Incidental Mutation 'R2128:Abca6'
ID |
227757 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Abca6
|
Ensembl Gene |
ENSMUSG00000044749 |
Gene Name |
ATP-binding cassette, sub-family A member 6 |
Synonyms |
6330565N06Rik |
MMRRC Submission |
040131-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R2128 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
11 |
Chromosomal Location |
110067646-110142602 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 110110475 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Threonine
at position 558
(I558T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000035458
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044003]
|
AlphaFold |
Q8K441 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000044003
AA Change: I558T
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000035458 Gene: ENSMUSG00000044749 AA Change: I558T
Domain | Start | End | E-Value | Type |
Pfam:ABC2_membrane_3
|
28 |
416 |
1.4e-42 |
PFAM |
low complexity region
|
484 |
495 |
N/A |
INTRINSIC |
AAA
|
506 |
691 |
1.13e-6 |
SMART |
transmembrane domain
|
854 |
876 |
N/A |
INTRINSIC |
transmembrane domain
|
971 |
990 |
N/A |
INTRINSIC |
transmembrane domain
|
1005 |
1027 |
N/A |
INTRINSIC |
Blast:AAA
|
1041 |
1176 |
4e-21 |
BLAST |
transmembrane domain
|
1191 |
1213 |
N/A |
INTRINSIC |
low complexity region
|
1243 |
1254 |
N/A |
INTRINSIC |
AAA
|
1312 |
1505 |
2.43e-6 |
SMART |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.4%
- 20x: 95.4%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] 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 intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This encoded protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This gene is clustered among 4 other ABC1 family members on 17q24 and may play a role in macrophage lipid homeostasis. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700113H08Rik |
A |
G |
10: 87,066,066 (GRCm39) |
E249G |
possibly damaging |
Het |
2610028H24Rik |
A |
G |
10: 76,293,349 (GRCm39) |
M136V |
possibly damaging |
Het |
4930523C07Rik |
A |
T |
1: 159,902,945 (GRCm39) |
K72* |
probably null |
Het |
Acot10 |
T |
C |
15: 20,666,712 (GRCm39) |
T10A |
probably benign |
Het |
Adgrl4 |
T |
A |
3: 151,205,838 (GRCm39) |
D233E |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,705,199 (GRCm39) |
F1537Y |
probably damaging |
Het |
Aqp3 |
T |
A |
4: 41,098,061 (GRCm39) |
I17F |
probably benign |
Het |
Arap1 |
T |
A |
7: 101,058,527 (GRCm39) |
L1375H |
probably damaging |
Het |
Aspm |
T |
C |
1: 139,385,373 (GRCm39) |
V339A |
probably benign |
Het |
Atp13a3 |
G |
A |
16: 30,173,094 (GRCm39) |
A261V |
probably damaging |
Het |
Casp8ap2 |
T |
C |
4: 32,640,142 (GRCm39) |
Y399H |
probably benign |
Het |
Cept1 |
A |
G |
3: 106,420,195 (GRCm39) |
V213A |
probably damaging |
Het |
Cit |
A |
G |
5: 116,123,566 (GRCm39) |
D1469G |
possibly damaging |
Het |
Cnga2 |
A |
G |
X: 71,051,394 (GRCm39) |
Y182C |
possibly damaging |
Het |
Cox20 |
A |
G |
1: 178,149,512 (GRCm39) |
I54V |
probably benign |
Het |
Dhx8 |
C |
A |
11: 101,629,235 (GRCm39) |
D261E |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,349,011 (GRCm39) |
