Incidental Mutation 'R1710:Hfm1'
ID |
190417 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Hfm1
|
Ensembl Gene |
ENSMUSG00000043410 |
Gene Name |
HFM1, ATP-dependent DNA helicase homolog |
Synonyms |
LOC381663, A330009G12Rik, Mer3, Sec63d1 |
MMRRC Submission |
039743-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.080)
|
Stock # |
R1710 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
106988058-107074187 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 107028380 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Leucine
at position 817
(F817L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000112590
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000112690]
[ENSMUST00000117588]
[ENSMUST00000148495]
|
AlphaFold |
D3Z4R1 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000112690
AA Change: F817L
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000108310 Gene: ENSMUSG00000043410 AA Change: F817L
Domain | Start | End | E-Value | Type |
DEXDc
|
276 |
490 |
3.66e-29 |
SMART |
HELICc
|
571 |
657 |
1.56e-14 |
SMART |
low complexity region
|
751 |
764 |
N/A |
INTRINSIC |
Sec63
|
775 |
1090 |
5.66e-60 |
SMART |
Blast:Sec63
|
1130 |
1188 |
2e-18 |
BLAST |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000117588
AA Change: F817L
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000112590 Gene: ENSMUSG00000043410 AA Change: F817L
Domain | Start | End | E-Value | Type |
DEXDc
|
276 |
490 |
3.66e-29 |
SMART |
HELICc
|
571 |
657 |
1.56e-14 |
SMART |
low complexity region
|
751 |
764 |
N/A |
INTRINSIC |
Sec63
|
775 |
1090 |
5.66e-60 |
SMART |
Blast:Sec63
|
1130 |
1188 |
2e-18 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000148495
|
Predicted Effect |
unknown
Transcript: ENSMUST00000155171
AA Change: F74L
|
SMART Domains |
Protein: ENSMUSP00000118674 Gene: ENSMUSG00000043410 AA Change: F74L
Domain | Start | End | E-Value | Type |
low complexity region
|
9 |
22 |
N/A |
INTRINSIC |
Sec63
|
33 |
304 |
3.04e-42 |
SMART |
Blast:Sec63
|
344 |
402 |
7e-19 |
BLAST |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183903
|
Meta Mutation Damage Score |
0.3558 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.5%
|
Validation Efficiency |
98% (117/120) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is thought to be an ATP-dependent DNA helicase and is expressed mainly in germ-line cells. Defects in this gene are a cause of premature ovarian failure 9 (POF9). [provided by RefSeq, Apr 2014] PHENOTYPE: Meiosis ais disrupted in homozygotes and bothe sexes are sterile [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503L19Rik |
A |
T |
18: 70,601,134 (GRCm39) |
S249R |
possibly damaging |
Het |
Acadvl |
T |
A |
11: 69,901,181 (GRCm39) |
I638F |
probably damaging |
Het |
Acnat2 |
T |
A |
4: 49,380,587 (GRCm39) |
T264S |
probably benign |
Het |
Acrv1 |
C |
T |
9: 36,605,551 (GRCm39) |
Q33* |
probably null |
Het |
Actrt3 |
T |
A |
3: 30,653,901 (GRCm39) |
N33I |
probably damaging |
Het |
Alyref2 |
T |
C |
1: 171,331,168 (GRCm39) |
|
probably benign |
Het |
Ank2 |
C |
A |
3: 126,726,709 (GRCm39) |
E3712* |
probably null |
Het |
Ano7 |
C |
A |
1: 93,313,346 (GRCm39) |
H161Q |
probably benign |
Het |
Arhgap10 |
C |
A |
8: 78,085,216 (GRCm39) |
E451* |
probably null |
Het |
Arhgap29 |
