TEX10 (testis expressed 10) - Rat Genome Database

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Gene: TEX10 (testis expressed 10) Homo sapiens
Analyze
Symbol: TEX10
Name: testis expressed 10
RGD ID: 1323824
HGNC Page HGNC:25988
Description: Predicted to be involved in rRNA processing. Located in mitochondrion and nucleoplasm. Part of MLL1 complex.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: bA208F1.2; FLJ20287; FLJ31157; FLJ34350; Ipi1; RP11-208F1.2; testis expressed gene 10; testis expressed sequence 10; testis-expressed protein 10; testis-expressed sequence 10 protein
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
GRCh389100,302,084 - 100,352,942 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl9100,302,077 - 100,352,942 (-)EnsemblGRCh38hg38GRCh38
GRCh379103,064,366 - 103,115,224 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 369102,104,190 - 102,154,995 (-)NCBINCBI36Build 36hg18NCBI36
Build 349100,143,923 - 100,194,729NCBI
Celera973,577,686 - 73,628,526 (-)NCBICelera
Cytogenetic Map9q31.1NCBI
HuRef972,663,398 - 72,714,298 (-)NCBIHuRef
CHM1_19103,210,798 - 103,261,707 (-)NCBICHM1_1
T2T-CHM13v2.09112,473,720 - 112,524,578 (-)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  (IEA)
intracellular organelle  (IEA)
mitochondrion  (IDA)
MLL1 complex  (IBA,IDA,IEA)
nucleolus  (IEA)
nucleoplasm  (IDA,IEA,TAS)
nucleus  (IBA,IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
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
3. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:12429849   PMID:12880961   PMID:14702039   PMID:15164053   PMID:15231748   PMID:15334068   PMID:15342556   PMID:15489334   PMID:15960975   PMID:19394292   PMID:19596235   PMID:19615732  
PMID:21326211   PMID:21873635   PMID:22190735   PMID:22586326   PMID:22872859   PMID:22939629   PMID:23481573   PMID:23667531   PMID:24332808   PMID:24457600   PMID:24711643   PMID:24981860  
PMID:25476789   PMID:25544563   PMID:25609649   PMID:25665578   PMID:25693804   PMID:25921289   PMID:25936917   PMID:26186194   PMID:26344197   PMID:26496610   PMID:27880917   PMID:27926873  
PMID:28077445   PMID:28514442   PMID:28695742   PMID:28700943   PMID:29180619   PMID:29298432   PMID:29395067   PMID:29467282   PMID:29511261   PMID:29568061   PMID:29656893   PMID:29802200  
PMID:29911972   PMID:30021884   PMID:30045663   PMID:30415952   PMID:30554943   PMID:30585729   PMID:31073040   PMID:31091453   PMID:31180492   PMID:31298480   PMID:31365120   PMID:31527615  
PMID:31586073   PMID:31638260   PMID:31871319   PMID:32160526   PMID:32235678   PMID:32296183   PMID:32416067   PMID:32538781   PMID:32707033   PMID:32807901   PMID:33301849   PMID:33462405  
PMID:33658012   PMID:33760161   PMID:33961781   PMID:34079125   PMID:34133714   PMID:34244565   PMID:34373451   PMID:34709727   PMID:34966825   PMID:35013218   PMID:35140242   PMID:35156514  
PMID:35241646   PMID:35271311   PMID:35439318   PMID:35509820   PMID:35545034   PMID:35850772   PMID:36114006   PMID:36215168   PMID:36244648   PMID:36351913   PMID:36424410   PMID:36526897  
PMID:36537216   PMID:36574265   PMID:36634849   PMID:36736316   PMID:36774506   PMID:36779763   PMID:36880596   PMID:36912080   PMID:37071664   PMID:37689310   PMID:37827155  


Genomics

Comparative Map Data
TEX10
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh389100,302,084 - 100,352,942 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl9100,302,077 - 100,352,942 (-)EnsemblGRCh38hg38GRCh38
GRCh379103,064,366 - 103,115,224 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 369102,104,190 - 102,154,995 (-)NCBINCBI36Build 36hg18NCBI36
Build 349100,143,923 - 100,194,729NCBI
Celera973,577,686 - 73,628,526 (-)NCBICelera
Cytogenetic Map9q31.1NCBI
HuRef972,663,398 - 72,714,298 (-)NCBIHuRef
CHM1_19103,210,798 - 103,261,707 (-)NCBICHM1_1
T2T-CHM13v2.09112,473,720 - 112,524,578 (-)NCBIT2T-CHM13v2.0
Tex10
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39448,430,805 - 48,473,492 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl448,430,858 - 48,473,459 (-)EnsemblGRCm39 Ensembl
GRCm38448,430,858 - 48,473,464 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl448,430,858 - 48,473,459 (-)EnsemblGRCm38mm10GRCm38
MGSCv37448,443,828 - 48,486,294 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36448,443,828 - 48,486,294 (-)NCBIMGSCv36mm8
Celera448,454,349 - 48,496,904 (-)NCBICelera
Cytogenetic Map4B1NCBI
cM Map426.13NCBI
Tex10
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8567,557,770 - 67,603,904 (-)NCBIGRCr8
