Incidental Mutation 'R4793:Abca6'
| ID |
368789 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Abca6
|
| Ensembl Gene |
ENSMUSG00000044749 |
| Gene Name |
ATP-binding cassette, sub-family A member 6 |
| Synonyms |
6330565N06Rik |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4793 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
110067646-110142602 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 110082544 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Valine
at position 1143
(E1143V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000035458
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044003]
|
| AlphaFold |
Q8K441 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000044003
AA Change: E1143V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000035458
Gene: ENSMUSG00000044749
AA Change: E1143V
| 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: 99.1%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.9%
|
| Validation Efficiency |
100% (91/91) |
| 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: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abi2 |
T |
A |
1: 60,448,963 (GRCm39) |
M1K |
probably null |
Het |
| Acp2 |
T |
C |
2: 91,037,134 (GRCm39) |
F205L |
probably benign |
Het |
| Adam17 |
T |
C |
12: 21,397,396 (GRCm39) |
N219D |
probably benign |
Het |
| Aldh2 |
T |
C |
5: 121,707,042 (GRCm39) |
S168G |
probably damaging |
Het |
| Arhgap15 |
A |
T |
2: 44,032,353 (GRCm39) |
E312D |
probably damaging |
Het |
| Calm5 |
T |
C |
13: 3,904,401 (GRCm39) |
S32P |
probably benign |
Het |
| Capn12 |
G |
A |
7: 28,592,094 (GRCm39) |
D671N |
probably benign |
Het |
| Ccdc73 |
A |
G |
2: 104,848,127 (GRCm39) |
|
probably null |
Het |
| Cdc20 |
T |
A |
4: 118,294,261 (GRCm39) |
I20F |
probably benign |
Het |
| Cdh23 |
A |
T |
10: 60,167,129 (GRCm39) |
I1841N |
probably damaging |
Het |
| Cftr |
T |
C |
6: 18,226,087 (GRCm39) |
V345A |
probably damaging |
Het |
| Col15a1 |
T |
C |
4: 47,262,997 (GRCm39) |
S550P |
possibly damaging |
Het |
| Col4a4 |
A |
G |
1: 82,516,820 (GRCm39) |
Y133H |
unknown |
Het |
| Csmd1 |
A |
G |
8: 16,138,277 (GRCm39) |
S1592P |
probably damaging |
Het |
| Cts6 |
T |
A |
13: 61,349,626 (GRCm39) |
M56L |
probably benign |
Het |
| Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
| Dock5 |
A |
G |
14: 68,037,803 (GRCm39) |
S947P |
probably benign |
Het |
| Dpysl2 |
G |
T |
14: 67,052,498 (GRCm39) |
A339D |
possibly damaging |
Het |
| Ebf2 |
A |
G |
14: 67,647,531 (GRCm39) |
D360G |
probably damaging |
Het |
| Ensa |
T |
C |
3: 95,532,489 (GRCm39) |
|
probably null |
Het |
| Fap |
C |
A |
2: 62,374,713 (GRCm39) |
V229F |
probably damaging |
Het |
| Fbn1 |
C |
A |
2: 125,163,155 (GRCm39) |
G2116* |
probably null |
Het |
| Frmd4b |
A |
T |
6: 97,272,822 (GRCm39) |
S857T |
probably damaging |
Het |
| Fsip2 |
T |
A |
2: 82,818,044 (GRCm39) |
Y4592* |
probably null |
Het |
| Fubp1 |
T |
A |
3: 151,928,966 (GRCm39) |
Y135N |
possibly damaging |
Het |
| Gdap2 |
T |
C |
3: 100,078,234 (GRCm39) |
L66P |
probably damaging |
Het |
| Gm10257 |
T |
C |
13: 101,083,305 (GRCm39) |
|
noncoding transcript |
Het |
| Gm1758 |
A |
T |
16: 14,325,036 (GRCm39) |
|
noncoding transcript |
Het |
| Gna13 |
T |
C |
11: 109,254,455 (GRCm39) |
|
probably benign |
Het |
| H2bc13 |
T |
C |
13: 21,900,088 (GRCm39) |
S76G |
probably benign |
Het |
| Heatr1 |
T |
C |
13: 12,446,718 (GRCm39) |
I1689T |
probably benign |
Het |
| Hephl1 |
A |
G |
9: 15,009,286 (GRCm39) |
I102T |
probably benign |
Het |
| Hltf |
T |
G |
3: 20,118,114 (GRCm39) |
Y121D |
possibly damaging |
Het |
| Hspg2 |
T |
C |
4: 137,256,784 (GRCm39) |
V1509A |
possibly damaging |
Het |
| Ifitm5 |
G |
T |
7: 140,530,077 (GRCm39) |
R16S |
probably benign |
Het |
| Il1rap |
A |
C |
16: 26,513,984 (GRCm39) |
D239A |
probably benign |
Het |
| Kalrn |
C |
T |
16: 33,810,180 (GRCm39) |
D2525N |
possibly damaging |
Het |
| Kcna6 |
T |
C |
6: 126,715,519 (GRCm39) |
I457V |
probably damaging |
Het |
| Kctd17 |
T |
A |
15: 78,317,224 (GRCm39) |
