Incidental Mutation 'R9717:Btaf1'
ID |
730574 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Btaf1
|
Ensembl Gene |
ENSMUSG00000040565 |
Gene Name |
B-TFIID TATA-box binding protein associated factor 1 |
Synonyms |
E430027O22Rik |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.967)
|
Stock # |
R9717 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
19 |
Chromosomal Location |
36903479-36990152 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 36922646 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Alanine
at position 17
(T17A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000097093
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099494]
|
AlphaFold |
E9QAE3 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000099494
AA Change: T17A
PolyPhen 2
Score 0.284 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000097093 Gene: ENSMUSG00000040565 AA Change: T17A
Domain | Start | End | E-Value | Type |
low complexity region
|
87 |
98 |
N/A |
INTRINSIC |
low complexity region
|
143 |
152 |
N/A |
INTRINSIC |
PDB:3OC3|B
|
276 |
414 |
3e-6 |
PDB |
low complexity region
|
438 |
454 |
N/A |
INTRINSIC |
Pfam:DUF3535
|
585 |
1051 |
1.1e-133 |
PFAM |
low complexity region
|
1099 |
1110 |
N/A |
INTRINSIC |
low complexity region
|
1177 |
1192 |
N/A |
INTRINSIC |
DEXDc
|
1261 |
1469 |
3.02e-30 |
SMART |
low complexity region
|
1630 |
1641 |
N/A |
INTRINSIC |
HELICc
|
1657 |
1743 |
2.22e-19 |
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 encodes a TAF (TATA box-binding protein-associated factor), which associates with TBP (TATA box-binding protein) to form the B-TFIID complex that is required for transcription initiation of genes by RNA polymerase II. This TAF has DNA-dependent ATPase activity, which drives the dissociation of TBP from DNA, freeing the TBP to associate with other TATA boxes or TATA-less promoters. [provided by RefSeq, Sep 2011] PHENOTYPE: Embryos homozygous for a gene-trapped allele display growth retardation. Embryos homozygous for an ENU-induced allele show growth retardation, edema, abnormal blood circulation, myocardial trabeculae hypoplasia, and delayed head and brain development. [provided by MGI curators]
|
Allele List at MGI |
All alleles(40) : Gene trapped(40) |
Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
T |
A |
13: 81,668,900 (GRCm39) |
N2552I |
probably damaging |
Het |
Amph |
G |
T |
13: 19,309,253 (GRCm39) |
A444S |
probably benign |
Het |
Ankrd52 |
A |
G |
10: 128,216,457 (GRCm39) |
N157S |
probably benign |
Het |
Arhgap29 |
T |
C |
3: 121,797,920 (GRCm39) |
F537L |
probably benign |
Het |
Asic1 |
A |
C |
15: 99,590,657 (GRCm39) |
T136P |
probably damaging |
Het |
Atg2b |
T |
C |
12: 105,605,561 (GRCm39) |
Y1468C |
probably benign |
Het |
Atm |
A |
G |
9: 53,427,817 (GRCm39) |
L431P |
probably damaging |
Het |
