SULT4A1 (sulfotransferase family 4A member 1) - Rat Genome Database

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Gene: SULT4A1 (sulfotransferase family 4A member 1) Homo sapiens
Analyze
Symbol: SULT4A1
Name: sulfotransferase family 4A member 1
RGD ID: 736677
HGNC Page HGNC:14903
Description: Enables identical protein binding activity. Predicted to be involved in sulfation. Predicted to act upstream of or within sulfur compound metabolic process. Predicted to be located in cytosol. Predicted to be active in cytoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: BR-STL-1; brain sulfotransferase-like protein; brain sulphotransferase-like; BRSTL1; DJ388M5.3; hBR-STL; hBR-STL-1; MGC40032; nervous system cytosolic sulfotransferase; nervous system sulfotransferase; NST; ST4A1; sulfotransferase 4A1; sulfotransferase family 4A, member 1; sulfotransferase-related protein; SULTX3
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382243,824,509 - 43,862,513 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2243,824,509 - 43,862,513 (-)EnsemblGRCh38hg38GRCh38
GRCh372244,220,389 - 44,258,393 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362242,551,720 - 42,589,711 (-)NCBINCBI36Build 36hg18NCBI36
Build 342242,545,289 - 42,583,257NCBI
Celera2228,131,680 - 28,168,899 (-)NCBICelera
Cytogenetic Map22q13.31NCBI
HuRef2227,174,799 - 27,191,668 (-)NCBIHuRef
CHM1_12244,179,106 - 44,216,628 (-)NCBICHM1_1
T2T-CHM13v2.02244,307,367 - 44,345,097 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytoplasm  (IBA,IEA)
cytosol  (IEA,TAS)
mitochondrion  (IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Molecular cloning and expression of novel sulphotransferase-like cDNAs from human and rat brain. Falany CN, etal., Biochem J 2000 Mar 15;346 Pt 3:857-64.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9034160   PMID:10591208   PMID:10720750   PMID:11154739   PMID:11535246   PMID:12039030   PMID:12477932   PMID:12529303   PMID:14623933   PMID:14702039   PMID:15461802   PMID:15489334  
PMID:16152568   PMID:17425406   PMID:18823757   PMID:19125109   PMID:19343046   PMID:19439498   PMID:20819778   PMID:20920535   PMID:21044950   PMID:21521020   PMID:21873635   PMID:23386860  
PMID:24956247   PMID:24988429   PMID:25340730   PMID:25640309   PMID:26186194   PMID:26760575   PMID:28514442   PMID:29791485   PMID:30606728   PMID:31266751   PMID:32152050   PMID:32296183  
PMID:33961781   PMID:35914814  


Genomics

Comparative Map Data
SULT4A1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382243,824,509 - 43,862,513 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2243,824,509 - 43,862,513 (-)EnsemblGRCh38hg38GRCh38
GRCh372244,220,389 - 44,258,393 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362242,551,720 - 42,589,711 (-)NCBINCBI36Build 36hg18NCBI36
Build 342242,545,289 - 42,583,257NCBI
Celera2228,131,680 - 28,168,899 (-)NCBICelera
Cytogenetic Map22q13.31NCBI
HuRef2227,174,799 - 27,191,668 (-)NCBIHuRef
CHM1_12244,179,106 - 44,216,628 (-)NCBICHM1_1
T2T-CHM13v2.02244,307,367 - 44,345,097 (-)NCBIT2T-CHM13v2.0
Sult4a1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391583,960,298 - 83,989,955 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1583,960,298 - 83,989,955 (-)EnsemblGRCm39 Ensembl
GRCm381584,076,097 - 84,105,754 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1584,076,097 - 84,105,754 (-)EnsemblGRCm38mm10GRCm38
MGSCv371583,906,527 - 83,936,184 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361583,903,863 - 83,933,520 (-)NCBIMGSCv36mm8
Celera1586,206,275 - 86,235,878 (-)NCBICelera
Cytogenetic Map15E2NCBI
cM Map1539.73NCBI
Sult4a1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr87117,096,064 - 117,120,714 (-)NCBIGRCr8
mRatBN7.27115,216,066 - 115,240,156 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl7115,216,066 - 115,240,085 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx7116,963,947 - 116,987,966 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.07119,189,653 - 119,213,672 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.07119,159,119 - 119,183,138 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.07124,958,546 - 124,982,602 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl7124,958,546 - 124,982,566 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.07124,946,961 - 124,971,011 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera7111,522,078 - 111,546,043 (-)NCBICelera
