Mutagenetix > Incidental Mutation

Incidental Mutation 'R7209:Entpd5'

560953

Institutional Source

Beutler Lab

Gene Symbol

Entpd5

Ensembl Gene

ENSMUSG00000021236

Gene Name

ectonucleoside triphosphate diphosphohydrolase 5

Synonyms

Pcph, NTPDase-5, mNTPase, ER-UDPase, NTPDase5, Cd39l4

MMRRC Submission

045338-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7209 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

84420649-84455803 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 84443702 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Cysteine at position 14 (S14C)

Ref Sequence

ENSEMBL: ENSMUSP00000071939 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021662] [ENSMUST00000072061] [ENSMUST00000110272] [ENSMUST00000117286] [ENSMUST00000120942] [ENSMUST00000122194]

AlphaFold

Q9WUZ9

Predicted Effect

probably benign
Transcript: ENSMUST00000021662

SMART Domains

Protein: ENSMUSP00000021662
Gene: ENSMUSG00000021236

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:GDA1_CD39	41	426	3.5e-76	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000072061
AA Change: S14C

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000071939
Gene: ENSMUSG00000021236
AA Change: S14C

Domain	Start	End	E-Value	Type
transmembrane domain	27	46	N/A	INTRINSIC
Pfam:GDA1_CD39	65	451	1.9e-77	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000110272

SMART Domains

Protein: ENSMUSP00000105901
Gene: ENSMUSG00000021236

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:GDA1_CD39	41	426	3.5e-76	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000117286

SMART Domains

Protein: ENSMUSP00000114011
Gene: ENSMUSG00000021236

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:GDA1_CD39	41	426	3.5e-76	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000120942

SMART Domains

Protein: ENSMUSP00000112516
Gene: ENSMUSG00000021236

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:GDA1_CD39	41	426	3.5e-76	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000122194

SMART Domains

Protein: ENSMUSP00000113106
Gene: ENSMUSG00000021236

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:GDA1_CD39	41	426	3.5e-76	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.8%

Validation Efficiency

100% (67/67)

