Incidental Mutation 'R1720:Med13l'
| ID |
191369 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Med13l
|
| Ensembl Gene |
ENSMUSG00000018076 |
| Gene Name |
mediator complex subunit 13-like |
| Synonyms |
9030618F05Rik, Trap240L, 6330591G05Rik, Thrap2, 2210413I17Rik |
| MMRRC Submission |
039752-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.966)
|
| Stock # |
R1720 (G1)
|
| Quality Score |
224 |
|
Status
|
Not validated
|
| Chromosome |
5 |
| Chromosomal Location |
118698744-118903503 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 118880060 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 1051
(T1051A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000144092
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000100816]
[ENSMUST00000201010]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000100816
AA Change: T1051A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000098379
Gene: ENSMUSG00000018076
AA Change: T1051A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Med13_N
|
1 |
380 |
2.5e-116 |
PFAM |
|
low complexity region
|
442 |
460 |
N/A |
INTRINSIC |
|
low complexity region
|
542 |
558 |
N/A |
INTRINSIC |
|
low complexity region
|
1020 |
1031 |
N/A |
INTRINSIC |
|
low complexity region
|
1044 |
1060 |
N/A |
INTRINSIC |
|
low complexity region
|
1541 |
1593 |
N/A |
INTRINSIC |
|
low complexity region
|
1601 |
1611 |
N/A |
INTRINSIC |
|
Pfam:Med13_C
|
1675 |
2197 |
1e-142 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000201010
AA Change: T1051A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000144092
Gene: ENSMUSG00000018076
AA Change: T1051A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Med13_N
|
1 |
380 |
1e-112 |
PFAM |
|
low complexity region
|
442 |
460 |
N/A |
INTRINSIC |
|
low complexity region
|
542 |
558 |
N/A |
INTRINSIC |
|
low complexity region
|
1020 |
1031 |
N/A |
INTRINSIC |
|
low complexity region
|
1044 |
1060 |
N/A |
INTRINSIC |
|
low complexity region
|
1541 |
1593 |
N/A |
INTRINSIC |
|
low complexity region
|
1601 |
1611 |
N/A |
INTRINSIC |
|
Pfam:Med13_C
|
1675 |
2206 |
1.7e-138 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.7%
- 20x: 93.8%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a subunit of the Mediator complex, a large complex of proteins that functions as a transcriptional coactivator for most RNA polymerase II-transcribed genes. The encoded protein is involved in early development of the heart and brain. Defects in this gene are a cause of transposition of the great arteries, dextro-looped (DTGA).[provided by RefSeq, Jul 2010]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 82 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acot5 |
A |
G |
12: 84,122,655 (GRCm39) |
D413G |
probably benign |
Het |
| Actr5 |
G |
T |
2: 158,478,057 (GRCm39) |
V476F |
possibly damaging |
Het |
| Adhfe1 |
G |
A |
1: 9,637,125 (GRCm39) |
D426N |
probably benign |
Het |
| Adra1a |
T |
C |
14: 66,875,727 (GRCm39) |
L234P |
probably damaging |
Het |
| Akap9 |
G |
T |
5: 4,022,791 (GRCm39) |
V1207L |
possibly damaging |
Het |
| Anapc2 |
A |
G |
2: 25,164,724 (GRCm39) |
D36G |
probably benign |
Het |
| Apol8 |
A |
G |
15: 77,633,566 (GRCm39) |
S337P |
possibly damaging |
Het |
| Asxl3 |
A |
T |
18: 22,585,492 (GRCm39) |
D139V |
probably damaging |
Het |
| Atp13a4 |
A |
T |
16: 29,227,746 (GRCm39) |
V1037E |
probably damaging |
Het |
| Baat |
A |
T |
4: 49,490,231 (GRCm39) |
F284L |
probably benign |
Het |
| Bltp3b |
T |
C |
10: 89,618,448 (GRCm39) |
