ZFAND1 (zinc finger AN1-type containing 1) - Rat Genome Database

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Gene: ZFAND1 (zinc finger AN1-type containing 1) Homo sapiens
Analyze
Symbol: ZFAND1
Name: zinc finger AN1-type containing 1
RGD ID: 1605942
HGNC Page HGNC:25858
Description: Enables proteasome binding activity. Involved in cellular response to arsenite ion; positive regulation of intracellular protein transport; and stress granule disassembly. Located in cytoplasmic stress granule.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: AN1-type zinc finger protein 1; FLJ14007; zinc finger AN1-type-containing protein 1; zinc finger, AN1-type domain 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: LOC100129734   LOC100289500  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38881,701,331 - 81,721,304 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl881,701,334 - 81,732,903 (-)EnsemblGRCh38hg38GRCh38
GRCh37882,613,566 - 82,633,539 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36882,776,513 - 82,796,085 (-)NCBINCBI36Build 36hg18NCBI36
Celera878,618,071 - 78,638,022 (-)NCBICelera
Cytogenetic Map8q21.13NCBI
HuRef878,103,461 - 78,123,472 (-)NCBIHuRef
CHM1_1882,665,188 - 82,685,124 (-)NCBICHM1_1
T2T-CHM13v2.0882,133,043 - 82,153,000 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (IBA,IEA)
cytoplasmic stress granule  (IBA,IDA,IEA)

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:8125298   PMID:8889548   PMID:12477932   PMID:14702039   PMID:15489334   PMID:17207965   PMID:19322201   PMID:21873635   PMID:23535730   PMID:24121501   PMID:28298427   PMID:29804830  
PMID:31932471   PMID:31980649   PMID:34315543   PMID:34739333   PMID:35256949   PMID:35563538   PMID:35831314   PMID:38537699  


Genomics

Comparative Map Data
ZFAND1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38881,701,331 - 81,721,304 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl881,701,334 - 81,732,903 (-)EnsemblGRCh38hg38GRCh38
GRCh37882,613,566 - 82,633,539 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36882,776,513 - 82,796,085 (-)NCBINCBI36Build 36hg18NCBI36
Celera878,618,071 - 78,638,022 (-)NCBICelera
Cytogenetic Map8q21.13NCBI
HuRef878,103,461 - 78,123,472 (-)NCBIHuRef
CHM1_1882,665,188 - 82,685,124 (-)NCBICHM1_1
T2T-CHM13v2.0882,133,043 - 82,153,000 (-)NCBIT2T-CHM13v2.0
Zfand1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39310,405,013 - 10,416,383 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl310,405,013 - 10,416,377 (-)EnsemblGRCm39 Ensembl
GRCm38310,339,956 - 10,351,334 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl310,339,953 - 10,351,317 (-)EnsemblGRCm38mm10GRCm38
MGSCv37310,339,956 - 10,351,301 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36310,322,488 - 10,333,833 (-)NCBIMGSCv36mm8
Celera310,373,905 - 10,385,278 (-)NCBICelera
Cytogenetic Map3A1NCBI
cM Map32.62NCBI
Zfand1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8293,351,918 - 93,364,959 (+)NCBIGRCr8
mRatBN7.2291,444,497 - 91,457,540 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl291,444,508 - 91,453,246 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx297,934,976 - 97,948,037 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0296,055,962 - 96,069,025 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0291,112,820 - 91,125,877 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0293,656,895 - 93,666,745 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl293,656,946 - 93,665,939 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02113,412,414 - 113,422,261 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4293,397,689 - 93,407,496 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1293,339,924 - 93,351,656 (+)NCBI
