Incidental Mutation 'R4082:Stard13'
ID |
316928 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Stard13
|
Ensembl Gene |
ENSMUSG00000016128 |
Gene Name |
StAR related lipid transfer domain containing 13 |
Synonyms |
GT650, DLC2 |
MMRRC Submission |
041624-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4082 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
150960975-151157301 bp(-) (GRCm39) |
Type of Mutation |
critical splice acceptor site |
DNA Base Change (assembly) |
C to A
at 151016294 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000143819
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000062015]
[ENSMUST00000062015]
[ENSMUST00000110483]
[ENSMUST00000110483]
[ENSMUST00000126770]
[ENSMUST00000126770]
[ENSMUST00000126770]
[ENSMUST00000126770]
[ENSMUST00000129088]
[ENSMUST00000129088]
[ENSMUST00000129088]
[ENSMUST00000129088]
[ENSMUST00000202111]
[ENSMUST00000202111]
[ENSMUST00000202111]
[ENSMUST00000202111]
[ENSMUST00000202365]
[ENSMUST00000202365]
[ENSMUST00000202365]
[ENSMUST00000202365]
|
AlphaFold |
Q923Q2 |
Predicted Effect |
probably null
Transcript: ENSMUST00000062015
|
SMART Domains |
Protein: ENSMUSP00000053232 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
Pfam:SAM_2
|
59 |
120 |
2.6e-6 |
PFAM |
low complexity region
|
197 |
216 |
N/A |
INTRINSIC |
low complexity region
|
322 |
340 |
N/A |
INTRINSIC |
low complexity region
|
473 |
486 |
N/A |
INTRINSIC |
low complexity region
|
612 |
624 |
N/A |
INTRINSIC |
RhoGAP
|
693 |
884 |
2.37e-50 |
SMART |
START
|
927 |
1129 |
2.08e-40 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000062015
|
SMART Domains |
Protein: ENSMUSP00000053232 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
Pfam:SAM_2
|
59 |
120 |
2.6e-6 |
PFAM |
low complexity region
|
197 |
216 |
N/A |
INTRINSIC |
low complexity region
|
322 |
340 |
N/A |
INTRINSIC |
low complexity region
|
473 |
486 |
N/A |
INTRINSIC |
low complexity region
|
612 |
624 |
N/A |
INTRINSIC |
RhoGAP
|
693 |
884 |
2.37e-50 |
SMART |
START
|
927 |
1129 |
2.08e-40 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000110483
|
SMART Domains |
Protein: ENSMUSP00000106109 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
PDB:2JW2|A
|
50 |
120 |
1e-37 |
PDB |
low complexity region
|
197 |
216 |
N/A |
INTRINSIC |
low complexity region
|
322 |
340 |
N/A |
INTRINSIC |
low complexity region
|
473 |
486 |
N/A |
INTRINSIC |
low complexity region
|
612 |
624 |
N/A |
INTRINSIC |
RhoGAP
|
674 |
865 |
2.37e-50 |
SMART |
START
|
908 |
1110 |
2.08e-40 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000110483
|
SMART Domains |
Protein: ENSMUSP00000106109 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
PDB:2JW2|A
|
50 |
120 |
1e-37 |
PDB |
low complexity region
|
197 |
216 |
N/A |
INTRINSIC |
low complexity region
|
322 |
340 |
N/A |
INTRINSIC |
low complexity region
|
473 |
486 |
N/A |
INTRINSIC |
low complexity region
|
612 |
624 |
N/A |
INTRINSIC |
RhoGAP
|
674 |
865 |
2.37e-50 |
SMART |
START
|
908 |
1110 |
2.08e-40 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000126770
|
SMART Domains |
Protein: ENSMUSP00000122468 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
Pfam:SAM_2
|
44 |
105 |
7.6e-8 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000126770
|
SMART Domains |
Protein: ENSMUSP00000122468 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
Pfam:SAM_2
|
44 |
105 |
7.6e-8 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000126770
|
SMART Domains |
Protein: ENSMUSP00000122468 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
Pfam:SAM_2
|
44 |
105 |
7.6e-8 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000126770
|
SMART Domains |
Protein: ENSMUSP00000122468 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
