Incidental Mutation 'R8725:Dscaml1'
| ID |
662363 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Dscaml1
|
| Ensembl Gene |
ENSMUSG00000032087 |
| Gene Name |
DS cell adhesion molecule like 1 |
| Synonyms |
4921507G06Rik, 4930435C18Rik |
| MMRRC Submission |
068574-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.481)
|
| Stock # |
R8725 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
45338735-45665011 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 45341759 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Asparagine
at position 57
(Y57N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000034592
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034592]
[ENSMUST00000213919]
[ENSMUST00000217538]
|
| AlphaFold |
Q4VA61 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000034592
AA Change: Y57N
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000034592
Gene: ENSMUSG00000032087
AA Change: Y57N
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
3 |
17 |
N/A |
INTRINSIC |
|
low complexity region
|
28 |
55 |
N/A |
INTRINSIC |
|
IG_like
|
96 |
168 |
1.22e0 |
SMART |
|
IG
|
189 |
277 |
1.15e-3 |
SMART |
|
IGc2
|
296 |
359 |
2.54e-14 |
SMART |
|
IGc2
|
385 |
451 |
8.12e-13 |
SMART |
|
IGc2
|
478 |
550 |
9.55e-10 |
SMART |
|
IGc2
|
575 |
640 |
9.78e-7 |
SMART |
|
IGc2
|
666 |
734 |
5.93e-6 |
SMART |
|
IGc2
|
760 |
832 |
6.75e-10 |
SMART |
|
IG
|
853 |
943 |
1e-3 |
SMART |
|
FN3
|
945 |
1029 |
6.64e-7 |
SMART |
|
FN3
|
1045 |
1133 |
9.46e-12 |
SMART |
|
FN3
|
1148 |
1234 |
3.2e-9 |
SMART |
|
FN3
|
1249 |
1332 |
3.48e-10 |
SMART |
|
IGc2
|
1363 |
1428 |
1.49e-11 |
SMART |
|
FN3
|
1442 |
1522 |
3.42e-9 |
SMART |
|
FN3
|
1537 |
1618 |
2.14e-1 |
SMART |
|
low complexity region
|
1671 |
1683 |
N/A |
INTRINSIC |
|
low complexity region
|
2018 |
2026 |
N/A |
INTRINSIC |
|
low complexity region
|
2035 |
2069 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213919
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217538
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.5%
|
| Validation Efficiency |
|
| 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 a member of the Ig superfamily of cell adhesion molecules and is involved in neuronal differentiation. The encoded membrane-bound protein localizes to the cell surface, where it forms aggregates that repel neuronal processes of the same cell type. [provided by RefSeq, Sep 2016]
PHENOTYPE: Mice homozygous for a gene trapped allele exhibit impaired self-avoidance in multiple cell types in the retina. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(4) : Gene trapped(4) |
| Other mutations in this stock |
Total: 74 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A630089N07Rik |
C |
T |
16: 97,867,651 (GRCm39) |
A104T |
probably damaging |
Het |
| Abhd18 |
T |
A |
3: 40,884,627 (GRCm39) |
L222Q |
probably damaging |
Het |
| Adam30 |
C |
T |
3: 98,070,348 (GRCm39) |
T727M |
possibly damaging |
Het |
| Adh6b |
A |
T |
3: 138,058,729 (GRCm39) |
Q137L |
probably damaging |
Het |
| Alpl |
C |
T |
4: 137,475,127 (GRCm39) |
V269I |
probably benign |
Het |
| Ang2 |
C |
T |
14: 51,432,996 (GRCm39) |
G129S |
probably benign |
Het |
| Atp6v0a1 |
A |
T |
11: 100,920,015 (GRCm39) |
H216L |
possibly damaging |
Het |
| BC030500 |
C |
T |
8: 59,366,049 (GRCm39) |
T61I |
unknown |
Het |
| Brpf1 |
T |
G |
6: 113,293,491 (GRCm39) |
L520R |
probably damaging |