T |
A |
3: 121,801,729 (GRCm39) |
Y748N |
probably damaging |
Het |
Arhgap45 |
C |
T |
10: 79,853,932 (GRCm39) |
Q149* |
probably null |
Het |
Asap2 |
C |
T |
12: 21,274,393 (GRCm39) |
H371Y |
probably damaging |
Het |
Atp6v1b1 |
T |
C |
6: 83,735,372 (GRCm39) |
I480T |
probably benign |
Het |
BC034090 |
T |
C |
1: 155,101,610 (GRCm39) |
D218G |
possibly damaging |
Het |
Brdt |
A |
T |
5: 107,491,450 (GRCm39) |
D74V |
probably damaging |
Het |
C4b |
A |
G |
17: 34,962,638 (GRCm39) |
|
probably benign |
Het |
Card11 |
T |
A |
5: 140,888,660 (GRCm39) |
K233* |
probably null |
Het |
Catip |
T |
G |
1: 74,401,929 (GRCm39) |
F35V |
possibly damaging |
Het |
Ccdc13 |
C |
T |
9: 121,648,647 (GRCm39) |
G247R |
probably damaging |
Het |
Cep97 |
T |
A |
16: 55,735,385 (GRCm39) |
D471V |
probably damaging |
Het |
Col17a1 |
A |
T |
19: 47,659,370 (GRCm39) |
L403Q |
probably damaging |
Het |
Crbn |
A |
G |
6: 106,767,906 (GRCm39) |
S194P |
possibly damaging |
Het |
Degs1l |
A |
G |
1: 180,878,884 (GRCm39) |
M1V |
probably null |
Het |
Dennd10 |
A |
G |
19: 60,806,021 (GRCm39) |
Y102C |
probably damaging |
Het |
Dhx58 |
T |
A |
11: 100,594,400 (GRCm39) |
H97L |
probably benign |
Het |
Dnah8 |
T |
C |
17: 31,073,914 (GRCm39) |
I4528T |
probably damaging |
Het |
Dpyd |
A |
G |
3: 118,404,092 (GRCm39) |
|
probably null |
Het |
Entpd1 |
A |
T |
19: 40,714,680 (GRCm39) |
Q263L |
probably benign |
Het |
Entrep1 |
A |
T |
19: 23,957,059 (GRCm39) |
I317N |
probably damaging |
Het |
Esyt3 |
T |
C |
9: 99,218,244 (GRCm39) |
I130M |
probably benign |
Het |
Etv1 |
T |
C |
12: 38,902,261 (GRCm39) |
F264S |
probably benign |
Het |
Fat1 |
T |
C |
8: 45,463,519 (GRCm39) |
S1354P |
probably benign |
Het |
Fat4 |
C |
A |
3: 39,005,304 (GRCm39) |
T1901N |
probably damaging |
Het |
Fbxw13 |
C |
T |
9: 109,010,586 (GRCm39) |
V351I |
probably damaging |
Het |
Fmo3 |
A |
G |
1: 162,795,356 (GRCm39) |
F160L |
possibly damaging |
Het |
Fyb2 |
T |
A |
4: 104,861,113 (GRCm39) |
D592E |
probably damaging |
Het |
Gjb4 |
T |
C |
4: 127,245,663 (GRCm39) |
M93V |
possibly damaging |
Het |
Gm5089 |
C |
A |
14: 122,673,566 (GRCm39) |
G52* |
probably null |
Het |
Gm6401 |
G |
T |
14: 41,788,840 (GRCm39) |
N76K |
probably benign |
Het |
Gm6871 |
A |
G |
7: 41,195,901 (GRCm39) |
S279P |
probably damaging |
Het |
Gtf2ird2 |
T |
G |
5: 134,240,081 (GRCm39) |
V301G |
probably benign |
Het |
H2bw2 |
A |
C |
X: 135,828,216 (GRCm39) |
D35A |
unknown |
Het |
Hivep2 |
A |
T |
10: 14,005,249 (GRCm39) |
K616* |
probably null |
Het |
Hmcn1 |
A |
T |
1: 150,551,735 (GRCm39) |
I2623N |
probably damaging |
Het |
Igf2bp3 |
G |
T |
6: 49,082,565 (GRCm39) |
A339E |
probably damaging |
Het |
Insyn2b |
T |
A |
11: 34,354,263 (GRCm39) |
|
probably null |
Het |
Irx4 |
T |
C |
13: 73,415,757 (GRCm39) |
I182T |
possibly damaging |
Het |
Jcad |
T |
C |
18: 4,674,511 (GRCm39) |
S758P |
probably damaging |
Het |
Klhdc4 |
A |
T |
8: 122,526,226 (GRCm39) |
Y304* |
probably null |
Het |
Lama1 |
A |
G |
17: 68,060,786 (GRCm39) |
I705V |
probably benign |
Het |
Mbd5 |
A |
G |
2: 49,147,044 (GRCm39) |
N418S |
probably benign |
Het |
Mmp21 |
C |
T |
7: 133,279,014 (GRCm39) |
V279I |
probably damaging |
Het |
Morc4 |
A |
C |
X: 138,755,279 (GRCm39) |
C272W |
probably damaging |
Het |
Mrm1 |
