Incidental Mutation 'R9432:Kat6b'
ID |
713049 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Kat6b
|
Ensembl Gene |
ENSMUSG00000021767 |
Gene Name |
K(lysine) acetyltransferase 6B |
Synonyms |
monocytic leukemia, Myst4, B130044K16Rik, Morf, qkf, querkopf |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.912)
|
Stock # |
R9432 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
14 |
Chromosomal Location |
21549284-21722546 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to C
at 21672077 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Proline
at position 329
(H329P)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000138511
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000069648]
[ENSMUST00000112458]
[ENSMUST00000182405]
[ENSMUST00000182855]
[ENSMUST00000182964]
|
AlphaFold |
Q8BRB7 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000069648
AA Change: H329P
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000066693 Gene: ENSMUSG00000021767 AA Change: H329P
Domain | Start | End | E-Value | Type |
H15
|
94 |
171 |
1.7e-12 |
SMART |
low complexity region
|
189 |
203 |
N/A |
INTRINSIC |
PHD
|
216 |
271 |
6.6e-5 |
SMART |
PHD
|
272 |
319 |
5.56e-12 |
SMART |
low complexity region
|
386 |
398 |
N/A |
INTRINSIC |
low complexity region
|
411 |
425 |
N/A |
INTRINSIC |
Blast:PHD
|
483 |
573 |
3e-51 |
BLAST |
Pfam:MOZ_SAS
|
594 |
772 |
4.5e-85 |
PFAM |
coiled coil region
|
811 |
845 |
N/A |
INTRINSIC |
coiled coil region
|
875 |
913 |
N/A |
INTRINSIC |
low complexity region
|
926 |
943 |
N/A |
INTRINSIC |
low complexity region
|
946 |
959 |
N/A |
INTRINSIC |
low complexity region
|
1153 |
1175 |
N/A |
INTRINSIC |
low complexity region
|
1207 |
1237 |
N/A |
INTRINSIC |
low complexity region
|
1391 |
1410 |
N/A |
INTRINSIC |
low complexity region
|
1450 |
1464 |
N/A |
INTRINSIC |
low complexity region
|
1490 |
1517 |
N/A |
INTRINSIC |
low complexity region
|
1676 |
1695 |
N/A |
INTRINSIC |
low complexity region
|
1811 |
1832 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000112458
|
SMART Domains |
Protein: ENSMUSP00000108077 Gene: ENSMUSG00000021767
Domain | Start | End | E-Value | Type |
H15
|
94 |
159 |
3.4e-1 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000182405
AA Change: H329P
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000138377 Gene: ENSMUSG00000021767 AA Change: H329P
Domain | Start | End | E-Value | Type |
H15
|
94 |
171 |
1.7e-12 |
SMART |
low complexity region
|
189 |
203 |
N/A |
INTRINSIC |
PHD
|
216 |
271 |
6.6e-5 |
SMART |
PHD
|
272 |
319 |
5.56e-12 |
SMART |
Pfam:MOZ_SAS
|
482 |
669 |
1.3e-89 |
PFAM |
coiled coil region
|
702 |
736 |
N/A |
INTRINSIC |
coiled coil region
|
766 |
804 |
N/A |
INTRINSIC |
low complexity region
|
817 |
834 |
N/A |
INTRINSIC |
low complexity region
|
837 |
850 |
N/A |
INTRINSIC |
low complexity region
|
1044 |
1066 |
N/A |
INTRINSIC |
low complexity region
|
1098 |
1128 |
N/A |
INTRINSIC |
low complexity region
|
1282 |
1301 |
N/A |
INTRINSIC |