Celera287,047,539 - 87,057,384 (+)NCBICelera
Cytogenetic Map2q23NCBI
Zfand1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541749,477 - 88,677 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541751,721 - 88,488 (-)NCBIChiLan1.0ChiLan1.0
ZFAND1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2797,438,463 - 97,462,514 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1873,067,820 - 73,091,865 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0878,224,428 - 78,248,625 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1879,844,701 - 79,868,716 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl879,837,970 - 79,868,716 (-)Ensemblpanpan1.1panPan2
ZFAND1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12928,799,635 - 28,825,494 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2928,808,423 - 28,825,748 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2929,086,361 - 29,106,418 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02928,939,673 - 28,959,401 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2928,938,544 - 28,959,664 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12929,008,849 - 29,028,893 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02929,022,792 - 29,042,770 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02929,379,575 - 29,399,635 (-)NCBIUU_Cfam_GSD_1.0
Zfand1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440530350,381,231 - 50,397,876 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366562,571,713 - 2,589,734 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366562,571,757 - 2,588,385 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZFAND1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl454,908,885 - 54,934,491 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1454,908,881 - 54,930,826 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
ZFAND1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1877,113,183 - 77,132,408 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl877,112,846 - 77,132,401 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603964,062,813 - 64,082,404 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Zfand1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247449,782,515 - 9,792,877 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247449,769,680 - 9,807,392 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ZFAND1
15 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8q21.11-21.13(chr8:73519300-82655582)x1 copy number loss See cases [RCV000051117] Chr8:73519300..82655582 [GRCh38]
Chr8:74431535..83567817 [GRCh37]
Chr8:74594089..83730372 [NCBI36]
Chr8:8q21.11-21.13		 pathogenic
GRCh38/hg38 8q12.3-21.13(chr8:61691800-82537696)x3 copy number gain See cases [RCV000053654] Chr8:61691800..82537696 [GRCh38]
Chr8:62604359..83449931 [GRCh37]
Chr8:62766913..83612486 [NCBI36]
Chr8:8q12.3-21.13		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8q21.11-21.2(chr8:73879385-85611466)x1 copy number loss See cases [RCV000054259] Chr8:73879385..85611466 [GRCh38]
Chr8:74791620..86523695 [GRCh37]
Chr8:74954174..86710947 [NCBI36]
Chr8:8q21.11-21.2		 pathogenic
GRCh38/hg38 8q21.13-21.3(chr8:77765431-91839285)x1 copy number loss See cases [RCV000054261] Chr8:77765431..91839285 [GRCh38]
Chr8:78677666..92851513 [GRCh37]
Chr8:78840221..92920689 [NCBI36]
Chr8:8q21.13-21.3		 pathogenic
GRCh38/hg38 8q21.13-22.1(chr8:78672463-95366868)x1 copy number loss See cases [RCV000054262] Chr8:78672463..95366868 [GRCh38]
Chr8:79584698..96379096 [GRCh37]
Chr8:79747253..96448272 [NCBI36]
Chr8:8q21.13-22.1		 pathogenic
