ANO4 (anoctamin 4) - Rat Genome Database

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Gene: ANO4 (anoctamin 4) Homo sapiens
Analyze
Symbol: ANO4
Name: anoctamin 4
RGD ID: 1321043
HGNC Page HGNC:23837
Description: Enables intracellular calcium activated chloride channel activity. Involved in chloride transport. Located in plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: anoctamin-4; FLJ34221; FLJ34272; FLJ35277; MGC130026; TMEM16D; transmembrane protein 16D
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3812100,717,261 - 101,128,641 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl12100,717,526 - 101,128,641 (+)EnsemblGRCh38hg38GRCh38
GRCh3712101,188,554 - 101,522,419 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361299,712,716 - 100,046,539 (+)NCBINCBI36Build 36hg18NCBI36
Build 341299,691,052 - 100,024,876NCBI
Celera12100,853,681 - 101,187,742 (+)NCBICelera
Cytogenetic Map12q23.1NCBI
HuRef1298,249,077 - 98,582,590 (+)NCBIHuRef
CHM1_112101,154,362 - 101,488,557 (+)NCBICHM1_1
T2T-CHM13v2.012100,678,611 - 101,090,362 (+)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

Cellular Component
membrane  (IEA)
plasma membrane  (IBA,IDA,IEA,TAS)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:12739008   PMID:14702039   PMID:15067359   PMID:16344560   PMID:19015192   PMID:21873635   PMID:22946059   PMID:23535033   PMID:24692353   PMID:24709693   PMID:29507755  
PMID:30021884   PMID:30783137   PMID:31564164   PMID:33800471   PMID:33961781  


Genomics

Comparative Map Data
ANO4
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3812100,717,261 - 101,128,641 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl12100,717,526 - 101,128,641 (+)EnsemblGRCh38hg38GRCh38
GRCh3712101,188,554 - 101,522,419 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361299,712,716 - 100,046,539 (+)NCBINCBI36Build 36hg18NCBI36
Build 341299,691,052 - 100,024,876NCBI
Celera12100,853,681 - 101,187,742 (+)NCBICelera
Cytogenetic Map12q23.1NCBI
HuRef1298,249,077 - 98,582,590 (+)NCBIHuRef
CHM1_112101,154,362 - 101,488,557 (+)NCBICHM1_1
T2T-CHM13v2.012100,678,611 - 101,090,362 (+)NCBIT2T-CHM13v2.0
Ano4
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391088,784,794 - 89,181,059 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1088,784,856 - 89,180,624 (-)EnsemblGRCm39 Ensembl
GRCm381088,948,932 - 89,345,205 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1088,948,994 - 89,344,762 (-)EnsemblGRCm38mm10GRCm38
MGSCv371088,411,739 - 88,720,535 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361088,378,793 - 88,687,589 (-)NCBIMGSCv36mm8
Celera1090,924,174 - 91,240,555 (-)NCBICelera
Cytogenetic Map10C1- C2NCBI
cM Map1044.42NCBI
Ano4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8725,216,389 - 25,625,811 (-)NCBIGRCr8
mRatBN7.2723,329,015 - 23,738,423 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl723,329,070 - 23,738,434 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx725,323,573 - 25,647,372 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0727,486,107 - 27,809,928 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0727,263,320 - 27,587,119 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0729,492,017 - 30,025,587 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl729,492,016 - 29,701,721 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0730,125,460 - 30,125,825 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.0729,593,754 - 29,766,992 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4725,641,745 - 25,971,720 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1725,661,960 - 25,796,163 (-)NCBI
Celera720,483,792 - 20,799,037 (-)NCBICelera
Cytogenetic Map7q13NCBI
Ano4
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540536,375,115 - 36,715,889 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540536,350,013 - 36,715,740 (+)NCBIChiLan1.0ChiLan1.0
ANO4
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v210108,857,881 - 109,194,980 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan112108,854,283 - 109,191,378 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01298,295,875 - 98,709,918 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.112101,700,830 - 102,113,378 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl12101,885,088 - 102,111,806 (+)Ensemblpanpan1.1panPan2
ANO4