mRatBN7.2562,762,230 - 62,808,373 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl562,762,230 - 62,808,373 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx564,739,864 - 64,786,013 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0566,559,162 - 66,605,312 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0566,528,626 - 66,574,780 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0564,179,247 - 64,225,844 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl564,179,247 - 64,225,844 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0568,695,431 - 68,742,028 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4565,118,575 - 65,165,336 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1565,124,068 - 65,160,400 (-)NCBI
Celera564,785,782 - 64,831,794 (+)NCBICelera
Cytogenetic Map5q22NCBI
Tex10
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541925,381,751 - 25,447,985 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495541925,382,222 - 25,445,492 (+)NCBIChiLan1.0ChiLan1.0
TEX10
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21139,100,927 - 39,151,881 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1939,103,298 - 39,154,252 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0971,394,926 - 71,445,750 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1999,509,642 - 99,560,447 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl999,509,648 - 99,560,447 (-)Ensemblpanpan1.1panPan2
TEX10
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11157,196,683 - 57,255,847 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1157,196,683 - 57,255,849 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1155,640,283 - 55,704,098 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01158,317,999 - 58,381,832 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1158,318,006 - 58,381,825 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11156,821,883 - 56,885,904 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01156,846,847 - 56,910,846 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01157,546,505 - 57,610,510 (-)NCBIUU_Cfam_GSD_1.0
Tex10
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947172,065,343 - 172,108,948 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365248,611,075 - 8,656,545 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365248,612,919 - 8,656,545 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TEX10
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1242,058,041 - 242,120,554 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11242,058,035 - 242,120,547 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21270,407,894 - 270,480,569 (-)NCBISscrofa10.2Sscrofa10.2susScr3
TEX10
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11239,087,506 - 39,138,134 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1239,091,085 - 39,138,027 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660353,417,617 - 3,468,710 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tex10
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624825640,971 - 701,039 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_004624825640,952 - 701,046 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TEX10
27 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1 copy number loss See cases [RCV000050315] Chr9:99138048..115011033 [GRCh38]
Chr9:101900330..117773312 [GRCh37]
Chr9:100940151..116813133 [NCBI36]
Chr9:9q22.33-33.1		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000050348] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q22.33-33.1(chr9:99349916-115767475)x1 copy number loss See cases [RCV000052921] Chr9:99349916..115767475 [GRCh38]
Chr9:102112198..118529754 [GRCh37]
Chr9:101152019..117569575 [NCBI36]
Chr9:9q22.33-33.1		 pathogenic
GRCh38/hg38 9q22.33-31.1(chr9:99465640-100394582)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052885]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052885]|See cases [RCV000052885] Chr9:99465640..100394582 [GRCh38]
Chr9:102227922..103156864 [GRCh37]
Chr9:101267743..102196685 [NCBI36]
Chr9:9q22.33-31.1		 uncertain significance
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124532)x3 copy number gain See cases [RCV000053745] Chr9:193412..138124532 [GRCh38]
Chr9:204193..141018984 [GRCh37]
Chr9:194193..140138805 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3 copy number gain See cases [RCV000053746] Chr9:193412..138114463 [GRCh38]
Chr9:214367..141008915 [GRCh37]
Chr9:204367..140128736 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|See cases [RCV000053748] Chr9:193412..138179445 [GRCh38]
Chr9:266045..141073897 [GRCh37]
Chr9:256045..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q22.32-31.2(chr9:94184266-106730550)x3 copy number gain See cases [RCV000053774] Chr9:94184266..106730550 [GRCh38]
Chr9:96946548..109492831 [GRCh37]
