Incidental Mutation 'R0532:Btaf1'
ID |
163264 |
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 |
038724-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.967)
|
Stock # |
R0532 (G1)
|
Quality Score |
53 |
Status
|
Validated
|
Chromosome |
19 |
Chromosomal Location |
36903479-36990152 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
T to C
at 36928586 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000097093
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099494]
|
AlphaFold |
E9QAE3 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000099494
|
SMART Domains |
Protein: ENSMUSP00000097093 Gene: ENSMUSG00000040565
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: 99.2%
- 3x: 98.4%
- 10x: 96.5%
- 20x: 93.2%
|
Validation Efficiency |
100% (90/90) |
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: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
A |
T |
18: 6,638,618 (GRCm39) |
E339V |
possibly damaging |
Het |
9230009I02Rik |
A |
T |
11: 50,982,405 (GRCm39) |
|
noncoding transcript |
Het |
9230112D13Rik |
A |
T |
14: 34,234,054 (GRCm39) |
I79K |
unknown |
Het |
Adam25 |
C |
T |
8: 41,208,987 (GRCm39) |
T751I |
probably benign |
Het |
Adgrv1 |
C |
A |
13: 81,727,015 (GRCm39) |
V446L |
probably damaging |
Het |
Afap1 |
C |
A |
5: 36,125,944 (GRCm39) |
A313D |
possibly damaging |
Het |
Akap6 |
A |
G |
12: 52,934,766 (GRCm39) |
T753A |
probably benign |
Het |
Aldh16a1 |
G |
T |
7: 44,792,262 (GRCm39) |
T730N |
probably damaging |
Het |
Amfr |
A |
T |
8: 94,725,736 (GRCm39) |
M215K |
probably damaging |
Het |
Apob |
A |
G |
12: 8,066,188 (GRCm39) |
R4386G |
possibly damaging |
Het |
Arhgap45 |
A |
T |
10: 79,857,917 (GRCm39) |
M217L |
possibly damaging |
Het |
Baiap2l2 |
C |
T |
15: 79,168,276 (GRCm39) |
E49K |
possibly damaging |
Het |
Baz1a |
C |
T |
12: 54,981,605 (GRCm39) |
E350K |
possibly damaging |
Het |
Bbx |
A |
T |
16: 50,086,647 (GRCm39) |
V83D |
probably damaging |
Het |
Cacna2d1 |
G |
A |
5: 16,567,271 (GRCm39) |
E942K |
probably benign |
Het |
Cad |
T |
C |
5: 31,219,531 (GRCm39) |
|
probably benign |
Het |
Ccdc96 |
A |
G |
5: 36,643,710 (GRCm39) |
K572R |
probably benign |
Het |
Cdc5l |
G |
A |
17: 45,726,610 (GRCm39) |
R321W |
probably damaging |
Het |
Cep164 |
G |
A |
9: 45,721,124 (GRCm39) |
R93* |
probably null |
Het |
Cir1 |
A |
G |
2: 73,140,799 (GRCm39) |
|
probably null |
Het |
Crocc |
A |
G |
4: 140,757,558 (GRCm39) |
S912P |
possibly damaging |
Het |
Cwf19l2 |
T |
C |
9: 3,431,057 (GRCm39) |
L463P |
probably benign |
Het |
Cyp3a59 |
C |
T |
5: 146,033,463 (GRCm39) |
Q200* |
probably null |
Het |
Cyp4b1 |
G |
T |
4: 115,484,073 (GRCm39) |
P303T |
probably damaging |
Het |
