Incidental Mutation 'R9711:Abcc12'
ID |
730170 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Abcc12
|
Ensembl Gene |
ENSMUSG00000036872 |
Gene Name |
ATP-binding cassette, sub-family C member 12 |
Synonyms |
MRP9, 4930467B22Rik |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.058)
|
Stock # |
R9711 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
8 |
Chromosomal Location |
87231197-87307317 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 87275388 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 430
(D430G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000079014
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000080115]
[ENSMUST00000129898]
[ENSMUST00000131423]
[ENSMUST00000131806]
[ENSMUST00000152438]
[ENSMUST00000156610]
|
AlphaFold |
Q80WJ6 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000080115
AA Change: D430G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000079014 Gene: ENSMUSG00000036872 AA Change: D430G
Domain | Start | End | E-Value | Type |
Pfam:ABC_membrane
|
123 |
392 |
3.6e-19 |
PFAM |
AAA
|
506 |
679 |
3.33e-13 |
SMART |
low complexity region
|
739 |
752 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
791 |
1079 |
1.3e-26 |
PFAM |
AAA
|
1153 |
1346 |
1.07e-11 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000129898
AA Change: D430G
PolyPhen 2
Score 0.074 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000122577 Gene: ENSMUSG00000036872 AA Change: D430G
Domain | Start | End | E-Value | Type |
Pfam:ABC_membrane
|
123 |
392 |
1.2e-19 |
PFAM |
AAA
|
506 |
679 |
3.33e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000131423
AA Change: D430G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000122402 Gene: ENSMUSG00000036872 AA Change: D430G
Domain | Start | End | E-Value | Type |
Pfam:ABC_membrane
|
123 |
392 |
1.1e-21 |
PFAM |
AAA
|
506 |
679 |
3.33e-13 |
SMART |
low complexity region
|
739 |
752 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
792 |
1077 |
1.6e-34 |
PFAM |
AAA
|
1153 |
1346 |
1.07e-11 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000131806
AA Change: D430G
PolyPhen 2
Score 0.115 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000116866 Gene: ENSMUSG00000036872 AA Change: D430G
Domain | Start | End | E-Value | Type |
Pfam:ABC_membrane
|
123 |
392 |
1.3e-19 |
PFAM |
AAA
|
506 |
679 |
3.33e-13 |
SMART |
low complexity region
|
739 |
752 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000152438
AA Change: D430G
PolyPhen 2
Score 0.074 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000114582 Gene: ENSMUSG00000036872 AA Change: D430G
Domain | Start | End | E-Value | Type |
Pfam:ABC_membrane
|
123 |
392 |
1.2e-19 |
PFAM |
AAA
|
506 |
679 |
3.33e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000156610
AA Change: D430G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000123578 Gene: ENSMUSG00000036872 AA Change: D430G
Domain | Start | End | E-Value | Type |
Pfam:ABC_membrane
|
123 |
392 |
5.9e-20 |
PFAM |
AAA
|
506 |
661 |
