Incidental Mutation 'R7241:Anks1b'
ID |
563218 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Anks1b
|
Ensembl Gene |
ENSMUSG00000058589 |
Gene Name |
ankyrin repeat and sterile alpha motif domain containing 1B |
Synonyms |
C030032C09Rik, Gm10937, AIDA-1b, LOC380650, E530015N03Rik |
MMRRC Submission |
045348-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7241 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
10 |
Chromosomal Location |
89709371-90809162 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to G
at 90348699 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Serine
at position 789
(I789S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000138539
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099368]
[ENSMUST00000182907]
[ENSMUST00000182936]
[ENSMUST00000183156]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000099368
AA Change: I789S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000096968 Gene: ENSMUSG00000058589 AA Change: I789S
Domain | Start | End | E-Value | Type |
low complexity region
|
21 |
46 |
N/A |
INTRINSIC |
ANK
|
58 |
87 |
1.88e-5 |
SMART |
ANK
|
91 |
123 |
3.13e-2 |
SMART |
ANK
|
127 |
156 |
6.92e-4 |
SMART |
ANK
|
160 |
189 |
3.08e-1 |
SMART |
ANK
|
193 |
222 |
1.43e-5 |
SMART |
ANK
|
225 |
254 |
4.75e-2 |
SMART |
low complexity region
|
498 |
513 |
N/A |
INTRINSIC |
low complexity region
|
551 |
577 |
N/A |
INTRINSIC |
low complexity region
|
659 |
670 |
N/A |
INTRINSIC |
SAM
|
806 |
875 |
2.06e-19 |
SMART |
SAM
|
880 |
931 |
4.44e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000182907
|
SMART Domains |
Protein: ENSMUSP00000138614 Gene: ENSMUSG00000058589
Domain | Start | End | E-Value | Type |
low complexity region
|
21 |
45 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000182936
|
SMART Domains |
Protein: ENSMUSP00000138209 Gene: ENSMUSG00000058589
Domain | Start | End | E-Value | Type |
low complexity region
|
21 |
46 |
N/A |
INTRINSIC |
ANK
|
58 |
87 |
1.88e-5 |
SMART |
ANK
|
91 |
123 |
3.13e-2 |
SMART |
ANK
|
127 |
156 |
6.92e-4 |
SMART |
ANK
|
160 |
189 |
3.08e-1 |
SMART |
ANK
|
193 |
222 |
1.43e-5 |
SMART |
ANK
|
225 |
254 |
5.03e2 |
SMART |
low complexity region
|
464 |
479 |
N/A |
INTRINSIC |
low complexity region
|
517 |
543 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000183156
AA Change: I789S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000138539 Gene: ENSMUSG00000058589 AA Change: I789S
Domain | Start | End | E-Value | Type |
low complexity region
|
21 |
46 |
N/A |
INTRINSIC |
ANK
|
58 |
87 |
1.88e-5 |
SMART |
ANK
|
91 |
123 |
3.13e-2 |
SMART |
ANK
|
127 |
156 |
6.92e-4 |
SMART |
ANK
|
160 |
189 |
3.08e-1 |
SMART |
ANK
|
193 |
222 |
1.43e-5 |
SMART |
ANK
|
225 |
254 |
4.75e-2 |
SMART |
low complexity region
|
498 |
513 |
N/A |
INTRINSIC |
low complexity region
|
551 |
577 |
N/A |
INTRINSIC |
low complexity region
|
659 |
670 |
N/A |
INTRINSIC |
SAM
|
806 |
875 |
2.06e-19 |
SMART |
SAM
|
880 |
948 |
5.66e-17 |
SMART |
low complexity region
|
968 |
983 |
N/A |
INTRINSIC |
PTB
|
1056 |
1194 |