L47Q |
probably damaging |
Het |
| Kdm1b |
C |
T |
13: 47,216,553 (GRCm39) |
R308W |
probably damaging |
Het |
| Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
| Lrrc63 |
A |
G |
14: 75,363,601 (GRCm39) |
S177P |
possibly damaging |
Het |
| Lrriq1 |
T |
C |
10: 103,006,327 (GRCm39) |
D1266G |
probably benign |
Het |
| Map3k2 |
G |
T |
18: 32,361,203 (GRCm39) |
M554I |
probably damaging |
Het |
| Mst1r |
T |
A |
9: 107,797,124 (GRCm39) |
V1331E |
probably damaging |
Het |
| Musk |
T |
C |
4: 58,373,400 (GRCm39) |
I775T |
probably damaging |
Het |
| Mybl2 |
A |
G |
2: 162,916,683 (GRCm39) |
K7E |
probably damaging |
Het |
| Nf1 |
T |
C |
11: 79,338,398 (GRCm39) |
S1137P |
probably damaging |
Het |
| Nlrp5 |
A |
G |
7: 23,117,055 (GRCm39) |
I260V |
probably damaging |
Het |
| Or13c7 |
A |
T |
4: 43,854,323 (GRCm39) |
N5Y |
probably benign |
Het |
| Or9g4 |
A |
C |
2: 85,504,842 (GRCm39) |
Y218D |
probably damaging |
Het |
| Or9s23 |
G |
T |
1: 92,501,207 (GRCm39) |
A105S |
possibly damaging |
Het |
| Pabpc1l |
C |
T |
2: 163,869,542 (GRCm39) |
A114V |
possibly damaging |
Het |
| Plac8l1 |
T |
A |
18: 42,311,973 (GRCm39) |
I149F |
possibly damaging |
Het |
| Pou6f1 |
T |
A |
15: 100,476,293 (GRCm39) |
N531I |
probably damaging |
Het |
| Prdm10 |
A |
G |
9: 31,264,701 (GRCm39) |
Y712C |
probably damaging |
Het |
| Ptbp3 |
T |
C |
4: 59,514,297 (GRCm39) |
T43A |
possibly damaging |
Het |
| Ptpn13 |
T |
C |
5: 103,730,644 (GRCm39) |
|
probably null |
Het |
| Rnf135 |
T |
C |
11: 80,087,775 (GRCm39) |
|
probably null |
Het |
| Rusf1 |
A |
T |
7: 127,887,374 (GRCm39) |
|
probably benign |
Het |
| Serpinb3d |
A |
G |
1: 107,005,951 (GRCm39) |
L379P |
probably damaging |
Het |
| Sh2d6 |
T |
A |
6: 72,494,581 (GRCm39) |
T124S |
probably benign |
Het |
| Slc26a5 |
G |
A |
5: 22,042,992 (GRCm39) |
P153S |
probably damaging |
Het |
| Slc5a7 |
A |
G |
17: 54,588,822 (GRCm39) |
F275S |
possibly damaging |
Het |
| Snx14 |
A |
G |
9: 88,276,495 (GRCm39) |
S606P |
probably damaging |
Het |
| Sphkap |
A |
T |
1: 83,255,805 (GRCm39) |
I648K |
possibly damaging |
Het |
| Spon2 |
T |
C |
5: 33,371,904 (GRCm39) |
T301A |
probably damaging |
Het |
| Srpra |
C |
T |
9: 35,124,447 (GRCm39) |
T48I |
probably benign |
Het |
| Taar9 |
G |
A |
10: 23,985,408 (GRCm39) |
P9S |
probably benign |
Het |
| Tacc1 |
A |
T |
8: 25,672,405 (GRCm39) |
S274R |
possibly damaging |
Het |
| Tc2n |
A |
G |
12: 101,617,376 (GRCm39) |
S348P |
possibly damaging |
Het |
| Timd2 |
G |
T |
11: 46,578,008 (GRCm39) |
T41K |
probably damaging |
Het |
| Tmem132a |
T |
A |
19: 10,842,857 (GRCm39) |
E206V |
probably damaging |
Het |
| Tmt1a3 |
A |
G |
15: 100,232,889 (GRCm39) |
M27V |
probably benign |
Het |
| Tpi1 |
A |
T |
6: 124,789,544 (GRCm39) |
|
probably benign |
Het |
| Traf5 |
T |
G |
1: 191,729,765 (GRCm39) |
T429P |
probably benign |
Het |
| Trav4-3 |
A |
G |
14: 53,836,615 (GRCm39) |
S27G |
possibly damaging |
Het |
| Tubd1 |
T |
C |
11: 86,457,895 (GRCm39) |
M462T |
probably benign |
Het |
| Ube4a |
T |
C |
9: 44,860,120 (GRCm39) |
D314G |
probably damaging |
Het |
| Utp25 |
T |
A |
1: 192,796,116 (GRCm39) |
Q50L |
probably null |
Het |
| Vmn2r58 |
G |
T |
7: 41,514,495 (GRCm39) |
T158K |
probably damaging |
Het |
| Vmn2r68 |
C |
A |
7: 84,883,648 (GRCm39) |
M152I |
probably benign |
Het |
| Vmn2r91 |
A |
G |
17: 18,325,658 (GRCm39) |
E92G |
probably damaging |
Het |
| Wdr20rt |
T |
C |
12: 65,273,395 (GRCm39) |
V113A |
probably damaging |
Het |
| Zfp729a |
T |
C |
13: 67,768,546 (GRCm39) |
H561R |
probably damaging |
Het |
| Zfp804a |
T |
A |
2: 82,066,186 (GRCm39) |
D52E |
probably damaging |
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 |
|
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 |
|
|
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'- AAGAGCAATACTTCTCTCCGAG -3'
(R):5'- AACTTTCTATTGGGGAGGTAGC -3'
Sequencing Primer
(F):5'- CACCTTCTATTTCTGTAAATCTAGGC -3'
(R):5'- ACTTTCTATTGGGGAGGTAGCATTTC -3'
|
| Posted On |
2016-02-04 |
Incidental Mutation