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11539,740,496 - 40,149,039 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1539,740,337 - 40,149,024 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1540,113,594 - 40,517,497 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01540,398,697 - 40,802,967 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1540,388,012 - 40,802,959 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11539,655,353 - 40,059,580 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01539,762,286 - 40,167,016 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01540,036,702 - 40,440,957 (+)NCBIUU_Cfam_GSD_1.0
Ano4
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494519,799,573 - 20,183,598 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493649212,809,987 - 13,000,661 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493649212,810,004 - 13,000,647 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ANO4
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl583,052,958 - 83,489,433 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1583,052,070 - 83,489,523 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2587,091,739 - 87,321,651 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ANO4
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11196,013,244 - 96,415,282 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1196,094,823 - 96,413,721 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666037148,609,881 - 149,020,706 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ano4
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247506,740,017 - 7,103,732 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247506,738,343 - 7,103,767 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ANO4
41 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 12q23.1-23.3(chr12:100670616-108583607)x1 copy number loss See cases [RCV000051320] Chr12:100670616..108583607 [GRCh38]
Chr12:101064394..108977383 [GRCh37]
Chr12:99588525..107501512 [NCBI36]
Chr12:12q23.1-23.3		 pathogenic
NM_178826.3(ANO4):c.107C>T (p.Pro36Leu) single nucleotide variant Malignant melanoma [RCV000070273] Chr12:100939366 [GRCh38]
Chr12:101333144 [GRCh37]
Chr12:99857275 [NCBI36]
Chr12:12q23.1		 not provided
NM_178826.3(ANO4):c.1578C>T (p.Ile526=) single nucleotide variant Malignant melanoma [RCV000069768] Chr12:101086806 [GRCh38]
Chr12:101480584 [GRCh37]
Chr12:100004715 [NCBI36]
Chr12:12q23.1		 not provided
NM_178826.3(ANO4):c.1687C>T (p.Leu563Phe) single nucleotide variant Malignant melanoma [RCV000069769] Chr12:101096589 [GRCh38]
Chr12:101490367 [GRCh37]
Chr12:100014498 [NCBI36]
Chr12:12q23.1		 not provided
NM_178826.3(ANO4):c.2386C>T (p.Arg796Ter) single nucleotide variant Malignant melanoma [RCV000069770] Chr12:101116719 [GRCh38]
Chr12:101510497 [GRCh37]
Chr12:100034628 [NCBI36]
Chr12:12q23.1		 not provided
NM_178826.3(ANO4):c.2642G>A (p.Arg881Gln) single nucleotide variant Malignant melanoma [RCV000069771] Chr12:101126949 [GRCh38]
Chr12:101520727 [GRCh37]
Chr12:100044858 [NCBI36]
Chr12:12q23.1		 not provided
NM_178826.3(ANO4):c.1325C>T (p.Ser442Phe) single nucleotide variant Malignant melanoma [RCV000062371] Chr12:101083712 [GRCh38]
Chr12:101477490 [GRCh37]
Chr12:100001621 [NCBI36]
Chr12:12q23.1		 not provided
NM_001286615.1(ANO4):c.-140-5970C>G single nucleotide variant Lung cancer [RCV000110528] Chr12:100895676 [GRCh38]
Chr12:101289454 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.1(ANO4):c.160+4564G>A single nucleotide variant Lung cancer [RCV000110529] Chr12:100926894 [GRCh38]
Chr12:101320672 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.1(ANO4):c.897+204C>T single nucleotide variant Lung cancer [RCV000110530] Chr12:101037354 [GRCh38]
Chr12:101431132 [GRCh37]
Chr12:12q23.1		 uncertain significance
GRCh38/hg38 12q23.1-23.2(chr12:97394550-101410225)x3 copy number gain See cases [RCV000137891] Chr12:97394550..101410225 [GRCh38]
Chr12:97788328..101804003 [GRCh37]
Chr12:96312459..100328134 [NCBI36]
Chr12:12q23.1-23.2		 likely pathogenic
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 copy number gain See cases [RCV000139555] Chr12:121271..133196807 [GRCh38]
Chr12:282465..133773393 [GRCh37]
Chr12:100698..132283466 [NCBI36]
Chr12:12p13.33-q24.33		 pathogenic
GRCh38/hg38 12q21.33-24.11(chr12:91044318-109133210)x3 copy number gain See cases [RCV000142447] Chr12:91044318..109133210 [GRCh38]
Chr12:91438095..109571015 [GRCh37]
Chr12:89962226..108055398 [NCBI36]
