Incidental Mutation 'R9746:Baz1a'
ID |
732148 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Baz1a
|
Ensembl Gene |
ENSMUSG00000035021 |
Gene Name |
bromodomain adjacent to zinc finger domain 1A |
Synonyms |
Gtl5, Wcrf180, Acf1 |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R9746 (G1)
|
Quality Score |
217.468 |
Status
|
Not validated
|
Chromosome |
12 |
Chromosomal Location |
54939774-55061133 bp(-) (GRCm39) |
Type of Mutation |
frame shift |
DNA Base Change (assembly) |
CCATT to CCATTCATT
at 55021895 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000134384
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000038926]
[ENSMUST00000172875]
[ENSMUST00000173177]
[ENSMUST00000173433]
[ENSMUST00000173529]
|
AlphaFold |
O88379 |
Predicted Effect |
probably null
Transcript: ENSMUST00000038926
|
SMART Domains |
Protein: ENSMUSP00000039757 Gene: ENSMUSG00000035021
Domain | Start | End | E-Value | Type |
Pfam:WAC_Acf1_DNA_bd
|
23 |
122 |
4.4e-36 |
PFAM |
low complexity region
|
164 |
175 |
N/A |
INTRINSIC |
coiled coil region
|
312 |
397 |
N/A |
INTRINSIC |
Pfam:DDT
|
423 |
485 |
2.3e-14 |
PFAM |
low complexity region
|
519 |
530 |
N/A |
INTRINSIC |
Pfam:WHIM1
|
593 |
641 |
1.5e-8 |
PFAM |
low complexity region
|
658 |
696 |
N/A |
INTRINSIC |
low complexity region
|
725 |
738 |
N/A |
INTRINSIC |
low complexity region
|
774 |
796 |
N/A |
INTRINSIC |
low complexity region
|
861 |
873 |
N/A |
INTRINSIC |
Pfam:WHIM3
|
894 |
932 |
2e-16 |
PFAM |
low complexity region
|
1058 |
1073 |
N/A |
INTRINSIC |
PHD
|
1151 |
1197 |
9.46e-15 |
SMART |
RING
|
1152 |
1196 |
6.88e-1 |
SMART |
low complexity region
|
1214 |
1257 |
N/A |
INTRINSIC |
BROMO
|
1426 |
1534 |
2.18e-31 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000172875
|
SMART Domains |
Protein: ENSMUSP00000134384 Gene: ENSMUSG00000035021
Domain | Start | End | E-Value | Type |
Pfam:WAC_Acf1_DNA_bd
|
22 |
122 |
3e-39 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000173177
|
SMART Domains |
Protein: ENSMUSP00000133796 Gene: ENSMUSG00000035021
Domain | Start | End | E-Value | Type |
Pfam:WAC_Acf1_DNA_bd
|
22 |
86 |
5.2e-27 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000173433
|
SMART Domains |
Protein: ENSMUSP00000133478 Gene: ENSMUSG00000035021
Domain | Start | End | E-Value | Type |
Pfam:WAC_Acf1_DNA_bd
|
22 |
122 |
1.1e-37 |
PFAM |
low complexity region
|
164 |
175 |
N/A |
INTRINSIC |
coiled coil region
|
312 |
397 |
N/A |
INTRINSIC |
DDT
|
422 |
487 |
1.54e-19 |
SMART |
low complexity region
|
518 |
529 |
N/A |
INTRINSIC |
Pfam:WHIM1
|
592 |
640 |
1.8e-8 |
PFAM |
low complexity region
|
657 |
695 |
N/A |
INTRINSIC |
low complexity region
|
722 |
735 |
N/A |
INTRINSIC |
low complexity region
|
771 |
793 |
N/A |
INTRINSIC |
low complexity region
|
858 |
870 |
N/A |
INTRINSIC |
low complexity region
|
1055 |
1070 |
N/A |
INTRINSIC |
PHD
|
1148 |
1194 |
9.46e-15 |
SMART |
RING
|
1149 |
1193 |
6.88e-1 |
SMART |
low complexity region
|
1211 |
1254 |
N/A |
INTRINSIC |
BROMO
|
1423 |
1531 |
