Incidental Mutation 'R1965:Hjurp'
ID |
218237 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Hjurp
|
Ensembl Gene |
ENSMUSG00000044783 |
Gene Name |
Holliday junction recognition protein |
Synonyms |
A730008H23Rik, C330011F01Rik, 6430706D22Rik |
MMRRC Submission |
039978-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.915)
|
Stock # |
R1965 (G1)
|
Quality Score |
217 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
88190193-88205355 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
GT to GTT
at 88194246 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000118659
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000054674]
[ENSMUST00000061013]
[ENSMUST00000065420]
[ENSMUST00000113130]
[ENSMUST00000127446]
[ENSMUST00000147393]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000054674
|
SMART Domains |
Protein: ENSMUSP00000054263 Gene: ENSMUSG00000044783
Domain | Start | End | E-Value | Type |
Pfam:Scm3
|
11 |
68 |
1.5e-10 |
PFAM |
low complexity region
|
159 |
175 |
N/A |
INTRINSIC |
low complexity region
|
215 |
232 |
N/A |
INTRINSIC |
Pfam:HJURP_mid
|
254 |
370 |
7.6e-54 |
PFAM |
Pfam:HJURP_C
|
385 |
446 |
3.1e-26 |
PFAM |
low complexity region
|
496 |
515 |
N/A |
INTRINSIC |
Pfam:HJURP_C
|
527 |
585 |
7.1e-21 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000061013
|
SMART Domains |
Protein: ENSMUSP00000130508 Gene: ENSMUSG00000079429
Domain | Start | End | E-Value | Type |
low complexity region
|
9 |
26 |
N/A |
INTRINSIC |
low complexity region
|
99 |
112 |
N/A |
INTRINSIC |
low complexity region
|
1235 |
1248 |
N/A |
INTRINSIC |
SCOP:d1jdha_
|
1371 |
1669 |
9e-8 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000065420
|
SMART Domains |
Protein: ENSMUSP00000070419 Gene: ENSMUSG00000044783
Domain | Start | End | E-Value | Type |
Pfam:Scm3
|
9 |
70 |
2.9e-11 |
PFAM |
low complexity region
|
83 |
99 |
N/A |
INTRINSIC |
low complexity region
|
139 |
156 |
N/A |
INTRINSIC |
Pfam:HJURP_mid
|
178 |
295 |
7.4e-64 |
PFAM |
Pfam:HJURP_C
|
309 |
371 |
1.2e-26 |
PFAM |
low complexity region
|
420 |
439 |
N/A |
INTRINSIC |
Pfam:HJURP_C
|
451 |
510 |
3e-26 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113130
|
SMART Domains |
Protein: ENSMUSP00000108755 Gene: ENSMUSG00000079429
Domain | Start | End | E-Value | Type |
low complexity region
|
9 |
26 |
N/A |
INTRINSIC |
low complexity region
|
99 |
112 |
N/A |
INTRINSIC |
low complexity region
|
1232 |
1245 |
N/A |
INTRINSIC |
SCOP:d1gw5a_
|
1446 |
1671 |
6e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000127446
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128532
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000147393
|
SMART Domains |
Protein: ENSMUSP00000120753 Gene: ENSMUSG00000044783
Domain | Start | End | E-Value | Type |
Pfam:Scm3
|
9 |
70 |
7.2e-13 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148384
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.6%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco1 |
T |
G |
4: 40,175,730 (GRCm39) |
L157R |
probably damaging |
Het |
Acot11 |
A |
T |
4: 106,606,550 (GRCm39) |
L513Q |
probably damaging |
Het |
Amd1 |
A |
G |
10: 40,170,755 (GRCm39) |
I52T |
probably benign |
Het |
Ap2b1 |
T |
C |
11: 83,237,721 (GRCm39) |
I557T |
probably benign |
Het |
Arel1 |
T |
A |
12: 84,987,173 (GRCm39) |
|
probably null |
Het |
Arg1 |
T |
A |
10: 24,792,762 (GRCm39) |
|
probably null |
Het |
Atf1 |
A |
T |
15: 100,152,052 (GRCm39) |
M135L |
probably benign |
Het |
Atf2 |
T |
C |
2: 73,681,242 (GRCm39) |
E77G |
possibly damaging |
Het |
Axin1 |
G |
T |
17: 26,403,199 (GRCm39) |
A394S |
probably damaging |
Het |
Axin1 |
A |
T |
17: 26,409,202 (GRCm39) |
Q734L |
probably damaging |
Het |
Brd8 |
G |
C |
18: 34,735,819 (GRCm39) |
A886G |
probably damaging |
Het |
Ccdc39 |
T |
C |
3: 33,880,629 (GRCm39) |
K446R |
probably damaging |
Het |
Celf3 |
T |
C |
3: 94,392,634 (GRCm39) |
V35A |
probably damaging |
Het |
Cfap299 |
T |
A |
5: 98,494,093 (GRCm39) |
D32E |
probably damaging |
Het |
Ckap2 |
T |
C |
8: 22,665,803 (GRCm39) |
T415A |
possibly damaging |
Het |
Crybg3 |
T |
C |
16: 59,323,600 (GRCm39) |