NM_001170796.1(ZFAND1):c.559G>A (p.Asp187Asn) single nucleotide variant Malignant melanoma [RCV000068418] Chr8:81703025 [GRCh38]
Chr8:82615260 [GRCh37]
Chr8:82777815 [NCBI36]
Chr8:8q21.13		 not provided
GRCh37/hg19 8q13.2-24.3(chr8:68912432-146295771)x2 copy number gain See cases [RCV002292707] Chr8:68912432..146295771 [GRCh37]
Chr8:8q13.2-24.3		 pathogenic
GRCh38/hg38 8q13.1-22.1(chr8:66171669-93505509)x3 copy number gain See cases [RCV000137050] Chr8:66171669..93505509 [GRCh38]
Chr8:67083904..94517737 [GRCh37]
Chr8:67246458..94586913 [NCBI36]
Chr8:8q13.1-22.1		 pathogenic
GRCh38/hg38 8q21.13(chr8:81188681-82043830)x3 copy number gain See cases [RCV000137815] Chr8:81188681..82043830 [GRCh38]
Chr8:82100916..82956065 [GRCh37]
Chr8:82263471..83118620 [NCBI36]
Chr8:8q21.13		 likely benign
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3 copy number gain See cases [RCV000139036] Chr8:77480050..145068712 [GRCh38]
Chr8:78392286..146294098 [GRCh37]
Chr8:78554841..146264902 [NCBI36]
Chr8:8q21.13-24.3		 pathogenic
GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3 copy number gain See cases [RCV000139539] Chr8:46031340..139285494 [GRCh38]
Chr8:46942962..140297737 [GRCh37]
Chr8:47062127..140366919 [NCBI36]
Chr8:8q11.1-24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3 copy number gain See cases [RCV000142597] Chr8:78614077..145054634 [GRCh38]
Chr8:79526312..146280020 [GRCh37]
Chr8:79688867..146250824 [NCBI36]
Chr8:8q21.13-24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8q21.13(chr8:82083686-82962356)x3 copy number gain See cases [RCV000449050] Chr8:82083686..82962356 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3 copy number gain not provided [RCV000848192] Chr8:31936551..146295771 [GRCh37]
Chr8:8p12-q24.3		 pathogenic
GRCh37/hg19 8q21.13(chr8:82349850-84358646)x1 copy number loss See cases [RCV000446913] Chr8:82349850..84358646 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3 copy number gain See cases [RCV000447507] Chr8:158991..146280828 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771) copy number gain See cases [RCV000510234] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8q21.11-21.13(chr8:77751515-83516216)x1 copy number loss See cases [RCV000511429] Chr8:77751515..83516216 [GRCh37]
Chr8:8q21.11-21.13		 pathogenic
GRCh37/hg19 8q21.13(chr8:82534933-83229899)x3 copy number gain See cases [RCV000511249] Chr8:82534933..83229899 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3 copy number gain See cases [RCV000511095] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
NM_024699.3(ZFAND1):c.503T>G (p.Val168Gly) single nucleotide variant not specified [RCV004331106] Chr8:81703102 [GRCh38]
Chr8:82615337 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_024699.3(ZFAND1):c.265A>G (p.Arg89Gly) single nucleotide variant not specified [RCV004320179] Chr8:81714988 [GRCh38]
Chr8:82627223 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3 copy number gain See cases [RCV000512169] Chr8:12490999..146295771 [GRCh37]
Chr8:8p23.1-q24.3		 pathogenic
GRCh37/hg19 8q21.13(chr8:82603894-82862754)x3 copy number gain not provided [RCV000682962] Chr8:82603894..82862754 [GRCh37]
Chr8:8q21.13		 likely benign
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3 copy number gain not provided [RCV000747254] Chr8:164984..146293414 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3 copy number gain not provided [RCV000747248] Chr8:10213..146293414 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8q21.13-21.2(chr8:82196649-85352499)x1 copy number loss not provided [RCV000847829] Chr8:82196649..85352499 [GRCh37]