Het |
| Btbd10 |
A |
G |
7: 112,927,626 (GRCm39) |
I243T |
possibly damaging |
Het |
| Bub1 |
C |
A |
2: 127,646,139 (GRCm39) |
C947F |
probably damaging |
Het |
| C4b |
T |
C |
17: 34,953,459 (GRCm39) |
E1008G |
probably damaging |
Het |
| Ccdc40 |
A |
G |
11: 119,155,323 (GRCm39) |
T1188A |
probably benign |
Het |
| Cdcp3 |
A |
G |
7: 130,875,485 (GRCm39) |
T1770A |
unknown |
Het |
| Cnn1 |
G |
T |
9: 22,010,557 (GRCm39) |
|
probably benign |
Het |
| Colgalt2 |
T |
C |
1: 152,360,662 (GRCm39) |
M233T |
probably damaging |
Het |
| Cox15 |
A |
T |
19: 43,735,181 (GRCm39) |
C195* |
probably null |
Het |
| Cped1 |
A |
T |
6: 22,059,941 (GRCm39) |
R202S |
possibly damaging |
Het |
| Dact2 |
A |
T |
17: 14,417,146 (GRCm39) |
C351* |
probably null |
Het |
| Dbnl |
A |
G |
11: 5,738,582 (GRCm39) |
N8S |
probably benign |
Het |
| Depdc1a |
T |
A |
3: 159,228,356 (GRCm39) |
N369K |
probably benign |
Het |
| Dnah2 |
A |
T |
11: 69,415,005 (GRCm39) |
L243Q |
probably damaging |
Het |
| Eif2b3 |
A |
G |
4: 116,927,944 (GRCm39) |
T388A |
probably benign |
Het |
| Eif4h |
A |
C |
5: 134,654,393 (GRCm39) |
|
probably null |
Het |
| Elf1 |
C |
T |
14: 79,810,667 (GRCm39) |
Q288* |
probably null |
Het |
| Fgl2 |
C |
T |
5: 21,580,677 (GRCm39) |
R340* |
probably null |
Het |
| Fut4 |
T |
C |
9: 14,662,082 (GRCm39) |
D404G |
probably damaging |
Het |
| Glmn |
G |
A |
5: 107,718,152 (GRCm39) |
P255L |
probably benign |
Het |
| Gm14322 |
C |
T |
2: 177,411,481 (GRCm39) |
T97I |
probably benign |
Het |
| Gm44511 |
C |
A |
6: 128,797,997 (GRCm39) |
C32F |
probably damaging |
Het |
| Gm5478 |
A |
G |
15: 101,553,871 (GRCm39) |
F247S |
probably damaging |
Het |
| Golgb1 |
T |
A |
16: 36,739,563 (GRCm39) |
M2675K |
probably damaging |
Het |
| Hectd1 |
T |
C |
12: 51,849,000 (GRCm39) |
D368G |
possibly damaging |
Het |
| Hnrnpul2 |
A |
G |
19: 8,798,064 (GRCm39) |
N140S |
probably benign |
Het |
| Htr4 |
A |
T |
18: 62,561,209 (GRCm39) |
I157L |
probably damaging |
Het |
| Kcnma1 |
T |
G |
14: 23,436,332 (GRCm39) |
M790L |
probably benign |
Het |
| Kcnv1 |
G |
A |
15: 44,977,999 (GRCm39) |
S13L |
unknown |
Het |
| Kctd20 |
C |
T |
17: 29,184,025 (GRCm39) |
R312* |
probably null |
Het |
| Kdm3b |
T |
A |
18: 34,960,435 (GRCm39) |
I1340N |
probably damaging |
Het |
| Kdm6b |
A |
G |
11: 69,292,919 (GRCm39) |
F1286L |
unknown |
Het |
| Knl1 |
T |
A |
2: 118,899,524 (GRCm39) |
F408L |
probably benign |
Het |
| Lypd5 |
G |
T |
7: 24,053,101 (GRCm39) |
G253W |
probably damaging |
Het |
| Mea1 |
A |
G |
17: 46,992,614 (GRCm39) |
T21A |
probably benign |
Het |
| Metrnl |
A |
G |
11: 121,606,842 (GRCm39) |
E299G |
possibly damaging |
Het |
| Muc5ac |
C |
T |
7: 141,363,481 (GRCm39) |
|
probably benign |
Het |
| Nbn |
G |
A |
4: 15,963,911 (GRCm39) |
S104N |
probably damaging |
Het |
| Nxpe2 |
A |
T |
9: 48,238,073 (GRCm39) |
F61I |
probably benign |
Het |
| Or6c1b |
T |
C |
10: 129,273,334 (GRCm39) |
Y218H |
probably benign |
Het |
| Or6c70 |
T |
A |
10: 129,710,092 (GRCm39) |
D178V |
probably damaging |
Het |
| Pgr |
C |
A |
9: 8,901,544 (GRCm39) |
P359Q |
probably damaging |
Het |
| Pi4k2b |
G |
A |
5: 52,908,031 (GRCm39) |
V157I |
probably benign |
Het |
| Plekhm1 |
A |
C |
11: 103,258,444 (GRCm39) |
F1031L |
probably damaging |
Het |
| Pltp |
A |
G |
2: 164,696,301 (GRCm39) |
S124P |
probably damaging |
Het |
| Polr3gl |
T |
A |
3: 96,487,154 (GRCm39) |