1.07e-7 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the superfamily of ATP-binding cassette (ABC) transporters and the encoded protein contains two ATP-binding domains and 12 transmembrane regions. 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 gene is a member of the MRP subfamily which is involved in multi-drug resistance. This gene and another subfamily member are arranged head-to-tail on chromosome 16q12.1. Increased expression of this gene is associated with breast cancer. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf1 |
T |
C |
17: 43,621,580 (GRCm39) |
S606P |
possibly damaging |
Het |
Afap1 |
A |
G |
5: 36,141,540 (GRCm39) |
N475D |
probably damaging |
Het |
Ahnak2 |
A |
G |
12: 112,739,468 (GRCm39) |
S1535P |
possibly damaging |
Het |
Akt1 |
G |
T |
12: 112,624,885 (GRCm39) |
H194N |
possibly damaging |
Het |
Api5 |
T |
A |
2: 94,251,812 (GRCm39) |
Q396L |
possibly damaging |
Het |
Aplp2 |
T |
C |
9: 31,083,303 (GRCm39) |
N148S |
probably benign |
Het |
Asb3 |
A |
G |
11: 31,031,400 (GRCm39) |
Y340C |
probably damaging |
Het |
Bbox1 |
A |
T |
2: 110,098,581 (GRCm39) |
M332K |
probably damaging |
Het |
Cabin1 |
A |
T |
10: 75,579,090 (GRCm39) |
S449T |
probably benign |
Het |
Carns1 |
A |
G |
19: 4,216,007 (GRCm39) |
V725A |
possibly damaging |
Het |
Cdkn1b |
A |
G |
6: 134,898,058 (GRCm39) |
K59R |
possibly damaging |
Het |
Cdv3 |
A |
T |
9: 103,233,539 (GRCm39) |
I212K |
probably damaging |
Het |
Clec14a |
T |
A |
12: 58,314,432 (GRCm39) |
I397F |
probably damaging |
Het |
Cnnm1 |
A |
G |
19: 43,483,469 (GRCm39) |
I950V |
possibly damaging |
Het |
Ddi2 |
A |
G |
4: 141,422,734 (GRCm39) |
M326T |
probably benign |
Het |
Dhx30 |
T |
C |
9: 109,914,103 (GRCm39) |
T1065A |
probably benign |
Het |
Eif3c |
A |
T |
7: 126,146,674 (GRCm39) |
M808K |
possibly damaging |
Het |
Evi2 |
G |
T |
11: 79,406,971 (GRCm39) |
H201Q |
possibly damaging |
Het |
Exoc4 |
A |
G |
6: 33,452,991 (GRCm39) |
T494A |
unknown |
Het |
Fam83f |
T |
A |
15: 80,574,819 (GRCm39) |
M242K |
probably damaging |
Het |
Fat4 |
T |
C |
3: 39,055,374 (GRCm39) |
Y4198H |
probably benign |
Het |
Fcgbp |
C |
A |
7: 27,793,000 (GRCm39) |
N1001K |
probably benign |
Het |
Gda |
G |
T |
19: 21,400,449 (GRCm39) |
A164E |
probably damaging |
Het |
Gm19410 |
T |
C |
8: 36,279,493 (GRCm39) |
V1786A |
possibly damaging |
Het |
Gm45871 |
A |
G |
18: 90,609,069 (GRCm39) |
N82S |
probably benign |
Het |
Gnas |
T |
A |
2: 174,141,392 (GRCm39) |
S580T |
unknown |
Het |
Gprin1 |
G |
A |
13: 54,886,714 (GRCm39) |
P520L |
probably benign |
Het |
Gramd4 |
C |
T |
15: 86,014,751 (GRCm39) |
R433C |
probably damaging |
Het |
Ighv5-12 |
T |
A |
12: 113,665,958 (GRCm39) |
T47S |
probably benign |
Het |
Itprid1 |
T |
G |
6: 55,864,018 (GRCm39) |
S115A |
probably damaging |
Het |
Kdm5a |
T |
A |
6: 120,367,658 (GRCm39) |
L451Q |
probably damaging |
Het |
Kif12 |
T |
A |
4: 63,084,126 (GRCm39) |
R624S |
probably benign |
Het |
Lepr |
T |
A |
4: 101,592,851 (GRCm39) |
Y155* |
probably null |
Het |
Lnx2 |
T |
A |
5: 146,961,376 (GRCm39) |
I519F |
probably damaging |
Het |
Marchf7 |
T |
A |
2: 60,060,175 (GRCm39) |
S101T |
probably damaging |
Het |
Miox |
A |
G |
15: 89,220,785 (GRCm39) |
D230G |
probably damaging |
Het |
Morc2a |
T |
A |
11: 3,600,381 (GRCm39) |
M1K |
probably null |
Het |
Mtus1 |
T |
C |
8: 41,536,222 (GRCm39) |
N498S |
probably damaging |
Het |
Mxd1 |
T |
A |
6: 86,645,554 (GRCm39) |
R46W |
probably damaging |
Het |
Ndufa11 |
G |
C |
17: 57,024,843 (GRCm39) |
A2P |
possibly damaging |
Het |
Necab2 |