A |
T |
11: 84,709,518 (GRCm39) |
C180S |
probably damaging |
Het |
Ncor1 |
T |
C |
11: 62,313,831 (GRCm39) |
D103G |
probably damaging |
Het |
Ndrg4 |
A |
G |
8: 96,437,314 (GRCm39) |
D251G |
probably damaging |
Het |
Ndufaf5 |
T |
C |
2: 140,035,522 (GRCm39) |
V246A |
possibly damaging |
Het |
Noa1 |
T |
C |
5: 77,457,572 (GRCm39) |
E111G |
possibly damaging |
Het |
Nod1 |
C |
A |
6: 54,921,044 (GRCm39) |
V425F |
probably damaging |
Het |
Nos1 |
A |
T |
5: 118,033,984 (GRCm39) |
I369F |
probably damaging |
Het |
Nsun5 |
C |
T |
5: 135,400,170 (GRCm39) |
H98Y |
probably damaging |
Het |
Optn |
G |
A |
2: 5,057,941 (GRCm39) |
T76I |
possibly damaging |
Het |
Or14c39 |
G |
A |
7: 86,344,318 (GRCm39) |
R218H |
probably benign |
Het |
Or4k15c |
C |
G |
14: 50,321,827 (GRCm39) |
V104L |
probably benign |
Het |
Or5k1b |
A |
G |
16: 58,581,504 (GRCm39) |
F12L |
probably benign |
Het |
Or8d1b |
A |
G |
9: 38,887,202 (GRCm39) |
I77V |
probably damaging |
Het |
Or8g28 |
T |
C |
9: 39,169,867 (GRCm39) |
I37V |
probably benign |
Het |
Or9g19 |
C |
T |
2: 85,600,199 (GRCm39) |
T18I |
probably benign |
Het |
Oscar |
C |
T |
7: 3,614,855 (GRCm39) |
W22* |
probably null |
Het |
Palmd |
T |
A |
3: 116,717,306 (GRCm39) |
Y397F |
probably damaging |
Het |
Plk1 |
A |
G |
7: 121,768,121 (GRCm39) |
D447G |
probably damaging |
Het |
Plscr5 |
T |
A |
9: 92,087,581 (GRCm39) |
N183K |
probably damaging |
Het |
Polk |
T |
G |
13: 96,625,712 (GRCm39) |
D364A |
probably damaging |
Het |
Polr3d |
T |
C |
14: 70,680,450 (GRCm39) |
T36A |
probably benign |
Het |
Ppp1r10 |
A |
T |
17: 36,237,428 (GRCm39) |
R199S |
probably damaging |
Het |
Prkcz |
C |
T |
4: 155,346,969 (GRCm39) |
D388N |
probably damaging |
Het |
Prrc2b |
T |
C |
2: 32,102,234 (GRCm39) |
L769P |
probably damaging |
Het |
Psg26 |
A |
G |
7: 18,213,966 (GRCm39) |
V232A |
probably damaging |
Het |
Pth2r |
T |
C |
1: 65,375,997 (GRCm39) |
V85A |
possibly damaging |
Het |
Rbpms2 |
T |
C |
9: 65,566,494 (GRCm39) |
|
probably benign |
Het |
Reps1 |
A |
T |
10: 17,994,698 (GRCm39) |
D514V |
possibly damaging |
Het |
Riok3 |
G |
T |
18: 12,276,018 (GRCm39) |
R238L |
probably benign |
Het |
Rnf19a |
T |
C |
15: 36,244,353 (GRCm39) |
Q569R |
probably damaging |
Het |
Rorb |
G |
A |
19: 18,937,865 (GRCm39) |
T267I |
probably damaging |
Het |
Rrm2b |
A |
T |
15: 37,929,340 (GRCm39) |
M70K |
probably damaging |
Het |
Rsf1 |
A |
T |
7: 97,311,556 (GRCm39) |
E762V |
possibly damaging |
Het |
S100a2 |
G |
A |
3: 90,498,699 (GRCm39) |
V67I |
probably benign |
Het |
Skp1 |
T |
A |
11: 52,133,442 (GRCm39) |
D42E |
probably benign |
Het |
Slc22a4 |
A |
T |
11: 53,918,801 (GRCm39) |
M1K |
probably null |
Het |
Slc2a9 |
T |
A |
5: 38,539,387 (GRCm39) |
Q371L |
probably damaging |
Het |
Slc4a9 |
A |
G |
18: 36,665,075 (GRCm39) |
T475A |
probably benign |
Het |
Slc8b1 |
A |
G |
5: 120,657,717 (GRCm39) |
N60S |
probably damaging |
Het |
Slx4 |
A |
C |
16: 3,817,022 (GRCm39) |
D66E |
probably benign |
Het |
Smg8 |
A |
T |
11: 86,977,113 (GRCm39) |
I156N |
probably damaging |
Het |
Snx25 |
A |
T |
8: 46,569,244 (GRCm39) |
C218S |
possibly damaging |
Het |
Sulf2 |
T |
C |
2: 165,920,992 (GRCm39) |
I784V |
probably benign |
Het |
Tatdn2 |
G |
T |
6: 113,674,888 (GRCm39) |
R72L |
possibly damaging |
Het |
