Incidental Mutation 'R7664:Spag9'
ID |
591808 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Spag9
|
Ensembl Gene |
ENSMUSG00000020859 |
Gene Name |
sperm associated antigen 9 |
Synonyms |
JLP, Mapk8ip4, 3110018C07Rik, JIP4, 4733401I23Rik, syd1, 4831406C20Rik |
MMRRC Submission |
045704-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.737)
|
Stock # |
R7664 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
93886917-94016911 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
T to C
at 93992986 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000042271
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000024979]
[ENSMUST00000041956]
[ENSMUST00000075695]
[ENSMUST00000092777]
[ENSMUST00000103168]
[ENSMUST00000132079]
[ENSMUST00000153076]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000024979
|
SMART Domains |
Protein: ENSMUSP00000024979 Gene: ENSMUSG00000020859
Domain | Start | End | E-Value | Type |
transmembrane domain
|
7 |
29 |
N/A |
INTRINSIC |
PDB:2W83|D
|
253 |
305 |
1e-25 |
PDB |
low complexity region
|
306 |
339 |
N/A |
INTRINSIC |
coiled coil region
|
572 |
606 |
N/A |
INTRINSIC |
low complexity region
|
735 |
751 |
N/A |
INTRINSIC |
SCOP:d1kb0a2
|
823 |
969 |
3e-5 |
SMART |
Blast:WD40
|
924 |
964 |
8e-18 |
BLAST |
low complexity region
|
1132 |
1150 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000041956
|
SMART Domains |
Protein: ENSMUSP00000042271 Gene: ENSMUSG00000020859
Domain | Start | End | E-Value | Type |
Pfam:Jnk-SapK_ap_N
|
24 |
179 |
2e-61 |
PFAM |
Pfam:JIP_LZII
|
390 |
460 |
5.3e-32 |
PFAM |
coiled coil region
|
710 |
744 |
N/A |
INTRINSIC |
low complexity region
|
873 |
889 |
N/A |
INTRINSIC |
SCOP:d1kb0a2
|
961 |
1107 |
1e-5 |
SMART |
Blast:WD40
|
1062 |
1102 |
1e-17 |
BLAST |
low complexity region
|
1270 |
1288 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000075695
|
SMART Domains |
Protein: ENSMUSP00000075115 Gene: ENSMUSG00000020859
Domain | Start | End | E-Value | Type |
transmembrane domain
|
7 |
29 |
N/A |
INTRINSIC |
PDB:2W83|D
|
253 |
305 |
1e-25 |
PDB |
low complexity region
|
306 |
339 |
N/A |
INTRINSIC |
coiled coil region
|
571 |
605 |
N/A |
INTRINSIC |
low complexity region
|
734 |
750 |
N/A |
INTRINSIC |
SCOP:d1kb0a2
|
822 |
968 |
3e-5 |
SMART |
Blast:WD40
|
923 |
963 |
7e-18 |
BLAST |
low complexity region
|
1131 |
1149 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000092777
|
SMART Domains |
Protein: ENSMUSP00000090452 Gene: ENSMUSG00000020859
Domain | Start | End | E-Value | Type |
transmembrane domain
|
7 |
29 |
N/A |
INTRINSIC |
PDB:2W83|D
|
254 |
306 |
1e-25 |
PDB |
low complexity region
|
307 |
340 |
N/A |
INTRINSIC |
coiled coil region
|
572 |
606 |
N/A |
INTRINSIC |
low complexity region
|
735 |
751 |
N/A |
INTRINSIC |
SCOP:d1kb0a2
|
823 |
969 |
3e-5 |
SMART |
Blast:WD40
|
924 |
964 |
7e-18 |
BLAST |
low complexity region
|
1132 |
1150 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000103168
|
SMART Domains |
Protein: ENSMUSP00000099457 Gene: ENSMUSG00000020859
Domain | Start | End | E-Value | Type |
transmembrane domain
|
7 |
29 |
N/A |
INTRINSIC |
PDB:2W83|D
|
249 |
301 |
1e-25 |
PDB |
low complexity region
|
302 |
335 |
N/A |
INTRINSIC |