2.18e-31 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000173529
|
SMART Domains |
Protein: ENSMUSP00000134445 Gene: ENSMUSG00000035021
Domain | Start | End | E-Value | Type |
Pfam:WAC_Acf1_DNA_bd
|
22 |
82 |
7.5e-26 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.7%
- 10x: 99.2%
- 20x: 98.2%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The BAZ1A gene encodes the accessory subunit of the ATP-dependent chromatin assembly factor (ACF), a member of the ISWI ('imitation switch') family of chromatin remodeling complexes (summarized by Racki et al., 2009 [PubMed 20033039]).[supplied by OMIM, Apr 2010] PHENOTYPE: Mice homozygous for a knock-out allele are viable and able to repair meiotic double-strand breaks but exhibit teratospermia, oligospermia, asthenospermia, and male infertility due to impaired spermiogenesis. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr1 |
T |
A |
1: 173,159,598 (GRCm39) |
H307L |
probably benign |
Het |
Acnat1 |
A |
T |
4: 49,450,652 (GRCm39) |
L153H |
probably damaging |
Het |
Actn4 |
A |
T |
7: 28,618,431 (GRCm39) |
D76E |
probably benign |
Het |
Afdn |
A |
C |
17: 14,066,782 (GRCm39) |
M640L |
probably benign |
Het |
Angpt1 |
A |
T |
15: 42,539,837 (GRCm39) |
F7L |
probably benign |
Het |
Ap3b2 |
A |
G |
7: 81,126,092 (GRCm39) |
F373S |
probably damaging |
Het |
Armc2 |
T |
A |
10: 41,800,457 (GRCm39) |
Y650F |
probably damaging |
Het |
Atg2b |
G |
T |
12: 105,630,197 (GRCm39) |
T398K |
possibly damaging |
Het |
Capn8 |
G |
A |
1: 182,438,670 (GRCm39) |
|
probably null |
Het |
Cdr1 |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
X: 60,228,130 (GRCm39) |
|
probably benign |
Het |
Cfap54 |
T |
C |
10: 92,637,081 (GRCm39) |
N3103D |
probably benign |
Het |
Chd9 |
G |
A |
8: 91,738,063 (GRCm39) |
R1565Q |
unknown |
Het |
Cir1 |
G |
A |
2: 73,134,152 (GRCm39) |
T139I |
probably damaging |
Het |
Cmah |
T |
C |
13: 24,619,673 (GRCm39) |
|
probably null |
Het |
Cnpy1 |
T |
C |
5: 28,450,800 (GRCm39) |
D2G |
probably damaging |
Het |
Dennd4a |
A |
T |
9: 64,801,793 (GRCm39) |
T979S |
probably benign |
Het |
Dnah11 |
T |
A |
12: 117,842,311 (GRCm39) |
K4423* |
probably null |
Het |
Dnajb4 |
A |
G |
3: 151,892,320 (GRCm39) |
I171T |
possibly damaging |
Het |
Dpm1 |
A |
T |
2: 168,072,307 (GRCm39) |
|
probably null |
Het |
Dtwd1 |
A |
G |
2: 125,996,595 (GRCm39) |
T27A |
probably benign |
Het |
Ep400 |
C |
T |
5: 110,889,872 (GRCm39) |
D464N |
unknown |
Het |
Epb42 |
A |
T |
2: 120,855,091 (GRCm39) |
I498N |
probably benign |
Het |
Fhod1 |
A |
G |
8: 106,064,048 (GRCm39) |
V219A |
unknown |
Het |
Gabrb2 |
A |
T |
11: 42,517,436 (GRCm39) |
E419D |
probably benign |
Het |
Galnt18 |
A |
T |
7: 111,071,168 (GRCm39) |
N615K |
possibly damaging |
Het |
Gm29106 |
T |
A |
1: 118,127,254 (GRCm39) |
H315Q |
possibly damaging |
Het |
Gprin2 |
G |
T |
14: 33,917,615 (GRCm39) |
Q52K |
probably benign |
Het |
Grm4 |
A |
T |
17: 27,657,765 (GRCm39) |
Y414N |
probably damaging |
Het |
Gulo |
C |
A |
14: 66,225,630 (GRCm39) |
|
probably null |
Het |
H2-M1 |
A |
C |
17: 36,980,997 (GRCm39) |