Chr12:12q21.33-24.11		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3 copy number gain See cases [RCV000258805] Chr12:1..133851895 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic|likely pathogenic
GRCh37/hg19 12q23.1-23.3(chr12:100580198-105804075)x3 copy number gain See cases [RCV000445929] Chr12:100580198..105804075 [GRCh37]
Chr12:12q23.1-23.3		 uncertain significance
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3 copy number gain See cases [RCV000510482] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902) copy number gain See cases [RCV000511643] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12q23.1-23.2(chr12:100667424-101651880)x3 copy number gain See cases [RCV000510816] Chr12:100667424..101651880 [GRCh37]
Chr12:12q23.1-23.2		 uncertain significance
GRCh37/hg19 12q23.1(chr12:96719383-101537641)x3 copy number gain not provided [RCV000683473] Chr12:96719383..101537641 [GRCh37]
Chr12:12q23.1		 likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3 copy number gain not provided [RCV000750253] Chr12:621220..133779118 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3 copy number gain not provided [RCV000750246] Chr12:191619..133777645 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12q22-23.2(chr12:94881995-103635998)x3 copy number gain not provided [RCV000750524] Chr12:94881995..103635998 [GRCh37]
Chr12:12q22-23.2		 pathogenic
NM_001286615.2(ANO4):c.1126G>A (p.Val376Ile) single nucleotide variant not provided [RCV000959342] Chr12:101042440 [GRCh38]
Chr12:101436218 [GRCh37]
Chr12:12q23.1		 likely benign
GRCh37/hg19 12q23.1-23.2(chr12:101447925-102593349)x3 copy number gain not provided [RCV000847334] Chr12:101447925..102593349 [GRCh37]
Chr12:12q23.1-23.2		 uncertain significance
NM_001286615.2(ANO4):c.2592G>A (p.Pro864=) single nucleotide variant not provided [RCV000888524] Chr12:101120541 [GRCh38]
Chr12:101514319 [GRCh37]
Chr12:12q23.1		 benign
GRCh37/hg19 12q23.1-23.2(chr12:101273182-101745632)x3 copy number gain not provided [RCV001006525] Chr12:101273182..101745632 [GRCh37]
Chr12:12q23.1-23.2		 uncertain significance
NM_001286615.2(ANO4):c.2148G>A (p.Met716Ile) single nucleotide variant Inborn genetic diseases [RCV003295481] Chr12:101099719 [GRCh38]
Chr12:101493497 [GRCh37]
Chr12:12q23.1		 uncertain significance
GRCh37/hg19 12q23.1-23.3(chr12:100580198-105804075) copy number gain not specified [RCV002053014] Chr12:100580198..105804075 [GRCh37]
Chr12:12q23.1-23.3		 uncertain significance
GRCh37/hg19 12q23.1-23.2(chr12:100564593-103021075) copy number loss not specified [RCV002053013] Chr12:100564593..103021075 [GRCh37]
Chr12:12q23.1-23.2		 uncertain significance
NM_001286615.2(ANO4):c.1158A>T (p.Lys386Asn) single nucleotide variant Inborn genetic diseases [RCV003275922] Chr12:101043542 [GRCh38]
Chr12:101437320 [GRCh37]
Chr12:12q23.1		 uncertain significance
GRCh37/hg19 12q23.1-23.2(chr12:101272963-101745632)x3 copy number gain not provided [RCV002473589] Chr12:101272963..101745632 [GRCh37]
Chr12:12q23.1-23.2		 uncertain significance
NM_001286615.2(ANO4):c.1496G>A (p.Cys499Tyr) single nucleotide variant Inborn genetic diseases [RCV002870659] Chr12:101083778 [GRCh38]
Chr12:101477556 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.1705T>C (p.Tyr569His) single nucleotide variant Inborn genetic diseases [RCV002737657] Chr12:101094259 [GRCh38]
Chr12:101488037 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.2102T>C (p.Leu701Pro) single nucleotide variant Inborn genetic diseases [RCV002889018] Chr12:101099673 [GRCh38]
Chr12:101493451 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.1529T>G (p.Phe510Cys) single nucleotide variant Inborn genetic diseases [RCV002924813] Chr12:101083811 [GRCh38]
Chr12:101477589 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.478A>G (p.Ile160Val) single nucleotide variant Inborn genetic diseases [RCV002984328] Chr12:100971327 [GRCh38]
Chr12:101365105 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.2059G>A (p.Glu687Lys) single nucleotide variant Inborn genetic diseases [RCV002665679] Chr12:101099630 [GRCh38]
Chr12:101493408 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.2108C>T (p.Pro703Leu) single nucleotide variant Inborn genetic diseases [RCV002644844] Chr12:101099679 [GRCh38]
Chr12:101493457 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.253A>C (p.Thr85Pro) single nucleotide variant Inborn genetic diseases [RCV002940761] Chr12:100939407 [GRCh38]