I2486N |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,408,467 (GRCm39) |
Q3484R |
probably benign |
Het |
Drd1 |
T |
C |
13: 54,207,572 (GRCm39) |
Y207C |
probably damaging |
Het |
Dtl |
C |
T |
1: 191,290,222 (GRCm39) |
V222I |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,607,316 (GRCm39) |
Y2636H |
probably damaging |
Het |
Endog |
C |
A |
2: 30,062,048 (GRCm39) |
D154E |
probably benign |
Het |
Epc1 |
A |
T |
18: 6,462,954 (GRCm39) |
V14E |
probably damaging |
Het |
Ercc4 |
C |
A |
16: 12,965,798 (GRCm39) |
T810K |
probably damaging |
Het |
Fam43b |
T |
A |
4: 138,123,299 (GRCm39) |
N7I |
possibly damaging |
Het |
Fgd1 |
T |
C |
X: 149,869,213 (GRCm39) |
|
probably null |
Het |
Filip1 |
G |
T |
9: 79,726,612 (GRCm39) |
T669N |
probably damaging |
Het |
Fndc1 |
A |
G |
17: 7,997,497 (GRCm39) |
|
probably benign |
Het |
Foxk1 |
C |
A |
5: 142,420,943 (GRCm39) |
S189* |
probably null |
Het |
Gatm |
T |
C |
2: 122,431,017 (GRCm39) |
N274S |
probably damaging |
Het |
Gdf9 |
A |
G |
11: 53,328,334 (GRCm39) |
Y430C |
probably damaging |
Het |
Gga1 |
C |
T |
15: 78,772,648 (GRCm39) |
P260S |
probably damaging |
Het |
Gm11595 |
A |
T |
11: 99,663,327 (GRCm39) |
C118S |
unknown |
Het |
Gm382 |
G |
T |
X: 125,970,274 (GRCm39) |
V820L |
possibly damaging |
Het |
Gzmk |
T |
A |
13: 113,308,548 (GRCm39) |
I179F |
probably damaging |
Het |
Hsp90b1 |
T |
C |
10: 86,531,570 (GRCm39) |
D421G |
probably damaging |
Het |
Hus1 |
A |
G |
11: 8,956,011 (GRCm39) |
M174T |
probably damaging |
Het |
Ifngr2 |
T |
A |
16: 91,359,761 (GRCm39) |
Y289* |
probably null |
Het |
Il6st |
T |
A |
13: 112,640,709 (GRCm39) |
H828Q |
probably benign |
Het |
Impg2 |
T |
A |
16: 56,038,742 (GRCm39) |
Y127N |
probably damaging |
Het |
Irf3 |
T |
A |
7: 44,651,168 (GRCm39) |
W345R |
probably damaging |
Het |
Kif1b |
G |
A |
4: 149,272,097 (GRCm39) |
S1568L |
possibly damaging |
Het |
Klhl42 |
A |
G |
6: 147,003,251 (GRCm39) |
T342A |
probably benign |
Het |
Kndc1 |
G |
T |
7: 139,510,025 (GRCm39) |
R1289L |
probably damaging |
Het |
Knl1 |
A |
T |
2: 118,902,300 (GRCm39) |
T1334S |
possibly damaging |
Het |
L3mbtl3 |
G |
T |
10: 26,189,766 (GRCm39) |
D499E |
unknown |
Het |
Ldhd |
T |
A |
8: 112,353,680 (GRCm39) |
M478L |
probably benign |
Het |
Loxl4 |
C |
G |
19: 42,592,402 (GRCm39) |
E385D |
probably damaging |
Het |
Lrriq1 |
G |
A |
10: 103,050,718 (GRCm39) |
T678I |
probably benign |
Het |
Macf1 |
T |
A |
4: 123,386,567 (GRCm39) |
I1017F |
probably benign |
Het |
Madcam1 |
A |
G |
10: 79,501,406 (GRCm39) |
E157G |
possibly damaging |
Het |
Mamdc4 |
T |
C |
2: 25,459,270 (GRCm39) |
D195G |
probably damaging |
Het |
Mctp1 |
A |
G |
13: 76,972,941 (GRCm39) |
D648G |
probably damaging |
Het |
Mycbp2 |
T |
C |
14: 103,438,666 (GRCm39) |
M2072V |
probably benign |
Het |
Nck1 |
A |
G |
9: 100,379,600 (GRCm39) |
|
probably null |
Het |
Ndufaf4 |
G |
T |
4: 24,898,608 (GRCm39) |
D55Y |
probably damaging |
Het |
Nek11 |
A |
T |
9: 105,177,560 (GRCm39) |
D230E |
probably benign |
Het |
Nit2 |
T |
C |
16: 56,981,559 (GRCm39) |
K67E |
possibly damaging |
Het |
Or12j2 |
C |
T |