coiled coil region
|
567 |
601 |
N/A |
INTRINSIC |
low complexity region
|
730 |
746 |
N/A |
INTRINSIC |
SCOP:d1kb0a2
|
818 |
964 |
3e-5 |
SMART |
Blast:WD40
|
919 |
959 |
8e-18 |
BLAST |
low complexity region
|
1127 |
1145 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000132079
|
SMART Domains |
Protein: ENSMUSP00000118850 Gene: ENSMUSG00000020859
Domain | Start | End | E-Value | Type |
transmembrane domain
|
7 |
29 |
N/A |
INTRINSIC |
coiled coil region
|
360 |
394 |
N/A |
INTRINSIC |
low complexity region
|
523 |
539 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000153076
|
SMART Domains |
Protein: ENSMUSP00000117502 Gene: ENSMUSG00000020859
Domain | Start | End | E-Value | Type |
PDB:2W83|D
|
1 |
25 |
4e-8 |
PDB |
low complexity region
|
26 |
59 |
N/A |
INTRINSIC |
coiled coil region
|
291 |
325 |
N/A |
INTRINSIC |
low complexity region
|
454 |
470 |
N/A |
INTRINSIC |
SCOP:d1kb0a2
|
542 |
688 |
3e-5 |
SMART |
Blast:WD40
|
643 |
683 |
1e-17 |
BLAST |
low complexity region
|
864 |
882 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000156019
|
SMART Domains |
Protein: ENSMUSP00000115864 Gene: ENSMUSG00000020859
Domain | Start | End | E-Value | Type |
Pfam:JIP_LZII
|
240 |
310 |
1.1e-32 |
PFAM |
coiled coil region
|
559 |
593 |
N/A |
INTRINSIC |
low complexity region
|
723 |
739 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
99% (83/84) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the cancer testis antigen gene family. The encoded protein functions as a scaffold protein that structurally organizes mitogen-activated protein kinases and mediates c-Jun-terminal kinase signaling. This protein also binds to kinesin-1 and may be involved in microtubule-based membrane transport. This protein may play a role in tumor growth and development. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2011] PHENOTYPE: Male mice homozygous for a null mutation display reduced fertility with oligoasthenozoospermia. [provided by MGI curators]
|
Allele List at MGI |
All alleles(5) : Targeted, knock-out(1) Gene trapped(4) |
Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
C |
T |
11: 84,136,175 (GRCm39) |
T510I |
probably damaging |
Het |
Akap12 |
G |
T |
10: 4,303,748 (GRCm39) |
W291L |
probably damaging |
Het |
Akip1 |
A |
T |
7: 109,308,187 (GRCm39) |
I152F |
probably benign |
Het |
Alpk2 |
T |
A |
18: 65,440,073 (GRCm39) |
Y440F |
probably benign |
Het |
Aox3 |
A |
G |
1: 58,158,698 (GRCm39) |
T90A |
probably damaging |
Het |
Arhgef18 |
A |
T |
8: 3,436,390 (GRCm39) |
E228V |
probably damaging |
Het |
B4galnt4 |
A |
G |
7: 140,647,626 (GRCm39) |
K405E |
probably damaging |
Het |
BC034090 |
T |
C |
1: 155,117,377 (GRCm39) |
E247G |
probably damaging |
Het |
Camkk2 |
A |
T |
5: 122,894,645 (GRCm39) |
F216I |
unknown |
Het |
Carm1 |
A |
C |
9: 21,498,286 (GRCm39) |
K430T |
probably benign |
Het |
Ccdc13 |
A |
G |
9: 121,643,279 (GRCm39) |
V374A |
probably benign |
Het |
Cdh26 |
T |
A |
2: 178,111,835 (GRCm39) |
M465K |
probably benign |
Het |
Ceacam10 |
A |
T |
7: 24,477,757 (GRCm39) |
M91L |
probably benign |
Het |
Chrnb1 |
T |
C |
11: 69,677,850 (GRCm39) |
T301A |
possibly damaging |
Het |
Clec4a3 |
A |
G |
6: 122,943,381 (GRCm39) |
D101G |