Y1066C |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,713,144 (GRCm39) |
H1506R |
probably benign |
Het |
Dnah10 |
A |
G |
5: 124,852,267 (GRCm39) |
D1808G |
probably damaging |
Het |
Dsc3 |
C |
T |
18: 20,113,729 (GRCm39) |
G398R |
probably damaging |
Het |
Emc2 |
A |
G |
15: 43,390,863 (GRCm39) |
Q293R |
probably damaging |
Het |
Evc2 |
A |
G |
5: 37,520,876 (GRCm39) |
N251D |
possibly damaging |
Het |
Fam151a |
A |
T |
4: 106,591,112 (GRCm39) |
|
probably benign |
Het |
Fbxw16 |
T |
A |
9: 109,270,289 (GRCm39) |
I151F |
probably damaging |
Het |
Fmnl2 |
A |
G |
2: 53,004,880 (GRCm39) |
D658G |
probably damaging |
Het |
Fnip2 |
G |
A |
3: 79,400,779 (GRCm39) |
T314I |
probably benign |
Het |
Foxc2 |
T |
A |
8: 121,843,413 (GRCm39) |
S20R |
probably damaging |
Het |
Fpr-rs6 |
C |
T |
17: 20,402,918 (GRCm39) |
G148R |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,823,124 (GRCm39) |
S6286P |
possibly damaging |
Het |
Fyb2 |
A |
T |
4: 104,770,846 (GRCm39) |
I54F |
probably benign |
Het |
Gbf1 |
T |
C |
19: 46,260,003 (GRCm39) |
F999L |
probably damaging |
Het |
Gldc |
G |
A |
19: 30,114,513 (GRCm39) |
R466* |
probably null |
Het |
Gm12695 |
T |
A |
4: 96,651,082 (GRCm39) |
S124C |
probably benign |
Het |
Gm4846 |
A |
T |
1: 166,314,533 (GRCm39) |
I370N |
possibly damaging |
Het |
Gsdmc3 |
T |
C |
15: 63,730,296 (GRCm39) |
T423A |
probably damaging |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Kcnmb3 |
T |
C |
3: 32,526,492 (GRCm39) |
Y233C |
probably damaging |
Het |
Kidins220 |
A |
G |
12: 25,044,905 (GRCm39) |
D191G |
probably damaging |
Het |
Kmt2a |
A |
G |
9: 44,732,757 (GRCm39) |
|
probably benign |
Het |
Krt1 |
T |
C |
15: 101,757,427 (GRCm39) |
D261G |
probably benign |
Het |
Lrba |
A |
G |
3: 86,513,175 (GRCm39) |
|
probably null |
Het |
Myo1f |
C |
T |
17: 33,817,146 (GRCm39) |
R730* |
probably null |
Het |
Ncoa7 |
C |
A |
10: 30,530,426 (GRCm39) |
E30* |
probably null |
Het |
Neurod4 |
T |
A |
10: 130,106,918 (GRCm39) |
K119* |
probably null |
Het |
Npy5r |
T |
C |
8: 67,133,929 (GRCm39) |
D288G |
probably benign |
Het |
Nr3c2 |
A |
T |
8: 77,636,092 (GRCm39) |
I398L |
probably damaging |
Het |
Or10a5 |
T |
C |
7: 106,635,565 (GRCm39) |
S68P |
probably damaging |
Het |
Or12j4 |
C |
A |
7: 140,046,574 (GRCm39) |
F153L |
probably benign |
Het |
Or4b1 |
T |
C |
2: 89,979,748 (GRCm39) |
S201G |
probably damaging |
Het |
Or4k35 |
T |
C |
2: 111,099,938 (GRCm39) |
Y258C |
probably damaging |
Het |
Or51v8 |
A |
T |
7: 103,320,103 (GRCm39) |
I45N |
probably damaging |
Het |
Or5g25 |
T |
C |
2: 85,478,090 (GRCm39) |
T192A |
possibly damaging |
Het |
Or5w8 |
A |
G |
2: 87,687,759 (GRCm39) |
K80R |
probably benign |
Het |
Or9m1b |
A |
G |
2: 87,836,648 (GRCm39) |
F149S |
probably damaging |
Het |
P3r3urf |
G |
A |
4: 116,031,376 (GRCm39) |
C82Y |
probably damaging |
Het |
Pcf11 |
A |
T |
7: 92,310,809 (GRCm39) |
M393K |
probably benign |
Het |
Pck2 |
T |
C |
14: 55,779,964 (GRCm39) |
V71A |
probably benign |
Het |
Pdzd8 |
G |
T |
19: 59,288,554 (GRCm39) |
L949I |
probably benign |
Het |
Pdzrn4 |
G |
A |
15: 92,644,190 (GRCm39) |
|
probably null |
Het |
Phospho1 |
A |
G |
11: 95,721,705 (GRCm39) |
N125S |
probably damaging |
Het |
Pirb |
A |
T |
7: 3,720,637 (GRCm39) |
L287Q |
probably benign |
Het |
Ppid |
A |
T |
3: 79,509,606 (GRCm39) |
K308* |
probably null |
Het |
Ppp1r1b |
A |
G |
11: 98,246,189 (GRCm39) |
E57G |
probably damaging |
Het |
Prtg |
T |
G |
9: 72,755,604 (GRCm39) |
S269A |
probably benign |
Het |
Rbbp5 |
T |
A |
1: 132,422,035 (GRCm39) |
S312T |
probably damaging |
Het |
Rbm11 |
T |
A |
16: 75,395,656 (GRCm39) |
|
probably null |
Het |
Retreg1 |
A |
G |
15: 25,970,250 (GRCm39) |
T139A |
probably damaging |
Het |
Riok3 |
T |
A |
18: 12,270,019 (GRCm39) |
H120Q |
probably damaging |
Het |
Rln1 |
A |
T |
19: 29,311,995 (GRCm39) |
M1K |
probably null |
Het |
Rpp30 |
C |
T |
19: 36,066,549 (GRCm39) |
S94L |
probably damaging |
Het |
Sccpdh |
C |
T |
1: 179,511,879 (GRCm39) |
P117L |
probably damaging |
Het |
Serac1 |
T |
C |
17: 6,099,274 (GRCm39) |
K506E |
possibly damaging |
Het |
Serping1 |
G |
T |
2: 84,596,072 (GRCm39) |
T454K |
probably damaging |