7: 139,916,342 (GRCm39) |
T189M |
probably damaging |
Het |
Or5ae1 |
T |
C |
7: 84,565,701 (GRCm39) |
F238S |
probably damaging |
Het |
Or6a2 |
T |
C |
7: 106,600,455 (GRCm39) |
D204G |
probably damaging |
Het |
Or6c1 |
A |
T |
10: 129,518,401 (GRCm39) |
V69E |
possibly damaging |
Het |
Pakap |
A |
G |
4: 57,854,890 (GRCm39) |
Y134C |
probably benign |
Het |
Pccb |
G |
C |
9: 100,867,884 (GRCm39) |
D347E |
probably damaging |
Het |
Plcl1 |
T |
A |
1: 55,736,997 (GRCm39) |
F779L |
probably damaging |
Het |
Prune2 |
C |
A |
19: 17,099,786 (GRCm39) |
D1763E |
probably benign |
Het |
Pwwp2a |
A |
G |
11: 43,596,145 (GRCm39) |
S437G |
probably benign |
Het |
Rabgap1l |
A |
T |
1: 160,566,527 (GRCm39) |
D90E |
probably benign |
Het |
Rapgef4 |
T |
A |
2: 72,056,897 (GRCm39) |
I552N |
possibly damaging |
Het |
Scn7a |
A |
T |
2: 66,528,330 (GRCm39) |
I720K |
probably damaging |
Het |
Scn9a |
T |
A |
2: 66,356,998 (GRCm39) |
N1101I |
probably damaging |
Het |
Siglec1 |
A |
T |
2: 130,922,417 (GRCm39) |
Y553N |
probably damaging |
Het |
Slc22a23 |
A |
G |
13: 34,387,953 (GRCm39) |
L381P |
possibly damaging |
Het |
Slc7a11 |
T |
A |
3: 50,338,558 (GRCm39) |
T284S |
probably damaging |
Het |
Slc8a2 |
T |
A |
7: 15,874,417 (GRCm39) |
|
probably null |
Het |
Snx29 |
T |
A |
16: 11,218,835 (GRCm39) |
S224T |
probably damaging |
Het |
Stimate |
T |
C |
14: 30,588,581 (GRCm39) |
Y103H |
probably damaging |
Het |
Stox1 |
T |
C |
10: 62,500,314 (GRCm39) |
T749A |
probably benign |
Het |
Tg |
A |
G |
15: 66,566,743 (GRCm39) |
I1264V |
probably benign |
Het |
Top2a |
A |
C |
11: 98,900,633 (GRCm39) |
V609G |
probably damaging |
Het |
Trmt44 |
G |
A |
5: 35,732,176 (GRCm39) |
P72S |
probably benign |
Het |
Ttll3 |
G |
C |
6: 113,389,895 (GRCm39) |
S760T |
probably benign |
Het |
Ttn |
T |
C |
2: 76,579,022 (GRCm39) |
D23957G |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,664,241 (GRCm39) |
|
probably benign |
Het |
Ubxn1 |
T |
G |
19: 8,849,434 (GRCm39) |
V59G |
probably benign |
Het |
Ubxn4 |
T |
C |
1: 128,172,247 (GRCm39) |
S14P |
probably benign |
Het |
Uso1 |
T |
A |
5: 92,343,229 (GRCm39) |
M771K |
probably benign |
Het |
Utp20 |
A |
G |
10: 88,649,917 (GRCm39) |
F431S |
probably damaging |
Het |
Vmn1r206 |
T |
C |
13: 22,804,782 (GRCm39) |
S142G |
probably benign |
Het |
Vmn2r19 |
A |
G |
6: 123,285,289 (GRCm39) |
|
probably null |
Het |
Vps36 |
G |
T |
8: 22,708,305 (GRCm39) |
|
probably null |
Het |
Wnt3 |
A |
G |
11: 103,703,474 (GRCm39) |
H319R |
possibly damaging |
Het |
Zbtb26 |
G |
T |
2: 37,326,563 (GRCm39) |
Q158K |
probably benign |
Het |
Zfp648 |
T |
C |
1: 154,080,353 (GRCm39) |
S171P |
probably benign |
Het |
|
Other mutations in Abca6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Abca6
|
APN |
11 |
110,075,535 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00569:Abca6
|
APN |
11 |
110,077,875 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00737:Abca6
|
APN |
11 |
110,087,823 (GRCm39) |
splice site |
probably benign |
|
IGL01024:Abca6
|
APN |
11 |
110,087,968 (GRCm39) |
missense |
probably benign |
|
IGL01087:Abca6
|
APN |
11 |
