Incidental Mutation 'R6244:Kdm3b'
| ID |
505492 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Kdm3b
|
| Ensembl Gene |
ENSMUSG00000038773 |
| Gene Name |
KDM3B lysine (K)-specific demethylase 3B |
| Synonyms |
JHDM2B, Jmjd1b, 5830462I21Rik |
| MMRRC Submission |
044435-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.942)
|
| Stock # |
R6244 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
18 |
| Chromosomal Location |
34777047-34838660 bp(+) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 34793005 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 66
(I66N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000153295
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043775]
[ENSMUST00000224715]
[ENSMUST00000225195]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000043775
AA Change: I66N
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000037628
Gene: ENSMUSG00000038773
AA Change: I66N
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
20 |
36 |
N/A |
INTRINSIC |
|
Blast:JmjC
|
149 |
944 |
N/A |
BLAST |
|
Blast:JmjC
|
946 |
1064 |
5e-40 |
BLAST |
|
Blast:JmjC
|
1069 |
1471 |
N/A |
BLAST |
|
JmjC
|
1499 |
1722 |
2.43e-65 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000180512
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000224715
AA Change: I66N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000225047
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000225195
AA Change: I66N
PolyPhen 2
Score 0.548 (Sensitivity: 0.88; Specificity: 0.91)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000225260
|
| Meta Mutation Damage Score |
0.5911 |
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.3%
- 20x: 95.1%
|
| Validation Efficiency |
96% (82/85) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 84 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4932438A13Rik |
T |
C |
3: 36,956,999 (GRCm38) |
V1782A |
probably benign |
Het |
| 6430550D23Rik |
T |
C |
2: 156,003,230 (GRCm38) |
H113R |
possibly damaging |
Het |
| Adgrf3 |
A |
T |
5: 30,197,533 (GRCm38) |
M499K |
probably benign |
Het |
| Adgrv1 |
G |
A |
13: 81,106,931 (GRCm38) |
T211I |
probably damaging |
Het |
| Adss |
C |
T |
1: 177,776,829 (GRCm38) |
E153K |
probably benign |
Het |
| Ago4 |
C |
A |
4: 126,511,487 (GRCm38) |
G431V |
possibly damaging |
Het |
| Araf |
G |
T |
X: 20,860,100 (GRCm38) |
R601L |
probably damaging |
Homo |
| Atp2b4 |
T |
A |
1: 133,726,561 (GRCm38) |
I769F |
probably damaging |
Het |
| Atp9a |
T |
C |
2: 168,689,352 (GRCm38) |
|
probably null |
Het |
| Brap |
C |
A |
5: 121,665,309 (GRCm38) |
D173E |
probably benign |
Het |
| Brca2 |
G |
T |
5: 150,566,978 (GRCm38) |
R3035L |
probably benign |
Het |
| Ccdc8 |
C |
A |
7: 16,996,251 (GRCm38) |
P555Q |
probably benign |
Het |
| Ccser2 |
A |
G |
14: 36,940,718 (GRCm38) |
S170P |
probably benign |
Het |
| Celsr2 |
T |
C |
3: 108,393,128 (GRCm38) |
H860R |
probably damaging |
Het |
| Cenpc1 |
C |
A |
5: 86,046,385 (GRCm38) |
R174M |
probably damaging |
Het |
| Cfap57 |
T |
G |
4: 118,579,410 (GRCm38) |
I930L |
probably damaging |
Het |
| Cx3cr1 |
C |
T |
9: 120,051,694 (GRCm38) |
R214H |
probably damaging |
Het |
| Cyp4f14 |
T |
A |
17: 32,906,317 (GRCm38) |
H429L |
probably benign |
Het |
| D5Ertd579e |
A |
G |
5: 36,615,276 (GRCm38) |
F592L |
probably damaging |
Het |
