Incidental Mutation 'R4960:Abcc9'
ID |
382268 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Abcc9
|
Ensembl Gene |
ENSMUSG00000030249 |
Gene Name |
ATP-binding cassette, sub-family C member 9 |
Synonyms |
SUR2A, Sur2, SUR2B |
MMRRC Submission |
042557-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.108)
|
Stock # |
R4960 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
6 |
Chromosomal Location |
142533588-142648041 bp(-) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
A to T
at 142566509 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000144779
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000073173]
[ENSMUST00000087527]
[ENSMUST00000100827]
[ENSMUST00000111771]
[ENSMUST00000205202]
|
AlphaFold |
P70170 |
Predicted Effect |
probably null
Transcript: ENSMUST00000073173
|
SMART Domains |
Protein: ENSMUSP00000072914 Gene: ENSMUSG00000030249
Domain | Start | End | E-Value | Type |
transmembrane domain
|
28 |
50 |
N/A |
INTRINSIC |
transmembrane domain
|
71 |
93 |
N/A |
INTRINSIC |
transmembrane domain
|
103 |
125 |
N/A |
INTRINSIC |
transmembrane domain
|
137 |
159 |
N/A |
INTRINSIC |
transmembrane domain
|
169 |
188 |
N/A |
INTRINSIC |
low complexity region
|
265 |
276 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
297 |
583 |
7.7e-33 |
PFAM |
AAA
|
659 |
867 |
3.11e-13 |
SMART |
coiled coil region
|
881 |
935 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
956 |
1228 |
6.6e-35 |
PFAM |
AAA
|
1300 |
1502 |
9.94e-12 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000087527
|
SMART Domains |
Protein: ENSMUSP00000084805 Gene: ENSMUSG00000030249
Domain | Start | End | E-Value | Type |
transmembrane domain
|
28 |
50 |
N/A |
INTRINSIC |
transmembrane domain
|
71 |
93 |
N/A |
INTRINSIC |
transmembrane domain
|
103 |
125 |
N/A |
INTRINSIC |
transmembrane domain
|
137 |
159 |
N/A |
INTRINSIC |
transmembrane domain
|
169 |
188 |
N/A |
INTRINSIC |
low complexity region
|
265 |
276 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
297 |
583 |
8e-33 |
PFAM |
AAA
|
694 |
902 |
3.11e-13 |
SMART |
coiled coil region
|
916 |
970 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
991 |
1263 |
6.8e-35 |
PFAM |
AAA
|
1335 |
1537 |
9.94e-12 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000100827
|
SMART Domains |
Protein: ENSMUSP00000098390 Gene: ENSMUSG00000030249
Domain | Start | End | E-Value | Type |
transmembrane domain
|
28 |
50 |
N/A |
INTRINSIC |
transmembrane domain
|
71 |
93 |
N/A |
INTRINSIC |
transmembrane domain
|
103 |
125 |
N/A |
INTRINSIC |
transmembrane domain
|
137 |
159 |
N/A |
INTRINSIC |
transmembrane domain
|
169 |
188 |
N/A |
INTRINSIC |
low complexity region
|
265 |
276 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
297 |
583 |
7.1e-35 |
PFAM |
AAA
|
694 |
902 |
3.11e-13 |
SMART |
coiled coil region
|
916 |
970 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
991 |
1263 |
5.2e-38 |
PFAM |
AAA
|
1335 |
1520 |
5.13e-14 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000111771
|
SMART Domains |
Protein: ENSMUSP00000107401 Gene: ENSMUSG00000030249
Domain | Start | End | E-Value | Type |
transmembrane domain
|
28 |
50 |
N/A |
INTRINSIC |
transmembrane domain
|
71 |
93 |
N/A |
INTRINSIC |
transmembrane domain
|
103 |
125 |
N/A |
INTRINSIC |
transmembrane domain
|
137 |
159 |
N/A |
INTRINSIC |
transmembrane domain
|
169 |
188 |
N/A |