Cytogenetic Map7q34NCBI
Sult4a1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541328,797,645 - 28,821,088 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541328,800,537 - 28,821,082 (-)NCBIChiLan1.0ChiLan1.0
SULT4A1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22353,651,729 - 53,690,705 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12256,345,149 - 56,383,037 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02224,712,960 - 24,751,078 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12242,905,463 - 42,922,260 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2242,906,959 - 42,927,236 (-)Ensemblpanpan1.1panPan2
SULT4A1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11021,781,562 - 21,815,059 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1021,781,487 - 21,814,006 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1021,722,268 - 21,755,762 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01022,530,422 - 22,563,935 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1022,530,347 - 22,562,882 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11022,249,779 - 22,283,267 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01022,569,893 - 22,603,392 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01022,743,989 - 22,777,510 (+)NCBIUU_Cfam_GSD_1.0
Sult4a1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244049455,420,418 - 5,442,706 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049367181,533,786 - 1,559,749 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049367181,537,459 - 1,559,743 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SULT4A1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl55,131,252 - 5,156,894 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.155,131,272 - 5,156,898 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.252,524,715 - 2,549,854 (+)NCBISscrofa10.2Sscrofa10.2susScr3
SULT4A1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11926,339,693 - 26,379,260 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1926,339,582 - 26,379,249 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604599,026,953 - 99,063,862 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Sult4a1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247525,272,276 - 5,294,615 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247525,272,212 - 5,301,350 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SULT4A1
6 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 22q13.2-13.33(chr22:42138114-50739836)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051370]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051370]|See cases [RCV000051370] Chr22:42138114..50739836 [GRCh38]
Chr22:42513525..51178264 [GRCh37]
Chr22:40843471..49525130 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42433752-50738932)x1 copy number loss See cases [RCV000051371] Chr22:42433752..50738932 [GRCh38]
Chr22:42829758..51177360 [GRCh37]
Chr22:41159702..49524226 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42826246-50739836)x1 copy number loss See cases [RCV000051407] Chr22:42826246..50739836 [GRCh38]
Chr22:43222252..51178264 [GRCh37]
Chr22:41552196..49525130 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q13.31-13.33(chr22:43807366-50739836)x1 copy number loss See cases [RCV000051408] Chr22:43807366..50739836 [GRCh38]
Chr22:44203246..51178264 [GRCh37]
Chr22:42534579..49525130 [NCBI36]
Chr22:22q13.31-13.33		 pathogenic
GRCh38/hg38 22q12.3-13.33(chr22:37061769-50738932)x3 copy number gain See cases [RCV000051684] Chr22:37061769..50738932 [GRCh38]
Chr22:37457809..51177360 [GRCh37]
Chr22:35787755..49524226 [NCBI36]
Chr22:22q12.3-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42599757-50725241)x3 copy number gain See cases [RCV000051686] Chr22:42599757..50725241 [GRCh38]
Chr22:42995763..51163669 [GRCh37]
Chr22:41325707..49510535 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42653747-50739836)x3 copy number gain See cases [RCV000051687] Chr22:42653747..50739836 [GRCh38]
Chr22:43049753..51178264 [GRCh37]
Chr22:41379697..49525130 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q12.3-13.33(chr22:33768441-50739977)x3 copy number gain See cases [RCV000051682] Chr22:33768441..50739977 [GRCh38]
Chr22:34164428..51178405 [GRCh37]
Chr22:32494428..49525271 [NCBI36]
Chr22:22q12.3-13.33		 pathogenic
GRCh38/hg38 22q13.31(chr22:43841416-44192863)x3 copy number gain See cases [RCV000052857] Chr22:43841416..44192863 [GRCh38]