Chr8:8q21.13-21.2		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not provided [RCV000848478] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8q21.13(chr8:82276728-82641699)x1 copy number loss not provided [RCV000846938] Chr8:82276728..82641699 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_024699.3(ZFAND1):c.127G>T (p.Gly43Cys) single nucleotide variant not specified [RCV004308136] Chr8:81717260 [GRCh38]
Chr8:82629495 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8q21.13(chr8:82581743-82652385)x1 copy number loss not provided [RCV001006116] Chr8:82581743..82652385 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_024699.3(ZFAND1):c.427G>T (p.Val143Phe) single nucleotide variant not specified [RCV004228591] Chr8:81713971 [GRCh38]
Chr8:82626206 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8q21.12-21.13(chr8:79876744-83112711)x3 copy number gain not provided [RCV002472757] Chr8:79876744..83112711 [GRCh37]
Chr8:8q21.12-21.13		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771) copy number gain Polydactyly [RCV002280629] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8q21.13(chr8:82353502-82673333) copy number gain not specified [RCV002053781] Chr8:82353502..82673333 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8q21.11-21.3(chr8:77906471-88917707) copy number loss not specified [RCV002053776] Chr8:77906471..88917707 [GRCh37]
Chr8:8q21.11-21.3		 pathogenic
GRCh37/hg19 8q21.13(chr8:82349850-84358646) copy number loss not specified [RCV002053779] Chr8:82349850..84358646 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8q21.13-21.2(chr8:81829690-85173253)x3 copy number gain not provided [RCV001827963] Chr8:81829690..85173253 [GRCh37]
Chr8:8q21.13-21.2		 uncertain significance
GRCh37/hg19 8q13.2-24.3(chr8:70382990-146295771) copy number gain not specified [RCV002053772] Chr8:70382990..146295771 [GRCh37]
Chr8:8q13.2-24.3		 pathogenic
GRCh37/hg19 8q21.11-21.3(chr8:75904944-87097083)x1 copy number loss Chromosome 8q21.11 deletion syndrome [RCV002279750] Chr8:75904944..87097083 [GRCh37]
Chr8:8q21.11-21.3		 pathogenic
NM_024699.3(ZFAND1):c.16A>T (p.Ile6Phe) single nucleotide variant not specified [RCV004316945] Chr8:81721266 [GRCh38]
Chr8:82633501 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8q21.12-24.11(chr8:79409349-119040631)x3 copy number gain not provided [RCV002474526] Chr8:79409349..119040631 [GRCh37]
Chr8:8q21.12-24.11		 pathogenic
NM_024699.3(ZFAND1):c.427G>A (p.Val143Ile) single nucleotide variant not specified [RCV004208923] Chr8:81713971 [GRCh38]
Chr8:82626206 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_024699.3(ZFAND1):c.271C>T (p.Arg91Cys) single nucleotide variant not specified [RCV004260453] Chr8:81714891 [GRCh38]
Chr8:82627126 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_024699.3(ZFAND1):c.577A>G (p.Ile193Val) single nucleotide variant not specified [RCV004265359] Chr8:81703028 [GRCh38]
Chr8:82615263 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8q21.12-22.3(chr8:79046933-102008860)x3 copy number gain not provided [RCV003484742] Chr8:79046933..102008860 [GRCh37]
Chr8:8q21.12-22.3		 pathogenic
GRCh37/hg19 8p21.2-q21.3(chr8:27024288-89410121)x3 copy number gain not specified [RCV003986754] Chr8:27024288..89410121 [GRCh37]
Chr8:8p21.2-q21.3		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not specified [RCV003986742] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8q21.13-21.2(chr8:81829690-85172228)x3 copy number gain not specified [RCV003986752] Chr8:81829690..85172228 [GRCh37]
Chr8:8q21.13-21.2		 uncertain significance
GRCh37/hg19 8q21.13(chr8:82540245-82662642)x1 copy number loss not specified [RCV003986738] Chr8:82540245..82662642 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_024699.3(ZFAND1):c.136G>A (p.Glu46Lys) single nucleotide variant not specified [RCV004483758] Chr8:81717251 [GRCh38]
