Mutagenetix > Incidental Mutation

Incidental Mutation 'R9032:Papss1'

687123

Institutional Source

Beutler Lab

Gene Symbol

Papss1

Ensembl Gene

ENSMUSG00000028032

Gene Name

3'-phosphoadenosine 5'-phosphosulfate synthase 1

Synonyms

Asapk, SK1

MMRRC Submission

068861-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.769) question?

Stock #

R9032 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

131270626-131349432 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 131324817 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Asparagine at position 425 (H425N)

Ref Sequence

ENSEMBL: ENSMUSP00000029666 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000029666] [ENSMUST00000197402] [ENSMUST00000199878] [ENSMUST00000200527]

AlphaFold

Q60967

Predicted Effect

probably damaging
Transcript: ENSMUST00000029666
AA Change: H425N

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000029666
Gene: ENSMUSG00000028032
AA Change: H425N

Domain	Start	End	E-Value	Type
Pfam:APS_kinase	51	209	5.6e-78	PFAM
Pfam:AAA_17	54	184	1.7e-7	PFAM
Pfam:AAA_33	55	182	4.4e-9	PFAM
Pfam:PUA_2	225	386	3.3e-51	PFAM
Pfam:ATP-sulfurylase	394	617	7.8e-74	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000197402

Predicted Effect

probably damaging
Transcript: ENSMUST00000199878
AA Change: H404N

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000142533
Gene: ENSMUSG00000028032
AA Change: H404N

Domain	Start	End	E-Value	Type
Pfam:APS_kinase	30	188	4.5e-75	PFAM
Pfam:AAA_33	33	169	8.5e-10	PFAM
Pfam:AAA_17	33	180	6.1e-6	PFAM
Pfam:PUA_2	204	365	2.7e-47	PFAM
Pfam:ATP-sulfurylase	372	597	6.6e-70	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000200527
AA Change: H404N

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000142616
Gene: ENSMUSG00000028032
AA Change: H404N

Domain	Start	End	E-Value	Type
Pfam:APS_kinase	30	188	4.5e-75	PFAM
Pfam:AAA_33	33	169	8.5e-10	PFAM
Pfam:AAA_17	33	180	6.1e-6	PFAM
Pfam:PUA_2	204	365	2.7e-47	PFAM
Pfam:ATP-sulfurylase	372	597	6.6e-70	PFAM

Meta Mutation Damage Score

0.9298

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

100% (56/56)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Three-prime-phosphoadenosine 5-prime-phosphosulfate (PAPS) is the sulfate donor cosubstrate for all sulfotransferase (SULT) enzymes (Xu et al., 2000 [PubMed 10679223]). SULTs catalyze the sulfate conjugation of many endogenous and exogenous compounds, including drugs and other xenobiotics. In humans, PAPS is synthesized from adenosine 5-prime triphosphate (ATP) and inorganic sulfate by 2 isoforms, PAPSS1 and PAPSS2 (MIM 603005).[supplied by OMIM, Mar 2008]

