Incidental Mutation 'IGL02544:Psap'
ID |
297767 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Psap
|
Ensembl Gene |
ENSMUSG00000004207 |
Gene Name |
prosaposin |
Synonyms |
SGP-1 |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
IGL02544
|
Quality Score |
|
Status
|
|
Chromosome |
10 |
Chromosomal Location |
60113449-60138376 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
G to T
at 60136405 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000137476
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000004316]
[ENSMUST00000073242]
[ENSMUST00000105461]
[ENSMUST00000105462]
[ENSMUST00000105463]
[ENSMUST00000105464]
[ENSMUST00000105465]
[ENSMUST00000177779]
[ENSMUST00000165878]
[ENSMUST00000179238]
|
AlphaFold |
Q61207 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000004316
|
SMART Domains |
Protein: ENSMUSP00000004316 Gene: ENSMUSG00000004207
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
16 |
N/A |
INTRINSIC |
SAPA
|
21 |
54 |
1.4e-18 |
SMART |
SapB
|
61 |
138 |
1.87e-27 |
SMART |
SapB
|
195 |
272 |
1.2e-16 |
SMART |
SapB
|
314 |
389 |
2.07e-20 |
SMART |
low complexity region
|
412 |
430 |
N/A |
INTRINSIC |
SapB
|
439 |
514 |
3.84e-24 |
SMART |
SAPA
|
523 |
556 |
3.19e-22 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000073242
|
SMART Domains |
Protein: ENSMUSP00000072973 Gene: ENSMUSG00000012819
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
CA
|
55 |
130 |
5.15e-13 |
SMART |
CA
|
154 |
234 |
3.19e-18 |
SMART |
CA
|
258 |
346 |
2.03e-11 |
SMART |
CA
|
371 |
458 |
8.11e-11 |
SMART |
CA
|
482 |
559 |
1.04e-22 |
SMART |
CA
|
583 |
669 |
3.55e-25 |
SMART |
CA
|
693 |
776 |
2.04e-25 |
SMART |
CA
|
800 |
888 |
5.03e-16 |
SMART |
CA
|
912 |
993 |
1.05e-27 |
SMART |
CA
|
1017 |
1100 |
1.99e-19 |
SMART |
CA
|
1124 |
1206 |
6.94e-19 |
SMART |
CA
|
1231 |
1311 |
1.99e-19 |
SMART |
CA
|
1335 |
1415 |
1.21e-18 |
SMART |
CA
|
1440 |
1524 |
2.38e-26 |
SMART |
CA
|
1549 |
1631 |
6.27e-26 |
SMART |
CA
|
1656 |
1741 |
6.99e-24 |
SMART |
CA
|
1765 |
1848 |
3.49e-24 |
SMART |
CA
|
1872 |
1956 |
2.78e-18 |
SMART |
CA
|
1984 |
2066 |
5.6e-14 |
SMART |
CA
|
2090 |
2171 |
2.59e-27 |
SMART |
CA
|
2195 |
2290 |
2.87e-11 |
SMART |
CA
|
2317 |
2399 |
1.01e-20 |
SMART |
CA
|
2423 |
2506 |
1.09e-25 |
SMART |
CA
|
2530 |
2608 |
7.91e-23 |
SMART |
CA
|
2634 |
2719 |
1.06e-23 |
SMART |
CA
|
2750 |
2843 |
2e-10 |
SMART |
Blast:CA
|
2867 |
2956 |
4e-51 |
BLAST |
transmembrane domain
|
3067 |
3089 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000105461
|
SMART Domains |
Protein: ENSMUSP00000101101 Gene: ENSMUSG00000012819
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
CA
|
55 |
130 |
5.15e-13 |
SMART |
CA
|
154 |
234 |
3.19e-18 |
SMART |
CA
|
258 |
346 |
2.03e-11 |
SMART |
CA
|
371 |
458 |
1.25e-11 |
SMART |
CA