Chr8:82629486 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_024699.3(ZFAND1):c.284A>C (p.Asp95Ala) single nucleotide variant not specified [RCV004483759] Chr8:81714878 [GRCh38]
Chr8:82627113 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_024699.3(ZFAND1):c.331A>G (p.Thr111Ala) single nucleotide variant not specified [RCV004483760] Chr8:81714831 [GRCh38]
Chr8:82627066 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_024699.3(ZFAND1):c.577A>C (p.Ile193Leu) single nucleotide variant not specified [RCV004483761] Chr8:81703028 [GRCh38]
Chr8:82615263 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_024699.3(ZFAND1):c.580G>T (p.Asp194Tyr) single nucleotide variant not specified [RCV004483762] Chr8:81703025 [GRCh38]
Chr8:82615260 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_024699.3(ZFAND1):c.645G>T (p.Arg215Ser) single nucleotide variant not specified [RCV004483763] Chr8:81702857 [GRCh38]
Chr8:82615092 [GRCh37]
Chr8:8q21.13		 uncertain significance
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR125Ahsa-miR-125a-5pTarbaseexternal_infoSequencingPOSITIVE

Predicted Target Of
Summary Value
Count of predictions:3654
Count of miRNA genes:961
Interacting mature miRNAs:1131
Transcripts:ENST00000220669, ENST00000517353, ENST00000517450, ENST00000517588, ENST00000518419, ENST00000519338, ENST00000519464, ENST00000519523, ENST00000519820, ENST00000520076, ENST00000520604, ENST00000520635, ENST00000520941, ENST00000521287, ENST00000521742, ENST00000521885, ENST00000521895, ENST00000522032, ENST00000522520, ENST00000523012, ENST00000523096, ENST00000523361, ENST00000523431, ENST00000524305, ENST00000524339
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
RH45131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37882,613,671 - 82,613,772UniSTSGRCh37
Build 36882,776,226 - 82,776,327RGDNCBI36
Celera878,618,176 - 78,618,277RGD
Cytogenetic Map8q21.13UniSTS
HuRef878,103,566 - 78,103,667UniSTS
GeneMap99-GB4 RH Map8413.36UniSTS
NCBI RH Map8888.8UniSTS
RH92477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37882,613,995 - 82,614,167UniSTSGRCh37
Build 36882,776,550 - 82,776,722RGDNCBI36
Celera878,618,500 - 78,618,672RGD
Cytogenetic Map8q21.13UniSTS
HuRef878,103,890 - 78,104,062UniSTS
GeneMap99-GB4 RH Map8413.26UniSTS
A009A23  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37882,614,918 - 82,615,022UniSTSGRCh37
GRCh37193,198,727 - 93,198,831UniSTSGRCh37
Build 36192,971,315 - 92,971,419RGDNCBI36
Celera191,452,320 - 91,452,424RGD
Celera878,619,423 - 78,619,527UniSTS
Cytogenetic Map8q21.13UniSTS
Cytogenetic Map1p22.1UniSTS
HuRef878,104,813 - 78,104,917UniSTS
HuRef191,319,941 - 91,320,045UniSTS
GeneMap99-GB4 RH Map8400.14UniSTS
NCBI RH Map8884.7UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001170796 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001170797 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_024699 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_033193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_033194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_033195 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_033196 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC132219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK024069 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225195 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL833030 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC022251 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC051857 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC056877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG618233 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ427843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ435400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU624414 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU678501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA412820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR457323 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000220669   ⟹   ENSP00000220669