Atosb |
T |
C |
4: 43,036,050 (GRCm39) |
H227R |
probably damaging |
Het |
Car10 |
A |
G |
11: 93,195,367 (GRCm39) |
N58S |
probably benign |
Het |
Cd79b |
A |
T |
11: 106,202,845 (GRCm39) |
D252E |
probably damaging |
Het |
Cdipt |
C |
T |
7: 126,576,202 (GRCm39) |
|
probably benign |
Het |
Cebpe |
T |
C |
14: 54,949,165 (GRCm39) |
D84G |
probably damaging |
Het |
Cenpj |
T |
C |
14: 56,790,453 (GRCm39) |
E532G |
probably benign |
Het |
Cherp |
A |
G |
8: 73,216,920 (GRCm39) |
|
probably null |
Het |
Chuk |
T |
C |
19: 44,071,109 (GRCm39) |
D532G |
possibly damaging |
Het |
Clec1b |
C |
T |
6: 129,374,603 (GRCm39) |
T9I |
probably benign |
Het |
Clspn |
G |
T |
4: 126,458,756 (GRCm39) |
A280S |
possibly damaging |
Het |
Cts3 |
T |
G |
13: 61,712,799 (GRCm39) |
Y307S |
probably benign |
Het |
Cyp2c39 |
T |
C |
19: 39,556,493 (GRCm39) |
M443T |
possibly damaging |
Het |
Dhx57 |
C |
T |
17: 80,582,447 (GRCm39) |
R386H |
probably damaging |
Het |
Dhx58 |
A |
T |
11: 100,592,133 (GRCm39) |
M305K |
probably benign |
Het |
Dlgap3 |
T |
C |
4: 127,129,287 (GRCm39) |
L894P |
probably damaging |
Het |
Dnah3 |
A |
T |
7: 119,574,299 (GRCm39) |
N2164K |
probably damaging |
Het |
Dnajb14 |
A |
G |
3: 137,608,044 (GRCm39) |
N183S |
probably benign |
Het |
Drd5 |
G |
T |
5: 38,478,090 (GRCm39) |
R361L |
probably damaging |
Het |
Duoxa1 |
T |
C |
2: 122,135,622 (GRCm39) |
E159G |
probably damaging |
Het |
Exoc1 |
T |
A |
5: 76,711,079 (GRCm39) |
S659R |
probably benign |
Het |
Fbln7 |
T |
C |
2: 128,719,314 (GRCm39) |
I37T |
probably benign |
Het |
Fcgrt |
T |
G |
7: 44,744,853 (GRCm39) |
E205A |
possibly damaging |
Het |
Fcho2 |
A |
T |
13: 98,900,202 (GRCm39) |
S304T |
probably damaging |
Het |
Gbp9 |
C |
A |
5: 105,253,587 (GRCm39) |
G43* |
probably null |
Het |
Gucy2d |
A |
G |
7: 98,123,868 (GRCm39) |
K151R |
probably benign |
Het |
Heatr4 |
T |
A |
12: 84,024,829 (GRCm39) |
I331F |
probably damaging |
Het |
Hmcn1 |
G |
A |
1: 150,485,378 (GRCm39) |
T4408I |
probably damaging |
Het |
Hoxc9 |
C |
T |
15: 102,890,551 (GRCm39) |
T156M |
probably benign |
Het |
Hrnr |
A |
T |
3: 93,227,987 (GRCm39) |
E35V |
probably damaging |
Het |
Idua |
C |
T |
5: 108,818,037 (GRCm39) |
Q70* |
probably null |
Het |
Klf5 |
A |
T |
14: 99,539,189 (GRCm39) |
I201F |
probably damaging |
Het |
Lonrf1 |
T |
C |
8: 36,701,164 (GRCm39) |
K349E |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,158,395 (GRCm39) |
D1721E |
|
Het |
Mdh1 |
T |
A |
11: 21,521,870 (GRCm39) |
|
probably benign |
Het |
Mllt11 |
T |
C |
3: 95,127,521 (GRCm39) |
H83R |
probably benign |
Het |
Mrgprb4 |
A |
C |
7: 47,848,583 (GRCm39) |
I115S |
possibly damaging |
Het |
Mrpl38 |
A |
G |
11: 116,023,296 (GRCm39) |
F319S |
probably damaging |
Het |
Naif1 |
A |
T |
2: 32,344,907 (GRCm39) |
M204L |
probably benign |
Het |
Ncan |
T |
A |