INTRINSIC |
low complexity region
|
265 |
276 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
297 |
583 |
1.4e-32 |
PFAM |
AAA
|
694 |
889 |
3.77e-12 |
SMART |
coiled coil region
|
903 |
957 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
978 |
1250 |
1.2e-34 |
PFAM |
AAA
|
1322 |
1524 |
9.94e-12 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000194811
|
Predicted Effect |
probably null
Transcript: ENSMUST00000205202
|
SMART Domains |
Protein: ENSMUSP00000144779 Gene: ENSMUSG00000030249
Domain | Start | End | E-Value | Type |
transmembrane domain
|
28 |
50 |
N/A |
INTRINSIC |
transmembrane domain
|
71 |
93 |
N/A |
INTRINSIC |
transmembrane domain
|
103 |
125 |
N/A |
INTRINSIC |
transmembrane domain
|
137 |
159 |
N/A |
INTRINSIC |
transmembrane domain
|
169 |
188 |
N/A |
INTRINSIC |
low complexity region
|
265 |
276 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
297 |
583 |
6.9e-35 |
PFAM |
AAA
|
659 |
867 |
3.11e-13 |
SMART |
coiled coil region
|
881 |
935 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
956 |
1228 |
5e-38 |
PFAM |
AAA
|
1300 |
1502 |
9.94e-12 |
SMART |
|
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.8%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. The human protein is thought to form ATP-sensitive potassium channels in cardiac, skeletal, and vascular and non-vascular smooth muscle. Protein structure suggests a role as the drug-binding channel-modulating subunit of the extrapancreatic ATP-sensitive potassium channels. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2015] PHENOTYPE: Mice homozygous for a null allele display lower serum glucose, enhanced insulin action, growth retardation, hypertension and spontaneous death due to episodic coronary artery vasospasm. Homozygous exon 5 deletion leads to cardiac mitochondrial defects, cardiomyopathy, and early postnatal death. [provided by MGI curators]
|
Allele List at MGI |
All alleles(4) : Targeted(4)
|
Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb3 |
A |
C |
10: 85,487,526 (GRCm39) |
N998T |
probably benign |
Het |
Adamts20 |
T |
C |
15: 94,277,655 (GRCm39) |
H269R |
probably benign |
Het |
Adamtsl1 |
C |
T |
4: 86,342,410 (GRCm39) |
Q1642* |
probably null |
Het |
Adamtsl3 |
A |
C |
7: 82,216,185 (GRCm39) |
T863P |
probably damaging |
Het |
Adcy3 |
G |
T |
12: 4,184,896 (GRCm39) |
V191L |
probably benign |
Het |
Akap9 |
G |
T |
5: 4,007,664 (GRCm39) |
R244L |
probably benign |
Het |
Anapc1 |
C |
T |
2: 128,526,514 (GRCm39) |
V95M |
probably benign |
Het |
Arhgap17 |
G |
T |
7: 122,886,149 (GRCm39) |
|
probably benign |
Het |
Art2b |
T |
A |
7: 101,229,437 (GRCm39) |
Y154F |
probably damaging |
Het |
Atrn |
C |
T |
2: 130,836,967 (GRCm39) |
R1144* |
probably null |
Het |
Atxn3 |
T |
C |
12: 101,914,638 (GRCm39) |
S29G |
possibly damaging |
Het |
Batf3 |
C |
T |
1: 190,830,707 (GRCm39) |
P18S |
probably benign |
Het |
Bmal1 |
T |
A |
7: 112,898,642 (GRCm39) |
|
probably null |
Het |
Bmpr1b |
A |
T |
3: 141,576,546 (GRCm39) |
C96S |
probably damaging |
Het |
Bola1 |
A |
G |
3: 96,104,370 (GRCm39) |
S75P |
probably benign |
Het |
Cela3a |
G |
A |
4: 137,129,959 (GRCm39) |
R221* |
probably null |
Het |
Chat |
A |
G |
14: 32,142,771 (GRCm39) |
V406A |
possibly damaging |
Het |
Chd1 |
T |
A |
17: 15,962,493 (GRCm39) |
M750K |
probably damaging |
Het |
Clip1 |
T |
A |
5: 123,792,066 (GRCm39) |
K35* |
