Incidental Mutation 'R7102:Abcb1a'
ID |
550898 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Abcb1a
|
Ensembl Gene |
ENSMUSG00000040584 |
Gene Name |
ATP-binding cassette, sub-family B member 1A |
Synonyms |
Evi32, multiple drug resistant 1a, Pgp, MDR3, Pgy-3, Mdr1a, P-glycoprotein, P-gp, Pgy3, mdr-3 |
MMRRC Submission |
045194-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.172)
|
Stock # |
R7102 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
5 |
Chromosomal Location |
8710077-8798575 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to G
at 8744072 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Alanine
at position 233
(S233A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000041204
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047753]
|
AlphaFold |
P21447 |
PDB Structure |
Structure of P-glycoprotein Reveals a Molecular Basis for Poly-Specific Drug Binding [X-RAY DIFFRACTION]
Structure of P-glycoprotein Reveals a Molecular Basis for Poly-Specific Drug Binding [X-RAY DIFFRACTION]
Structure of P-glycoprotein Reveals a Molecular Basis for Poly-Specific Drug Binding [X-RAY DIFFRACTION]
Structures of P-glycoprotein reveal its conformational flexibility and an epitope on the nucleotide-binding domain [X-RAY DIFFRACTION]
Structures of P-glycoprotein reveal its conformational flexibility and an epitope on the nucleotide-binding domain [X-RAY DIFFRACTION]
Structures of P-glycoprotein reveal its conformational flexibility and an epitope on the nucleotide-binding domain [X-RAY DIFFRACTION]
Structure of Mouse P-Glycoprotein [X-RAY DIFFRACTION]
Corrected Structure of Mouse P-glycoprotein [X-RAY DIFFRACTION]
Corrected Structure of Mouse P-glycoprotein bound to QZ59-RRR [X-RAY DIFFRACTION]
Corrected Structure of Mouse P-glycoprotein bound to QZ59-SSS [X-RAY DIFFRACTION]
>> 5 additional structures at PDB <<
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000047753
AA Change: S233A
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
SMART Domains |
Protein: ENSMUSP00000041204 Gene: ENSMUSG00000040584 AA Change: S233A
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
30 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
50 |
339 |
8.3e-97 |
PFAM |
AAA
|
415 |
607 |
1.22e-20 |
SMART |
Pfam:ABC_membrane
|
707 |
982 |
4.8e-79 |
PFAM |
AAA
|
1058 |
1246 |
8.85e-18 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.0%
|
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 MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This gene encodes a p-glycoprotein which actively transports a variety of hydrophobic amphipathic drugs and plays a major role in the blood-brain barrier permeability of certain drugs. [provided by RefSeq, Jul 2008] PHENOTYPE: Mutations in this gene result in increased sensitivity to various drugs, including avermectins and vinblastine. Mice with a null allele develop spontanous colitis. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,285,215 (GRCm39) |