|
482 |
559 |
1.04e-22 |
SMART |
CA
|
583 |
669 |
3.55e-25 |
SMART |
CA
|
693 |
776 |
2.04e-25 |
SMART |
CA
|
800 |
888 |
5.03e-16 |
SMART |
CA
|
912 |
993 |
1.05e-27 |
SMART |
CA
|
1017 |
1100 |
1.99e-19 |
SMART |
CA
|
1124 |
1206 |
6.94e-19 |
SMART |
CA
|
1231 |
1311 |
1.99e-19 |
SMART |
CA
|
1335 |
1416 |
5.26e-19 |
SMART |
CA
|
1441 |
1525 |
2.38e-26 |
SMART |
CA
|
1550 |
1632 |
6.27e-26 |
SMART |
CA
|
1657 |
1742 |
6.99e-24 |
SMART |
CA
|
1766 |
1849 |
3.49e-24 |
SMART |
CA
|
1873 |
1957 |
2.78e-18 |
SMART |
CA
|
1985 |
2067 |
5.6e-14 |
SMART |
CA
|
2091 |
2172 |
2.59e-27 |
SMART |
CA
|
2196 |
2291 |
2.87e-11 |
SMART |
CA
|
2318 |
2400 |
1.01e-20 |
SMART |
CA
|
2424 |
2507 |
1.09e-25 |
SMART |
CA
|
2531 |
2609 |
7.91e-23 |
SMART |
CA
|
2635 |
2720 |
1.06e-23 |
SMART |
CA
|
2751 |
2844 |
2e-10 |
SMART |
Blast:CA
|
2868 |
2957 |
4e-51 |
BLAST |
transmembrane domain
|
3068 |
3090 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000105462
|
SMART Domains |
Protein: ENSMUSP00000101102 Gene: ENSMUSG00000012819
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
CA
|
55 |
130 |
5.15e-13 |
SMART |
CA
|
154 |
234 |
3.19e-18 |
SMART |
CA
|
261 |
349 |
2.03e-11 |
SMART |
CA
|
374 |
461 |
8.11e-11 |
SMART |
CA
|
485 |
562 |
1.04e-22 |
SMART |
CA
|
586 |
672 |
3.55e-25 |
SMART |
CA
|
696 |
779 |
2.04e-25 |
SMART |
CA
|
803 |
891 |
5.03e-16 |
SMART |
CA
|
915 |
996 |
1.05e-27 |
SMART |
CA
|
1020 |
1103 |
1.99e-19 |
SMART |
CA
|
1127 |
1209 |
6.94e-19 |
SMART |
CA
|
1234 |
1314 |
1.99e-19 |
SMART |
CA
|
1338 |
1418 |
1.21e-18 |
SMART |
CA
|
1443 |
1527 |
2.38e-26 |
SMART |
CA
|
1552 |
1634 |
6.27e-26 |
SMART |
CA
|
1659 |
1744 |
6.99e-24 |
SMART |
CA
|
1768 |
1851 |
3.49e-24 |
SMART |
CA
|
1875 |
1959 |
2.78e-18 |
SMART |
CA
|
1987 |
2069 |
5.6e-14 |
SMART |
CA
|
2093 |
2174 |
2.59e-27 |
SMART |
CA
|
2198 |
2293 |
2.87e-11 |
SMART |
CA
|
2320 |
2402 |
1.01e-20 |
SMART |
CA
|
2426 |
2509 |
1.09e-25 |
SMART |
CA
|
2533 |
2611 |
7.91e-23 |
SMART |
CA
|
2637 |
2722 |
1.06e-23 |
SMART |
CA
|
2753 |
2846 |
2e-10 |
SMART |
Blast:CA
|
2870 |
2959 |
4e-51 |
BLAST |
transmembrane domain
|
3070 |
3092 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000105463
|
SMART Domains |
Protein: ENSMUSP00000101103 Gene: ENSMUSG00000012819
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
CA
|
55 |
130 |
5.15e-13 |
SMART |
CA
|
154 |
234 |
3.19e-18 |
SMART |
CA
|
258 |
346 |
2.03e-11 |
SMART |
CA
|
371 |
458 |
1.25e-11 |
SMART |
CA
|
482 |
559 |
1.04e-22 |
SMART |
CA
|
583 |
669 |
3.55e-25 |
SMART |
CA
|
693 |
776 |
2.04e-25 |
SMART |
CA
|
800 |
888 |
5.03e-16 |
SMART |
CA
|
912 |
993 |
1.05e-27 |
SMART |
CA
|
1017 |
1100 |
1.99e-19 |
SMART |
CA
|
1124 |
1206 |
6.94e-19 |
SMART |
CA
|
1231 |
1311 |
1.99e-19 |
SMART |
CA
|
1335 |
1416 |
5.26e-19 |
SMART |
CA
|