Tbc1d8 |
T |
C |
1: 39,445,918 (GRCm39) |
D91G |
possibly damaging |
Het |
Tifab |
C |
A |
13: 56,324,433 (GRCm39) |
R3S |
probably benign |
Het |
Tm4sf1 |
A |
T |
3: 57,200,304 (GRCm39) |
S104T |
probably damaging |
Het |
Tmem132e |
T |
A |
11: 82,334,343 (GRCm39) |
I618N |
probably damaging |
Het |
Ttc7b |
A |
T |
12: 100,369,667 (GRCm39) |
D367E |
probably damaging |
Het |
Txlnb |
A |
G |
10: 17,719,203 (GRCm39) |
D678G |
possibly damaging |
Het |
Vgll4 |
A |
G |
6: 114,934,895 (GRCm39) |
|
probably null |
Het |
Vmn2r124 |
A |
T |
17: 18,282,187 (GRCm39) |
|
probably benign |
Het |
Vmn2r2 |
T |
C |
3: 64,024,820 (GRCm39) |
D587G |
probably benign |
Het |
Vmn2r84 |
G |
A |
10: 130,226,968 (GRCm39) |
A290V |
probably benign |
Het |
Vps13c |
T |
A |
9: 67,818,811 (GRCm39) |
S1077R |
probably benign |
Het |
Vsig10 |
C |
T |
5: 117,489,719 (GRCm39) |
A495V |
probably benign |
Het |
Vwa3a |
A |
T |
7: 120,403,254 (GRCm39) |
|
probably null |
Het |
Zfhx2 |
C |
A |
14: 55,303,455 (GRCm39) |
A1510S |
possibly damaging |
Het |
Zfp142 |
T |
A |
1: 74,611,389 (GRCm39) |
D601V |
probably damaging |
Het |
Zfp62 |
T |
C |
11: 49,108,510 (GRCm39) |
I867T |
probably benign |
Het |
|
Other mutations in Hfm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00944:Hfm1
|
APN |
5 |
107,049,996 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01295:Hfm1
|
APN |
5 |
107,065,472 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01725:Hfm1
|
APN |
5 |
107,065,245 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01758:Hfm1
|
APN |
5 |
107,052,659 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01911:Hfm1
|
APN |
5 |
107,059,410 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02337:Hfm1
|
APN |
5 |
107,052,133 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02472:Hfm1
|
APN |
5 |
107,021,794 (GRCm39) |
splice site |
probably benign |
|
IGL02496:Hfm1
|
APN |
5 |
107,049,627 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02545:Hfm1
|
APN |
5 |
107,043,153 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02584:Hfm1
|
APN |
5 |
107,026,528 (GRCm39) |
splice site |
probably null |
|
IGL02728:Hfm1
|
APN |
5 |
107,026,689 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02881:Hfm1
|
APN |
5 |
107,022,118 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03108:Hfm1
|
APN |
5 |
107,043,800 (GRCm39) |
unclassified |
probably benign |
|
IGL03351:Hfm1
|
APN |
5 |
107,059,441 (GRCm39) |
nonsense |
probably null |
|
IGL03353:Hfm1
|
APN |
5 |
107,004,795 (GRCm39) |
missense |
probably damaging |
0.99 |
R0024:Hfm1
|
UTSW |
5 |
107,004,790 (GRCm39) |
missense |
probably benign |
0.41 |
R0024:Hfm1
|
UTSW |
5 |
107,004,790 (GRCm39) |
missense |
probably benign |
0.41 |
R0094:Hfm1
|
UTSW |
5 |
107,065,344 (GRCm39) |
missense |
probably benign |
|
R0633:Hfm1
|
UTSW |
5 |
107,065,467 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0644:Hfm1
|
UTSW |
5 |
107,046,122 (GRCm39) |
critical splice donor site |
probably null |
|
R1078:Hfm1
|
UTSW |
5 |
107,026,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R1120:Hfm1
|
UTSW |
5 |
107,052,084 (GRCm39) |
splice site |
probably benign |
|
R1166:Hfm1
|
UTSW |
5 |
107,059,277 (GRCm39) |
missense |
probably benign |
0.00 |
R1242:Hfm1
|
UTSW |
5 |
107,022,767 (GRCm39) |