probably benign |
Het |
Cmss1 |
G |
A |
16: 57,138,310 (GRCm39) |
P59S |
probably benign |
Het |
Crhr1 |
T |
A |
11: 104,059,968 (GRCm39) |
F138L |
probably benign |
Het |
Cxcl5 |
A |
T |
5: 90,907,890 (GRCm39) |
I107F |
probably damaging |
Het |
Cxcr1 |
A |
G |
1: 74,231,834 (GRCm39) |
S63P |
probably damaging |
Het |
Cxcr5 |
A |
G |
9: 44,424,607 (GRCm39) |
L350P |
probably benign |
Het |
D5Ertd579e |
A |
T |
5: 36,771,961 (GRCm39) |
H811Q |
probably benign |
Het |
Ddx46 |
T |
G |
13: 55,806,864 (GRCm39) |
I499S |
probably damaging |
Het |
Ddx51 |
T |
G |
5: 110,804,785 (GRCm39) |
|
probably null |
Het |
Dnaja1 |
C |
T |
4: 40,724,090 (GRCm39) |
P84S |
probably benign |
Het |
Dnajc27 |
A |
G |
12: 4,153,132 (GRCm39) |
K203E |
possibly damaging |
Het |
Fam107b |
T |
A |
2: 3,571,747 (GRCm39) |
C24S |
probably damaging |
Het |
Fancg |
T |
C |
4: 43,010,066 (GRCm39) |
K11R |
probably benign |
Het |
Fnip1 |
T |
C |
11: 54,356,951 (GRCm39) |
L44P |
probably damaging |
Het |
Fthl17b |
C |
T |
X: 8,829,043 (GRCm39) |
R9Q |
possibly damaging |
Het |
Fthl17b |
C |
T |
X: 8,829,047 (GRCm39) |
V8M |
possibly damaging |
Het |
Heca |
A |
T |
10: 17,778,118 (GRCm39) |
L493Q |
probably damaging |
Het |
Hrh2 |
C |
T |
13: 54,368,875 (GRCm39) |
P284S |
probably damaging |
Het |
Ifnar1 |
C |
G |
16: 91,292,082 (GRCm39) |
A141G |
probably damaging |
Het |
Igkv6-32 |
T |
A |
6: 70,051,282 (GRCm39) |
T25S |
probably damaging |
Het |
Inppl1 |
T |
C |
7: 101,479,304 (GRCm39) |
H525R |
probably damaging |
Het |
Itga2b |
A |
G |
11: 102,351,666 (GRCm39) |
L553P |
probably damaging |
Het |
Itgbl1 |
A |
G |
14: 124,083,962 (GRCm39) |
Y280C |
probably damaging |
Het |
Kap |
T |
C |
6: 133,828,920 (GRCm39) |
I54V |
probably benign |
Het |
Kcnh4 |
G |
T |
11: 100,641,148 (GRCm39) |
L434M |
probably damaging |
Het |
Klhl14 |
T |
C |
18: 21,687,706 (GRCm39) |
D572G |
probably damaging |
Het |
Klhl41 |
T |
A |
2: 69,501,061 (GRCm39) |
L174Q |
probably damaging |
Het |
Lrp2 |
T |
G |
2: 69,337,076 (GRCm39) |
H1232P |
probably damaging |
Het |
Lyar |
A |
G |
5: 38,388,161 (GRCm39) |
E229G |
probably benign |
Het |
Mark4 |
A |
T |
7: 19,177,151 (GRCm39) |
L226Q |
probably damaging |
Het |
Mcm8 |
A |
G |
2: 132,685,453 (GRCm39) |
K823R |
probably damaging |
Het |
Mfsd6 |
A |
T |
1: 52,748,212 (GRCm39) |
S218T |
probably benign |
Het |
Mlip |
A |
T |
9: 77,045,828 (GRCm39) |
I884N |
possibly damaging |
Het |
Mmrn1 |
A |
G |
6: 60,953,689 (GRCm39) |
T657A |
probably benign |
Het |
Morc2b |
A |
G |
17: 33,355,376 (GRCm39) |
Y799H |
probably benign |
Het |
Muc16 |
A |
T |
9: 18,519,018 (GRCm39) |
I6304N |
probably benign |
Het |
Mug1 |
C |
A |
6: 121,838,179 (GRCm39) |
H470N |
possibly damaging |
Het |
Naaladl2 |
T |
C |
3: 24,112,303 (GRCm39) |
Y593C |
probably damaging |
Het |
Ncor1 |
T |
C |
11: 62,289,154 (GRCm39) |
E341G |
probably damaging |
Het |
Nrg1 |
G |
T |
8: 32,499,169 (GRCm39) |
|
probably null |
Het |
Nudt3 |
A |
G |
17: 27,842,149 (GRCm39) |
L4P |
probably benign |
Het |
Odf2l |
T |
A |
3: 144,854,345 (GRCm39) |
H493Q |
probably benign |
Het |
Ost4 |
A |
C |
5: 31,065,007 (GRCm39) |
|
probably null |
Het |
Patj |
A |
T |
4: 98,385,187 (GRCm39) |
Q840L |
possibly damaging |