Pfam:SAM_2
|
44 |
105 |
7.6e-8 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000129088
|
SMART Domains |
Protein: ENSMUSP00000116705 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
Blast:SAM
|
40 |
104 |
6e-32 |
BLAST |
PDB:2JW2|A
|
42 |
104 |
8e-33 |
PDB |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000129088
|
SMART Domains |
Protein: ENSMUSP00000116705 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
Blast:SAM
|
40 |
104 |
6e-32 |
BLAST |
PDB:2JW2|A
|
42 |
104 |
8e-33 |
PDB |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000129088
|
SMART Domains |
Protein: ENSMUSP00000116705 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
Blast:SAM
|
40 |
104 |
6e-32 |
BLAST |
PDB:2JW2|A
|
42 |
104 |
8e-33 |
PDB |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000129088
|
SMART Domains |
Protein: ENSMUSP00000116705 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
Blast:SAM
|
40 |
104 |
6e-32 |
BLAST |
PDB:2JW2|A
|
42 |
104 |
8e-33 |
PDB |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141117
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000146814
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000201680
|
Predicted Effect |
probably null
Transcript: ENSMUST00000202111
|
SMART Domains |
Protein: ENSMUSP00000144056 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
low complexity region
|
79 |
98 |
N/A |
INTRINSIC |
low complexity region
|
204 |
222 |
N/A |
INTRINSIC |
low complexity region
|
355 |
368 |
N/A |
INTRINSIC |
low complexity region
|
494 |
506 |
N/A |
INTRINSIC |
RhoGAP
|
556 |
747 |
1.4e-52 |
SMART |
START
|
790 |
992 |
1.4e-42 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000202111
|
SMART Domains |
Protein: ENSMUSP00000144056 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
low complexity region
|
79 |
98 |
N/A |
INTRINSIC |
low complexity region
|
204 |
222 |
N/A |
INTRINSIC |
low complexity region
|
355 |
368 |
N/A |
INTRINSIC |
low complexity region
|
494 |
506 |
N/A |
INTRINSIC |
RhoGAP
|
556 |
747 |
1.4e-52 |
SMART |
START
|
790 |
992 |
1.4e-42 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000202111
|
SMART Domains |
Protein: ENSMUSP00000144056 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
low complexity region
|
79 |
98 |
N/A |
INTRINSIC |
low complexity region
|
204 |
222 |
N/A |
INTRINSIC |
low complexity region
|
355 |
368 |
N/A |
INTRINSIC |
low complexity region
|
494 |
506 |
N/A |
INTRINSIC |
RhoGAP
|
556 |
747 |
1.4e-52 |
SMART |
START
|
790 |
992 |
1.4e-42 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000202111
|
SMART Domains |
Protein: ENSMUSP00000144056 Gene: ENSMUSG00000016128
Domain | Start | End | E-Value | Type |
low complexity region
|
79 |
98 |
N/A |
INTRINSIC |
low complexity region
|
204 |
222 |
N/A |
INTRINSIC |
low complexity region
|
355 |
368 |
N/A |
INTRINSIC |
low complexity region
|
494 |
506 |
N/A |
INTRINSIC |
RhoGAP
|
556 |
747 |
1.4e-52 |
SMART |
START
|
790 |
992 |
1.4e-42 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000202365
|
Predicted Effect |
probably null
Transcript: ENSMUST00000202365
|
Predicted Effect |
probably null
Transcript: ENSMUST00000202365
|
Predicted Effect |
probably null
Transcript: ENSMUST00000202365
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000202385
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000202866
|
Meta Mutation Damage Score |
0.9489 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.4%
|
Validation Efficiency |
