Incidental Mutation 'R5024:Hjurp'
| ID |
452884 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Hjurp
|
| Ensembl Gene |
ENSMUSG00000044783 |
| Gene Name |
Holliday junction recognition protein |
| Synonyms |
A730008H23Rik, C330011F01Rik, 6430706D22Rik |
| MMRRC Submission |
042615-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.915)
|
| Stock # |
R5024 (G1)
|
| Quality Score |
69 |
|
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: 99.2%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.4%
|
| Validation Efficiency |
99% (95/96) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 85 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrd1 |
A |
G |
5: 129,248,959 (GRCm39) |
N575S |
probably damaging |
Het |
| Akap6 |
C |
T |
12: 53,189,345 (GRCm39) |
T2253M |
probably benign |
Het |
| Arhgef37 |
A |
C |
18: 61,639,511 (GRCm39) |
N289K |
probably damaging |
Het |
| Atad2b |
A |
C |
12: 4,987,534 (GRCm39) |
T121P |
probably benign |
Het |
| Atp4a |
A |
C |
7: 30,415,289 (GRCm39) |
D303A |
possibly damaging |
Het |
| Calu |
A |
T |
6: 29,374,518 (GRCm39) |
|
probably benign |
Het |
| Ccdc141 |
A |
C |
2: 76,885,047 (GRCm39) |
N531K |
probably benign |
Het |
| Ccdc146 |
T |
C |
5: 21,604,612 (GRCm39) |
|
probably null |
Het |
| Cd207 |
G |
A |
6: 83,651,301 (GRCm39) |
T218I |
probably damaging |
Het |
| Cd2ap |
A |
C |
17: 43,116,236 (GRCm39) |
|
probably null |
Het |
| Ceacam23 |
A |
G |
7: 17,644,607 (GRCm39) |
I575V |
probably benign |
Het |
| Clip3 |
G |
A |
7: 29,991,644 (GRCm39) |
|
probably benign |
Het |
| Clstn1 |
G |
A |
4: 149,719,751 (GRCm39) |
R432H |
possibly damaging |
Het |
| Csmd2 |
A |
G |
4: 128,215,141 (GRCm39) |
Y521C |
possibly damaging |
Het |
| Dnah8 |
A |
T |
17: 30,955,070 (GRCm39) |
E2033V |
probably damaging |
Het |
| Eng |
T |
G |
2: 32,563,404 (GRCm39) |
V319G |
probably benign |
Het |
| Erp44 |
C |
T |
4: 48,241,296 (GRCm39) |
W57* |
probably null |
Het |
| Etv1 |
T |
A |
12: 38,904,233 (GRCm39) |
|
probably null |
Het |
| Eva1c |
T |
C |
16: 90,673,081 (GRCm39) |
|
probably null |
Het |
| Fam221b |
T |
A |
4: 43,659,674 (GRCm39) |
N482I |
probably damaging |
Het |
| Fam83h |
T |
C |
15: 75,876,991 (GRCm39) |
H202R |
probably damaging |
Het |
| Fbxw13 |
T |
C |
9: 109,008,403 (GRCm39) |
T449A |
probably benign |
Het |
| Fbxw25 |
A |
T |
9: 109,492,442 (GRCm39) |
|
probably null |
Het |
| Frmd3 |
T |
A |
4: 74,016,381 (GRCm39) |
S99T |
probably benign |
Het |
| Gm5174 |
G |
T |
10: 86,492,451 (GRCm39) |
|
noncoding transcript |
Het |
| Gm815 |
C |
T |
19: 26,865,175 (GRCm39) |
Q49* |
probably null |
Het |
| H2-DMa |
A |
T |
17: 34,357,461 (GRCm39) |
I245F |
possibly damaging |
Het |
| Herc1 |
A |
T |
9: 66,377,608 (GRCm39) |
K3458M |
possibly damaging |
Het |
| Hirip3 |
A |
G |
7: 126,463,661 (GRCm39) |
|
probably null |
Het |
| Hmcn1 |
T |
A |
1: 150,556,439 (GRCm39) |
E2449V |
possibly damaging |
Het |
| Igll1 |
G |
T |
16: 16,681,657 (GRCm39) |
H33N |
probably benign |
Het |
| Il6 |
T |
C |
5: 30,224,512 (GRCm39) |
L184P |
probably damaging |
Het |
| Impg2 |
T |
A |
16: 56,080,463 (GRCm39) |
S756T |
probably damaging |
Het |
| Insyn2a |
A |
G |
7: 134,520,207 (GRCm39) |
S108P |
probably damaging |
Het |
| Kank4 |
T |
G |
4: 98,673,898 (GRCm39) |
D5A |
probably damaging |
Het |
| Kcna7 |
G |
A |
7: 45,056,015 (GRCm39) |
R77H |
probably damaging |
Het |
| Kcns2 |
A |
T |
15: 34,839,683 (GRCm39) |
T349S |
probably benign |
Het |
| Keap1 |
A |
G |
9: 21,148,522 (GRCm39) |
Y162H |
probably damaging |
Het |
| Kif9 |
T |
C |
9: 110,312,161 (GRCm39) |
F10L |
possibly damaging |
Het |
| Klhdc8b |
ACACGCACGCACGCACGCACGCACGCACGCACGCACGCAC |
ACACGCACGCACGCACGCACGCACGCACGCACGCACGCACGCAC |
9: 108,326,184 (GRCm39) |
|
probably benign |
Het |
| Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
| Lpar6 |
A |
G |
14: 73,476,809 (GRCm39) |
T257A |
probably damaging |
Het |
| Lpin1 |
A |
T |
12: 16,604,007 (GRCm39) |
L608Q |
probably benign |
Het |
| Lyst |
T |
C |
13: 13,808,989 (GRCm39) |
S220P |
probably benign |
Het |
| M1ap |
A |
G |
6: 83,005,339 (GRCm39) |
|
probably benign |
Het |
| Mbd6 |
C |
T |
10: 127,122,310 (GRCm39) |
V173I |
probably benign |
Het |
| Myo5b |
A |
T |
18: 74,849,105 (GRCm39) |
T1115S |
possibly damaging |
Het |
| Mysm1 |
C |
A |
4: 94,839,253 (GRCm39) |
V683F |
possibly damaging |
Het |
| Nlrp4g |
T |
A |
9: 124,350,155 (GRCm38) |
|
noncoding transcript |
Het |
| Odad2 |
T |
C |
18: 7,088,555 (GRCm39) |
M1005V |
probably benign |
Het |
| Or14c39 |
A |
T |
7: 86,344,089 (GRCm39) |
M142L |
probably benign |
Het |
| Or2ak5 |
T |
A |
11: 58,611,776 (GRCm39) |
I33F |
probably benign |
Het |
| Or5al6 |
G |
T |
2: 85,976,877 (GRCm39) |
A67E |
probably damaging |
Het |
| Or8j3c |
C |
T |
2: 86,253,805 (GRCm39) |
G72S |
possibly damaging |
Het |
| Otud6b |
T |
A |
4: 14,826,293 (GRCm39) |
Q34L |
probably damaging |
Het |
| Parp11 |
C |
T |
6: 127,448,599 (GRCm39) |
T72I |
probably damaging |
Het |
| Pbx1 |
T |
A |
1: 168,011,158 (GRCm39) |
D343V |
possibly damaging |
Het |
| Phf11 |
T |
C |
14: 59,495,932 (GRCm39) |
|
probably null |
Het |
| Ppp1r12b |
G |
T |
1: 134,883,471 (GRCm39) |
A17E |
probably benign |
Het |
| Pramel15 |
C |
A |
4: 144,099,878 (GRCm39) |
E296* |
probably null |
Het |
| Ranbp9 |
A |
T |
13: 43,588,331 (GRCm39) |
I67N |
probably damaging |
Het |
| Rasgrp4 |
A |
G |
7: 28,847,832 (GRCm39) |
E414G |
probably damaging |
Het |
| Rbbp5 |
A |
G |
1: 132,418,226 (GRCm39) |
H15R |
possibly damaging |
Het |
| Scd2 |
A |
G |
19: 44,289,710 (GRCm39) |
Y235C |
probably benign |
Het |
| Sdr16c5 |
C |
T |
4: 4,010,365 (GRCm39) |
G170S |
probably damaging |
Het |
| Sh3bp4 |
G |
T |
1: 89,073,317 (GRCm39) |
G722C |
probably damaging |
Het |
| Shmt1 |
A |
T |
11: 60,688,305 (GRCm39) |
|
probably benign |
Het |
| Slc12a1 |
A |
G |
2: 125,008,057 (GRCm39) |
I206V |
probably benign |
Het |
| Slc26a3 |
A |
G |
12: 31,503,907 (GRCm39) |
D304G |
probably benign |
Het |
| Slc26a7 |
T |
A |
4: 14,532,572 (GRCm39) |
D434V |
possibly damaging |
Het |
| Slc6a16 |
G |
T |
7: 44,909,390 (GRCm39) |
M185I |
probably benign |
Het |
| Stat4 |
A |
G |
1: 52,121,729 (GRCm39) |
I363V |
possibly damaging |
Het |
| Tgfb1i1 |
G |
T |
7: 127,847,389 (GRCm39) |
M1I |
probably null |
Het |
| Thoc2l |
A |
G |
5: 104,670,124 (GRCm39) |
K1549E |
possibly damaging |
Het |
| Tmem225 |
T |
C |
9: 40,060,639 (GRCm39) |
V66A |
probably benign |
Het |
| Tmtc4 |
T |
C |
14: 123,178,714 (GRCm39) |
|
probably null |
Het |
| Trpc4 |
T |
A |
3: 54,102,217 (GRCm39) |
N38K |
probably benign |
Het |
| Ttll12 |
A |
T |
15: 83,471,314 (GRCm39) |
Y218N |
probably damaging |
Het |
| Ttn |
A |
T |
2: 76,778,769 (GRCm39) |
|
probably null |
Het |
| Tulp1 |
A |
C |
17: 28,570,969 (GRCm39) |
Y178* |
probably null |
Het |
| Vmn2r58 |
A |
G |
7: 41,513,746 (GRCm39) |
V299A |
probably damaging |
Het |
| Washc4 |
C |
A |
10: 83,419,200 (GRCm39) |
Q911K |
possibly damaging |
Het |
| Wdr3 |
T |
C |
3: 100,062,252 (GRCm39) |
D221G |
probably benign |
Het |
| Zan |
A |
T |
5: 137,460,155 (GRCm39) |
C1245* |
probably null |
Het |
| Zfyve9 |
A |
C |
4: 108,548,866 (GRCm39) |
S773A |
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 |
88,194,000 (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 |
|
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'- TCGGTACACATGGCTTGCTG -3'
(R):5'- GGATTGCTCTGAACGCTTGC -3'
Sequencing Primer
(F):5'- ACACATGGCTTGCTGTGGAC -3'
(R):5'- GAACGCTTGCTTGCCTTTCG -3'
|
| Posted On |
2017-01-23 |
Incidental Mutation