Chr22:44237296..44588743 [GRCh37]
Chr22:42568629..42920076 [NCBI36]
Chr22:22q13.31		 uncertain significance
NM_014351.3(SULT4A1):c.170-7547T>G single nucleotide variant Lung cancer [RCV000102079] Chr22:43849479 [GRCh38]
Chr22:44245359 [GRCh37]
Chr22:22q13.31		 uncertain significance
GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3 copy number gain See cases [RCV000133646] Chr22:16916608..50739836 [GRCh38]
Chr22:17397498..51178264 [GRCh37]
Chr22:15777498..49525130 [NCBI36]
Chr22:22q11.1-13.33		 pathogenic
GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3 copy number gain See cases [RCV000134730] Chr22:16916743..50739785 [GRCh38]
Chr22:17397633..51178213 [GRCh37]
Chr22:15777633..49525079 [NCBI36]
Chr22:22q11.1-13.33		 pathogenic
GRCh38/hg38 22q13.1-13.33(chr22:40202014-50735806)x3 copy number gain See cases [RCV000134513] Chr22:40202014..50735806 [GRCh38]
Chr22:40598018..51174234 [GRCh37]
Chr22:38927964..49521100 [NCBI36]
Chr22:22q13.1-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.31(chr22:42197923-47305564)x4 copy number gain See cases [RCV000135528] Chr22:42197923..47305564 [GRCh38]
Chr22:42593929..47701314 [GRCh37]
Chr22:40923873..46079978 [NCBI36]
Chr22:22q13.2-13.31		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:41871143-50739836)x1 copy number loss See cases [RCV000136921] Chr22:41871143..50739836 [GRCh38]
Chr22:42267147..51178264 [GRCh37]
Chr22:40597093..49525130 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42710276-50739836)x3 copy number gain See cases [RCV000137136] Chr22:42710276..50739836 [GRCh38]
Chr22:43106282..51178264 [GRCh37]
Chr22:41436226..49525130 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42493445-50268479)x1 copy number loss See cases [RCV000136786] Chr22:42493445..50268479 [GRCh38]
Chr22:42889451..50706908 [GRCh37]
Chr22:41219395..49049035 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42837094-50735806)x1 copy number loss See cases [RCV000141415] Chr22:42837094..50735806 [GRCh38]
Chr22:43233100..51174234 [GRCh37]
Chr22:41563044..49521100 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:43187980-50745444)x1 copy number loss See cases [RCV000140901] Chr22:43187980..50745444 [GRCh38]
Chr22:43583986..51183872 [GRCh37]
Chr22:41913930..49530738 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42380961-50759410)x3 copy number gain See cases [RCV000141659] Chr22:42380961..50759410 [GRCh38]
Chr22:42776967..51197838 [GRCh37]
Chr22:41106911..49544704 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42080077-50739836)x3 copy number gain See cases [RCV000142755] Chr22:42080077..50739836 [GRCh38]
Chr22:42476081..51178264 [GRCh37]
Chr22:40806027..49525130 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3 copy number gain See cases [RCV000240091] Chr22:16054691..51237518 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q12.3-13.33(chr22:35728929-51220961)x3 copy number gain See cases [RCV000240469] Chr22:35728929..51220961 [GRCh37]
Chr22:22q12.3-13.33		 pathogenic
GRCh37/hg19 22q13.1-13.33(chr22:40425714-51220961)x3 copy number gain See cases [RCV000240459] Chr22:40425714..51220961 [GRCh37]
Chr22:22q13.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3 copy number gain See cases [RCV000446956] Chr22:16054691..51220902 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3 copy number gain See cases [RCV000448847] Chr22:16054691..51237463 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:43381459-51197838)x1 copy number loss See cases [RCV000512121] Chr22:43381459..51197838 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:43875989-51197838)x1 copy number loss See cases [RCV000511015] Chr22:43875989..51197838 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:43050743-51197838)x1 copy number loss See cases [RCV000511256] Chr22:43050743..51197838 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:42441918-51197838)x1 copy number loss See cases [RCV000510765] Chr22:42441918..51197838 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838) copy number gain See cases [RCV000510873] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3 copy number gain See cases [RCV000512333] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:43320284-51183840)x1 copy number loss not provided [RCV000684527] Chr22:43320284..51183840 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:43111156-51183840)x1 copy number loss not provided [RCV000684528] Chr22:43111156..51183840 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:42955616-51183840)x1 copy number loss not provided [RCV000684529] Chr22:42955616..51183840 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.31(chr22:44023172-44744568)x3 copy number gain not provided [RCV000684483] Chr22:44023172..44744568 [GRCh37]