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 similar to E-type nucleotidases (NTPases)/ecto-ATPase/apyrases. NTPases, such as CD39, mediate catabolism of extracellular nucleotides. ENTPD5 contains 4 apyrase-conserved regions which is characteristic of NTPases. [provided by RefSeq, Jan 2009]
PHENOTYPE: Mice homozygous for a null allele develop progressive hepatopathy, hepatocellular tumors, and spermatogenic arrest. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam7	A	G	14: 68,767,268 (GRCm39)	Y61H	probably damaging	Het
Adgrb1	T	G	15: 74,441,797 (GRCm39)	V966G	possibly damaging	Het
Adh5	G	A	3: 138,148,909 (GRCm39)		probably benign	Het
Akr1b8	T	C	6: 34,333,207 (GRCm39)	V28A	probably damaging	Het
Apbb1	T	A	7: 105,215,292 (GRCm39)	I450F	probably damaging	Het
Arhgap23	C	T	11: 97,366,911 (GRCm39)	T1064I	probably damaging	Het
Arhgap23	G	C	11: 97,383,273 (GRCm39)		probably null	Het
Atg4b	A	G	1: 93,702,955 (GRCm39)	I128M	probably damaging	Het
Baat	A	T	4: 49,503,065 (GRCm39)	I19N	probably damaging	Het
Bspry	T	G	4: 62,404,852 (GRCm39)	I216S	possibly damaging	Het
Commd9	T	A	2: 101,725,483 (GRCm39)	S19T	possibly damaging	Het
Cr2	A	G	1: 194,851,032 (GRCm39)	C145R	probably damaging	Het
Cyp2c68	A	G	19: 39,677,649 (GRCm39)	L447P	probably damaging	Het
Depdc1b	T	C	13: 108,519,389 (GRCm39)	M333T	possibly damaging	Het
Dhx9	T	C	1: 153,340,369 (GRCm39)	T710A	possibly damaging	Het
Dnah5	T	C	15: 28,459,371 (GRCm39)	V4530A	possibly damaging	Het
Dohh	T	A	10: 81,221,874 (GRCm39)	H89Q	probably damaging	Het
Dop1b	T	A	16: 93,566,733 (GRCm39)	N1171K	probably benign	Het
Dscam	T	C	16: 96,451,544 (GRCm39)		probably null	Het
Eqtn	G	A	4: 94,813,806 (GRCm39)	S125F	probably damaging	Het
Erp44	A	T	4: 48,211,704 (GRCm39)	D197E	probably benign	Het
Fgf18	A	T	11: 33,084,315 (GRCm39)	D46E	probably benign	Het
Foxa1	T	A	12: 57,590,077 (GRCm39)	M48L	probably benign	Het
Gabrg1	C	A	5: 70,911,513 (GRCm39)	C417F	probably damaging	Het
Glrp1	T	A	1: 88,431,004 (GRCm39)	Q122L	unknown	Het
Gm5622	A	G	14: 51,893,363 (GRCm39)	I97V	possibly damaging	Het
Gusb	A	G	5: 130,027,387 (GRCm39)	V306A	probably benign	Het
Hars1	A	G	18: 36,906,593 (GRCm39)	S126P	probably benign	Het
Herc1	A	G	9: 66,292,314 (GRCm39)	S356G	possibly damaging	Het
Hydin	C	A	8: 111,216,424 (GRCm39)	Y1336*	probably null	Het
Iftap	T	C	2: 101,396,727 (GRCm39)	*217W	probably null	Het
Kin	T	C	2: 10,096,564 (GRCm39)	Y138H	possibly damaging	Het
Lypd2	C	T	15: 74,604,266 (GRCm39)	V101M	probably benign	Het
Madcam1	A	T	10: 79,500,892 (GRCm39)	T70S	possibly damaging	Het
Man1a2	A	G	3: 100,554,395 (GRCm39)	C112R	unknown	Het
Mia2	T	A	12: 59,201,176 (GRCm39)	V198E	possibly damaging	Het
Mpdz	C	T	4: 81,225,114 (GRCm39)	V1438M	possibly damaging	Het
Mtif2	G	A	11: 29,479,996 (GRCm39)	V21M	probably benign	Het
Nbeal1	G	C	1: 60,276,310 (GRCm39)	V684L	probably benign	Het
Nln	G	A	13: 104,209,406 (GRCm39)	Q56*	probably null	Het
Nlrp4b	T	C	7: 10,444,297 (GRCm39)	V82A	probably benign	Het
Obscn	C	A	11: 58,975,933 (GRCm39)	E2065*	probably null	Het
Or10g1	A	G	14: 52,647,550 (GRCm39)	C260R	possibly damaging	Het
Pilrb2	C	T	5: 137,869,126 (GRCm39)		probably null	Het
Plekhh1	C	A	12: 79,097,150 (GRCm39)	D99E	probably benign	Het
Polr2b	T	A	5: 77,491,026 (GRCm39)	F956I	probably damaging	Het
Ppp3cc	A	G	14: 70,504,947 (GRCm39)	F20L	probably benign	Het
Prmt9	T	C	8: 78,291,627 (GRCm39)	V333A	probably benign	Het
Psd4	T	C	2: 24,287,357 (GRCm39)	S430P	probably damaging	Het
Relch	C	A	1: 105,678,082 (GRCm39)	P1136T	probably damaging	Het
Rrp12	A	C	19: 41,861,388 (GRCm39)	V973G	possibly damaging	Het
Rxfp2	A	G	5: 149,976,563 (GRCm39)		probably null	Het
S100a6	G	A	3: 90,521,095 (GRCm39)	A8T	possibly damaging	Het
Sgsm2	C	A	11: 74,745,151 (GRCm39)	G717V	probably damaging	Het
Sipa1	A	G	19: 5,705,003 (GRCm39)	Y531H	probably damaging	Het
Slc45a1	A	C	4: 150,719,669 (GRCm39)		probably null	Het
Spopfm3	A	T	3: 94,106,012 (GRCm39)	Q110L	probably benign	Het
Srbd1	C	A	17: 86,308,948 (GRCm39)	L743F	probably damaging	Het
Taar2	A	T	10: 23,816,597 (GRCm39)	I46F	possibly damaging	Het
Tmem241	A	T	18: 12,237,229 (GRCm39)	V69D	probably damaging	Het
Tns1	T	C	1: 73,993,074 (GRCm39)	S535G	possibly damaging	Het
Trgc3	A	G	13: 19,445,334 (GRCm39)	N94S	probably benign	Het
Ttc34	C	A	4: 154,923,585 (GRCm39)	P98Q	probably damaging	Het
Ubr1	C	A	2: 120,693,246 (GRCm39)	R1720L	probably benign	Het
Ubr3	T	A	2: 69,846,478 (GRCm39)	D1597E	probably benign	Het
Unc79	T	C	12: 103,091,883 (GRCm39)	M1930T	probably benign	Het
Vmn2r100	A	T	17: 19,751,576 (GRCm39)	I603F	not run	Het
Vps26b	A	T	9: 26,921,288 (GRCm39)	S304T	probably benign	Het
Zfp952	A	T	17: 33,222,444 (GRCm39)	T308S	possibly damaging	Het