2.94e-38 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a multi-domain protein that is predominantly expressed in brain and testis. This protein interacts with amyloid beta protein precursor (AbetaPP) and may have a role in normal brain development, and in the pathogenesis of Alzheimer's disease. Expression of this gene has been shown to be elevated in patients with pre-B cell acute lymphocytic leukemia associated with t(1;19) translocation. Alternatively spliced transcript variants encoding different isoforms (some with different subcellular localization, PMID:15004329) have been described for this gene. [provided by RefSeq, Aug 2011] PHENOTYPE: Mice homozygous for a conditional allele activated in neurons alters hippocampal synaptic transmission. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
G |
7: 119,846,184 (GRCm39) |
T612A |
probably damaging |
Het |
Acacb |
G |
A |
5: 114,383,161 (GRCm39) |
A2115T |
possibly damaging |
Het |
Adam32 |
T |
C |
8: 25,388,510 (GRCm39) |
K398R |
probably benign |
Het |
Adam9 |
T |
A |
8: 25,441,002 (GRCm39) |
I824F |
possibly damaging |
Het |
Ahnak |
A |
G |
19: 8,986,395 (GRCm39) |
I2560V |
possibly damaging |
Het |
Ank3 |
G |
A |
10: 69,542,644 (GRCm39) |
M1I |
probably null |
Het |
Ap2b1 |
T |
A |
11: 83,241,931 (GRCm39) |
N641K |
probably benign |
Het |
Arhgap33 |
A |
G |
7: 30,228,146 (GRCm39) |
L412P |
probably damaging |
Het |
Atp13a3 |
T |
A |
16: 30,171,095 (GRCm39) |
M317L |
possibly damaging |
Het |
B4galt5 |
A |
G |
2: 167,148,617 (GRCm39) |
L167P |
probably damaging |
Het |
Bace2 |
T |
C |
16: 97,237,998 (GRCm39) |
I483T |
possibly damaging |
Het |
C2cd3 |
A |
C |
7: 100,056,257 (GRCm39) |
K177T |
|
Het |
Ccr4 |
T |
C |
9: 114,322,024 (GRCm39) |
T14A |
probably benign |
Het |
Cep250 |
A |
T |
2: 155,833,472 (GRCm39) |
H1799L |
probably benign |
Het |
Cgnl1 |
T |
C |
9: 71,632,052 (GRCm39) |
Q433R |
probably benign |
Het |
Copb1 |
C |
T |
7: 113,836,591 (GRCm39) |
V384M |
probably damaging |
Het |
Cyp2c50 |
T |
A |
19: 40,079,012 (GRCm39) |
N118K |
probably benign |
Het |
Cyp4a32 |
A |
G |
4: 115,459,499 (GRCm39) |
I78V |
probably benign |
Het |
Cyth4 |
A |
G |
15: 78,491,245 (GRCm39) |
K108R |
probably benign |
Het |
Dnah1 |
T |
C |
14: 30,986,896 (GRCm39) |
H3632R |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,542,856 (GRCm39) |
I540V |
probably benign |
Het |
Dock4 |
A |
G |
12: 40,844,859 (GRCm39) |
Y1174C |
probably damaging |
Het |
Drd5 |
A |
G |
5: 38,477,879 (GRCm39) |
T291A |
probably damaging |
Het |
Eeig1 |
A |
G |
2: 32,448,076 (GRCm39) |
R62G |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,148,415 (GRCm39) |
N2611S |
possibly damaging |
Het |
Fcsk |
A |
G |
8: 111,622,529 (GRCm39) |
I133T |
probably benign |
Het |
Fhod3 |
A |
G |
18: 25,193,409 (GRCm39) |
E640G |
probably damaging |
Het |
Flvcr2 |
T |
A |
12: 85,852,013 (GRCm39) |
D522E |
probably benign |
Het |
Ganc |
T |
A |
2: 120,272,010 (GRCm39) |
I556K |
probably damaging |
Het |
Gjc2 |
T |
A |
11: 59,067,960 (GRCm39) |
E174V |
unknown |
Het |
Gzmd |
G |
A |
14: 56,368,799 (GRCm39) |
R32C |
probably damaging |
Het |
Hltf |
T |
A |
3: 20,119,556 (GRCm39) |
H200Q |
probably benign |
Het |
Ift88 |
A |
G |
14: 57,717,454 (GRCm39) |
I559M |
probably damaging |
Het |
Ighv1-62-1 |
C |
A |
12: 115,350,322 (GRCm39) |
C115F |
probably damaging |
Het |
Impdh2 |
A |
G |
9: 108,440,636 (GRCm39) |
N279S |
possibly damaging |
Het |
Itpr1 |
T |
C |
6: 108,494,581 (GRCm39) |
|
probably null |
Het |
Kansl1l |
T |
C |
1: 66,840,787 (GRCm39) |
N171S |
possibly damaging |
Het |
Kif14 |
T |
A |
1: 136,396,491 (GRCm39) |
C266S |
probably benign |
Het |
Kif19b |
A |
G |
5: 140,447,943 (GRCm39) |
T137A |
probably damaging |
Het |
Lrriq1 |
A |
C |
10: 103,051,834 (GRCm39) |
V306G |
probably damaging |
Het |
Mast4 |
G |
A |