Chr22:22q13.2-13.31		 uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16054667-51243435)x3 copy number gain not provided [RCV000741689] Chr22:16054667..51243435 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51195728)x3 copy number gain not provided [RCV000741691] Chr22:16114244..51195728 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:42151555-51195728)x1 copy number loss not provided [RCV000741989] Chr22:42151555..51195728 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51211392)x3 copy number gain not provided [RCV000741692] Chr22:16114244..51211392 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NM_014351.4(SULT4A1):c.258C>T (p.Leu86=) single nucleotide variant not provided [RCV000924095] Chr22:43841844 [GRCh38]
Chr22:44237724 [GRCh37]
Chr22:22q13.31		 likely benign
GRCh37/hg19 22q13.1-13.33(chr22:40502364-51197838)x3 copy number gain not provided [RCV001007502] Chr22:40502364..51197838 [GRCh37]
Chr22:22q13.1-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:42416026-51181759) copy number loss Phelan-McDermid syndrome [RCV000767745] Chr22:42416026..51181759 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
NM_014351.4(SULT4A1):c.740G>A (p.Arg247Gln) single nucleotide variant not specified [RCV004318387] Chr22:43829062 [GRCh38]
Chr22:44224942 [GRCh37]
Chr22:22q13.31		 uncertain significance
GRCh37/hg19 22q12.2-13.33(chr22:30654764-51197838)x3 copy number gain not provided [RCV001007181] Chr22:30654764..51197838 [GRCh37]
Chr22:22q12.2-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3 copy number gain not provided [RCV000846344] Chr22:16888899..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NC_000022.11:g.43802117_50806121del deletion Phelan-McDermid syndrome [RCV001254364] Chr22:43802117..50806121 [GRCh38]
Chr22:22q13.31-13.33		 pathogenic
NC_000022.11:g.43032129_50739836del deletion Phelan-McDermid syndrome [RCV001254356] Chr22:43032129..50739836 [GRCh38]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.31(chr22:43471921-44241041)x1 copy number loss not provided [RCV001258785] Chr22:43471921..44241041 [GRCh37]
Chr22:22q13.2-13.31		 uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3 copy number gain See cases [RCV001263056] Chr22:16197005..51224252 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
Single allele deletion Intellectual disability [RCV001293376] Chr22:42333802..51195728 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:42321321-51244066)x1 copy number loss Phelan-McDermid syndrome [RCV001801178] Chr22:42321321..51244066 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:42972719-51197838) copy number loss not specified [RCV002052757] Chr22:42972719..51197838 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.31(chr22:43451316-46662660) copy number loss not specified [RCV002052758] Chr22:43451316..46662660 [GRCh37]
Chr22:22q13.2-13.31		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:44178749-51183840)x1 copy number loss not provided [RCV002472623] Chr22:44178749..51183840 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:43436847-51188164)x3 copy number gain not provided [RCV002468433] Chr22:43436847..51188164 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
NM_014351.4(SULT4A1):c.602G>A (p.Arg201Gln) single nucleotide variant not specified [RCV004214029] Chr22:43833641 [GRCh38]
Chr22:44229521 [GRCh37]
Chr22:22q13.31		 uncertain significance
NM_014351.4(SULT4A1):c.488G>A (p.Arg163Gln) single nucleotide variant not specified [RCV004107272] Chr22:43838887 [GRCh38]
Chr22:44234767 [GRCh37]
Chr22:22q13.31		 uncertain significance
NM_014351.4(SULT4A1):c.571G>A (p.Val191Met) single nucleotide variant not specified [RCV004165598] Chr22:43833672 [GRCh38]
Chr22:44229552 [GRCh37]
Chr22:22q13.31		 uncertain significance
GRCh37/hg19 22q13.2-13.33(chr22:43820992-51218654)x1 copy number loss not provided [RCV003457366] Chr22:43820992..51218654 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.2-13.31(chr22:43920110-46548382)x1 copy number loss not specified [RCV003986192] Chr22:43920110..46548382 [GRCh37]
