Incidental Mutation 'IGL02958:Efhc2'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Efhc2
Ensembl Gene ENSMUSG00000025038
Gene NameEF-hand domain (C-terminal) containing 2
Synonyms4933407D04Rik, mRib72-2
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.249) question?
Stock #IGL02958
Quality Score
Chromosomal Location17132049-17319368 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) C to T at 17161246 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000026014 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026014]
Predicted Effect probably benign
Transcript: ENSMUST00000026014
SMART Domains Protein: ENSMUSP00000026014
Gene: ENSMUSG00000025038

DM10 75 182 2.04e-51 SMART
DM10 226 368 6.9e-49 SMART
DM10 430 537 2.52e-42 SMART
SCOP:d2mysb_ 560 693 9e-5 SMART
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 protein which contains three DM10 domains and three calcium-binding EF-hand motifs. A related protein is encoded by a gene on chromosome 6. It has been suggested that both proteins are involved in the development of epilepsy (PMID: 15258581, 16112844) and that this gene may be associated with fear recognition in individuals with Turner syndrome. [provided by RefSeq, Aug 2011]
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aars2 G T 17: 45,518,172 V755L probably benign Het
Abhd15 T C 11: 77,515,965 V256A possibly damaging Het
Agtr1b A T 3: 20,316,094 V116E possibly damaging Het
Ahi1 A T 10: 20,963,799 D203V probably damaging Het
Aplp2 G T 9: 31,164,676 probably benign Het
Arid4a T C 12: 71,097,563 S1249P probably benign Het
Asz1 T A 6: 18,073,814 K298M possibly damaging Het
C4bp A G 1: 130,636,795 I384T probably damaging Het
Cacna1e C A 1: 154,465,741 A1236S probably damaging Het
Cdh13 T C 8: 119,312,721 I634T possibly damaging Het
Cemip A T 7: 83,975,055 F524L probably damaging Het
Dnah7c G A 1: 46,657,111 R2051H probably damaging Het
Dnajc17 T C 2: 119,185,762 K77E probably benign Het
Ergic2 A T 6: 148,181,943 *50K probably null Het
Fam83g C T 11: 61,707,722 P812S probably damaging Het
Flg2 C T 3: 93,203,613 R983W unknown Het
Gm7102 G T 19: 61,175,680 Q106K possibly damaging Het
Gm9047 G A 6: 29,471,626 G34R probably damaging Het
Itih3 T C 14: 30,913,182 T73A probably benign Het
Kcnj1 A G 9: 32,396,555 S72G probably damaging Het
Kcnn4 T C 7: 24,374,745 V78A probably benign Het
Lrp1b T A 2: 41,302,916 D1353V probably damaging Het
Lrrc2 T A 9: 110,962,673 probably null Het
Ndufs8 T C 19: 3,911,232 E45G probably benign Het
Nell1 G A 7: 50,220,337 probably null Het
Nxt1 A G 2: 148,675,772 probably benign Het
Olfr1039 T A 2: 86,131,007 I219F probably benign Het
Olfr1390 A G 11: 49,341,300 Y256C probably benign Het
Pdzd8 A T 19: 59,300,372 C865* probably null Het
Pop1 G T 15: 34,530,363 C969F probably damaging Het
Rc3h2 A C 2: 37,414,700 I16S probably damaging Het
Shank1 T C 7: 44,354,473 V1863A possibly damaging Het
Slc15a4 A T 5: 127,604,665 L296Q possibly damaging Het
Ssr4 T C X: 73,787,250 probably benign Het
Supt20 T A 3: 54,713,723 probably benign Het
Ttc8 A T 12: 98,964,544 K282N probably benign Het
Usp40 A T 1: 87,978,485 V676E probably damaging Het
Vmn1r43 T C 6: 89,870,049 I152V probably benign Het
Vmn2r61 A T 7: 42,299,937 I594F probably benign Het
Vps53 A C 11: 76,117,711 I261S probably damaging Het
Wdr19 T A 5: 65,212,807 probably null Het
Zc3hav1 T A 6: 38,332,984 D301V probably damaging Het
Other mutations in Efhc2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01293:Efhc2 APN X 17207695 missense probably benign 0.04
IGL01317:Efhc2 APN X 17204959 splice site probably benign
IGL02215:Efhc2 APN X 17230578 missense probably damaging 1.00
R2867:Efhc2 UTSW X 17161245 splice site probably benign
R4052:Efhc2 UTSW X 17230550 missense possibly damaging 0.94
R4207:Efhc2 UTSW X 17230550 missense possibly damaging 0.94
R4208:Efhc2 UTSW X 17230550 missense possibly damaging 0.94
X0063:Efhc2 UTSW X 17162820 missense probably damaging 1.00
Posted On2015-12-18