99% (73/74) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein which contains an N-terminal sterile alpha motif (SAM) for protein-protein interactions, followed by an ATP/GTP-binding motif, a GTPase-activating protein (GAP) domain, and a C-terminal STAR-related lipid transfer (START) domain. It may be involved in regulation of cytoskeletal reorganization, cell proliferation, and cell motility, and acts as a tumor suppressor in hepatoma cells. The gene is located in a region of chromosome 13 that is associated with loss of heterozygosity in hepatocellular carcinomas. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011] PHENOTYPE: Mice homozygous for a knock-out allele exhibit small body size, decreased weight, and reduced adipose tissue. Mice homozygous for another knock-out allele exhibit increased angiogenesis in matrigel plugs and implanted tumors. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700021P04Rik |
T |
G |
19: 24,043,366 (GRCm39) |
|
noncoding transcript |
Het |
a |
A |
T |
2: 154,887,678 (GRCm39) |
D46V |
probably damaging |
Het |
Aass |
A |
T |
6: 23,109,497 (GRCm39) |
D324E |
possibly damaging |
Het |
Abca12 |
G |
T |
1: 71,306,622 (GRCm39) |
T2028K |
possibly damaging |
Het |
Abt1 |
T |
C |
13: 23,606,316 (GRCm39) |
T213A |
probably benign |
Het |
Adcy1 |
A |
C |
11: 7,014,117 (GRCm39) |
Y173S |
probably damaging |
Het |
Aim2 |
T |
C |
1: 173,287,417 (GRCm39) |
|
probably null |
Het |
Akr1d1 |
G |
A |
6: 37,534,424 (GRCm39) |
V193M |
probably damaging |
Het |
Cars1 |
C |
T |
7: 143,123,234 (GRCm39) |
E461K |
probably damaging |
Het |
Ccdc80 |
T |
C |
16: 44,943,290 (GRCm39) |
L800P |
probably damaging |
Het |
Ccl22 |
A |
G |
8: 95,473,536 (GRCm39) |
Y27C |
probably damaging |
Het |
Cdc123 |
G |
A |
2: 5,815,566 (GRCm39) |
|
probably benign |
Het |
Cldn11 |
A |
T |
3: 31,217,278 (GRCm39) |
I149F |
probably benign |
Het |
Col14a1 |
T |
C |
15: 55,300,429 (GRCm39) |
Y986H |
unknown |
Het |
Col6a3 |
G |
A |
1: 90,749,605 (GRCm39) |
L410F |
probably damaging |
Het |
Crocc |
T |
C |
4: 140,761,282 (GRCm39) |
|
probably null |
Het |
Cubn |
A |
G |
2: 13,433,374 (GRCm39) |
|
probably benign |
Het |
Cwc25 |
G |
T |
11: 97,644,744 (GRCm39) |
Q205K |
probably benign |
Het |
Cyp2e1 |
T |
C |
7: 140,350,991 (GRCm39) |
I321T |
possibly damaging |
Het |
Eps8l1 |
T |
A |
7: 4,473,797 (GRCm39) |
|
probably null |
Het |
Fasl |
C |
T |
1: 161,609,420 (GRCm39) |
V189M |
probably damaging |
Het |
Fbxw5 |
T |
C |
2: 25,394,643 (GRCm39) |
|
probably null |
Het |
Flg2 |
A |
C |
3: 93,110,828 (GRCm39) |
E952A |
unknown |
Het |
Gpd1l |
A |
T |
9: 114,746,146 (GRCm39) |
L90Q |
probably damaging |
Het |
Grik4 |
G |
T |
9: 42,509,180 (GRCm39) |
F414L |
probably benign |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Klhl3 |
C |
T |
13: 58,166,611 (GRCm39) |
G407S |
probably null |
Het |
Lmbr1 |
T |
C |
5: 29,463,753 (GRCm39) |
E157G |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,343,617 (GRCm39) |
H914L |
probably damaging |
Het |
Mrpl20 |
A |
T |
4: 155,892,970 (GRCm39) |
D67V |
probably damaging |
Het |
Myo15a |
A |
G |
11: 60,378,022 (GRCm39) |
T1346A |
possibly damaging |
Het |
Naip5 |
A |
T |
13: 100,382,338 (GRCm39) |
C124S |
probably damaging |
Het |
Or10ag2 |
T |
A |
2: 87,248,801 (GRCm39) |
Y134* |
probably null |
Het |
Or13n4 |
T |
C |
7: 106,423,245 (GRCm39) |
T163A |
possibly damaging |
Het |
Or52u1 |
T |
A |
7: 104,237,830 (GRCm39) |
V290D |
probably damaging |
Het |
Osbp |
A |
G |
19: 11,956,030 (GRCm39) |
D385G |
probably benign |
Het |
Paip1 |
G |
A |
13: 119,593,540 (GRCm39) |
D460N |
probably damaging |
Het |
Pde3b |
T |
C |
7: 114,093,823 (GRCm39) |
S356P |
probably benign |
Het |
Pms2 |
A |
G |
5: 143,867,837 (GRCm39) |
M814V |
probably damaging |
Het |
Polg |
C |
A |
7: 79,114,576 (GRCm39) |
K128N |
probably damaging |
Het |
Polk |
G |
T |
13: 96,620,181 (GRCm39) |
T694K |
probably benign |
Het |
Pom121 |
T |
C |
5: 135,417,491 (GRCm39) |
K342R |
unknown |
Het |
Pou5f2 |
T |
C |
13: 78,174,024 (GRCm39) |
L322P |
