Incidental Mutation 'R7552:Adcy4'
ID |
584510 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Adcy4
|
Ensembl Gene |
ENSMUSG00000022220 |
Gene Name |
adenylate cyclase 4 |
Synonyms |
|
MMRRC Submission |
045621-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7552 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
14 |
Chromosomal Location |
56006514-56021552 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 56010922 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Methionine
at position 665
(T665M)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000002398
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000002398]
[ENSMUST00000057569]
[ENSMUST00000170223]
|
AlphaFold |
Q91WF3 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000002398
AA Change: T665M
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
SMART Domains |
Protein: ENSMUSP00000002398 Gene: ENSMUSG00000022220 AA Change: T665M
Domain | Start | End | E-Value | Type |
low complexity region
|
28 |
48 |
N/A |
INTRINSIC |
low complexity region
|
66 |
80 |
N/A |
INTRINSIC |
low complexity region
|
145 |
161 |
N/A |
INTRINSIC |
CYCc
|
218 |
426 |
1.56e-62 |
SMART |
Pfam:DUF1053
|
479 |
581 |
2.4e-35 |
PFAM |
transmembrane domain
|
607 |
629 |
N/A |
INTRINSIC |
transmembrane domain
|
661 |
683 |
N/A |
INTRINSIC |
transmembrane domain
|
717 |
739 |
N/A |
INTRINSIC |
transmembrane domain
|
746 |
768 |
N/A |
INTRINSIC |
transmembrane domain
|
792 |
809 |
N/A |
INTRINSIC |
CYCc
|
835 |
1057 |
4.46e-40 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000057569
|
SMART Domains |
Protein: ENSMUSP00000051368 Gene: ENSMUSG00000046908
Domain | Start | End | E-Value | Type |
Pfam:7TM_GPCR_Srx
|
28 |
196 |
7.4e-7 |
PFAM |
Pfam:7TM_GPCR_Srsx
|
31 |
249 |
2e-8 |
PFAM |
Pfam:7tm_1
|
37 |
285 |
1.3e-42 |
PFAM |
Pfam:Serpentine_r_xa
|
54 |
201 |
2.8e-4 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000170223
AA Change: T665M
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
SMART Domains |
Protein: ENSMUSP00000130530 Gene: ENSMUSG00000022220 AA Change: T665M
Domain | Start | End | E-Value | Type |
transmembrane domain
|
29 |
51 |
N/A |
INTRINSIC |
transmembrane domain
|
61 |
80 |
N/A |
INTRINSIC |
transmembrane domain
|
92 |
114 |
N/A |
INTRINSIC |
transmembrane domain
|
119 |
138 |
N/A |
INTRINSIC |
transmembrane domain
|
145 |
162 |
N/A |
INTRINSIC |
transmembrane domain
|
172 |
194 |
N/A |
INTRINSIC |
CYCc
|
218 |
426 |
1.56e-62 |
SMART |
Pfam:DUF1053
|
479 |
581 |
1.6e-24 |
PFAM |
transmembrane domain
|
607 |
629 |
N/A |
INTRINSIC |
transmembrane domain
|
661 |
683 |
N/A |
INTRINSIC |
transmembrane domain
|
717 |
739 |
N/A |
INTRINSIC |
transmembrane domain
|
746 |
768 |
N/A |
INTRINSIC |
transmembrane domain
|
792 |
809 |
N/A |
INTRINSIC |
CYCc
|
835 |
1057 |
4.46e-40 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
100% (89/89) |
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 family of adenylate cyclases, which are membrane-associated enzymes that catalyze the formation of the secondary messenger cyclic adenosine monophosphate (cAMP). Mouse studies show that adenylate cyclase 4, along with adenylate cyclases 2 and 3, is expressed in olfactory cilia, suggesting that several different adenylate cyclases may couple to olfactory receptors and that there may be multiple receptor-mediated mechanisms for the generation of cAMP signals. Alternative splicing results in transcript variants. [provided by RefSeq, Nov 2010] PHENOTYPE: Mice homozygous for disruptions of this gene display a normal phenotype. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd17a |