8: 70,554,628 (GRCm39) |
D1063V |
probably damaging |
Het |
Noto |
A |
T |
6: 85,401,327 (GRCm39) |
R119W |
possibly damaging |
Het |
Or4c115 |
G |
A |
2: 88,927,573 (GRCm39) |
L233F |
probably benign |
Het |
Or51h7 |
A |
T |
7: 102,591,165 (GRCm39) |
D206E |
probably damaging |
Het |
Or6c69 |
T |
A |
10: 129,748,048 (GRCm39) |
Y33F |
probably damaging |
Het |
Or8b3 |
A |
T |
9: 38,314,841 (GRCm39) |
I224F |
probably damaging |
Het |
Ovch2 |
A |
G |
7: 107,393,584 (GRCm39) |
W181R |
probably damaging |
Het |
Palm |
G |
C |
10: 79,655,117 (GRCm39) |
G292R |
probably damaging |
Het |
Pdgfrb |
T |
A |
18: 61,205,787 (GRCm39) |
L591* |
probably null |
Het |
Pik3c2g |
T |
C |
6: 139,841,910 (GRCm39) |
S772P |
|
Het |
Prx |
C |
A |
7: 27,217,411 (GRCm39) |
D776E |
probably benign |
Het |
Ptpra |
A |
G |
2: 130,384,366 (GRCm39) |
E562G |
possibly damaging |
Het |
Rbm4b |
A |
G |
19: 4,807,359 (GRCm39) |
Y25C |
probably damaging |
Het |
Reln |
T |
C |
5: 22,136,427 (GRCm39) |
T2534A |
probably benign |
Het |
Rnf123 |
T |
C |
9: 107,954,963 (GRCm39) |
S14G |
probably benign |
Het |
Rock2 |
A |
G |
12: 17,015,602 (GRCm39) |
H833R |
probably benign |
Het |
Rxfp3 |
A |
G |
15: 11,037,111 (GRCm39) |
V87A |
possibly damaging |
Het |
S100b |
G |
A |
10: 76,092,936 (GRCm39) |
G23D |
probably damaging |
Het |
Scn9a |
T |
A |
2: 66,357,002 (GRCm39) |
M1100L |
probably benign |
Het |
Septin11 |
T |
A |
5: 93,296,266 (GRCm39) |
S55T |
possibly damaging |
Het |
Speer4a3 |
T |
C |
5: 26,154,829 (GRCm39) |
E257G |
probably damaging |
Het |
Sv2b |
T |
A |
7: 74,769,676 (GRCm39) |
Q622L |
probably benign |
Het |
Taar7a |
T |
C |
10: 23,868,799 (GRCm39) |
D194G |
probably benign |
Het |
Trappc3 |
T |
C |
4: 126,169,014 (GRCm39) |
I168T |
probably benign |
Het |
Trim27 |
T |
C |
13: 21,374,296 (GRCm39) |
|
probably null |
Het |
Wdr49 |
G |
A |
3: 75,304,359 (GRCm39) |
T109I |
probably benign |
Het |
Wdr64 |
T |
C |
1: 175,544,854 (GRCm39) |
Y96H |
probably damaging |
Het |
Zfp219 |
A |
T |
14: 52,247,049 (GRCm39) |
L26Q |
probably damaging |
Het |
Zfp758 |
T |
A |
17: 22,593,829 (GRCm39) |
V105D |
possibly damaging |
Het |
Zfp975 |
C |
G |
7: 42,312,332 (GRCm39) |
E94Q |
possibly damaging |
Het |
Zfyve9 |
C |
T |
4: 108,539,334 (GRCm39) |
A289T |
probably benign |
Het |
Zscan5b |
T |
C |
7: 6,234,525 (GRCm39) |
S184P |
possibly damaging |
Het |
|
Other mutations in Btaf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Btaf1
|
APN |
19 |
36,987,102 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00535:Btaf1
|
APN |
19 |
36,974,935 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00574:Btaf1
|
APN |
19 |
36,947,330 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00969:Btaf1
|
APN |
19 |
36,988,652 (GRCm39) |
splice site |
probably benign |
|
IGL01325:Btaf1
|
APN |
19 |
36,982,049 (GRCm39) |
