Incidental Mutation 'R1496:Hjurp'
ID |
250612 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Hjurp
|
Ensembl Gene |
ENSMUSG00000044783 |
Gene Name |
Holliday junction recognition protein |
Synonyms |
A730008H23Rik, C330011F01Rik, 6430706D22Rik |
MMRRC Submission |
039547-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.915)
|
Stock # |
R1496 (G1)
|
Quality Score |
46 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
88190193-88205355 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 88202772 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Asparagine
at position 71
(Y71N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000070419
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000054674]
[ENSMUST00000065420]
[ENSMUST00000147393]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000054674
AA Change: Y71N
PolyPhen 2
Score 0.034 (Sensitivity: 0.95; Specificity: 0.82)
|
SMART Domains |
Protein: ENSMUSP00000054263 Gene: ENSMUSG00000044783 AA Change: Y71N
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 |
possibly damaging
Transcript: ENSMUST00000065420
AA Change: Y71N
PolyPhen 2
Score 0.593 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000070419 Gene: ENSMUSG00000044783 AA Change: Y71N
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 |
noncoding transcript
Transcript: ENSMUST00000126739
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128532
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000147393
AA Change: Y71N
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000120753 Gene: ENSMUSG00000044783 AA Change: Y71N
Domain | Start | End | E-Value | Type |
Pfam:Scm3
|
9 |
70 |
7.2e-13 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148138
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148384
|
Meta Mutation Damage Score |
0.1795 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.3%
- 20x: 92.9%
|
Validation Efficiency |
98% (94/96) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429L15Rik |
A |
G |
9: 46,221,552 (GRCm39) |
|
probably benign |
Het |
4933411K16Rik |
T |
C |
19: 42,041,489 (GRCm39) |
Y207H |
probably damaging |
Het |
Abcc1 |
T |
A |
16: 14,266,298 (GRCm39) |
L832Q |
probably damaging |
Het |
Acan |
T |
A |
7: 78,750,552 (GRCm39) |
H1774Q |
probably benign |
Het |
Adss2 |
T |
C |
1: 177,599,760 (GRCm39) |
T275A |
probably benign |
Het |
Ano5 |
G |
A |
7: 51,233,523 (GRCm39) |
R595H |
probably damaging |
Het |
Araf |
G |
T |
X: 20,725,943 (GRCm39) |
R522L |
probably damaging |
Het |
Arhgef28 |
C |
T |
13: 98,102,054 (GRCm39) |
V807I |
possibly damaging |
Het |
Bin1 |
T |
C |
18: 32,545,757 (GRCm39) |
I103T |
probably damaging |
Het |
C4b |
C |
T |
17: 34,958,995 (GRCm39) |
R478Q |
probably benign |
Het |
Cacna1b |
G |
A |
2: 24,568,047 (GRCm39) |
P1015S |
probably benign |
Het |
Capn1 |
A |
G |
19: 6,057,528 (GRCm39) |
|
probably null |
Het |
Cep290 |
A |
G |
10: 100,374,828 (GRCm39) |
Q1358R |
probably damaging |
Het |
Cfap126 |
T |
C |
1: 170,953,386 (GRCm39) |
|
probably benign |
Het |