A |
G |
10: 80,419,737 (GRCm39) |
Y290H |
probably benign |
Het |
Aco2 |
T |
C |
15: 81,788,142 (GRCm39) |
V257A |
probably damaging |
Het |
Adam26a |
C |
A |
8: 44,023,007 (GRCm39) |
C161F |
possibly damaging |
Het |
Adam9 |
G |
A |
8: 25,445,988 (GRCm39) |
P820S |
unknown |
Het |
Ahnak |
T |
A |
19: 8,984,188 (GRCm39) |
M1824K |
probably benign |
Het |
Alpi |
T |
C |
1: 87,026,795 (GRCm39) |
N428D |
probably benign |
Het |
Ano5 |
C |
T |
7: 51,196,528 (GRCm39) |
P153L |
probably benign |
Het |
Atp1a1 |
A |
T |
3: 101,489,437 (GRCm39) |
L725* |
probably null |
Het |
Atp8b2 |
G |
A |
3: 89,854,071 (GRCm39) |
T595I |
probably damaging |
Het |
Ccdc66 |
T |
C |
14: 27,220,820 (GRCm39) |
I35V |
possibly damaging |
Het |
Cd163 |
A |
G |
6: 124,284,187 (GRCm39) |
T120A |
probably benign |
Het |
Cmah |
A |
T |
13: 24,640,938 (GRCm39) |
T396S |
possibly damaging |
Het |
Cmya5 |
C |
T |
13: 93,205,820 (GRCm39) |
V3350I |
probably benign |
Het |
Commd9 |
A |
C |
2: 101,731,410 (GRCm39) |
K198N |
probably damaging |
Het |
Cxcr1 |
A |
G |
1: 74,231,773 (GRCm39) |
V83A |
probably benign |
Het |
D630045J12Rik |
A |
G |
6: 38,125,383 (GRCm39) |
S1544P |
probably damaging |
Het |
Ddt |
A |
T |
10: 75,609,048 (GRCm39) |
|
probably null |
Het |
Depdc7 |
A |
G |
2: 104,557,585 (GRCm39) |
S222P |
possibly damaging |
Het |
Ehd2 |
A |
G |
7: 15,684,431 (GRCm39) |
I456T |
probably damaging |
Het |
Epas1 |
A |
T |
17: 87,136,471 (GRCm39) |
M748L |
probably benign |
Het |
Esr1 |
G |
A |
10: 4,806,903 (GRCm39) |
R273H |
probably damaging |
Het |
Fras1 |
G |
A |
5: 96,916,297 (GRCm39) |
D3444N |
probably damaging |
Het |
Hand2 |
A |
G |
8: 57,775,272 (GRCm39) |
R111G |
probably damaging |
Het |
Hecw1 |
A |
T |
13: 14,490,835 (GRCm39) |
V306E |
probably damaging |
Het |
Ift140 |
T |
C |
17: 25,252,089 (GRCm39) |
I312T |
probably benign |
Het |
Ikbke |
A |
T |
1: 131,199,887 (GRCm39) |
L257* |
probably null |
Het |
Kcnk5 |
G |
A |
14: 20,192,349 (GRCm39) |
P271S |
probably benign |
Het |
Lama1 |
T |
C |
17: 68,044,662 (GRCm39) |
V187A |
|
Het |
Lemd2 |
A |
T |
17: 27,412,810 (GRCm39) |
|
probably null |
Het |
Lig3 |
T |
A |
11: 82,679,717 (GRCm39) |
D341E |
probably benign |
Het |
Lpcat1 |
C |
T |
13: 73,643,014 (GRCm39) |
S196L |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 40,567,582 (GRCm39) |
D4048E |
|
Het |
Lrrfip1 |
G |
A |
1: 91,033,005 (GRCm39) |
E158K |
probably damaging |
Het |
Mcm5 |
T |
C |
8: 75,848,220 (GRCm39) |
S490P |
probably damaging |
Het |
Mia3 |
A |
C |
1: 183,147,036 (GRCm39) |
Y73* |
probably null |
Het |
Minar1 |
T |
A |
9: 89,483,888 (GRCm39) |
H503L |
probably benign |
Het |
Msr1 |
A |
T |
8: 40,077,003 (GRCm39) |
N202K |
probably benign |
Het |
N4bp2l2 |
A |
T |
5: 150,585,286 (GRCm39) |
Y231* |
probably null |
Het |
Nbeal2 |
A |
G |
9: 110,482,985 (GRCm39) |
W11R |
probably benign |
Het |
Ncor1 |
T |
C |
11: 62,264,250 (GRCm39) |
E384G |
possibly damaging |
Het |
Neb |
A |
G |
2: 52,137,202 (GRCm39) |
V254A |
|
Het |
Nlrp9b |
T |
C |
7: 19,779,691 (GRCm39) |
S785P |
probably benign |
Het |
Oprd1 |
T |
G |
4: 131,841,092 (GRCm39) |
I289L |