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5031439G07Rik	C	T	15: 84,844,782 (GRCm39)	M78I	probably benign	Het
Abca8b	C	T	11: 109,848,073 (GRCm39)	V803M	probably benign	Het
Acap1	T	C	11: 69,772,491 (GRCm39)	E728G	probably damaging	Het
Afg1l	G	A	10: 42,194,637 (GRCm39)	T385M	probably damaging	Het
Ankib1	T	C	5: 3,819,641 (GRCm39)	I93V	probably benign	Het
Aopep	C	T	13: 63,444,681 (GRCm39)	R752*	probably null	Het
Apoa4	T	A	9: 46,154,275 (GRCm39)	L292Q	probably damaging	Het
Arhgap29	T	A	3: 121,808,249 (GRCm39)	D1142E	probably benign	Het
Asb5	A	T	8: 55,038,929 (GRCm39)	D265V	probably benign	Het
Ash1l	C	T	3: 88,889,294 (GRCm39)	A391V	probably benign	Het
Ash1l	T	C	3: 88,891,529 (GRCm39)	V1136A	probably benign	Het
Cacna1c	G	T	6: 118,615,466 (GRCm39)	Y1308*	probably null	Het
Ctif	CGGGGCACACTTTGCTCTTACCTCCCGGAGGCACGTGTAGATGGGGCACACTTTGCTCTTACCTCCCGGAGGCACGTGTAGATGGGGCACAC	CGGGGCACACTTTGCTCTTACCTCCCGGAGGCACGTGTAGATGGGGCACAC	18: 75,604,874 (GRCm39)		probably benign	Het
Dmtn	A	G	14: 70,853,534 (GRCm39)	S92P	probably damaging	Het
Edc4	T	C	8: 106,613,639 (GRCm39)	F353S	probably damaging	Het
Emc1	T	C	4: 139,094,474 (GRCm39)	Y676H	possibly damaging	Het
Epb41l4b	A	T	4: 57,041,064 (GRCm39)		probably null	Het
Fat1	A	T	8: 45,492,894 (GRCm39)	N3872I	probably benign	Het
Fer	T	A	17: 64,228,767 (GRCm39)	M214K	probably damaging	Het
Fgf17	A	G	14: 70,874,436 (GRCm39)	F129L	probably damaging	Het
Fnbp1	T	C	2: 30,973,017 (GRCm39)	D161G	probably damaging	Het
Frmd4b	A	C	6: 97,269,334 (GRCm39)	S993A	probably benign	Het
Hsh2d	T	C	8: 72,954,385 (GRCm39)	S256P	probably benign	Het
Il31ra	T	C	13: 112,660,628 (GRCm39)	S654G		Het
Lmnb2	T	C	10: 80,740,091 (GRCm39)	D442G	probably benign	Het
Med19	A	G	2: 84,515,660 (GRCm39)	M115V	probably damaging	Het
Mroh5	T	C	15: 73,655,302 (GRCm39)	Y641C	probably benign	Het
Mrpl18	A	T	17: 13,134,582 (GRCm39)	V61E	probably damaging	Het
Mrtfb	A	C	16: 13,230,092 (GRCm39)	T926P	probably damaging	Het
Mtap	AC	A	4: 89,090,515 (GRCm39)		probably null	Het
Muc2	T	A	7: 141,287,058 (GRCm39)	C154S	probably damaging	Het
Mypn	T	G	10: 62,983,894 (GRCm39)		probably null	Het
Naip5	T	A	13: 100,356,338 (GRCm39)	E1092D	probably benign	Het
Nes	T	G	3: 87,887,069 (GRCm39)	V1776G	possibly damaging	Het
Nxn	A	G	11: 76,169,383 (GRCm39)	I132T	probably damaging	Het
Oxr1	G	A	15: 41,718,317 (GRCm39)	V798I	probably benign	Het
Pde4dip	T	C	3: 97,601,385 (GRCm39)	N2344S	probably benign	Het
Pfas	C	T	11: 68,879,421 (GRCm39)	G263S		Het
Pknox1	C	T	17: 31,822,229 (GRCm39)	T332M	possibly damaging	Het
Plch2	T	C	4: 155,084,976 (GRCm39)	D321G	probably damaging	Het
Pnma1	T	C	12: 84,193,806 (GRCm39)	N299S	probably benign	Het
Psg23	T	G	7: 18,348,660 (GRCm39)	N49T	possibly damaging	Het
Qrfpr	A	G	3: 36,276,099 (GRCm39)	F97S	probably damaging	Het
Rbl1	A	G	2: 157,035,073 (GRCm39)	F336L	probably benign	Het
Rpap1	G	A	2: 119,608,776 (GRCm39)	P143S	probably benign	Het
Rsph6a	A	T	7: 18,799,250 (GRCm39)	N294Y	probably damaging	Het
Serpinb9h	T	C	13: 33,581,781 (GRCm39)	Y113H	probably damaging	Het
Sesn1	C	T	10: 41,686,835 (GRCm39)		probably benign	Het
Sh3d19	T	C	3: 86,033,992 (GRCm39)	Y782H	probably damaging	Het
Siglecg	T	C	7: 43,061,049 (GRCm39)	V374A	probably benign	Het
Slc35d2	A	G	13: 64,256,227 (GRCm39)	F156S	probably damaging	Het
Slc6a11	A	T	6: 114,202,808 (GRCm39)	I301F	probably damaging	Het
Slx4ip	A	G	2: 136,910,240 (GRCm39)	K412E	possibly damaging	Het
Tas2r115	A	T	6: 132,714,327 (GRCm39)	V208E	probably benign	Het
Tlcd5	C	T	9: 43,022,664 (GRCm39)	R230Q	probably benign	Het
Tmem132a	G	T	19: 10,843,835 (GRCm39)	Q174K	probably damaging	Het
Tmtc1	A	T	6: 148,237,749 (GRCm39)	Y338*	probably null	Het
Vav3	C	T	3: 109,413,722 (GRCm39)	A220V	probably benign	Het
Wt1	C	A	2: 104,957,160 (GRCm39)	Q7K	probably benign	Het
Zbtb4	T	A	11: 69,672,650 (GRCm39)	F204L	probably benign	Het
Zfp51	T	A	17: 21,684,660 (GRCm39)	L425H	probably damaging	Het

