Incidental Mutation 'R8968:Hjurp'
| ID |
682824 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Hjurp
|
| Ensembl Gene |
ENSMUSG00000044783 |
| Gene Name |
Holliday junction recognition protein |
| Synonyms |
A730008H23Rik, C330011F01Rik, 6430706D22Rik |
| MMRRC Submission |
068802-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.917)
|
| Stock # |
R8968 (G1)
|
| Quality Score |
217.468 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
88190193-88205355 bp(-) (GRCm39) |
| Type of Mutation |
utr 3 prime |
| DNA Base Change (assembly) |
CTCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCT to C
at 88193999 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000120753
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000054674]
[ENSMUST00000061013]
[ENSMUST00000065420]
[ENSMUST00000113130]
[ENSMUST00000127446]
[ENSMUST00000147393]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
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 benign
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 benign
Transcript: ENSMUST00000127446
|
| 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 |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.4%
- 20x: 97.9%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2210408I21Rik |
T |
A |
13: 77,480,429 (GRCm39) |
L1153* |
probably null |
Het |
| Adamts2 |
T |
C |
11: 50,683,550 (GRCm39) |
I944T |
possibly damaging |
Het |
| Aqp9 |
A |
T |
9: 71,045,485 (GRCm39) |
C67* |
probably null |
Het |
| Armt1 |
G |
T |
10: 4,404,150 (GRCm39) |
G412W |
probably damaging |
Het |
| B4galt1 |
T |
C |
4: 40,807,243 (GRCm39) |
D381G |
probably benign |
Het |
| Bmp5 |
A |
T |
9: 75,780,579 (GRCm39) |
H292L |
probably benign |
Het |
| Brpf1 |
T |
C |
6: 113,299,510 (GRCm39) |
F1181S |
probably damaging |
Het |
| Btbd7 |
C |
A |
12: 102,779,025 (GRCm39) |
G414C |
probably damaging |
Het |
| Ccdc65 |
A |
T |
15: 98,616,723 (GRCm39) |
K204* |
probably null |
Het |
| Cdk5 |
T |
A |
5: 24,627,379 (GRCm39) |
K88M |
probably damaging |
Het |
| Cdrt4 |
T |
A |
11: 62,883,634 (GRCm39) |
L112Q |
probably damaging |
Het |
| Cenpb |
T |
C |
2: 131,020,547 (GRCm39) |
E417G |
unknown |
Het |
| Cep135 |
T |
C |
5: 76,754,576 (GRCm39) |
I351T |
possibly damaging |
Het |
| Ces1d |
A |
T |
8: 93,914,383 (GRCm39) |
S226R |
probably damaging |
Het |
| Cfap97 |
T |
A |
8: 46,623,114 (GRCm39) |
V168E |
possibly damaging |
Het |
| CN725425 |
T |
C |
15: 91,130,090 (GRCm39) |
C318R |
possibly damaging |
Het |
| Cnga3 |
T |
A |
1: 37,300,460 (GRCm39) |
D393E |
probably benign |
Het |
| Cplane1 |
A |
T |
15: 8,230,765 (GRCm39) |
H1014L |
possibly damaging |
Het |
| Cpsf1 |
G |
A |
15: 76,486,169 (GRCm39) |
R358* |
probably null |
Het |
| Cyp2b23 |
G |
A |
7: 26,378,963 (GRCm39) |
P167L |
probably damaging |
Het |
| Cyp2c70 |
A |
T |
19: 40,142,059 (GRCm39) |
H477Q |
probably benign |
Het |
| D930020B18Rik |
A |
C |
10: 121,490,721 (GRCm39) |
Y107S |
probably damaging |
Het |
| Dhrs1 |
A |
T |
14: 55,978,192 (GRCm39) |
F216I |
probably benign |
Het |
| Dmgdh |
A |
T |
13: 93,845,767 (GRCm39) |
K474* |
probably null |
Het |
| Dsp |
T |
C |
13: 38,335,596 (GRCm39) |
I11T |
possibly damaging |
Het |
| Erh |
G |
T |
12: 80,684,282 (GRCm39) |
A65E |
probably benign |
Het |
| Fmnl1 |
AGGCTCTGG |
AGG |
11: 103,077,444 (GRCm39) |
|
probably benign |
Het |
| Grid2 |
A |
C |
6: 64,643,139 (GRCm39) |
H967P |
probably benign |
Het |
| Hc |
A |
G |
2: 34,922,317 (GRCm39) |
I503T |
possibly damaging |
Het |
| Herc3 |
T |
C |
6: 58,867,183 (GRCm39) |
L824S |
probably damaging |
Het |
| Hfm1 |
T |
C |
5: 107,065,439 (GRCm39) |
D80G |
probably benign |
Het |
| Hspa1l |
A |
G |
17: 35,196,230 (GRCm39) |
K90E |
possibly damaging |
Het |
| Impa2 |
G |
A |
18: 67,451,497 (GRCm39) |
V264I |
probably benign |
Het |
| Ipmk |
C |
T |
10: 71,199,333 (GRCm39) |
R65W |
probably damaging |
Het |
| Klhl38 |
C |
T |
