Incidental Mutation 'IGL03006:Prkar2a'
| ID |
407564 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Prkar2a
|
| Ensembl Gene |
ENSMUSG00000032601 |
| Gene Name |
protein kinase, cAMP dependent regulatory, type II alpha |
| Synonyms |
1110061A24Rik, RII(alpha) |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL03006
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
108569342-108627643 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 108617640 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Leucine
at position 233
(V233L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000141869
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035220]
[ENSMUST00000195405]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000035220
AA Change: V233L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000035220
Gene: ENSMUSG00000032601
AA Change: V233L
| Domain | Start | End | E-Value | Type |
|---|
|
RIIa
|
8 |
45 |
7.15e-16 |
SMART |
|
low complexity region
|
70 |
85 |
N/A |
INTRINSIC |
|
low complexity region
|
104 |
114 |
N/A |
INTRINSIC |
|
cNMP
|
137 |
257 |
2.27e-23 |
SMART |
|
cNMP
|
259 |
384 |
2.02e-29 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000083740
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000192068
AA Change: V132L
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000193215
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000195405
AA Change: V233L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000141869
Gene: ENSMUSG00000032601
AA Change: V233L
| Domain | Start | End | E-Value | Type |
|---|
|
RIIa
|
8 |
45 |
4.3e-18 |
SMART |
|
low complexity region
|
70 |
85 |
N/A |
INTRINSIC |
|
low complexity region
|
104 |
114 |
N/A |
INTRINSIC |
|
cNMP
|
137 |
257 |
1.1e-25 |
SMART |
|
cNMP
|
259 |
362 |
3.9e-12 |
SMART |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] cAMP is a signaling molecule important for a variety of cellular functions. cAMP exerts its effects by activating the cAMP-dependent protein kinase, which transduces the signal through phosphorylation of different target proteins. The inactive kinase holoenzyme is a tetramer composed of two regulatory and two catalytic subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different regulatory subunits and three catalytic subunits have been identified in humans. The protein encoded by this gene is one of the regulatory subunits. This subunit can be phosphorylated by the activated catalytic subunit. It may interact with various A-kinase anchoring proteins and determine the subcellular localization of cAMP-dependent protein kinase. This subunit has been shown to regulate protein transport from endosomes to the Golgi apparatus and further to the endoplasmic reticulum (ER). [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous null mice are viable and appear healthy. They have normal growth and no deficits in locomotor activity, muscle strength, or exploratory behavior. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700012B07Rik |
T |
A |
11: 109,718,671 (GRCm39) |
S21C |
probably damaging |
Het |
| 2210408I21Rik |
T |
C |
13: 77,471,891 (GRCm39) |
|
probably null |
Het |
| Abcc3 |
T |
C |
11: 94,259,421 (GRCm39) |
D340G |
probably benign |
Het |
| Adamts17 |
G |
T |
7: 66,728,095 (GRCm39) |
R879L |
possibly damaging |
Het |
| Adissp |
A |
C |
2: 130,993,634 (GRCm39) |
D22E |
probably damaging |
Het |
| Cacna1f |
C |
A |
X: 7,493,142 (GRCm39) |
T1275K |
probably damaging |
Het |
| Csmd2 |
T |
A |
4: 128,374,558 (GRCm39) |
|
probably benign |
Het |
| Dll1 |
C |
T |
17: 15,593,854 (GRCm39) |
R171Q |
probably benign |
Het |
| Dnm1 |
T |
A |
2: 32,243,133 (GRCm39) |
D30V |
possibly damaging |
Het |
| Fam184a |
G |
A |
10: 53,574,793 (GRCm39) |
S216L |
probably damaging |
Het |
| Fbxo33 |
G |
A |
12: 59,251,105 (GRCm39) |
A470V |
probably benign |
Het |
| Gm6401 |
C |
T |
14: 41,788,851 (GRCm39) |
E73K |
possibly damaging |
Het |
| Ighv7-1 |
A |
T |
12: 113,860,145 (GRCm39) |
S82R |
probably damaging |
Het |
| Klk1b4 |
A |
G |
7: 43,861,019 (GRCm39) |
I221V |
probably benign |
Het |
| Lama3 |
T |
C |
18: 12,601,425 (GRCm39) |
|
probably benign |
Het |
| Lrch1 |
A |
G |
14: 75,051,060 (GRCm39) |
L359P |
probably damaging |
Het |
| Mapk8ip3 |
T |
C |
17: 25,120,489 (GRCm39) |
T882A |
probably benign |
Het |
| Med12 |
C |
T |
X: 100,321,684 (GRCm39) |
R456W |
