Incidental Mutation 'R2044:Sema6a'
ID |
221743 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Sema6a
|
Ensembl Gene |
ENSMUSG00000019647 |
Gene Name |
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A |
Synonyms |
VIa, Semaq, Sema6A-1, sema, A730020P05Rik |
MMRRC Submission |
040051-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R2044 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
18 |
Chromosomal Location |
47378321-47504267 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
A to T
at 47439496 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Stop codon
at position 9
(C9*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000121442
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000019791]
[ENSMUST00000076043]
[ENSMUST00000115449]
[ENSMUST00000126684]
[ENSMUST00000135790]
[ENSMUST00000156422]
|
AlphaFold |
O35464 |
Predicted Effect |
probably null
Transcript: ENSMUST00000019791
AA Change: C9*
|
SMART Domains |
Protein: ENSMUSP00000019791 Gene: ENSMUSG00000019647 AA Change: C9*
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
Sema
|
56 |
487 |
1.06e-185 |
SMART |
PSI
|
514 |
569 |
9.57e-1 |
SMART |
transmembrane domain
|
648 |
670 |
N/A |
INTRINSIC |
low complexity region
|
932 |
951 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000076043
AA Change: C9*
|
SMART Domains |
Protein: ENSMUSP00000075420 Gene: ENSMUSG00000019647 AA Change: C9*
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
Sema
|
56 |
487 |
1.06e-185 |
SMART |
PSI
|
514 |
569 |
9.57e-1 |
SMART |
transmembrane domain
|
593 |
615 |
N/A |
INTRINSIC |
low complexity region
|
877 |
896 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000115449
AA Change: C9*
|
SMART Domains |
Protein: ENSMUSP00000111109 Gene: ENSMUSG00000019647 AA Change: C9*
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
Sema
|
56 |
461 |
1.24e-168 |
SMART |
PSI
|
488 |
543 |
9.57e-1 |
SMART |
transmembrane domain
|
622 |
644 |
N/A |
INTRINSIC |
low complexity region
|
906 |
925 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000126684
AA Change: C9*
|
SMART Domains |
Protein: ENSMUSP00000118655 Gene: ENSMUSG00000019647 AA Change: C9*
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
Pfam:Sema
|
56 |
216 |
2.5e-51 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000135790
AA Change: C9*
|
SMART Domains |
Protein: ENSMUSP00000120011 Gene: ENSMUSG00000019647 AA Change: C9*
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
Sema
|
56 |
487 |
1.06e-185 |
SMART |
PSI
|
514 |
569 |
9.57e-1 |
SMART |
transmembrane domain
|
665 |
687 |
N/A |
INTRINSIC |
low complexity region
|
949 |
968 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141224
|
Predicted Effect |
probably null
Transcript: ENSMUST00000156422
AA Change: C9*
|
SMART Domains |
Protein: ENSMUSP00000121442 Gene: ENSMUSG00000019647 AA Change: C9*
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
Sema
|
56 |
487 |
1.06e-185 |
SMART |
PSI
|
514 |
569 |
9.57e-1 |
SMART |
transmembrane domain
|
648 |
670 |
N/A |
INTRINSIC |
low complexity region
|
932 |
951 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144223
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000151382
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.7%
|
Validation Efficiency |