splice site |
probably benign |
|
IGL01399:Btaf1
|
APN |
19 |
36,977,570 (GRCm39) |
nonsense |
probably null |
|
IGL02024:Btaf1
|
APN |
19 |
36,969,826 (GRCm39) |
splice site |
probably benign |
|
IGL02471:Btaf1
|
APN |
19 |
36,977,592 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02664:Btaf1
|
APN |
19 |
36,955,828 (GRCm39) |
splice site |
probably benign |
|
IGL02898:Btaf1
|
APN |
19 |
36,946,468 (GRCm39) |
missense |
probably benign |
|
IGL02995:Btaf1
|
APN |
19 |
36,958,535 (GRCm39) |
splice site |
probably benign |
|
IGL03023:Btaf1
|
APN |
19 |
36,987,415 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03188:Btaf1
|
APN |
19 |
36,926,508 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03353:Btaf1
|
APN |
19 |
36,969,900 (GRCm39) |
missense |
probably damaging |
1.00 |
freudenberg
|
UTSW |
19 |
36,965,573 (GRCm39) |
critical splice donor site |
probably null |
|
Galanos
|
UTSW |
19 |
36,926,502 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Btaf1
|
UTSW |
19 |
36,987,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Btaf1
|
UTSW |
19 |
36,935,773 (GRCm39) |
missense |
probably benign |
|
R0048:Btaf1
|
UTSW |
19 |
36,980,924 (GRCm39) |
missense |
probably benign |
0.01 |
R0117:Btaf1
|
UTSW |
19 |
36,947,368 (GRCm39) |
missense |
probably benign |
0.06 |
R0207:Btaf1
|
UTSW |
19 |
36,987,048 (GRCm39) |
nonsense |
probably null |
|
R0310:Btaf1
|
UTSW |
19 |
36,981,934 (GRCm39) |
missense |
probably damaging |
0.96 |
R0377:Btaf1
|
UTSW |
19 |
36,966,402 (GRCm39) |
missense |
probably benign |
|
R0419:Btaf1
|
UTSW |
19 |
36,922,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R0440:Btaf1
|
UTSW |
19 |
36,964,053 (GRCm39) |
missense |
probably damaging |
0.99 |
R0532:Btaf1
|
UTSW |
19 |
36,928,586 (GRCm39) |
splice site |
probably benign |
|
R0612:Btaf1
|
UTSW |
19 |
36,946,537 (GRCm39) |
missense |
probably damaging |
0.99 |
R0731:Btaf1
|
UTSW |
19 |
36,974,895 (GRCm39) |
splice site |
probably null |
|
R0780:Btaf1
|
UTSW |
19 |
36,966,322 (GRCm39) |
missense |
probably damaging |
0.99 |
R0919:Btaf1
|
UTSW |
19 |
36,968,143 (GRCm39) |
missense |
probably benign |
0.03 |
R1104:Btaf1
|
UTSW |
19 |
36,982,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R1263:Btaf1
|
UTSW |
19 |
36,933,924 (GRCm39) |
missense |
probably benign |
0.10 |
R1325:Btaf1
|
UTSW |
19 |
36,946,562 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1447:Btaf1
|
UTSW |
19 |
36,969,854 (GRCm39) |
missense |
probably benign |
0.00 |
R1554:Btaf1
|
UTSW |
19 |
36,973,998 (GRCm39) |
missense |
probably benign |
0.02 |
R1649:Btaf1
|
UTSW |
19 |
36,959,122 (GRCm39) |
missense |
probably benign |
|
R1715:Btaf1
|
UTSW |
19 |
36,946,521 (GRCm39) |
missense |
probably damaging |
0.99 |
R1733:Btaf1
|
UTSW |
19 |
36,972,362 (GRCm39) |
missense |
probably benign |
|
R1764:Btaf1
|
UTSW |
19 |
