Incidental Mutation 'R9798:Entpd1'
| ID |
735075 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Entpd1
|
| Ensembl Gene |
ENSMUSG00000048120 |
| Gene Name |
ectonucleoside triphosphate diphosphohydrolase 1 |
| Synonyms |
2610206B08Rik, ectoapyrase, NTPDase-1, Cd39 |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R9798 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
19 |
| Chromosomal Location |
40600810-40730046 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 40715789 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Methionine
at position 319
(V319M)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000116285
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000112231]
[ENSMUST00000127828]
[ENSMUST00000134063]
[ENSMUST00000156598]
|
| AlphaFold |
P55772 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000112231
AA Change: V290M
PolyPhen 2
Score 0.448 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000107850
Gene: ENSMUSG00000048120
AA Change: V290M
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:GDA1_CD39
|
40 |
471 |
7.8e-160 |
PFAM |
|
transmembrane domain
|
477 |
499 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000127268
AA Change: V89M
PolyPhen 2
Score 0.963 (Sensitivity: 0.78; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000116895
Gene: ENSMUSG00000048120
AA Change: V89M
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:GDA1_CD39
|
1 |
217 |
4.6e-72 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000127828
|
| SMART Domains |
Protein: ENSMUSP00000117213
Gene: ENSMUSG00000048120
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:GDA1_CD39
|
1 |
63 |
1.2e-21 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000134063
AA Change: V319M
PolyPhen 2
Score 0.812 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000116285
Gene: ENSMUSG00000048120
AA Change: V319M
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:GDA1_CD39
|
69 |
500 |
6.9e-170 |
PFAM |
|
transmembrane domain
|
506 |
528 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000156598
|
| SMART Domains |
Protein: ENSMUSP00000116349
Gene: ENSMUSG00000048120
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:GDA1_CD39
|
40 |
281 |
6.1e-101 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.8%
- 10x: 99.4%
- 20x: 98.3%
|
| 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 plasma membrane protein that hydrolyzes extracellular ATP and ADP to AMP. Inhibition of this protein's activity may confer anticancer benefits. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]
PHENOTYPE: Mice homozygous for disruptions in this gene display abnormalities in muscle contraction, synaptic transmitter release and blood coagulation. [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 |
|---|
| 4930486L24Rik |
A |
T |
13: 61,000,934 (GRCm39) |
S201T |
possibly damaging |
Het |
| Adamtsl1 |
A |
G |
4: 86,074,927 (GRCm39) |
D98G |
probably damaging |
Het |
| Ahnak |
A |
G |
19: 8,990,983 (GRCm39) |
D4089G |
probably damaging |
Het |
| Alpk3 |
T |
A |
7: 80,742,400 (GRCm39) |
M739K |
probably benign |
Het |
| Asns |
T |
C |
6: 7,689,395 (GRCm39) |
N36D |
possibly damaging |
Het |
| Bbs7 |
A |
T |
3: 36,652,439 (GRCm39) |
M338K |
probably benign |
Het |
| Bbx |
T |
C |
16: 50,045,121 (GRCm39) |
D480G |
probably damaging |
Het |
| Cc2d2b |
G |
A |
19: 40,783,080 (GRCm39) |
V626I |
unknown |
Het |
| Celsr3 |
A |
T |
9: 108,705,794 (GRCm39) |
D759V |
probably damaging |
Het |
| Espnl |
G |
T |
1: 91,251,286 (GRCm39) |
G127V |
probably damaging |
Het |
| Fgfr1 |
C |
T |
8: 26,053,523 (GRCm39) |
T266I |
unknown |
Het |
| Fktn |
C |
T |
4: 53,747,128 (GRCm39) |
H344Y |
probably damaging |
Het |
| Fryl |
T |
C |
5: 73,192,402 (GRCm39) |
M2678V |
probably benign |
Het |
| Fsip2 |
T |
A |
2: 82,810,225 (GRCm39) |
Y2181* |
probably null |
Het |
| Gm21698 |
A |
T |
5: 26,189,184 (GRCm39) |
D256E |
probably damaging |
Het |
| Hipk1 |
C |
T |
3: 103,651,431 (GRCm39) |
V1156I |
possibly damaging |
Het |
| Igsf10 |
T |
A |
3: 59,239,126 (GRCm39) |
I352F |
probably damaging |
Het |
| Igsf5 |
C |
A |
16: 96,174,075 (GRCm39) |
T35K |
probably damaging |
Het |
| Il23a |
G |
C |
10: 128,132,829 (GRCm39) |
R143G |
probably benign |
Het |
| Kctd11 |
T |
G |
11: 69,770,732 (GRCm39) |
H102P |
probably damaging |
Het |
| Msln |
T |
C |
17: 25,972,771 (GRCm39) |
T37A |
probably benign |
Het |
| Or7g29 |
T |
A |
9: 19,286,577 (GRCm39) |
Y200F |
probably benign |
Het |
