Incidental Mutation 'R1901:Abca15'
ID |
212213 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Abca15
|
Ensembl Gene |
ENSMUSG00000054746 |
Gene Name |
ATP-binding cassette, sub-family A member 15 |
Synonyms |
4930500I12Rik |
MMRRC Submission |
039921-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.059)
|
Stock # |
R1901 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
119927893-120006910 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 119945322 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Glycine
at position 466
(E466G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000112821
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000076272]
[ENSMUST00000121265]
|
AlphaFold |
E9PWH4 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000076272
AA Change: E466G
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000075621 Gene: ENSMUSG00000054746 AA Change: E466G
Domain | Start | End | E-Value | Type |
Pfam:ABC2_membrane_3
|
24 |
464 |
5.7e-21 |
PFAM |
AAA
|
550 |
732 |
9.14e-11 |
SMART |
Pfam:ABC2_membrane_3
|
892 |
1293 |
7.9e-24 |
PFAM |
AAA
|
1381 |
1565 |
1.16e-3 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000121265
AA Change: E466G
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000112821 Gene: ENSMUSG00000054746 AA Change: E466G
Domain | Start | End | E-Value | Type |
Pfam:ABC2_membrane_3
|
24 |
464 |
2.1e-21 |
PFAM |
AAA
|
550 |
732 |
9.14e-11 |
SMART |
Pfam:ABC2_membrane_3
|
907 |
1293 |
1e-25 |
PFAM |
AAA
|
1381 |
1565 |
1.16e-3 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000140459
|
Coding Region Coverage |
- 1x: 97.3%
- 3x: 96.8%
- 10x: 95.2%
- 20x: 92.5%
|
Validation Efficiency |
|
Allele List at MGI |
All alleles(2) : Targeted(2)
|
Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
A |
T |
5: 114,303,795 (GRCm39) |
R73* |
probably null |
Het |
Acta1 |
A |
T |
8: 124,619,900 (GRCm39) |
S147T |
probably benign |
Het |
Adh1 |
G |
A |
3: 137,994,558 (GRCm39) |
V293I |
probably benign |
Het |
Aldh3b3 |
T |
C |
19: 4,015,130 (GRCm39) |
Y170H |
probably damaging |
Het |
Ank3 |
A |
T |
10: 69,658,167 (GRCm39) |
T198S |
probably damaging |
Het |
Ankrd12 |
A |
T |
17: 66,293,698 (GRCm39) |
N578K |
possibly damaging |
Het |
Ano2 |
A |
T |
6: 125,849,647 (GRCm39) |
E126D |
probably damaging |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Arhgef7 |
C |
A |
8: 11,858,713 (GRCm39) |
|
probably null |
Het |
Cfap44 |
A |
C |
16: 44,242,737 (GRCm39) |
T714P |
probably benign |
Het |
Cnot1 |
T |
C |
8: 96,469,749 (GRCm39) |
I1369V |
possibly damaging |
Het |
Col19a1 |
A |
T |
1: 24,576,078 (GRCm39) |
I88K |
unknown |
Het |
Col1a1 |
G |
A |
11: 94,837,458 (GRCm39) |
|
probably null |
Het |
Col5a1 |
A |
G |
2: 27,850,456 (GRCm39) |
T518A |
unknown |
Het |
Cul7 |
T |
C |
17: 46,966,666 (GRCm39) |
L365P |
probably damaging |
Het |
Dlec1 |
T |
C |
9: 118,931,712 (GRCm39) |
S44P |
probably damaging |
Het |
Dock9 |
T |
C |
14: 121,862,565 (GRCm39) |
|
probably null |
Het |
Fbxl9 |
T |
C |
8: 106,039,707 (GRCm39) |
N556S |
probably damaging |
Het |
Flrt2 |
C |
A |
12: 95,745,904 (GRCm39) |