possibly damaging |
Het |
Or4c10 |
G |
T |
2: 89,761,064 (GRCm39) |
D304Y |
probably benign |
Het |
Or4s2 |
A |
G |
2: 88,473,752 (GRCm39) |
I214V |
probably benign |
Het |
Or5m12 |
A |
G |
2: 85,734,447 (GRCm39) |
V317A |
probably benign |
Het |
Or6a2 |
T |
C |
7: 106,600,534 (GRCm39) |
T178A |
probably benign |
Het |
Or6c2 |
T |
A |
10: 129,362,429 (GRCm39) |
F111Y |
possibly damaging |
Het |
Orc1 |
A |
G |
4: 108,445,951 (GRCm39) |
N23S |
probably benign |
Het |
Paip1 |
A |
T |
13: 119,577,356 (GRCm39) |
H149L |
possibly damaging |
Het |
Pdhx |
A |
T |
2: 102,877,099 (GRCm39) |
D103E |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,109,080 (GRCm39) |
Y1614C |
|
Het |
Pias3 |
ACC |
AC |
3: 96,608,701 (GRCm39) |
|
probably null |
Het |
Pigb |
A |
G |
9: 72,941,770 (GRCm39) |
V163A |
probably benign |
Het |
Pla2g4d |
A |
G |
2: 120,114,620 (GRCm39) |
I37T |
possibly damaging |
Het |
Ppfia1 |
A |
T |
7: 144,059,982 (GRCm39) |
V610D |
probably damaging |
Het |
Pramel41 |
G |
A |
5: 94,596,394 (GRCm39) |
C477Y |
probably damaging |
Het |
Prss1 |
T |
C |
6: 41,439,507 (GRCm39) |
V80A |
probably benign |
Het |
Psph |
G |
A |
5: 129,847,800 (GRCm39) |
R49W |
probably benign |
Het |
Qrich2 |
T |
C |
11: 116,347,080 (GRCm39) |
Y1248C |
possibly damaging |
Het |
Rlbp1 |
T |
A |
7: 79,029,861 (GRCm39) |
Y124F |
probably damaging |
Het |
Scn4a |
T |
A |
11: 106,239,995 (GRCm39) |
E74V |
probably benign |
Het |
Sdk2 |
A |
T |
11: 113,764,039 (GRCm39) |
I249N |
possibly damaging |
Het |
Sgsh |
A |
T |
11: 119,237,378 (GRCm39) |
L412Q |
probably damaging |
Het |
Shank1 |
C |
A |
7: 44,002,452 (GRCm39) |
D1390E |
probably benign |
Het |
Slc12a6 |
A |
G |
2: 112,172,319 (GRCm39) |
D421G |
probably damaging |
Het |
Snx29 |
T |
A |
16: 11,238,649 (GRCm39) |
|
probably null |
Het |
Spata31d1c |
A |
G |
13: 65,183,937 (GRCm39) |
Y493C |
probably damaging |
Het |
Stmn4 |
G |
A |
14: 66,593,727 (GRCm39) |
G40E |
probably damaging |
Het |
Stox2 |
A |
G |
8: 47,656,154 (GRCm39) |
|
probably null |
Het |
Strada |
T |
C |
11: 106,077,830 (GRCm39) |
S45G |
unknown |
Het |
Taco1 |
G |
A |
11: 105,962,774 (GRCm39) |
G154S |
probably benign |
Het |
Tas2r121 |
T |
C |
6: 132,677,505 (GRCm39) |
M156V |
probably benign |
Het |
Tbc1d31 |
A |
G |
15: 57,804,136 (GRCm39) |
S384G |
probably benign |
Het |
Tbc1d9 |
A |
T |
8: 83,966,560 (GRCm39) |
D387V |
probably damaging |
Het |
Tet3 |
A |
G |
6: 83,345,289 (GRCm39) |
L1716P |
probably damaging |
Het |
Thbs1 |
A |
G |
2: 117,943,843 (GRCm39) |
K154E |
possibly damaging |
Het |
Ush2a |
T |
C |
1: 187,999,241 (GRCm39) |
Y184H |
possibly damaging |
Het |
Vmn1r235 |
C |
A |
17: 21,481,713 (GRCm39) |
Q13K |
probably benign |
Het |
Vmn2r15 |
A |
T |
5: 109,440,774 (GRCm39) |
Y361* |
probably null |
Het |
Vmn2r88 |
A |
T |
14: 51,648,315 (GRCm39) |
|
probably null |
Het |
Vps54 |
T |
C |
11: 21,248,831 (GRCm39) |
V460A |
probably benign |
Het |
Wdr64 |
A |
G |
1: 175,613,147 (GRCm39) |
N674S |
possibly damaging |
Het |
Zfp592 |
A |
G |
7: 80,673,390 (GRCm39) |
D118G |
probably benign |
Het |
Zfp763 |
A |
G |
17: 33,237,625 (GRCm39) |
Y507H |
probably benign |
Het |
Zfp934 |
T |
C |
13: 62,640,705 (GRCm39) |
E16G |
probably damaging |
Het |
Zfyve26 |
G |
A |
12: 79,337,731 (GRCm39) |
L94F |
probably damaging |
Het |
|
Other mutations in Adcy4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00917:Adcy4