36,928,518 (GRCm39) |
missense |
probably benign |
0.12 |
R1874:Btaf1
|
UTSW |
19 |
36,957,983 (GRCm39) |
missense |
probably benign |
|
R1911:Btaf1
|
UTSW |
19 |
36,964,030 (GRCm39) |
missense |
probably benign |
|
R1933:Btaf1
|
UTSW |
19 |
36,950,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Btaf1
|
UTSW |
19 |
36,928,548 (GRCm39) |
missense |
probably benign |
0.09 |
R2483:Btaf1
|
UTSW |
19 |
36,958,486 (GRCm39) |
missense |
probably benign |
0.02 |
R2510:Btaf1
|
UTSW |
19 |
36,979,845 (GRCm39) |
missense |
probably benign |
0.08 |
R3623:Btaf1
|
UTSW |
19 |
36,958,486 (GRCm39) |
missense |
probably benign |
0.02 |
R3624:Btaf1
|
UTSW |
19 |
36,958,486 (GRCm39) |
missense |
probably benign |
0.02 |
R3801:Btaf1
|
UTSW |
19 |
36,966,373 (GRCm39) |
missense |
probably benign |
0.00 |
R3801:Btaf1
|
UTSW |
19 |
36,963,948 (GRCm39) |
missense |
probably benign |
|
R3802:Btaf1
|
UTSW |
19 |
36,966,373 (GRCm39) |
missense |
probably benign |
0.00 |
R3802:Btaf1
|
UTSW |
19 |
36,963,948 (GRCm39) |
missense |
probably benign |
|
R3803:Btaf1
|
UTSW |
19 |
36,966,373 (GRCm39) |
missense |
probably benign |
0.00 |
R3803:Btaf1
|
UTSW |
19 |
36,963,948 (GRCm39) |
missense |
probably benign |
|
R4077:Btaf1
|
UTSW |
19 |
36,963,879 (GRCm39) |
missense |
probably benign |
0.00 |
R4079:Btaf1
|
UTSW |
19 |
36,963,879 (GRCm39) |
missense |
probably benign |
0.00 |
R4133:Btaf1
|
UTSW |
19 |
36,939,138 (GRCm39) |
missense |
probably benign |
0.00 |
R4673:Btaf1
|
UTSW |
19 |
36,955,772 (GRCm39) |
missense |
probably benign |
0.00 |
R4731:Btaf1
|
UTSW |
19 |
36,958,478 (GRCm39) |
missense |
probably benign |
0.03 |
R4796:Btaf1
|
UTSW |
19 |
36,933,828 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4824:Btaf1
|
UTSW |
19 |
36,958,448 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4835:Btaf1
|
UTSW |
19 |
36,979,858 (GRCm39) |
missense |
probably benign |
0.00 |
R4837:Btaf1
|
UTSW |
19 |
36,944,185 (GRCm39) |
missense |
probably benign |
|
R4925:Btaf1
|
UTSW |
19 |
36,988,733 (GRCm39) |
missense |
probably benign |
|
R4968:Btaf1
|
UTSW |
19 |
36,947,351 (GRCm39) |
missense |
probably null |
0.71 |
R4976:Btaf1
|
UTSW |
19 |
36,963,979 (GRCm39) |
missense |
probably benign |
|
R5001:Btaf1
|
UTSW |
19 |
36,964,052 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5037:Btaf1
|
UTSW |
19 |
36,980,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R5039:Btaf1
|
UTSW |
19 |
36,968,162 (GRCm39) |
missense |
probably benign |
|
R5211:Btaf1
|
UTSW |
19 |
36,973,962 (GRCm39) |
missense |
probably benign |
0.32 |
R5422:Btaf1
|
UTSW |
19 |
36,928,507 (GRCm39) |
missense |
probably benign |
0.09 |
R5429:Btaf1
|
UTSW |
19 |
36,972,257 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5530:Btaf1
|
UTSW |
19 |
36,968,175 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5582:Btaf1
|
UTSW |