low complexity region
|
1341 |
1355 |
N/A |
INTRINSIC |
low complexity region
|
1381 |
1408 |
N/A |
INTRINSIC |
low complexity region
|
1567 |
1586 |
N/A |
INTRINSIC |
low complexity region
|
1702 |
1723 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000182855
AA Change: H329P
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000138511 Gene: ENSMUSG00000021767 AA Change: H329P
Domain | Start | End | E-Value | Type |
H15
|
94 |
171 |
1.7e-12 |
SMART |
low complexity region
|
189 |
203 |
N/A |
INTRINSIC |
PHD
|
216 |
271 |
6.6e-5 |
SMART |
PHD
|
272 |
319 |
5.56e-12 |
SMART |
Pfam:MOZ_SAS
|
482 |
669 |
1.3e-89 |
PFAM |
coiled coil region
|
702 |
736 |
N/A |
INTRINSIC |
coiled coil region
|
766 |
804 |
N/A |
INTRINSIC |
low complexity region
|
817 |
834 |
N/A |
INTRINSIC |
low complexity region
|
837 |
850 |
N/A |
INTRINSIC |
low complexity region
|
1044 |
1066 |
N/A |
INTRINSIC |
low complexity region
|
1098 |
1128 |
N/A |
INTRINSIC |
low complexity region
|
1282 |
1301 |
N/A |
INTRINSIC |
low complexity region
|
1341 |
1355 |
N/A |
INTRINSIC |
low complexity region
|
1381 |
1408 |
N/A |
INTRINSIC |
low complexity region
|
1567 |
1586 |
N/A |
INTRINSIC |
low complexity region
|
1702 |
1723 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000182964
AA Change: H329P
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000138421 Gene: ENSMUSG00000021767 AA Change: H329P
Domain | Start | End | E-Value | Type |
H15
|
94 |
171 |
1.7e-12 |
SMART |
low complexity region
|
189 |
203 |
N/A |
INTRINSIC |
PHD
|
216 |
271 |
6.6e-5 |
SMART |
PHD
|
272 |
319 |
5.56e-12 |
SMART |
low complexity region
|
386 |
398 |
N/A |
INTRINSIC |
low complexity region
|
411 |
425 |
N/A |
INTRINSIC |
Blast:PHD
|
483 |
573 |
3e-51 |
BLAST |
Pfam:MOZ_SAS
|
591 |
778 |
1.4e-89 |
PFAM |
coiled coil region
|
811 |
845 |
N/A |
INTRINSIC |
coiled coil region
|
875 |
913 |
N/A |
INTRINSIC |
low complexity region
|
926 |
943 |
N/A |
INTRINSIC |
low complexity region
|
946 |
959 |
N/A |
INTRINSIC |
low complexity region
|
1153 |
1175 |
N/A |
INTRINSIC |
low complexity region
|
1207 |
1237 |
N/A |
INTRINSIC |
low complexity region
|
1391 |
1410 |
N/A |
INTRINSIC |
low complexity region
|
1450 |
1464 |
N/A |
INTRINSIC |
low complexity region
|
1490 |
1517 |
N/A |
INTRINSIC |
low complexity region
|
1676 |
1695 |
N/A |
INTRINSIC |
low complexity region
|
1811 |
1832 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Reduced expression of this gene results in developmental defects of the skeleton and brain, particularly the cerebral cortex. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
T |
C |
5: 109,884,917 (GRCm39) |
R314G |
unknown |
Het |
Abca13 |
G |
A |
11: 9,244,559 (GRCm39) |
V2141M |
probably benign |
Het |
Abcc10 |
G |
A |
17: 46,634,710 (GRCm39) |
A431V |
possibly damaging |
Het |
Acod1 |
A |
G |
14: 103,292,414 (GRCm39) |
R313G |
probably damaging |
Het |
Adam3 |
G |
T |
8: 25,193,928 (GRCm39) |
S361R |
probably damaging |
Het |
Ahcyl2 |
C |
T |
6: 29,768,874 (GRCm39) |