Het |
Pcdh20 |
T |
A |
14: 88,706,803 (GRCm39) |
T166S |
probably benign |
Het |
Pcdhb4 |
T |
A |
18: 37,442,293 (GRCm39) |
D534E |
probably damaging |
Het |
Pik3ap1 |
T |
C |
19: 41,310,069 (GRCm39) |
D417G |
possibly damaging |
Het |
Ppwd1 |
A |
T |
13: 104,356,798 (GRCm39) |
V239E |
probably damaging |
Het |
Prdm9 |
T |
A |
17: 15,775,833 (GRCm39) |
Y206F |
probably damaging |
Het |
Ranbp6 |
A |
G |
19: 29,789,476 (GRCm39) |
V292A |
possibly damaging |
Het |
Rgs21 |
T |
A |
1: 144,416,987 (GRCm39) |
M22L |
probably benign |
Het |
Rnf17 |
A |
T |
14: 56,676,335 (GRCm39) |
I399F |
probably damaging |
Het |
Rph3a |
T |
A |
5: 121,099,339 (GRCm39) |
Q184L |
probably benign |
Het |
Scrn3 |
T |
C |
2: 73,149,714 (GRCm39) |
Y137H |
possibly damaging |
Het |
Sec14l4 |
C |
A |
11: 3,994,178 (GRCm39) |
Y342* |
probably null |
Het |
Serpinb11 |
G |
A |
1: 107,307,718 (GRCm39) |
G383D |
probably damaging |
Het |
Sf3b1 |
A |
G |
1: 55,026,626 (GRCm39) |
V1261A |
probably damaging |
Het |
Sh3tc2 |
C |
T |
18: 62,148,042 (GRCm39) |
Q1251* |
probably null |
Het |
Skor1 |
A |
T |
9: 63,049,045 (GRCm39) |
D845E |
probably benign |
Het |
Slc39a7 |
A |
G |
17: 34,248,551 (GRCm39) |
L364P |
probably damaging |
Het |
Snrpn |
T |
C |
7: 59,637,239 (GRCm39) |
I26V |
probably benign |
Het |
Snx5 |
A |
T |
2: 144,099,924 (GRCm39) |
|
probably null |
Het |
Srrm2 |
T |
C |
17: 24,039,955 (GRCm39) |
S2200P |
probably damaging |
Het |
Stx11 |
T |
C |
10: 12,817,070 (GRCm39) |
E218G |
probably damaging |
Het |
Tmem151b |
T |
C |
17: 45,856,861 (GRCm39) |
N193S |
probably damaging |
Het |
Tmem87b |
A |
T |
2: 128,690,974 (GRCm39) |
D525V |
possibly damaging |
Het |
Ubtfl1 |
A |
T |
9: 18,320,782 (GRCm39) |
R103S |
possibly damaging |
Het |
Vmn1r196 |
T |
A |
13: 22,477,932 (GRCm39) |
D190E |
probably damaging |
Het |
Vmn2r67 |
T |
A |
7: 84,805,019 (GRCm39) |
D31V |
probably benign |
Het |
Zbtb22 |
T |
A |
17: 34,137,553 (GRCm39) |
M566K |
probably benign |
Het |
Zfp568 |
A |
T |
7: 29,721,715 (GRCm39) |
H220L |
probably benign |
Het |
Zfp974 |
A |
T |
7: 27,610,137 (GRCm39) |
S529R |
possibly damaging |
Het |
|
Other mutations in Spag9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00422:Spag9
|
APN |
11 |
93,988,692 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01776:Spag9
|
APN |
11 |
94,007,553 (GRCm39) |
splice site |
probably benign |
|
IGL02095:Spag9
|
APN |
11 |
93,999,408 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02307:Spag9
|
APN |
11 |
93,992,986 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02417:Spag9
|
APN |
11 |
94,007,567 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02480:Spag9
|
APN |
11 |
93,999,413 (GRCm39) |
nonsense |
probably null |
|
IGL02864:Spag9
|
APN |
11 |
93,997,487 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02976:Spag9
|
APN |
11 |
93,974,779 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02979:Spag9
|
APN |
11 |
93,988,190 (GRCm39) |
missense |
probably benign |
|
IGL03349:Spag9
|
APN |
11 |
93,984,335 (GRCm39) |
missense |
possibly damaging |
0.51 |
dazzle
|
UTSW |
11 |
93,984,450 (GRCm39) |
nonsense |
probably null |
|
R0128:Spag9
|
UTSW |
11 |
93,984,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R0418:Spag9