110,082,476 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01511:Abca6
|
APN |
11 |
110,135,136 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01516:Abca6
|
APN |
11 |
110,109,043 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01621:Abca6
|
APN |
11 |
110,075,534 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01749:Abca6
|
APN |
11 |
110,135,050 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01934:Abca6
|
APN |
11 |
110,079,481 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02010:Abca6
|
APN |
11 |
110,110,442 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02121:Abca6
|
APN |
11 |
110,073,750 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02423:Abca6
|
APN |
11 |
110,109,832 (GRCm39) |
splice site |
probably benign |
|
IGL02428:Abca6
|
APN |
11 |
110,069,618 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02491:Abca6
|
APN |
11 |
110,067,794 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02541:Abca6
|
APN |
11 |
110,103,093 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02792:Abca6
|
APN |
11 |
110,079,507 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02836:Abca6
|
APN |
11 |
110,139,374 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02965:Abca6
|
APN |
11 |
110,071,439 (GRCm39) |
missense |
probably benign |
|
IGL03094:Abca6
|
APN |
11 |
110,074,938 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03109:Abca6
|
APN |
11 |
110,071,173 (GRCm39) |
missense |
probably damaging |
0.96 |
R0068:Abca6
|
UTSW |
11 |
110,073,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R0142:Abca6
|
UTSW |
11 |
110,079,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R0165:Abca6
|
UTSW |
11 |
110,110,430 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0254:Abca6
|
UTSW |
11 |
110,127,615 (GRCm39) |
missense |
probably benign |
0.16 |
R0598:Abca6
|
UTSW |
11 |
110,087,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R0992:Abca6
|
UTSW |
11 |
110,102,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1386:Abca6
|
UTSW |
11 |
110,135,081 (GRCm39) |
missense |
probably benign |
0.02 |
R1642:Abca6
|
UTSW |
11 |
110,109,107 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1673:Abca6
|
UTSW |
11 |
110,103,165 (GRCm39) |
missense |
probably benign |
0.01 |
R1792:Abca6
|
UTSW |
11 |
110,074,870 (GRCm39) |
missense |
probably benign |
0.00 |
R1813:Abca6
|
UTSW |
11 |
110,124,671 (GRCm39) |
splice site |
probably benign |
|
R1817:Abca6
|
UTSW |
11 |
110,110,144 (GRCm39) |
missense |
probably benign |
0.00 |
R1842:Abca6
|
UTSW |
11 |
110,087,865 (GRCm39) |
missense |
probably benign |
0.00 |
R1898:Abca6
|
UTSW |
11 |
110,099,625 (GRCm39) |
missense |
probably damaging |
0.99 |
R1914:Abca6
|
UTSW |
11 |
110,103,036 (GRCm39) |
missense |
probably benign |
0.06 |
R1915:Abca6
|
UTSW |
11 |
110,103,036 (GRCm39) |
missense |
probably benign |
0.06 |
R1934:Abca6
|
UTSW |
11 |
110,100,909 (GRCm39) |
critical splice donor site |
probably null |
|
R1964:Abca6
|
UTSW |
11 |
110,075,502 (GRCm39) |
missense |
probably damaging |
0.98 |
R1967:Abca6
|
UTSW |
11 |
110,077,974 (GRCm39) |
missense |
probably benign |
0.09 |
R2127:Abca6
|
UTSW |
11 |