98% (92/94) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The transmembrane semaphorin SEMA6A is expressed in developing neural tissue and is required for proper development of the thalamocortical projection (Leighton et al., 2001 [PubMed 11242070]).[supplied by OMIM, Feb 2011] PHENOTYPE: Mice homozygous for a gene trapped allele exhibit defects in lamina-specific neurite stratification of specific retinal neuron subtypes and disruption of the dendritic plexus organization of On but not Off starburst amacrine cells. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410137M14Rik |
G |
A |
17: 37,288,986 (GRCm39) |
|
probably benign |
Het |
Abhd15 |
A |
G |
11: 77,409,164 (GRCm39) |
T293A |
probably benign |
Het |
Aldh1l1 |
C |
T |
6: 90,539,647 (GRCm39) |
P192L |
probably benign |
Het |
Aldoart1 |
T |
G |
4: 72,770,779 (GRCm39) |
I10L |
probably benign |
Het |
Ankhd1 |
G |
A |
18: 36,778,166 (GRCm39) |
G1653D |
probably benign |
Het |
Ankk1 |
A |
C |
9: 49,330,664 (GRCm39) |
|
probably null |
Het |
Astn1 |
A |
G |
1: 158,428,072 (GRCm39) |
T748A |
possibly damaging |
Het |
Bmp7 |
C |
A |
2: 172,781,708 (GRCm39) |
R52L |
possibly damaging |
Het |
Ccdc33 |
G |
A |
9: 57,938,395 (GRCm39) |
P859S |
possibly damaging |
Het |
Ccny |
A |
G |
18: 9,449,644 (GRCm39) |
S10P |
probably damaging |
Het |
Cdc6 |
C |
A |
11: 98,801,287 (GRCm39) |
F179L |
probably benign |
Het |
Cdc7 |
T |
A |
5: 107,130,998 (GRCm39) |
V491E |
probably benign |
Het |
Cdh23 |
G |
T |
10: 60,432,509 (GRCm39) |
S138R |
possibly damaging |
Het |
Cenpc1 |
T |
C |
5: 86,185,614 (GRCm39) |
H299R |
probably benign |
Het |
Ciart |
A |
T |
3: 95,786,013 (GRCm39) |
M354K |
probably benign |
Het |
Clasrp |
G |
T |
7: 19,320,640 (GRCm39) |
|
probably benign |
Het |
Col4a3 |
G |
A |
1: 82,674,040 (GRCm39) |
G1132E |
unknown |
Het |
Crebbp |
G |
A |
16: 3,902,687 (GRCm39) |
T2184I |
probably benign |
Het |
Cyp2r1 |
A |
C |
7: 114,149,640 (GRCm39) |
M458R |
probably damaging |
Het |
Cyp7a1 |
C |
A |
4: 6,275,492 (GRCm39) |
R27M |
probably null |
Het |
Ddhd2 |
A |
G |
8: 26,242,192 (GRCm39) |
F116L |
probably damaging |
Het |
Dgkd |
G |
A |
1: 87,855,413 (GRCm39) |
R685K |
probably benign |
Het |
Dnah2 |
A |
G |
11: 69,415,066 (GRCm39) |
S223P |
probably benign |
Het |
Exph5 |
A |
T |
9: 53,283,979 (GRCm39) |
R353S |
possibly damaging |
Het |
F11 |
C |
A |
8: 45,705,155 (GRCm39) |
V129F |
probably benign |
Het |
F830045P16Rik |
A |
T |
2: 129,301,317 (GRCm39) |
S454T |
possibly damaging |
Het |
Fam124a |
T |
C |
14: 62,824,656 (GRCm39) |
I50T |
probably damaging |
Het |
Fam20c |
T |
C |
5: 138,741,982 (GRCm39) |
|
probably null |
Het |
Fam234b |
A |
G |
6: 135,203,912 (GRCm39) |
T405A |
probably benign |
Het |
Fbh1 |
C |
A |
2: 11,767,781 (GRCm39) |
V356L |
possibly damaging |
Het |
Flywch1 |
G |
A |
17: 23,981,287 (GRCm39) |
Q132* |
probably null |
Het |
Foxo6 |
T |
C |
4: 120,144,166 (GRCm39) |
D95G |
probably benign |
Het |
Ggt5 |
T |
C |
10: 75,439,921 (GRCm39) |
F174S |
probably damaging |
Het |
Gm7104 |
G |
A |
12: 88,252,551 (GRCm39) |
|
noncoding transcript |
Het |
Gpr155 |
A |
G |
2: 73,203,977 (GRCm39) |
L279P |
probably damaging |
Het |
H2-T23 |
A |
G |
17: 36,343,083 (GRCm39) |
L98P |
probably damaging |
Het |
H4c16 |
G |
C |
6: 136,781,101 (GRCm39) |
R93G |
possibly damaging |
Het |
Heatr5a |
A |
G |
12: 52,002,186 (GRCm39) |
V250A |
probably benign |
Het |
Heyl |
A |
T |
4: 123,135,156 (GRCm39) |
I50F |
probably damaging |
Het |
Ifitm10 |
A |
T |
7: 141,909,771 (GRCm39) |
S179R |
probably damaging |
Het |
Isg15 |
A |
T |
4: 156,284,249 (GRCm39) |
I93N |
probably benign |
Het |
Itga10 |
C |
T |
3: 96,559,054 (GRCm39) |
|
probably benign |
Het |
Itga10 |
G |
A |
3: 96,565,006 (GRCm39) |