P81T |
probably damaging |
Het |
Flrt2 |
C |
T |
12: 95,745,905 (GRCm39) |
P81L |
probably damaging |
Het |
Ginm1 |
A |
G |
10: 7,650,980 (GRCm39) |
|
probably null |
Het |
Glis3 |
T |
C |
19: 28,508,985 (GRCm39) |
N333S |
probably damaging |
Het |
Glo1 |
T |
G |
17: 30,815,382 (GRCm39) |
E144D |
probably benign |
Het |
Golga1 |
A |
T |
2: 38,937,792 (GRCm39) |
|
probably null |
Het |
H2-Aa |
A |
G |
17: 34,502,207 (GRCm39) |
I155T |
possibly damaging |
Het |
Haus5 |
A |
G |
7: 30,356,670 (GRCm39) |
S479P |
probably damaging |
Het |
Il10ra |
A |
T |
9: 45,167,654 (GRCm39) |
V299D |
probably benign |
Het |
Il17re |
T |
C |
6: 113,446,665 (GRCm39) |
V472A |
probably damaging |
Het |
Il22ra1 |
A |
T |
4: 135,478,219 (GRCm39) |
Q430L |
probably damaging |
Het |
Il23r |
A |
C |
6: 67,400,718 (GRCm39) |
D537E |
probably benign |
Het |
Inppl1 |
T |
C |
7: 101,472,584 (GRCm39) |
E1237G |
possibly damaging |
Het |
Ip6k1 |
G |
A |
9: 107,918,195 (GRCm39) |
E77K |
possibly damaging |
Het |
Klhl35 |
T |
C |
7: 99,119,427 (GRCm39) |
L304P |
probably damaging |
Het |
Krt78 |
A |
T |
15: 101,855,398 (GRCm39) |
C804* |
probably null |
Het |
Med15 |
G |
T |
16: 17,491,018 (GRCm39) |
|
probably benign |
Het |
Mettl25 |
A |
G |
10: 105,661,948 (GRCm39) |
S341P |
probably damaging |
Het |
Mroh1 |
A |
G |
15: 76,320,249 (GRCm39) |
T1008A |
probably benign |
Het |
Mug1 |
A |
G |
6: 121,858,780 (GRCm39) |
D1166G |
probably benign |
Het |
Mug2 |
C |
A |
6: 122,048,801 (GRCm39) |
H856N |
probably benign |
Het |
Naca |
T |
A |
10: 127,879,590 (GRCm39) |
|
probably benign |
Het |
Nagk |
G |
T |
6: 83,776,336 (GRCm39) |
V184F |
probably damaging |
Het |
Nav1 |
T |
G |
1: 135,400,148 (GRCm39) |
N474T |
probably benign |
Het |
Ncor2 |
T |
A |
5: 125,102,489 (GRCm39) |
H2089L |
probably benign |
Het |
Nek6 |
A |
G |
2: 38,472,458 (GRCm39) |
I261V |
probably damaging |
Het |
Neurod2 |
G |
A |
11: 98,218,558 (GRCm39) |
T202M |
probably damaging |
Het |
Nlgn2 |
A |
G |
11: 69,716,726 (GRCm39) |
V605A |
probably damaging |
Het |
Nlrp5 |
A |
C |
7: 23,123,335 (GRCm39) |
E732A |
possibly damaging |
Het |
Nt5dc1 |
A |
T |
10: 34,189,667 (GRCm39) |
V340D |
probably damaging |
Het |
Ntn4 |
A |
G |
10: 93,543,234 (GRCm39) |
D320G |
possibly damaging |
Het |
Or10al3 |
T |
A |
17: 38,012,312 (GRCm39) |
H250Q |
probably damaging |
Het |
Or10x1 |
A |
T |
1: 174,196,734 (GRCm39) |
I84L |
probably benign |
Het |
Or52l1 |
A |
G |
7: 104,830,079 (GRCm39) |
I162T |
possibly damaging |
Het |
Or52z15 |
T |
C |
7: 103,332,750 (GRCm39) |
I265T |
probably damaging |
Het |
Or5ac25 |
A |
T |
16: 59,182,526 (GRCm39) |
D18E |
probably benign |
Het |
Osbpl5 |
T |
C |
7: 143,256,918 (GRCm39) |
D404G |
possibly damaging |
Het |
Pcdhb12 |
T |
A |
18: 37,570,683 (GRCm39) |
W610R |
possibly damaging |
Het |
Pias2 |
T |
A |
18: 77,185,139 (GRCm39) |
C66* |
probably null |
Het |
Plec |
T |
A |
15: 76,059,751 (GRCm39) |
E3417D |
probably damaging |
Het |
Plekhm3 |
CCTGCTGCTGCTGCTGCTGCTGCTGC |
CCTGCTGCTGCTGCTGCTGCTGC |
1: 64,976,940 (GRCm39) |
|
probably benign |
Het |
Ppp1r12a |
T |
A |
10: 108,034,752 (GRCm39) |
