Incidental Mutation 'R4700:Hjurp'
ID |
394784 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Hjurp
|
Ensembl Gene |
ENSMUSG00000044783 |
Gene Name |
Holliday junction recognition protein |
Synonyms |
A730008H23Rik, C330011F01Rik, 6430706D22Rik |
MMRRC Submission |
041948-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.915)
|
Stock # |
R4700 (G1)
|
Quality Score |
112 |
Status
|
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: 96.8%
- 20x: 94.0%
|
Validation Efficiency |
97% (127/131) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A530084C06Rik |
A |
G |
13: 31,742,795 (GRCm39) |
|
probably benign |
Het |
Abca13 |
A |
G |
11: 9,242,306 (GRCm39) |
T1390A |
possibly damaging |
Het |
Abca14 |
T |
A |
7: 119,911,928 (GRCm39) |
|
probably null |
Het |
Abca8a |
A |
C |
11: 109,961,308 (GRCm39) |
V538G |
probably damaging |
Het |
Acy1 |
C |
T |
9: 106,310,782 (GRCm39) |
G329R |
probably benign |
Het |
Adamts17 |
T |
C |
7: 66,691,636 (GRCm39) |
C607R |
probably damaging |
Het |
Adamts20 |
A |
T |
15: 94,292,503 (GRCm39) |
C202* |
probably null |
Het |
Adcy5 |
A |
G |
16: 35,099,586 (GRCm39) |
N712S |
possibly damaging |
Het |
Ahnak |
A |
G |
19: 8,982,045 (GRCm39) |
K1110E |
probably benign |
Het |
Anks6 |
T |
A |
4: 47,033,127 (GRCm39) |
H578L |
possibly damaging |
Het |
Appl1 |
C |
A |
14: 26,647,928 (GRCm39) |
L626F |
probably benign |
Het |
Arl1 |
A |
G |
10: 88,566,499 (GRCm39) |
|
probably benign |
Het |
Atf4 |
T |
A |
15: 80,141,618 (GRCm39) |
I336K |
probably damaging |
Het |
Atp7b |
A |
T |
8: 22,490,137 (GRCm39) |
S1044T |
probably benign |
Het |
Carm1 |
A |
G |
9: 21,498,480 (GRCm39) |
N466S |
probably benign |
Het |
Cbl |
A |
G |
9: 44,084,677 (GRCm39) |
S153P |
probably damaging |
Het |
Ccdc159 |
A |
G |
9: 21,839,027 (GRCm39) |
|
probably null |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Cdc7 |
T |
C |
5: 107,121,707 (GRCm39) |
F207L |
probably benign |
Het |
Celsr2 |
T |
C |
3: 108,304,547 (GRCm39) |
R2271G |
probably benign |
Het |
Cep162 |
T |
C |
9: 87,088,915 (GRCm39) |
Q989R |
probably damaging |
Het |
Cep89 |
A |
G |
7: 35,137,862 (GRCm39) |
T749A |
probably benign |
Het |
Clcn5 |
T |
C |
X: 7,032,591 (GRCm39) |
|
probably null |
Het |
Clu |
A |
T |
14: 66,217,313 (GRCm39) |
Y382F |
probably benign |
Het |
Cnih4 |
A |
G |
1: 180,993,808 (GRCm39) |
|
probably benign |
Het |
Crb1 |
A |
G |
1: 139,126,509 (GRCm39) |
L1340P |
probably damaging |
Het |
Ddx4 |
T |
C |
13: 112,750,269 (GRCm39) |
T421A |
probably damaging |
Het |
Dennd5a |
T |
C |
7: 109,520,405 (GRCm39) |
E484G |
probably benign |
Het |
Dsg4 |
G |
T |
18: 20,589,965 (GRCm39) |
V372L |
possibly damaging |
Het |
Dyrk2 |
T |
C |
10: 118,704,191 (GRCm39) |
D21G |
probably benign |
Het |
E2f1 |
C |
G |
2: 154,405,942 (GRCm39) |
G144R |
probably damaging |
Het |
Epb41l4a |
A |
T |
18: 33,935,560 (GRCm39) |
|
probably null |
Het |
F10 |
G |
T |
8: 13,089,621 (GRCm39) |
V67F |
possibly damaging |
Het |
Fat3 |
A |
G |
9: 15,942,469 (GRCm39) |
I1301T |
probably damaging |
Het |
Filip1l |
A |
G |
16: 57,391,058 (GRCm39) |
T549A |
probably benign |