Chr9:95986369..108532652 [NCBI36]
Chr9:9q22.32-31.2		 pathogenic
GRCh38/hg38 9q22.1-32(chr9:88522292-113687796)x3 copy number gain See cases [RCV000053752] Chr9:88522292..113687796 [GRCh38]
Chr9:91137207..116450076 [GRCh37]
Chr9:90327027..115489897 [NCBI36]
Chr9:9q22.1-32		 pathogenic
NM_001161584.1(TEX10):c.2594C>T (p.Ala865Val) single nucleotide variant Malignant melanoma [RCV000061844] Chr9:100303666 [GRCh38]
Chr9:103065948 [GRCh37]
Chr9:102105769 [NCBI36]
Chr9:9q31.1		 not provided
GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445) copy number gain See cases [RCV000133791] Chr9:204193..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q22.32-31.3(chr9:95061030-108695569)x1 copy number loss See cases [RCV000134375] Chr9:95061030..108695569 [GRCh38]
Chr9:97823312..111457849 [GRCh37]
Chr9:96863133..110497670 [NCBI36]
Chr9:9q22.32-31.3		 pathogenic
GRCh38/hg38 9q21.11-31.2(chr9:68420430-106579493)x3 copy number gain See cases [RCV000136788] Chr9:68420430..106579493 [GRCh38]
Chr9:71130848..109341774 [GRCh37]
Chr9:70225166..108381595 [NCBI36]
Chr9:9q21.11-31.2		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3 copy number gain See cases [RCV000138783] Chr9:193412..138124524 [GRCh38]
Chr9:204090..141018976 [GRCh37]
Chr9:194090..140138797 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q22.33-31.3(chr9:99024205-109947890)x1 copy number loss See cases [RCV000138281] Chr9:99024205..109947890 [GRCh38]
Chr9:101786487..112710170 [GRCh37]
Chr9:100826308..111749991 [NCBI36]
Chr9:9q22.33-31.3		 pathogenic|likely pathogenic
GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000139207] Chr9:193412..138159073 [GRCh38]
Chr9:68420641..141053525 [GRCh37]
Chr9:67910461..140173346 [NCBI36]
Chr9:9p11.2-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000138962] Chr9:193412..138159073 [GRCh38]
Chr9:204104..141053525 [GRCh37]
Chr9:194104..140173346 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic|conflicting data from submitters
GRCh38/hg38 9q21.12-31.3(chr9:69627642-111454304)x3 copy number gain See cases [RCV000139789] Chr9:69627642..111454304 [GRCh38]
Chr9:72242558..114216584 [GRCh37]
Chr9:71432378..113256405 [NCBI36]
Chr9:9q21.12-31.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3 copy number gain See cases [RCV000141876] Chr9:203861..138125937 [GRCh38]
Chr9:203861..141020389 [GRCh37]
Chr9:193861..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3 copy number gain See cases [RCV000143476] Chr9:203862..138125937 [GRCh38]
Chr9:203862..141020389 [GRCh37]
Chr9:193862..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1 copy number loss See cases [RCV000148264] Chr9:99138048..115011033 [GRCh38]
Chr9:101900330..117773312 [GRCh37]
Chr9:100940151..116813133 [NCBI36]
Chr9:9q22.33-33.1		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000148113] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3 copy number gain See cases [RCV000240081] Chr9:163131..141122114 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407) copy number gain See cases [RCV000449375] Chr9:62525..141006407 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3 copy number gain not specified [RCV003986800] Chr9:203861..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203864-141020389)x3 copy number gain See cases [RCV000448978] Chr9:203864..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
NC_000009.11:g.(?_102339410)_(109549354_?)del deletion Schizophrenia [RCV000416788] Chr9:102339410..109549354 [GRCh37]
Chr9:101379231..108589175 [NCBI36]
Chr9:9q22.33-31.2		 likely pathogenic
NM_017746.4(TEX10):c.1169A>C (p.Asp390Ala) single nucleotide variant Inborn genetic diseases [RCV003286977] Chr9:100340338 [GRCh38]
Chr9:103102620 [GRCh37]
Chr9:9q31.1		 uncertain significance
GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928) copy number gain Global developmental delay [RCV000626548] Chr9:71069743..140999928 [GRCh37]
Chr9:9q21.11-34.3		 likely pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389) copy number gain See cases [RCV000512392] Chr9:203862..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141114095)x2 copy number gain not provided [RCV000748054] Chr9:10590..141114095 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141122247)x3 copy number gain not provided [RCV000748055] Chr9:10590..141122247 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141107672)x3 copy number gain not provided [RCV000748053] Chr9:10590..141107672 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:46587-141066491)x3 copy number gain not provided [RCV000748063] Chr9:46587..141066491 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3 copy number gain not provided [RCV000847808] Chr9:71416475..141020389 [GRCh37]