1441 |
1525 |
2.38e-26 |
SMART |
CA
|
1550 |
1632 |
6.27e-26 |
SMART |
CA
|
1657 |
1742 |
6.99e-24 |
SMART |
CA
|
1766 |
1849 |
3.49e-24 |
SMART |
CA
|
1873 |
1957 |
2.78e-18 |
SMART |
CA
|
1985 |
2067 |
5.6e-14 |
SMART |
CA
|
2091 |
2172 |
2.59e-27 |
SMART |
CA
|
2196 |
2291 |
2.87e-11 |
SMART |
CA
|
2318 |
2400 |
1.01e-20 |
SMART |
CA
|
2424 |
2507 |
1.09e-25 |
SMART |
CA
|
2531 |
2609 |
7.91e-23 |
SMART |
CA
|
2635 |
2720 |
1.06e-23 |
SMART |
CA
|
2751 |
2844 |
2e-10 |
SMART |
Blast:CA
|
2868 |
2957 |
4e-51 |
BLAST |
transmembrane domain
|
3068 |
3090 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000105464
|
SMART Domains |
Protein: ENSMUSP00000101104 Gene: ENSMUSG00000012819
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
CA
|
55 |
130 |
5.15e-13 |
SMART |
CA
|
154 |
234 |
3.19e-18 |
SMART |
CA
|
258 |
346 |
2.03e-11 |
SMART |
CA
|
371 |
456 |
3.58e-12 |
SMART |
CA
|
480 |
557 |
1.04e-22 |
SMART |
CA
|
581 |
667 |
3.55e-25 |
SMART |
CA
|
691 |
774 |
2.04e-25 |
SMART |
CA
|
798 |
886 |
5.03e-16 |
SMART |
CA
|
910 |
991 |
1.05e-27 |
SMART |
CA
|
1015 |
1098 |
1.99e-19 |
SMART |
CA
|
1122 |
1204 |
6.94e-19 |
SMART |
CA
|
1229 |
1309 |
1.99e-19 |
SMART |
CA
|
1333 |
1414 |
5.26e-19 |
SMART |
CA
|
1439 |
1523 |
2.38e-26 |
SMART |
CA
|
1548 |
1630 |
6.27e-26 |
SMART |
CA
|
1655 |
1740 |
6.99e-24 |
SMART |
CA
|
1764 |
1847 |
3.49e-24 |
SMART |
CA
|
1871 |
1955 |
2.78e-18 |
SMART |
CA
|
1983 |
2065 |
5.6e-14 |
SMART |
CA
|
2089 |
2170 |
2.59e-27 |
SMART |
CA
|
2194 |
2289 |
2.87e-11 |
SMART |
CA
|
2316 |
2398 |
1.01e-20 |
SMART |
CA
|
2422 |
2505 |
1.09e-25 |
SMART |
CA
|
2529 |
2607 |
7.91e-23 |
SMART |
CA
|
2633 |
2718 |
1.06e-23 |
SMART |
CA
|
2749 |
2842 |
2e-10 |
SMART |
Blast:CA
|
2866 |
2955 |
3e-51 |
BLAST |
transmembrane domain
|
3066 |
3088 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000105465
|
SMART Domains |
Protein: ENSMUSP00000101105 Gene: ENSMUSG00000004207
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
16 |
N/A |
INTRINSIC |
SAPA
|
21 |
54 |
1.4e-18 |
SMART |
SapB
|
61 |
138 |
1.87e-27 |
SMART |
SapB
|
195 |
270 |
2.76e-16 |
SMART |
SapB
|
312 |
387 |
2.07e-20 |
SMART |
low complexity region
|
410 |
428 |
N/A |
INTRINSIC |
SapB
|
437 |
512 |
3.84e-24 |
SMART |
SAPA
|
521 |
554 |
3.19e-22 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000177779
|
SMART Domains |
Protein: ENSMUSP00000137286 Gene: ENSMUSG00000004207
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
16 |
N/A |
INTRINSIC |
SAPA
|
21 |
54 |
1.4e-18 |
SMART |
SapB
|
61 |
138 |
1.87e-27 |
SMART |
SapB
|
195 |
273 |
2.37e-15 |
SMART |
SapB
|
315 |
390 |
2.07e-20 |
SMART |
low complexity region
|
413 |
431 |
N/A |
INTRINSIC |
SapB
|
440 |
515 |
3.84e-24 |
SMART |
SAPA
|
524 |
557 |
3.19e-22 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000165878
