Incidental Mutation 'R5560:Hjurp'
| ID |
501191 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Hjurp
|
| Ensembl Gene |
ENSMUSG00000044783 |
| Gene Name |
Holliday junction recognition protein |
| Synonyms |
A730008H23Rik, C330011F01Rik, 6430706D22Rik |
| MMRRC Submission |
043117-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.915)
|
| Stock # |
R5560 (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: 99.9%
- 3x: 99.6%
- 10x: 97.7%
- 20x: 92.8%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 81 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
| Adipor1 |
T |
C |
1: 134,353,778 (GRCm39) |
W188R |
possibly damaging |
Het |
| Agrn |
T |
C |
4: 156,262,954 (GRCm39) |
D441G |
probably damaging |
Het |
| Ankrd55 |
T |
C |
13: 112,520,024 (GRCm39) |
S570P |
probably benign |
Het |
| Ano9 |
C |
G |
7: 140,690,395 (GRCm39) |
G80R |
probably damaging |
Het |
| Arhgef2 |
T |
A |
3: 88,541,744 (GRCm39) |
V250E |
probably damaging |
Het |
| Atp2b2 |
T |
C |
6: 113,751,319 (GRCm39) |
D583G |
possibly damaging |
Het |
| Bcar3 |
T |
A |
3: 122,220,224 (GRCm39) |
D40E |
possibly damaging |
Het |
| Capn12 |
A |
G |
7: 28,582,285 (GRCm39) |
D133G |
probably benign |
Het |
| Ccna1 |
A |
T |
3: 54,955,990 (GRCm39) |
Y269N |
probably damaging |
Het |
| Cct6b |
A |
T |
11: 82,632,239 (GRCm39) |
Y250N |
probably damaging |
Het |
| Cep112 |
A |
C |
11: 108,328,061 (GRCm39) |
K98Q |
probably damaging |
Het |
| Chst13 |
T |
C |
6: 90,295,251 (GRCm39) |
D54G |
probably damaging |
Het |
| Clstn2 |
G |
T |
9: 97,351,872 (GRCm39) |
H518N |
possibly damaging |
Het |
| Cntnap1 |
T |
A |
11: 101,073,261 (GRCm39) |
L581M |
probably damaging |
Het |
| Cog3 |
T |
A |
14: 75,966,833 (GRCm39) |
M446L |
probably damaging |
Het |
| Dennd2c |
T |
A |
3: 103,068,871 (GRCm39) |
I756K |
probably damaging |
Het |
| Dennd3 |
T |
G |
15: 73,404,744 (GRCm39) |
L273R |
probably damaging |
Het |
| Dhx34 |
C |
A |
7: 15,952,466 (GRCm39) |
R53L |
probably benign |
Het |
| Dnah9 |
G |
A |
11: 65,772,566 (GRCm39) |
T3722I |
probably benign |
Het |
| Dnajb12 |
GC |
G |
10: 59,728,574 (GRCm39) |
|
probably null |
Het |
| Dusp6 |
A |
G |
10: 99,102,103 (GRCm39) |
Y217C |
probably damaging |
Het |
| Dync2i1 |
T |
C |
12: 116,181,733 (GRCm39) |
S769G |
probably damaging |
Het |
| Dyrk1b |
G |
A |
7: 27,883,678 (GRCm39) |
R178Q |
possibly damaging |
Het |
| Eif4g1 |
T |
A |
16: 20,505,645 (GRCm39) |
C1009S |
probably benign |
Het |
| Frmpd1 |
A |
T |
4: 45,243,697 (GRCm39) |
T57S |
probably damaging |
Het |
| Gask1a |
T |
C |
9: 121,807,289 (GRCm39) |
F478L |
possibly damaging |
Het |
| Gjc2 |
A |
G |
11: 59,068,185 (GRCm39) |
V99A |
possibly damaging |
Het |
| Gm9955 |
A |
T |
18: 24,842,149 (GRCm39) |
|
probably benign |
Het |
| Gpr158 |
A |
G |
2: 21,831,101 (GRCm39) |
I734V |
possibly damaging |
Het |
| H1f2 |
A |
G |
13: 23,923,390 (GRCm39) |
S187G |
probably benign |
Het |
| Herc1 |
A |
T |
9: 66,358,401 (GRCm39) |
H2494L |
probably benign |
Het |
| Hmgcs1 |
A |
G |
13: 120,161,351 (GRCm39) |
|
probably null |
Het |
| Invs |
A |
T |
4: 48,416,084 (GRCm39) |
T655S |
probably benign |
Het |
| Ipo9 |
G |
A |
1: 135,329,983 (GRCm39) |
L486F |
probably damaging |
Het |
| Katnip |
T |
C |
7: 125,453,733 (GRCm39) |
V1150A |
probably benign |
Het |
| Kcnj6 |
A |
T |
16: 94,633,824 (GRCm39) |
L96M |
probably benign |
Het |
| Lfng |
A |
G |
5: 140,600,022 (GRCm39) |
D354G |
possibly damaging |
Het |
| Lgsn |
T |
C |
1: 31,235,953 (GRCm39) |