13: 103,470,508 (GRCm39) |
R65W |
possibly damaging |
Het |
Mex3d |
T |
C |
10: 80,223,091 (GRCm39) |
D55G |
|
Het |
Mrps27 |
A |
T |
13: 99,547,788 (GRCm39) |
K233* |
probably null |
Het |
Myo1f |
A |
G |
17: 33,798,902 (GRCm39) |
N189S |
probably damaging |
Het |
Nbn |
A |
T |
4: 15,991,190 (GRCm39) |
K729N |
probably benign |
Het |
Or1e35 |
T |
C |
11: 73,798,058 (GRCm39) |
S87G |
probably benign |
Het |
Or8k35 |
C |
A |
2: 86,424,498 (GRCm39) |
V225F |
possibly damaging |
Het |
Pgghg |
T |
C |
7: 140,525,633 (GRCm39) |
S479P |
|
Het |
Plaat5 |
A |
G |
19: 7,591,946 (GRCm39) |
T121A |
probably benign |
Het |
Polr1e |
A |
C |
4: 45,029,340 (GRCm39) |
H315P |
probably damaging |
Het |
Pou6f2 |
A |
G |
13: 18,299,874 (GRCm39) |
V595A |
|
Het |
Prdm15 |
T |
C |
16: 97,596,941 (GRCm39) |
D960G |
possibly damaging |
Het |
Prkcz |
A |
T |
4: 155,353,516 (GRCm39) |
M460K |
probably benign |
Het |
Prkd2 |
G |
T |
7: 16,591,730 (GRCm39) |
R587L |
probably benign |
Het |
Prkn |
C |
A |
17: 12,073,748 (GRCm39) |
N355K |
possibly damaging |
Het |
Rabep1 |
C |
A |
11: 70,830,815 (GRCm39) |
T829N |
probably damaging |
Het |
Rptn |
A |
G |
3: 93,303,261 (GRCm39) |
E198G |
probably benign |
Het |
Ryr2 |
A |
T |
13: 11,680,799 (GRCm39) |
I3182N |
possibly damaging |
Het |
Sectm1a |
T |
A |
11: 120,960,708 (GRCm39) |
I36F |
possibly damaging |
Het |
Sez6l |
T |
C |
5: 112,621,346 (GRCm39) |
S243G |
probably benign |
Het |
Spata31h1 |
T |
C |
10: 82,122,876 (GRCm39) |
E3378G |
probably benign |
Het |
Taf2 |
T |
A |
15: 54,925,537 (GRCm39) |
H235L |
probably benign |
Het |
Tbc1d7 |
T |
C |
13: 43,306,493 (GRCm39) |
Q161R |
probably benign |
Het |
Tfcp2 |
T |
C |
15: 100,416,468 (GRCm39) |
T271A |
possibly damaging |
Het |
Thrsp |
G |
T |
7: 97,066,295 (GRCm39) |
T139K |
probably damaging |
Het |
Timm10 |
T |
A |
2: 84,660,333 (GRCm39) |
*91R |
probably null |
Het |
Tlr11 |
T |
A |
14: 50,599,598 (GRCm39) |
I528N |
possibly damaging |
Het |
Tnnt2 |
T |
A |
1: 135,779,444 (GRCm39) |
L278Q |
probably damaging |
Het |
Toe1 |
A |
T |
4: 116,664,715 (GRCm39) |
M1K |
probably null |
Het |
Trpv5 |
G |
A |
6: 41,652,242 (GRCm39) |
R148* |
probably null |
Het |
Ttll13 |
A |
C |
7: 79,903,911 (GRCm39) |
K280Q |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,783,550 (GRCm39) |
V860A |
unknown |
Het |
Txnip |
T |
C |
3: 96,466,991 (GRCm39) |
Y222H |
probably damaging |
Het |
Ubr4 |
G |
A |
4: 139,170,725 (GRCm39) |
S1600N |
probably damaging |
Het |
Uhrf1 |
T |
C |
17: 56,622,193 (GRCm39) |
Y364H |
probably damaging |
Het |
Unc5a |
A |
T |
13: 55,138,833 (GRCm39) |
T71S |
probably damaging |
Het |
Vmn1r123 |
A |
T |
7: 20,896,537 (GRCm39) |
Y143F |
possibly damaging |
Het |
Vmn1r180 |
T |
A |
7: 23,651,891 (GRCm39) |
I18N |
probably damaging |
Het |
Washc2 |
A |
G |
6: 116,185,168 (GRCm39) |
M1V |
probably null |
Het |
Zfp174 |
C |
A |
16: 3,666,111 (GRCm39) |
H125Q |
probably benign |
Het |
Zfpl1 |
T |
C |
19: 6,131,943 (GRCm39) |
H227R |
possibly damaging |
Het |
|
Other mutations in Anks1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01669:Anks1b
|
APN |
10 |
90,733,100 (GRCm39) |
splice site |
probably benign |
|
IGL01890:Anks1b
|
APN |
10 |
90,480,389 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01966:Anks1b
|
APN |
10 |
90,730,994 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02176:Anks1b
|
APN |
10 |
89,878,530 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02205:Anks1b
|
APN |
