Incidental Mutation 'IGL01531:Adcy1'
ID 89766
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Adcy1
Ensembl Gene ENSMUSG00000020431
Gene Name adenylate cyclase 1
Synonyms AC1, I-AC, D11Bwg1392e
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01531
Quality Score
Status
Chromosome 11
Chromosomal Location 7013489-7128506 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 7119414 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 1019 (V1019A)
Ref Sequence ENSEMBL: ENSMUSP00000020706 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020706]
AlphaFold O88444
Predicted Effect possibly damaging
Transcript: ENSMUST00000020706
AA Change: V1019A

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000020706
Gene: ENSMUSG00000020431
AA Change: V1019A

DomainStartEndE-ValueType
low complexity region 2 36 N/A INTRINSIC
low complexity region 58 90 N/A INTRINSIC
low complexity region 112 135 N/A INTRINSIC
CYCc 257 455 2.05e-80 SMART
transmembrane domain 608 630 N/A INTRINSIC
transmembrane domain 634 656 N/A INTRINSIC
transmembrane domain 676 698 N/A INTRINSIC
CYCc 827 1038 1.71e-50 SMART
low complexity region 1090 1104 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135398
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 of adenylate cyclase gene family that is primarily expressed in the brain. This protein is regulated by calcium/calmodulin concentration and may be involved in brain development. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]
PHENOTYPE: Mice homozygous for an insertional or null mutation fail to develop normal patterned distribution of neurons in the brain and display behavioral and learning abnormalities. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4833420G17Rik T A 13: 119,603,494 (GRCm39) probably null Het
Abtb3 T C 10: 85,465,069 (GRCm39) probably benign Het
Blm A G 7: 80,123,819 (GRCm39) Y1004H probably damaging Het
Cachd1 A C 4: 100,810,231 (GRCm39) I278L probably benign Het
Ddx18 T A 1: 121,492,315 (GRCm39) T131S probably benign Het
Dgkd T C 1: 87,808,133 (GRCm39) F67S probably damaging Het
Dlgap1 A G 17: 70,823,374 (GRCm39) T120A probably damaging Het
Dnaja3 T G 16: 4,512,268 (GRCm39) V224G probably damaging Het
Dntt A T 19: 41,041,677 (GRCm39) R454* probably null Het
Dync2h1 T A 9: 7,071,111 (GRCm39) T3083S probably benign Het
Eea1 C A 10: 95,867,539 (GRCm39) T1045K probably damaging Het
Gpnmb T A 6: 49,024,392 (GRCm39) probably benign Het
Hirip3 A G 7: 126,462,548 (GRCm39) E108G possibly damaging Het
Il33 C A 19: 29,929,381 (GRCm39) Q35K possibly damaging Het
Il6ra G A 3: 89,793,350 (GRCm39) L267F probably damaging Het
Impact C T 18: 13,109,076 (GRCm39) S69F probably benign Het
Klk1b9 G A 7: 43,441,675 (GRCm39) G39D probably damaging Het
Ldah A G 12: 8,277,337 (GRCm39) D91G probably benign Het
Lrp4 T C 2: 91,341,898 (GRCm39) L1837P probably damaging Het
Mov10l1 T A 15: 88,938,555 (GRCm39) H1204Q probably damaging Het
Nlrp4c A G 7: 6,063,655 (GRCm39) E21G probably damaging Het
Or12k8 T C 2: 36,975,407 (GRCm39) M118V possibly damaging Het
Or52ae9 T A 7: 103,390,321 (GRCm39) N42I probably damaging Het
Osbpl1a T G 18: 13,066,638 (GRCm39) K40N probably damaging Het
Ptprd T C 4: 76,003,757 (GRCm39) T1010A probably damaging Het
Rp1 A G 1: 4,419,168 (GRCm39) V648A probably benign Het
