Incidental Mutation 'R1817:Abca6'
ID |
204526 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Abca6
|
Ensembl Gene |
ENSMUSG00000044749 |
Gene Name |
ATP-binding cassette, sub-family A member 6 |
Synonyms |
6330565N06Rik |
MMRRC Submission |
039845-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1817 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
110067646-110142602 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 110110144 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Threonine
at position 600
(S600T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000035458
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044003]
|
AlphaFold |
Q8K441 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000044003
AA Change: S600T
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
SMART Domains |
Protein: ENSMUSP00000035458 Gene: ENSMUSG00000044749 AA Change: S600T
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: 97.4%
- 3x: 96.9%
- 10x: 95.2%
- 20x: 91.9%
|
Validation Efficiency |
95% (90/95) |
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: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acly |
T |
A |
11: 100,386,717 (GRCm39) |
Q615L |
probably benign |
Het |
Adgrf1 |
C |
A |
17: 43,620,924 (GRCm39) |
T387K |
probably benign |
Het |
Afg3l1 |
G |
T |
8: 124,228,670 (GRCm39) |
K745N |
probably damaging |
Het |
Armc8 |
T |
C |
9: 99,418,312 (GRCm39) |
T39A |
possibly damaging |
Het |
Atm |
C |
A |
9: 53,403,533 (GRCm39) |
|
probably benign |
Het |
Babam2 |
A |
G |
5: 32,214,890 (GRCm39) |
T324A |
probably damaging |
Het |
Btd |
C |
A |
14: 31,384,246 (GRCm39) |
D77E |
possibly damaging |
Het |
Cadm1 |
T |
A |
9: 47,740,668 (GRCm39) |
|
probably benign |
Het |
Card11 |
A |
T |
5: 140,871,315 (GRCm39) |
D729E |
probably benign |
Het |
Ccni |
G |
T |
5: 93,335,967 (GRCm39) |
T144K |
possibly damaging |
Het |
Ceacam23 |
C |
T |
7: 17,607,255 (GRCm39) |
|
noncoding transcript |
Het |
Cecr2 |
A |
G |
6: 120,708,228 (GRCm39) |
T77A |
probably damaging |
Het |
Cgas |
A |
G |
9: 78,341,593 (GRCm39) |
|
probably null |
Het |
Cpsf7 |
T |
C |
19: 10,512,803 (GRCm39) |
F296L |
possibly damaging |
Het |
Cyfip1 |
C |
A |
7: 55,523,196 (GRCm39) |
N70K |
possibly damaging |
Het |
Cyp4a12b |
A |
G |
4: 115,271,259 (GRCm39) |
|
probably benign |
Het |
Ddx20 |
A |
T |
3: 105,585,896 (GRCm39) |
Y816* |
probably null |
Het |
Ddx59 |
A |
G |
1: 136,360,245 (GRCm39) |
I420V |
probably damaging |
Het |
Dgat1 |
T |
A |
15: 76,386,703 (GRCm39) |
M445L |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,246,546 (GRCm39) |
L628* |
probably null |
Het |
Dnah7a |
A |
C |
1: 53,598,307 (GRCm39) |
D1409E |
probably benign |
Het |
Dnmt1 |
T |
C |
9: 20,838,422 (GRCm39) |
T215A |
probably benign |
Het |
Dsg4 |
C |
T |
18: 20,604,302 (GRCm39) |
T923M |
probably damaging |
Het |
Enox1 |
A |
G |
14: 77,852,915 (GRCm39) |
I394V |
possibly damaging |
Het |
Esrp2 |
A |
T |
8: 106,861,250 (GRCm39) |
M183K |
probably damaging |
Het |
Fam171a1 |
C |
T |
2: 3,179,410 (GRCm39) |
P79S |
probably benign |
Het |
Fga |
A |
G |
3: 82,939,082 (GRCm39) |
T486A |
probably benign |
Het |
Fkbp10 |
G |
T |
11: 100,306,715 (GRCm39) |
A36S |
probably benign |
Het |
Fnip1 |
A |
G |
11: 54,393,279 (GRCm39) |
T572A |
probably benign |
Het |
Fxn |
A |
C |
19: 24,257,765 (GRCm39) |
|
probably null |
Het |
Gaa |
C |
T |
11: 119,175,324 (GRCm39) |
Q901* |
probably null |
Het |
Gabrg1 |
A |
G |
5: 70,911,594 (GRCm39) |
M344T |
probably benign |
Het |
Galnt7 |
C |
T |
8: 57,991,212 (GRCm39) |
V433M |
probably damaging |
Het |
Gin1 |
A |
G |
1: 97,712,951 (GRCm39) |
|
probably null |
Het |
Hydin |
A |
C |
8: 111,259,459 (GRCm39) |
D2477A |
probably benign |
Het |
Igsf6 |
T |
C |
7: 120,670,031 (GRCm39) |
Y37C |
probably damaging |
Het |
Il18rap |
A |
G |
1: 40,570,687 (GRCm39) |
I210V |
probably benign |
Het |
Kif3a |
T |
C |
11: 53,489,561 (GRCm39) |
Y138H |
probably damaging |
Het |
Klra17 |
A |
G |
6: 129,845,681 (GRCm39) |
|
probably null |