L139P |
probably damaging |
Het |
| Madd |
C |
A |
2: 90,993,890 (GRCm39) |
V923L |
probably damaging |
Het |
| Mical1 |
A |
T |
10: 41,354,961 (GRCm39) |
I157F |
probably damaging |
Het |
| Mis18bp1 |
T |
C |
12: 65,199,590 (GRCm39) |
N154S |
possibly damaging |
Het |
| Mrps14 |
A |
G |
1: 160,023,105 (GRCm39) |
K6R |
probably benign |
Het |
| Mug1 |
T |
A |
6: 121,838,032 (GRCm39) |
C421S |
probably damaging |
Het |
| Myo18b |
A |
G |
5: 113,016,161 (GRCm39) |
I696T |
probably damaging |
Het |
| Naf1 |
T |
C |
8: 67,336,197 (GRCm39) |
Y375H |
probably damaging |
Het |
| Nsf |
T |
A |
11: 103,754,081 (GRCm39) |
E485V |
possibly damaging |
Het |
| Nup188 |
A |
G |
2: 30,199,897 (GRCm39) |
D307G |
probably damaging |
Het |
| Ocel1 |
C |
A |
8: 71,825,122 (GRCm39) |
P108T |
probably damaging |
Het |
| Oip5 |
A |
G |
2: 119,443,540 (GRCm39) |
S177P |
probably damaging |
Het |
| Omg |
A |
G |
11: 79,392,584 (GRCm39) |
W425R |
possibly damaging |
Het |
| Or1ad8 |
A |
C |
11: 50,898,350 (GRCm39) |
I184L |
possibly damaging |
Het |
| Or1l4 |
A |
G |
2: 37,091,942 (GRCm39) |
I230V |
probably benign |
Het |
| Or5an10 |
G |
A |
19: 12,276,008 (GRCm39) |
Q163* |
probably null |
Het |
| Or8g26 |
A |
C |
9: 39,095,480 (GRCm39) |
E2A |
probably benign |
Het |
| Pikfyve |
A |
G |
1: 65,292,566 (GRCm39) |
Y1339C |
probably damaging |
Het |
| Polr3e |
A |
G |
7: 120,522,172 (GRCm39) |
D6G |
possibly damaging |
Het |
| Pou4f3 |
C |
A |
18: 42,528,480 (GRCm39) |
P141Q |
probably benign |
Het |
| Rcsd1 |
T |
A |
1: 165,483,070 (GRCm39) |
N337I |
possibly damaging |
Het |
| Rhoj |
C |
T |
12: 75,438,486 (GRCm39) |
P91S |
probably damaging |
Het |
| Rnf10 |
A |
G |
5: 115,388,057 (GRCm39) |
F367S |
probably damaging |
Het |
| Rnft1 |
A |
T |
11: 86,384,022 (GRCm39) |
R307S |
probably benign |
Het |
| Ryr3 |
A |
T |
2: 112,585,222 (GRCm39) |
F2788Y |
probably damaging |
Het |
| Scgb1c1 |
A |
G |
7: 140,426,137 (GRCm39) |
K78E |
possibly damaging |
Het |
| Scn5a |
G |
T |
9: 119,389,352 (GRCm39) |
A123E |
probably damaging |
Het |
| Setd2 |
T |
A |
9: 110,378,907 (GRCm39) |
Y623* |
probably null |
Het |
| Slc49a3 |
A |
T |
5: 108,596,729 (GRCm39) |
M1K |
probably null |
Het |
| Spmap2l |
A |
G |
5: 77,164,333 (GRCm39) |
D112G |
possibly damaging |
Het |
| Tbl2 |
C |
T |
5: 135,186,445 (GRCm39) |
Q216* |
probably null |
Het |
| Tnc |
A |
G |
4: 63,926,946 (GRCm39) |
I860T |
probably damaging |
Het |
| Trafd1 |
T |
C |
5: 121,511,366 (GRCm39) |
K484R |
possibly damaging |
Het |
| Trank1 |
T |
C |
9: 111,219,635 (GRCm39) |
V2124A |
probably damaging |
Het |
| Trpm4 |
A |
T |
7: 44,959,756 (GRCm39) |
W713R |
probably damaging |
Het |
| Uap1l1 |
T |
C |
2: 25,252,688 (GRCm39) |
T451A |
probably benign |
Het |
| Uba6 |
A |
T |
5: 86,279,119 (GRCm39) |
C668S |
probably damaging |
Het |
| Ubxn11 |
T |
C |
4: 133,853,935 (GRCm39) |
F441S |
probably damaging |
Het |
| Vmn1r22 |
C |
T |
6: 57,877,723 (GRCm39) |
V85M |
probably damaging |
Het |
| Vmn2r72 |
T |
A |
7: 85,401,150 (GRCm39) |
I90L |
probably damaging |
Het |
| Zfp330 |
T |
C |
8: 83,491,585 (GRCm39) |
E196G |
probably benign |
Het |
| Zfp746 |
A |
G |
6: 48,059,108 (GRCm39) |
V167A |
possibly damaging |
Het |
| Zfp994 |
T |
C |
17: 22,420,694 (GRCm39) |
E85G |
possibly 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 |
|
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 |
|
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 |
2017-12-01 |
Incidental Mutation