C |
T |
8: 120,198,513 (GRCm39) |
H362Y |
probably damaging |
Het |
Nphp4 |
G |
A |
4: 152,623,434 (GRCm39) |
V703I |
possibly damaging |
Het |
Nup54 |
T |
C |
5: 92,582,218 (GRCm39) |
N31S |
unknown |
Het |
Or13a23-ps1 |
T |
A |
7: 140,118,497 (GRCm39) |
S22R |
probably benign |
Het |
Or1ad6 |
T |
C |
11: 50,860,316 (GRCm39) |
L157P |
probably damaging |
Het |
Or1e34 |
A |
T |
11: 73,778,696 (GRCm39) |
C167* |
probably null |
Het |
Or8b4 |
A |
C |
9: 37,830,066 (GRCm39) |
T38P |
probably damaging |
Het |
P2rx2 |
T |
C |
5: 110,490,388 (GRCm39) |
E109G |
possibly damaging |
Het |
Pcdha7 |
T |
C |
18: 37,107,409 (GRCm39) |
S145P |
probably damaging |
Het |
Pdlim5 |
A |
T |
3: 141,948,529 (GRCm39) |
V586E |
probably damaging |
Het |
Pex5l |
T |
C |
3: 33,136,204 (GRCm39) |
E5G |
probably benign |
Het |
Plch1 |
T |
A |
3: 63,615,176 (GRCm39) |
D774V |
probably damaging |
Het |
Plekhg3 |
A |
T |
12: 76,611,726 (GRCm39) |
D335V |
possibly damaging |
Het |
Pop1 |
A |
G |
15: 34,530,227 (GRCm39) |
H905R |
probably benign |
Het |
Ppm1k |
T |
C |
6: 57,492,720 (GRCm39) |
T189A |
probably damaging |
Het |
Pramel13 |
A |
G |
4: 144,122,517 (GRCm39) |
L9P |
probably damaging |
Het |
Recql5 |
A |
G |
11: 115,784,367 (GRCm39) |
V911A |
probably damaging |
Het |
Rnf145 |
T |
A |
11: 44,415,830 (GRCm39) |
L15* |
probably null |
Het |
Rpl13a |
A |
G |
7: 44,776,673 (GRCm39) |
V29A |
probably benign |
Het |
Rps6ka5 |
A |
G |
12: 100,540,250 (GRCm39) |
V491A |
probably benign |
Het |
Setbp1 |
T |
C |
18: 78,900,142 (GRCm39) |
H1175R |
probably benign |
Het |
Setd5 |
T |
C |
6: 113,093,063 (GRCm39) |
S372P |
probably damaging |
Het |
Slc1a3 |
T |
C |
15: 8,675,177 (GRCm39) |
E276G |
probably damaging |
Het |
Slc36a2 |
T |
C |
11: 55,070,169 (GRCm39) |
N136S |
probably benign |
Het |
Spag1 |
G |
A |
15: 36,190,683 (GRCm39) |
|
probably null |
Het |
Spon1 |
A |
C |
7: 113,387,685 (GRCm39) |
T81P |
probably damaging |
Het |
Sv2b |
A |
T |
7: 74,856,238 (GRCm39) |
D17E |
probably benign |
Het |
Tasor2 |
A |
G |
13: 3,649,667 (GRCm39) |
V44A |
probably benign |
Het |
Tax1bp1 |
C |
T |
6: 52,704,215 (GRCm39) |
T65I |
probably damaging |
Het |
Tenm2 |
C |
A |
11: 35,915,341 (GRCm39) |
K2065N |
probably damaging |
Het |
Ticam2 |
T |
C |
18: 46,693,658 (GRCm39) |
D143G |
probably damaging |
Het |
Tmem132d |
T |
C |
5: 127,869,579 (GRCm39) |
E585G |
possibly damaging |
Het |
Tnfrsf8 |
C |
T |
4: 145,019,668 (GRCm39) |
|
probably null |
Het |
Trim44 |
C |
T |
2: 102,230,813 (GRCm39) |
G73R |
unknown |
Het |
Trpc3 |
C |
T |
3: 36,692,713 (GRCm39) |
D760N |
possibly damaging |
Het |
Tspan9 |
T |
A |
6: 127,942,715 (GRCm39) |
M171L |
probably benign |
Het |
Ugt2b37 |
A |
G |
5: 87,402,532 (GRCm39) |
F33S |
possibly damaging |
Het |
Vav2 |
A |
T |
2: 27,159,027 (GRCm39) |
V734E |
probably damaging |
Het |
Vmn1r214 |
A |
G |
13: 23,218,508 (GRCm39) |
M1V |
probably null |
Het |
Vmn1r24 |
A |
T |
6: 57,932,804 (GRCm39) |
V238E |
probably damaging |
Het |
Vmn2r107 |
A |
G |
17: 20,577,262 (GRCm39) |
Q420R |
probably damaging |
Het |
Vmn2r31 |
G |
A |
7: 7,387,085 (GRCm39) |
P829S |
probably damaging |
Het |
Xpo6 |
A |
G |
7: 125,712,873 (GRCm39) |
F703L |
probably benign |
Het |
Zfp442 |
T |
A |
2: 150,250,207 (GRCm39) |
H565L |
possibly damaging |
Het |