probably null |
Het |
Cnr2 |
G |
A |
4: 135,644,918 (GRCm39) |
G332D |
probably benign |
Het |
Cnrip1 |
A |
G |
11: 17,002,228 (GRCm39) |
D20G |
probably damaging |
Het |
Col2a1 |
T |
C |
15: 97,874,030 (GRCm39) |
Y1384C |
unknown |
Het |
Col6a3 |
T |
A |
1: 90,731,940 (GRCm39) |
I831F |
probably damaging |
Het |
Cp |
G |
A |
3: 20,027,961 (GRCm39) |
V456I |
probably damaging |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Ctbp2 |
T |
C |
7: 132,615,967 (GRCm39) |
I323V |
probably benign |
Het |
Ctnna2 |
C |
T |
6: 77,630,094 (GRCm39) |
R120H |
probably damaging |
Het |
Cyp2a12 |
A |
G |
7: 26,733,575 (GRCm39) |
H318R |
probably benign |
Het |
Cyp2c66 |
A |
T |
19: 39,151,766 (GRCm39) |
|
probably null |
Het |
Cyp2j8 |
T |
C |
4: 96,395,614 (GRCm39) |
T4A |
probably benign |
Het |
Cyp4v3 |
A |
G |
8: 45,773,674 (GRCm39) |
V165A |
possibly damaging |
Het |
D5Ertd579e |
G |
A |
5: 36,773,571 (GRCm39) |
R275* |
probably null |
Het |
Deup1 |
G |
T |
9: 15,512,264 (GRCm39) |
Q160K |
possibly damaging |
Het |
Dhx36 |
A |
T |
3: 62,404,280 (GRCm39) |
I221K |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,272,886 (GRCm39) |
M2338K |
probably benign |
Het |
Dync2li1 |
T |
G |
17: 84,940,969 (GRCm39) |
L62V |
probably benign |
Het |
Ephb3 |
A |
G |
16: 21,039,245 (GRCm39) |
K367R |
probably benign |
Het |
Etv3 |
A |
G |
3: 87,435,368 (GRCm39) |
K80E |
probably damaging |
Het |
Flacc1 |
T |
A |
1: 58,706,965 (GRCm39) |
E234V |
probably damaging |
Het |
Gdap1l1 |
T |
C |
2: 163,295,779 (GRCm39) |
F346L |
probably benign |
Het |
Gm4787 |
C |
T |
12: 81,426,090 (GRCm39) |
V23M |
probably damaging |
Het |
Greb1l |
T |
A |
18: 10,547,306 (GRCm39) |
I1508N |
probably damaging |
Het |
Heatr5b |
G |
A |
17: 79,139,013 (GRCm39) |
T43I |
probably benign |
Het |
Hephl1 |
T |
C |
9: 14,997,586 (GRCm39) |
Y360C |
probably damaging |
Het |
Itgam |
A |
C |
7: 127,715,012 (GRCm39) |
T865P |
possibly damaging |
Het |
Kcnma1 |
T |
C |
14: 24,054,186 (GRCm39) |
|
probably benign |
Het |
Kidins220 |
T |
A |
12: 25,042,259 (GRCm39) |
C185* |
probably null |
Het |
Klhl35 |
G |
T |
7: 99,118,275 (GRCm39) |
G273V |
probably damaging |
Het |
Lama5 |
A |
G |
2: 179,850,045 (GRCm39) |
|
probably null |
Het |
Lamc3 |
A |
G |
2: 31,805,966 (GRCm39) |
Q689R |
probably benign |
Het |
Lnx2 |
C |
T |
5: 146,955,850 (GRCm39) |
V649I |
probably benign |
Het |
Lrrc43 |
A |
G |
5: 123,637,675 (GRCm39) |
I281V |
probably benign |
Het |
Ly6g6d |
C |
A |
17: 35,290,730 (GRCm39) |
A67S |
probably benign |
Het |
Map1b |
A |
G |
13: 99,568,720 (GRCm39) |
S1334P |
probably benign |
Het |
Mast1 |
T |
A |
8: 85,644,500 (GRCm39) |
T810S |
probably benign |
Het |
Matcap1 |
G |
T |
8: 106,009,843 (GRCm39) |
R369S |
probably damaging |
Het |
Mbnl1 |
A |
G |
3: 60,503,117 (GRCm39) |
M1V |
probably null |
Het |
Mc5r |
T |
G |
18: 68,471,890 (GRCm39) |
M83R |
possibly damaging |
Het |
Mkln1 |
T |
C |
6: 31,435,941 (GRCm39) |
F300S |
probably damaging |
Het |
Mrgpre |
A |
T |
7: 143,335,088 (GRCm39) |
C138* |
probably null |
Het |
Mtarc2 |
T |
A |
1: 184,566,116 (GRCm39) |
M186L |
probably benign |
Het |
Ncbp1 |
C |
T |
4: 46,165,273 (GRCm39) |
Q529* |
probably null |
Het |
Nherf1 |
A |
G |
11: 115,067,289 (GRCm39) |
D180G |
probably benign |
Het |
Nrcam |
A |
G |
12: 44,613,082 (GRCm39) |
D591G |
probably benign |
Het |
Nrxn3 |
A |
T |
12: 88,761,971 (GRCm39) |
