Incidental Mutation 'R1488:Ctsh'
| ID |
165509 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ctsh
|
| Ensembl Gene |
ENSMUSG00000032359 |
| Gene Name |
cathepsin H |
| Synonyms |
Cat H |
| MMRRC Submission |
039540-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R1488 (G1)
|
| Quality Score |
215 |
|
Status
|
Validated
|
| Chromosome |
9 |
| Chromosomal Location |
89936320-89958148 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 89953944 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Asparagine
at position 218
(D218N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000140437
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034915]
[ENSMUST00000123320]
[ENSMUST00000185459]
|
| AlphaFold |
P49935 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000034915
AA Change: D256N
PolyPhen 2
Score 0.412 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000034915
Gene: ENSMUSG00000032359
AA Change: D256N
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
21 |
N/A |
INTRINSIC |
|
Inhibitor_I29
|
33 |
88 |
7.24e-17 |
SMART |
|
Pept_C1
|
114 |
330 |
7.46e-108 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000123320
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127842
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142750
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000151219
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000185459
AA Change: D218N
PolyPhen 2
Score 0.894 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000140437
Gene: ENSMUSG00000032359
AA Change: D218N
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
Inhibitor_I29
|
30 |
85 |
5.3e-21 |
SMART |
|
Pept_C1
|
85 |
291 |
9.4e-87 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000190338
|
| Meta Mutation Damage Score |
0.4191 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.2%
- 10x: 96.1%
- 20x: 92.3%
|
| Validation Efficiency |
100% (53/53) |
| MGI Phenotype |
FUNCTION: This gene encodes a member of the peptidase C1 (papain) family of cysteine proteases. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate multiple protein products. These products include the cathepsin H mini, heavy, and light chains. In rat and human, these three chains can associate to form the mature enzyme, which has both aminopeptidase and endopeptidase activities. Homozygous knockout mice for this gene exhibit impaired lung surfactant processing and reduced tumorigenesis in a pancreatic cancer model. Multiple pseudogenes of this gene have been identified in the genome. [provided by RefSeq, Aug 2015]
PHENOTYPE: Mice homozygous for a reporter allele exhibit impaired lung surfactant and an abnormal eye globe with elongated axial length. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 50 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aoc1l2 |
A |
G |
6: 48,910,381 (GRCm39) |
N691S |
possibly damaging |
Het |
| Arhgap23 |
A |
G |
11: 97,391,685 (GRCm39) |
S1401G |
possibly damaging |
Het |
| Art2b |
A |
C |
7: 101,229,414 (GRCm39) |
F162V |
probably damaging |
Het |
| Atg4c |
T |
A |
4: 99,109,479 (GRCm39) |
W149R |
probably damaging |
Het |
| Atxn1l |
A |
G |
8: 110,460,049 (GRCm39) |
I71T |
probably benign |
Het |
| Axdnd1 |
T |
A |
1: 156,176,530 (GRCm39) |
L748F |
probably damaging |
Het |
| Bdh2 |
A |
G |
3: 135,002,602 (GRCm39) |
Y157C |
probably damaging |
Het |
| C2cd4a |
G |
T |
9: 67,738,990 (GRCm39) |
R18S |
probably benign |
Het |
| Catsperb |
A |
G |
12: 101,560,526 (GRCm39) |
H839R |
probably damaging |
Het |
| Ccdc24 |
C |
A |
4: 117,727,765 (GRCm39) |
S134I |
possibly damaging |
Het |
| Cd55 |
G |
T |
1: 130,376,115 (GRCm39) |
T70K |
probably damaging |
Het |
| Cdh10 |
A |
T |
15: 19,013,349 (GRCm39) |
I650F |
probably damaging |
Het |
| Clca3a2 |
T |
A |
3: 144,789,925 (GRCm39) |
K470N |
possibly damaging |
Het |
| Csn2 |
G |
A |
5: 87,842,755 (GRCm39) |
Q91* |
probably null |
Het |
| Cyb5r4 |
C |
G |
9: 86,911,591 (GRCm39) |
Y88* |
probably null |
Het |
| Dgkq |
A |
G |
5: 108,798,743 (GRCm39) |
F601S |
probably damaging |
Het |
| Eci2 |
A |
G |
13: 35,161,916 (GRCm39) |
V352A |
probably benign |
Het |
| Krt28 |
T |
C |
11: 99,255,997 (GRCm39) |
T421A |
probably benign |
Het |
| Lamp5 |
T |
C |
2: 135,911,011 (GRCm39) |
V248A |
probably benign |
Het |
| Lin9 |
T |
A |
1: 180,515,850 (GRCm39) |
L483Q |
possibly damaging |
Het |
| Lrp1b |
C |
A |
2: 41,392,036 (GRCm39) |
M509I |
probably benign |
Het |
| Lrrfip1 |
T |
C |
1: 91,042,354 (GRCm39) |
V253A |
probably damaging |
Het |