I99N |
probably damaging |
Het |
Prpf8 |
T |
G |
11: 75,395,570 (GRCm39) |
V1899G |
probably damaging |
Het |
Prr13 |
C |
A |
15: 102,369,133 (GRCm39) |
|
probably benign |
Het |
Ptchd4 |
A |
T |
17: 42,814,507 (GRCm39) |
I803L |
probably benign |
Het |
R3hdm2 |
T |
C |
10: 127,334,337 (GRCm39) |
I947T |
possibly damaging |
Het |
Raet1d |
A |
G |
10: 22,247,350 (GRCm39) |
D142G |
probably damaging |
Het |
Rbbp8nl |
C |
T |
2: 179,925,106 (GRCm39) |
R33Q |
probably damaging |
Het |
Robo1 |
A |
G |
16: 72,757,092 (GRCm39) |
Q351R |
probably null |
Het |
Rptn |
A |
T |
3: 93,304,017 (GRCm39) |
H450L |
possibly damaging |
Het |
Scn11a |
T |
A |
9: 119,608,102 (GRCm39) |
K1010* |
probably null |
Het |
Slc16a10 |
G |
A |
10: 39,932,602 (GRCm39) |
Q33* |
probably null |
Het |
Slc31a1 |
C |
T |
4: 62,303,842 (GRCm39) |
|
probably benign |
Het |
Slc34a1 |
A |
T |
13: 55,548,963 (GRCm39) |
K138* |
probably null |
Het |
Slc6a18 |
T |
A |
13: 73,818,162 (GRCm39) |
E285V |
probably benign |
Het |
Slco6c1 |
T |
A |
1: 97,000,707 (GRCm39) |
T515S |
probably damaging |
Het |
Snrnp40 |
T |
A |
4: 130,279,768 (GRCm39) |
S295T |
probably damaging |
Het |
Snx4 |
A |
T |
16: 33,104,808 (GRCm39) |
Y252F |
possibly damaging |
Het |
Spata18 |
T |
A |
5: 73,828,482 (GRCm39) |
F348I |
probably damaging |
Het |
Spef2 |
G |
T |
15: 9,607,463 (GRCm39) |
R1319S |
probably damaging |
Het |
Tas2r125 |
T |
C |
6: 132,887,139 (GRCm39) |
F176L |
probably benign |
Het |
Tcp10b |
A |
G |
17: 13,300,513 (GRCm39) |
K399E |
possibly damaging |
Het |
Tcstv3 |
A |
G |
13: 120,779,260 (GRCm39) |
H53R |
probably damaging |
Het |
Tnrc6c |
A |
G |
11: 117,613,831 (GRCm39) |
K823R |
probably damaging |
Het |
Trim31 |
A |
G |
17: 37,212,692 (GRCm39) |
E221G |
probably benign |
Het |
Trim47 |
T |
A |
11: 115,998,605 (GRCm39) |
Q338L |
probably damaging |
Het |
Tubgcp6 |
C |
A |
15: 89,000,444 (GRCm39) |
R307L |
possibly damaging |
Het |
Usp9y |
A |
G |
Y: 1,303,371 (GRCm39) |
|
probably null |
Het |
Utp20 |
G |
T |
10: 88,588,888 (GRCm39) |
T2427K |
probably benign |
Het |
Vldlr |
T |
C |
19: 27,218,709 (GRCm39) |
V147A |
probably damaging |
Het |
Vmn1r115 |
C |
T |
7: 20,578,198 (GRCm39) |
R238H |
probably benign |
Het |
Vmn1r175 |
C |
A |
7: 23,508,218 (GRCm39) |
R136S |
probably benign |
Het |
Vmn1r53 |
A |
G |
6: 90,201,268 (GRCm39) |
S19P |
possibly damaging |
Het |
Vwa5b2 |
G |
T |
16: 20,423,582 (GRCm39) |
S1165I |
possibly damaging |
Het |
Zfp362 |
G |
T |
4: 128,684,069 (GRCm39) |
P13T |
probably damaging |
Het |
Zfp825 |
A |
G |
13: 74,629,064 (GRCm39) |
C151R |
probably damaging |
Het |
|
Other mutations in Abca15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Abca15
|
APN |
7 |
119,996,277 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00505:Abca15
|
APN |
7 |
119,968,459 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00851:Abca15
|
APN |
7 |
119,939,230 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00985:Abca15
|
APN |
7 |
119,996,241 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01114:Abca15
|
APN |
7 |