Other mutations in Entpd5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00924:Entpd5	APN	12	84,433,828 (GRCm39)	missense	probably damaging	1.00
IGL01455:Entpd5	APN	12	84,441,451 (GRCm39)	missense	probably benign	0.00
IGL02168:Entpd5	APN	12	84,433,752 (GRCm39)	critical splice donor site	probably null
IGL02183:Entpd5	APN	12	84,427,154 (GRCm39)	splice site	probably benign
IGL03104:Entpd5	APN	12	84,431,022 (GRCm39)	missense	probably damaging	0.97
IGL03332:Entpd5	APN	12	84,429,002 (GRCm39)	splice site	probably null
aventi	UTSW	12	84,429,069 (GRCm39)	nonsense	probably null
eatsy	UTSW	12	84,429,069 (GRCm39)	nonsense	probably null
magenschonend	UTSW	12	84,441,464 (GRCm39)	missense	probably benign	0.00
R0024:Entpd5	UTSW	12	84,420,507 (GRCm39)	missense	probably benign	0.01
R0103:Entpd5	UTSW	12	84,443,717 (GRCm39)	nonsense	probably null
R0103:Entpd5	UTSW	12	84,443,717 (GRCm39)	nonsense	probably null
R0644:Entpd5	UTSW	12	84,432,915 (GRCm39)	missense	probably benign	0.00
R1533:Entpd5	UTSW	12	84,441,434 (GRCm39)	missense	probably damaging	1.00
R1536:Entpd5	UTSW	12	84,429,069 (GRCm39)	nonsense	probably null
R1740:Entpd5	UTSW	12	84,443,545 (GRCm39)	missense	probably benign	0.01
R1768:Entpd5	UTSW	12	84,432,985 (GRCm39)	missense	probably benign
R2049:Entpd5	UTSW	12	84,443,632 (GRCm39)	missense	probably benign	0.00
R5128:Entpd5	UTSW	12	84,441,464 (GRCm39)	missense	probably benign	0.00
R6562:Entpd5	UTSW	12	84,432,974 (GRCm39)	missense	probably damaging	1.00
R6907:Entpd5	UTSW	12	84,424,127 (GRCm39)	missense	probably benign	0.23
R7605:Entpd5	UTSW	12	84,443,482 (GRCm39)	missense	probably damaging	1.00
R8700:Entpd5	UTSW	12	84,443,508 (GRCm39)	missense	probably damaging	1.00
X0057:Entpd5	UTSW	12	84,430,994 (GRCm39)	splice site	probably null

Predicted Primers

PCR Primer
(F):5'- TGAATCCGAGTTCCAGTGCTG -3'
(R):5'- GCCTGTTGTACTGGTTATTCGAAATAC -3'

Sequencing Primer
(F):5'- TTCCATAAAAGGTGCCGGC -3'
(R):5'- GGTTATTCGAAATACATCAGGAACAC -3'

Posted On

2019-06-26