E177V |
probably benign |
Het |
| Pstk |
G |
T |
7: 130,973,024 (GRCm39) |
R41L |
possibly damaging |
Het |
| Rasgrp1 |
T |
C |
2: 117,119,158 (GRCm39) |
E493G |
probably benign |
Het |
| Rtn3 |
A |
G |
19: 7,434,726 (GRCm39) |
L422P |
probably benign |
Het |
| Rusc2 |
C |
T |
4: 43,401,351 (GRCm39) |
|
probably benign |
Het |
| Sbno2 |
A |
G |
10: 79,911,090 (GRCm39) |
F6S |
probably benign |
Het |
| Sh2d4a |
A |
G |
8: 68,798,695 (GRCm39) |
Y348C |
probably damaging |
Het |
| Sh3rf3 |
A |
G |
10: 58,939,992 (GRCm39) |
|
probably null |
Het |
| Sipa1l2 |
T |
C |
8: 126,177,125 (GRCm39) |
E1163G |
probably benign |
Het |
| Strip1 |
G |
C |
3: 107,521,964 (GRCm39) |
A738G |
probably damaging |
Het |
| Tdrkh |
C |
T |
3: 94,333,299 (GRCm39) |
R255C |
probably benign |
Het |
| Tln1 |
A |
T |
4: 43,555,911 (GRCm39) |
M101K |
possibly damaging |
Het |
| Trav6-2 |
A |
C |
14: 52,905,028 (GRCm39) |
|
probably benign |
Het |
| Tspan11 |
A |
T |
6: 127,900,674 (GRCm39) |
I82F |
possibly damaging |
Het |
| Ttn |
T |
C |
2: 76,779,320 (GRCm39) |
K1233E |
unknown |
Het |
| Usp29 |
A |
T |
7: 6,965,917 (GRCm39) |
S587C |
probably damaging |
Het |
| Vmn1r235 |
A |
T |
17: 21,482,056 (GRCm39) |
Q127L |
probably damaging |
Het |
| Vmn1r65 |
C |
A |
7: 6,011,503 (GRCm39) |
A244S |
probably damaging |
Het |
| Vmn2r18 |
A |
G |
5: 151,508,462 (GRCm39) |
S221P |
probably damaging |
Het |
| Zfp229 |
T |
C |
17: 21,964,828 (GRCm39) |
S353P |
probably damaging |
Het |
| Zpld2 |
T |
C |
4: 133,930,150 (GRCm39) |
K52E |
probably benign |
Het |
|
| Other mutations in Dscaml1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00418:Dscaml1
|
APN |
9 |
45,581,498 (GRCm39) |
nonsense |
probably null |
|
|
IGL00497:Dscaml1
|
APN |
9 |
45,663,536 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00895:Dscaml1
|
APN |
9 |
45,662,551 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01011:Dscaml1
|
APN |
9 |
45,594,970 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
IGL01086:Dscaml1
|
APN |
9 |
45,613,960 (GRCm39) |
splice site |
probably benign |
|
|
IGL01125:Dscaml1
|
APN |
9 |
45,660,930 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL01132:Dscaml1
|
APN |
9 |
45,663,626 (GRCm39) |
nonsense |
probably null |
|
|
IGL01356:Dscaml1
|
APN |
9 |
45,658,155 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL01459:Dscaml1
|
APN |
9 |
45,653,981 (GRCm39) |
nonsense |
probably null |
|
|
IGL01552:Dscaml1
|
APN |
9 |
45,359,206 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02033:Dscaml1
|
APN |
9 |
45,595,080 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02044:Dscaml1
|
APN |
9 |
45,658,241 (GRCm39) |
nonsense |
probably null |
|
|
IGL02095:Dscaml1
|
APN |
9 |
45,359,001 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02166:Dscaml1
|
APN |
9 |
45,594,999 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02262:Dscaml1
|
APN |
9 |
45,643,378 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02262:Dscaml1
|
APN |
9 |
45,656,414 (GRCm39) |
missense |
probably benign |
|
|
IGL02340:Dscaml1
|
APN |
9 |
45,581,474 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
IGL02604:Dscaml1
|
APN |
9 |
45,655,626 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02619:Dscaml1
|
APN |
9 |
45,359,094 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02805:Dscaml1
|
APN |
9 |
45,359,195 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL03409:Dscaml1