Zfp950 |
A |
T |
19: 61,116,000 (GRCm39) |
D2E |
probably damaging |
Het |
Zfp992 |
T |
A |
4: 146,551,345 (GRCm39) |
S355R |
probably damaging |
Het |
Zwilch |
A |
T |
9: 64,063,303 (GRCm39) |
F309Y |
probably damaging |
Het |
|
Other mutations in Abcc12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01362:Abcc12
|
APN |
8 |
87,261,322 (GRCm39) |
missense |
probably benign |
0.45 |
IGL01504:Abcc12
|
APN |
8 |
87,284,231 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01593:Abcc12
|
APN |
8 |
87,284,279 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02164:Abcc12
|
APN |
8 |
87,254,033 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02173:Abcc12
|
APN |
8 |
87,293,071 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02175:Abcc12
|
APN |
8 |
87,261,642 (GRCm39) |
splice site |
probably null |
|
IGL02405:Abcc12
|
APN |
8 |
87,284,782 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02620:Abcc12
|
APN |
8 |
87,231,943 (GRCm39) |
splice site |
probably null |
|
IGL02635:Abcc12
|
APN |
8 |
87,236,311 (GRCm39) |
splice site |
probably benign |
|
IGL03241:Abcc12
|
APN |
8 |
87,236,436 (GRCm39) |
missense |
possibly damaging |
0.77 |
PIT4544001:Abcc12
|
UTSW |
8 |
87,231,875 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0023:Abcc12
|
UTSW |
8 |
87,264,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0023:Abcc12
|
UTSW |
8 |
87,264,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0116:Abcc12
|
UTSW |
8 |
87,261,627 (GRCm39) |
missense |
probably benign |
0.00 |
R0131:Abcc12
|
UTSW |
8 |
87,258,197 (GRCm39) |
missense |
probably benign |
|
R0131:Abcc12
|
UTSW |
8 |
87,258,197 (GRCm39) |
missense |
probably benign |
|
R0132:Abcc12
|
UTSW |
8 |
87,258,197 (GRCm39) |
missense |
probably benign |
|
R0308:Abcc12
|
UTSW |
8 |
87,284,381 (GRCm39) |
splice site |
probably benign |
|
R0589:Abcc12
|
UTSW |
8 |
87,287,101 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1451:Abcc12
|
UTSW |
8 |
87,284,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R1564:Abcc12
|
UTSW |
8 |
87,244,115 (GRCm39) |
missense |
probably benign |
0.10 |
R1740:Abcc12
|
UTSW |
8 |
87,236,400 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1740:Abcc12
|
UTSW |
8 |
87,232,126 (GRCm39) |
nonsense |
probably null |
|
R1970:Abcc12
|
UTSW |
8 |
87,253,910 (GRCm39) |
missense |
probably benign |
0.27 |
R2017:Abcc12
|
UTSW |
8 |
87,290,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R2026:Abcc12
|
UTSW |
8 |
87,284,862 (GRCm39) |
missense |
probably benign |
0.30 |
R2402:Abcc12
|
UTSW |
8 |
87,235,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R3085:Abcc12
|
UTSW |
8 |
87,270,536 (GRCm39) |
splice site |
probably benign |
|
R3115:Abcc12
|
UTSW |
8 |
87,266,653 (GRCm39) |
critical splice donor site |
probably null |
|
R3176:Abcc12
|
UTSW |
8 |
87,233,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R3276:Abcc12
|
UTSW |
8 |
87,233,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R3847:Abcc12
|
UTSW |
8 |
87,280,020 (GRCm39) |
missense |
probably benign |
0.05 |
R3911:Abcc12
|
UTSW |
8 |
87,255,048 (GRCm39) |
splice site |
probably benign |
|
R4031:Abcc12
|
UTSW |
8 |
87,244,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R4297:Abcc12
|
UTSW |
8 |
87,258,154 (GRCm39) |
splice site |
probably null |