V313G |
possibly damaging |
Het |
Hectd3 |
T |
C |
4: 116,852,951 (GRCm39) |
W118R |
probably damaging |
Het |
Hs6st3 |
G |
A |
14: 120,106,492 (GRCm39) |
C300Y |
probably damaging |
Het |
Il1rl2 |
T |
A |
1: 40,404,519 (GRCm39) |
S547T |
possibly damaging |
Het |
Kank1 |
G |
T |
19: 25,386,872 (GRCm39) |
V182F |
probably damaging |
Het |
Kif20b |
T |
A |
19: 34,928,149 (GRCm39) |
L1137* |
probably null |
Het |
Klhl7 |
A |
G |
5: 24,331,818 (GRCm39) |
|
probably null |
Het |
Krt13 |
T |
A |
11: 100,011,987 (GRCm39) |
D112V |
possibly damaging |
Het |
Ltbr |
A |
G |
6: 125,290,064 (GRCm39) |
V71A |
probably benign |
Het |
Ly6g |
T |
C |
15: 75,030,458 (GRCm39) |
V92A |
probably benign |
Het |
Map2k3 |
G |
A |
11: 60,822,929 (GRCm39) |
|
probably benign |
Het |
Mast2 |
A |
C |
4: 116,168,927 (GRCm39) |
D842E |
probably benign |
Het |
Mpo |
T |
G |
11: 87,694,349 (GRCm39) |
M693R |
probably benign |
Het |
Myo15a |
C |
A |
11: 60,378,234 (GRCm39) |
S212* |
probably null |
Het |
Nadk2 |
C |
T |
15: 9,106,824 (GRCm39) |
R37* |
probably null |
Het |
Ncapd3 |
G |
A |
9: 26,974,655 (GRCm39) |
R709H |
probably benign |
Het |
Nck2 |
T |
A |
1: 43,572,892 (GRCm39) |
Y55* |
probably null |
Het |
Neurl4 |
A |
G |
11: 69,798,301 (GRCm39) |
D777G |
probably damaging |
Het |
Npr2 |
G |
A |
4: 43,633,527 (GRCm39) |
V224M |
possibly damaging |
Het |
Nptx2 |
T |
A |
5: 144,484,950 (GRCm39) |
S148T |
probably benign |
Het |
Nr1d1 |
T |
C |
11: 98,661,160 (GRCm39) |
T369A |
probably benign |
Het |
Nub1 |
T |
G |
5: 24,908,483 (GRCm39) |
F411V |
probably damaging |
Het |
Nup188 |
T |
A |
2: 30,194,300 (GRCm39) |
Y158N |
probably damaging |
Het |
Or2d36 |
A |
T |
7: 106,746,660 (GRCm39) |
I46F |
probably benign |
Het |
Or5e1 |
A |
G |
7: 108,354,639 (GRCm39) |
N192S |
probably benign |
Het |
Or5m8 |
A |
G |
2: 85,823,091 (GRCm39) |
Y310C |
probably benign |
Het |
Or6c6c |
A |
T |
10: 129,541,208 (GRCm39) |
I154F |
probably damaging |
Het |
Or8c19-ps1 |
T |
A |
9: 38,220,928 (GRCm39) |
I279K |
unknown |
Het |
Orc2 |
C |
T |
1: 58,536,610 (GRCm39) |
G85S |
probably damaging |
Het |
Pak1ip1 |
T |
A |
13: 41,162,743 (GRCm39) |
V182D |
probably damaging |
Het |
Parvg |
T |
G |
15: 84,210,424 (GRCm39) |
C30W |
probably benign |
Het |
Pcdha1 |
T |
A |
18: 37,065,713 (GRCm39) |
D792E |
probably benign |
Het |
Ppp1r13b |
G |
T |
12: 111,800,242 (GRCm39) |
Q635K |
probably benign |
Het |
Pramel26 |
T |
C |
4: 143,536,886 (GRCm39) |
T482A |
probably benign |
Het |
Psg16 |
A |
G |
7: 16,832,086 (GRCm39) |
I341V |
probably benign |
Het |
Psme4 |
C |
T |
11: 30,826,868 (GRCm39) |
Q1796* |
probably null |
Het |
Ptn |
T |
G |
6: 36,692,699 (GRCm39) |
|
probably null |
Het |
Rapsn |
C |
T |
2: 90,875,823 (GRCm39) |
P400L |
probably damaging |
Het |
Rasal1 |
G |
A |
5: 120,800,358 (GRCm39) |
G207D |
probably damaging |
Het |
Rdx |
A |
G |
9: 51,974,878 (GRCm39) |
I5V |
probably benign |
Het |
Rpf1 |
A |
G |
3: 146,223,533 (GRCm39) |
I105T |
probably damaging |
Het |
Rps15a |
A |
T |
7: 117,709,220 (GRCm39) |
F79I |