Het |
Slc1a2 |
T |
A |
2: 102,570,245 (GRCm39) |
N174K |
probably damaging |
Het |
Slc2a2 |
A |
G |
3: 28,773,634 (GRCm39) |
Q313R |
probably damaging |
Het |
Slc46a2 |
T |
A |
4: 59,914,249 (GRCm39) |
S225C |
probably damaging |
Het |
Smarcc2 |
G |
A |
10: 128,310,627 (GRCm39) |
E419K |
probably damaging |
Het |
Stkld1 |
T |
A |
2: 26,836,744 (GRCm39) |
|
probably null |
Het |
Szt2 |
A |
G |
4: 118,241,162 (GRCm39) |
M1704T |
probably benign |
Het |
Tasor |
T |
G |
14: 27,164,511 (GRCm39) |
C272W |
probably damaging |
Het |
Tfcp2l1 |
C |
T |
1: 118,580,653 (GRCm39) |
Q116* |
probably null |
Het |
Timm44 |
A |
G |
8: 4,310,603 (GRCm39) |
M383T |
possibly damaging |
Het |
Tnpo2 |
G |
A |
8: 85,771,946 (GRCm39) |
|
probably null |
Het |
Tnrc6b |
A |
G |
15: 80,764,640 (GRCm39) |
K714R |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 102,099,178 (GRCm39) |
L290P |
probably damaging |
Het |
Wdr59 |
A |
G |
8: 112,177,709 (GRCm39) |
F898L |
probably damaging |
Het |
Zfp120 |
A |
T |
2: 149,959,318 (GRCm39) |
C335S |
probably damaging |
Het |
Zfp518a |
T |
C |
19: 40,901,954 (GRCm39) |
S628P |
probably benign |
Het |
Zfp879 |
A |
T |
11: 50,724,355 (GRCm39) |
C234S |
probably damaging |
Het |
|
Other mutations in Hjurp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Hjurp
|
APN |
1 |
88,197,991 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03099:Hjurp
|
APN |
1 |
88,194,011 (GRCm39) |
missense |
probably benign |
0.09 |
BB003:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03097:Hjurp
|
UTSW |
1 |
88,194,002 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03098:Hjurp
|
UTSW |
1 |
88,194,002 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03147:Hjurp
|
UTSW |
1 |
88,194,002 (GRCm39) |
utr 3 prime |
probably benign |
|
PIT4131001:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
PIT4142001:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
PIT4142001:Hjurp
|
UTSW |
1 |
88,193,768 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4142001:Hjurp
|
UTSW |
1 |
88,194,338 (GRCm39) |
missense |
probably benign |
0.04 |
PIT4142001:Hjurp
|
UTSW |
1 |
88,194,283 (GRCm39) |
utr 3 prime |
probably benign |
|
PIT4378001:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
PIT4812001:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
R0053:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R0371:Hjurp
|
UTSW |
1 |
88,205,090 (GRCm39) |
splice site |
probably benign |
|
R0442:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R0762:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R0928:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R1333:Hjurp
|
UTSW |
1 |
88,193,768 (GRCm39) |
missense |
probably damaging |
0.98 |
R1342:Hjurp
|
UTSW |
1 |
88,205,090 (GRCm39) |
splice site |
probably benign |
|
R1364:Hjurp
|
UTSW |
1 |
88,194,247 (GRCm39) |
frame shift |
probably null |
|
R1496:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1637:Hjurp
|
UTSW |
1 |
88,193,843 (GRCm39) |
missense |
probably benign |
0.03 |
R1905:Hjurp
|
UTSW |
1 |
88,194,338 (GRCm39) |
missense |
probably benign |
0.04 |
R1992:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R2002:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R2023:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R2024:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R2332:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R2420:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R2422:Hjurp
|
UTSW |
1 |
88,194,283 (GRCm39) |
utr 3 prime |
probably benign |
|
R2869:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R2870:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R2871:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R2872:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R3019:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R3021:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R3150:Hjurp
|
UTSW |
1 |
88,194,283 (GRCm39) |
utr 3 prime |
probably benign |
|