Chr12:101333185 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.2100C>A (p.Asn700Lys) single nucleotide variant Inborn genetic diseases [RCV002832189] Chr12:101099671 [GRCh38]
Chr12:101493449 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.320C>T (p.Ser107Leu) single nucleotide variant Inborn genetic diseases [RCV002936469] Chr12:100942399 [GRCh38]
Chr12:101336177 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.2591C>T (p.Pro864Leu) single nucleotide variant Inborn genetic diseases [RCV002657064] Chr12:101120540 [GRCh38]
Chr12:101514318 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.862A>G (p.Asn288Asp) single nucleotide variant Inborn genetic diseases [RCV003201599] Chr12:101037115 [GRCh38]
Chr12:101430893 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.2089A>G (p.Lys697Glu) single nucleotide variant Inborn genetic diseases [RCV003185325] Chr12:101099660 [GRCh38]
Chr12:101493438 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.1510G>A (p.Val504Ile) single nucleotide variant Inborn genetic diseases [RCV003212175] Chr12:101083792 [GRCh38]
Chr12:101477570 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.1402A>T (p.Ile468Leu) single nucleotide variant Inborn genetic diseases [RCV003342645] Chr12:101083684 [GRCh38]
Chr12:101477462 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.2742G>T (p.Arg914Ser) single nucleotide variant Inborn genetic diseases [RCV003281261] Chr12:101126944 [GRCh38]
Chr12:101520722 [GRCh37]
Chr12:12q23.1		 uncertain significance
NM_001286615.2(ANO4):c.1441C>T (p.Arg481Trp) single nucleotide variant Inborn genetic diseases [RCV003185562] Chr12:101083723 [GRCh38]
Chr12:101477501 [GRCh37]
Chr12:12q23.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2081
Count of miRNA genes:776
Interacting mature miRNAs:894
Transcripts:ENST00000299222, ENST00000392977, ENST00000392979, ENST00000538618, ENST00000546991, ENST00000548940, ENST00000549155, ENST00000549234, ENST00000550015, ENST00000551148
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
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
D12S1041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712101,458,361 - 101,458,505UniSTSGRCh37
Build 361299,982,492 - 99,982,636RGDNCBI36
Celera12101,123,706 - 101,123,853RGD
Cytogenetic Map12q23.1UniSTS
HuRef1298,518,521 - 98,518,668UniSTS
Marshfield Genetic Map12106.52RGD
Marshfield Genetic Map12106.52UniSTS
deCODE Assembly Map12112.36UniSTS
Whitehead-YAC Contig Map12 UniSTS
RH99125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712101,382,093 - 101,382,212UniSTSGRCh37
Build 361299,906,224 - 99,906,343RGDNCBI36
Celera12101,047,411 - 101,047,530RGD
Cytogenetic Map12q23.1UniSTS
HuRef1298,442,586 - 98,442,705UniSTS
GeneMap99-GB4 RH Map12399.56UniSTS
SHGC-106784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712101,264,173 - 101,264,503UniSTSGRCh37
Build 361299,788,304 - 99,788,634RGDNCBI36
Celera12100,929,487 - 100,929,817RGD
Cytogenetic Map12q23.1UniSTS
HuRef1298,324,875 - 98,325,205UniSTS
WI-15132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712101,521,865 - 101,522,014UniSTSGRCh37
Build 3612100,045,996 - 100,046,145RGDNCBI36
Celera12101,187,188 - 101,187,337RGD
Cytogenetic Map12q23.1UniSTS
HuRef1298,582,036 - 98,582,185UniSTS
GeneMap99-GB4 RH Map12400.32UniSTS
Whitehead-RH Map12496.3UniSTS
NCBI RH Map12689.3UniSTS
G17618  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712101,288,799 - 101,288,996UniSTSGRCh37
Build 361299,812,930 - 99,813,127RGDNCBI36
Celera12100,954,113 - 100,954,310RGD
Cytogenetic Map12q23.1UniSTS
HuRef1298,349,327 - 98,349,524UniSTS
SHGC-153536  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712101,264,020 - 101,264,295UniSTSGRCh37
Build 361299,788,151 - 99,788,426RGDNCBI36
Celera12100,929,334 - 100,929,609RGD
Cytogenetic Map12q23.1UniSTS
HuRef1298,324,722 - 98,324,997UniSTS
D12S1835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712101,468,045 - 101,468,281UniSTSGRCh37
Build 361299,992,176 - 99,992,412RGDNCBI36
Celera12101,133,393 - 101,133,629RGD
Cytogenetic Map12q23.1UniSTS
HuRef1298,528,209 - 98,528,445UniSTS
Stanford-G3 RH Map124193.0UniSTS
D12S1101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712101,491,339 - 101,491,504UniSTSGRCh37
Build 3612100,015,470 - 100,015,635RGDNCBI36
Celera12101,156,697 - 101,156,862RGD
Cytogenetic Map12q23.1UniSTS
HuRef1298,551,513 - 98,551,678UniSTS