H3283L |
probably damaging |
Het |
Actr10 |
T |
C |
12: 70,999,805 (GRCm39) |
|
probably null |
Het |
Acvr2b |
C |
T |
9: 119,261,619 (GRCm39) |
A380V |
probably damaging |
Het |
Adcy5 |
A |
G |
16: 35,119,995 (GRCm39) |
E1168G |
probably damaging |
Het |
Akap12 |
C |
T |
10: 4,303,226 (GRCm39) |
T117I |
probably damaging |
Het |
Alox5 |
T |
A |
6: 116,390,429 (GRCm39) |
Y516F |
probably benign |
Het |
Amigo2 |
T |
C |
15: 97,143,741 (GRCm39) |
N227S |
probably damaging |
Het |
Anpep |
C |
A |
7: 79,486,061 (GRCm39) |
V554L |
probably benign |
Het |
Ap5b1 |
T |
A |
19: 5,620,215 (GRCm39) |
V545E |
possibly damaging |
Het |
Bbs9 |
C |
T |
9: 22,490,849 (GRCm39) |
L326F |
probably damaging |
Het |
Bltp1 |
T |
G |
3: 36,994,947 (GRCm39) |
Y990D |
probably damaging |
Het |
Cadps |
C |
T |
14: 12,603,738 (GRCm38) |
G361R |
probably damaging |
Het |
Ccdc57 |
C |
A |
11: 120,812,557 (GRCm39) |
E66* |
probably null |
Het |
Ccr6 |
G |
A |
17: 8,475,019 (GRCm39) |
V75I |
probably benign |
Het |
Cdk6 |
T |
C |
5: 3,570,709 (GRCm39) |
F300S |
probably damaging |
Het |
Cenpb |
A |
C |
2: 131,020,799 (GRCm39) |
V333G |
probably damaging |
Het |
Clca4a |
T |
C |
3: 144,667,670 (GRCm39) |
I434V |
probably benign |
Het |
Coro2b |
T |
A |
9: 62,328,667 (GRCm39) |
D447V |
possibly damaging |
Het |
Cpeb3 |
T |
C |
19: 37,152,119 (GRCm39) |
S86G |
probably benign |
Het |
Cry2 |
C |
A |
2: 92,243,438 (GRCm39) |
A468S |
probably damaging |
Het |
Csf2rb2 |
T |
C |
15: 78,181,272 (GRCm39) |
Y40C |
probably damaging |
Het |
Ddx49 |
T |
A |
8: 70,753,726 (GRCm39) |
T48S |
probably damaging |
Het |
Dennd10 |
T |
A |
19: 60,821,034 (GRCm39) |
M272K |
probably damaging |
Het |
Dip2c |
A |
G |
13: 9,654,572 (GRCm39) |
T727A |
probably benign |
Het |
Dnai3 |
A |
T |
3: 145,761,459 (GRCm39) |
S632R |
possibly damaging |
Het |
Ebf4 |
A |
T |
2: 130,151,651 (GRCm39) |
I183F |
probably benign |
Het |
Elavl3 |
G |
T |
9: 21,930,025 (GRCm39) |
P293Q |
possibly damaging |
Het |
Esyt1 |
A |
T |
10: 128,352,105 (GRCm39) |
L768Q |
probably damaging |
Het |
Fat2 |
G |
A |
11: 55,174,260 (GRCm39) |
P2151L |
probably damaging |
Het |
Fgfbp3 |
G |
T |
19: 36,896,606 (GRCm39) |
A4E |
possibly damaging |
Het |
Flg |
T |
A |
3: 93,200,335 (GRCm39) |
V277D |
unknown |
Het |
Fndc3b |
T |
C |
3: 27,524,383 (GRCm39) |
D459G |
possibly damaging |
Het |
Fras1 |
A |
G |
5: 96,718,900 (GRCm39) |
Q438R |
probably benign |
Het |
Glipr1l2 |
A |
T |
10: 111,928,330 (GRCm39) |
|
probably null |
Het |
Gm7347 |
T |
A |
5: 26,262,382 (GRCm39) |
|
probably null |
Het |
Grm6 |
G |
A |
11: 50,753,804 (GRCm39) |
V703I |
possibly damaging |
Het |
Gtf2h1 |
T |
A |
7: 46,468,550 (GRCm39) |
V496E |
probably benign |
Het |
Ifna12 |
A |
G |
4: 88,521,388 (GRCm39) |
L53P |
probably damaging |
Het |
Invs |
T |
A |
4: 48,407,674 (GRCm39) |
S550T |
probably benign |
Het |
Irak2 |
G |
T |
6: 113,663,810 (GRCm39) |
C453F |
probably damaging |
Het |
Itih2 |
G |
T |
2: 10,110,574 (GRCm39) |
Q506K |