| Ddb1 |
A |
G |
19: 10,625,923 (GRCm38) |
E865G |
probably damaging |
Het |
| Ddx50 |
A |
T |
10: 62,621,566 (GRCm38) |
|
probably null |
Het |
| Dpp6 |
A |
G |
5: 27,049,628 (GRCm38) |
T14A |
probably damaging |
Het |
| Echs1 |
C |
A |
7: 140,113,069 (GRCm38) |
Q51H |
possibly damaging |
Het |
| Ecm2 |
A |
T |
13: 49,530,307 (GRCm38) |
D587V |
probably damaging |
Het |
| Ect2l |
A |
T |
10: 18,140,397 (GRCm38) |
Y666N |
possibly damaging |
Het |
| Epha2 |
G |
A |
4: 141,316,912 (GRCm38) |
G342S |
probably benign |
Het |
| Fbxo33 |
C |
A |
12: 59,206,079 (GRCm38) |
K211N |
probably benign |
Het |
| Fchsd2 |
A |
G |
7: 101,259,776 (GRCm38) |
|
probably null |
Het |
| Fen1 |
A |
G |
19: 10,200,687 (GRCm38) |
V131A |
probably damaging |
Het |
| Fetub |
C |
T |
16: 22,932,331 (GRCm38) |
R143C |
probably damaging |
Het |
| Flnb |
A |
G |
14: 7,892,092 (GRCm38) |
E587G |
probably damaging |
Het |
| Foxd3 |
A |
G |
4: 99,657,240 (GRCm38) |
T206A |
possibly damaging |
Het |
| Fut1 |
A |
G |
7: 45,619,306 (GRCm38) |
E228G |
possibly damaging |
Het |
| Galnt13 |
T |
C |
2: 54,933,548 (GRCm38) |
F379L |
probably damaging |
Het |
| Gcnt2 |
A |
C |
13: 40,861,241 (GRCm38) |
E296A |
probably damaging |
Het |
| Gm7145 |
T |
A |
1: 117,986,140 (GRCm38) |
C251S |
probably damaging |
Het |
| Gpam |
G |
A |
19: 55,070,985 (GRCm38) |
P810L |
probably damaging |
Het |
| Il1rl2 |
T |
A |
1: 40,327,566 (GRCm38) |
L87M |
possibly damaging |
Het |
| Itgae |
A |
G |
11: 73,145,601 (GRCm38) |
S1122G |
probably damaging |
Het |
| Kcnh7 |
T |
A |
2: 63,182,226 (GRCm38) |
D46V |
probably damaging |
Het |
| Kcnn3 |
T |
G |
3: 89,645,523 (GRCm38) |
Y511* |
probably null |
Het |
| Klk1b27 |
A |
T |
7: 44,054,550 (GRCm38) |
H39L |
probably benign |
Het |
| Kmo |
C |
T |
1: 175,659,695 (GRCm38) |
T404I |
possibly damaging |
Het |
| Krt222 |
C |
T |
11: 99,235,058 (GRCm38) |
|
probably null |
Het |
| Magi3 |
G |
C |
3: 104,015,697 (GRCm38) |
H1235D |
probably benign |
Het |
| Mapk8ip1 |
C |
A |
2: 92,389,244 (GRCm38) |
G81C |
probably damaging |
Het |
| Med15 |
G |
A |
16: 17,652,745 (GRCm38) |
Q583* |
probably null |
Het |
| Mroh2a |
T |
C |
1: 88,256,754 (GRCm38) |
V1453A |
probably benign |
Het |
| Myh13 |
A |
G |
11: 67,362,501 (GRCm38) |
M1488V |
probably benign |
Het |
| Naip2 |
A |
T |
13: 100,152,137 (GRCm38) |
F1193L |
probably damaging |
Het |
| Nop58 |
T |
A |
1: 59,702,855 (GRCm38) |
M181K |
probably damaging |
Het |
| Npepps |
A |
T |
11: 97,213,790 (GRCm38) |
V796D |
probably damaging |
Het |
| Nr1d1 |
A |
G |
11: 98,770,537 (GRCm38) |
F301S |
probably damaging |
Het |
| Nynrin |
G |
A |
14: 55,868,028 (GRCm38) |
V832I |
probably damaging |
Het |
| Olfr1046 |
T |
A |
2: 86,217,222 (GRCm38) |
T163S |
possibly damaging |
Het |
| Olfr1508 |
T |
A |
14: 52,463,895 (GRCm38) |
Y38F |
probably damaging |
Het |
| Olfr320 |
A |
T |
11: 58,684,004 (GRCm38) |
T44S |
possibly damaging |
Het |
| Olfr342 |
T |
A |
2: 36,528,341 (GRCm38) |
C310S |
probably benign |
Het |
| Olfr61 |
C |
A |
7: 140,638,433 (GRCm38) |
S244Y |
probably damaging |
Het |
| Phrf1 |
T |
A |
7: 141,237,673 (GRCm38) |
C132S |
probably damaging |
Het |
| Plekhn1 |
T |
C |
4: 156,230,558 (GRCm38) |
|
probably null |
Het |
| Polr2a |
G |
A |
11: 69,744,226 (GRCm38) |
T569M |
probably damaging |
Het |
| Prr29 |
A |
G |
11: 106,376,632 (GRCm38) |