probably damaging |
Het |
Prorp |
G |
T |
12: 55,351,398 (GRCm39) |
V236F |
possibly damaging |
Het |
Ptpn6 |
T |
C |
6: 124,705,382 (GRCm39) |
D183G |
probably damaging |
Het |
Pygb |
G |
A |
2: 150,668,391 (GRCm39) |
|
probably null |
Het |
Ralgds |
C |
T |
2: 28,442,283 (GRCm39) |
|
probably benign |
Het |
Ret |
T |
C |
6: 118,130,927 (GRCm39) |
T1079A |
possibly damaging |
Het |
Rspo2 |
A |
C |
15: 42,885,933 (GRCm39) |
V241G |
probably benign |
Het |
Smg1 |
T |
A |
7: 117,759,469 (GRCm39) |
|
probably benign |
Het |
Snph |
T |
C |
2: 151,435,722 (GRCm39) |
D402G |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,041,632 (GRCm39) |
D1334G |
probably benign |
Het |
Sufu |
A |
G |
19: 46,413,541 (GRCm39) |
M141V |
probably damaging |
Het |
Sytl2 |
T |
A |
7: 90,057,635 (GRCm39) |
V831D |
possibly damaging |
Het |
Tc2n |
T |
C |
12: 101,617,414 (GRCm39) |
E335G |
possibly damaging |
Het |
Tex11 |
C |
A |
X: 99,977,021 (GRCm39) |
A487S |
possibly damaging |
Het |
Tmcc1 |
T |
A |
6: 116,020,441 (GRCm39) |
H118L |
probably damaging |
Het |
Tulp4 |
C |
T |
17: 6,282,055 (GRCm39) |
H695Y |
probably damaging |
Het |
Vmn1r209 |
A |
C |
13: 22,989,785 (GRCm39) |
L302V |
probably null |
Het |
Vmn2r117 |
C |
T |
17: 23,679,080 (GRCm39) |
V715I |
probably benign |
Het |
Vopp1 |
A |
T |
6: 57,766,964 (GRCm39) |
Y37* |
probably null |
Het |
Xrn1 |
A |
G |
9: 95,863,973 (GRCm39) |
T528A |
probably benign |
Het |
Zfhx2 |
T |
C |
14: 55,302,662 (GRCm39) |
D1774G |
probably benign |
Het |
Zfp955b |
T |
A |
17: 33,521,129 (GRCm39) |
D199E |
probably benign |
Het |
Zp2 |
T |
C |
7: 119,734,475 (GRCm39) |
S525G |
probably benign |
Het |
|
Other mutations in Stard13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00639:Stard13
|
APN |
5 |
150,965,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01362:Stard13
|
APN |
5 |
151,113,417 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01588:Stard13
|
APN |
5 |
150,968,702 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01947:Stard13
|
APN |
5 |
150,986,309 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02294:Stard13
|
APN |
5 |
150,986,580 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02713:Stard13
|
APN |
5 |
150,965,651 (GRCm39) |
nonsense |
probably null |
|
IGL02746:Stard13
|
APN |
5 |
150,970,322 (GRCm39) |
splice site |
probably benign |
|
IGL02827:Stard13
|
APN |
5 |
150,986,591 (GRCm39) |
missense |
probably benign |
0.07 |
R0498:Stard13
|
UTSW |
5 |
150,975,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R1427:Stard13
|
UTSW |
5 |
150,969,456 (GRCm39) |
missense |
probably damaging |
0.99 |
R1785:Stard13
|
UTSW |
5 |
150,968,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1857:Stard13
|
UTSW |
5 |
151,018,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Stard13
|
UTSW |
5 |
151,018,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:Stard13
|
UTSW |
5 |
150,968,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Stard13
|
UTSW |
5 |
150,968,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Stard13
|
UTSW |
5 |
150,968,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Stard13
|
UTSW |
5 |
150,968,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:Stard13
|
UTSW |
5 |
150,963,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R3435:Stard13
|
UTSW |
5 |
150,965,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R4080:Stard13
|
UTSW |
5 |
151,016,294 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4081:Stard13
|
UTSW |
5 |
151,016,294 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4233:Stard13
|
UTSW |
5 |
150,986,164 (GRCm39) |
missense |
probably benign |
0.00 |
R4288:Stard13
|
UTSW |
5 |
150,968,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R4303:Stard13
|
UTSW |