Chn1 |
T |
C |
2: 73,509,951 (GRCm39) |
|
probably benign |
Het |
Cldn8 |
T |
C |
16: 88,359,289 (GRCm39) |
E212G |
probably benign |
Het |
Cpb1 |
T |
C |
3: 20,317,696 (GRCm39) |
N249S |
probably damaging |
Het |
Cxcr6 |
A |
T |
9: 123,639,412 (GRCm39) |
I138F |
probably benign |
Het |
Dab2ip |
G |
A |
2: 35,608,803 (GRCm39) |
R579H |
probably damaging |
Het |
Dcaf8 |
T |
C |
1: 172,021,422 (GRCm39) |
M538T |
probably benign |
Het |
Dhrs4 |
T |
G |
14: 55,725,107 (GRCm39) |
L201V |
probably damaging |
Het |
Dnah12 |
C |
T |
14: 26,431,403 (GRCm39) |
A407V |
probably benign |
Het |
Elavl3 |
T |
A |
9: 21,937,461 (GRCm39) |
|
probably benign |
Het |
Elp4 |
T |
C |
2: 105,662,506 (GRCm39) |
H88R |
probably benign |
Het |
Ercc3 |
T |
C |
18: 32,394,350 (GRCm39) |
|
probably benign |
Het |
Eri1 |
A |
G |
8: 35,936,335 (GRCm39) |
S329P |
possibly damaging |
Het |
Erich2 |
A |
T |
2: 70,343,117 (GRCm39) |
|
probably benign |
Het |
Esyt1 |
A |
G |
10: 128,348,297 (GRCm39) |
S864P |
possibly damaging |
Het |
Fam170b |
A |
G |
14: 32,557,588 (GRCm39) |
E141G |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,486,427 (GRCm39) |
Y3304C |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,151,415 (GRCm39) |
T2531A |
probably benign |
Het |
Fgfr3 |
T |
C |
5: 33,887,094 (GRCm39) |
V166A |
probably damaging |
Het |
Glt8d2 |
T |
C |
10: 82,495,372 (GRCm39) |
D194G |
probably damaging |
Het |
Gpr89 |
A |
G |
3: 96,812,526 (GRCm39) |
I5T |
probably benign |
Het |
Gpx6 |
A |
T |
13: 21,503,090 (GRCm39) |
H168L |
probably benign |
Het |
Gusb |
T |
C |
5: 130,027,385 (GRCm39) |
T307A |
probably benign |
Het |
Ifngr1 |
A |
G |
10: 19,477,193 (GRCm39) |
D118G |
probably benign |
Het |
Ipcef1 |
A |
T |
10: 6,885,173 (GRCm39) |
|
probably null |
Het |
Kbtbd3 |
A |
T |
9: 4,330,276 (GRCm39) |
T217S |
probably benign |
Het |
Kmt5a |
GAA |
GA |
5: 124,597,948 (GRCm39) |
|
probably null |
Het |
Lrp1 |
T |
C |
10: 127,374,880 (GRCm39) |
D4526G |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 42,213,674 (GRCm39) |
V46D |
probably damaging |
Het |
Lsm8 |
T |
A |
6: 18,849,658 (GRCm39) |
M22K |
probably benign |
Het |
Map1lc3b |
C |
T |
8: 122,323,339 (GRCm39) |
R70C |
possibly damaging |
Het |
Meiob |
T |
A |
17: 25,032,026 (GRCm39) |
S14T |
possibly damaging |
Het |
Mkx |
G |
T |
18: 6,992,330 (GRCm39) |
Y183* |
probably null |
Het |
Mrs2 |
T |
C |
13: 25,189,017 (GRCm39) |
Y99C |
probably benign |
Het |
Mycbpap |
T |
C |
11: 94,396,387 (GRCm39) |
K151R |
probably benign |
Het |
Neb |
T |
G |
2: 52,218,746 (GRCm39) |
Q88P |
probably damaging |
Het |
Noc4l |
T |
A |
5: 110,797,944 (GRCm39) |
H319L |
probably damaging |
Het |
Nt5c2 |
G |
A |
19: 46,893,417 (GRCm39) |
T122I |
probably damaging |
Het |
Nuggc |
A |
T |
14: 65,861,582 (GRCm39) |
N476I |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,921,862 (GRCm39) |
H5978L |
probably benign |
Het |
Oc90 |
G |
T |
15: 65,748,370 (GRCm39) |
A412D |
probably damaging |
Het |
Or2l13b |
T |
A |
16: 19,349,133 (GRCm39) |
D179V |