|
UTSW |
11 |
93,982,579 (GRCm39) |
splice site |
probably benign |
|
R1463:Spag9
|
UTSW |
11 |
94,007,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R1593:Spag9
|
UTSW |
11 |
93,988,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Spag9
|
UTSW |
11 |
93,939,365 (GRCm39) |
missense |
probably damaging |
0.99 |
R1649:Spag9
|
UTSW |
11 |
93,999,278 (GRCm39) |
splice site |
probably null |
|
R1697:Spag9
|
UTSW |
11 |
93,887,391 (GRCm39) |
missense |
probably benign |
0.00 |
R1952:Spag9
|
UTSW |
11 |
93,988,184 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2011:Spag9
|
UTSW |
11 |
93,983,201 (GRCm39) |
nonsense |
probably null |
|
R2012:Spag9
|
UTSW |
11 |
93,983,201 (GRCm39) |
nonsense |
probably null |
|
R2351:Spag9
|
UTSW |
11 |
93,983,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R2367:Spag9
|
UTSW |
11 |
94,007,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R3027:Spag9
|
UTSW |
11 |
93,977,203 (GRCm39) |
missense |
probably null |
1.00 |
R3766:Spag9
|
UTSW |
11 |
93,951,109 (GRCm39) |
intron |
probably benign |
|
R3777:Spag9
|
UTSW |
11 |
93,989,852 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3937:Spag9
|
UTSW |
11 |
93,935,305 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3937:Spag9
|
UTSW |
11 |
93,935,243 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4417:Spag9
|
UTSW |
11 |
93,951,172 (GRCm39) |
intron |
probably benign |
|
R4445:Spag9
|
UTSW |
11 |
93,988,079 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4711:Spag9
|
UTSW |
11 |
94,005,177 (GRCm39) |
critical splice donor site |
probably null |
|
R4799:Spag9
|
UTSW |
11 |
93,939,343 (GRCm39) |
missense |
probably damaging |
0.96 |
R4799:Spag9
|
UTSW |
11 |
93,939,342 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4816:Spag9
|
UTSW |
11 |
93,939,425 (GRCm39) |
intron |
probably benign |
|
R4843:Spag9
|
UTSW |
11 |
93,988,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R5020:Spag9
|
UTSW |
11 |
93,988,612 (GRCm39) |
missense |
probably benign |
0.08 |
R5119:Spag9
|
UTSW |
11 |
94,013,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5298:Spag9
|
UTSW |
11 |
93,990,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R5304:Spag9
|
UTSW |
11 |
93,959,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5305:Spag9
|
UTSW |
11 |
93,959,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5395:Spag9
|
UTSW |
11 |
93,982,577 (GRCm39) |
splice site |
probably null |
|
R5636:Spag9
|
UTSW |
11 |
93,959,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5638:Spag9
|
UTSW |
11 |
93,959,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5654:Spag9
|
UTSW |
11 |
93,981,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R5779:Spag9
|
UTSW |
11 |
94,005,079 (GRCm39) |
missense |
probably benign |
0.20 |
R5814:Spag9
|
UTSW |
11 |
93,973,654 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5912:Spag9
|
UTSW |
11 |
93,935,251 (GRCm39) |
missense |
probably damaging |
0.98 |
R6038:Spag9
|
UTSW |
11 |
94,002,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R6038:Spag9
|
UTSW |
11 |
94,002,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R6269:Spag9
|
UTSW |
11 |
93,935,333 (GRCm39) |
missense |
probably benign |