H6L |
possibly damaging |
Het |
Nsmaf |
T |
A |
4: 6,423,342 (GRCm39) |
D342V |
probably damaging |
Het |
Oip5 |
TGAGAAA |
T |
2: 119,448,342 (GRCm39) |
|
probably benign |
Het |
Omt2a |
T |
A |
9: 78,220,305 (GRCm39) |
E31D |
possibly damaging |
Het |
Or4f62 |
A |
G |
2: 111,986,697 (GRCm39) |
T134A |
probably benign |
Het |
Or52n2b |
A |
G |
7: 104,565,915 (GRCm39) |
I196T |
probably benign |
Het |
Or5ac20 |
A |
G |
16: 59,104,348 (GRCm39) |
S171P |
probably benign |
Het |
Or6c88 |
A |
C |
10: 129,406,895 (GRCm39) |
I124L |
probably damaging |
Het |
Or9a2 |
C |
A |
6: 41,749,003 (GRCm39) |
V77F |
probably damaging |
Het |
Phyhipl |
A |
G |
10: 70,404,815 (GRCm39) |
V131A |
probably benign |
Het |
Pik3r5 |
A |
G |
11: 68,384,464 (GRCm39) |
M619V |
probably benign |
Het |
Pramel19 |
T |
C |
4: 101,798,661 (GRCm39) |
Y211H |
probably benign |
Het |
Ptprg |
A |
T |
14: 12,237,837 (GRCm38) |
E1431D |
probably benign |
Het |
Rnf20 |
A |
G |
4: 49,638,029 (GRCm39) |
T85A |
probably damaging |
Het |
Rtn3 |
A |
T |
19: 7,433,886 (GRCm39) |
I683K |
probably damaging |
Het |
Rwdd3 |
A |
G |
3: 120,952,470 (GRCm39) |
F174L |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,778,208 (GRCm39) |
Q2096R |
possibly damaging |
Het |
Scrn1 |
T |
C |
6: 54,511,407 (GRCm39) |
D111G |
probably damaging |
Het |
Sema3e |
A |
G |
5: 14,302,646 (GRCm39) |
R724G |
possibly damaging |
Het |
She |
A |
G |
3: 89,741,544 (GRCm39) |
M232V |
possibly damaging |
Het |
Skic3 |
T |
A |
13: 76,333,275 (GRCm39) |
V1508E |
possibly damaging |
Het |
Slc25a54 |
A |
T |
3: 109,020,132 (GRCm39) |
N382I |
possibly damaging |
Het |
Slc26a2 |
T |
C |
18: 61,331,875 (GRCm39) |
M519V |
probably damaging |
Het |
Slc9a1 |
T |
A |
4: 133,097,967 (GRCm39) |
L38H |
probably damaging |
Het |
Snap47 |
A |
T |
11: 59,319,369 (GRCm39) |
D256E |
probably damaging |
Het |
Tacc3 |
A |
G |
5: 33,829,326 (GRCm39) |
T610A |
probably benign |
Het |
Tbc1d30 |
G |
A |
10: 121,103,121 (GRCm39) |
T637M |
probably benign |
Het |
Tbcd |
T |
A |
11: 121,464,681 (GRCm39) |
M572K |
probably benign |
Het |
Thoc7 |
A |
T |
14: 13,953,460 (GRCm38) |
D68E |
probably benign |
Het |
Tmpo |
G |
A |
10: 90,989,171 (GRCm39) |
T250M |
probably damaging |
Het |
Tmtc1 |
TGTCCGCCAGGCCCTTGCCCCAGAAGTC |
TGTC |
6: 148,345,445 (GRCm39) |
|
probably benign |
Het |
Tnfaip1 |
A |
T |
11: 78,418,396 (GRCm39) |
C224S |
possibly damaging |
Het |
Tshz1 |
T |
C |
18: 84,032,987 (GRCm39) |
T474A |
probably benign |
Het |
Tspoap1 |
C |
T |
11: 87,657,222 (GRCm39) |
Q345* |
probably null |
Het |
Ttc21a |
A |
G |
9: 119,774,067 (GRCm39) |
E258G |
possibly damaging |
Het |
Ttyh1 |
T |
C |
7: 4,131,225 (GRCm39) |
L232P |
probably damaging |
Het |
Usp2 |
T |
A |
9: 43,987,110 (GRCm39) |
L136Q |
probably damaging |
Het |
Usp31 |
T |
C |
7: 121,247,868 (GRCm39) |
S1192G |
probably damaging |
Het |
|
Other mutations in Abcc9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Abcc9
|
APN |
6 |
142,578,916 (GRCm39) |
splice site |
probably benign |
|
IGL00670:Abcc9
|
APN |
6 |
142,633,007 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00675:Abcc9
|
APN |
6 |
142,610,347 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00741:Abcc9
|
APN |
6 |
142,632,956 (GRCm39) |
missense |
probably benign |
|
IGL01371:Abcc9
|
APN |
6 |
142,602,340 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01686:Abcc9
|
APN |