SHGC-64282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372017,922,369 - 17,922,584UniSTSGRCh37
GRCh3712101,463,430 - 101,463,648UniSTSGRCh37
Build 361299,987,561 - 99,987,779RGDNCBI36
Celera2017,996,916 - 17,997,131UniSTS
Celera12101,128,778 - 101,128,996RGD
Cytogenetic Map20p11UniSTS
Cytogenetic Map12q23.1UniSTS
HuRef2017,885,239 - 17,885,454UniSTS
HuRef1298,523,594 - 98,523,812UniSTS
D12S1083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712101,313,948 - 101,314,183UniSTSGRCh37
Build 361299,838,079 - 99,838,314RGDNCBI36
Celera12100,979,271 - 100,979,506RGD
Cytogenetic Map12q23.1UniSTS
HuRef1298,374,481 - 98,374,716UniSTS
Whitehead-YAC Contig Map12 UniSTS
SHGC-33403  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712101,522,273 - 101,522,406UniSTSGRCh37
Build 3612100,046,404 - 100,046,537RGDNCBI36
Celera12101,187,596 - 101,187,729RGD
Cytogenetic Map12q23.1UniSTS
HuRef1298,582,444 - 98,582,577UniSTS
GeneMap99-GB4 RH Map12399.39UniSTS
Whitehead-RH Map12495.2UniSTS
NCBI RH Map12689.3UniSTS
TKY933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712101,430,229 - 101,430,321UniSTSGRCh37
Celera12101,095,576 - 101,095,668UniSTS
HuRef5147,124,452 - 147,124,540UniSTS


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 adipose tissue appendage entire extraembryonic component
High
Medium 2 4 63 2 2 2 32 10 195 37 85 15
Low 124 71 817 123 27 51 1141 35 3378 162 1048 467 75 574 596
Below cutoff 2148 2131 621 298 731 211 2932 2026 136 190 262 1018 92 629 1994 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001286615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001286616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_178826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537911 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537912 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537913 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537914 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537915 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537916 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537918 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448841 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428302 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428303 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428305 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428307 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428308 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371110 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371112 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371116 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371117 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC010209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC063947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC079953 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC125628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC127893 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC138360 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC225709 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI140598 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK092596 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302962 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC109308 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA213819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA811418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC325277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF570266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000392977   ⟹   ENSP00000376703
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12100,794,776 - 101,128,629 (+)Ensembl
RefSeq Acc Id: ENST00000392979   ⟹   ENSP00000376705
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12100,794,807 - 101,128,641 (+)Ensembl
RefSeq Acc Id: ENST00000546991   ⟹   ENSP00000447867
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12100,794,778 - 100,901,818 (+)Ensembl
RefSeq Acc Id: ENST00000548940
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12101,042,380 - 101,086,813 (+)Ensembl
RefSeq Acc Id: ENST00000549155   ⟹   ENSP00000449116
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12100,717,526 - 101,020,124 (+)Ensembl
RefSeq Acc Id: ENST00000549234
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12100,987,119 - 101,042,381 (+)Ensembl