| Mpdz |
C |
A |
4: 81,266,945 (GRCm39) |
E981* |
probably null |
Het |
| Mpo |
A |
C |
11: 87,688,256 (GRCm39) |
N305T |
probably damaging |
Het |
| Or2y1 |
A |
G |
11: 49,385,945 (GRCm39) |
E195G |
probably benign |
Het |
| Or51a24 |
T |
C |
7: 103,733,859 (GRCm39) |
I143V |
probably benign |
Het |
| Or5p79 |
A |
T |
7: 108,221,696 (GRCm39) |
I226F |
probably damaging |
Het |
| Papss2 |
T |
C |
19: 32,614,490 (GRCm39) |
S69P |
probably benign |
Het |
| Pcdhb22 |
A |
G |
18: 37,652,941 (GRCm39) |
T470A |
possibly damaging |
Het |
| Plce1 |
A |
G |
19: 38,705,247 (GRCm39) |
D884G |
possibly damaging |
Het |
| Prex2 |
T |
A |
1: 11,263,752 (GRCm39) |
I1239K |
probably benign |
Het |
| Prkd2 |
T |
A |
7: 16,592,364 (GRCm39) |
F625I |
probably damaging |
Het |
| Rab20 |
A |
T |
8: 11,504,268 (GRCm39) |
V144E |
probably benign |
Het |
| Rnf213 |
A |
G |
11: 119,371,715 (GRCm39) |
N4840S |
probably benign |
Het |
| Scaf8 |
T |
G |
17: 3,247,872 (GRCm39) |
M1065R |
probably damaging |
Het |
| Slco3a1 |
A |
G |
7: 73,996,449 (GRCm39) |
L319P |
possibly damaging |
Het |
| Slit1 |
A |
G |
19: 41,596,824 (GRCm39) |
C1092R |
probably damaging |
Het |
| Tlr4 |
A |
G |
4: 66,757,786 (GRCm39) |
D193G |
probably damaging |
Het |
| Tmem145 |
T |
A |
7: 25,006,860 (GRCm39) |
|
probably null |
Het |
| Tmem184a |
T |
A |
5: 139,793,395 (GRCm39) |
K235N |
probably benign |
Het |
| Tnpo1 |
A |
T |
13: 98,993,415 (GRCm39) |
D590E |
probably damaging |
Het |
| Trio |
C |
A |
15: 27,741,053 (GRCm39) |
G2724V |
probably damaging |
Het |
| Ttc6 |
A |
T |
12: 57,696,301 (GRCm39) |
Y34F |
possibly damaging |
Het |
| Tuba4a |
T |
C |
1: 75,193,045 (GRCm39) |
T190A |
probably benign |
Het |
| Tubgcp4 |
T |
G |
2: 121,007,031 (GRCm39) |
V136G |
possibly damaging |
Het |
| Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
| Vmn1r74 |
T |
C |
7: 11,581,510 (GRCm39) |
I270T |
probably benign |
Het |
| Vmn2r103 |
A |
T |
17: 20,013,922 (GRCm39) |
E238V |
probably damaging |
Het |
| Vmn2r60 |
T |
A |
7: 41,786,137 (GRCm39) |
F313L |
probably benign |
Het |
| Zfp710 |
T |
C |
7: 79,731,752 (GRCm39) |
Y310H |
probably damaging |
Het |
|
| Other mutations in Ctsh |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00786:Ctsh
|
APN |
9 |
89,946,291 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01875:Ctsh
|
APN |
9 |
89,946,260 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02008:Ctsh
|
APN |
9 |
89,943,600 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0336:Ctsh
|
UTSW |
9 |
89,957,791 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0632:Ctsh
|
UTSW |
9 |
89,943,635 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R1847:Ctsh
|
UTSW |
9 |
89,943,618 (GRCm39) |
missense |
probably benign |
0.04 |
|
R3613:Ctsh
|
UTSW |
9 |
89,957,763 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4270:Ctsh
|
UTSW |
9 |
89,943,651 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4860:Ctsh
|
UTSW |
9 |
89,936,601 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5187:Ctsh
|
UTSW |
9 |
89,936,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5469:Ctsh
|
UTSW |
9 |
89,942,564 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5900:Ctsh
|
UTSW |
9 |
89,946,621 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5937:Ctsh
|
UTSW |
9 |
89,943,509 (GRCm39) |
missense |
probably benign |
|
|
R6303:Ctsh
|
UTSW |
9 |
89,944,796 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R6657:Ctsh
|
UTSW |
9 |
89,942,555 (GRCm39) |
missense |
probably benign |
0.30 |
|
R6905:Ctsh
|
UTSW |
9 |
89,944,819 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6985:Ctsh
|
UTSW |
9 |
89,936,657 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7171:Ctsh
|
UTSW |
9 |
89,949,154 (GRCm39) |
missense |
probably benign |
|
|
R7342:Ctsh
|
UTSW |
9 |
89,957,040 (GRCm39) |
missense |
probably benign |
|
|
R7819:Ctsh
|
UTSW |
9 |
89,942,556 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R7884:Ctsh
|
UTSW |
9 |
89,943,476 (GRCm39) |
missense |
probably benign |
|
|
R8099:Ctsh
|
UTSW |
9 |
89,946,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8294:Ctsh
|
UTSW |
9 |
89,950,489 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R9195:Ctsh
|
UTSW |
9 |
89,944,815 (GRCm39) |
missense |
probably benign |
0.06 |
|
| Predicted Primers |
PCR Primer
(F):5'- GGTTGTTGTCCCTCAAGGTTACCTG -3'
(R):5'- AGACTTGGTCCCTGACACTCAGAG -3'
Sequencing Primer
(F):5'- AAGGTTACCTGCACAGCTCTG -3'
(R):5'- CCTGACACTCAGAGCTGAAGG -3'
|
| Posted On |
2014-03-28 |
Incidental Mutation