|
SMART Domains |
Protein: ENSMUSP00000126407 Gene: ENSMUSG00000004207
Domain | Start | End | E-Value | Type |
SAPA
|
18 |
51 |
1.4e-18 |
SMART |
SapB
|
58 |
135 |
1.87e-27 |
SMART |
SapB
|
192 |
267 |
2.76e-16 |
SMART |
SapB
|
309 |
384 |
2.07e-20 |
SMART |
low complexity region
|
407 |
425 |
N/A |
INTRINSIC |
SapB
|
434 |
509 |
3.84e-24 |
SMART |
SAPA
|
518 |
551 |
3.19e-22 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000179238
|
SMART Domains |
Protein: ENSMUSP00000137476 Gene: ENSMUSG00000004207
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
16 |
N/A |
INTRINSIC |
SAPA
|
21 |
54 |
1.4e-18 |
SMART |
SapB
|
61 |
138 |
1.87e-27 |
SMART |
SapB
|
195 |
273 |
8.5e-17 |
SMART |
SapB
|
315 |
390 |
2.07e-20 |
SMART |
low complexity region
|
413 |
431 |
N/A |
INTRINSIC |
SapB
|
440 |
515 |
3.84e-24 |
SMART |
SAPA
|
524 |
557 |
3.19e-22 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135638
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128249
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000151194
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153525
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156501
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: This gene encodes a multifunctional glycoprotein that plays a role in the intracellular metabolism of various sphingolipids or secreted into the plasma, milk or cerebrospinal fluid. The encoded protein undergoes proteolytic processing to generate four different polypeptides known as saposin A, B, C or D, that are required for the hydrolysis of certain sphingolipids by lysosomal hydrolases. Alternately, the encoded protein is secreted into body fluids where it exhibits neurotrophic and myelinotrophic activities. A complete lack of the encoded protein is fatal to mice either at the neonatal stage or within the first month due to severe leukodystrophy and sphingolipid accumulation. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate the mature saposins. [provided by RefSeq, Sep 2015] PHENOTYPE: Homozygotes for a targeted null mutation die either neonatally or around 7 weeks. At 30 days, mutants show hypomyelination, PAS-positive material in the nervous system, and accumulation of ceramides in brain, liver, and kidney. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
C |
5: 77,049,961 (GRCm39) |
S12A |
probably benign |
Het |
Abcb5 |
A |
T |
12: 118,870,003 (GRCm39) |
|
probably benign |
Het |
Acap3 |
G |
A |
4: 155,976,867 (GRCm39) |
E6K |
possibly damaging |
Het |
Ano3 |
A |
T |
2: 110,488,594 (GRCm39) |
I946K |
possibly damaging |
Het |
Arid1a |
A |
G |
4: 133,409,059 (GRCm39) |
V1816A |
unknown |
Het |
Cacna1c |
C |
T |
6: 118,728,440 (GRCm39) |
G335R |
probably damaging |
Het |
Ccnh |
C |
A |
13: 85,350,460 (GRCm39) |
Y118* |