|
APN |
9 |
45,581,401 (GRCm39) |
missense |
probably damaging |
1.00 |
|
D3080:Dscaml1
|
UTSW |
9 |
45,595,623 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL03050:Dscaml1
|
UTSW |
9 |
45,654,297 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0149:Dscaml1
|
UTSW |
9 |
45,653,978 (GRCm39) |
nonsense |
probably null |
|
|
R0582:Dscaml1
|
UTSW |
9 |
45,579,562 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R0629:Dscaml1
|
UTSW |
9 |
45,632,716 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0632:Dscaml1
|
UTSW |
9 |
45,643,432 (GRCm39) |
missense |
probably benign |
0.06 |
|
R0815:Dscaml1
|
UTSW |
9 |
45,656,372 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1162:Dscaml1
|
UTSW |
9 |
45,663,647 (GRCm39) |
splice site |
probably benign |
|
|
R1449:Dscaml1
|
UTSW |
9 |
45,653,521 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1474:Dscaml1
|
UTSW |
9 |
45,596,519 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1481:Dscaml1
|
UTSW |
9 |
45,583,941 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1533:Dscaml1
|
UTSW |
9 |
45,361,882 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1542:Dscaml1
|
UTSW |
9 |
45,660,738 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R1572:Dscaml1
|
UTSW |
9 |
45,632,631 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1627:Dscaml1
|
UTSW |
9 |
45,664,445 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1634:Dscaml1
|
UTSW |
9 |
45,584,047 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1713:Dscaml1
|
UTSW |
9 |
45,663,988 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R1777:Dscaml1
|
UTSW |
9 |
45,595,054 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R1812:Dscaml1
|
UTSW |
9 |
45,662,584 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1834:Dscaml1
|
UTSW |
9 |
45,594,930 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1907:Dscaml1
|
UTSW |
9 |
45,651,778 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1953:Dscaml1
|
UTSW |
9 |
45,581,522 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2056:Dscaml1
|
UTSW |
9 |
45,661,430 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2193:Dscaml1
|
UTSW |
9 |
45,596,532 (GRCm39) |
missense |
probably benign |
0.21 |
|
R2497:Dscaml1
|
UTSW |
9 |
45,656,376 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3768:Dscaml1
|
UTSW |
9 |
45,643,435 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R3891:Dscaml1
|
UTSW |
9 |
45,628,782 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R4110:Dscaml1
|
UTSW |
9 |
45,643,366 (GRCm39) |
missense |
probably benign |
0.07 |
|
R4706:Dscaml1
|
UTSW |
9 |
45,361,878 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4716:Dscaml1
|
UTSW |
9 |
45,361,890 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4719:Dscaml1
|
UTSW |
9 |
45,583,993 (GRCm39) |
missense |
probably benign |
0.13 |
|
R4770:Dscaml1
|
UTSW |
9 |
45,581,404 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4924:Dscaml1
|
UTSW |
9 |
45,656,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5167:Dscaml1
|
UTSW |
9 |
45,628,730 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5346:Dscaml1
|
UTSW |
9 |
45,361,857 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R5737:Dscaml1
|
UTSW |
9 |
45,656,483 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5977:Dscaml1
|
UTSW |
9 |
45,632,596 (GRCm39) |
missense |
probably benign |