probably benign |
Het |
Kidins220 |
T |
C |
12: 25,107,662 (GRCm39) |
I1614T |
probably benign |
Het |
Krtap5-3 |
T |
A |
7: 141,755,992 (GRCm39) |
C276* |
probably null |
Het |
Lama3 |
T |
A |
18: 12,685,870 (GRCm39) |
M1128K |
possibly damaging |
Het |
Lhfpl4 |
C |
T |
6: 113,171,106 (GRCm39) |
A27T |
possibly damaging |
Het |
Lyplal1 |
A |
G |
1: 185,832,524 (GRCm39) |
V77A |
probably damaging |
Het |
Malrd1 |
A |
T |
2: 16,147,114 (GRCm39) |
E1985D |
unknown |
Het |
Mlx |
A |
C |
11: 100,979,802 (GRCm39) |
Q161P |
probably benign |
Het |
Mroh2b |
T |
A |
15: 4,977,485 (GRCm39) |
M1279K |
probably benign |
Het |
Myh7b |
A |
G |
2: 155,464,119 (GRCm39) |
E540G |
probably damaging |
Het |
Neb |
T |
A |
2: 52,194,067 (GRCm39) |
D653V |
probably damaging |
Het |
Nek10 |
T |
A |
14: 14,828,517 (GRCm38) |
L113Q |
probably damaging |
Het |
Nlrp4c |
T |
A |
7: 6,068,708 (GRCm39) |
L203* |
probably null |
Het |
Nscme3l |
T |
A |
19: 5,553,623 (GRCm39) |
T53S |
probably benign |
Het |
Ntpcr |
T |
A |
8: 126,456,794 (GRCm39) |
C5S |
unknown |
Het |
Nwd1 |
A |
G |
8: 73,421,957 (GRCm39) |
D1001G |
probably damaging |
Het |
Or12j5 |
T |
A |
7: 140,084,229 (GRCm39) |
T48S |
probably benign |
Het |
Or14a256 |
C |
T |
7: 86,265,475 (GRCm39) |
C126Y |
probably benign |
Het |
Or4p22 |
T |
A |
2: 88,317,492 (GRCm39) |
C139S |
probably damaging |
Het |
Or6c208 |
A |
C |
10: 129,224,036 (GRCm39) |
D178A |
probably damaging |
Het |
Osbpl3 |
T |
A |
6: 50,297,115 (GRCm39) |
S564C |
probably damaging |
Het |
Pax6 |
C |
A |
2: 105,522,604 (GRCm39) |
P264T |
probably damaging |
Het |
Plppr4 |
T |
C |
3: 117,116,832 (GRCm39) |
R342G |
probably damaging |
Het |
Prg4 |
C |
T |
1: 150,328,005 (GRCm39) |
C220Y |
probably damaging |
Het |
Prune2 |
T |
A |
19: 17,098,577 (GRCm39) |
D1360E |
probably benign |
Het |
Ranbp2 |
T |
A |
10: 58,299,772 (GRCm39) |
S469T |
probably damaging |
Het |
Rbfox1 |
A |
T |
16: 7,187,698 (GRCm39) |
K43N |
probably benign |
Het |
Rgs22 |
T |
C |
15: 36,122,459 (GRCm39) |
D25G |
probably damaging |
Het |
Rnf113a2 |
G |
A |
12: 84,464,545 (GRCm39) |
G146S |
probably damaging |
Het |
Sbpl |
T |
A |
17: 24,173,608 (GRCm39) |
K55* |
probably null |
Het |
Scel |
G |
A |
14: 103,781,268 (GRCm39) |
W138* |
probably null |
Het |
Scgb2b19 |
T |
C |
7: 32,979,711 (GRCm39) |
I12V |
probably null |
Het |
Scn9a |
T |
A |
2: 66,379,359 (GRCm39) |
M358L |
probably damaging |
Het |
Sdk2 |
C |
A |
11: 113,733,516 (GRCm39) |
E924* |
probably null |
Het |
Sipa1l3 |
T |
C |
7: 29,048,012 (GRCm39) |
Q1292R |
possibly damaging |
Het |
Skint4 |
G |
A |
4: 111,975,298 (GRCm39) |
G86D |
probably damaging |
Het |
Slc28a3 |
C |
T |
13: 58,736,028 (GRCm39) |
V57I |
probably benign |
Het |
Slc9a4 |
T |
C |
1: 40,662,559 (GRCm39) |
S609P |
probably damaging |
Het |
Slc9a4 |
C |
T |
1: 40,619,799 (GRCm39) |
P42S |
probably benign |
Het |
Slitrk1 |
T |
A |
14: 109,150,061 (GRCm39) |
T217S |
probably benign |
Het |
Spindoc |
C |
T |
19: 7,335,807 (GRCm39) |