possibly damaging |
Het |
Rwdd2b |
G |
A |
16: 87,233,641 (GRCm39) |
P153L |
probably benign |
Het |
Scaf11 |
G |
A |
15: 96,318,298 (GRCm39) |
S422L |
probably damaging |
Het |
Serpinb3b |
T |
A |
1: 107,082,403 (GRCm39) |
E287V |
possibly damaging |
Het |
Sgta |
T |
C |
10: 80,887,118 (GRCm39) |
D49G |
possibly damaging |
Het |
Sin3a |
T |
A |
9: 57,025,358 (GRCm39) |
M1068K |
probably benign |
Het |
Slc12a9 |
G |
A |
5: 137,319,671 (GRCm39) |
R615W |
probably damaging |
Het |
Slc26a3 |
T |
A |
12: 31,499,145 (GRCm39) |
S151T |
probably benign |
Het |
Slc4a8 |
C |
A |
15: 100,681,721 (GRCm39) |
H111N |
probably damaging |
Het |
Syngr1 |
G |
A |
15: 79,975,659 (GRCm39) |
R22K |
probably benign |
Het |
Tars2 |
A |
T |
3: 95,662,077 (GRCm39) |
V25E |
probably benign |
Het |
Tbx15 |
A |
G |
3: 99,259,647 (GRCm39) |
Y506C |
probably damaging |
Het |
Tgm4 |
A |
T |
9: 122,875,634 (GRCm39) |
K162N |
possibly damaging |
Het |
Tmem253 |
A |
G |
14: 52,255,439 (GRCm39) |
E83G |
probably damaging |
Het |
Trp73 |
G |
A |
4: 154,165,859 (GRCm39) |
T118I |
probably damaging |
Het |
Trpm7 |
A |
G |
2: 126,664,578 (GRCm39) |
S934P |
possibly damaging |
Het |
Ttc23l |
G |
A |
15: 10,523,729 (GRCm39) |
S330L |
probably benign |
Het |
Tub |
A |
C |
7: 108,624,845 (GRCm39) |
D199A |
probably benign |
Het |
Uri1 |
A |
C |
7: 37,696,110 (GRCm39) |
|
probably null |
Het |
Usp16 |
C |
T |
16: 87,276,120 (GRCm39) |
A486V |
probably benign |
Het |
Vmn1r12 |
A |
G |
6: 57,136,526 (GRCm39) |
I208V |
probably benign |
Het |
Vmn2r116 |
A |
T |
17: 23,620,797 (GRCm39) |
M844L |
probably benign |
Het |
Vmn2r13 |
C |
T |
5: 109,339,773 (GRCm39) |
|
probably null |
Het |
Xpnpep1 |
T |
C |
19: 53,001,892 (GRCm39) |
D118G |
probably damaging |
Het |
Zfp111 |
G |
A |
7: 23,898,067 (GRCm39) |
P516S |
possibly damaging |
Het |
|
Other mutations in Baz1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01108:Baz1a
|
APN |
12 |
54,963,516 (GRCm39) |
missense |
probably benign |
|
IGL01138:Baz1a
|
APN |
12 |
54,977,110 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01298:Baz1a
|
APN |
12 |
55,001,594 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02639:Baz1a
|
APN |
12 |
54,942,810 (GRCm39) |
splice site |
probably benign |
|
IGL02995:Baz1a
|
APN |
12 |
54,947,232 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03001:Baz1a
|
APN |
12 |
54,969,896 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL03104:Baz1a
|
APN |
12 |
54,941,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03135:Baz1a
|
APN |
12 |
54,976,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03151:Baz1a
|
APN |
12 |
54,955,934 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03235:Baz1a
|
APN |
12 |
54,945,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03240:Baz1a
|
APN |
12 |
54,974,352 (GRCm39) |
nonsense |
probably null |
|
Bezos
|
UTSW |
12 |
54,941,816 (GRCm39) |
nonsense |
probably null |
|
Flavia
|
UTSW |
12 |
55,022,093 (GRCm39) |
missense |
probably damaging |
1.00 |
gumdrops
|
UTSW |
12 |
54,947,233 (GRCm39) |