V985I |
probably benign |
Het |
Kcnt2 |
T |
C |
1: 140,302,892 (GRCm39) |
I144T |
probably benign |
Het |
Klk1 |
A |
C |
7: 43,878,458 (GRCm39) |
K104T |
possibly damaging |
Het |
Lemd3 |
C |
A |
10: 120,769,347 (GRCm39) |
R654L |
probably damaging |
Het |
Lmod1 |
A |
T |
1: 135,292,125 (GRCm39) |
M327L |
probably benign |
Het |
Lonrf2 |
T |
C |
1: 38,846,131 (GRCm39) |
E347G |
probably benign |
Het |
Ltbp1 |
A |
G |
17: 75,583,427 (GRCm39) |
Y409C |
probably damaging |
Het |
Mecom |
A |
T |
3: 30,034,741 (GRCm39) |
Y312N |
probably damaging |
Het |
Mmut |
A |
G |
17: 41,252,342 (GRCm39) |
T295A |
probably benign |
Het |
Mrgprb3 |
C |
T |
7: 48,293,482 (GRCm39) |
C23Y |
possibly damaging |
Het |
Nadk |
C |
A |
4: 155,669,898 (GRCm39) |
L194I |
probably damaging |
Het |
Naxd |
A |
G |
8: 11,559,510 (GRCm39) |
I182V |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,358,846 (GRCm39) |
I1176K |
probably damaging |
Het |
Nol4l |
C |
A |
2: 153,371,441 (GRCm39) |
R81L |
possibly damaging |
Het |
Odad3 |
T |
G |
9: 21,903,154 (GRCm39) |
T419P |
possibly damaging |
Het |
Or4k47 |
T |
A |
2: 111,452,159 (GRCm39) |
R87W |
probably benign |
Het |
Or8g36 |
A |
T |
9: 39,422,674 (GRCm39) |
M114K |
probably damaging |
Het |
Or9s15 |
G |
T |
1: 92,524,691 (GRCm39) |
R150L |
probably benign |
Het |
Pcdh18 |
A |
G |
3: 49,709,389 (GRCm39) |
V642A |
probably benign |
Het |
Pdzk1 |
G |
A |
3: 96,763,164 (GRCm39) |
|
probably benign |
Het |
Per3 |
C |
T |
4: 151,118,395 (GRCm39) |
V233I |
probably benign |
Het |
Pisd |
G |
A |
5: 32,922,140 (GRCm39) |
P267S |
possibly damaging |
Het |
Prm1 |
T |
A |
16: 10,614,357 (GRCm39) |
|
probably benign |
Het |
Ptprj |
A |
G |
2: 90,293,439 (GRCm39) |
V548A |
probably damaging |
Het |
Ranbp3 |
G |
A |
17: 56,980,367 (GRCm39) |
|
probably benign |
Het |
Raver2 |
T |
A |
4: 100,960,009 (GRCm39) |
V163D |
probably damaging |
Het |
Rbm14 |
A |
T |
19: 4,853,905 (GRCm39) |
I159N |
possibly damaging |
Het |
Rfx6 |
G |
A |
10: 51,594,222 (GRCm39) |
V381I |
probably benign |
Het |
Rhobtb1 |
T |
C |
10: 69,108,693 (GRCm39) |
|
probably benign |
Het |
Rpl28-ps4 |
T |
A |
6: 117,190,856 (GRCm39) |
|
noncoding transcript |
Het |
Rsph10b |
A |
G |
5: 143,904,068 (GRCm39) |
|
probably null |
Het |
Rspo4 |
A |
G |
2: 151,715,013 (GRCm39) |
K217E |
unknown |
Het |
Scgb2b27 |
G |
A |
7: 33,712,710 (GRCm39) |
A44V |
possibly damaging |
Het |
Sec14l2 |
G |
A |
11: 4,061,435 (GRCm39) |
|
probably benign |
Het |
Sec31b |
T |
C |
19: 44,524,595 (GRCm39) |
N101D |
probably benign |
Het |
Septin5 |
A |
C |
16: 18,441,762 (GRCm39) |
L331R |
probably benign |
Het |
Slc16a11 |
C |
A |
11: 70,106,477 (GRCm39) |
Y238* |
probably null |
Het |
Slc25a12 |
T |
C |
2: 71,142,892 (GRCm39) |
T210A |
probably benign |
Het |
Slc35f1 |
A |
T |
10: 52,965,443 (GRCm39) |
Y286F |
probably damaging |
Het |
Szt2 |
A |
T |
4: 118,233,645 (GRCm39) |
L2225* |
probably null |
Het |
Thap12 |
T |
C |
7: 98,365,827 (GRCm39) |
L665P |
probably damaging |
Het |
Tpsb2 |
T |
A |
17: 25,586,698 (GRCm39) |
W237R |
probably damaging |
Het |
Tyk2 |
T |
C |
9: 21,031,637 (GRCm39) |
D451G |
probably damaging |
Het |
Ube2j1 |
T |
A |
4: 33,049,696 (GRCm39) |
N231K |
probably benign |
Het |
Vmn1r225 |
A |
T |
17: 20,722,852 (GRCm39) |
T98S |
possibly damaging |
Het |
Vmn1r87 |
A |
T |
7: 12,865,748 (GRCm39) |
S180T |
probably benign |
Het |
Vmn2r6 |
A |
G |
3: 64,445,262 (GRCm39) |
V821A |
probably damaging |
Het |
Zfp689 |
C |
A |
7: 127,043,998 (GRCm39) |
G211C |
probably damaging |