Het |
Flt4 |
C |
A |
11: 49,517,271 (GRCm39) |
|
probably benign |
Het |
Fndc1 |
G |
A |
17: 7,990,312 (GRCm39) |
T1128I |
unknown |
Het |
Fos |
T |
C |
12: 85,522,936 (GRCm39) |
S283P |
probably benign |
Het |
Fryl |
T |
C |
5: 73,222,881 (GRCm39) |
Y1900C |
possibly damaging |
Het |
Fsip2 |
C |
A |
2: 82,817,373 (GRCm39) |
Q4369K |
probably benign |
Het |
Gad2 |
A |
T |
2: 22,563,982 (GRCm39) |
H395L |
probably damaging |
Het |
Grm2 |
T |
A |
9: 106,531,130 (GRCm39) |
I120F |
probably benign |
Het |
Igsf10 |
A |
T |
3: 59,227,751 (GRCm39) |
I1974N |
probably damaging |
Het |
Il23r |
T |
C |
6: 67,450,834 (GRCm39) |
N215S |
probably damaging |
Het |
Jph1 |
T |
A |
1: 17,161,928 (GRCm39) |
M245L |
possibly damaging |
Het |
Loxl4 |
G |
A |
19: 42,596,052 (GRCm39) |
H147Y |
probably benign |
Het |
Lsg1 |
A |
G |
16: 30,384,267 (GRCm39) |
I521T |
probably damaging |
Het |
Ltc4s |
C |
T |
11: 50,127,908 (GRCm39) |
G83R |
probably damaging |
Het |
Map2 |
A |
G |
1: 66,449,796 (GRCm39) |
E173G |
probably damaging |
Het |
Med29 |
T |
A |
7: 28,086,352 (GRCm39) |
D152V |
possibly damaging |
Het |
Megf8 |
A |
G |
7: 25,062,940 (GRCm39) |
D2432G |
probably damaging |
Het |
Mrpl38 |
G |
A |
11: 116,025,978 (GRCm39) |
|
probably benign |
Het |
Myh7 |
A |
G |
14: 55,225,778 (GRCm39) |
I521T |
possibly damaging |
Het |
Mylk |
G |
T |
16: 34,742,805 (GRCm39) |
V1106L |
probably benign |
Het |
Myo15b |
A |
T |
11: 115,752,761 (GRCm39) |
D753V |
possibly damaging |
Het |
Myo1g |
T |
C |
11: 6,466,785 (GRCm39) |
|
probably null |
Het |
Myrfl |
A |
G |
10: 116,613,247 (GRCm39) |
|
probably null |
Het |
Naip5 |
A |
G |
13: 100,359,922 (GRCm39) |
V438A |
possibly damaging |
Het |
Nav3 |
A |
G |
10: 109,600,796 (GRCm39) |
V1277A |
probably benign |
Het |
Nek10 |
T |
A |
14: 14,842,841 (GRCm38) |
V182E |
possibly damaging |
Het |
Ngly1 |
T |
C |
14: 16,281,809 (GRCm38) |
V355A |
probably benign |
Het |
Nol6 |
T |
C |
4: 41,118,944 (GRCm39) |
E683G |
possibly damaging |
Het |
Obsl1 |
A |
T |
1: 75,480,085 (GRCm39) |
V487E |
probably damaging |
Het |
Oc90 |
T |
A |
15: 65,753,354 (GRCm39) |
R322W |
possibly damaging |
Het |
Or1q1 |
C |
A |
2: 36,887,515 (GRCm39) |
A231D |
probably benign |
Het |
Or4f60 |
A |
G |
2: 111,902,097 (GRCm39) |
V277A |
possibly damaging |
Het |
Or52e4 |
A |
T |
7: 104,705,483 (GRCm39) |
H10L |
possibly damaging |
Het |
Or8b4 |
A |
G |
9: 37,830,217 (GRCm39) |
E93G |
possibly damaging |
Het |
Osbp2 |
T |
C |
11: 3,662,160 (GRCm39) |
H231R |
probably damaging |
Het |
Pate6 |
A |
T |
9: 35,701,021 (GRCm39) |
C22S |
probably damaging |
Het |
Pdzph1 |
T |
C |
17: 59,281,541 (GRCm39) |
H247R |
probably damaging |
Het |
Pidd1 |
T |
C |
7: 141,022,162 (GRCm39) |
N209S |
probably damaging |
Het |
Pknox1 |
C |
T |
17: 31,822,286 (GRCm39) |
A351V |
probably damaging |
Het |
Plxnd1 |
C |
A |
6: 115,935,576 (GRCm39) |
V1737F |
probably damaging |
Het |
Prkdc |
A |
T |
16: 15,519,976 (GRCm39) |
K1138M |
probably damaging |
Het |
Rad54l2 |
T |
C |
9: 106,631,224 (GRCm39) |
D21G |
possibly damaging |
Het |
Recql4 |
C |
T |
15: 76,592,785 (GRCm39) |