|
probably null |
Het |
| Rsf1 |
CG |
CGACGGCGGAG |
7: 97,579,908 (GRCm38) |
|
probably benign |
Homo |
| Sc5d |
T |
C |
9: 42,255,421 (GRCm38) |
E274G |
probably benign |
Het |
| Serpina1d |
A |
T |
12: 103,764,828 (GRCm38) |
|
probably null |
Het |
| Serpinb11 |
T |
A |
1: 107,372,242 (GRCm38) |
I106N |
probably damaging |
Het |
| Setd2 |
G |
A |
9: 110,548,665 (GRCm38) |
R516K |
probably damaging |
Het |
| Sirt2 |
G |
T |
7: 28,787,797 (GRCm38) |
C291F |
probably damaging |
Het |
| Stac3 |
T |
C |
10: 127,508,175 (GRCm38) |
V314A |
probably damaging |
Het |
| Stat6 |
C |
T |
10: 127,657,712 (GRCm38) |
|
probably null |
Het |
| Strn3 |
A |
G |
12: 51,610,107 (GRCm38) |
V712A |
probably damaging |
Het |
| Tmc5 |
G |
T |
7: 118,634,214 (GRCm38) |
G84C |
possibly damaging |
Het |
| Tnik |
C |
A |
3: 28,650,179 (GRCm38) |
L996I |
probably damaging |
Het |
| Trim30d |
G |
T |
7: 104,487,610 (GRCm38) |
T129K |
probably damaging |
Het |
| Triml1 |
G |
T |
8: 43,138,756 (GRCm38) |
Y188* |
probably null |
Het |
| Trpc7 |
A |
G |
13: 56,773,892 (GRCm38) |
Y760H |
probably damaging |
Het |
| Uaca |
G |
A |
9: 60,870,044 (GRCm38) |
R571Q |
probably damaging |
Het |
| Ubash3a |
A |
T |
17: 31,239,272 (GRCm38) |
Q575L |
possibly damaging |
Het |
| Usp49 |
T |
A |
17: 47,672,902 (GRCm38) |
C61* |
probably null |
Het |
| Vmn2r18 |
A |
T |
5: 151,584,651 (GRCm38) |
V336E |
probably damaging |
Het |
| Vwa8 |
T |
C |
14: 79,086,662 (GRCm38) |
V1135A |
probably benign |
Het |
| Zcchc4 |
T |
C |
5: 52,783,161 (GRCm38) |
V24A |
probably benign |
Het |
| Zfp354c |
A |
G |
11: 50,814,971 (GRCm38) |
Y426H |
probably benign |
Het |
|
| Other mutations in Kdm3b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00162:Kdm3b
|
APN |
18 |
34,809,409 (GRCm38) |
missense |
probably benign |
0.03 |
|
IGL01357:Kdm3b
|
APN |
18 |
34,793,014 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01615:Kdm3b
|
APN |
18 |
34,829,231 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01980:Kdm3b
|
APN |
18 |
34,834,236 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02277:Kdm3b
|
APN |
18 |
34,823,664 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02346:Kdm3b
|
APN |
18 |
34,834,238 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02417:Kdm3b
|
APN |
18 |
34,808,577 (GRCm38) |
missense |
probably benign |
0.03 |
|
IGL02531:Kdm3b
|
APN |
18 |
34,795,729 (GRCm38) |
missense |
probably benign |
|
|
IGL02589:Kdm3b
|
APN |
18 |
34,812,418 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
IGL02793:Kdm3b
|
APN |
18 |
34,829,019 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL03121:Kdm3b
|
APN |
18 |
34,795,709 (GRCm38) |
missense |
probably damaging |
0.98 |
|
IGL03123:Kdm3b
|
APN |
18 |
34,809,491 (GRCm38) |
critical splice donor site |
probably null |
|
|
IGL03128:Kdm3b
|
APN |
18 |
34,827,427 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Affable
|
UTSW |
18 |
34,793,005 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Dotage
|
UTSW |
18 |
34,827,382 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Endearing
|
UTSW |
18 |
34,827,328 (GRCm38) |
splice site |
probably null |
|
|
Oldtimer
|
UTSW |
18 |
34,823,699 (GRCm38) |
nonsense |
probably null |
|
|
PIT4382001:Kdm3b
|
UTSW |
18 |
34,809,087 (GRCm38) |
missense |
probably damaging |
1.00 |
|
PIT4445001:Kdm3b