Chr22:22q13.2-13.31		 likely pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:44034281-51197838)x1 copy number loss not specified [RCV003986178] Chr22:44034281..51197838 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
GRCh37/hg19 22q13.1-13.31(chr22:39044105-45794212)x3 copy number gain not specified [RCV003986179] Chr22:39044105..45794212 [GRCh37]
Chr22:22q13.1-13.31		 pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:43107363-51156692)x1 copy number loss not specified [RCV003986180] Chr22:43107363..51156692 [GRCh37]
Chr22:22q13.2-13.33		 pathogenic
NM_014351.4(SULT4A1):c.368A>G (p.Asn123Ser) single nucleotide variant not specified [RCV004461028] Chr22:43839958 [GRCh38]
Chr22:44235838 [GRCh37]
Chr22:22q13.31		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2516
Count of miRNA genes:804
Interacting mature miRNAs:919
Transcripts:ENST00000249130, ENST00000330884, ENST00000422525, ENST00000432404, ENST00000475131, ENST00000540422
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
D22S1165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,223,609 - 44,223,706UniSTSGRCh37
Build 362242,554,942 - 42,555,039RGDNCBI36
Celera2228,134,906 - 28,135,006RGD
Cytogenetic Map22q13.2UniSTS
HuRef2227,178,024 - 27,178,127UniSTS
Marshfield Genetic Map2248.19UniSTS
Marshfield Genetic Map2248.19RGD
Genethon Genetic Map2242.1UniSTS
deCODE Assembly Map2250.81UniSTS
A003P41  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,221,543 - 44,221,674UniSTSGRCh37
Build 362242,552,876 - 42,553,007RGDNCBI36
Celera2228,132,836 - 28,132,971RGD
Cytogenetic Map22q13.2UniSTS
HuRef2227,175,954 - 27,176,089UniSTS
GeneMap99-GB4 RH Map22145.82UniSTS
Whitehead-RH Map22165.8UniSTS
D22S1012E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,221,569 - 44,221,738UniSTSGRCh37
Build 362242,552,902 - 42,553,071RGDNCBI36
Celera2228,132,866 - 28,133,035RGD
Cytogenetic Map22q13.2UniSTS
HuRef2227,175,984 - 27,176,153UniSTS
D22S297  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,248,868 - 44,249,120UniSTSGRCh37
Build 362242,580,201 - 42,580,453RGDNCBI36
Celera2228,159,390 - 28,159,642RGD
Cytogenetic Map22q13.2UniSTS
HuRef2227,202,732 - 27,202,984UniSTS
G65394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,248,429 - 44,248,681UniSTSGRCh37
Build 362242,579,762 - 42,580,014RGDNCBI36
Celera2228,158,951 - 28,159,203RGD
Cytogenetic Map22q13.2UniSTS
HuRef2227,202,293 - 27,202,545UniSTS
G65436  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,249,069 - 44,249,465UniSTSGRCh37
Build 362242,580,402 - 42,580,798RGDNCBI36
Celera2228,159,591 - 28,159,987RGD
Cytogenetic Map22q13.2UniSTS
HuRef2227,202,933 - 27,203,329UniSTS
G65437  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,251,454 - 44,251,805UniSTSGRCh37
Build 362242,582,787 - 42,583,138RGDNCBI36
Celera2228,161,976 - 28,162,327RGD
Cytogenetic Map22q13.2UniSTS
HuRef2227,205,319 - 27,205,670UniSTS
G65391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,222,367 - 44,222,626UniSTSGRCh37
Build 362242,553,700 - 42,553,959RGDNCBI36
Celera2228,133,664 - 28,133,923RGD
Cytogenetic Map22q13.2UniSTS
HuRef2227,176,782 - 27,177,041UniSTS
G65392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,228,310 - 44,228,697UniSTSGRCh37
Build 362242,559,643 - 42,560,030RGDNCBI36
Celera2228,139,610 - 28,139,997RGD
Cytogenetic Map22q13.2UniSTS
HuRef2227,182,754 - 27,183,141UniSTS
G65393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,240,494 - 44,240,874UniSTSGRCh37
Build 362242,571,827 - 42,572,207RGDNCBI36
Celera2228,151,016 - 28,151,396RGD
Cytogenetic Map22q13.2UniSTS
HuRef2227,194,356 - 27,194,736UniSTS
IB1320  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,220,427 - 44,220,631UniSTSGRCh37
Build 362242,551,760 - 42,551,964RGDNCBI36
Celera2228,131,720 - 28,131,924RGD
Cytogenetic Map22q13.2UniSTS
HuRef2227,174,839 - 27,175,042UniSTS
GeneMap99-GB4 RH Map22141.87UniSTS
Whitehead-RH Map22170.9UniSTS
NCBI RH Map22212.8UniSTS
SULT4A1_2458  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,220,224 - 44,220,971UniSTSGRCh37
Build 362242,551,557 - 42,552,304RGDNCBI36
Celera2228,131,517 - 28,132,264RGD
HuRef2227,174,636 - 27,175,382UniSTS
G19733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,220,448 - 44,220,648UniSTSGRCh37
Build 362242,551,781 - 42,551,981RGDNCBI36
Celera2228,131,741 - 28,131,941RGD
Cytogenetic Map22q13.2UniSTS
A001X01  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,220,448 - 44,220,648UniSTSGRCh37