V141A |
probably damaging |
Het |
| C1qtnf6 |
A |
T |
15: 78,411,640 (GRCm39) |
F40Y |
probably damaging |
Het |
| Caskin2 |
G |
A |
11: 115,693,608 (GRCm39) |
H508Y |
probably damaging |
Het |
| Cass4 |
A |
T |
2: 172,269,654 (GRCm39) |
I579F |
probably damaging |
Het |
| Cdk15 |
A |
G |
1: 59,328,917 (GRCm39) |
Y277C |
probably damaging |
Het |
| Cit |
G |
A |
5: 116,105,956 (GRCm39) |
D947N |
probably damaging |
Het |
| Clint1 |
T |
A |
11: 45,778,237 (GRCm39) |
I126K |
probably damaging |
Het |
| Col6a4 |
C |
T |
9: 105,903,671 (GRCm39) |
G1640E |
probably damaging |
Het |
| Ddx10 |
T |
C |
9: 53,149,371 (GRCm39) |
K119E |
probably damaging |
Het |
| Dennd1a |
G |
A |
2: 37,690,209 (GRCm39) |
Q964* |
probably null |
Het |
| Dnhd1 |
T |
C |
7: 105,343,035 (GRCm39) |
F1460L |
probably benign |
Het |
| Edc3 |
T |
C |
9: 57,655,462 (GRCm39) |
|
probably null |
Het |
| Edn1 |
A |
G |
13: 42,458,826 (GRCm39) |
E163G |
probably benign |
Het |
| Efl1 |
A |
T |
7: 82,332,929 (GRCm39) |
D317V |
possibly damaging |
Het |
| Elapor2 |
T |
G |
5: 9,478,407 (GRCm39) |
C424G |
probably damaging |
Het |
| F2 |
A |
T |
2: 91,459,175 (GRCm39) |
Y430* |
probably null |
Het |
| Faap100 |
C |
T |
11: 120,265,407 (GRCm39) |
V490M |
probably damaging |
Het |
| Fuz |
G |
T |
7: 44,546,415 (GRCm39) |
G104W |
probably damaging |
Het |
| Greb1l |
C |
A |
18: 10,553,848 (GRCm39) |
H1616Q |
probably benign |
Het |
| Grm1 |
G |
T |
10: 10,622,538 (GRCm39) |
|
probably null |
Het |
| Gucy2d |
G |
T |
7: 98,126,437 (GRCm39) |
A1098S |
probably benign |
Het |
| H1f0 |
T |
A |
15: 78,913,195 (GRCm39) |
S92T |
possibly damaging |
Het |
| Hbb-bt |
T |
A |
7: 103,463,083 (GRCm39) |
|
probably benign |
Het |
| Heg1 |
G |
A |
16: 33,527,549 (GRCm39) |
A170T |
probably benign |
Het |
| Hspa4l |
A |
T |
3: 40,736,049 (GRCm39) |
K578* |
probably null |
Het |
| Ikbke |
A |
G |
1: 131,186,947 (GRCm39) |
S582P |
possibly damaging |
Het |
| Itga6 |
T |
A |
2: 71,650,510 (GRCm39) |
F185L |
probably damaging |
Het |
| Itgal |
T |
A |
7: 126,906,099 (GRCm39) |
D396E |
probably benign |
Het |
| Kif5b |
T |
C |
18: 6,213,427 (GRCm39) |
H687R |
probably benign |
Het |
| Kmt2c |
T |
C |
5: 25,504,182 (GRCm39) |
N3709D |
probably benign |
Het |
| Lipf |
A |
T |
19: 33,943,066 (GRCm39) |
K125* |
probably null |
Het |
| Lrif1 |
A |
T |
3: 106,640,452 (GRCm39) |
E512D |
probably damaging |
Het |
| Matn2 |
T |
A |
15: 34,345,420 (GRCm39) |
Y142* |
probably null |
Het |
| Mpp3 |
T |
A |
11: 101,916,582 (GRCm39) |
M1L |
possibly damaging |
Het |
| Mro |
C |
T |
18: 74,009,806 (GRCm39) |
S159L |
probably benign |
Het |
| Myh15 |
T |
A |
16: 48,913,145 (GRCm39) |
D367E |
probably damaging |
Het |
| Myo1g |
T |
C |
11: 6,462,490 (GRCm39) |
Q547R |
probably benign |
Het |
| Neb |
T |
C |
2: 52,097,733 (GRCm39) |
I902M |
probably benign |
Het |
| Nsd1 |
G |
A |
13: 55,394,711 (GRCm39) |
D771N |
probably damaging |
Het |
| Or10x4 |
A |
G |
1: 174,219,486 (GRCm39) |
I284V |
probably benign |
Het |
| Or14a256 |
T |
C |
7: 86,265,664 (GRCm39) |
N63S |
probably damaging |
Het |
| Or2a20 |
T |
C |
6: 43,194,494 (GRCm39) |
S216P |
probably damaging |
Het |
| Or4e5 |
A |
C |
14: 52,728,051 (GRCm39) |
Y40* |
probably null |
Het |
| Or8b48 |
C |
T |
9: 38,492,585 (GRCm39) |
T4I |
probably benign |
Het |
| Penk |
A |
G |
4: 4,134,240 (GRCm39) |
Y136H |
probably damaging |
Het |
| Prdm6 |
C |
T |
18: 53,673,272 (GRCm39) |
S144L |
probably benign |
Het |
| Ptprq |
T |
A |
10: 107,522,155 (GRCm39) |