|
APN |
14 |
56,011,120 (GRCm39) |
splice site |
probably null |
|
IGL02406:Adcy4
|
APN |
14 |
56,007,504 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL02503:Adcy4
|
APN |
14 |
56,008,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02543:Adcy4
|
APN |
14 |
56,006,627 (GRCm39) |
missense |
probably benign |
|
IGL02616:Adcy4
|
APN |
14 |
56,020,971 (GRCm39) |
splice site |
probably null |
|
IGL03002:Adcy4
|
APN |
14 |
56,011,013 (GRCm39) |
missense |
probably benign |
0.31 |
IGL03026:Adcy4
|
APN |
14 |
56,015,467 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03190:Adcy4
|
APN |
14 |
56,016,510 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03247:Adcy4
|
APN |
14 |
56,007,553 (GRCm39) |
missense |
probably damaging |
1.00 |
stressed
|
UTSW |
14 |
56,016,556 (GRCm39) |
splice site |
probably null |
|
IGL03098:Adcy4
|
UTSW |
14 |
56,019,038 (GRCm39) |
missense |
probably null |
0.82 |
R0098:Adcy4
|
UTSW |
14 |
56,007,284 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0102:Adcy4
|
UTSW |
14 |
56,008,990 (GRCm39) |
missense |
probably benign |
0.29 |
R0396:Adcy4
|
UTSW |
14 |
56,009,745 (GRCm39) |
missense |
probably benign |
0.00 |
R0482:Adcy4
|
UTSW |
14 |
56,012,029 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0634:Adcy4
|
UTSW |
14 |
56,019,054 (GRCm39) |
missense |
probably benign |
|
R0691:Adcy4
|
UTSW |
14 |
56,010,104 (GRCm39) |
splice site |
probably benign |
|
R0704:Adcy4
|
UTSW |
14 |
56,010,213 (GRCm39) |
missense |
probably benign |
|
R0815:Adcy4
|
UTSW |
14 |
56,021,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R0863:Adcy4
|
UTSW |
14 |
56,021,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R1446:Adcy4
|
UTSW |
14 |
56,007,480 (GRCm39) |
critical splice donor site |
probably null |
|
R1462:Adcy4
|
UTSW |
14 |
56,015,765 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1462:Adcy4
|
UTSW |
14 |
56,015,765 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1463:Adcy4
|
UTSW |
14 |
56,016,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R1624:Adcy4
|
UTSW |
14 |
56,019,384 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1799:Adcy4
|
UTSW |
14 |
56,008,929 (GRCm39) |
missense |
probably benign |
0.01 |
R1878:Adcy4
|
UTSW |
14 |
56,007,362 (GRCm39) |
missense |
probably damaging |
0.96 |
R2007:Adcy4
|
UTSW |
14 |
56,015,770 (GRCm39) |
missense |
possibly damaging |
0.45 |
R2156:Adcy4
|
UTSW |
14 |
56,006,627 (GRCm39) |
missense |
probably benign |
0.09 |
R2425:Adcy4
|
UTSW |
14 |
56,015,474 (GRCm39) |
missense |
probably damaging |
0.99 |
R2517:Adcy4
|
UTSW |
14 |
56,019,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R3882:Adcy4
|
UTSW |
14 |
56,012,003 (GRCm39) |
missense |
probably benign |
0.27 |
R4021:Adcy4
|
UTSW |
14 |
56,012,635 (GRCm39) |
splice site |
probably null |
|
R4022:Adcy4
|
UTSW |
14 |
56,012,635 (GRCm39) |
splice site |
probably null |
|
R4411:Adcy4
|
UTSW |
14 |
56,006,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R4530:Adcy4
|
UTSW |
14 |
56,016,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R4560:Adcy4
|
UTSW |
14 |
56,016,407 (GRCm39) |
splice site |
probably null |
|
R4704:Adcy4
|
UTSW |
14 |
56,012,482 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4780:Adcy4
|
UTSW |
14 |
56,012,493 (GRCm39) |
missense |
probably benign |
0.07 |
R4860:Adcy4
|
UTSW |
14 |