RefSeq Acc Id: ENST00000550015
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12101,047,988 - 101,128,627 (+)Ensembl
RefSeq Acc Id: ENST00000551148
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12100,794,596 - 100,901,681 (+)Ensembl
RefSeq Acc Id: ENST00000644049   ⟹   ENSP00000494481
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12100,717,526 - 101,128,287 (+)Ensembl
RefSeq Acc Id: NM_001286615   ⟹   NP_001273544
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,794,776 - 101,128,629 (+)NCBI
HuRef1298,249,077 - 98,582,590 (+)NCBI
CHM1_112101,154,362 - 101,488,557 (+)NCBI
T2T-CHM13v2.012100,756,168 - 101,090,350 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001286616   ⟹   NP_001273545
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,901,646 - 101,128,641 (+)NCBI
HuRef1298,249,077 - 98,582,590 (+)NCBI
CHM1_112101,261,388 - 101,488,557 (+)NCBI
T2T-CHM13v2.012100,863,074 - 101,090,362 (+)NCBI
Sequence:
RefSeq Acc Id: NM_178826   ⟹   NP_849148
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,794,776 - 101,128,629 (+)NCBI
GRCh3712101,133,841 - 101,522,419 (+)NCBI
Build 361299,712,716 - 100,046,539 (+)NCBI Archive
Celera12100,853,681 - 101,187,742 (+)RGD
HuRef1298,249,077 - 98,582,590 (+)ENTREZGENE
CHM1_112101,154,362 - 101,488,557 (+)NCBI
T2T-CHM13v2.012100,756,168 - 101,090,350 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011537911   ⟹   XP_011536213
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,717,261 - 101,128,641 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011537912   ⟹   XP_011536214
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,717,261 - 101,128,641 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011537913   ⟹   XP_011536215
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,717,261 - 101,128,641 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011537915   ⟹   XP_011536217
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,717,261 - 101,128,641 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011537916   ⟹   XP_011536218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,885,454 - 101,128,641 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011537918   ⟹   XP_011536220
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,717,261 - 101,053,404 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024448841   ⟹   XP_024304609
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,971,322 - 101,128,641 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024448842   ⟹   XP_024304610
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,971,322 - 101,128,641 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047428302   ⟹   XP_047284258
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,717,261 - 101,128,641 (+)NCBI
RefSeq Acc Id: XM_047428303   ⟹   XP_047284259
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,717,261 - 101,128,641 (+)NCBI
RefSeq Acc Id: XM_047428305   ⟹   XP_047284261
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,717,261 - 101,128,641 (+)NCBI
RefSeq Acc Id: XM_047428306   ⟹   XP_047284262
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,717,261 - 101,128,641 (+)NCBI
RefSeq Acc Id: XM_047428307   ⟹   XP_047284263
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,717,261 - 101,128,641 (+)NCBI
RefSeq Acc Id: XM_047428308   ⟹   XP_047284264
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812100,717,261 - 101,128,641 (+)NCBI
RefSeq Acc Id: XM_054371104   ⟹   XP_054227079
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,678,635 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371105   ⟹   XP_054227080
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,678,616 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371106   ⟹   XP_054227081
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,678,616 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371107   ⟹   XP_054227082
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,678,616 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371108   ⟹   XP_054227083
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,678,611 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371109   ⟹   XP_054227084
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,678,635 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371110   ⟹   XP_054227085
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,678,635 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371111   ⟹   XP_054227086