Scn9a T C 2: 66,367,722 (GRCm39) K654E probably benign Het
Sema3d A G 5: 12,591,047 (GRCm39) I309V probably benign Het
Slc6a2 T C 8: 93,722,310 (GRCm39) L519P probably damaging Het
Stard9 A G 2: 120,504,085 (GRCm39) I211V possibly damaging Het
Stau2 T C 1: 16,415,922 (GRCm39) *480W probably null Het
Svopl T C 6: 38,003,876 (GRCm39) probably benign Het
Virma A G 4: 11,528,753 (GRCm39) E1330G probably damaging Het
Zan G A 5: 137,422,874 (GRCm39) T2713I unknown Het
Other mutations in Adcy1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01149:Adcy1 APN 11 7,087,385 (GRCm39) missense probably damaging 0.99
IGL01325:Adcy1 APN 11 7,014,102 (GRCm39) missense possibly damaging 0.58
IGL01585:Adcy1 APN 11 7,117,143 (GRCm39) missense probably damaging 1.00
IGL01932:Adcy1 APN 11 7,050,565 (GRCm39) splice site probably benign
IGL01945:Adcy1 APN 11 7,111,891 (GRCm39) missense probably damaging 1.00
IGL02532:Adcy1 APN 11 7,094,737 (GRCm39) missense probably benign 0.26
IGL02649:Adcy1 APN 11 7,117,156 (GRCm39) missense probably damaging 1.00
IGL02658:Adcy1 APN 11 7,088,279 (GRCm39) splice site probably benign
IGL02813:Adcy1 APN 11 7,096,591 (GRCm39) missense possibly damaging 0.83
IGL02931:Adcy1 APN 11 7,029,012 (GRCm39) missense probably benign 0.19
IGL03116:Adcy1 APN 11 7,100,071 (GRCm39) missense probably benign
IGL03119:Adcy1 APN 11 7,059,051 (GRCm39) missense probably damaging 1.00
IGL03214:Adcy1 APN 11 7,117,054 (GRCm39) splice site probably benign
PIT4431001:Adcy1 UTSW 11 7,014,089 (GRCm39) missense possibly damaging 0.93
PIT4520001:Adcy1 UTSW 11 7,117,133 (GRCm39) missense probably damaging 1.00
R0032:Adcy1 UTSW 11 7,094,729 (GRCm39) missense possibly damaging 0.93
R0032:Adcy1 UTSW 11 7,094,729 (GRCm39) missense possibly damaging 0.93
R0080:Adcy1 UTSW 11 7,099,497 (GRCm39) splice site probably benign
R0082:Adcy1 UTSW 11 7,099,497 (GRCm39) splice site probably benign
R0238:Adcy1 UTSW 11 7,089,162 (GRCm39) missense possibly damaging 0.80
R0238:Adcy1 UTSW 11 7,089,162 (GRCm39) missense possibly damaging 0.80
R0312:Adcy1 UTSW 11 7,099,538 (GRCm39) missense probably benign 0.08
R0569:Adcy1 UTSW 11 7,096,514 (GRCm39) missense probably benign 0.34
R1055:Adcy1 UTSW 11 7,059,075 (GRCm39) missense probably damaging 1.00
R1144:Adcy1 UTSW 11 7,087,400 (GRCm39) missense probably damaging 1.00
R1179:Adcy1 UTSW 11 7,117,054 (GRCm39) splice site probably null
R1245:Adcy1 UTSW 11 7,119,410 (GRCm39) splice site probably benign
R1467:Adcy1 UTSW 11 7,088,396 (GRCm39) missense probably damaging 0.97
R1467:Adcy1 UTSW 11 7,088,396 (GRCm39) missense probably damaging 0.97
R1823:Adcy1 UTSW 11 7,111,312 (GRCm39) missense probably benign 0.23
R1953:Adcy1 UTSW 11 7,028,991 (GRCm39) missense probably benign 0.01
R1957:Adcy1 UTSW 11 7,111,945 (GRCm39) missense probably benign 0.00
R2029:Adcy1 UTSW 11 7,089,142 (GRCm39) missense probably benign 0.10
R2051:Adcy1 UTSW 11 7,111,885 (GRCm39) nonsense probably null
R2483:Adcy1 UTSW 11 7,080,348 (GRCm39) missense probably benign 0.01
R3108:Adcy1 UTSW 11 7,119,453 (GRCm39) missense probably damaging 1.00
R3623:Adcy1 UTSW 11 7,080,348 (GRCm39) missense probably benign 0.01
R3624:Adcy1 UTSW 11 7,080,348 (GRCm39) missense probably benign 0.01
R4082:Adcy1 UTSW 11 7,014,117 (GRCm39) missense probably damaging 1.00