missense |
probably damaging |
1.00 |
Kilter
|
UTSW |
12 |
54,947,317 (GRCm39) |
missense |
probably damaging |
0.99 |
Kisses
|
UTSW |
12 |
55,021,922 (GRCm39) |
missense |
probably damaging |
1.00 |
liverlips
|
UTSW |
12 |
54,967,928 (GRCm39) |
missense |
possibly damaging |
0.68 |
smooch
|
UTSW |
12 |
54,963,608 (GRCm39) |
missense |
probably damaging |
1.00 |
Smootch
|
UTSW |
12 |
54,958,170 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4458001:Baz1a
|
UTSW |
12 |
54,977,095 (GRCm39) |
missense |
probably benign |
0.03 |
R0127:Baz1a
|
UTSW |
12 |
54,945,491 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0183:Baz1a
|
UTSW |
12 |
54,958,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R0393:Baz1a
|
UTSW |
12 |
54,965,221 (GRCm39) |
critical splice donor site |
probably null |
|
R0532:Baz1a
|
UTSW |
12 |
54,981,605 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0614:Baz1a
|
UTSW |
12 |
54,988,304 (GRCm39) |
nonsense |
probably null |
|
R0626:Baz1a
|
UTSW |
12 |
55,022,055 (GRCm39) |
missense |
probably damaging |
0.99 |
R0654:Baz1a
|
UTSW |
12 |
54,958,182 (GRCm39) |
missense |
probably benign |
0.01 |
R0782:Baz1a
|
UTSW |
12 |
54,941,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0826:Baz1a
|
UTSW |
12 |
54,977,097 (GRCm39) |
nonsense |
probably null |
|
R0855:Baz1a
|
UTSW |
12 |
54,947,348 (GRCm39) |
splice site |
probably benign |
|
R0927:Baz1a
|
UTSW |
12 |
54,941,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R0941:Baz1a
|
UTSW |
12 |
54,945,216 (GRCm39) |
missense |
probably benign |
0.00 |
R1079:Baz1a
|
UTSW |
12 |
54,941,785 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1157:Baz1a
|
UTSW |
12 |
54,976,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Baz1a
|
UTSW |
12 |
55,021,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R1731:Baz1a
|
UTSW |
12 |
54,965,330 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1739:Baz1a
|
UTSW |
12 |
54,945,573 (GRCm39) |
nonsense |
probably null |
|
R1762:Baz1a
|
UTSW |
12 |
54,955,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R1770:Baz1a
|
UTSW |
12 |
54,945,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Baz1a
|
UTSW |
12 |
54,947,122 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2037:Baz1a
|
UTSW |
12 |
54,976,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Baz1a
|
UTSW |
12 |
54,958,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R2215:Baz1a
|
UTSW |
12 |
55,022,154 (GRCm39) |
nonsense |
probably null |
|
R2282:Baz1a
|
UTSW |
12 |
54,963,597 (GRCm39) |
nonsense |
probably null |
|
R2875:Baz1a
|
UTSW |
12 |
54,969,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R2890:Baz1a
|
UTSW |
12 |
54,945,302 (GRCm39) |
missense |
probably benign |
|
R2971:Baz1a
|
UTSW |
12 |
54,970,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R3404:Baz1a
|
UTSW |
12 |
54,963,774 (GRCm39) |
missense |
probably benign |
0.00 |
R3419:Baz1a
|
UTSW |
12 |
54,993,684 (GRCm39) |
missense |
probably benign |
0.05 |
R3699:Baz1a
|
UTSW |
12 |
54,963,831 (GRCm39) |
missense |
probably benign |