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,678,611 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371112   ⟹   XP_054227087
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,678,635 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371113   ⟹   XP_054227088
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,678,635 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371114   ⟹   XP_054227089
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,846,878 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371115   ⟹   XP_054227090
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,932,691 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371116   ⟹   XP_054227091
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,932,691 - 101,090,362 (+)NCBI
RefSeq Acc Id: XM_054371117   ⟹   XP_054227092
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012100,678,635 - 101,014,783 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001273544 (Get FASTA)   NCBI Sequence Viewer  
  NP_001273545 (Get FASTA)   NCBI Sequence Viewer  
  NP_849148 (Get FASTA)   NCBI Sequence Viewer  
  XP_011536213 (Get FASTA)   NCBI Sequence Viewer  
  XP_011536214 (Get FASTA)   NCBI Sequence Viewer  
  XP_011536215 (Get FASTA)   NCBI Sequence Viewer  
  XP_011536217 (Get FASTA)   NCBI Sequence Viewer  
  XP_011536218 (Get FASTA)   NCBI Sequence Viewer  
  XP_011536220 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304609 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304610 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284258 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284259 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284261 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284262 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284263 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284264 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227079 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227080 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227081 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227082 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227083 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227084 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227085 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227086 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227087 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227088 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227089 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227090 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227091 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227092 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI09309 (Get FASTA)   NCBI Sequence Viewer  
  BAC03688 (Get FASTA)   NCBI Sequence Viewer  
  BAC03704 (Get FASTA)   NCBI Sequence Viewer  
  BAC03924 (Get FASTA)   NCBI Sequence Viewer  
  BAH11602 (Get FASTA)   NCBI Sequence Viewer  
  BAH13859 (Get FASTA)   NCBI Sequence Viewer  
  BAH14476 (Get FASTA)   NCBI Sequence Viewer  
  EAW97645 (Get FASTA)   NCBI Sequence Viewer  
  EAW97646 (Get FASTA)   NCBI Sequence Viewer  
  EAW97647 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000376703
  ENSP00000376703.3
  ENSP00000376705
  ENSP00000376705.3
  ENSP00000447867.1
  ENSP00000449116.2
  ENSP00000469449.2
  ENSP00000470039.2
  ENSP00000471431.2
  ENSP00000494481
  ENSP00000494481.1
GenBank Protein Q32M45 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_849148   ⟸   NM_178826
- Peptide Label: isoform 2
- UniProtKB: B7Z9Z0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001273544   ⟸   NM_001286615
- Peptide Label: isoform 1
- UniProtKB: Q8NB39 (UniProtKB/Swiss-Prot),   Q8NAJ0 (UniProtKB/Swiss-Prot),   Q8NB53 (UniProtKB/Swiss-Prot),   Q32M45 (UniProtKB/Swiss-Prot),   B7Z9Z0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001273545   ⟸   NM_001286616
- Peptide Label: isoform 1
- UniProtKB: Q8NB39 (UniProtKB/Swiss-Prot),   Q8NAJ0 (UniProtKB/Swiss-Prot),   Q8NB53 (UniProtKB/Swiss-Prot),   Q32M45 (UniProtKB/Swiss-Prot),   B7Z9Z0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011536214   ⟸   XM_011537912
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011536213   ⟸   XM_011537911
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011536215   ⟸   XM_011537913