119,960,643 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01287:Abca15
|
APN |
7 |
119,932,081 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01333:Abca15
|
APN |
7 |
119,981,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01482:Abca15
|
APN |
7 |
119,981,969 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01610:Abca15
|
APN |
7 |
119,939,867 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02238:Abca15
|
APN |
7 |
119,995,829 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02377:Abca15
|
APN |
7 |
119,965,133 (GRCm39) |
splice site |
probably benign |
|
IGL02666:Abca15
|
APN |
7 |
119,934,431 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02836:Abca15
|
APN |
7 |
119,987,439 (GRCm39) |
missense |
probably benign |
|
IGL03337:Abca15
|
APN |
7 |
119,995,930 (GRCm39) |
missense |
probably benign |
0.24 |
IGL03354:Abca15
|
APN |
7 |
119,993,711 (GRCm39) |
nonsense |
probably null |
|
H8562:Abca15
|
UTSW |
7 |
119,974,077 (GRCm39) |
splice site |
probably benign |
|
IGL03098:Abca15
|
UTSW |
7 |
119,987,499 (GRCm39) |
splice site |
probably null |
|
R0029:Abca15
|
UTSW |
7 |
119,945,225 (GRCm39) |
missense |
probably benign |
0.01 |
R0029:Abca15
|
UTSW |
7 |
119,945,225 (GRCm39) |
missense |
probably benign |
0.01 |
R0076:Abca15
|
UTSW |
7 |
119,972,908 (GRCm39) |
splice site |
probably benign |
|
R0165:Abca15
|
UTSW |
7 |
119,950,126 (GRCm39) |
splice site |
probably benign |
|
R0311:Abca15
|
UTSW |
7 |
120,002,127 (GRCm39) |
missense |
probably damaging |
0.98 |
R0387:Abca15
|
UTSW |
7 |
119,932,075 (GRCm39) |
critical splice donor site |
probably null |
|
R0610:Abca15
|
UTSW |
7 |
119,965,009 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0612:Abca15
|
UTSW |
7 |
119,936,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R0704:Abca15
|
UTSW |
7 |
119,953,746 (GRCm39) |
missense |
probably damaging |
0.98 |
R0890:Abca15
|
UTSW |
7 |
119,972,936 (GRCm39) |
missense |
probably benign |
0.01 |
R0961:Abca15
|
UTSW |
7 |
119,960,208 (GRCm39) |
nonsense |
probably null |
|
R1144:Abca15
|
UTSW |
7 |
119,960,083 (GRCm39) |
splice site |
probably benign |
|
R1412:Abca15
|
UTSW |
7 |
119,944,546 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1419:Abca15
|
UTSW |
7 |
119,974,125 (GRCm39) |
missense |
probably benign |
0.10 |
R1467:Abca15
|
UTSW |
7 |
119,939,761 (GRCm39) |
splice site |
probably null |
|
R1467:Abca15
|
UTSW |
7 |
119,939,761 (GRCm39) |
splice site |
probably null |
|
R1469:Abca15
|
UTSW |
7 |
119,981,720 (GRCm39) |
missense |
probably benign |
0.00 |
R1469:Abca15
|
UTSW |
7 |
119,981,720 (GRCm39) |
missense |
probably benign |
0.00 |
R1493:Abca15
|
UTSW |
7 |
119,981,513 (GRCm39) |
missense |
probably benign |
0.00 |
R1513:Abca15
|
UTSW |
7 |
119,939,322 (GRCm39) |
missense |
probably damaging |
0.96 |
R1702:Abca15
|
UTSW |
7 |
119,981,925 (GRCm39) |
missense |
probably benign |
0.10 |
R1857:Abca15
|
UTSW |
7 |
119,960,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1893:Abca15
|
UTSW |
7 |
119,939,776 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1951:Abca15
|
UTSW |
7 |