R327H |
probably benign |
Het |
Stk36 |
T |
C |
1: 74,661,382 (GRCm39) |
S470P |
probably benign |
Het |
Sypl1 |
C |
T |
12: 33,024,254 (GRCm39) |
P196L |
probably benign |
Het |
Tekt4 |
T |
A |
17: 25,693,718 (GRCm39) |
I285N |
probably damaging |
Het |
Tgm5 |
T |
A |
2: 120,876,979 (GRCm39) |
I686F |
possibly damaging |
Het |
Thsd4 |
C |
A |
9: 59,883,587 (GRCm39) |
R933L |
probably damaging |
Het |
Treml1 |
T |
A |
17: 48,673,700 (GRCm39) |
I237N |
probably damaging |
Het |
Txndc16 |
T |
C |
14: 45,442,839 (GRCm39) |
I119V |
probably benign |
Het |
Ubr3 |
C |
A |
2: 69,728,166 (GRCm39) |
N176K |
probably damaging |
Het |
Vit |
A |
G |
17: 78,932,426 (GRCm39) |
Y511C |
probably damaging |
Het |
Vwa5b2 |
G |
A |
16: 20,422,984 (GRCm39) |
G994D |
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,925,268 (GRCm39) |
T1648A |
unknown |
Het |
Ythdf1 |
G |
A |
2: 180,553,315 (GRCm39) |
T300I |
probably damaging |
Het |
Zan |
A |
G |
5: 137,452,462 (GRCm39) |
|
probably null |
Het |
Zbbx |
A |
G |
3: 75,019,401 (GRCm39) |
L103P |
probably benign |
Het |
Zfp105 |
A |
G |
9: 122,758,869 (GRCm39) |
D180G |
probably damaging |
Het |
Zfp114 |
T |
A |
7: 23,880,083 (GRCm39) |
L144Q |
possibly damaging |
Het |
Zfp128 |
T |
C |
7: 12,624,399 (GRCm39) |
C256R |
probably damaging |
Het |
|
Other mutations in Abcb1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00704:Abcb1a
|
APN |
5 |
8,736,257 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00898:Abcb1a
|
APN |
5 |
8,783,690 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01064:Abcb1a
|
APN |
5 |
8,782,388 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01118:Abcb1a
|
APN |
5 |
8,724,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01150:Abcb1a
|
APN |
5 |
8,752,550 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01584:Abcb1a
|
APN |
5 |
8,748,637 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01654:Abcb1a
|
APN |
5 |
8,765,065 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01820:Abcb1a
|
APN |
5 |
8,765,896 (GRCm39) |
splice site |
probably benign |
|
IGL02499:Abcb1a
|
APN |
5 |
8,776,807 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02711:Abcb1a
|
APN |
5 |
8,773,245 (GRCm39) |
splice site |
probably null |
|
IGL02954:Abcb1a
|
APN |
5 |
8,782,341 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03018:Abcb1a
|
APN |
5 |
8,752,451 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03119:Abcb1a
|
APN |
5 |
8,764,887 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03292:Abcb1a
|
APN |
5 |
8,765,827 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03338:Abcb1a
|
APN |
5 |
8,744,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R0418:Abcb1a
|
UTSW |
5 |
8,763,281 (GRCm39) |
missense |
probably damaging |
0.96 |
R0559:Abcb1a
|
UTSW |
5 |
8,748,535 (GRCm39) |
missense |
probably benign |
0.01 |
R0595:Abcb1a
|
UTSW |
5 |
8,790,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0599:Abcb1a
|
UTSW |
5 |