Het |
Zfp827 |
A |
G |
8: 79,802,865 (GRCm39) |
D479G |
probably benign |
Het |
Zfp995 |
A |
C |
17: 22,099,575 (GRCm39) |
F220V |
probably damaging |
Het |
|
Other mutations in Sema6a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Sema6a
|
APN |
18 |
47,423,042 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01351:Sema6a
|
APN |
18 |
47,414,369 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01594:Sema6a
|
APN |
18 |
47,381,884 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01953:Sema6a
|
APN |
18 |
47,423,187 (GRCm39) |
nonsense |
probably null |
|
IGL02077:Sema6a
|
APN |
18 |
47,416,465 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02632:Sema6a
|
APN |
18 |
47,423,222 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02957:Sema6a
|
APN |
18 |
47,382,291 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03013:Sema6a
|
APN |
18 |
47,381,461 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03279:Sema6a
|
APN |
18 |
47,433,157 (GRCm39) |
nonsense |
probably null |
|
saphire
|
UTSW |
18 |
47,439,496 (GRCm39) |
nonsense |
probably null |
|
IGL02988:Sema6a
|
UTSW |
18 |
47,431,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R0114:Sema6a
|
UTSW |
18 |
47,423,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R0311:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0312:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0347:Sema6a
|
UTSW |
18 |
47,424,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R0350:Sema6a
|
UTSW |
18 |
47,403,785 (GRCm39) |
missense |
probably benign |
|
R0366:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0368:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0391:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0403:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0466:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0515:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0517:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0542:Sema6a
|
UTSW |
18 |
47,381,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R0557:Sema6a
|
UTSW |
18 |
47,382,567 (GRCm39) |
missense |
probably benign |
0.01 |
R0569:Sema6a
|
UTSW |
18 |
47,403,872 (GRCm39) |
splice site |
probably null |
|
R0650:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0689:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0694:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0726:Sema6a
|
UTSW |
18 |
47,425,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R0741:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0821:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0824:Sema6a
|
UTSW |
18 |
47,423,112 (GRCm39) |
splice site |
probably null |
|
R0924:Sema6a
|
UTSW |
18 |
47,381,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R1108:Sema6a
|
UTSW |
18 |
47,439,498 (GRCm39) |
missense |
probably benign |
0.02 |
R1255:Sema6a
|
UTSW |
18 |
47,382,366 (GRCm39) |
missense |
probably damaging |
0.98 |
R1422:Sema6a
|
UTSW |
18 |
47,439,498 (GRCm39) |
missense |
probably benign |
0.02 |
R1531:Sema6a
|
UTSW |
18 |
47,382,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R1707:Sema6a
|
UTSW |
18 |
47,416,512 (GRCm39) |
missense |
probably benign |
0.04 |
R1746:Sema6a
|
UTSW |
18 |
47,439,416 (GRCm39) |
splice site |
probably benign |
|
R1807:Sema6a
|
UTSW |
18 |
47,409,491 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1974:Sema6a
|
UTSW |
18 |
47,403,696 (GRCm39) |
missense |
probably benign |
0.04 |
R1987:Sema6a
|
UTSW |
18 |