110,110,475 (GRCm39) |
missense |
probably benign |
0.00 |
R2164:Abca6
|
UTSW |
11 |
110,101,019 (GRCm39) |
frame shift |
probably null |
|
R2895:Abca6
|
UTSW |
11 |
110,093,252 (GRCm39) |
missense |
probably benign |
0.00 |
R3110:Abca6
|
UTSW |
11 |
110,069,655 (GRCm39) |
nonsense |
probably null |
|
R3111:Abca6
|
UTSW |
11 |
110,069,655 (GRCm39) |
nonsense |
probably null |
|
R3112:Abca6
|
UTSW |
11 |
110,069,655 (GRCm39) |
nonsense |
probably null |
|
R4094:Abca6
|
UTSW |
11 |
110,071,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R4432:Abca6
|
UTSW |
11 |
110,132,414 (GRCm39) |
missense |
probably benign |
0.11 |
R4474:Abca6
|
UTSW |
11 |
110,124,598 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4572:Abca6
|
UTSW |
11 |
110,107,374 (GRCm39) |
missense |
probably benign |
0.31 |
R4629:Abca6
|
UTSW |
11 |
110,121,375 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4793:Abca6
|
UTSW |
11 |
110,082,544 (GRCm39) |
missense |
probably benign |
|
R4852:Abca6
|
UTSW |
11 |
110,135,029 (GRCm39) |
missense |
probably benign |
0.09 |
R4867:Abca6
|
UTSW |
11 |
110,093,205 (GRCm39) |
missense |
probably benign |
0.01 |
R4879:Abca6
|
UTSW |
11 |
110,110,526 (GRCm39) |
missense |
probably damaging |
0.98 |
R4918:Abca6
|
UTSW |
11 |
110,071,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R5060:Abca6
|
UTSW |
11 |
110,110,430 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5062:Abca6
|
UTSW |
11 |
110,067,892 (GRCm39) |
missense |
probably benign |
0.12 |
R5083:Abca6
|
UTSW |
11 |
110,109,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R5173:Abca6
|
UTSW |
11 |
110,082,546 (GRCm39) |
missense |
probably benign |
|
R5393:Abca6
|
UTSW |
11 |
110,135,121 (GRCm39) |
missense |
probably benign |
0.00 |
R5484:Abca6
|
UTSW |
11 |
110,074,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R5498:Abca6
|
UTSW |
11 |
110,099,670 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5503:Abca6
|
UTSW |
11 |
110,109,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R5645:Abca6
|
UTSW |
11 |
110,141,234 (GRCm39) |
missense |
probably damaging |
0.99 |
R5680:Abca6
|
UTSW |
11 |
110,127,471 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5761:Abca6
|
UTSW |
11 |
110,100,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R5779:Abca6
|
UTSW |
11 |
110,075,496 (GRCm39) |
missense |
probably benign |
0.37 |
R5818:Abca6
|
UTSW |
11 |
110,110,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R6282:Abca6
|
UTSW |
11 |
110,099,650 (GRCm39) |
missense |
probably damaging |
0.98 |
R6455:Abca6
|
UTSW |
11 |
110,132,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R6826:Abca6
|
UTSW |
11 |
110,107,431 (GRCm39) |
missense |
probably benign |
0.15 |
R6857:Abca6
|
UTSW |
11 |
110,110,514 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6914:Abca6
|
UTSW |
11 |
110,081,064 (GRCm39) |
missense |
probably benign |
|
R6931:Abca6
|
UTSW |
11 |
110,135,154 (GRCm39) |
missense |
probably benign |
0.27 |
R7222:Abca6
|
UTSW |
11 |
110,082,519 (GRCm39) |
missense |
probably benign |
0.29 |
R7242:Abca6
|
UTSW |
11 |
110,132,479 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7297:Abca6