probably null |
Het |
Cep76 |
C |
T |
18: 67,768,020 (GRCm39) |
|
probably benign |
Het |
Cyp2c65 |
T |
C |
19: 39,079,082 (GRCm39) |
V387A |
probably damaging |
Het |
Dapk1 |
T |
G |
13: 60,899,031 (GRCm39) |
S834A |
probably benign |
Het |
Ddx39a |
T |
C |
8: 84,449,402 (GRCm39) |
S367P |
probably benign |
Het |
Dicer1 |
A |
G |
12: 104,681,091 (GRCm39) |
I474T |
probably damaging |
Het |
Dnah10 |
G |
A |
5: 124,876,069 (GRCm39) |
R2579H |
probably benign |
Het |
Dnajc16 |
T |
C |
4: 141,491,958 (GRCm39) |
N622D |
probably damaging |
Het |
Eif3c |
G |
T |
7: 126,146,784 (GRCm39) |
S799* |
probably null |
Het |
Fbxo9 |
A |
G |
9: 77,994,541 (GRCm39) |
Y259H |
probably damaging |
Het |
Fpr-rs4 |
A |
T |
17: 18,242,473 (GRCm39) |
H160L |
probably benign |
Het |
Galc |
A |
T |
12: 98,197,701 (GRCm39) |
V336D |
probably benign |
Het |
Matcap1 |
C |
T |
8: 106,010,092 (GRCm39) |
V286M |
probably benign |
Het |
Mfrp |
T |
C |
9: 44,014,091 (GRCm39) |
L153P |
probably damaging |
Het |
Mtx1 |
C |
A |
3: 89,117,703 (GRCm39) |
W30L |
probably damaging |
Het |
Mysm1 |
A |
T |
4: 94,840,543 (GRCm39) |
D624E |
probably damaging |
Het |
Naa16 |
A |
G |
14: 79,573,260 (GRCm39) |
F837L |
probably damaging |
Het |
Or10ag56 |
C |
T |
2: 87,139,471 (GRCm39) |
R113C |
possibly damaging |
Het |
Or1j17 |
A |
G |
2: 36,578,848 (GRCm39) |
Y278C |
probably damaging |
Het |
Or2ag1 |
T |
C |
7: 106,313,742 (GRCm39) |
I49V |
probably benign |
Het |
Or5h25 |
A |
T |
16: 58,930,507 (GRCm39) |
H155Q |
probably damaging |
Het |
Pde4d |
G |
T |
13: 109,877,057 (GRCm39) |
D137Y |
probably damaging |
Het |
Pik3r1 |
G |
T |
13: 101,823,784 (GRCm39) |
R534S |
probably damaging |
Het |
Pira12 |
T |
A |
7: 3,900,185 (GRCm39) |
Y139F |
probably damaging |
Het |
Plekha5 |
A |
C |
6: 140,535,454 (GRCm39) |
E239A |
possibly damaging |
Het |
Rap2b |
T |
C |
3: 61,272,560 (GRCm39) |
F28S |
probably damaging |
Het |
Rfc5 |
A |
T |
5: 117,524,931 (GRCm39) |
|
probably benign |
Het |
Ryr1 |
C |
T |
7: 28,815,024 (GRCm39) |
D175N |
probably benign |
Het |
Sbno1 |
T |
G |
5: 124,542,046 (GRCm39) |
I370L |
probably damaging |
Het |
Slc17a6 |
T |
A |
7: 51,315,903 (GRCm39) |
C390* |
probably null |
Het |
Srsf7 |
A |
T |
17: 80,511,620 (GRCm39) |
|
probably benign |
Het |
Tbc1d10c |
C |
T |
19: 4,237,959 (GRCm39) |
D272N |
probably benign |
Het |
Tll2 |
A |
G |
19: 41,124,404 (GRCm39) |
F204L |
probably damaging |
Het |
Tmc1 |
T |
A |
19: 20,884,327 (GRCm39) |
T38S |
probably benign |
Het |
Tmem184b |
A |
T |
15: 79,250,007 (GRCm39) |
I256K |
probably damaging |
Het |
Tmem214 |
G |
A |
5: 31,030,090 (GRCm39) |
A296T |
probably benign |
Het |
Trip11 |
G |
A |
12: 101,859,780 (GRCm39) |
R365W |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,142,429 (GRCm39) |
P1339S |
probably damaging |