19 |
36,965,573 (GRCm39) |
critical splice donor site |
probably null |
|
R5654:Btaf1
|
UTSW |
19 |
36,961,015 (GRCm39) |
missense |
probably benign |
0.35 |
R5744:Btaf1
|
UTSW |
19 |
36,981,890 (GRCm39) |
missense |
probably benign |
0.02 |
R6082:Btaf1
|
UTSW |
19 |
36,960,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R6243:Btaf1
|
UTSW |
19 |
36,958,520 (GRCm39) |
missense |
probably benign |
0.02 |
R6291:Btaf1
|
UTSW |
19 |
36,950,408 (GRCm39) |
missense |
probably benign |
0.00 |
R6502:Btaf1
|
UTSW |
19 |
36,961,017 (GRCm39) |
missense |
probably benign |
|
R7034:Btaf1
|
UTSW |
19 |
36,981,869 (GRCm39) |
missense |
probably benign |
|
R7036:Btaf1
|
UTSW |
19 |
36,981,869 (GRCm39) |
missense |
probably benign |
|
R7085:Btaf1
|
UTSW |
19 |
36,950,318 (GRCm39) |
missense |
probably benign |
|
R7097:Btaf1
|
UTSW |
19 |
36,926,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R7248:Btaf1
|
UTSW |
19 |
36,922,714 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7386:Btaf1
|
UTSW |
19 |
36,935,782 (GRCm39) |
missense |
probably benign |
0.02 |
R7402:Btaf1
|
UTSW |
19 |
36,980,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R7452:Btaf1
|
UTSW |
19 |
36,946,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7493:Btaf1
|
UTSW |
19 |
36,987,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Btaf1
|
UTSW |
19 |
36,955,803 (GRCm39) |
missense |
probably benign |
0.30 |
R7888:Btaf1
|
UTSW |
19 |
36,943,036 (GRCm39) |
missense |
probably benign |
0.10 |
R7944:Btaf1
|
UTSW |
19 |
36,926,565 (GRCm39) |
missense |
probably benign |
|
R8062:Btaf1
|
UTSW |
19 |
36,969,865 (GRCm39) |
missense |
probably benign |
0.00 |
R8559:Btaf1
|
UTSW |
19 |
36,964,273 (GRCm39) |
missense |
probably benign |
0.00 |
R8793:Btaf1
|
UTSW |
19 |
36,958,429 (GRCm39) |
missense |
probably benign |
0.21 |
R8855:Btaf1
|
UTSW |
19 |
36,935,901 (GRCm39) |
missense |
probably benign |
|
R8866:Btaf1
|
UTSW |
19 |
36,935,901 (GRCm39) |
missense |
probably benign |
|
R9016:Btaf1
|
UTSW |
19 |
36,971,705 (GRCm39) |
missense |
probably benign |
0.00 |
R9028:Btaf1
|
UTSW |
19 |
36,946,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R9109:Btaf1
|
UTSW |
19 |
36,964,114 (GRCm39) |
missense |
probably benign |
|
R9172:Btaf1
|
UTSW |
19 |
36,977,630 (GRCm39) |
missense |
probably damaging |
0.98 |
R9298:Btaf1
|
UTSW |
19 |
36,964,114 (GRCm39) |
missense |
probably benign |
|
W0251:Btaf1
|
UTSW |
19 |
36,980,904 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Btaf1
|
UTSW |
19 |
36,926,496 (GRCm39) |
nonsense |
probably null |
|
Z1088:Btaf1
|
UTSW |
19 |
36,964,018 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- GCATCTCTTATACCCACAGCTTTTAAG -3'
(R):5'- ACCCCAAGGTCACTTAGGAC -3'
Sequencing Primer
(F):5'- TGTCAGAATTCAGAAATCCGCCTG -3'
(R):5'- GGTCACTTAGGACGATTTTTACC -3'
|
Posted On |
2022-10-06 |