0.19 |
|
R6073:Dscaml1
|
UTSW |
9 |
45,361,881 (GRCm39) |
missense |
probably benign |
0.22 |
|
R6276:Dscaml1
|
UTSW |
9 |
45,579,458 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R6415:Dscaml1
|
UTSW |
9 |
45,594,975 (GRCm39) |
nonsense |
probably null |
|
|
R6527:Dscaml1
|
UTSW |
9 |
45,623,482 (GRCm39) |
nonsense |
probably null |
|
|
R6582:Dscaml1
|
UTSW |
9 |
45,664,104 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6655:Dscaml1
|
UTSW |
9 |
45,658,235 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6772:Dscaml1
|
UTSW |
9 |
45,621,609 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6799:Dscaml1
|
UTSW |
9 |
45,361,881 (GRCm39) |
missense |
probably benign |
0.22 |
|
R6892:Dscaml1
|
UTSW |
9 |
45,595,128 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6918:Dscaml1
|
UTSW |
9 |
45,341,805 (GRCm39) |
missense |
probably benign |
|
|
R6967:Dscaml1
|
UTSW |
9 |
45,585,821 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7214:Dscaml1
|
UTSW |
9 |
45,581,437 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7286:Dscaml1
|
UTSW |
9 |
45,654,044 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7315:Dscaml1
|
UTSW |
9 |
45,656,423 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7338:Dscaml1
|
UTSW |
9 |
45,585,802 (GRCm39) |
missense |
probably benign |
0.12 |
|
R7343:Dscaml1
|
UTSW |
9 |
45,664,214 (GRCm39) |
missense |
probably benign |
|
|
R7395:Dscaml1
|
UTSW |
9 |
45,613,703 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R7439:Dscaml1
|
UTSW |
9 |
45,621,624 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7484:Dscaml1
|
UTSW |
9 |
45,660,744 (GRCm39) |
splice site |
probably null |
|
|
R7545:Dscaml1
|
UTSW |
9 |
45,596,681 (GRCm39) |
missense |
probably benign |
0.11 |
|
R7979:Dscaml1
|
UTSW |
9 |
45,595,029 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8005:Dscaml1
|
UTSW |
9 |
45,628,808 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8181:Dscaml1
|
UTSW |
9 |
45,658,140 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R8262:Dscaml1
|
UTSW |
9 |
45,658,438 (GRCm39) |
intron |
probably benign |
|
|
R8428:Dscaml1
|
UTSW |
9 |
45,653,884 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8727:Dscaml1
|
UTSW |
9 |
45,341,759 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8796:Dscaml1
|
UTSW |
9 |
45,359,026 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8840:Dscaml1
|
UTSW |
9 |
45,634,718 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9291:Dscaml1
|
UTSW |
9 |
45,359,251 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9394:Dscaml1
|
UTSW |
9 |
45,661,354 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R9610:Dscaml1
|
UTSW |
9 |
45,579,522 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9611:Dscaml1
|
UTSW |
9 |
45,579,522 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9653:Dscaml1
|
UTSW |
9 |
45,643,466 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9699:Dscaml1
|
UTSW |
9 |
45,654,315 (GRCm39) |
missense |
probably damaging |
0.97 |
|
X0058:Dscaml1
|
UTSW |
9 |
45,663,426 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1177:Dscaml1
|
UTSW |
9 |
45,584,089 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- TAAGCTTGTGGGACTAAGTGAC -3'
(R):5'- AAACCAGGGGTTCCTTTGCC -3'
Sequencing Primer
(F):5'- ACTAAGTGACCCCAGGCTG -3'
(R):5'- AGACCCTTCTCTCGGAACCG -3'
|
| Posted On |
2021-03-08 |
Incidental Mutation