possibly damaging |
Het |
Or3a4 |
A |
G |
11: 73,944,650 (GRCm39) |
*312Q |
probably null |
Het |
Or4a76 |
A |
G |
2: 89,460,358 (GRCm39) |
S295P |
possibly damaging |
Het |
Or5w18 |
T |
G |
2: 87,633,212 (GRCm39) |
S160A |
probably benign |
Het |
Or7a42 |
T |
A |
10: 78,791,682 (GRCm39) |
S214R |
probably benign |
Het |
Or8k33 |
A |
T |
2: 86,384,096 (GRCm39) |
V124E |
probably damaging |
Het |
Pdzrn3 |
A |
T |
6: 101,127,930 (GRCm39) |
V912E |
probably benign |
Het |
Phactr1 |
T |
A |
13: 43,248,466 (GRCm39) |
Y387N |
probably damaging |
Het |
Picalm |
T |
A |
7: 89,779,859 (GRCm39) |
C27S |
probably benign |
Het |
Pkd1l1 |
T |
A |
11: 8,891,077 (GRCm39) |
I314F |
possibly damaging |
Het |
Pold2 |
T |
C |
11: 5,824,175 (GRCm39) |
E210G |
possibly damaging |
Het |
Ptprz1 |
C |
T |
6: 23,049,523 (GRCm39) |
|
probably benign |
Het |
Rac1 |
G |
T |
5: 143,493,093 (GRCm39) |
A165E |
probably damaging |
Het |
Rpap3 |
G |
T |
15: 97,584,364 (GRCm39) |
T360K |
possibly damaging |
Het |
Scn9a |
G |
A |
2: 66,357,232 (GRCm39) |
T1012I |
probably benign |
Het |
Sdad1 |
A |
G |
5: 92,457,682 (GRCm39) |
I20T |
possibly damaging |
Het |
Setbp1 |
T |
G |
18: 78,903,127 (GRCm39) |
K180T |
probably damaging |
Het |
Sgpl1 |
T |
C |
10: 60,938,368 (GRCm39) |
N475S |
probably damaging |
Het |
Shroom3 |
T |
C |
5: 93,090,693 (GRCm39) |
S1148P |
possibly damaging |
Het |
Sin3a |
T |
A |
9: 57,026,442 (GRCm39) |
H1119Q |
possibly damaging |
Het |
Slc26a7 |
T |
A |
4: 14,506,489 (GRCm39) |
Y620F |
probably benign |
Het |
Slc4a1 |
T |
C |
11: 102,251,997 (GRCm39) |
I36V |
probably benign |
Het |
Smarca2 |
C |
G |
19: 26,608,501 (GRCm39) |
P263A |
possibly damaging |
Het |
Sp100 |
T |
C |
1: 85,591,242 (GRCm39) |
|
probably benign |
Het |
Spag6l |
A |
G |
16: 16,598,478 (GRCm39) |
|
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,071,498 (GRCm39) |
N1491S |
probably damaging |
Het |
Tbl1xr1 |
T |
G |
3: 22,245,115 (GRCm39) |
V155G |
possibly damaging |
Het |
Tmc1 |
A |
G |
19: 20,845,719 (GRCm39) |
I168T |
probably damaging |
Het |
Tmem87b |
G |
A |
2: 128,668,313 (GRCm39) |
|
probably null |
Het |
Tnfrsf9 |
T |
A |
4: 151,017,561 (GRCm39) |
|
probably null |
Het |
Tnni3k |
T |
C |
3: 154,645,295 (GRCm39) |
D530G |
probably damaging |
Het |
Vmn1r209 |
G |
A |
13: 22,989,934 (GRCm39) |
S252F |
probably damaging |
Het |
Zbtb3 |
A |
T |
19: 8,780,714 (GRCm39) |
N109I |
probably damaging |
Het |
Zdhhc17 |
T |
G |
10: 110,782,071 (GRCm39) |
H541P |
probably damaging |
Het |
Zfp84 |
A |
G |
7: 29,476,039 (GRCm39) |
I244V |
possibly damaging |
Het |
Zyx |
A |
G |
6: 42,333,246 (GRCm39) |
Y393C |
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 |
|
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 |
R1965:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
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'- ACATGGCTTGCTGTGGACTATGATG -3'
(R):5'- GCCAATGCCTGGATTGCTCTGAAC -3'
Sequencing Primer
(F):5'- CTGTGGACTATGATGAAGAAATAGC -3'
(R):5'- GATTGCTCTGAACGCTTGC -3'
|
Posted On |
2014-11-26 |