Incidental Mutation 'IGL03136:Akap5'
ID410544
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Akap5
Ensembl Gene ENSMUSG00000021057
Gene NameA kinase (PRKA) anchor protein 5
SynonymsLOC238276, AKAP150, 3526401B18Rik
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.236) question?
Stock #IGL03136
Quality Score
Status
Chromosome12
Chromosomal Location76324891-76334153 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) G to T at 76329875 bp
ZygosityHeterozygous
Amino Acid Change Glutamic Acid to Stop codon at position 694 (E694*)
Ref Sequence ENSEMBL: ENSMUSP00000134127 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095610] [ENSMUST00000154078] [ENSMUST00000172992]
Predicted Effect probably null
Transcript: ENSMUST00000095610
AA Change: E694*
SMART Domains Protein: ENSMUSP00000093270
Gene: ENSMUSG00000021057
AA Change: E694*

DomainStartEndE-ValueType
low complexity region 45 57 N/A INTRINSIC
Pfam:WSK 78 108 4.7e-13 PFAM
SCOP:d1k28a2 386 573 6e-21 SMART
Predicted Effect probably null
Transcript: ENSMUST00000154078
AA Change: E687*
SMART Domains Protein: ENSMUSP00000114495
Gene: ENSMUSG00000021057
AA Change: E687*

DomainStartEndE-ValueType
low complexity region 38 50 N/A INTRINSIC
Pfam:WSK 71 101 3.3e-13 PFAM
SCOP:d1k28a2 379 566 8e-21 SMART
Predicted Effect probably null
Transcript: ENSMUST00000172992
AA Change: E694*
SMART Domains Protein: ENSMUSP00000134127
Gene: ENSMUSG00000021057
AA Change: E694*

DomainStartEndE-ValueType
low complexity region 45 57 N/A INTRINSIC
Pfam:WSK 79 107 8.7e-15 PFAM
SCOP:d1k28a2 386 573 6e-21 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. The encoded protein binds to the RII-beta regulatory subunit of PKA, and also to protein kinase C and the phosphatase calcineurin. It is predominantly expressed in cerebral cortex and may anchor the PKA protein at postsynaptic densities (PSD) and be involved in the regulation of postsynaptic events. It is also expressed in T lymphocytes and may function to inhibit interleukin-2 transcription by disrupting calcineurin-dependent dephosphorylation of NFAT. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit reduced long term potentiation, improved glucose handling and heightened insulin sensitivity. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5730522E02Rik A G 11: 25,769,122 L7S unknown Het
Abr C T 11: 76,425,295 W571* probably null Het
Adam18 A T 8: 24,641,836 C420S probably damaging Het
Bbs1 T C 19: 4,890,991 K565R probably benign Het
Brix1 A G 15: 10,478,766 F189S probably damaging Het
Cnot4 C A 6: 35,051,241 R480L probably damaging Het
Ctu2 A G 8: 122,479,201 probably benign Het
Dhcr7 A G 7: 143,847,366 H422R probably damaging Het
Dock1 A G 7: 135,168,389 M1793V probably benign Het
Dock7 A G 4: 99,003,791 F853L probably damaging Het
Fkbp15 G A 4: 62,340,229 probably benign Het
Ftsj3 C T 11: 106,253,813 D117N probably damaging Het
Gphn A G 12: 78,481,333 I142V possibly damaging Het
Hsd3b1 G A 3: 98,852,985 A230V probably damaging Het
Hydin G A 8: 110,418,524 A836T probably benign Het
Ift52 G T 2: 163,025,334 E71* probably null Het
Ms4a14 T C 19: 11,304,411 D261G possibly damaging Het
Nid1 G A 13: 13,500,499 V935I probably benign Het
Nrap T C 19: 56,342,255 K1008E possibly damaging Het
Nup210 A C 6: 91,028,861 V1340G probably benign Het
Olfr1442 T A 19: 12,674,967 I254N probably damaging Het
Olfr169 A T 16: 19,566,353 F177I probably damaging Het
Olfr974 T C 9: 39,943,036 Y259H probably damaging Het
Pcdhb15 C A 18: 37,475,014 T433N probably damaging Het
Pdcd6ip T A 9: 113,691,499 N139I probably damaging Het
Pgbd1 A G 13: 21,433,439 V80A possibly damaging Het
Pigw A G 11: 84,877,777 I242T probably benign Het
Prtg T G 9: 72,856,985 V580G possibly damaging Het
Ptpn13 T A 5: 103,543,463 N1065K possibly damaging Het
Qrich1 G A 9: 108,544,918 R577H probably damaging Het
Ryr3 G A 2: 112,675,974 probably benign Het
Selenoi T C 5: 30,257,727 Y197H probably damaging Het
Slc47a2 A G 11: 61,310,765 C343R probably benign Het
Smurf2 A T 11: 106,831,048 D527E probably benign Het
Spam1 C T 6: 24,797,011 probably benign Het
Stkld1 T C 2: 26,951,423 V460A probably benign Het
Tgoln1 G A 6: 72,614,113 R339W probably damaging Het
Tprg T C 16: 25,412,762 probably benign Het
Treml1 T G 17: 48,364,851 probably benign Het
Ttc39b A T 4: 83,237,280 V497E probably damaging Het
Vmn1r223 A G 13: 23,249,763 T176A possibly damaging Het
Vmn2r75 A T 7: 86,148,703 I634N possibly damaging Het
Vps13c A G 9: 67,950,310 E2608G probably damaging Het
Zfp575 A G 7: 24,585,956 C87R probably damaging Het
Zfp790 T A 7: 29,829,895 Y668* probably null Het
Other mutations in Akap5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02194:Akap5 APN 12 76328033 missense probably damaging 0.99
IGL02309:Akap5 APN 12 76328855 missense possibly damaging 0.91
IGL02801:Akap5 APN 12 76328995 missense probably benign 0.25
PIT4802001:Akap5 UTSW 12 76329932 missense probably damaging 1.00
R1517:Akap5 UTSW 12 76329262 missense possibly damaging 0.91
R1694:Akap5 UTSW 12 76329924 missense probably damaging 0.99
R2012:Akap5 UTSW 12 76329348 missense possibly damaging 0.53
R4507:Akap5 UTSW 12 76327907 missense possibly damaging 0.91
R4755:Akap5 UTSW 12 76327807 nonsense probably null
R4893:Akap5 UTSW 12 76329969 missense probably damaging 0.99
R4905:Akap5 UTSW 12 76328433 missense probably damaging 0.96
R5482:Akap5 UTSW 12 76328826 missense probably benign 0.26
R5886:Akap5 UTSW 12 76327845 missense possibly damaging 0.88
R7151:Akap5 UTSW 12 76328249 missense probably benign 0.08
R7413:Akap5 UTSW 12 76328904 missense possibly damaging 0.65
R7514:Akap5 UTSW 12 76328529 missense probably benign 0.00
X0067:Akap5 UTSW 12 76328198 missense possibly damaging 0.93
Posted On2016-08-02