Dcbld1 |
C |
A |
10: 52,193,173 (GRCm39) |
T306K |
probably benign |
Het |
Dgat2 |
A |
G |
7: 98,818,988 (GRCm39) |
V56A |
possibly damaging |
Het |
Dnajc16 |
A |
C |
4: 141,516,320 (GRCm39) |
L16R |
probably damaging |
Het |
Dnmt1 |
A |
C |
9: 20,829,852 (GRCm39) |
|
probably benign |
Het |
Dus3l |
A |
G |
17: 57,076,308 (GRCm39) |
I528V |
probably damaging |
Het |
Egflam |
T |
C |
15: 7,263,718 (GRCm39) |
D744G |
probably benign |
Het |
Epb41 |
A |
C |
4: 131,706,106 (GRCm39) |
|
probably benign |
Het |
Eri2 |
C |
T |
7: 119,385,206 (GRCm39) |
V432I |
probably benign |
Het |
Esyt2 |
A |
G |
12: 116,320,818 (GRCm39) |
|
probably benign |
Het |
Extl3 |
A |
T |
14: 65,315,122 (GRCm39) |
M20K |
probably benign |
Het |
Fam32a |
A |
G |
8: 72,976,063 (GRCm39) |
Y103C |
probably damaging |
Het |
Fat4 |
T |
C |
3: 39,035,870 (GRCm39) |
V3174A |
probably benign |
Het |
Fbxo40 |
T |
A |
16: 36,789,984 (GRCm39) |
E375D |
possibly damaging |
Het |
Frrs1 |
A |
G |
3: 116,676,813 (GRCm39) |
T182A |
probably benign |
Het |
Fry |
A |
G |
5: 150,357,172 (GRCm39) |
|
probably benign |
Het |
Fry |
T |
C |
5: 150,402,226 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,808,129 (GRCm39) |
I1483V |
probably benign |
Het |
Glra3 |
T |
A |
8: 56,578,111 (GRCm39) |
D389E |
probably benign |
Het |
Gpr3 |
A |
T |
4: 132,937,796 (GRCm39) |
I292N |
probably damaging |
Het |
Grina |
T |
C |
15: 76,133,045 (GRCm39) |
M230T |
probably damaging |
Het |
Igkv11-125 |
G |
A |
6: 67,890,603 (GRCm39) |
W16* |
probably null |
Het |
Il18r1 |
T |
C |
1: 40,514,061 (GRCm39) |
V89A |
probably damaging |
Het |
Ino80 |
T |
C |
2: 119,212,464 (GRCm39) |
E1286G |
possibly damaging |
Het |
Iqch |
G |
A |
9: 63,415,514 (GRCm39) |
|
probably benign |
Het |
Itpr2 |
G |
T |
6: 146,013,898 (GRCm39) |
Q2666K |
probably damaging |
Het |
Kcnh3 |
A |
G |
15: 99,130,844 (GRCm39) |
D487G |
probably damaging |
Het |
Kdm1a |
A |
G |
4: 136,288,377 (GRCm39) |
L402P |
probably damaging |
Het |
Klhl10 |
T |
G |
11: 100,337,937 (GRCm39) |
|
probably benign |
Het |
Krt39 |
T |
C |
11: 99,405,617 (GRCm39) |
T428A |
possibly damaging |
Het |
Mapk3 |
G |
A |
7: 126,362,558 (GRCm39) |
|
probably benign |
Het |
Med13l |
T |
A |
5: 118,897,188 (GRCm39) |
S2089T |
possibly damaging |
Het |
Mex3c |
G |
A |
18: 73,723,124 (GRCm39) |
D406N |
possibly damaging |
Het |
Mki67 |
G |
A |
7: 135,299,893 (GRCm39) |
R1714* |
probably null |
Het |
Mmp9 |
C |
A |
2: 164,791,740 (GRCm39) |
S211* |
probably null |
Het |
Nat8f2 |
G |
T |
6: 85,844,784 (GRCm39) |
Q193K |
probably benign |
Het |
Omt2a |
C |
A |
9: 78,220,187 (GRCm39) |
A71S |
possibly damaging |
Het |
Or10ak11 |
T |
G |
4: 118,686,897 (GRCm39) |