I599F |
probably damaging |
Het |
| Racgap1 |
A |
T |
15: 99,526,650 (GRCm39) |
C304* |
probably null |
Het |
| Rbp3 |
T |
C |
14: 33,678,866 (GRCm39) |
V938A |
probably benign |
Het |
| Rpp30 |
A |
G |
19: 36,071,827 (GRCm39) |
K132E |
probably damaging |
Het |
| Rxfp2 |
A |
T |
5: 149,966,564 (GRCm39) |
R101* |
probably null |
Het |
| Ryr1 |
A |
T |
7: 28,801,295 (GRCm39) |
V823E |
probably damaging |
Het |
| S100pbp |
A |
T |
4: 129,075,886 (GRCm39) |
D146E |
probably damaging |
Het |
| Sdr9c7 |
T |
A |
10: 127,738,127 (GRCm39) |
V135E |
probably damaging |
Het |
| Serpinb12 |
A |
G |
1: 106,874,344 (GRCm39) |
D23G |
probably damaging |
Het |
| Serpinf1 |
T |
A |
11: 75,304,807 (GRCm39) |
T185S |
probably null |
Het |
| Slc23a1 |
A |
C |
18: 35,758,904 (GRCm39) |
C96G |
possibly damaging |
Het |
| Slc5a4a |
C |
T |
10: 76,025,103 (GRCm39) |
|
probably null |
Het |
| Spmap1 |
A |
G |
11: 97,662,435 (GRCm39) |
F146L |
probably damaging |
Het |
| Suco |
A |
T |
1: 161,661,623 (GRCm39) |
L936Q |
probably damaging |
Het |
| Tmem144 |
T |
C |
3: 79,732,606 (GRCm39) |
Y224C |
probably damaging |
Het |
| Tpm4 |
T |
A |
8: 72,898,598 (GRCm39) |
|
probably null |
Het |
| Ttn |
T |
C |
2: 76,560,414 (GRCm39) |
E29329G |
probably damaging |
Het |
| Txn1 |
T |
C |
4: 57,943,922 (GRCm39) |
I101V |
probably benign |
Het |
| Ube2o |
A |
T |
11: 116,435,433 (GRCm39) |
C452S |
probably benign |
Het |
| Uxs1 |
A |
T |
1: 43,804,081 (GRCm39) |
I278N |
probably damaging |
Het |
| Vps54 |
T |
C |
11: 21,256,519 (GRCm39) |
F663L |
probably damaging |
Het |
| Wdfy3 |
CG |
C |
5: 102,074,391 (GRCm39) |
|
probably null |
Het |
| Zc3h11a |
A |
G |
1: 133,549,439 (GRCm39) |
S741P |
probably damaging |
Het |
| Zdbf2 |
G |
A |
1: 63,342,436 (GRCm39) |
V272I |
possibly damaging |
Het |
| Zdhhc24 |
A |
G |
19: 4,928,979 (GRCm39) |
N68S |
probably damaging |
Het |
| Znfx1 |
A |
T |
2: 166,885,986 (GRCm39) |
L858* |
probably null |
Het |
|
| Other mutations in Med13l |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00232:Med13l
|
APN |
5 |
118,862,136 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01012:Med13l
|
APN |
5 |
118,872,093 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01316:Med13l
|
APN |
5 |
118,900,846 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01529:Med13l
|
APN |
5 |
118,880,400 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01731:Med13l
|
APN |
5 |
118,880,472 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL01790:Med13l
|
APN |
5 |
118,731,587 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02394:Med13l
|
APN |
5 |
118,886,898 (GRCm39) |
missense |
probably benign |
0.37 |
|
IGL02432:Med13l
|
APN |
5 |
118,876,465 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL02698:Med13l
|
APN |
5 |
118,900,894 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02801:Med13l
|
APN |
5 |
118,883,178 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03242:Med13l
|
APN |
5 |
118,885,510 (GRCm39) |
missense |
probably benign |
|
|
IGL03270:Med13l
|
APN |
5 |
118,869,495 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Basics
|
UTSW |
5 |
118,897,329 (GRCm39) |
critical splice donor site |
probably null |
|
|
firmament
|
UTSW |
5 |
118,883,071 (GRCm39) |
splice site |
probably null |
|
|
Fundament
|
UTSW |
5 |
118,859,539 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Root
|
UTSW |
5 |
118,731,510 (GRCm39) |
missense |
probably damaging |
1.00 |
|
P0035:Med13l
|
UTSW |
5 |