|
R4298:Abcc12
|
UTSW |
8 |
87,258,154 (GRCm39) |
splice site |
probably null |
|
R4299:Abcc12
|
UTSW |
8 |
87,258,154 (GRCm39) |
splice site |
probably null |
|
R4688:Abcc12
|
UTSW |
8 |
87,275,323 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4810:Abcc12
|
UTSW |
8 |
87,287,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R4863:Abcc12
|
UTSW |
8 |
87,265,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R4892:Abcc12
|
UTSW |
8 |
87,236,431 (GRCm39) |
missense |
probably benign |
0.28 |
R5288:Abcc12
|
UTSW |
8 |
87,293,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R5303:Abcc12
|
UTSW |
8 |
87,236,415 (GRCm39) |
missense |
probably benign |
0.15 |
R5332:Abcc12
|
UTSW |
8 |
87,251,459 (GRCm39) |
splice site |
probably null |
|
R5386:Abcc12
|
UTSW |
8 |
87,244,118 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5457:Abcc12
|
UTSW |
8 |
87,236,473 (GRCm39) |
missense |
probably benign |
0.03 |
R5900:Abcc12
|
UTSW |
8 |
87,293,149 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6035:Abcc12
|
UTSW |
8 |
87,244,033 (GRCm39) |
missense |
probably damaging |
0.98 |
R6035:Abcc12
|
UTSW |
8 |
87,244,033 (GRCm39) |
missense |
probably damaging |
0.98 |
R6291:Abcc12
|
UTSW |
8 |
87,293,173 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6518:Abcc12
|
UTSW |
8 |
87,235,718 (GRCm39) |
|
|
|
R6677:Abcc12
|
UTSW |
8 |
87,261,381 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7258:Abcc12
|
UTSW |
8 |
87,287,486 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7411:Abcc12
|
UTSW |
8 |
87,287,479 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7619:Abcc12
|
UTSW |
8 |
87,293,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Abcc12
|
UTSW |
8 |
87,234,568 (GRCm39) |
missense |
probably benign |
0.03 |
R7828:Abcc12
|
UTSW |
8 |
87,254,904 (GRCm39) |
missense |
probably benign |
0.08 |
R7834:Abcc12
|
UTSW |
8 |
87,284,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7834:Abcc12
|
UTSW |
8 |
87,258,179 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7939:Abcc12
|
UTSW |
8 |
87,275,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R7989:Abcc12
|
UTSW |
8 |
87,232,108 (GRCm39) |
missense |
probably benign |
0.02 |
R8290:Abcc12
|
UTSW |
8 |
87,238,911 (GRCm39) |
missense |
probably damaging |
0.99 |
R8681:Abcc12
|
UTSW |
8 |
87,231,908 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8795:Abcc12
|
UTSW |
8 |
87,258,213 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8811:Abcc12
|
UTSW |
8 |
87,280,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R8939:Abcc12
|
UTSW |
8 |
87,243,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R8940:Abcc12
|
UTSW |
8 |
87,287,440 (GRCm39) |
missense |
probably benign |
0.45 |
X0027:Abcc12
|
UTSW |
8 |
87,279,920 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Abcc12
|
UTSW |
8 |
87,286,908 (GRCm39) |
splice site |
probably null |
|
Z1176:Abcc12
|
UTSW |
8 |
87,277,230 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Abcc12
|
UTSW |
8 |
87,254,013 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
Predicted Primers |
PCR Primer
(F):5'- ACTGATGTTGTGTAGCACTGAC -3'
(R):5'- GGGAATAACTTCTGGTCAGTCC -3'
Sequencing Primer
(F):5'- ACTTTGCCACTCCGGGCTAG -3'
(R):5'- CCTGATTGTCTTGAGTAGAAATGCC -3'
|
Posted On |
2022-10-06 |