R4159:Adcy1 UTSW 11 7,013,889 (GRCm39) missense probably damaging 1.00
R4470:Adcy1 UTSW 11 7,094,804 (GRCm39) missense probably benign 0.17
R4472:Adcy1 UTSW 11 7,080,369 (GRCm39) missense probably damaging 1.00
R4951:Adcy1 UTSW 11 7,088,336 (GRCm39) missense possibly damaging 0.83
R4997:Adcy1 UTSW 11 7,111,298 (GRCm39) missense probably benign 0.25
R5237:Adcy1 UTSW 11 7,099,553 (GRCm39) missense probably benign 0.00
R5288:Adcy1 UTSW 11 7,111,351 (GRCm39) missense probably benign 0.01
R5304:Adcy1 UTSW 11 7,014,198 (GRCm39) missense probably benign 0.00
R5341:Adcy1 UTSW 11 7,080,375 (GRCm39) missense probably damaging 0.99
R5379:Adcy1 UTSW 11 7,096,532 (GRCm39) missense probably damaging 1.00
R5592:Adcy1 UTSW 11 7,089,088 (GRCm39) nonsense probably null
R5677:Adcy1 UTSW 11 7,111,914 (GRCm39) missense probably damaging 1.00
R5680:Adcy1 UTSW 11 7,059,020 (GRCm39) missense probably damaging 1.00
R5753:Adcy1 UTSW 11 7,080,300 (GRCm39) missense probably damaging 1.00
R5888:Adcy1 UTSW 11 7,089,095 (GRCm39) missense possibly damaging 0.66
R5943:Adcy1 UTSW 11 7,111,337 (GRCm39) missense probably damaging 1.00
R6435:Adcy1 UTSW 11 7,111,367 (GRCm39) missense possibly damaging 0.60
R6931:Adcy1 UTSW 11 7,100,884 (GRCm39) missense possibly damaging 0.81
R6998:Adcy1 UTSW 11 7,029,026 (GRCm39) missense probably damaging 1.00
R7368:Adcy1 UTSW 11 7,094,765 (GRCm39) missense probably damaging 1.00
R7378:Adcy1 UTSW 11 7,119,543 (GRCm39) missense possibly damaging 0.56
R7393:Adcy1 UTSW 11 7,087,381 (GRCm39) missense probably damaging 1.00
R7500:Adcy1 UTSW 11 7,094,762 (GRCm39) missense probably damaging 1.00
R7529:Adcy1 UTSW 11 7,089,157 (GRCm39) missense probably damaging 0.98
R8681:Adcy1 UTSW 11 7,111,328 (GRCm39) missense probably damaging 1.00
R8682:Adcy1 UTSW 11 7,111,328 (GRCm39) missense probably damaging 1.00
R8683:Adcy1 UTSW 11 7,111,328 (GRCm39) missense probably damaging 1.00
R8831:Adcy1 UTSW 11 7,111,362 (GRCm39) missense probably benign 0.02
R8859:Adcy1 UTSW 11 7,111,877 (GRCm39) missense probably benign 0.06
R8894:Adcy1 UTSW 11 7,087,375 (GRCm39) missense probably damaging 0.97
R8904:Adcy1 UTSW 11 7,059,075 (GRCm39) missense probably damaging 1.00
R8970:Adcy1 UTSW 11 7,099,983 (GRCm39) missense probably benign 0.00
R9037:Adcy1 UTSW 11 7,087,325 (GRCm39) missense possibly damaging 0.78
R9172:Adcy1 UTSW 11 7,110,317 (GRCm39) missense probably damaging 0.97
R9303:Adcy1 UTSW 11 7,094,766 (GRCm39) missense probably damaging 1.00
R9448:Adcy1 UTSW 11 7,099,575 (GRCm39) missense possibly damaging 0.94
R9694:Adcy1 UTSW 11 7,094,774 (GRCm39) missense probably damaging 1.00
R9763:Adcy1 UTSW 11 7,014,126 (GRCm39) missense probably damaging 1.00
X0027:Adcy1 UTSW 11 7,111,930 (GRCm39) missense possibly damaging 0.47
Z1088:Adcy1 UTSW 11 7,100,019 (GRCm39) missense probably benign 0.19
Z1176:Adcy1 UTSW 11 7,100,857 (GRCm39) missense probably damaging 0.96
Z1176:Adcy1 UTSW 11 7,099,536 (GRCm39) missense probably damaging 0.99
Z1176:Adcy1 UTSW 11 7,059,098 (GRCm39) missense probably damaging 1.00
Z1176:Adcy1 UTSW 11 7,100,858 (GRCm39) missense possibly damaging 0.62
Z1177:Adcy1 UTSW 11 7,094,802 (GRCm39) missense probably damaging 1.00
Z1177:Adcy1 UTSW 11 7,050,642 (GRCm39) nonsense probably null
Posted On 2013-12-03