10 |
89,906,956 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02465:Anks1b
|
APN |
10 |
89,999,127 (GRCm39) |
nonsense |
probably null |
|
IGL02534:Anks1b
|
APN |
10 |
90,730,979 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02554:Anks1b
|
APN |
10 |
90,757,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02820:Anks1b
|
APN |
10 |
89,912,921 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03164:Anks1b
|
APN |
10 |
89,878,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Anks1b
|
UTSW |
10 |
89,909,924 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0096:Anks1b
|
UTSW |
10 |
89,909,924 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0482:Anks1b
|
UTSW |
10 |
90,195,057 (GRCm39) |
missense |
probably benign |
0.00 |
R0542:Anks1b
|
UTSW |
10 |
89,909,829 (GRCm39) |
splice site |
probably benign |
|
R0848:Anks1b
|
UTSW |
10 |
89,906,987 (GRCm39) |
missense |
probably damaging |
0.99 |
R1056:Anks1b
|
UTSW |
10 |
90,757,291 (GRCm39) |
splice site |
probably null |
|
R1398:Anks1b
|
UTSW |
10 |
89,885,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R1446:Anks1b
|
UTSW |
10 |
90,346,935 (GRCm39) |
missense |
probably benign |
0.00 |
R1548:Anks1b
|
UTSW |
10 |
89,885,847 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1551:Anks1b
|
UTSW |
10 |
89,912,843 (GRCm39) |
missense |
probably benign |
0.00 |
R1607:Anks1b
|
UTSW |
10 |
89,878,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R1667:Anks1b
|
UTSW |
10 |
90,347,046 (GRCm39) |
critical splice donor site |
probably null |
|
R1701:Anks1b
|
UTSW |
10 |
89,885,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1843:Anks1b
|
UTSW |
10 |
90,348,751 (GRCm39) |
critical splice donor site |
probably null |
|
R1899:Anks1b
|
UTSW |
10 |
90,096,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R1957:Anks1b
|
UTSW |
10 |
89,885,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R2036:Anks1b
|
UTSW |
10 |
90,805,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R2279:Anks1b
|
UTSW |
10 |
89,885,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R2280:Anks1b
|
UTSW |
10 |
90,802,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R2937:Anks1b
|
UTSW |
10 |
89,912,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R3739:Anks1b
|
UTSW |
10 |
89,869,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R4061:Anks1b
|
UTSW |
10 |
90,143,484 (GRCm39) |
missense |
probably damaging |
0.98 |
R4459:Anks1b
|
UTSW |
10 |
90,346,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R4479:Anks1b
|
UTSW |
10 |
89,885,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Anks1b
|
UTSW |
10 |
90,346,652 (GRCm39) |
missense |
probably benign |
0.01 |
R4511:Anks1b
|
UTSW |
10 |
90,346,652 (GRCm39) |
missense |
probably benign |
0.01 |
R4780:Anks1b
|
UTSW |
10 |
89,709,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Anks1b
|
UTSW |
10 |
90,750,612 (GRCm39) |
missense |
probably null |
0.88 |
R4790:Anks1b
|
UTSW |
10 |
89,999,137 (GRCm39) |
missense |
probably damaging |
0.99 |
R5012:Anks1b
|
UTSW |
10 |
90,194,999 (GRCm39) |
missense |
probably benign |
0.06 |
R5400:Anks1b
|
UTSW |
10 |
90,348,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Anks1b
|
UTSW |
10 |
89,912,926 (GRCm39) |
missense |
probably damaging |
0.98 |
R5687:Anks1b
|
UTSW |
10 |
90,750,573 (GRCm39) |
missense |
probably benign |
0.03 |
R5899:Anks1b
|
UTSW |
10 |
90,759,379 (GRCm39) |
splice site |
probably null |
|
R5917:Anks1b