T113M |
possibly damaging |
Het |
Ano8 |
C |
A |
8: 71,933,561 (GRCm39) |
R577L |
unknown |
Het |
Arhgef7 |
T |
A |
8: 11,869,646 (GRCm39) |
S653R |
probably damaging |
Het |
Atp10a |
G |
A |
7: 58,469,418 (GRCm39) |
V1090I |
possibly damaging |
Het |
Birc6 |
A |
G |
17: 74,966,216 (GRCm39) |
M4048V |
probably benign |
Het |
C3 |
G |
A |
17: 57,530,950 (GRCm39) |
P384S |
probably damaging |
Het |
Camkk1 |
A |
T |
11: 72,928,757 (GRCm39) |
E432V |
probably damaging |
Het |
Celsr3 |
T |
A |
9: 108,726,032 (GRCm39) |
V3087D |
probably benign |
Het |
Ckap4 |
A |
G |
10: 84,363,543 (GRCm39) |
S507P |
probably damaging |
Het |
Coq6 |
G |
A |
12: 84,420,464 (GRCm39) |
M471I |
probably benign |
Het |
Csmd2 |
C |
A |
4: 128,171,004 (GRCm39) |
H332Q |
|
Het |
Cxcr1 |
T |
A |
1: 74,231,231 (GRCm39) |
N264Y |
probably damaging |
Het |
Dchs2 |
C |
A |
3: 83,036,032 (GRCm39) |
R260S |
possibly damaging |
Het |
Elmod2 |
C |
A |
8: 84,057,761 (GRCm39) |
A41S |
possibly damaging |
Het |
Emilin2 |
G |
A |
17: 71,581,781 (GRCm39) |
T315I |
probably benign |
Het |
Eml1 |
A |
G |
12: 108,482,842 (GRCm39) |
N487S |
probably benign |
Het |
Epn1 |
G |
T |
7: 5,096,369 (GRCm39) |
R221L |
probably benign |
Het |
Faah |
A |
G |
4: 115,874,772 (GRCm39) |
V28A |
probably benign |
Het |
Fbl |
G |
A |
7: 27,876,689 (GRCm39) |
R230H |
probably benign |
Het |
Fsip2 |
C |
T |
2: 82,805,907 (GRCm39) |
S742F |
probably damaging |
Het |
Gm5460 |
A |
G |
14: 33,767,769 (GRCm39) |
D184G |
possibly damaging |
Het |
Gpatch2l |
T |
C |
12: 86,307,408 (GRCm39) |
V262A |
probably damaging |
Het |
Grin2c |
A |
T |
11: 115,142,052 (GRCm39) |
L789* |
probably null |
Het |
H1f0 |
C |
T |
15: 78,912,947 (GRCm39) |
P9L |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,460,864 (GRCm39) |
T948A |
probably benign |
Het |
Herc2 |
G |
A |
7: 55,780,932 (GRCm39) |
G1199D |
probably damaging |
Het |
Hoxb7 |
G |
T |
11: 96,177,617 (GRCm39) |
A22S |
possibly damaging |
Het |
Ifih1 |
T |
A |
2: 62,439,618 (GRCm39) |
I519F |
probably damaging |
Het |
Ifit1bl1 |
T |
A |
19: 34,571,498 (GRCm39) |
I320F |
possibly damaging |
Het |
Iqgap2 |
T |
C |
13: 95,774,261 (GRCm39) |
T1320A |
probably benign |
Het |
Kat2a |
A |
G |
11: 100,602,178 (GRCm39) |
V192A |
probably damaging |
Het |
Klhl29 |
A |
G |
12: 5,260,056 (GRCm39) |
L54P |
probably benign |
Het |
Kntc1 |
A |
T |
5: 123,925,112 (GRCm39) |
I1142F |
possibly damaging |
Het |
Lipo3 |
A |
G |
19: 33,533,864 (GRCm39) |
Y323H |
probably damaging |
Het |
Lmtk3 |
G |
A |
7: 45,441,994 (GRCm39) |
V351I |
probably damaging |
Het |
Lrrc8b |
T |
C |
5: 105,633,888 (GRCm39) |
S787P |
probably benign |
Het |
Magi1 |
A |
G |
6: 93,660,058 (GRCm39) |
I1179T |
probably damaging |
Het |
Mapk11 |
T |
C |
15: 89,028,631 (GRCm39) |
D269G |
probably benign |
Het |
Mfsd13a |
T |
G |
19: 46,354,868 (GRCm39) |
I15R |
probably benign |
Het |
Myo1h |
G |
A |
5: 114,499,366 (GRCm39) |
V143I |
possibly damaging |
Het |
Naaladl1 |
T |
C |
19: 6,156,917 (GRCm39) |
I187T |