|
UTSW |
11 |
110,073,852 (GRCm39) |
critical splice donor site |
probably null |
|
R7387:Abca6
|
UTSW |
11 |
110,093,246 (GRCm39) |
missense |
probably benign |
|
R7420:Abca6
|
UTSW |
11 |
110,141,303 (GRCm39) |
missense |
probably benign |
0.24 |
R7494:Abca6
|
UTSW |
11 |
110,099,571 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7603:Abca6
|
UTSW |
11 |
110,071,084 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7637:Abca6
|
UTSW |
11 |
110,109,778 (GRCm39) |
missense |
probably benign |
0.00 |
R7674:Abca6
|
UTSW |
11 |
110,110,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R7753:Abca6
|
UTSW |
11 |
110,074,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7800:Abca6
|
UTSW |
11 |
110,078,698 (GRCm39) |
missense |
probably benign |
0.00 |
R7842:Abca6
|
UTSW |
11 |
110,087,523 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7855:Abca6
|
UTSW |
11 |
110,082,454 (GRCm39) |
missense |
probably benign |
0.01 |
R8119:Abca6
|
UTSW |
11 |
110,087,930 (GRCm39) |
missense |
probably benign |
0.00 |
R8139:Abca6
|
UTSW |
11 |
110,074,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R8176:Abca6
|
UTSW |
11 |
110,135,020 (GRCm39) |
missense |
probably benign |
0.01 |
R8179:Abca6
|
UTSW |
11 |
110,136,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R8197:Abca6
|
UTSW |
11 |
110,102,641 (GRCm39) |
missense |
probably damaging |
0.99 |
R8241:Abca6
|
UTSW |
11 |
110,079,456 (GRCm39) |
missense |
probably null |
1.00 |
R8404:Abca6
|
UTSW |
11 |
110,110,145 (GRCm39) |
missense |
probably damaging |
0.99 |
R8429:Abca6
|
UTSW |
11 |
110,093,208 (GRCm39) |
missense |
probably benign |
|
R8502:Abca6
|
UTSW |
11 |
110,110,145 (GRCm39) |
missense |
probably damaging |
0.99 |
R8816:Abca6
|
UTSW |
11 |
110,127,513 (GRCm39) |
missense |
probably benign |
0.04 |
R8964:Abca6
|
UTSW |
11 |
110,139,363 (GRCm39) |
missense |
probably benign |
0.00 |
R9153:Abca6
|
UTSW |
11 |
110,107,481 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9233:Abca6
|
UTSW |
11 |
110,082,496 (GRCm39) |
missense |
probably benign |
0.31 |
R9407:Abca6
|
UTSW |
11 |
110,093,210 (GRCm39) |
nonsense |
probably null |
|
R9412:Abca6
|
UTSW |
11 |
110,103,059 (GRCm39) |
missense |
probably damaging |
0.99 |
R9453:Abca6
|
UTSW |
11 |
110,138,090 (GRCm39) |
critical splice donor site |
probably null |
|
R9533:Abca6
|
UTSW |
11 |
110,102,582 (GRCm39) |
missense |
probably benign |
0.16 |
R9546:Abca6
|
UTSW |
11 |
110,135,042 (GRCm39) |
nonsense |
probably null |
|
R9650:Abca6
|
UTSW |
11 |
110,071,446 (GRCm39) |
missense |
probably benign |
0.32 |
R9702:Abca6
|
UTSW |
11 |
110,107,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R9709:Abca6
|
UTSW |
11 |
110,102,589 (GRCm39) |
missense |
probably benign |
0.01 |
X0024:Abca6
|
UTSW |
11 |
110,135,081 (GRCm39) |
missense |
probably benign |
0.02 |
X0064:Abca6
|
UTSW |
11 |
110,087,968 (GRCm39) |
missense |
probably benign |
0.01 |
|
Predicted Primers |
PCR Primer
(F):5'- CTGAGGTCATGATTGAACATGG -3'
(R):5'- CTCAGAGAGAACGTGCTACACAG -3'
Sequencing Primer
(F):5'- CATGATTGAACATGGTTAATGATGGG -3'
(R):5'- GTGCTACACAGTATCTACACTAGG -3'
|
Posted On |
2014-09-17 |