0.05 |
R6294:Spag9
|
UTSW |
11 |
93,984,311 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6389:Spag9
|
UTSW |
11 |
93,977,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R6420:Spag9
|
UTSW |
11 |
93,977,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R6460:Spag9
|
UTSW |
11 |
93,959,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R6482:Spag9
|
UTSW |
11 |
93,984,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6860:Spag9
|
UTSW |
11 |
93,972,196 (GRCm39) |
missense |
probably benign |
0.25 |
R7086:Spag9
|
UTSW |
11 |
93,988,690 (GRCm39) |
missense |
probably benign |
|
R7179:Spag9
|
UTSW |
11 |
93,980,258 (GRCm39) |
splice site |
probably null |
|
R7225:Spag9
|
UTSW |
11 |
93,988,184 (GRCm39) |
missense |
probably damaging |
0.98 |
R7351:Spag9
|
UTSW |
11 |
93,983,802 (GRCm39) |
missense |
probably benign |
0.00 |
R7366:Spag9
|
UTSW |
11 |
93,999,347 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7378:Spag9
|
UTSW |
11 |
94,005,177 (GRCm39) |
critical splice donor site |
probably null |
|
R7401:Spag9
|
UTSW |
11 |
93,988,515 (GRCm39) |
missense |
probably benign |
|
R7506:Spag9
|
UTSW |
11 |
93,999,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R7507:Spag9
|
UTSW |
11 |
93,958,906 (GRCm39) |
missense |
probably benign |
0.00 |
R7513:Spag9
|
UTSW |
11 |
94,002,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R7655:Spag9
|
UTSW |
11 |
93,887,389 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7656:Spag9
|
UTSW |
11 |
93,887,389 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7665:Spag9
|
UTSW |
11 |
93,904,480 (GRCm39) |
missense |
probably damaging |
0.98 |
R7862:Spag9
|
UTSW |
11 |
94,002,892 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8074:Spag9
|
UTSW |
11 |
94,002,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Spag9
|
UTSW |
11 |
93,989,870 (GRCm39) |
missense |
probably benign |
|
R8469:Spag9
|
UTSW |
11 |
93,982,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R8547:Spag9
|
UTSW |
11 |
94,013,647 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8709:Spag9
|
UTSW |
11 |
93,958,916 (GRCm39) |
missense |
probably benign |
0.02 |
R8732:Spag9
|
UTSW |
11 |
93,962,514 (GRCm39) |
critical splice donor site |
probably null |
|
R8899:Spag9
|
UTSW |
11 |
93,983,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R8983:Spag9
|
UTSW |
11 |
93,958,815 (GRCm39) |
missense |
probably benign |
|
R9043:Spag9
|
UTSW |
11 |
93,951,085 (GRCm39) |
missense |
|
|
R9050:Spag9
|
UTSW |
11 |
93,935,294 (GRCm39) |
missense |
probably damaging |
0.97 |
R9502:Spag9
|
UTSW |
11 |
93,959,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R9575:Spag9
|
UTSW |
11 |
93,962,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R9667:Spag9
|
UTSW |
11 |
93,887,119 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9683:Spag9
|
UTSW |
11 |
93,988,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R9774:Spag9
|
UTSW |
11 |
94,005,062 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Predicted Primers |
PCR Primer
(F):5'- CACAAACTGGCCTTGGAGAG -3'
(R):5'- GGCAGAGAAAATGCTAAACTCTTC -3'
Sequencing Primer
(F):5'- TTGGAGAGGGCTGCACCAG -3'
(R):5'- GTTCATTGCAATAAACACACTTGTCC -3'
|
Posted On |
2019-11-12 |