Incidental Mutation 'IGL00960:Cckar'
| ID |
27489 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Cckar
|
| Ensembl Gene |
ENSMUSG00000029193 |
| Gene Name |
cholecystokinin A receptor |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.113)
|
| Stock # |
IGL00960
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
5 |
| Chromosomal Location |
53855827-53865046 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 53858634 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Histidine
at position 158
(Y158H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000144103
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000031093]
[ENSMUST00000200691]
|
| AlphaFold |
O08786 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000031093
AA Change: Y229H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000031093
Gene: ENSMUSG00000029193
AA Change: Y229H
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CholecysA-Rec_N
|
1 |
47 |
8.8e-29 |
PFAM |
|
Pfam:7tm_4
|
48 |
252 |
7.2e-12 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
52 |
393 |
2.6e-10 |
PFAM |
|
Pfam:7tm_1
|
58 |
378 |
1.1e-66 |
PFAM |
|
low complexity region
|
399 |
416 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000200691
AA Change: Y158H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000144103
Gene: ENSMUSG00000029193
AA Change: Y158H
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_1
|
1 |
307 |
1.6e-59 |
PFAM |
|
Pfam:7tm_4
|
3 |
181 |
1.8e-6 |
PFAM |
|
low complexity region
|
328 |
345 |
N/A |
INTRINSIC |
|
| 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 G-protein coupled receptor that binds non-sulfated members of the cholecystokinin (CCK) family of peptide hormones. This receptor is a major physiologic mediator of pancreatic enzyme secretion and smooth muscle contraction of the gallbladder and stomach. In the central and peripheral nervous system this receptor regulates satiety and the release of beta-endorphin and dopamine. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutant mice cannot regulate core body temperature in response to changes in ambient temperature. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcc10 |
C |
A |
17: 46,634,671 (GRCm39) |
R444L |
probably damaging |
Het |
| Baiap2 |
T |
A |
11: 119,890,118 (GRCm39) |
S460T |
possibly damaging |
Het |
| Cdk4 |
A |
G |
10: 126,900,166 (GRCm39) |
Y21C |
probably damaging |
Het |
| Entpd1 |
C |
T |
19: 40,699,714 (GRCm39) |
P42S |
probably benign |
Het |
| Epha8 |
A |
T |
4: 136,679,150 (GRCm39) |
|
probably null |
Het |
| Fastkd1 |
A |
T |
2: 69,524,997 (GRCm39) |
|
probably benign |
Het |
| Fmnl2 |
A |
G |
2: 53,013,494 (GRCm39) |
D951G |
probably damaging |
Het |
| Hnrnpm |
C |
A |
17: 33,868,876 (GRCm39) |
R517L |
probably damaging |
Het |
| Kcnj5 |
T |
A |
9: 32,233,719 (GRCm39) |
T199S |
probably damaging |
Het |
| Med13 |
T |
C |
11: 86,181,866 (GRCm39) |
|
probably benign |
Het |
| Mycbp2 |
G |
T |
14: 103,466,820 (GRCm39) |
H1314Q |
possibly damaging |
Het |
| Ncapd2 |
A |
T |
6: 125,150,811 (GRCm39) |
S795T |
probably benign |
Het |
| Nf1 |
T |
C |
11: 79,335,947 (GRCm39) |
S1042P |
probably damaging |
Het |
| Nlgn1 |
C |
A |
3: 25,966,861 (GRCm39) |
L197F |
probably damaging |
Het |
| Nsun7 |
A |
G |
5: 66,446,846 (GRCm39) |
Y428C |
probably benign |
Het |
| Or10d5j |
A |
G |
9: 39,867,455 (GRCm39) |
Y259H |
probably damaging |
Het |
| Parp14 |
T |
C |
16: 35,661,589 (GRCm39) |
D1453G |
probably benign |
Het |
| Pcdhb8 |
A |
T |
18: 37,489,026 (GRCm39) |
I235F |
probably benign |
Het |
| Pclo |
T |
C |
5: 14,725,234 (GRCm39) |
V1364A |
unknown |
Het |
| Polq |
T |
C |
16: 36,880,874 (GRCm39) |
S734P |
probably damaging |
Het |
| Sco1 |
T |
C |
11: 66,954,864 (GRCm39) |
*290Q |
probably null |
Het |
| Slc22a3 |
A |
T |
17: 12,644,497 (GRCm39) |
I496N |
probably damaging |
Het |
| Slc5a8 |
T |
G |
10: 88,757,627 (GRCm39) |
I539S |