56,019,384 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4860:Adcy4
|
UTSW |
14 |
56,019,384 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4868:Adcy4
|
UTSW |
14 |
56,011,179 (GRCm39) |
missense |
probably benign |
|
R4890:Adcy4
|
UTSW |
14 |
56,016,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4920:Adcy4
|
UTSW |
14 |
56,016,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4948:Adcy4
|
UTSW |
14 |
56,016,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4952:Adcy4
|
UTSW |
14 |
56,016,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4953:Adcy4
|
UTSW |
14 |
56,016,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4987:Adcy4
|
UTSW |
14 |
56,010,934 (GRCm39) |
missense |
probably benign |
0.01 |
R4991:Adcy4
|
UTSW |
14 |
56,010,922 (GRCm39) |
missense |
probably benign |
0.03 |
R5080:Adcy4
|
UTSW |
14 |
56,009,832 (GRCm39) |
missense |
probably damaging |
0.98 |
R5620:Adcy4
|
UTSW |
14 |
56,009,824 (GRCm39) |
nonsense |
probably null |
|
R5652:Adcy4
|
UTSW |
14 |
56,010,900 (GRCm39) |
missense |
probably benign |
|
R5726:Adcy4
|
UTSW |
14 |
56,021,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R5910:Adcy4
|
UTSW |
14 |
56,016,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R5958:Adcy4
|
UTSW |
14 |
56,016,556 (GRCm39) |
splice site |
probably null |
|
R6280:Adcy4
|
UTSW |
14 |
56,016,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Adcy4
|
UTSW |
14 |
56,006,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R6598:Adcy4
|
UTSW |
14 |
56,007,502 (GRCm39) |
missense |
probably benign |
0.03 |
R6947:Adcy4
|
UTSW |
14 |
56,015,848 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7012:Adcy4
|
UTSW |
14 |
56,017,376 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7147:Adcy4
|
UTSW |
14 |
56,017,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R7386:Adcy4
|
UTSW |
14 |
56,015,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R7414:Adcy4
|
UTSW |
14 |
56,019,090 (GRCm39) |
missense |
probably benign |
0.15 |
R7431:Adcy4
|
UTSW |
14 |
56,010,129 (GRCm39) |
missense |
probably benign |
0.01 |
R7490:Adcy4
|
UTSW |
14 |
56,007,890 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7672:Adcy4
|
UTSW |
14 |
56,018,362 (GRCm39) |
missense |
probably benign |
0.14 |
R8003:Adcy4
|
UTSW |
14 |
56,019,092 (GRCm39) |
missense |
probably benign |
0.00 |
R8042:Adcy4
|
UTSW |
14 |
56,012,696 (GRCm39) |
missense |
probably benign |
0.01 |
R8100:Adcy4
|
UTSW |
14 |
56,009,722 (GRCm39) |
nonsense |
probably null |
|
R8343:Adcy4
|
UTSW |
14 |
56,012,697 (GRCm39) |
missense |
probably benign |
0.02 |
R8801:Adcy4
|
UTSW |
14 |
56,009,452 (GRCm39) |
missense |
probably benign |
0.05 |
R8811:Adcy4
|
UTSW |
14 |
56,010,221 (GRCm39) |
missense |
probably benign |
|
R8993:Adcy4
|
UTSW |
14 |
56,016,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R8993:Adcy4
|
UTSW |
14 |
56,008,835 (GRCm39) |
missense |
probably null |
1.00 |
R9026:Adcy4
|
UTSW |
14 |
56,016,426 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Adcy4
|
UTSW |
14 |
56,007,848 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Adcy4
|
UTSW |
14 |
56,018,413 (GRCm39) |
missense |
probably benign |
0.06 |
|
Predicted Primers |
PCR Primer
(F):5'- GATTATTCCTGGAGGGCAGG -3'
(R):5'- TAGTGACAAGCTGAAGCCC -3'
Sequencing Primer
(F):5'- CTGGAGGGCAGGACACACAC -3'
(R):5'- TGAAGCCCTGGCCTTGAACTG -3'
|
Posted On |
2019-10-17 |