C302Y |
probably damaging |
Het |
Scgb2b6 |
T |
C |
7: 31,318,908 (GRCm39) |
|
noncoding transcript |
Het |
Sdc1 |
A |
G |
12: 8,840,541 (GRCm39) |
E106G |
possibly damaging |
Het |
Slc10a5 |
T |
G |
3: 10,400,360 (GRCm39) |
Q100P |
probably damaging |
Het |
Slc10a5 |
C |
A |
3: 10,400,359 (GRCm39) |
Q100H |
probably damaging |
Het |
Slc5a9 |
A |
T |
4: 111,748,134 (GRCm39) |
L226Q |
possibly damaging |
Het |
Slfn1 |
T |
C |
11: 83,012,475 (GRCm39) |
V197A |
probably benign |
Het |
Spire1 |
T |
C |
18: 67,645,935 (GRCm39) |
M244V |
probably benign |
Het |
St3gal3 |
C |
T |
4: 117,817,232 (GRCm39) |
V141I |
probably benign |
Het |
St6galnac4 |
G |
T |
2: 32,477,172 (GRCm39) |
|
probably benign |
Het |
Svep1 |
T |
C |
4: 58,097,323 (GRCm39) |
K1407E |
possibly damaging |
Het |
Tbc1d32 |
A |
G |
10: 56,100,745 (GRCm39) |
C78R |
probably damaging |
Het |
Tcstv5 |
T |
C |
13: 120,411,378 (GRCm39) |
Y76C |
probably benign |
Het |
Tln2 |
A |
G |
9: 67,253,809 (GRCm39) |
V754A |
probably benign |
Het |
Tmeff1 |
A |
T |
4: 48,636,869 (GRCm39) |
Y189F |
possibly damaging |
Het |
Tmem131l |
C |
T |
3: 83,806,519 (GRCm39) |
A1433T |
probably benign |
Het |
Tnfrsf8 |
T |
C |
4: 145,029,692 (GRCm39) |
Y36C |
probably damaging |
Het |
Trp53i11 |
G |
T |
2: 93,030,245 (GRCm39) |
R184L |
probably damaging |
Het |
Trpv1 |
A |
T |
11: 73,142,110 (GRCm39) |
M214L |
possibly damaging |
Het |
Tsnax |
T |
A |
8: 125,755,533 (GRCm39) |
S132T |
probably benign |
Het |
Ttc28 |
T |
C |
5: 111,424,909 (GRCm39) |
L1547P |
probably damaging |
Het |
Ttc3 |
A |
G |
16: 94,240,100 (GRCm39) |
|
probably null |
Het |
Tubal3 |
T |
A |
13: 3,983,514 (GRCm39) |
D431E |
probably damaging |
Het |
Ugt2b36 |
A |
T |
5: 87,240,301 (GRCm39) |
|
probably null |
Het |
Vmn1r23 |
A |
T |
6: 57,903,190 (GRCm39) |
I196K |
probably benign |
Het |
Vmn1r55 |
A |
C |
7: 5,149,586 (GRCm39) |
L279R |
probably damaging |
Het |
Vmn1r55 |
G |
T |
7: 5,149,587 (GRCm39) |
L279M |
probably damaging |
Het |
Vmn2r89 |
G |
A |
14: 51,694,942 (GRCm39) |
G474E |
probably damaging |
Het |
Vps26b |
T |
C |
9: 26,926,511 (GRCm39) |
K163E |
probably damaging |
Het |
Zfp142 |
A |
G |
1: 74,609,431 (GRCm39) |
F1352L |
probably damaging |
Het |
Zfp422 |
C |
T |
6: 116,603,844 (GRCm39) |
E52K |
possibly damaging |
Het |
Zfp423 |
T |
A |
8: 88,508,338 (GRCm39) |
|
probably null |
Het |
Zfp493 |
T |
C |
13: 67,934,736 (GRCm39) |
F230L |
probably damaging |
Het |
Zfp760 |
T |
C |
17: 21,941,388 (GRCm39) |
C188R |
probably benign |
Het |
Zfyve28 |
G |
T |
5: 34,375,189 (GRCm39) |
T275K |
probably damaging |
Het |
Znhit3 |
T |
C |
11: 84,807,155 (GRCm39) |
N5D |
probably benign |
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 |
88,194,283 (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 |
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 |
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 |
|
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'- ACTGTCATGGTTTGTGATGCCC -3'
Sequencing Primer
(F):5'- AGGTCTTGGTGGAGATGATGCAG -3'
(R):5'- CCTGCCCGGTGGGTAAGTATG -3'
|
Posted On |
2016-06-17 |