Het |
Vmn2r83 |
T |
A |
10: 79,317,293 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Psap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00926:Psap
|
APN |
10 |
60,128,316 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01100:Psap
|
APN |
10 |
60,135,708 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01122:Psap
|
APN |
10 |
60,135,253 (GRCm39) |
missense |
probably benign |
0.04 |
twerk
|
UTSW |
10 |
60,136,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R0591:Psap
|
UTSW |
10 |
60,136,634 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0624:Psap
|
UTSW |
10 |
60,135,345 (GRCm39) |
splice site |
probably benign |
|
R1018:Psap
|
UTSW |
10 |
60,136,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R1896:Psap
|
UTSW |
10 |
60,130,826 (GRCm39) |
nonsense |
probably null |
|
R3161:Psap
|
UTSW |
10 |
60,113,575 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3162:Psap
|
UTSW |
10 |
60,113,575 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3162:Psap
|
UTSW |
10 |
60,113,575 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3615:Psap
|
UTSW |
10 |
60,130,383 (GRCm39) |
missense |
probably benign |
0.06 |
R3616:Psap
|
UTSW |
10 |
60,130,383 (GRCm39) |
missense |
probably benign |
0.06 |
R4622:Psap
|
UTSW |
10 |
60,136,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Psap
|
UTSW |
10 |
60,136,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Psap
|
UTSW |
10 |
60,136,324 (GRCm39) |
missense |
probably benign |
|
R5131:Psap
|
UTSW |
10 |
60,135,736 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5203:Psap
|
UTSW |
10 |
60,130,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R5251:Psap
|
UTSW |
10 |
60,137,479 (GRCm39) |
missense |
probably damaging |
0.99 |
R5511:Psap
|
UTSW |
10 |
60,134,959 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5764:Psap
|
UTSW |
10 |
60,129,186 (GRCm39) |
missense |
probably benign |
0.18 |
R6207:Psap
|
UTSW |
10 |
60,136,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R7003:Psap
|
UTSW |
10 |
60,135,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R7494:Psap
|
UTSW |
10 |
60,135,275 (GRCm39) |
missense |
probably benign |
0.00 |
R7525:Psap
|
UTSW |
10 |
60,135,253 (GRCm39) |
missense |
probably benign |
0.04 |
R7711:Psap
|
UTSW |
10 |
60,135,634 (GRCm39) |
missense |
probably damaging |
0.96 |
R8252:Psap
|
UTSW |
10 |
60,113,511 (GRCm39) |
start gained |
probably benign |
|
R8894:Psap
|
UTSW |
10 |
60,135,736 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9062:Psap
|
UTSW |
10 |
60,131,738 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9756:Psap
|
UTSW |
10 |
60,130,784 (GRCm39) |
missense |
possibly damaging |
0.70 |
X0019:Psap
|
UTSW |
10 |
60,135,694 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Posted On |
2015-04-16 |