118,880,685 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0051:Med13l
|
UTSW |
5 |
118,880,720 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0051:Med13l
|
UTSW |
5 |
118,880,720 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0136:Med13l
|
UTSW |
5 |
118,862,115 (GRCm39) |
missense |
probably benign |
0.15 |
|
R0158:Med13l
|
UTSW |
5 |
118,880,514 (GRCm39) |
missense |
unknown |
|
|
R0197:Med13l
|
UTSW |
5 |
118,809,067 (GRCm39) |
splice site |
probably benign |
|
|
R0370:Med13l
|
UTSW |
5 |
118,879,891 (GRCm39) |
missense |
probably benign |
0.14 |
|
R0492:Med13l
|
UTSW |
5 |
118,876,560 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0532:Med13l
|
UTSW |
5 |
118,897,188 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R0726:Med13l
|
UTSW |
5 |
118,886,749 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0738:Med13l
|
UTSW |
5 |
118,889,698 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0827:Med13l
|
UTSW |
5 |
118,864,312 (GRCm39) |
splice site |
probably benign |
|
|
R0883:Med13l
|
UTSW |
5 |
118,809,067 (GRCm39) |
splice site |
probably benign |
|
|
R0959:Med13l
|
UTSW |
5 |
118,892,350 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R1458:Med13l
|
UTSW |
5 |
118,876,524 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1562:Med13l
|
UTSW |
5 |
118,876,584 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1577:Med13l
|
UTSW |
5 |
118,859,457 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1661:Med13l
|
UTSW |
5 |
118,887,813 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1665:Med13l
|
UTSW |
5 |
118,887,813 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1929:Med13l
|
UTSW |
5 |
118,866,898 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1967:Med13l
|
UTSW |
5 |
118,899,387 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2301:Med13l
|
UTSW |
5 |
118,731,512 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3691:Med13l
|
UTSW |
5 |
118,859,562 (GRCm39) |
missense |
probably benign |
0.16 |
|
R3895:Med13l
|
UTSW |
5 |
118,899,388 (GRCm39) |
missense |
probably null |
0.99 |
|
R4043:Med13l
|
UTSW |
5 |
118,731,528 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4593:Med13l
|
UTSW |
5 |
118,880,625 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4902:Med13l
|
UTSW |
5 |
118,883,195 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4995:Med13l
|
UTSW |
5 |
118,869,014 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5010:Med13l
|
UTSW |
5 |
118,731,615 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5057:Med13l
|
UTSW |
5 |
118,856,558 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5369:Med13l
|
UTSW |
5 |
118,862,075 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5446:Med13l
|
UTSW |
5 |
118,880,462 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R5564:Med13l
|
UTSW |
5 |
118,880,105 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5566:Med13l
|
UTSW |
5 |
118,866,730 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5580:Med13l
|
UTSW |
5 |
118,889,695 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5634:Med13l
|
UTSW |
5 |
118,698,915 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R5748:Med13l
|
UTSW |
5 |
118,731,510 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5764:Med13l
|
UTSW |
5 |
118,866,707 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5765:Med13l
|
UTSW |
5 |
118,866,707 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6083:Med13l
|
UTSW |
5 |
118,859,551 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R6504:Med13l