119,960,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R1953:Abca15
|
UTSW |
7 |
119,960,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Abca15
|
UTSW |
7 |
119,940,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R2063:Abca15
|
UTSW |
7 |
119,960,127 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2141:Abca15
|
UTSW |
7 |
120,006,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R2145:Abca15
|
UTSW |
7 |
119,953,701 (GRCm39) |
missense |
probably benign |
0.08 |
R2182:Abca15
|
UTSW |
7 |
119,939,450 (GRCm39) |
nonsense |
probably null |
|
R2425:Abca15
|
UTSW |
7 |
119,959,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R2444:Abca15
|
UTSW |
7 |
119,965,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R3023:Abca15
|
UTSW |
7 |
119,982,002 (GRCm39) |
missense |
probably benign |
0.40 |
R3079:Abca15
|
UTSW |
7 |
119,984,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R3106:Abca15
|
UTSW |
7 |
119,995,856 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3622:Abca15
|
UTSW |
7 |
119,950,036 (GRCm39) |
nonsense |
probably null |
|
R4085:Abca15
|
UTSW |
7 |
119,981,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R4233:Abca15
|
UTSW |
7 |
120,002,202 (GRCm39) |
nonsense |
probably null |
|
R4591:Abca15
|
UTSW |
7 |
119,981,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Abca15
|
UTSW |
7 |
119,934,384 (GRCm39) |
missense |
probably benign |
0.03 |
R4721:Abca15
|
UTSW |
7 |
119,949,998 (GRCm39) |
missense |
probably benign |
0.01 |
R4838:Abca15
|
UTSW |
7 |
119,944,523 (GRCm39) |
missense |
probably benign |
0.00 |
R4940:Abca15
|
UTSW |
7 |
119,931,917 (GRCm39) |
missense |
probably benign |
|
R4963:Abca15
|
UTSW |
7 |
119,960,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R4993:Abca15
|
UTSW |
7 |
120,000,941 (GRCm39) |
missense |
probably damaging |
0.99 |
R5022:Abca15
|
UTSW |
7 |
119,945,319 (GRCm39) |
missense |
probably damaging |
0.98 |
R5030:Abca15
|
UTSW |
7 |
119,939,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Abca15
|
UTSW |
7 |
120,006,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R5090:Abca15
|
UTSW |
7 |
119,984,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R5309:Abca15
|
UTSW |
7 |
119,944,592 (GRCm39) |
missense |
probably damaging |
0.96 |
R5310:Abca15
|
UTSW |
7 |
119,931,839 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5312:Abca15
|
UTSW |
7 |
119,944,592 (GRCm39) |
missense |
probably damaging |
0.96 |
R5482:Abca15
|
UTSW |
7 |
119,968,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R5596:Abca15
|
UTSW |
7 |
120,000,972 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5853:Abca15
|
UTSW |
7 |
119,939,806 (GRCm39) |
missense |
probably benign |
0.00 |
R5950:Abca15
|
UTSW |
7 |
119,981,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R5953:Abca15
|
UTSW |
7 |
119,960,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R6072:Abca15
|
UTSW |
7 |
119,987,481 (GRCm39) |
missense |
probably damaging |
0.98 |
R6131:Abca15
|
UTSW |
7 |
119,939,428 (GRCm39) |
missense |
probably benign |
0.03 |
R6132:Abca15
|
UTSW |
7 |
119,960,643 (GRCm39) |
missense |
probably benign |