R3411:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R3552:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R3704:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R3730:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R3733:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R3764:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R3799:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R3819:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R3857:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R3930:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R3952:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R4090:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R4159:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R4207:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R4322:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R4391:Hjurp
|
UTSW |
1 |
88,194,283 (GRCm39) |
utr 3 prime |
probably benign |
|
R4392:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R4393:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R4393:Hjurp
|
UTSW |
1 |
88,194,283 (GRCm39) |
utr 3 prime |
probably benign |
|
R4397:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R4700:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R4808:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R4900:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R4901:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R5023:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5024:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5076:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R5123:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5236:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R5300:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R5318:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R5370:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R5410:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R5445:Hjurp
|
UTSW |
1 |
88,194,038 (GRCm39) |
missense |
probably benign |
0.43 |
R5457:Hjurp
|
UTSW |
1 |
88,194,247 (GRCm39) |
frame shift |
probably null |
|
R5497:Hjurp
|
UTSW |
1 |
88,194,042 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5560:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R5561:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R5615:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R5661:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
R5722:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R6087:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R6089:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R6090:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R6125:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R6175:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R6362:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6659:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R7016:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
R7016:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
R7045:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
R7179:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
R7200:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
R7463:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
R7912:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
R8215:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R8968:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
R9038:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
R9115:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
R9133:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9146:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
R9221:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
R9475:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
R9482:Hjurp
|
UTSW |
1 |
88,193,996 (GRCm39) |
utr 3 prime |
probably benign |
|
R9565:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
R9599:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
V5622:Hjurp
|
UTSW |
1 |
88,205,247 (GRCm39) |
unclassified |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- CCAGCTCTGGTTGATGTAGG -3'
(R):5'- AACTGTCATGGTTTGTGATGCC -3'
Sequencing Primer
(F):5'- AGGTCTTGGTGGAGATGATGCAG -3'
(R):5'- CCTGCCCGGTGGGTAAGTATG -3'
|
Posted On |
2014-08-01 |