6 |
142,548,801 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01724:Abcc9
|
APN |
6 |
142,610,259 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01807:Abcc9
|
APN |
6 |
142,551,640 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01941:Abcc9
|
APN |
6 |
142,551,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01946:Abcc9
|
APN |
6 |
142,571,763 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02210:Abcc9
|
APN |
6 |
142,633,097 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02498:Abcc9
|
APN |
6 |
142,617,265 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02535:Abcc9
|
APN |
6 |
142,574,152 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02552:Abcc9
|
APN |
6 |
142,551,645 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02812:Abcc9
|
APN |
6 |
142,643,516 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02954:Abcc9
|
APN |
6 |
142,592,007 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03035:Abcc9
|
APN |
6 |
142,573,319 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03040:Abcc9
|
APN |
6 |
142,598,323 (GRCm39) |
nonsense |
probably null |
|
IGL03100:Abcc9
|
APN |
6 |
142,640,270 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03157:Abcc9
|
APN |
6 |
142,551,649 (GRCm39) |
splice site |
probably benign |
|
R0054:Abcc9
|
UTSW |
6 |
142,547,500 (GRCm39) |
critical splice donor site |
probably null |
|
R0054:Abcc9
|
UTSW |
6 |
142,547,500 (GRCm39) |
critical splice donor site |
probably null |
|
R0084:Abcc9
|
UTSW |
6 |
142,604,277 (GRCm39) |
missense |
probably damaging |
0.97 |
R0211:Abcc9
|
UTSW |
6 |
142,634,710 (GRCm39) |
missense |
probably benign |
0.01 |
R0349:Abcc9
|
UTSW |
6 |
142,610,351 (GRCm39) |
missense |
probably benign |
0.00 |
R0387:Abcc9
|
UTSW |
6 |
142,585,230 (GRCm39) |
nonsense |
probably null |
|
R0393:Abcc9
|
UTSW |
6 |
142,591,604 (GRCm39) |
splice site |
probably benign |
|
R0528:Abcc9
|
UTSW |
6 |
142,638,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R0588:Abcc9
|
UTSW |
6 |
142,548,787 (GRCm39) |
nonsense |
probably null |
|
R0646:Abcc9
|
UTSW |
6 |
142,627,830 (GRCm39) |
missense |
probably benign |
0.05 |
R0691:Abcc9
|
UTSW |
6 |
142,584,979 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0881:Abcc9
|
UTSW |
6 |
142,592,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R1264:Abcc9
|
UTSW |
6 |
142,592,103 (GRCm39) |
splice site |
probably benign |
|
R1340:Abcc9
|
UTSW |
6 |
142,628,581 (GRCm39) |
splice site |
probably benign |
|
R1413:Abcc9
|
UTSW |
6 |
142,573,245 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1413:Abcc9
|
UTSW |
6 |
142,536,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R1535:Abcc9
|
UTSW |
6 |
142,610,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R1595:Abcc9
|
UTSW |
6 |
142,578,821 (GRCm39) |
missense |
probably benign |
0.02 |
R1670:Abcc9
|
UTSW |
6 |
142,540,448 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1769:Abcc9
|
UTSW |
6 |
142,573,194 (GRCm39) |
splice site |
probably benign |
|
R1888:Abcc9
|
UTSW |
6 |
142,625,040 (GRCm39) |
missense |
probably benign |
|
R1888:Abcc9
|
UTSW |
6 |
142,625,040 (GRCm39) |
missense |
probably benign |
|
R1918:Abcc9
|
UTSW |
6 |
142,643,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R1925:Abcc9
|
UTSW |
6 |
142,617,333 (GRCm39) |
missense |
probably damaging |
0.98 |
R2019:Abcc9
|
UTSW |
6 |