|
UTSW |
18 |
34,793,115 (GRCm38) |
nonsense |
probably null |
|
|
R0068:Kdm3b
|
UTSW |
18 |
34,824,774 (GRCm38) |
missense |
probably benign |
0.18 |
|
R0068:Kdm3b
|
UTSW |
18 |
34,824,774 (GRCm38) |
missense |
probably benign |
0.18 |
|
R0233:Kdm3b
|
UTSW |
18 |
34,809,420 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R0265:Kdm3b
|
UTSW |
18 |
34,795,663 (GRCm38) |
splice site |
probably benign |
|
|
R0306:Kdm3b
|
UTSW |
18 |
34,804,017 (GRCm38) |
missense |
probably benign |
0.35 |
|
R0941:Kdm3b
|
UTSW |
18 |
34,803,552 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R0970:Kdm3b
|
UTSW |
18 |
34,809,039 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1061:Kdm3b
|
UTSW |
18 |
34,796,862 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1104:Kdm3b
|
UTSW |
18 |
34,819,811 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1221:Kdm3b
|
UTSW |
18 |
34,808,245 (GRCm38) |
missense |
possibly damaging |
0.57 |
|
R1486:Kdm3b
|
UTSW |
18 |
34,834,304 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1523:Kdm3b
|
UTSW |
18 |
34,793,173 (GRCm38) |
critical splice donor site |
probably null |
|
|
R1558:Kdm3b
|
UTSW |
18 |
34,809,096 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1585:Kdm3b
|
UTSW |
18 |
34,809,292 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1601:Kdm3b
|
UTSW |
18 |
34,808,731 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1650:Kdm3b
|
UTSW |
18 |
34,809,115 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R1772:Kdm3b
|
UTSW |
18 |
34,803,504 (GRCm38) |
missense |
probably benign |
0.01 |
|
R1853:Kdm3b
|
UTSW |
18 |
34,833,393 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1934:Kdm3b
|
UTSW |
18 |
34,813,544 (GRCm38) |
missense |
probably benign |
0.04 |
|
R1959:Kdm3b
|
UTSW |
18 |
34,812,395 (GRCm38) |
missense |
possibly damaging |
0.55 |
|
R2079:Kdm3b
|
UTSW |
18 |
34,803,517 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2102:Kdm3b
|
UTSW |
18 |
34,830,147 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2121:Kdm3b
|
UTSW |
18 |
34,796,780 (GRCm38) |
splice site |
probably benign |
|
|
R2281:Kdm3b
|
UTSW |
18 |
34,808,419 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R3719:Kdm3b
|
UTSW |
18 |
34,808,671 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R3755:Kdm3b
|
UTSW |
18 |
34,808,296 (GRCm38) |
missense |
probably benign |
|
|
R3857:Kdm3b
|
UTSW |
18 |
34,833,387 (GRCm38) |
missense |
probably benign |
|
|
R4165:Kdm3b
|
UTSW |
18 |
34,795,744 (GRCm38) |
missense |
probably benign |
0.01 |
|
R4166:Kdm3b
|
UTSW |
18 |
34,795,744 (GRCm38) |
missense |
probably benign |
0.01 |
|
R4372:Kdm3b
|
UTSW |
18 |
34,827,444 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4672:Kdm3b
|
UTSW |
18 |
34,808,577 (GRCm38) |
missense |
probably benign |
|
|
R4933:Kdm3b
|
UTSW |
18 |
34,810,393 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4969:Kdm3b
|
UTSW |
18 |
34,822,375 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5009:Kdm3b
|
UTSW |
18 |
34,824,710 (GRCm38) |
missense |
probably benign |
0.42 |
|
R5059:Kdm3b
|
UTSW |
18 |
34,777,197 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
R5092:Kdm3b
|
UTSW |
18 |
34,813,462 (GRCm38) |
missense |
probably benign |
0.16 |
|
R5270:Kdm3b
|
UTSW |
18 |
34,827,414 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5816:Kdm3b