probably damaging |
Het |
| Mms22l |
T |
C |
4: 24,521,253 (GRCm39) |
S267P |
probably damaging |
Het |
| Mtpap |
G |
A |
18: 4,375,721 (GRCm39) |
G34R |
possibly damaging |
Het |
| Nf1 |
G |
A |
11: 79,436,257 (GRCm39) |
D1966N |
probably damaging |
Het |
| Nlrp9c |
G |
A |
7: 26,071,507 (GRCm39) |
T867I |
probably damaging |
Het |
| Nrap |
C |
T |
19: 56,335,596 (GRCm39) |
V941I |
probably benign |
Het |
| Or5k1b |
T |
A |
16: 58,581,511 (GRCm39) |
K9N |
probably benign |
Het |
| Pcdh10 |
A |
G |
3: 45,333,937 (GRCm39) |
I84V |
probably damaging |
Het |
| Polr3d |
T |
A |
14: 70,678,603 (GRCm39) |
|
probably null |
Het |
| Prl4a1 |
T |
C |
13: 28,207,359 (GRCm39) |
V211A |
probably damaging |
Het |
| Qpct |
T |
C |
17: 79,378,151 (GRCm39) |
V107A |
probably benign |
Het |
| Rai1 |
T |
C |
11: 60,079,031 (GRCm39) |
S1032P |
possibly damaging |
Het |
| Rims1 |
G |
T |
1: 22,367,178 (GRCm39) |
T1113K |
probably damaging |
Het |
| Rxra |
C |
T |
2: 27,649,657 (GRCm39) |
T454I |
probably damaging |
Het |
| S100z |
T |
C |
13: 95,615,127 (GRCm39) |
I13V |
probably damaging |
Het |
| Scp2 |
T |
C |
4: 107,948,477 (GRCm39) |
K167E |
probably benign |
Het |
| Sephs2 |
A |
G |
7: 126,872,206 (GRCm39) |
F296L |
probably benign |
Het |
| Setd1b |
A |
G |
5: 123,286,514 (GRCm39) |
E520G |
unknown |
Het |
| Slc28a2 |
G |
A |
2: 122,283,019 (GRCm39) |
V308M |
possibly damaging |
Het |
| Smarcad1 |
T |
A |
6: 65,060,873 (GRCm39) |
I451K |
probably benign |
Het |
| Tarbp1 |
C |
T |
8: 127,170,881 (GRCm39) |
D1040N |
probably damaging |
Het |
| Tdrd6 |
T |
C |
17: 43,936,323 (GRCm39) |
D1575G |
probably damaging |
Het |
| Tll1 |
T |
A |
8: 64,527,251 (GRCm39) |
|
probably benign |
Het |
| Tsks |
A |
T |
7: 44,600,198 (GRCm39) |
|
probably benign |
Het |
| Ttc1 |
A |
T |
11: 43,636,147 (GRCm39) |
M32K |
probably benign |
Het |
| Txlnb |
C |
T |
10: 17,714,723 (GRCm39) |
A385V |
probably damaging |
Het |
| Zc4h2 |
T |
C |
X: 94,687,019 (GRCm39) |
H98R |
probably damaging |
Het |
|
| Other mutations in Prkar2a |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02064:Prkar2a
|
APN |
9 |
108,610,403 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL02073:Prkar2a
|
APN |
9 |
108,610,322 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02117:Prkar2a
|
APN |
9 |
108,596,460 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02268:Prkar2a
|
APN |
9 |
108,624,152 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL02635:Prkar2a
|
APN |
9 |
108,605,476 (GRCm39) |
missense |
probably damaging |
0.99 |
|
PIT4486001:Prkar2a
|
UTSW |
9 |
108,610,326 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0335:Prkar2a
|
UTSW |
9 |
108,596,457 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0920:Prkar2a
|
UTSW |
9 |
108,596,496 (GRCm39) |
splice site |
probably benign |
|
|
R0943:Prkar2a
|
UTSW |
9 |
108,610,475 (GRCm39) |
splice site |
probably benign |
|
|
R1513:Prkar2a
|
UTSW |
9 |
108,605,469 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R2178:Prkar2a
|
UTSW |
9 |
108,617,737 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3820:Prkar2a
|
UTSW |
9 |
108,624,155 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3842:Prkar2a
|
UTSW |
9 |
108,605,467 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4807:Prkar2a
|
UTSW |
9 |
108,617,584 (GRCm39) |
intron |
probably benign |
|
|
R4886:Prkar2a
|
UTSW |
9 |
108,622,823 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5051:Prkar2a
|
UTSW |
9 |
108,622,690 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5435:Prkar2a
|
UTSW |
9 |
108,617,682 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6979:Prkar2a
|
UTSW |
9 |
108,610,342 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R7121:Prkar2a
|
UTSW |
9 |
108,569,821 (GRCm39) |
missense |
probably benign |
|
|
R7199:Prkar2a
|
UTSW |
9 |
108,617,669 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7819:Prkar2a
|
UTSW |
9 |
108,622,744 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8194:Prkar2a
|
UTSW |
9 |
108,569,710 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8218:Prkar2a
|
UTSW |
9 |
108,596,448 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8253:Prkar2a
|
UTSW |
9 |
108,617,638 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0060:Prkar2a
|
UTSW |
9 |
108,622,781 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2016-08-02 |
Incidental Mutation