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011536217   ⟸   XM_011537915
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_011536220   ⟸   XM_011537918
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: XP_011536218   ⟸   XM_011537916
- Peptide Label: isoform X6
- UniProtKB: B7Z9Z0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024304610   ⟸   XM_024448842
- Peptide Label: isoform X7
- UniProtKB: B7Z1R6 (UniProtKB/TrEMBL),   B7Z9Z0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024304609   ⟸   XM_024448841
- Peptide Label: isoform X7
- UniProtKB: B7Z1R6 (UniProtKB/TrEMBL),   B7Z9Z0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000447867   ⟸   ENST00000546991
RefSeq Acc Id: ENSP00000449116   ⟸   ENST00000549155
RefSeq Acc Id: ENSP00000376705   ⟸   ENST00000392979
RefSeq Acc Id: ENSP00000376703   ⟸   ENST00000392977
RefSeq Acc Id: ENSP00000494481   ⟸   ENST00000644049
RefSeq Acc Id: XP_047284258   ⟸   XM_047428302
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047284264   ⟸   XM_047428308
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047284261   ⟸   XM_047428305
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047284259   ⟸   XM_047428303
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047284263   ⟸   XM_047428307
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047284262   ⟸   XM_047428306
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054227083   ⟸   XM_054371108
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054227086   ⟸   XM_054371111
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054227080   ⟸   XM_054371105
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054227082   ⟸   XM_054371107
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054227081   ⟸   XM_054371106
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054227079   ⟸   XM_054371104
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054227088   ⟸   XM_054371113
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054227087   ⟸   XM_054371112
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054227084   ⟸   XM_054371109
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054227085   ⟸   XM_054371110
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054227092   ⟸   XM_054371117
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054227089   ⟸   XM_054371114
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054227091   ⟸   XM_054371116
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054227090   ⟸   XM_054371115
- Peptide Label: isoform X7
Protein Domains
Anoctamin dimerisation   Anoctamin transmembrane

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q32M45-F1-model_v2 AlphaFold Q32M45 1-955 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:23837 AgrOrtholog
COSMIC ANO4 COSMIC
Ensembl Genes ENSG00000151572 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000262139 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000392977 ENTREZGENE
  ENST00000392977.8 UniProtKB/Swiss-Prot
  ENST00000392979 ENTREZGENE
  ENST00000392979.7 UniProtKB/Swiss-Prot
  ENST00000546991.1 UniProtKB/TrEMBL
  ENST00000549155.6 UniProtKB/TrEMBL
  ENST00000570509.4 UniProtKB/Swiss-Prot
  ENST00000573650.8 UniProtKB/Swiss-Prot
  ENST00000575847.8 UniProtKB/Swiss-Prot
  ENST00000644049 ENTREZGENE
  ENST00000644049.1 UniProtKB/TrEMBL
GTEx ENSG00000151572 GTEx
  ENSG00000262139 GTEx
HGNC ID HGNC:23837 ENTREZGENE
Human Proteome Map ANO4 Human Proteome Map
InterPro Anoct_dimer UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Anoctamin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Anoctamin_TM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:121601 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 121601 ENTREZGENE
OMIM 610111 OMIM
PANTHER PTHR12308 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR12308:SF28 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Anoct_dimer UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Anoctamin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA164715582 PharmGKB
UniProt A0A2R8Y532_HUMAN UniProtKB/TrEMBL
  ANO4_HUMAN UniProtKB/Swiss-Prot
  B7Z1R6 ENTREZGENE, UniProtKB/TrEMBL
  B7Z9Z0 ENTREZGENE, UniProtKB/TrEMBL
  F8VUH1_HUMAN UniProtKB/TrEMBL
  F8VW62_HUMAN UniProtKB/TrEMBL
  Q32M45 ENTREZGENE
  Q8NAJ0 ENTREZGENE
  Q8NB39 ENTREZGENE
  Q8NB53 ENTREZGENE
UniProt Secondary Q8NAJ0 UniProtKB/Swiss-Prot
  Q8NB39 UniProtKB/Swiss-Prot
  Q8NB53 UniProtKB/Swiss-Prot