0.14 |
R6136:Abca15
|
UTSW |
7 |
119,939,272 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6207:Abca15
|
UTSW |
7 |
119,973,017 (GRCm39) |
missense |
probably benign |
0.01 |
R6315:Abca15
|
UTSW |
7 |
119,945,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R6417:Abca15
|
UTSW |
7 |
119,996,351 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6420:Abca15
|
UTSW |
7 |
119,996,351 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6595:Abca15
|
UTSW |
7 |
119,993,710 (GRCm39) |
missense |
probably benign |
0.00 |
R6653:Abca15
|
UTSW |
7 |
119,945,229 (GRCm39) |
missense |
probably benign |
0.03 |
R6859:Abca15
|
UTSW |
7 |
120,002,217 (GRCm39) |
nonsense |
probably null |
|
R6983:Abca15
|
UTSW |
7 |
119,953,686 (GRCm39) |
missense |
probably benign |
0.26 |
R7127:Abca15
|
UTSW |
7 |
119,931,825 (GRCm39) |
missense |
probably benign |
0.06 |
R7205:Abca15
|
UTSW |
7 |
119,993,587 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7336:Abca15
|
UTSW |
7 |
119,987,456 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7426:Abca15
|
UTSW |
7 |
119,945,221 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7745:Abca15
|
UTSW |
7 |
119,931,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R7751:Abca15
|
UTSW |
7 |
119,965,044 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7806:Abca15
|
UTSW |
7 |
119,932,059 (GRCm39) |
missense |
probably damaging |
0.96 |
R8042:Abca15
|
UTSW |
7 |
120,002,233 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8098:Abca15
|
UTSW |
7 |
119,960,619 (GRCm39) |
missense |
probably benign |
0.09 |
R8153:Abca15
|
UTSW |
7 |
119,999,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Abca15
|
UTSW |
7 |
119,936,445 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8259:Abca15
|
UTSW |
7 |
119,939,422 (GRCm39) |
missense |
probably benign |
0.00 |
R8272:Abca15
|
UTSW |
7 |
120,006,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R8295:Abca15
|
UTSW |
7 |
119,974,188 (GRCm39) |
missense |
probably benign |
0.00 |
R8757:Abca15
|
UTSW |
7 |
120,006,631 (GRCm39) |
missense |
probably damaging |
0.96 |
R8759:Abca15
|
UTSW |
7 |
120,006,631 (GRCm39) |
missense |
probably damaging |
0.96 |
R8905:Abca15
|
UTSW |
7 |
119,960,771 (GRCm39) |
missense |
probably benign |
0.28 |
R9145:Abca15
|
UTSW |
7 |
119,987,388 (GRCm39) |
missense |
probably benign |
0.13 |
R9217:Abca15
|
UTSW |
7 |
119,987,439 (GRCm39) |
missense |
probably benign |
|
R9264:Abca15
|
UTSW |
7 |
120,001,056 (GRCm39) |
missense |
probably benign |
0.14 |
R9517:Abca15
|
UTSW |
7 |
119,987,424 (GRCm39) |
missense |
probably benign |
0.07 |
RF018:Abca15
|
UTSW |
7 |
119,993,683 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1176:Abca15
|
UTSW |
7 |
119,981,728 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Abca15
|
UTSW |
7 |
119,945,249 (GRCm39) |
missense |
probably benign |
0.22 |
|
Predicted Primers |
PCR Primer
(F):5'- CTCTAGAAAGGACCAACAAGTGATTC -3'
(R):5'- AAGAATGGTTCTCTTGTCTGCTTC -3'
Sequencing Primer
(F):5'- ACAGTTGTAGAACTATCTTAGTCCCC -3'
(R):5'- GTCTGCTTCACTACCTCAGTAATAG -3'
|
Posted On |
2014-06-30 |