47,433,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R3719:Sema6a
|
UTSW |
18 |
47,382,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R4491:Sema6a
|
UTSW |
18 |
47,439,524 (GRCm39) |
utr 5 prime |
probably benign |
|
R4552:Sema6a
|
UTSW |
18 |
47,424,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:Sema6a
|
UTSW |
18 |
47,381,779 (GRCm39) |
missense |
probably benign |
0.43 |
R4710:Sema6a
|
UTSW |
18 |
47,403,750 (GRCm39) |
missense |
probably benign |
0.00 |
R4713:Sema6a
|
UTSW |
18 |
47,382,363 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4963:Sema6a
|
UTSW |
18 |
47,431,318 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5088:Sema6a
|
UTSW |
18 |
47,382,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Sema6a
|
UTSW |
18 |
47,433,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R5135:Sema6a
|
UTSW |
18 |
47,424,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R5141:Sema6a
|
UTSW |
18 |
47,381,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R5277:Sema6a
|
UTSW |
18 |
47,409,611 (GRCm39) |
intron |
probably benign |
|
R5551:Sema6a
|
UTSW |
18 |
47,381,595 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5618:Sema6a
|
UTSW |
18 |
47,415,015 (GRCm39) |
missense |
probably damaging |
0.98 |
R5717:Sema6a
|
UTSW |
18 |
47,382,330 (GRCm39) |
missense |
probably benign |
0.01 |
R5729:Sema6a
|
UTSW |
18 |
47,414,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R5779:Sema6a
|
UTSW |
18 |
47,381,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R5917:Sema6a
|
UTSW |
18 |
47,414,405 (GRCm39) |
missense |
probably benign |
0.05 |
R6054:Sema6a
|
UTSW |
18 |
47,416,470 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6142:Sema6a
|
UTSW |
18 |
47,414,266 (GRCm39) |
missense |
probably benign |
0.00 |
R6209:Sema6a
|
UTSW |
18 |
47,431,369 (GRCm39) |
splice site |
probably null |
|
R6307:Sema6a
|
UTSW |
18 |
47,382,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R6734:Sema6a
|
UTSW |
18 |
47,412,236 (GRCm39) |
missense |
probably benign |
0.31 |
R7014:Sema6a
|
UTSW |
18 |
47,431,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Sema6a
|
UTSW |
18 |
47,381,637 (GRCm39) |
missense |
probably damaging |
0.96 |
R7574:Sema6a
|
UTSW |
18 |
47,424,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:Sema6a
|
UTSW |
18 |
47,424,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R8250:Sema6a
|
UTSW |
18 |
47,423,182 (GRCm39) |
missense |
probably damaging |
0.99 |
R8408:Sema6a
|
UTSW |
18 |
47,381,958 (GRCm39) |
missense |
probably benign |
0.34 |
R8411:Sema6a
|
UTSW |
18 |
47,382,022 (GRCm39) |
missense |
probably benign |
0.00 |
R8900:Sema6a
|
UTSW |
18 |
47,424,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R9140:Sema6a
|
UTSW |
18 |
47,415,009 (GRCm39) |
missense |
probably benign |
|
R9158:Sema6a
|
UTSW |
18 |
47,431,330 (GRCm39) |
missense |
probably damaging |
0.98 |
R9488:Sema6a
|
UTSW |
18 |
47,437,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Sema6a
|
UTSW |
18 |
47,382,594 (GRCm39) |
missense |
probably null |
1.00 |
R9652:Sema6a
|
UTSW |
18 |
47,382,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R9732:Sema6a
|
UTSW |
18 |
47,381,925 (GRCm39) |
missense |
probably damaging |
0.96 |
X0065:Sema6a
|
UTSW |
18 |
47,416,386 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
Predicted Primers |
PCR Primer
(F):5'- ACCTGCTGTGAAATCACCTATCC -3'
(R):5'- AGGGAACAGAAGCCTTTTGTC -3'
Sequencing Primer
(F):5'- CATGCAGTTGAAAATGACTGGGTCTC -3'
(R):5'- GGAACAGAAGCCTTTTGTCTTGAATC -3'
|
Posted On |
2014-08-25 |