Incidental Mutation 'R3695:Arsi'
ID 268961
Institutional Source Beutler Lab
Gene Symbol Arsi
Ensembl Gene ENSMUSG00000036412
Gene Name arylsulfatase i
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # R3695 (G1)
Quality Score 225
Status Not validated
Chromosome 18
Chromosomal Location 61045063-61051633 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 61049723 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Glutamic Acid at position 202 (G202E)
Ref Sequence ENSEMBL: ENSMUSP00000043966 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040359]
AlphaFold Q32KI9
Predicted Effect probably benign
Transcript: ENSMUST00000040359
AA Change: G202E

PolyPhen 2 Score 0.068 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000043966
Gene: ENSMUSG00000036412
AA Change: G202E

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
Pfam:Sulfatase 47 360 8.2e-73 PFAM
low complexity region 526 537 N/A INTRINSIC
low complexity region 547 556 N/A INTRINSIC
Meta Mutation Damage Score 0.0626 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.4%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that belongs to a large family of sulfatases that hydrolyze sulfate esters and sulfamates. Members of this family play a role in several cellular processes, including hormone synthesis, cell signaling in development and degradation of macromolecules. The protein encoded by this gene is thought to be secreted, and to function in extracellular space. [provided by RefSeq, Jul 2016]
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2010106E10Rik A T X: 111,466,012 (GRCm39) L187F probably damaging Het
Abca17 G C 17: 24,508,481 (GRCm39) T1018R probably damaging Het
Atxn7l1 A G 12: 33,408,696 (GRCm39) N286S probably damaging Het
B430306N03Rik C T 17: 48,626,194 (GRCm39) T129I possibly damaging Het
Cabp2 A G 19: 4,133,593 (GRCm39) T12A probably benign Het
Crygs C T 16: 22,624,301 (GRCm39) G102D possibly damaging Het
Dmrta1 T A 4: 89,580,415 (GRCm39) Y458* probably null Het
Gabrr2 A G 4: 33,071,430 (GRCm39) D65G probably damaging Het
Grin3a G T 4: 49,792,704 (GRCm39) T343K possibly damaging Het
Hsp90ab1 T C 17: 45,882,403 (GRCm39) D97G probably damaging Het
Mageb4 G T X: 85,296,000 (GRCm39) R10S probably damaging Het
Mdm4 A G 1: 132,919,731 (GRCm39) L379S probably benign Het
Or8j3c T C 2: 86,253,987 (GRCm39) E11G probably damaging Het
Or8k40 A T 2: 86,584,215 (GRCm39) I289N probably damaging Het
Pde4b C T 4: 102,458,742 (GRCm39) A466V probably damaging Het
Pkd2l2 A G 18: 34,571,843 (GRCm39) N614S possibly damaging Het
Ppp2r2a C A 14: 67,257,199 (GRCm39) D344Y probably damaging Het
Rbm4 A G 19: 4,837,411 (GRCm39) Y358H probably damaging Het
Skic2 A G 17: 35,066,888 (GRCm39) F154S probably damaging Het
St3gal2 A G 8: 111,688,973 (GRCm39) D171G probably damaging Het
Strn T C 17: 78,964,421 (GRCm39) N515D probably damaging Het
Stxbp5l A T 16: 37,061,708 (GRCm39) Y367* probably null Het
Syk A G 13: 52,776,801 (GRCm39) probably null Het
Tgs1 A G 4: 3,604,949 (GRCm39) probably null Het
Tlr5 A T 1: 182,802,912 (GRCm39) R739W probably damaging Het
Tns2 G T 15: 102,021,184 (GRCm39) V942L probably null Het
Tsnaxip1 A G 8: 106,560,167 (GRCm39) T40A possibly damaging Het
Tub A G 7: 108,627,039 (GRCm39) S313G probably benign Het
Vmn2r77 A G 7: 86,450,044 (GRCm39) N97D probably damaging Het
Wscd2 T A 5: 113,689,078 (GRCm39) I28N possibly damaging Het
Other mutations in Arsi
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00897:Arsi APN 18 61,045,502 (GRCm39) missense probably damaging 1.00
IGL02519:Arsi APN 18 61,050,139 (GRCm39) missense probably damaging 1.00
IGL03186:Arsi APN 18 61,050,545 (GRCm39) missense probably damaging 1.00
IGL03134:Arsi UTSW 18 61,050,424 (GRCm39) missense probably damaging 1.00
R0003:Arsi UTSW 18 61,050,058 (GRCm39) missense probably benign 0.29
R0003:Arsi UTSW 18 61,050,058 (GRCm39) missense probably benign 0.29
R0448:Arsi UTSW 18 61,050,374 (GRCm39) missense probably damaging 0.98
R1147:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1147:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1148:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1148:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1190:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1261:Arsi UTSW 18 61,049,743 (GRCm39) missense probably damaging 1.00
R1511:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1538:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1635:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1641:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1759:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1794:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1822:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1824:Arsi UTSW 18 61,045,369 (GRCm39) missense probably damaging 1.00