|
UTSW |
5 |
118,892,386 (GRCm39) |
missense |
probably benign |
0.34 |
|
R6546:Med13l
|
UTSW |
5 |
118,859,539 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6797:Med13l
|
UTSW |
5 |
118,897,329 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6911:Med13l
|
UTSW |
5 |
118,893,723 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6942:Med13l
|
UTSW |
5 |
118,883,071 (GRCm39) |
splice site |
probably null |
|
|
R7018:Med13l
|
UTSW |
5 |
118,890,051 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7096:Med13l
|
UTSW |
5 |
118,859,991 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7113:Med13l
|
UTSW |
5 |
118,864,330 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7136:Med13l
|
UTSW |
5 |
118,859,587 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7140:Med13l
|
UTSW |
5 |
118,880,037 (GRCm39) |
missense |
probably benign |
0.27 |
|
R7345:Med13l
|
UTSW |
5 |
118,880,825 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7409:Med13l
|
UTSW |
5 |
118,892,386 (GRCm39) |
missense |
probably benign |
0.34 |
|
R7410:Med13l
|
UTSW |
5 |
118,698,897 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7432:Med13l
|
UTSW |
5 |
118,890,003 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7486:Med13l
|
UTSW |
5 |
118,866,539 (GRCm39) |
missense |
probably benign |
0.17 |
|
R7509:Med13l
|
UTSW |
5 |
118,886,995 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7722:Med13l
|
UTSW |
5 |
118,885,472 (GRCm39) |
missense |
probably benign |
0.32 |
|
R7802:Med13l
|
UTSW |
5 |
118,866,655 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8081:Med13l
|
UTSW |
5 |
118,866,333 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8260:Med13l
|
UTSW |
5 |
118,886,794 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8266:Med13l
|
UTSW |
5 |
118,880,174 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8347:Med13l
|
UTSW |
5 |
118,880,662 (GRCm39) |
missense |
probably benign |
|
|
R8365:Med13l
|
UTSW |
5 |
118,866,709 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R8508:Med13l
|
UTSW |
5 |
118,892,386 (GRCm39) |
missense |
probably benign |
0.34 |
|
R8920:Med13l
|
UTSW |
5 |
118,885,543 (GRCm39) |
nonsense |
probably null |
|
|
R8970:Med13l
|
UTSW |
5 |
118,883,164 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8994:Med13l
|
UTSW |
5 |
118,866,226 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R9045:Med13l
|
UTSW |
5 |
118,880,816 (GRCm39) |
missense |
probably benign |
|
|
R9401:Med13l
|
UTSW |
5 |
118,883,089 (GRCm39) |
missense |
probably benign |
0.14 |
|
R9445:Med13l
|
UTSW |
5 |
118,862,214 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9446:Med13l
|
UTSW |
5 |
118,876,567 (GRCm39) |
missense |
probably benign |
0.11 |
|
R9714:Med13l
|
UTSW |
5 |
118,866,438 (GRCm39) |
missense |
probably benign |
0.44 |
|
R9777:Med13l
|
UTSW |
5 |
118,887,024 (GRCm39) |
missense |
probably benign |
|
|
R9781:Med13l
|
UTSW |
5 |
118,868,032 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R9797:Med13l
|
UTSW |
5 |
118,880,144 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0065:Med13l
|
UTSW |
5 |
118,867,948 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1088:Med13l
|
UTSW |
5 |
118,887,706 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGATATTCAGTGCAGGGCTATGGGG -3'
(R):5'- TTGCAGGCACAAATGCAACAGC -3'
Sequencing Primer
(F):5'- CCAAAGCTACTTTGTATCTGTTGC -3'
(R):5'- GTCAAAGTTCCTGTCCTTGAAGAC -3'
|
| Posted On |
2014-05-14 |
Incidental Mutation