possibly damaging |
Het |
Nos1 |
G |
A |
5: 118,034,871 (GRCm39) |
V416M |
probably damaging |
Het |
Or14a256 |
G |
A |
7: 86,265,065 (GRCm39) |
R263C |
possibly damaging |
Het |
Or14j8 |
A |
G |
17: 38,263,559 (GRCm39) |
S119P |
probably damaging |
Het |
Or8k30 |
T |
G |
2: 86,338,914 (GRCm39) |
I37S |
probably benign |
Het |
Pcdh15 |
A |
G |
10: 74,460,170 (GRCm39) |
T1373A |
probably damaging |
Het |
Pcdh18 |
T |
G |
3: 49,699,667 (GRCm39) |
M932L |
probably damaging |
Het |
Pcdhb15 |
T |
A |
18: 37,608,683 (GRCm39) |
H638Q |
probably benign |
Het |
Pcdhb19 |
A |
G |
18: 37,630,628 (GRCm39) |
E141G |
possibly damaging |
Het |
Pds5b |
T |
G |
5: 150,693,256 (GRCm39) |
L656R |
probably damaging |
Het |
Plcl1 |
T |
C |
1: 55,445,587 (GRCm39) |
L14P |
probably benign |
Het |
Pzp |
A |
T |
6: 128,499,128 (GRCm39) |
I173N |
|
Het |
Rnf123 |
C |
T |
9: 107,937,008 (GRCm39) |
R849H |
probably damaging |
Het |
Sfrp5 |
T |
C |
19: 42,188,225 (GRCm39) |
D198G |
probably damaging |
Het |
Sftpb |
G |
C |
6: 72,283,843 (GRCm39) |
A147P |
probably benign |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Slc30a6 |
A |
G |
17: 74,719,699 (GRCm39) |
T220A |
possibly damaging |
Het |
Slc5a3 |
T |
A |
16: 91,874,615 (GRCm39) |
V224D |
probably benign |
Het |
Smad5 |
T |
A |
13: 56,875,417 (GRCm39) |
Y202N |
probably benign |
Het |
Smok2b |
A |
G |
17: 13,453,881 (GRCm39) |
I14V |
probably damaging |
Het |
Tas2r108 |
T |
A |
6: 40,471,121 (GRCm39) |
I199K |
probably damaging |
Het |
Tcea2 |
A |
G |
2: 181,322,227 (GRCm39) |
I10V |
probably damaging |
Het |
Tfg |
G |
A |
16: 56,524,868 (GRCm39) |
R113* |
probably null |
Het |
Tubb4a |
A |
T |
17: 57,388,034 (GRCm39) |
L331I |
probably benign |
Het |
Ugt2b37 |
A |
G |
5: 87,402,046 (GRCm39) |
V195A |
probably damaging |
Het |
Umad1 |
A |
G |
6: 8,401,096 (GRCm39) |
H55R |
unknown |
Het |
Vmn1r176 |
A |
T |
7: 23,534,743 (GRCm39) |
Y137N |
probably damaging |
Het |
Vmn1r44 |
T |
A |
6: 89,870,473 (GRCm39) |
M73K |
possibly damaging |
Het |
Vmn2r112 |
A |
G |
17: 22,821,233 (GRCm39) |
T69A |
|
Het |
Vmn2r59 |
A |
T |
7: 41,696,254 (GRCm39) |
Y163N |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,830,137 (GRCm39) |
D1514E |
probably benign |
Het |
Vsir |
A |
G |
10: 60,193,732 (GRCm39) |
D65G |
possibly damaging |
Het |
Ypel3 |
A |
T |
7: 126,379,262 (GRCm39) |
M112L |
probably benign |
Het |
Zfp26 |
T |
A |
9: 20,347,830 (GRCm39) |
K911N |
probably damaging |
Het |
Zfp362 |
C |
T |
4: 128,670,980 (GRCm39) |
R346Q |
probably damaging |
Het |
Zfp595 |
A |
T |
13: 67,465,407 (GRCm39) |
Y288* |
probably null |
Het |
Zfyve28 |
G |
T |
5: 34,400,633 (GRCm39) |
Q22K |
possibly damaging |
Het |
Zswim4 |
T |
G |
8: 84,963,539 (GRCm39) |
D32A |
probably damaging |
Het |
|
Other mutations in Kat6b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00264:Kat6b
|
APN |
14 |
21,718,627 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01128:Kat6b
|
APN |
14 |
21,710,928 (GRCm39) |
missense |
probably benign |
|