| Or8u10 |
T |
C |
2: 85,915,606 (GRCm39) |
N172D |
probably damaging |
Het |
| Phtf1 |
T |
C |
3: 103,904,869 (GRCm39) |
S506P |
probably benign |
Het |
| Pias3 |
T |
C |
3: 96,606,881 (GRCm39) |
I57T |
probably damaging |
Het |
| Psmc2 |
A |
G |
5: 22,000,806 (GRCm39) |
I94V |
probably benign |
Het |
| Ripor1 |
T |
C |
8: 106,342,798 (GRCm39) |
Y224H |
possibly damaging |
Het |
| Rrh |
C |
T |
3: 129,605,421 (GRCm39) |
V229M |
probably damaging |
Het |
| Scaf4 |
G |
A |
16: 90,045,533 (GRCm39) |
R526C |
unknown |
Het |
| Slc1a6 |
G |
A |
10: 78,629,167 (GRCm39) |
|
probably null |
Het |
| Slc4a7 |
A |
G |
14: 14,782,056 (GRCm38) |
D937G |
probably damaging |
Het |
| Slco1b2 |
C |
A |
6: 141,601,079 (GRCm39) |
T134K |
probably damaging |
Het |
| Sptbn4 |
T |
C |
7: 27,056,717 (GRCm39) |
*2562W |
probably null |
Het |
| Ston1 |
T |
C |
17: 88,944,472 (GRCm39) |
V626A |
probably damaging |
Het |
| Synpo |
A |
T |
18: 60,736,832 (GRCm39) |
D371E |
possibly damaging |
Het |
| Tex15 |
T |
A |
8: 34,062,721 (GRCm39) |
V717D |
probably damaging |
Het |
| Tmod3 |
A |
C |
9: 75,436,805 (GRCm39) |
N43K |
probably damaging |
Het |
| Tmod3 |
G |
T |
9: 75,436,801 (GRCm39) |
L45I |
possibly damaging |
Het |
| Tmod3 |
G |
C |
9: 75,436,803 (GRCm39) |
A44G |
probably damaging |
Het |
| Top2b |
T |
C |
14: 16,389,845 (GRCm38) |
F228L |
probably damaging |
Het |
| Trappc14 |
A |
G |
5: 138,259,940 (GRCm39) |
M372T |
possibly damaging |
Het |
| Ush2a |
A |
G |
1: 188,644,002 (GRCm39) |
T4455A |
possibly damaging |
Het |
| Vmn1r178 |
C |
A |
7: 23,593,733 (GRCm39) |
Y260* |
probably null |
Het |
| Vps13c |
T |
A |
9: 67,826,646 (GRCm39) |
I1429N |
probably damaging |
Het |
| Wdr31 |
A |
G |
4: 62,381,651 (GRCm39) |
V60A |
probably benign |
Het |
|
| Other mutations in Entpd1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00960:Entpd1
|
APN |
19 |
40,699,714 (GRCm39) |
missense |
probably benign |
0.21 |
|
IGL02624:Entpd1
|
APN |
19 |
40,714,502 (GRCm39) |
nonsense |
probably null |
|
|
IGL02893:Entpd1
|
APN |
19 |
40,715,961 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0413:Entpd1
|
UTSW |
19 |
40,699,729 (GRCm39) |
missense |
probably benign |
|
|
R0626:Entpd1
|
UTSW |
19 |
40,715,769 (GRCm39) |
missense |
probably benign |
0.36 |
|
R0666:Entpd1
|
UTSW |
19 |
40,648,350 (GRCm39) |
splice site |
probably benign |
|
|
R1460:Entpd1
|
UTSW |
19 |
40,714,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1518:Entpd1
|
UTSW |
19 |
40,713,507 (GRCm39) |
nonsense |
probably null |
|
|
R1710:Entpd1
|
UTSW |
19 |
40,714,680 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1757:Entpd1
|
UTSW |
19 |
40,727,450 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1759:Entpd1
|
UTSW |
19 |
40,600,968 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2143:Entpd1
|
UTSW |
19 |
40,725,227 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3876:Entpd1
|
UTSW |
19 |
40,725,264 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4937:Entpd1
|
UTSW |
19 |
40,727,965 (GRCm39) |
unclassified |
probably benign |
|
|
R5082:Entpd1
|
UTSW |
19 |
40,713,473 (GRCm39) |
splice site |
probably null |
|
|
R5764:Entpd1
|
UTSW |
19 |
40,727,417 (GRCm39) |
splice site |
probably null |
|
|
R5906:Entpd1
|
UTSW |
19 |
40,727,283 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6052:Entpd1
|
UTSW |
19 |
40,708,928 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7154:Entpd1
|
UTSW |
19 |
40,713,430 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7408:Entpd1
|
UTSW |
19 |
40,727,309 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7814:Entpd1
|
UTSW |
19 |
40,715,891 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7976:Entpd1
|
UTSW |
19 |
40,600,865 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
|
R8438:Entpd1
|
UTSW |
19 |
40,725,224 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R8951:Entpd1
|
UTSW |
19 |
40,727,319 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9126:Entpd1
|
UTSW |
19 |
40,714,608 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
W0251:Entpd1
|
UTSW |
19 |
40,714,697 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Z1176:Entpd1
|
UTSW |
19 |
40,727,408 (GRCm39) |
missense |
probably benign |
0.02 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGGTTCTTGCTTGTAAGACCTACTG -3'
(R):5'- CATTGAAGGCACACTGGGAG -3'
Sequencing Primer
(F):5'- TGCTTAGCACTGTGAGACCAG -3'
(R):5'- CACACTGGGAGTAAGGGCAGTG -3'
|
| Posted On |
2022-11-14 |
Incidental Mutation