R1824:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1930:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1932:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R1983:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2035:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2036:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2108:Arsi UTSW 18 61,049,443 (GRCm39) missense possibly damaging 0.75
R2166:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2168:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2261:Arsi UTSW 18 61,049,737 (GRCm39) missense probably damaging 1.00
R2263:Arsi UTSW 18 61,049,737 (GRCm39) missense probably damaging 1.00
R2299:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2300:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2393:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2402:Arsi UTSW 18 61,049,539 (GRCm39) missense possibly damaging 0.88
R2484:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2511:Arsi UTSW 18 61,049,666 (GRCm39) missense probably damaging 1.00
R2994:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2995:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2996:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R2997:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R3625:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R3694:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R3883:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R3884:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R3907:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R3932:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R3954:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4212:Arsi UTSW 18 61,049,773 (GRCm39) missense probably damaging 1.00
R4256:Arsi UTSW 18 61,050,388 (GRCm39) missense probably damaging 1.00
R4257:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4258:Arsi UTSW 18 61,050,388 (GRCm39) missense probably damaging 1.00
R4459:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4469:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4601:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4603:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4610:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4649:Arsi UTSW 18 61,050,170 (GRCm39) missense probably damaging 1.00
R4649:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4650:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4651:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4652:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4749:Arsi UTSW 18 61,050,533 (GRCm39) missense probably benign 0.23
R4766:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4807:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4808:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4856:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4860:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4860:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R4886:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R5015:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R5121:Arsi UTSW 18 61,050,511 (GRCm39) missense probably damaging 1.00
R5185:Arsi UTSW 18 61,049,984 (GRCm39) missense probably damaging 1.00
R6191:Arsi UTSW 18 61,045,544 (GRCm39) missense probably damaging 1.00
R6197:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R6218:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R6219:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R6220:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R6378:Arsi UTSW 18 61,049,573 (GRCm39) missense probably damaging 1.00
R6612:Arsi UTSW 18 61,045,528 (GRCm39) missense probably benign 0.12
R6871:Arsi UTSW 18 61,049,723 (GRCm39) missense probably benign 0.07
R7813:Arsi UTSW 18 61,049,726 (GRCm39) missense possibly damaging 0.58
R7974:Arsi UTSW 18 61,045,478 (GRCm39) missense probably damaging 1.00
R8035:Arsi UTSW 18 61,049,442 (GRCm39) missense probably damaging 1.00
R9162:Arsi UTSW 18 61,050,569 (GRCm39) missense probably damaging 0.96
R9200:Arsi UTSW 18 61,049,836 (GRCm39) missense possibly damaging 0.87
R9581:Arsi UTSW 18 61,050,160 (GRCm39) missense probably damaging 1.00
Z1176:Arsi UTSW 18 61,049,852 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CATACAGGATTGCAGCACTCC -3'
(R):5'- TCACCATGGCTGCGTACTTG -3'

Sequencing Primer
(F):5'- AGGATTGCAGCACTCCATTATC -3'
(R):5'- TACTTGCGCCGTGCTACG -3'
Posted On 2015-02-19