IGL02272:Kat6b
|
APN |
14 |
21,676,846 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02349:Kat6b
|
APN |
14 |
21,687,661 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02402:Kat6b
|
APN |
14 |
21,681,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02474:Kat6b
|
APN |
14 |
21,719,107 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02516:Kat6b
|
APN |
14 |
21,659,936 (GRCm39) |
splice site |
probably benign |
|
IGL02666:Kat6b
|
APN |
14 |
21,678,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02971:Kat6b
|
APN |
14 |
21,719,826 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03075:Kat6b
|
APN |
14 |
21,711,638 (GRCm39) |
nonsense |
probably null |
|
IGL03274:Kat6b
|
APN |
14 |
21,659,831 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03308:Kat6b
|
APN |
14 |
21,674,902 (GRCm39) |
missense |
probably damaging |
0.99 |
R0118:Kat6b
|
UTSW |
14 |
21,720,042 (GRCm39) |
missense |
probably damaging |
0.99 |
R0383:Kat6b
|
UTSW |
14 |
21,719,149 (GRCm39) |
missense |
probably benign |
0.02 |
R0441:Kat6b
|
UTSW |
14 |
21,720,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R0457:Kat6b
|
UTSW |
14 |
21,720,598 (GRCm39) |
missense |
probably damaging |
0.96 |
R0558:Kat6b
|
UTSW |
14 |
21,719,489 (GRCm39) |
missense |
probably benign |
0.03 |
R0662:Kat6b
|
UTSW |
14 |
21,712,417 (GRCm39) |
small deletion |
probably benign |
|
R0684:Kat6b
|
UTSW |
14 |
21,718,849 (GRCm39) |
missense |
probably benign |
|
R0755:Kat6b
|
UTSW |
14 |
21,687,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R1216:Kat6b
|
UTSW |
14 |
21,672,108 (GRCm39) |
nonsense |
probably null |
|
R1479:Kat6b
|
UTSW |
14 |
21,669,024 (GRCm39) |
missense |
probably benign |
0.19 |
R1873:Kat6b
|
UTSW |
14 |
21,567,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R1957:Kat6b
|
UTSW |
14 |
21,678,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Kat6b
|
UTSW |
14 |
21,718,735 (GRCm39) |
missense |
probably benign |
0.02 |
R2152:Kat6b
|
UTSW |
14 |
21,718,735 (GRCm39) |
missense |
probably benign |
0.02 |
R2153:Kat6b
|
UTSW |
14 |
21,718,735 (GRCm39) |
missense |
probably benign |
0.02 |
R2154:Kat6b
|
UTSW |
14 |
21,718,735 (GRCm39) |
missense |
probably benign |
0.02 |
R2399:Kat6b
|
UTSW |
14 |
21,712,417 (GRCm39) |
small deletion |
probably benign |
|
R3740:Kat6b
|
UTSW |
14 |
21,720,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R3771:Kat6b
|
UTSW |
14 |
21,567,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R4178:Kat6b
|
UTSW |
14 |
21,668,972 (GRCm39) |
nonsense |
probably null |
|
R4261:Kat6b
|
UTSW |
14 |
21,719,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R4551:Kat6b
|
UTSW |
14 |
21,711,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R4724:Kat6b
|
UTSW |
14 |
21,711,030 (GRCm39) |
missense |
probably benign |
|
R5055:Kat6b
|
UTSW |
14 |
21,567,062 (GRCm39) |
missense |
probably damaging |
0.99 |
R5098:Kat6b
|
UTSW |
14 |
21,669,083 (GRCm39) |
splice site |
probably benign |
|
R5121:Kat6b
|
UTSW |
14 |
21,669,326 (GRCm39) |