|
UTSW |
10 |
90,412,803 (GRCm39) |
intron |
probably benign |
|
R5999:Anks1b
|
UTSW |
10 |
90,194,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R6080:Anks1b
|
UTSW |
10 |
90,802,211 (GRCm39) |
nonsense |
probably null |
|
R6216:Anks1b
|
UTSW |
10 |
90,096,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Anks1b
|
UTSW |
10 |
90,777,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R6298:Anks1b
|
UTSW |
10 |
90,516,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R6337:Anks1b
|
UTSW |
10 |
90,757,158 (GRCm39) |
missense |
probably benign |
0.27 |
R6522:Anks1b
|
UTSW |
10 |
90,733,189 (GRCm39) |
intron |
probably benign |
|
R6843:Anks1b
|
UTSW |
10 |
90,784,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R6852:Anks1b
|
UTSW |
10 |
90,096,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6933:Anks1b
|
UTSW |
10 |
89,905,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R7114:Anks1b
|
UTSW |
10 |
90,143,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R7211:Anks1b
|
UTSW |
10 |
90,346,932 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7264:Anks1b
|
UTSW |
10 |
90,348,732 (GRCm39) |
missense |
probably benign |
0.08 |
R7325:Anks1b
|
UTSW |
10 |
90,777,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R7392:Anks1b
|
UTSW |
10 |
90,516,648 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7578:Anks1b
|
UTSW |
10 |
89,885,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R7604:Anks1b
|
UTSW |
10 |
90,096,708 (GRCm39) |
splice site |
probably null |
|
R7633:Anks1b
|
UTSW |
10 |
90,784,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R7881:Anks1b
|
UTSW |
10 |
90,802,880 (GRCm39) |
missense |
probably benign |
0.07 |
R7910:Anks1b
|
UTSW |
10 |
90,516,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R7941:Anks1b
|
UTSW |
10 |
90,413,017 (GRCm39) |
missense |
probably damaging |
0.98 |
R8045:Anks1b
|
UTSW |
10 |
90,516,722 (GRCm39) |
missense |
probably benign |
|
R8146:Anks1b
|
UTSW |
10 |
90,143,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R8176:Anks1b
|
UTSW |
10 |
89,905,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R8535:Anks1b
|
UTSW |
10 |
90,784,493 (GRCm39) |
missense |
probably benign |
0.00 |
R8681:Anks1b
|
UTSW |
10 |
89,885,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R9300:Anks1b
|
UTSW |
10 |
90,412,966 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9469:Anks1b
|
UTSW |
10 |
90,733,205 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9541:Anks1b
|
UTSW |
10 |
90,412,947 (GRCm39) |
missense |
probably benign |
0.02 |
R9550:Anks1b
|
UTSW |
10 |
90,412,360 (GRCm39) |
start codon destroyed |
probably null |
|
R9653:Anks1b
|
UTSW |
10 |
90,346,524 (GRCm39) |
missense |
probably damaging |
1.00 |
RF004:Anks1b
|
UTSW |
10 |
89,869,087 (GRCm39) |
missense |
probably damaging |
1.00 |
RF008:Anks1b
|
UTSW |
10 |
89,869,087 (GRCm39) |
missense |
probably damaging |
1.00 |
RF017:Anks1b
|
UTSW |
10 |
89,869,087 (GRCm39) |
missense |
probably damaging |
1.00 |
RF018:Anks1b
|
UTSW |
10 |
89,869,087 (GRCm39) |
missense |
probably damaging |
1.00 |
RF023:Anks1b
|
UTSW |
10 |
89,869,087 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Anks1b
|
UTSW |
10 |
90,348,707 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- ACCTTGACACTGAACCTGTCC -3'
(R):5'- GAAGGAAATCATTTGCAGCTACTC -3'
Sequencing Primer
(F):5'- CCTAAGTTAATGGGTCACATATGC -3'
(R):5'- TGCAGCTACTCATTATAAAATAGGAC -3'
|
Posted On |
2019-06-26 |