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,701,337 - 81,721,300 (-)Ensembl
Ensembl Acc Id: ENST00000517353
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,714,440 - 81,732,903 (-)Ensembl
Ensembl Acc Id: ENST00000517450   ⟹   ENSP00000427811
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,713,918 - 81,721,300 (-)Ensembl
Ensembl Acc Id: ENST00000517588   ⟹   ENSP00000430214
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,702,914 - 81,721,263 (-)Ensembl
Ensembl Acc Id: ENST00000518419   ⟹   ENSP00000428527
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,713,948 - 81,721,241 (-)Ensembl
Ensembl Acc Id: ENST00000519338
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,702,159 - 81,703,128 (-)Ensembl
Ensembl Acc Id: ENST00000519464   ⟹   ENSP00000428375
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,702,544 - 81,721,287 (-)Ensembl
Ensembl Acc Id: ENST00000519523   ⟹   ENSP00000429167
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,702,914 - 81,721,288 (-)Ensembl
Ensembl Acc Id: ENST00000519820
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,714,599 - 81,721,300 (-)Ensembl
Ensembl Acc Id: ENST00000520076   ⟹   ENSP00000430719
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,713,951 - 81,721,283 (-)Ensembl
Ensembl Acc Id: ENST00000520604   ⟹   ENSP00000428101
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,702,993 - 81,732,345 (-)Ensembl
Ensembl Acc Id: ENST00000520635   ⟹   ENSP00000428278
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,702,825 - 81,732,407 (-)Ensembl
Ensembl Acc Id: ENST00000520941
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,714,987 - 81,732,619 (-)Ensembl
Ensembl Acc Id: ENST00000521287   ⟹   ENSP00000428139
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,702,682 - 81,721,295 (-)Ensembl
Ensembl Acc Id: ENST00000521742   ⟹   ENSP00000430405
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,713,918 - 81,732,387 (-)Ensembl
Ensembl Acc Id: ENST00000521885
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,714,674 - 81,732,373 (-)Ensembl
Ensembl Acc Id: ENST00000521895   ⟹   ENSP00000429527
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,702,548 - 81,721,282 (-)Ensembl
Ensembl Acc Id: ENST00000522032   ⟹   ENSP00000430499
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,702,324 - 81,714,040 (-)Ensembl
Ensembl Acc Id: ENST00000522520   ⟹   ENSP00000429999
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,701,765 - 81,721,289 (-)Ensembl
Ensembl Acc Id: ENST00000523012
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,717,252 - 81,721,244 (-)Ensembl
Ensembl Acc Id: ENST00000523096   ⟹   ENSP00000430736
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,701,722 - 81,721,300 (-)Ensembl
Ensembl Acc Id: ENST00000523361   ⟹   ENSP00000427957
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,703,099 - 81,732,881 (-)Ensembl
Ensembl Acc Id: ENST00000523431   ⟹   ENSP00000428927
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,702,729 - 81,721,290 (-)Ensembl
Ensembl Acc Id: ENST00000524305
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,701,334 - 81,715,039 (-)Ensembl
Ensembl Acc Id: ENST00000524339