T247P |
probably damaging |
Het |
Or5ac22 |
T |
C |
16: 59,134,964 (GRCm39) |
K269E |
probably benign |
Het |
Pdgfra |
G |
A |
5: 75,331,434 (GRCm39) |
V315I |
probably benign |
Het |
Pdgfrb |
A |
G |
18: 61,216,337 (GRCm39) |
D1065G |
probably damaging |
Het |
Pfas |
A |
T |
11: 68,893,455 (GRCm39) |
|
probably benign |
Het |
Pramel5 |
T |
C |
4: 143,999,310 (GRCm39) |
E259G |
probably benign |
Het |
Prpf6 |
A |
G |
2: 181,264,004 (GRCm39) |
Y222C |
possibly damaging |
Het |
Rbck1 |
C |
A |
2: 152,166,250 (GRCm39) |
Q229H |
probably damaging |
Het |
Rdm1 |
T |
A |
11: 101,526,661 (GRCm39) |
C278S |
probably benign |
Het |
Sall1 |
T |
C |
8: 89,759,819 (GRCm39) |
D95G |
probably benign |
Het |
Scn1a |
T |
A |
2: 66,148,167 (GRCm39) |
D1126V |
probably damaging |
Het |
Scn4a |
C |
T |
11: 106,221,226 (GRCm39) |
G811D |
probably benign |
Het |
Sh2b1 |
A |
G |
7: 126,071,444 (GRCm39) |
I247T |
probably benign |
Het |
Shprh |
C |
A |
10: 11,038,556 (GRCm39) |
T437K |
possibly damaging |
Het |
Slc13a4 |
A |
T |
6: 35,264,339 (GRCm39) |
|
probably null |
Het |
Slc16a1 |
C |
A |
3: 104,560,734 (GRCm39) |
Y346* |
probably null |
Het |
Slc25a38 |
G |
T |
9: 119,949,772 (GRCm39) |
A163S |
probably damaging |
Het |
Slc6a12 |
G |
A |
6: 121,333,877 (GRCm39) |
V238I |
probably damaging |
Het |
Slc8b1 |
C |
A |
5: 120,657,736 (GRCm39) |
D66E |
probably damaging |
Het |
Snapin |
A |
G |
3: 90,396,893 (GRCm39) |
L106P |
probably damaging |
Het |
Tas2r122 |
G |
A |
6: 132,688,791 (GRCm39) |
S34F |
possibly damaging |
Het |
Tiam2 |
A |
G |
17: 3,471,921 (GRCm39) |
K521R |
probably damaging |
Het |
Tmem81 |
C |
G |
1: 132,435,567 (GRCm39) |
I124M |
probably damaging |
Het |
Ttc3 |
T |
C |
16: 94,188,189 (GRCm39) |
|
probably benign |
Het |
Uba1y |
T |
C |
Y: 820,911 (GRCm39) |
F31L |
probably benign |
Het |
Ucp3 |
A |
G |
7: 100,131,186 (GRCm39) |
|
probably benign |
Het |
Vcan |
T |
C |
13: 89,851,891 (GRCm39) |
E1023G |
probably damaging |
Het |
Vmn2r45 |
A |
G |
7: 8,474,820 (GRCm39) |
I736T |
probably damaging |
Het |
Vps36 |
T |
C |
8: 22,708,261 (GRCm39) |
F342L |
probably benign |
Het |
Zc3hc1 |
A |
G |
6: 30,374,929 (GRCm39) |
|
probably benign |
Het |
Zmym4 |
G |
A |
4: 126,792,194 (GRCm39) |
Q596* |
probably null |
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 |
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 |
|
R9717:Btaf1
|
UTSW |
19 |
36,922,646 (GRCm39) |
missense |
probably benign |
0.28 |
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'- ACTCATGCTGTAACCCTGGAGGTC -3'
(R):5'- GCAGCTTTAGAACAAGCACTGTTGG -3'
Sequencing Primer
(F):5'- GCAGGTAACACTATGCCATGTTC -3'
(R):5'- ACAAGCACTGTTGGTCACTTTG -3'
|
Posted On |
2014-03-19 |