missense |
probably damaging |
0.99 |
R1414:Hfm1
|
UTSW |
5 |
107,020,219 (GRCm39) |
missense |
probably benign |
0.01 |
R1450:Hfm1
|
UTSW |
5 |
107,066,324 (GRCm39) |
missense |
probably damaging |
0.99 |
R1529:Hfm1
|
UTSW |
5 |
107,000,989 (GRCm39) |
missense |
probably benign |
0.00 |
R1622:Hfm1
|
UTSW |
5 |
107,041,389 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1710:Hfm1
|
UTSW |
5 |
107,043,869 (GRCm39) |
missense |
probably damaging |
0.96 |
R1757:Hfm1
|
UTSW |
5 |
107,028,226 (GRCm39) |
splice site |
probably null |
|
R1856:Hfm1
|
UTSW |
5 |
106,995,542 (GRCm39) |
missense |
probably benign |
0.00 |
R1984:Hfm1
|
UTSW |
5 |
107,046,442 (GRCm39) |
missense |
probably damaging |
0.98 |
R1985:Hfm1
|
UTSW |
5 |
107,046,442 (GRCm39) |
missense |
probably damaging |
0.98 |
R2040:Hfm1
|
UTSW |
5 |
107,049,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Hfm1
|
UTSW |
5 |
107,044,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R2426:Hfm1
|
UTSW |
5 |
106,995,519 (GRCm39) |
splice site |
probably null |
|
R2474:Hfm1
|
UTSW |
5 |
107,020,282 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2926:Hfm1
|
UTSW |
5 |
107,022,148 (GRCm39) |
nonsense |
probably null |
|
R2944:Hfm1
|
UTSW |
5 |
107,020,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R3705:Hfm1
|
UTSW |
5 |
107,040,705 (GRCm39) |
unclassified |
probably benign |
|
R4256:Hfm1
|
UTSW |
5 |
107,052,663 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4455:Hfm1
|
UTSW |
5 |
107,034,374 (GRCm39) |
splice site |
probably null |
|
R4538:Hfm1
|
UTSW |
5 |
107,022,756 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4540:Hfm1
|
UTSW |
5 |
107,022,087 (GRCm39) |
nonsense |
probably null |
|
R4591:Hfm1
|
UTSW |
5 |
106,995,533 (GRCm39) |
missense |
probably benign |
0.08 |
R4745:Hfm1
|
UTSW |
5 |
107,049,709 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4747:Hfm1
|
UTSW |
5 |
107,065,389 (GRCm39) |
missense |
probably benign |
|
R4765:Hfm1
|
UTSW |
5 |
106,990,405 (GRCm39) |
missense |
probably benign |
0.21 |
R4821:Hfm1
|
UTSW |
5 |
107,002,606 (GRCm39) |
critical splice donor site |
probably null |
|
R4842:Hfm1
|
UTSW |
5 |
107,040,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R4944:Hfm1
|
UTSW |
5 |
107,022,079 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5093:Hfm1
|
UTSW |
5 |
107,049,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Hfm1
|
UTSW |
5 |
107,065,428 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5414:Hfm1
|
UTSW |
5 |
107,049,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Hfm1
|
UTSW |
5 |
107,040,638 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5459:Hfm1
|
UTSW |
5 |
107,052,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5485:Hfm1
|
UTSW |
5 |
106,995,528 (GRCm39) |
critical splice donor site |
probably null |
|
R5585:Hfm1
|
UTSW |
5 |
107,059,305 (GRCm39) |
missense |
probably benign |
0.05 |
R5631:Hfm1
|
UTSW |
5 |
107,052,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5705:Hfm1
|
UTSW |
5 |
107,059,319 (GRCm39) |
missense |
probably benign |
0.21 |
R5804:Hfm1
|
UTSW |
5 |
107,026,455 (GRCm39) |
splice site |
probably null |
|
R5959:Hfm1
|
UTSW |
5 |
107,022,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R6046:Hfm1
|
UTSW |
5 |
107,046,509 (GRCm39) |