Build 362242,551,781 - 42,551,981RGDNCBI36
Celera2228,131,741 - 28,131,941RGD
Cytogenetic Map22q13.2UniSTS
GeneMap99-GB4 RH Map22145.42UniSTS
NCBI RH Map22210.6UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High
Medium 33 3 309 11 29 11 189 19 2705 14 520 79 3 3 2
Low 1840 287 197 110 364 67 583 752 448 131 418 325 46 1 286 230 1
Below cutoff 464 2132 1003 384 698 269 3245 1289 552 168 443 1031 116 880 2275

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_014351 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011530120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011530121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452212 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047441321 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047441322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054325505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054325506 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054325507 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054325508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001755207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008485384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_937838 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_937839 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF115311 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF176342 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF188698 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF251263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091700 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313048 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL590119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832543 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC022459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC028171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC030665 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471138 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR456588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z97055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000330884   ⟹   ENSP00000332565
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2243,824,509 - 43,862,513 (-)Ensembl
RefSeq Acc Id: ENST00000422525   ⟹   ENSP00000388285
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2243,824,510 - 43,862,470 (-)Ensembl
RefSeq Acc Id: ENST00000432404   ⟹   ENSP00000414220
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2243,824,510 - 43,862,406 (-)Ensembl
RefSeq Acc Id: ENST00000475131
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2243,828,806 - 43,838,913 (-)Ensembl
RefSeq Acc Id: NM_014351   ⟹   NP_055166
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382243,824,509 - 43,862,513 (-)NCBI
GRCh372244,220,387 - 44,258,378 (-)ENTREZGENE
Build 362242,551,720 - 42,589,711 (-)NCBI Archive
HuRef2227,174,799 - 27,191,668 (-)ENTREZGENE
CHM1_12244,179,106 - 44,216,628 (-)NCBI
T2T-CHM13v2.02244,307,367 - 44,345,097 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011530120   ⟹   XP_011528422
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382243,835,096 - 43,862,513 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011530121   ⟹   XP_011528423
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382243,824,509 - 43,862,513 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047441321   ⟹   XP_047297277
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382243,827,514 - 43,862,513 (-)NCBI
RefSeq Acc Id: XM_047441322   ⟹   XP_047297278
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382243,827,514 - 43,862,513 (-)NCBI
RefSeq Acc Id: XM_054325505   ⟹   XP_054181480
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02244,310,381 - 44,345,097 (-)NCBI
RefSeq Acc Id: XM_054325506   ⟹   XP_054181481
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02244,307,367 - 44,345,097 (-)NCBI
RefSeq Acc Id: XM_054325507   ⟹   XP_054181482
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02244,317,751 - 44,345,097 (-)NCBI
RefSeq Acc Id: XM_054325508   ⟹   XP_054181483
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02244,310,381 - 44,345,097 (-)NCBI
RefSeq Acc Id: XR_008485384
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02244,317,752 - 44,345,097 (-)NCBI
RefSeq Acc Id: XR_937839