probably benign |
Het |
| Tecta |
A |
G |
9: 42,270,376 (GRCm39) |
F1311L |
possibly damaging |
Het |
| Tex261 |
A |
T |
6: 83,752,650 (GRCm39) |
I19N |
possibly damaging |
Het |
| Tfr2 |
T |
C |
5: 137,569,954 (GRCm39) |
V120A |
probably benign |
Het |
| Vmn2r71 |
A |
T |
7: 85,273,582 (GRCm39) |
S799C |
probably damaging |
Het |
| Zar1 |
G |
A |
5: 72,734,628 (GRCm39) |
T197I |
probably damaging |
Het |
| Zfa-ps |
A |
G |
10: 52,420,043 (GRCm39) |
|
noncoding transcript |
Het |
|
| Other mutations in Cckar |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00422:Cckar
|
APN |
5 |
53,857,171 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL00568:Cckar
|
APN |
5 |
53,864,643 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL00766:Cckar
|
APN |
5 |
53,857,378 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02424:Cckar
|
APN |
5 |
53,863,770 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
IGL03002:Cckar
|
APN |
5 |
53,860,247 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0167:Cckar
|
UTSW |
5 |
53,863,795 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0302:Cckar
|
UTSW |
5 |
53,857,641 (GRCm39) |
frame shift |
probably null |
|
|
R0366:Cckar
|
UTSW |
5 |
53,857,507 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0391:Cckar
|
UTSW |
5 |
53,863,595 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0981:Cckar
|
UTSW |
5 |
53,863,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1619:Cckar
|
UTSW |
5 |
53,857,409 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1644:Cckar
|
UTSW |
5 |
53,857,215 (GRCm39) |
missense |
probably benign |
|
|
R1779:Cckar
|
UTSW |
5 |
53,857,321 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2184:Cckar
|
UTSW |
5 |
53,860,254 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4290:Cckar
|
UTSW |
5 |
53,863,839 (GRCm39) |
missense |
probably benign |
|
|
R4291:Cckar
|
UTSW |
5 |
53,863,839 (GRCm39) |
missense |
probably benign |
|
|
R4292:Cckar
|
UTSW |
5 |
53,863,839 (GRCm39) |
missense |
probably benign |
|
|
R4294:Cckar
|
UTSW |
5 |
53,863,839 (GRCm39) |
missense |
probably benign |
|
|
R4518:Cckar
|
UTSW |
5 |
53,857,264 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4583:Cckar
|
UTSW |
5 |
53,857,124 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5139:Cckar
|
UTSW |
5 |
53,860,265 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5505:Cckar
|
UTSW |
5 |
53,860,410 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6207:Cckar
|
UTSW |
5 |
53,857,186 (GRCm39) |
missense |
probably benign |
|
|
R6415:Cckar
|
UTSW |
5 |
53,860,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7127:Cckar
|
UTSW |
5 |
53,863,817 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7372:Cckar
|
UTSW |
5 |
53,864,624 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7966:Cckar
|
UTSW |
5 |
53,858,580 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R8790:Cckar
|
UTSW |
5 |
53,857,291 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8897:Cckar
|
UTSW |
5 |
53,864,583 (GRCm39) |
start gained |
probably benign |
|
|
R9010:Cckar
|
UTSW |
5 |
53,857,163 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9054:Cckar
|
UTSW |
5 |
53,860,424 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9205:Cckar
|
UTSW |
5 |
53,864,587 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9396:Cckar
|
UTSW |
5 |
53,864,623 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9646:Cckar
|
UTSW |
5 |
53,863,608 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9656:Cckar
|
UTSW |
5 |
53,857,318 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9709:Cckar
|
UTSW |
5 |
53,860,201 (GRCm39) |
critical splice donor site |
probably null |
|
|
X0028:Cckar
|
UTSW |
5 |
53,864,616 (GRCm39) |
missense |
probably benign |
0.01 |
|
X0028:Cckar
|
UTSW |
5 |
53,864,615 (GRCm39) |
missense |
probably benign |
0.22 |
|
| Posted On |
2013-04-17 |
Incidental Mutation