0.09 |
R3899:Baz1a
|
UTSW |
12 |
54,981,589 (GRCm39) |
missense |
probably benign |
0.01 |
R3927:Baz1a
|
UTSW |
12 |
54,967,928 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4050:Baz1a
|
UTSW |
12 |
54,976,404 (GRCm39) |
missense |
probably benign |
0.00 |
R4072:Baz1a
|
UTSW |
12 |
54,988,345 (GRCm39) |
missense |
probably benign |
0.18 |
R4196:Baz1a
|
UTSW |
12 |
54,958,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R4289:Baz1a
|
UTSW |
12 |
54,947,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R4455:Baz1a
|
UTSW |
12 |
54,958,153 (GRCm39) |
missense |
probably benign |
0.26 |
R4583:Baz1a
|
UTSW |
12 |
54,969,325 (GRCm39) |
missense |
probably damaging |
0.99 |
R4622:Baz1a
|
UTSW |
12 |
54,988,300 (GRCm39) |
missense |
probably benign |
0.00 |
R4807:Baz1a
|
UTSW |
12 |
54,945,267 (GRCm39) |
missense |
probably benign |
0.28 |
R4998:Baz1a
|
UTSW |
12 |
55,021,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R5239:Baz1a
|
UTSW |
12 |
54,945,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R5379:Baz1a
|
UTSW |
12 |
54,941,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R5408:Baz1a
|
UTSW |
12 |
54,969,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R5678:Baz1a
|
UTSW |
12 |
54,947,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R5810:Baz1a
|
UTSW |
12 |
54,974,500 (GRCm39) |
intron |
probably benign |
|
R6092:Baz1a
|
UTSW |
12 |
54,955,868 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6317:Baz1a
|
UTSW |
12 |
55,001,585 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6332:Baz1a
|
UTSW |
12 |
54,965,339 (GRCm39) |
missense |
probably benign |
0.01 |
R6803:Baz1a
|
UTSW |
12 |
54,988,340 (GRCm39) |
missense |
probably null |
0.99 |
R7185:Baz1a
|
UTSW |
12 |
55,022,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R7248:Baz1a
|
UTSW |
12 |
54,947,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R7392:Baz1a
|
UTSW |
12 |
54,945,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R8009:Baz1a
|
UTSW |
12 |
54,941,816 (GRCm39) |
nonsense |
probably null |
|
R8025:Baz1a
|
UTSW |
12 |
54,955,921 (GRCm39) |
missense |
probably benign |
0.34 |
R8392:Baz1a
|
UTSW |
12 |
54,969,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R8862:Baz1a
|
UTSW |
12 |
55,032,624 (GRCm39) |
unclassified |
probably benign |
|
R8949:Baz1a
|
UTSW |
12 |
54,941,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R9340:Baz1a
|
UTSW |
12 |
54,963,372 (GRCm39) |
missense |
probably damaging |
0.97 |
R9389:Baz1a
|
UTSW |
12 |
54,963,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R9401:Baz1a
|
UTSW |
12 |
54,963,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R9666:Baz1a
|
UTSW |
12 |
54,988,345 (GRCm39) |
missense |
probably benign |
0.18 |
R9722:Baz1a
|
UTSW |
12 |
54,946,882 (GRCm39) |
missense |
probably benign |
0.43 |
|
Predicted Primers |
PCR Primer
(F):5'- AGGAAAGGTTTCATCACATCTCC -3'
(R):5'- GTATCAGGAAGCTCTTGAATCCG -3'
Sequencing Primer
(F):5'- GAAAGGTTTCATCACATCTCCTTTTC -3'
(R):5'- GCTCTTGAATCCGAAAGAAAAGC -3'
|
Posted On |
2022-11-14 |