Het |
Lcorl |
A |
T |
5: 45,952,688 (GRCm39) |
I55N |
probably damaging |
Het |
Lrrc49 |
A |
G |
9: 60,510,059 (GRCm39) |
S398P |
possibly damaging |
Het |
Ltv1 |
A |
G |
10: 13,055,018 (GRCm39) |
L384S |
probably damaging |
Het |
Mageb3 |
A |
T |
2: 121,784,918 (GRCm39) |
Y261* |
probably null |
Het |
Mical3 |
T |
G |
6: 121,019,196 (GRCm39) |
T9P |
probably benign |
Het |
Myrip |
C |
T |
9: 120,217,228 (GRCm39) |
S49L |
probably damaging |
Het |
Nrap |
T |
C |
19: 56,372,487 (GRCm39) |
|
probably benign |
Het |
Or2m12 |
T |
C |
16: 19,104,627 (GRCm39) |
N289D |
probably damaging |
Het |
Or4k5 |
A |
G |
14: 50,385,728 (GRCm39) |
V201A |
probably benign |
Het |
Otoa |
A |
T |
7: 120,759,753 (GRCm39) |
|
probably benign |
Het |
Pals2 |
T |
G |
6: 50,140,411 (GRCm39) |
F144V |
probably benign |
Het |
Parp11 |
T |
A |
6: 127,467,008 (GRCm39) |
I133N |
probably damaging |
Het |
Pcnx1 |
A |
G |
12: 81,965,416 (GRCm39) |
T528A |
probably benign |
Het |
Pde4c |
A |
G |
8: 71,179,638 (GRCm39) |
H63R |
probably benign |
Het |
Pdpk1 |
T |
C |
17: 24,329,878 (GRCm39) |
K53E |
probably damaging |
Het |
Pdzd7 |
A |
T |
19: 45,024,615 (GRCm39) |
M468K |
probably damaging |
Het |
Perm1 |
C |
A |
4: 156,303,061 (GRCm39) |
P535Q |
possibly damaging |
Het |
Pgap1 |
C |
A |
1: 54,575,128 (GRCm39) |
A265S |
probably benign |
Het |
Pik3c2a |
A |
T |
7: 115,975,747 (GRCm39) |
|
probably null |
Het |
Plxnd1 |
T |
C |
6: 115,957,562 (GRCm39) |
T491A |
possibly damaging |
Het |
Pms1 |
A |
T |
1: 53,246,128 (GRCm39) |
D470E |
probably benign |
Het |
Prf1 |
C |
A |
10: 61,138,762 (GRCm39) |
T240N |
probably damaging |
Het |
Prune2 |
A |
G |
19: 17,099,445 (GRCm39) |
T1650A |
probably benign |
Het |
Ptprf |
A |
G |
4: 118,080,462 (GRCm39) |
L1264P |
probably benign |
Het |
Ptprs |
A |
G |
17: 56,726,527 (GRCm39) |
S948P |
probably damaging |
Het |
Rapgef1 |
T |
C |
2: 29,576,268 (GRCm39) |
V117A |
probably damaging |
Het |
Rnf123 |
A |
G |
9: 107,940,125 (GRCm39) |
V756A |
probably benign |
Het |
Sez6l2 |
A |
G |
7: 126,566,291 (GRCm39) |
E741G |
probably damaging |
Het |
Shc3 |
A |
T |
13: 51,626,888 (GRCm39) |
I125K |
possibly damaging |
Het |
Smr3a |
A |
T |
5: 88,155,917 (GRCm39) |
|
probably benign |
Het |
Spef2 |
C |
T |
15: 9,584,194 (GRCm39) |
E1624K |
probably damaging |
Het |
St6gal1 |
A |
T |
16: 23,140,083 (GRCm39) |
K85* |
probably null |
Het |
Taf1b |
T |
G |
12: 24,597,121 (GRCm39) |
D353E |
possibly damaging |
Het |
Tcp10b |
C |
T |
17: 13,286,590 (GRCm39) |
P180S |
possibly damaging |
Het |
Tlr9 |
A |
T |
9: 106,102,142 (GRCm39) |
M478L |
probably benign |
Het |
Tpr |
A |
T |
1: 150,295,654 (GRCm39) |
E892D |
probably damaging |
Het |
Trio |
C |
T |
15: 27,742,581 (GRCm39) |
W22* |
probably null |
Het |
Usp14 |
A |
G |
18: 10,024,673 (GRCm39) |
V8A |
probably damaging |
Het |
Vmn2r19 |
A |
T |
6: 123,307,011 (GRCm39) |
K506N |
possibly damaging |
Het |
Vmn2r45 |
T |
A |
7: 8,475,372 (GRCm39) |
N552I |
probably damaging |
Het |
Vmn2r56 |
A |
T |
7: 12,449,542 (GRCm39) |
M232K |
probably benign |
Het |
Vps13b |
T |
A |
15: 35,910,788 (GRCm39) |
F3517L |
possibly damaging |
Het |
Yif1a |
C |
T |
19: 5,142,333 (GRCm39) |
R247* |
probably null |
Het |
Zbtb5 |
A |
G |
4: 44,993,767 (GRCm39) |
V539A |
probably benign |
Het |
Zfp180 |
G |
A |
7: 23,804,652 (GRCm39) |
R357Q |
probably damaging |
Het |
Zfp536 |
A |
G |
7: 37,268,042 (GRCm39) |
L458P |
probably damaging |
Het |
Zfp646 |
G |
A |
7: 127,482,292 (GRCm39) |
G1490S |
probably benign |
Het |
Zfp970 |
C |
T |
2: 177,167,976 (GRCm39) |
H517Y |
probably damaging |
Het |
Zranb3 |
A |
T |
1: 127,945,293 (GRCm39) |
|
probably null |
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 |
|
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 |
R2128: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'- AAGCCCTGCATGACTCTTAC -3'
(R):5'- CTTCCACAGGACGTAGAGCAAG -3'
Sequencing Primer
(F):5'- TACTGAGTCACTTACAACCTCCG -3'
(R):5'- TAACCATGTTCAATCATGACCTCAG -3'
|
Posted On |
2014-06-23 |