENOTYPE: Homozygous mutants exhibit an increase in intracellular calcium concentration and in the frequency of intracellular calcium oscillations in pancreatic acinar cells. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adat3 T A 10: 80,606,859 M177K probably damaging Het
Ankrd28 G T 14: 31,755,767 T48K probably damaging Het
BC005561 A T 5: 104,520,663 Y1017F probably benign Het
Capn3 T C 2: 120,480,708 I112T probably damaging Het
Clec3a T A 8: 114,425,542 I96N probably damaging Het
Clic4 C T 4: 135,217,193 A224T probably damaging Het
Eif2b3 T C 4: 117,028,542 Y94H probably benign Het
Ep300 A T 15: 81,632,464 probably benign Het
Errfi1 C A 4: 150,867,030 T305N probably damaging Het
Fam131c T A 4: 141,379,673 probably null Het
Fbxo11 G A 17: 88,002,896 T494I probably benign Het
Hpf1 C A 8: 60,890,479 probably benign Het
Hspa1b T C 17: 34,957,549 N487D probably benign Het
Ikbke C A 1: 131,257,921 A617S probably benign Het
Jade1 G T 3: 41,596,649 R174S possibly damaging Het
Lcmt1 T C 7: 123,404,440 F139S probably benign Het
Lipo2 T C 19: 33,721,024 T318A probably benign Het
Lrp1b C T 2: 40,677,486 probably benign Het
Lsm14a T C 7: 34,389,355 probably benign Het
Mpp2 T C 11: 102,061,519 D393G probably benign Het
Nfyb T C 10: 82,752,426 Y137C probably damaging Het
Olfr1161 A T 2: 88,025,304 H194L probably benign Het
Olfr1510 T C 14: 52,410,842 D10G probably benign Het
Olfr476 T C 7: 107,967,991 I198T probably benign Het
Scn3a A C 2: 65,461,446 I1652S probably damaging Het
Slc33a1 C T 3: 63,943,347 V519I probably benign Het
Strada G T 11: 106,173,292 N66K probably damaging Het
Tlr1 T A 5: 64,925,846 I463F probably damaging Het
Tnfrsf19 G T 14: 60,974,609 F197L possibly damaging Het
Tph1 T A 7: 46,650,881 probably benign Het
Ttn A T 2: 76,816,578 L3287H probably damaging Het
Vmn2r18 A T 5: 151,585,168 S164T possibly damaging Het
Zan C T 5: 137,446,733 V1755I unknown Het
Zmym4 T C 4: 126,911,280 I396V possibly damaging Het
Other mutations in Homer2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02197:Homer2 APN 7 81610399 missense probably benign 0.01
IGL02865:Homer2 APN 7 81610332 missense probably damaging 1.00
IGL02948:Homer2 APN 7 81649645 missense probably damaging 1.00
IGL03035:Homer2 APN 7 81624278 missense possibly damaging 0.57
R0148:Homer2 UTSW 7 81624278 missense probably benign 0.11
R0480:Homer2 UTSW 7 81618603 missense possibly damaging 0.86
R0544:Homer2 UTSW 7 81649678 missense probably damaging 1.00
R1872:Homer2 UTSW 7 81636402 missense probably damaging 0.99
R1873:Homer2 UTSW 7 81636363 missense probably damaging 1.00
R2060:Homer2 UTSW 7 81618703 missense probably benign 0.00
R2148:Homer2 UTSW 7 81624295 missense possibly damaging 0.50
R4096:Homer2 UTSW 7 81611304 critical splice donor site probably null
R4888:Homer2 UTSW 7 81649563 missense probably benign 0.02
R5121:Homer2 UTSW 7 81649563 missense probably benign 0.02
R6033:Homer2 UTSW 7 81618679 missense possibly damaging 0.92
R6033:Homer2 UTSW 7 81618679 missense possibly damaging 0.92
R6489:Homer2 UTSW 7 81624278 missense probably benign 0.11
R7652:Homer2 UTSW 7 81649666 missense probably damaging 1.00
R8306:Homer2 UTSW 7 81624266 missense possibly damaging 0.78
Posted On2013-12-09