15: 58,185,500 (GRCm39) |
V410I |
probably benign |
Het |
| Lcn4 |
A |
G |
2: 26,558,360 (GRCm39) |
I175T |
possibly damaging |
Het |
| Lipo2 |
C |
A |
19: 33,726,917 (GRCm39) |
W40L |
probably damaging |
Het |
| Mgam |
A |
T |
6: 40,734,745 (GRCm39) |
|
probably null |
Het |
| Myo16 |
T |
A |
8: 10,619,700 (GRCm39) |
I1417N |
unknown |
Het |
| Or2n1d |
A |
T |
17: 38,646,320 (GRCm39) |
T91S |
possibly damaging |
Het |
| Or4a66 |
T |
A |
2: 88,531,137 (GRCm39) |
I179F |
probably benign |
Het |
| Or52e19b |
A |
T |
7: 103,032,667 (GRCm39) |
C181S |
probably damaging |
Het |
| Or5j3 |
G |
A |
2: 86,128,526 (GRCm39) |
R122H |
probably benign |
Het |
| Pcdha11 |
A |
G |
18: 37,145,307 (GRCm39) |
N466S |
probably damaging |
Het |
| Pif1 |
C |
T |
9: 65,499,076 (GRCm39) |
T432M |
probably damaging |
Het |
| Pigt |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
2: 164,341,589 (GRCm39) |
|
probably null |
Het |
| Pkd1l3 |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
8: 110,350,420 (GRCm39) |
|
probably benign |
Het |
| Pole |
T |
C |
5: 110,459,949 (GRCm39) |
S1118P |
possibly damaging |
Het |
| Ppp4r4 |
T |
C |
12: 103,566,706 (GRCm39) |
M652T |
probably benign |
Het |
| Prex2 |
A |
T |
1: 11,180,562 (GRCm39) |
K376* |
probably null |
Het |
| Prps1l1 |
A |
T |
12: 35,035,205 (GRCm39) |
I107F |
probably damaging |
Het |
| Resf1 |
T |
A |
6: 149,228,664 (GRCm39) |
V570D |
probably damaging |
Het |
| Rfc1 |
C |
T |
5: 65,432,778 (GRCm39) |
V761I |
probably benign |
Het |
| Ripk4 |
T |
C |
16: 97,547,203 (GRCm39) |
E353G |
probably benign |
Het |
| Robo2 |
C |
A |
16: 73,767,941 (GRCm39) |
|
probably null |
Het |
| Rrm1 |
C |
T |
7: 102,117,545 (GRCm39) |
A745V |
probably benign |
Het |
| Sash1 |
A |
T |
10: 8,606,179 (GRCm39) |
V737D |
probably benign |
Het |
| Sel1l2 |
T |
C |
2: 140,127,209 (GRCm39) |
K101E |
probably benign |
Het |
| Selenbp2 |
A |
T |
3: 94,607,337 (GRCm39) |
I253F |
probably benign |
Het |
| Setd1a |
C |
T |
7: 127,385,279 (GRCm39) |
P662L |
possibly damaging |
Het |
| Slc16a6 |
C |
T |
11: 109,345,776 (GRCm39) |
V496I |
possibly damaging |
Het |
| Slc4a4 |
A |
T |
5: 89,232,512 (GRCm39) |
M239L |
probably benign |
Het |
| Slc7a8 |
G |
C |
14: 55,018,750 (GRCm39) |
A12G |
probably benign |
Het |
| Snx30 |
T |
C |
4: 59,886,517 (GRCm39) |
S309P |
possibly damaging |
Het |
| Spen |
T |
C |
4: 141,197,701 (GRCm39) |
N3389S |
probably benign |
Het |
| Spg11 |
T |
C |
2: 121,922,687 (GRCm39) |
T921A |
probably damaging |
Het |
| Tanc2 |
T |
A |
11: 105,758,400 (GRCm39) |
D720E |
possibly damaging |
Het |
| Tmprss9 |
A |
T |
10: 80,730,163 (GRCm39) |
I688F |
possibly damaging |
Het |
| Trap1 |
A |
G |
16: 3,862,490 (GRCm39) |
V596A |
possibly damaging |
Het |
| Ttc32 |
G |
T |
12: 9,080,187 (GRCm39) |
R44L |
probably benign |
Het |
| Tusc3 |
T |
A |
8: 39,597,898 (GRCm39) |
N288K |
probably benign |
Het |
| Ush2a |
G |
A |
1: 188,127,956 (GRCm39) |
G656E |
probably damaging |
Het |
| Vill |
T |
C |
9: 118,892,671 (GRCm39) |
|
probably null |
Het |
| Vmn1r5 |
A |
T |
6: 56,963,182 (GRCm39) |
R286* |
probably null |
Het |
| Vmn2r14 |
T |
C |
5: 109,365,533 (GRCm39) |
T514A |
probably benign |
Het |
| Vmn2r32 |
G |
A |
7: 7,477,204 (GRCm39) |
H396Y |
probably benign |
Het |
| Vmn2r75 |
A |
T |
7: 85,820,765 (GRCm39) |
Y56* |
probably null |
Het |
| Wdfy3 |
C |
T |
5: 102,011,983 (GRCm39) |
S2668N |
probably benign |
Het |
| Wdr72 |
G |
A |
9: 74,059,729 (GRCm39) |
D392N |
probably benign |
Het |
| Zfp518a |
A |
C |
19: 40,901,870 (GRCm39) |
K600Q |
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 |
|
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 |
|
|
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'- AAGTCCAAGTCCTTCTGCGG -3'
(R):5'- TTTGCAATGTGACAATCAGCG -3'
Sequencing Primer
(F):5'- CTTCTGCGGCATCATCTGGAG -3'
(R):5'- GCAATGTGACAATCAGCGATTTG -3'
|
| Posted On |
2021-10-11 |
Incidental Mutation