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl881,714,325 - 81,721,295 (-)Ensembl
RefSeq Acc Id: NM_001170796   ⟹   NP_001164267
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38881,701,331 - 81,721,304 (-)NCBI
GRCh37882,613,566 - 82,633,539 (-)RGD
Celera878,618,071 - 78,638,022 (-)RGD
HuRef878,103,461 - 78,123,472 (-)ENTREZGENE
CHM1_1882,665,188 - 82,685,124 (-)NCBI
T2T-CHM13v2.0882,133,043 - 82,153,000 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001170797   ⟹   NP_001164268
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38881,702,914 - 81,721,300 (-)NCBI
GRCh37882,613,566 - 82,633,539 (-)RGD
Celera878,618,071 - 78,638,022 (-)RGD
HuRef878,103,461 - 78,123,472 (-)ENTREZGENE
CHM1_1882,666,771 - 82,685,124 (-)NCBI
T2T-CHM13v2.0882,134,626 - 82,152,996 (-)NCBI
Sequence:
RefSeq Acc Id: NM_024699   ⟹   NP_078975
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38881,701,337 - 81,721,300 (-)NCBI
GRCh37882,613,566 - 82,633,539 (-)RGD
Build 36882,776,513 - 82,796,085 (-)NCBI Archive
Celera878,618,071 - 78,638,022 (-)RGD
HuRef878,103,461 - 78,123,472 (-)ENTREZGENE
CHM1_1882,665,188 - 82,685,124 (-)NCBI
T2T-CHM13v2.0882,133,049 - 82,152,996 (-)NCBI
Sequence:
RefSeq Acc Id: NR_033193
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38881,701,331 - 81,721,304 (-)NCBI
GRCh37882,613,566 - 82,633,539 (-)RGD
Celera878,618,071 - 78,638,022 (-)RGD
HuRef878,103,461 - 78,123,472 (-)ENTREZGENE
CHM1_1882,665,188 - 82,685,124 (-)NCBI
T2T-CHM13v2.0882,133,043 - 82,153,000 (-)NCBI
Sequence:
RefSeq Acc Id: NR_033194
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38881,701,331 - 81,721,304 (-)NCBI
GRCh37882,613,566 - 82,633,539 (-)RGD
Celera878,618,071 - 78,638,022 (-)RGD
HuRef878,103,461 - 78,123,472 (-)ENTREZGENE
CHM1_1882,665,188 - 82,685,124 (-)NCBI
T2T-CHM13v2.0882,133,043 - 82,153,000 (-)NCBI
Sequence:
RefSeq Acc Id: NR_033195
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38881,701,331 - 81,721,304 (-)NCBI
GRCh37882,613,566 - 82,633,539 (-)RGD
Celera878,618,071 - 78,638,022 (-)RGD
HuRef878,103,461 - 78,123,472 (-)ENTREZGENE
CHM1_1882,665,188 - 82,685,124 (-)NCBI
T2T-CHM13v2.0882,133,043 - 82,153,000 (-)NCBI
Sequence:
RefSeq Acc Id: NR_033196
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38881,702,914 - 81,721,300 (-)NCBI
GRCh37882,613,566 - 82,633,539 (-)RGD
Celera878,618,071 - 78,638,022 (-)RGD
HuRef878,103,461 - 78,123,472 (-)ENTREZGENE
CHM1_1882,666,771 - 82,685,124 (-)NCBI
T2T-CHM13v2.0882,134,626 - 82,152,996 (-)NCBI
Sequence:
RefSeq Acc Id: NP_078975   ⟸   NM_024699
- Peptide Label: isoform a
- UniProtKB: Q6PGQ6 (UniProtKB/Swiss-Prot),   Q6IA32 (UniProtKB/Swiss-Prot),   Q658R7 (UniProtKB/Swiss-Prot),   E5RJ99 (UniProtKB/Swiss-Prot),   E5RIG0 (UniProtKB/Swiss-Prot),   Q9H810 (UniProtKB/Swiss-Prot),   Q8TCF1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001164267   ⟸   NM_001170796
- Peptide Label: isoform b
- UniProtKB: Q8TCF1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001164268   ⟸   NM_001170797
- Peptide Label: isoform c
- UniProtKB: Q8TCF1 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000430214   ⟸   ENST00000517588
Ensembl Acc Id: ENSP00000427811   ⟸   ENST00000517450
Ensembl Acc Id: ENSP00000428527   ⟸   ENST00000518419
Ensembl Acc Id: ENSP00000428375   ⟸   ENST00000519464
Ensembl Acc Id: ENSP00000429167   ⟸   ENST00000519523
Ensembl Acc Id: ENSP00000430719   ⟸   ENST00000520076
Ensembl Acc Id: ENSP00000428278   ⟸   ENST00000520635
Ensembl Acc Id: ENSP00000428101   ⟸   ENST00000520604
Ensembl Acc Id: ENSP00000428139   ⟸   ENST00000521287
Ensembl Acc Id: ENSP00000430405   ⟸   ENST00000521742
Ensembl Acc Id: ENSP00000429527   ⟸   ENST00000521895