142,621,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R2698:Abcc9
|
UTSW |
6 |
142,578,862 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2860:Abcc9
|
UTSW |
6 |
142,571,736 (GRCm39) |
missense |
probably benign |
0.01 |
R2861:Abcc9
|
UTSW |
6 |
142,571,736 (GRCm39) |
missense |
probably benign |
0.01 |
R2980:Abcc9
|
UTSW |
6 |
142,633,034 (GRCm39) |
missense |
probably benign |
0.00 |
R3115:Abcc9
|
UTSW |
6 |
142,634,755 (GRCm39) |
missense |
probably benign |
0.08 |
R3617:Abcc9
|
UTSW |
6 |
142,625,015 (GRCm39) |
missense |
probably damaging |
0.97 |
R3880:Abcc9
|
UTSW |
6 |
142,584,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R4063:Abcc9
|
UTSW |
6 |
142,551,645 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4065:Abcc9
|
UTSW |
6 |
142,591,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R4290:Abcc9
|
UTSW |
6 |
142,539,738 (GRCm39) |
missense |
probably benign |
0.08 |
R4538:Abcc9
|
UTSW |
6 |
142,560,138 (GRCm39) |
critical splice donor site |
probably null |
|
R4615:Abcc9
|
UTSW |
6 |
142,634,833 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4659:Abcc9
|
UTSW |
6 |
142,618,321 (GRCm39) |
splice site |
probably null |
|
R4774:Abcc9
|
UTSW |
6 |
142,585,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R4788:Abcc9
|
UTSW |
6 |
142,566,456 (GRCm39) |
nonsense |
probably null |
|
R4832:Abcc9
|
UTSW |
6 |
142,617,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R4844:Abcc9
|
UTSW |
6 |
142,634,824 (GRCm39) |
missense |
probably benign |
0.09 |
R4903:Abcc9
|
UTSW |
6 |
142,546,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Abcc9
|
UTSW |
6 |
142,536,162 (GRCm39) |
missense |
probably benign |
|
R4983:Abcc9
|
UTSW |
6 |
142,627,867 (GRCm39) |
missense |
probably benign |
0.44 |
R4986:Abcc9
|
UTSW |
6 |
142,573,317 (GRCm39) |
missense |
probably benign |
0.00 |
R5060:Abcc9
|
UTSW |
6 |
142,571,836 (GRCm39) |
intron |
probably benign |
|
R5120:Abcc9
|
UTSW |
6 |
142,602,344 (GRCm39) |
missense |
probably benign |
0.00 |
R5198:Abcc9
|
UTSW |
6 |
142,571,726 (GRCm39) |
missense |
probably benign |
0.00 |
R5301:Abcc9
|
UTSW |
6 |
142,536,207 (GRCm39) |
missense |
probably benign |
0.41 |
R5328:Abcc9
|
UTSW |
6 |
142,627,785 (GRCm39) |
missense |
probably benign |
0.25 |
R5568:Abcc9
|
UTSW |
6 |
142,634,742 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5654:Abcc9
|
UTSW |
6 |
142,571,371 (GRCm39) |
intron |
probably benign |
|
R5694:Abcc9
|
UTSW |
6 |
142,546,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R5734:Abcc9
|
UTSW |
6 |
142,571,457 (GRCm39) |
intron |
probably benign |
|
R5774:Abcc9
|
UTSW |
6 |
142,574,285 (GRCm39) |
missense |
probably damaging |
0.98 |
R5802:Abcc9
|
UTSW |
6 |
142,602,402 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5890:Abcc9
|
UTSW |
6 |
142,550,554 (GRCm39) |
critical splice donor site |
probably null |
|
R5946:Abcc9
|
UTSW |
6 |
142,571,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R5971:Abcc9
|
UTSW |
6 |
142,585,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R6078:Abcc9
|
UTSW |
6 |
142,585,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R6392:Abcc9
|
UTSW |
6 |
142,627,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R6400:Abcc9
|
UTSW |
6 |
142,638,435 (GRCm39) |
makesense |
probably null |
|
R6478:Abcc9
|
UTSW |
6 |
142,625,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R6481:Abcc9
|
UTSW |
6 |