missense |
probably damaging |
0.98 |
R5158:Kat6b
|
UTSW |
14 |
21,720,054 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5488:Kat6b
|
UTSW |
14 |
21,719,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5489:Kat6b
|
UTSW |
14 |
21,719,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5653:Kat6b
|
UTSW |
14 |
21,719,440 (GRCm39) |
missense |
probably benign |
0.10 |
R5742:Kat6b
|
UTSW |
14 |
21,718,503 (GRCm39) |
missense |
probably damaging |
0.99 |
R5868:Kat6b
|
UTSW |
14 |
21,684,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R5969:Kat6b
|
UTSW |
14 |
21,720,860 (GRCm39) |
missense |
probably damaging |
0.97 |
R6110:Kat6b
|
UTSW |
14 |
21,720,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R6427:Kat6b
|
UTSW |
14 |
21,567,480 (GRCm39) |
missense |
probably benign |
0.24 |
R6457:Kat6b
|
UTSW |
14 |
21,720,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6639:Kat6b
|
UTSW |
14 |
21,567,562 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6891:Kat6b
|
UTSW |
14 |
21,719,104 (GRCm39) |
missense |
probably benign |
0.01 |
R7784:Kat6b
|
UTSW |
14 |
21,710,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R7916:Kat6b
|
UTSW |
14 |
21,712,417 (GRCm39) |
small deletion |
probably benign |
|
R7977:Kat6b
|
UTSW |
14 |
21,719,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7987:Kat6b
|
UTSW |
14 |
21,719,931 (GRCm39) |
missense |
probably benign |
0.00 |
R8167:Kat6b
|
UTSW |
14 |
21,719,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8266:Kat6b
|
UTSW |
14 |
21,566,913 (GRCm39) |
start gained |
probably benign |
|
R8483:Kat6b
|
UTSW |
14 |
21,719,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R8902:Kat6b
|
UTSW |
14 |
21,719,629 (GRCm39) |
missense |
probably benign |
0.30 |
R8909:Kat6b
|
UTSW |
14 |
21,719,214 (GRCm39) |
missense |
probably benign |
|
R8931:Kat6b
|
UTSW |
14 |
21,674,995 (GRCm39) |
missense |
probably damaging |
0.98 |
R9112:Kat6b
|
UTSW |
14 |
21,675,256 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9182:Kat6b
|
UTSW |
14 |
21,567,187 (GRCm39) |
missense |
probably benign |
0.20 |
R9224:Kat6b
|
UTSW |
14 |
21,720,031 (GRCm39) |
missense |
probably benign |
0.14 |
R9273:Kat6b
|
UTSW |
14 |
21,711,551 (GRCm39) |
missense |
probably benign |
0.07 |
R9332:Kat6b
|
UTSW |
14 |
21,720,093 (GRCm39) |
missense |
probably benign |
0.00 |
R9380:Kat6b
|
UTSW |
14 |
21,678,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R9397:Kat6b
|
UTSW |
14 |
21,675,244 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9400:Kat6b
|
UTSW |
14 |
21,659,826 (GRCm39) |
missense |
probably damaging |
0.99 |
R9481:Kat6b
|
UTSW |
14 |
21,712,417 (GRCm39) |
small deletion |
probably benign |
|
R9526:Kat6b
|
UTSW |
14 |
21,567,564 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
Predicted Primers |
PCR Primer
(F):5'- TTTCCTAGAGAAAGAGCTGCATACAG -3'
(R):5'- CTCAGAAGCTACTATTTTGGAGAAG -3'
Sequencing Primer
(F):5'- TGCATACAGACATCCTTGGTCAG -3'
(R):5'- GCTTGAAACATGTCACTCGG -3'
|
Posted On |
2022-05-16 |