splice site |
probably null |
|
R6191:Hfm1
|
UTSW |
5 |
107,034,419 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6345:Hfm1
|
UTSW |
5 |
106,989,504 (GRCm39) |
missense |
probably benign |
|
R6580:Hfm1
|
UTSW |
5 |
106,995,575 (GRCm39) |
missense |
probably benign |
0.00 |
R6651:Hfm1
|
UTSW |
5 |
106,995,553 (GRCm39) |
missense |
probably benign |
0.00 |
R6761:Hfm1
|
UTSW |
5 |
107,043,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R6835:Hfm1
|
UTSW |
5 |
107,026,681 (GRCm39) |
nonsense |
probably null |
|
R6891:Hfm1
|
UTSW |
5 |
107,065,240 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6924:Hfm1
|
UTSW |
5 |
106,998,276 (GRCm39) |
splice site |
probably null |
|
R6980:Hfm1
|
UTSW |
5 |
107,028,343 (GRCm39) |
missense |
probably benign |
0.31 |
R7054:Hfm1
|
UTSW |
5 |
107,043,909 (GRCm39) |
missense |
probably benign |
0.01 |
R7058:Hfm1
|
UTSW |
5 |
107,059,306 (GRCm39) |
missense |
probably benign |
0.04 |
R7189:Hfm1
|
UTSW |
5 |
107,049,569 (GRCm39) |
critical splice donor site |
probably null |
|
R7250:Hfm1
|
UTSW |
5 |
107,052,197 (GRCm39) |
missense |
probably benign |
0.00 |
R7376:Hfm1
|
UTSW |
5 |
107,043,084 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7577:Hfm1
|
UTSW |
5 |
107,043,909 (GRCm39) |
missense |
probably benign |
0.01 |
R7636:Hfm1
|
UTSW |
5 |
107,065,332 (GRCm39) |
missense |
probably benign |
0.02 |
R7639:Hfm1
|
UTSW |
5 |
107,046,341 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7639:Hfm1
|
UTSW |
5 |
107,037,791 (GRCm39) |
missense |
probably benign |
0.03 |
R7763:Hfm1
|
UTSW |
5 |
107,029,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R7828:Hfm1
|
UTSW |
5 |
107,029,657 (GRCm39) |
critical splice donor site |
probably null |
|
R7905:Hfm1
|
UTSW |
5 |
107,046,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R8160:Hfm1
|
UTSW |
5 |
107,043,899 (GRCm39) |
missense |
probably null |
0.00 |
R8477:Hfm1
|
UTSW |
5 |
107,029,684 (GRCm39) |
missense |
probably benign |
0.01 |
R8739:Hfm1
|
UTSW |
5 |
107,046,371 (GRCm39) |
missense |
probably damaging |
0.96 |
R8968:Hfm1
|
UTSW |
5 |
107,065,439 (GRCm39) |
missense |
probably benign |
0.00 |
R9072:Hfm1
|
UTSW |
5 |
107,046,146 (GRCm39) |
missense |
probably benign |
0.04 |
R9073:Hfm1
|
UTSW |
5 |
107,046,146 (GRCm39) |
missense |
probably benign |
0.04 |
R9152:Hfm1
|
UTSW |
5 |
106,989,611 (GRCm39) |
missense |
probably benign |
0.01 |
R9234:Hfm1
|
UTSW |
5 |
107,041,334 (GRCm39) |
missense |
probably benign |
|
R9244:Hfm1
|
UTSW |
5 |
107,022,766 (GRCm39) |
missense |
probably damaging |
0.96 |
R9576:Hfm1
|
UTSW |
5 |
107,021,938 (GRCm39) |
missense |
probably benign |
0.00 |
R9649:Hfm1
|
UTSW |
5 |
107,066,329 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9743:Hfm1
|
UTSW |
5 |
107,022,125 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9782:Hfm1
|
UTSW |
5 |
107,021,896 (GRCm39) |
missense |
probably benign |
0.38 |
R9789:Hfm1
|
UTSW |
5 |
107,065,346 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Hfm1
|
UTSW |
5 |
107,019,686 (GRCm39) |
missense |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- GCAGCTACTGTAATGAAGGGACCAAC -3'
(R):5'- CCGTCTCAACGTCTGCCATATAGAAG -3'
Sequencing Primer
(F):5'- CAGACTTCTGCTGGAAACATGG -3'
(R):5'- TGTTAGTGAGTGAATCCTTAAAGAAG -3'
|
Posted On |
2014-05-14 |