|
UTSW |
18 |
34,828,469 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5970:Kdm3b
|
UTSW |
18 |
34,829,289 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6705:Kdm3b
|
UTSW |
18 |
34,819,873 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6723:Kdm3b
|
UTSW |
18 |
34,793,005 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R6909:Kdm3b
|
UTSW |
18 |
34,827,328 (GRCm38) |
splice site |
probably null |
|
|
R6958:Kdm3b
|
UTSW |
18 |
34,808,283 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7026:Kdm3b
|
UTSW |
18 |
34,822,464 (GRCm38) |
missense |
possibly damaging |
0.90 |
|
R7289:Kdm3b
|
UTSW |
18 |
34,794,504 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7488:Kdm3b
|
UTSW |
18 |
34,824,881 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R7587:Kdm3b
|
UTSW |
18 |
34,797,027 (GRCm38) |
splice site |
probably null |
|
|
R7695:Kdm3b
|
UTSW |
18 |
34,794,559 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R7846:Kdm3b
|
UTSW |
18 |
34,809,240 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R7984:Kdm3b
|
UTSW |
18 |
34,823,699 (GRCm38) |
nonsense |
probably null |
|
|
R7997:Kdm3b
|
UTSW |
18 |
34,808,283 (GRCm38) |
missense |
probably benign |
0.00 |
|
R8035:Kdm3b
|
UTSW |
18 |
34,808,728 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8064:Kdm3b
|
UTSW |
18 |
34,813,407 (GRCm38) |
critical splice acceptor site |
probably null |
|
|
R8141:Kdm3b
|
UTSW |
18 |
34,828,546 (GRCm38) |
nonsense |
probably null |
|
|
R8302:Kdm3b
|
UTSW |
18 |
34,834,335 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8328:Kdm3b
|
UTSW |
18 |
34,793,070 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8443:Kdm3b
|
UTSW |
18 |
34,793,076 (GRCm38) |
missense |
probably benign |
0.04 |
|
R8513:Kdm3b
|
UTSW |
18 |
34,793,076 (GRCm38) |
missense |
probably benign |
0.04 |
|
R8515:Kdm3b
|
UTSW |
18 |
34,793,076 (GRCm38) |
missense |
probably benign |
0.04 |
|
R8523:Kdm3b
|
UTSW |
18 |
34,793,076 (GRCm38) |
missense |
probably benign |
0.04 |
|
R8717:Kdm3b
|
UTSW |
18 |
34,819,787 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R8725:Kdm3b
|
UTSW |
18 |
34,827,382 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8727:Kdm3b
|
UTSW |
18 |
34,827,382 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8762:Kdm3b
|
UTSW |
18 |
34,804,104 (GRCm38) |
missense |
probably benign |
|
|
R8835:Kdm3b
|
UTSW |
18 |
34,808,749 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8918:Kdm3b
|
UTSW |
18 |
34,837,597 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9015:Kdm3b
|
UTSW |
18 |
34,830,159 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9144:Kdm3b
|
UTSW |
18 |
34,794,505 (GRCm38) |
missense |
probably benign |
|
|
R9246:Kdm3b
|
UTSW |
18 |
34,808,427 (GRCm38) |
nonsense |
probably null |
|
|
R9376:Kdm3b
|
UTSW |
18 |
34,837,665 (GRCm38) |
missense |
probably damaging |
0.99 |
|
X0028:Kdm3b
|
UTSW |
18 |
34,799,266 (GRCm38) |
splice site |
probably null |
|
|
X0067:Kdm3b
|
UTSW |
18 |
34,823,517 (GRCm38) |
missense |
probably benign |
0.00 |
|
Z1176:Kdm3b
|
UTSW |
18 |
34,809,069 (GRCm38) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TCCCAATAAGTCAGTTTCCTTTTAAT -3'
(R):5'- AAAGCTACTTACCAGGGCTG -3'
Sequencing Primer
(F):5'- TTTAATCCCAGCACTCGGGAG -3'
(R):5'- CCAGGGCTGGCCACTGG -3'
|
| Posted On |
2018-02-28 |
Incidental Mutation