8,748,539 (GRCm39) |
missense |
probably benign |
0.13 |
R0811:Abcb1a
|
UTSW |
5 |
8,763,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R0812:Abcb1a
|
UTSW |
5 |
8,763,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R0894:Abcb1a
|
UTSW |
5 |
8,724,856 (GRCm39) |
splice site |
probably benign |
|
R0948:Abcb1a
|
UTSW |
5 |
8,790,621 (GRCm39) |
splice site |
probably null |
|
R1292:Abcb1a
|
UTSW |
5 |
8,763,343 (GRCm39) |
missense |
probably benign |
0.00 |
R1318:Abcb1a
|
UTSW |
5 |
8,751,621 (GRCm39) |
missense |
probably benign |
0.31 |
R1459:Abcb1a
|
UTSW |
5 |
8,752,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R1489:Abcb1a
|
UTSW |
5 |
8,736,300 (GRCm39) |
critical splice donor site |
probably null |
|
R1514:Abcb1a
|
UTSW |
5 |
8,724,791 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2100:Abcb1a
|
UTSW |
5 |
8,763,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R2409:Abcb1a
|
UTSW |
5 |
8,788,747 (GRCm39) |
missense |
probably benign |
0.30 |
R2844:Abcb1a
|
UTSW |
5 |
8,736,164 (GRCm39) |
missense |
probably benign |
0.02 |
R3709:Abcb1a
|
UTSW |
5 |
8,788,738 (GRCm39) |
missense |
probably benign |
0.03 |
R3755:Abcb1a
|
UTSW |
5 |
8,797,403 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4193:Abcb1a
|
UTSW |
5 |
8,765,068 (GRCm39) |
splice site |
probably null |
|
R4401:Abcb1a
|
UTSW |
5 |
8,752,390 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4463:Abcb1a
|
UTSW |
5 |
8,769,981 (GRCm39) |
splice site |
probably benign |
|
R4539:Abcb1a
|
UTSW |
5 |
8,765,793 (GRCm39) |
missense |
probably benign |
|
R4635:Abcb1a
|
UTSW |
5 |
8,764,927 (GRCm39) |
missense |
probably benign |
|
R4740:Abcb1a
|
UTSW |
5 |
8,752,280 (GRCm39) |
critical splice donor site |
probably null |
|
R4757:Abcb1a
|
UTSW |
5 |
8,787,632 (GRCm39) |
missense |
probably damaging |
0.99 |
R4764:Abcb1a
|
UTSW |
5 |
8,765,732 (GRCm39) |
splice site |
probably null |
|
R4792:Abcb1a
|
UTSW |
5 |
8,796,657 (GRCm39) |
critical splice donor site |
probably null |
|
R4829:Abcb1a
|
UTSW |
5 |
8,773,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R4935:Abcb1a
|
UTSW |
5 |
8,787,773 (GRCm39) |
critical splice donor site |
probably null |
|
R5140:Abcb1a
|
UTSW |
5 |
8,752,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R5181:Abcb1a
|
UTSW |
5 |
8,764,937 (GRCm39) |
missense |
probably benign |
|
R5355:Abcb1a
|
UTSW |
5 |
8,776,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R5406:Abcb1a
|
UTSW |
5 |
8,752,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R5496:Abcb1a
|
UTSW |
5 |
8,724,818 (GRCm39) |
missense |
probably benign |
|
R5557:Abcb1a
|
UTSW |
5 |
8,764,949 (GRCm39) |
missense |
probably benign |
0.01 |
R5572:Abcb1a
|
UTSW |
5 |
8,765,108 (GRCm39) |
splice site |
probably null |
|
R5702:Abcb1a
|
UTSW |
5 |
8,787,752 (GRCm39) |
missense |
probably benign |
0.15 |
R5753:Abcb1a
|
UTSW |
5 |
8,773,160 (GRCm39) |
missense |
probably damaging |
0.98 |
R5769:Abcb1a
|
UTSW |
5 |
8,733,426 (GRCm39) |
missense |