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382243,835,096 - 43,862,513 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_055166 (Get FASTA)   NCBI Sequence Viewer  
  XP_011528422 (Get FASTA)   NCBI Sequence Viewer  
  XP_011528423 (Get FASTA)   NCBI Sequence Viewer  
  XP_047297277 (Get FASTA)   NCBI Sequence Viewer  
  XP_047297278 (Get FASTA)   NCBI Sequence Viewer  
  XP_054181480 (Get FASTA)   NCBI Sequence Viewer  
  XP_054181481 (Get FASTA)   NCBI Sequence Viewer  
  XP_054181482 (Get FASTA)   NCBI Sequence Viewer  
  XP_054181483 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF21970 (Get FASTA)   NCBI Sequence Viewer  
  AAF61197 (Get FASTA)   NCBI Sequence Viewer  
  AAF98152 (Get FASTA)   NCBI Sequence Viewer  
  AAH22459 (Get FASTA)   NCBI Sequence Viewer  
  AAH28171 (Get FASTA)   NCBI Sequence Viewer  
  AAH30665 (Get FASTA)   NCBI Sequence Viewer  
  AAK64595 (Get FASTA)   NCBI Sequence Viewer  
  BAG35880 (Get FASTA)   NCBI Sequence Viewer  
  BAH11827 (Get FASTA)   NCBI Sequence Viewer  
  BAH12056 (Get FASTA)   NCBI Sequence Viewer  
  CAC34872 (Get FASTA)   NCBI Sequence Viewer  
  CAG30474 (Get FASTA)   NCBI Sequence Viewer  
  EAW73317 (Get FASTA)   NCBI Sequence Viewer  
  EAW73318 (Get FASTA)   NCBI Sequence Viewer  
  EAW73319 (Get FASTA)   NCBI Sequence Viewer  
  EAW73320 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000332565
  ENSP00000332565.4
  ENSP00000388285
  ENSP00000388285.1
  ENSP00000414220.1
GenBank Protein Q9BR01 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_055166   ⟸   NM_014351
- UniProtKB: B2R7N3 (UniProtKB/Swiss-Prot),   O43728 (UniProtKB/Swiss-Prot),   Q9BR01 (UniProtKB/Swiss-Prot),   B7Z320 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011528423   ⟸   XM_011530121
- Peptide Label: isoform X2
- UniProtKB: B7Z2E1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011528422   ⟸   XM_011530120
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: ENSP00000332565   ⟸   ENST00000330884
RefSeq Acc Id: ENSP00000414220   ⟸   ENST00000432404
RefSeq Acc Id: ENSP00000388285   ⟸   ENST00000422525
RefSeq Acc Id: XP_047297278   ⟸   XM_047441322
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047297277   ⟸   XM_047441321
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054181481   ⟸   XM_054325506
- Peptide Label: isoform X2
- UniProtKB: B7Z2E1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054181483   ⟸   XM_054325508
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054181480   ⟸   XM_054325505
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054181482   ⟸   XM_054325507
- Peptide Label: isoform X3
Protein Domains
Sulfotransferase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9BR01-F1-model_v2 AlphaFold Q9BR01 1-284 view protein structure

Promoters
RGD ID:13604356
Promoter ID:EPDNEW_H28362
Type:initiation region
Name:SULT4A1_1
Description:sulfotransferase family 4A member 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382243,862,513 - 43,862,573EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14903 AgrOrtholog
COSMIC SULT4A1 COSMIC
Ensembl Genes ENSG00000130540 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000330884 ENTREZGENE
  ENST00000330884.9 UniProtKB/Swiss-Prot
  ENST00000422525 ENTREZGENE
  ENST00000422525.1 UniProtKB/Swiss-Prot
  ENST00000432404.5 UniProtKB/TrEMBL
Gene3D-CATH 3.40.50.300 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000130540 GTEx
HGNC ID HGNC:14903 ENTREZGENE
Human Proteome Map SULT4A1 Human Proteome Map
InterPro P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sulfotransferase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:25830 UniProtKB/Swiss-Prot
NCBI Gene 25830 ENTREZGENE
OMIM 608359 OMIM
PANTHER SULFOTRANSFERASE 4A1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SULFOTRANSFERASE SULT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Sulfotransfer_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA412 PharmGKB
Superfamily-SCOP SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B2R7N3 ENTREZGENE
  B7Z2E1 ENTREZGENE, UniProtKB/TrEMBL
  B7Z320 ENTREZGENE, UniProtKB/TrEMBL
  F8WE22_HUMAN UniProtKB/TrEMBL
  O43728 ENTREZGENE
  Q9BR01 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B2R7N3 UniProtKB/Swiss-Prot
  O43728 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-10 SULT4A1  sulfotransferase family 4A member 1  SULT4A1  sulfotransferase family 4A, member 1  Symbol and/or name change 5135510 APPROVED