142,550,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R6564:Abcc9
|
UTSW |
6 |
142,548,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R6700:Abcc9
|
UTSW |
6 |
142,633,013 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6902:Abcc9
|
UTSW |
6 |
142,624,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6946:Abcc9
|
UTSW |
6 |
142,624,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6989:Abcc9
|
UTSW |
6 |
142,634,707 (GRCm39) |
missense |
probably damaging |
0.97 |
R7052:Abcc9
|
UTSW |
6 |
142,604,261 (GRCm39) |
missense |
probably benign |
0.00 |
R7062:Abcc9
|
UTSW |
6 |
142,544,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Abcc9
|
UTSW |
6 |
142,634,853 (GRCm39) |
nonsense |
probably null |
|
R7284:Abcc9
|
UTSW |
6 |
142,628,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R7296:Abcc9
|
UTSW |
6 |
142,617,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R7353:Abcc9
|
UTSW |
6 |
142,546,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R7359:Abcc9
|
UTSW |
6 |
142,617,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7815:Abcc9
|
UTSW |
6 |
142,598,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R7894:Abcc9
|
UTSW |
6 |
142,539,733 (GRCm39) |
makesense |
probably null |
|
R8095:Abcc9
|
UTSW |
6 |
142,590,048 (GRCm39) |
missense |
probably benign |
0.22 |
R8099:Abcc9
|
UTSW |
6 |
142,621,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R8245:Abcc9
|
UTSW |
6 |
142,539,870 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8355:Abcc9
|
UTSW |
6 |
142,638,478 (GRCm39) |
missense |
probably benign |
0.00 |
R8356:Abcc9
|
UTSW |
6 |
142,536,096 (GRCm39) |
missense |
probably benign |
0.06 |
R8365:Abcc9
|
UTSW |
6 |
142,544,798 (GRCm39) |
missense |
probably benign |
0.03 |
R8846:Abcc9
|
UTSW |
6 |
142,551,610 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8886:Abcc9
|
UTSW |
6 |
142,546,420 (GRCm39) |
intron |
probably benign |
|
R8939:Abcc9
|
UTSW |
6 |
142,624,977 (GRCm39) |
missense |
probably damaging |
0.99 |
R9049:Abcc9
|
UTSW |
6 |
142,628,658 (GRCm39) |
missense |
probably damaging |
0.99 |
R9113:Abcc9
|
UTSW |
6 |
142,591,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R9368:Abcc9
|
UTSW |
6 |
142,640,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9401:Abcc9
|
UTSW |
6 |
142,543,836 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9407:Abcc9
|
UTSW |
6 |
142,574,229 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9597:Abcc9
|
UTSW |
6 |
142,578,813 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9600:Abcc9
|
UTSW |
6 |
142,536,102 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9687:Abcc9
|
UTSW |
6 |
142,578,889 (GRCm39) |
missense |
probably benign |
0.00 |
R9698:Abcc9
|
UTSW |
6 |
142,571,757 (GRCm39) |
missense |
probably benign |
|
R9761:Abcc9
|
UTSW |
6 |
142,544,854 (GRCm39) |
missense |
possibly damaging |
0.78 |
U15987:Abcc9
|
UTSW |
6 |
142,585,301 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Abcc9
|
UTSW |
6 |
142,591,664 (GRCm39) |
missense |
probably null |
0.96 |
Z1177:Abcc9
|
UTSW |
6 |
142,571,708 (GRCm39) |
missense |
probably benign |
0.07 |
Z1177:Abcc9
|
UTSW |
6 |
142,540,484 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GAGCAACACAGTGTGCCTTC -3'
(R):5'- GATCTGTAGTACAGCTAAGATCAGG -3'
Sequencing Primer
(F):5'- CCTTCAAAAGGGTGTCCGTTAG -3'
(R):5'- CTAAGATCAGGTATGGTGGTACC -3'
|
Posted On |
2016-04-27 |