Other mutations in Papss1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00955:Papss1	APN	3	131,305,710 (GRCm39)	missense	probably benign	0.00
IGL01642:Papss1	APN	3	131,288,996 (GRCm39)	splice site	probably benign
IGL02249:Papss1	APN	3	131,307,772 (GRCm39)	missense	probably damaging	1.00
IGL02832:Papss1	APN	3	131,288,280 (GRCm39)	missense	probably damaging	1.00
IGL03008:Papss1	APN	3	131,290,860 (GRCm39)	missense	possibly damaging	0.55
IGL03180:Papss1	APN	3	131,313,143 (GRCm39)	missense	probably damaging	1.00
IGL03343:Papss1	APN	3	131,288,950 (GRCm39)	missense	probably benign	0.27
IGL03384:Papss1	APN	3	131,285,113 (GRCm39)	missense	probably damaging	0.96
R0549:Papss1	UTSW	3	131,324,974 (GRCm39)	missense	possibly damaging	0.87
R0685:Papss1	UTSW	3	131,288,854 (GRCm39)	missense	possibly damaging	0.61
R0800:Papss1	UTSW	3	131,305,615 (GRCm39)	splice site	probably benign
R1225:Papss1	UTSW	3	131,285,062 (GRCm39)	splice site	probably benign
R1458:Papss1	UTSW	3	131,311,615 (GRCm39)	missense	probably damaging	1.00
R1718:Papss1	UTSW	3	131,324,946 (GRCm39)	missense	probably damaging	1.00
R1728:Papss1	UTSW	3	131,311,728 (GRCm39)	missense	probably benign	0.00
R1784:Papss1	UTSW	3	131,311,728 (GRCm39)	missense	probably benign	0.00
R1862:Papss1	UTSW	3	131,288,945 (GRCm39)	missense	possibly damaging	0.93
R1937:Papss1	UTSW	3	131,305,632 (GRCm39)	missense	probably benign	0.38
R2349:Papss1	UTSW	3	131,305,627 (GRCm39)	missense	probably benign
R3859:Papss1	UTSW	3	131,313,096 (GRCm39)	missense	probably benign	0.30
R4698:Papss1	UTSW	3	131,313,092 (GRCm39)	missense	probably damaging	0.97
R4741:Papss1	UTSW	3	131,324,860 (GRCm39)	missense	probably damaging	1.00
R5333:Papss1	UTSW	3	131,348,805 (GRCm39)	missense	probably damaging	1.00
R5642:Papss1	UTSW	3	131,337,565 (GRCm39)	nonsense	probably null
R6658:Papss1	UTSW	3	131,311,696 (GRCm39)	missense	probably benign
R6932:Papss1	UTSW	3	131,305,732 (GRCm39)	missense	probably damaging	1.00
R7051:Papss1	UTSW	3	131,307,811 (GRCm39)	missense	probably damaging	1.00
R7199:Papss1	UTSW	3	131,290,899 (GRCm39)	missense	probably benign	0.01
R7201:Papss1	UTSW	3	131,305,687 (GRCm39)	missense	probably damaging	1.00
R7276:Papss1	UTSW	3	131,324,995 (GRCm39)	missense	probably benign	0.11
R7575:Papss1	UTSW	3	131,348,857 (GRCm39)	missense	probably damaging	0.99
R7627:Papss1	UTSW	3	131,290,873 (GRCm39)	missense	probably benign	0.01
R8325:Papss1	UTSW	3	131,288,372 (GRCm39)	missense	probably benign
R8380:Papss1	UTSW	3	131,337,456 (GRCm39)	missense	probably damaging	1.00
R9085:Papss1	UTSW	3	131,324,817 (GRCm39)	missense	probably damaging	0.99
R9425:Papss1	UTSW	3	131,270,708 (GRCm39)	nonsense	probably null
R9469:Papss1	UTSW	3	131,288,959 (GRCm39)	missense	possibly damaging	0.62
Z1088:Papss1	UTSW	3	131,348,728 (GRCm39)	missense	possibly damaging	0.62

Predicted Primers

PCR Primer
(F):5'- TAAGCAGTCACCAGTCCATG -3'
(R):5'- GCCCAGCATACATCATAGGAG -3'

Sequencing Primer
(F):5'- CCATGGCTTTACCCGTTTGTGATG -3'
(R):5'- CACTGTCGTTTCAGGATCCAGG -3'

Posted On

2021-11-19