Ensembl Acc Id: ENSP00000430499   ⟸   ENST00000522032
Ensembl Acc Id: ENSP00000429999   ⟸   ENST00000522520
Ensembl Acc Id: ENSP00000428927   ⟸   ENST00000523431
Ensembl Acc Id: ENSP00000427957   ⟸   ENST00000523361
Ensembl Acc Id: ENSP00000430736   ⟸   ENST00000523096
Ensembl Acc Id: ENSP00000220669   ⟸   ENST00000220669
Protein Domains
AN1-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8TCF1-F1-model_v2 AlphaFold Q8TCF1 1-268 view protein structure

Promoters
RGD ID:7213645
Promoter ID:EPDNEW_H12569
Type:initiation region
Name:ZFAND1_1
Description:zinc finger AN1-type containing 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12572  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38881,721,300 - 81,721,360EPDNEW
RGD ID:6807166
Promoter ID:HG_KWN:61600
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001170796,   NM_001170797,   NM_024699,   NR_033193,   NR_033194,   NR_033195,   NR_033196
Position:
Human AssemblyChrPosition (strand)Source
Build 36882,795,769 - 82,796,269 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:25858 AgrOrtholog
COSMIC ZFAND1 COSMIC
Ensembl Genes ENSG00000104231 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000220669 ENTREZGENE
  ENST00000220669.10 UniProtKB/Swiss-Prot
  ENST00000517450.5 UniProtKB/TrEMBL
  ENST00000517588 ENTREZGENE
  ENST00000517588.5 UniProtKB/TrEMBL
  ENST00000518419.5 UniProtKB/TrEMBL
  ENST00000519464.5 UniProtKB/TrEMBL
  ENST00000519523 ENTREZGENE
  ENST00000519523.5 UniProtKB/Swiss-Prot
  ENST00000520076.5 UniProtKB/TrEMBL
  ENST00000520604.5 UniProtKB/TrEMBL
  ENST00000520635.5 UniProtKB/TrEMBL
  ENST00000521287.5 UniProtKB/Swiss-Prot
  ENST00000521742.5 UniProtKB/TrEMBL
  ENST00000521895.5 UniProtKB/TrEMBL
  ENST00000522032.1 UniProtKB/TrEMBL
  ENST00000522520.5 UniProtKB/Swiss-Prot
  ENST00000523096 ENTREZGENE
  ENST00000523096.5 UniProtKB/Swiss-Prot
  ENST00000523361.5 UniProtKB/TrEMBL
  ENST00000523431.5 UniProtKB/TrEMBL
Gene3D-CATH 4.10.1110.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000104231 GTEx
HGNC ID HGNC:25858 ENTREZGENE
Human Proteome Map ZFAND1 Human Proteome Map
InterPro AN1-like_Znf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_AN1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:79752 UniProtKB/Swiss-Prot
NCBI Gene 79752 ENTREZGENE
PANTHER AN1-TYPE ZINC FINGER PROTEIN 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ARSENITE INDUCUBLE RNA ASSOCIATED PROTEIN AIP-1-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam zf-AN1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142670532 PharmGKB
PROSITE ZF_AN1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART ZnF_AN1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF118310 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt E5RFE5_HUMAN UniProtKB/TrEMBL
  E5RFU1_HUMAN UniProtKB/TrEMBL
  E5RG60_HUMAN UniProtKB/TrEMBL
  E5RGE5_HUMAN UniProtKB/TrEMBL
  E5RHR9_HUMAN UniProtKB/TrEMBL
  E5RI74_HUMAN UniProtKB/TrEMBL
  E5RIG0 ENTREZGENE
  E5RIH7_HUMAN UniProtKB/TrEMBL
  E5RIS3_HUMAN UniProtKB/TrEMBL
  E5RJ74_HUMAN UniProtKB/TrEMBL
  E5RJ99 ENTREZGENE
  E5RK75_HUMAN UniProtKB/TrEMBL
  H0YBX7_HUMAN UniProtKB/TrEMBL
  Q05BD2_HUMAN UniProtKB/TrEMBL
  Q658R7 ENTREZGENE
  Q6IA32 ENTREZGENE
  Q6PGQ6 ENTREZGENE
  Q8TCF1 ENTREZGENE
  Q9H810 ENTREZGENE
  ZFAN1_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary E5RIG0 UniProtKB/Swiss-Prot
  E5RJ99 UniProtKB/Swiss-Prot
  Q658R7 UniProtKB/Swiss-Prot
  Q6IA32 UniProtKB/Swiss-Prot
  Q6PGQ6 UniProtKB/Swiss-Prot
  Q9H810 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-16 ZFAND1  zinc finger AN1-type containing 1    zinc finger, AN1-type domain 1  Symbol and/or name change 5135510 APPROVED