probably benign |
0.01 |
R5895:Abcb1a
|
UTSW |
5 |
8,752,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R6536:Abcb1a
|
UTSW |
5 |
8,769,030 (GRCm39) |
missense |
probably benign |
0.01 |
R6555:Abcb1a
|
UTSW |
5 |
8,752,468 (GRCm39) |
missense |
probably damaging |
0.97 |
R6798:Abcb1a
|
UTSW |
5 |
8,782,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R6875:Abcb1a
|
UTSW |
5 |
8,751,628 (GRCm39) |
missense |
probably benign |
0.28 |
R7000:Abcb1a
|
UTSW |
5 |
8,752,823 (GRCm39) |
missense |
probably benign |
0.19 |
R7172:Abcb1a
|
UTSW |
5 |
8,752,399 (GRCm39) |
missense |
probably benign |
0.00 |
R7313:Abcb1a
|
UTSW |
5 |
8,773,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Abcb1a
|
UTSW |
5 |
8,765,771 (GRCm39) |
nonsense |
probably null |
|
R7718:Abcb1a
|
UTSW |
5 |
8,765,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R7816:Abcb1a
|
UTSW |
5 |
8,736,132 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7829:Abcb1a
|
UTSW |
5 |
8,748,623 (GRCm39) |
missense |
probably benign |
0.06 |
R7943:Abcb1a
|
UTSW |
5 |
8,736,222 (GRCm39) |
missense |
probably benign |
|
R8040:Abcb1a
|
UTSW |
5 |
8,765,035 (GRCm39) |
missense |
probably benign |
0.00 |
R8086:Abcb1a
|
UTSW |
5 |
8,724,833 (GRCm39) |
missense |
probably benign |
|
R8271:Abcb1a
|
UTSW |
5 |
8,736,212 (GRCm39) |
missense |
probably benign |
0.41 |
R8367:Abcb1a
|
UTSW |
5 |
8,736,221 (GRCm39) |
missense |
probably benign |
0.00 |
R8520:Abcb1a
|
UTSW |
5 |
8,735,346 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8680:Abcb1a
|
UTSW |
5 |
8,735,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R8820:Abcb1a
|
UTSW |
5 |
8,773,204 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8996:Abcb1a
|
UTSW |
5 |
8,769,069 (GRCm39) |
missense |
probably benign |
0.00 |
R9114:Abcb1a
|
UTSW |
5 |
8,788,702 (GRCm39) |
nonsense |
probably null |
|
R9127:Abcb1a
|
UTSW |
5 |
8,724,707 (GRCm39) |
missense |
probably benign |
|
R9187:Abcb1a
|
UTSW |
5 |
8,765,016 (GRCm39) |
missense |
probably benign |
|
R9294:Abcb1a
|
UTSW |
5 |
8,736,171 (GRCm39) |
missense |
probably benign |
0.02 |
R9459:Abcb1a
|
UTSW |
5 |
8,735,414 (GRCm39) |
critical splice donor site |
probably null |
|
R9581:Abcb1a
|
UTSW |
5 |
8,790,428 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9617:Abcb1a
|
UTSW |
5 |
8,797,353 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9676:Abcb1a
|
UTSW |
5 |
8,714,548 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9682:Abcb1a
|
UTSW |
5 |
8,752,507 (GRCm39) |
missense |
probably benign |
0.44 |
R9790:Abcb1a
|
UTSW |
5 |
8,748,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R9791:Abcb1a
|
UTSW |
5 |
8,748,604 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Abcb1a
|
UTSW |
5 |
8,796,544 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- CAACTTGGAGACATCTTACATAGTG -3'
(R):5'- CCATCCTAAATGTCATGTGGGCTG -3'
Sequencing Primer
(F):5'- CATCTTACATAGTGatatatatatat -3'
(R):5'- CCTAAATGTCATGTGGGCTGATAAAC -3'
|
Posted On |
2019-05-15 |