5 |
150,986,334 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4659:Stard13
|
UTSW |
5 |
150,986,253 (GRCm39) |
missense |
probably benign |
0.01 |
R4695:Stard13
|
UTSW |
5 |
150,984,280 (GRCm39) |
missense |
probably benign |
0.08 |
R4910:Stard13
|
UTSW |
5 |
150,985,992 (GRCm39) |
missense |
probably benign |
|
R5135:Stard13
|
UTSW |
5 |
150,986,232 (GRCm39) |
nonsense |
probably null |
|
R5338:Stard13
|
UTSW |
5 |
150,983,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Stard13
|
UTSW |
5 |
150,971,266 (GRCm39) |
nonsense |
probably null |
|
R5546:Stard13
|
UTSW |
5 |
150,969,366 (GRCm39) |
missense |
probably benign |
0.03 |
R5685:Stard13
|
UTSW |
5 |
150,986,592 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5771:Stard13
|
UTSW |
5 |
151,113,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Stard13
|
UTSW |
5 |
151,018,965 (GRCm39) |
splice site |
probably null |
|
R6034:Stard13
|
UTSW |
5 |
151,018,965 (GRCm39) |
splice site |
probably null |
|
R6141:Stard13
|
UTSW |
5 |
150,965,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R6171:Stard13
|
UTSW |
5 |
151,016,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R6296:Stard13
|
UTSW |
5 |
150,986,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Stard13
|
UTSW |
5 |
150,970,384 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6508:Stard13
|
UTSW |
5 |
150,986,754 (GRCm39) |
missense |
probably benign |
0.06 |
R7252:Stard13
|
UTSW |
5 |
150,986,634 (GRCm39) |
missense |
probably benign |
0.01 |
R7318:Stard13
|
UTSW |
5 |
150,986,038 (GRCm39) |
nonsense |
probably null |
|
R7459:Stard13
|
UTSW |
5 |
150,971,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R7571:Stard13
|
UTSW |
5 |
150,982,967 (GRCm39) |
missense |
probably damaging |
0.97 |
R7696:Stard13
|
UTSW |
5 |
150,984,267 (GRCm39) |
missense |
probably damaging |
0.99 |
R7809:Stard13
|
UTSW |
5 |
151,113,489 (GRCm39) |
missense |
probably damaging |
0.98 |
R7962:Stard13
|
UTSW |
5 |
150,975,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R7970:Stard13
|
UTSW |
5 |
150,986,726 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8103:Stard13
|
UTSW |
5 |
150,970,435 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8113:Stard13
|
UTSW |
5 |
150,986,970 (GRCm39) |
missense |
probably damaging |
0.99 |
R8263:Stard13
|
UTSW |
5 |
151,157,106 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8392:Stard13
|
UTSW |
5 |
150,965,627 (GRCm39) |
missense |
probably benign |
0.24 |
R8490:Stard13
|
UTSW |
5 |
150,987,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R8726:Stard13
|
UTSW |
5 |
150,986,607 (GRCm39) |
missense |
probably benign |
0.28 |
R8896:Stard13
|
UTSW |
5 |
150,986,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R8939:Stard13
|
UTSW |
5 |
150,968,574 (GRCm39) |
critical splice donor site |
probably null |
|
R8946:Stard13
|
UTSW |
5 |
150,984,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R9157:Stard13
|
UTSW |
5 |
151,157,152 (GRCm39) |
missense |
probably benign |
0.00 |
R9257:Stard13
|
UTSW |
5 |
150,985,956 (GRCm39) |
missense |
probably benign |
|
R9387:Stard13
|
UTSW |
5 |
151,113,483 (GRCm39) |
missense |
probably benign |
0.27 |
R9586:Stard13
|
UTSW |
5 |
150,985,832 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9708:Stard13
|
UTSW |
5 |
150,986,961 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9771:Stard13
|
UTSW |
5 |
150,983,048 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Stard13
|
UTSW |
5 |
150,986,799 (GRCm39) |
missense |
probably benign |
0.18 |
|
Predicted Primers |
PCR Primer
(F):5'- CAGTGACCACAATAAACGTATTTCC -3'
(R):5'- GCACTTACACTGCACTCTCAAG -3'
Sequencing Primer
(F):5'- CCACAATAAACGTATTTCCAAAGTTG -3'
(R):5'- GCACTCTCAAGAGCATTTTCTGTG -3'
|
Posted On |
2015-05-15 |