Chr9:9q21.11-34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3 copy number gain not provided [RCV000845900] Chr9:203861..141020388 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q22.31-31.2(chr9:96126075-108535272)x1 copy number loss See cases [RCV001194520] Chr9:96126075..108535272 [GRCh37]
Chr9:9q22.31-31.2		 pathogenic
Single allele deletion Intellectual disability [RCV001293373] Chr9:97834573..107199088 [GRCh37]
Chr9:9q22.32-31.1		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389) copy number gain not specified [RCV002053823] Chr9:353349..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q31.1-31.2(chr9:102858276-110624997)x3 copy number gain not provided [RCV001834515] Chr9:102858276..110624997 [GRCh37]
Chr9:9q31.1-31.2		 uncertain significance
GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410) copy number gain not specified [RCV002053853] Chr9:71349994..122603410 [GRCh37]
Chr9:9q21.11-33.2		 likely pathogenic
GRCh37/hg19 9q22.2-31.1(chr9:93864974-106661581)x1 copy number loss Gorlin syndrome [RCV002279743] Chr9:93864974..106661581 [GRCh37]
Chr9:9q22.2-31.1		 pathogenic
GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3 copy number gain See cases [RCV002292402] Chr9:203861..131603223 [GRCh37]
Chr9:9p24.3-q34.11		 pathogenic
GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311) copy number loss Distal tetrasomy 15q [RCV002280776] Chr9:19356861..119513311 [GRCh37]
Chr9:9p22.1-q33.1		 uncertain significance
NM_017746.4(TEX10):c.1439A>G (p.Asn480Ser) single nucleotide variant Inborn genetic diseases [RCV002682313] Chr9:100329981 [GRCh38]
Chr9:103092263 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.1946T>G (p.Leu649Trp) single nucleotide variant Inborn genetic diseases [RCV002778674] Chr9:100326335 [GRCh38]
Chr9:103088617 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.1588A>C (p.Ile530Leu) single nucleotide variant Inborn genetic diseases [RCV002772763] Chr9:100329177 [GRCh38]
Chr9:103091459 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.2111G>A (p.Gly704Glu) single nucleotide variant Inborn genetic diseases [RCV002859278] Chr9:100320356 [GRCh38]
Chr9:103082638 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.840G>C (p.Gln280His) single nucleotide variant Inborn genetic diseases [RCV002733589] Chr9:100346747 [GRCh38]
Chr9:103109029 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.2744T>C (p.Ile915Thr) single nucleotide variant Inborn genetic diseases [RCV002822978] Chr9:100302237 [GRCh38]
Chr9:103064519 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.659C>T (p.Ser220Phe) single nucleotide variant Inborn genetic diseases [RCV002868791] Chr9:100346928 [GRCh38]
Chr9:103109210 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.1496C>T (p.Thr499Ile) single nucleotide variant Inborn genetic diseases [RCV002784183] Chr9:100329269 [GRCh38]
Chr9:103091551 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.1565T>C (p.Leu522Ser) single nucleotide variant Inborn genetic diseases [RCV002919544] Chr9:100329200 [GRCh38]
Chr9:103091482 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.2269A>G (p.Ile757Val) single nucleotide variant Inborn genetic diseases [RCV002875453] Chr9:100310313 [GRCh38]
Chr9:103072595 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.2429C>G (p.Thr810Ser) single nucleotide variant Inborn genetic diseases [RCV002769033] Chr9:100308536 [GRCh38]
Chr9:103070818 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.85A>G (p.Thr29Ala) single nucleotide variant Inborn genetic diseases [RCV002964873] Chr9:100349279 [GRCh38]
Chr9:103111561 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.2206G>A (p.Val736Ile) single nucleotide variant Inborn genetic diseases [RCV002812536] Chr9:100310376 [GRCh38]
Chr9:103072658 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.835A>G (p.Ile279Val) single nucleotide variant Inborn genetic diseases [RCV002961004] Chr9:100346752 [GRCh38]
Chr9:103109034 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.2031T>A (p.Asp677Glu) single nucleotide variant Inborn genetic diseases [RCV002668596] Chr9:100321720 [GRCh38]
Chr9:103084002 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.2677A>G (p.Thr893Ala) single nucleotide variant Inborn genetic diseases [RCV002936324] Chr9:100302304 [GRCh38]
Chr9:103064586 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.1265C>T (p.Thr422Ile) single nucleotide variant Inborn genetic diseases [RCV002855012] Chr9:100330155 [GRCh38]
Chr9:103092437 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.19C>T (p.Arg7Cys) single nucleotide variant Inborn genetic diseases [RCV002674516] Chr9:100349345 [GRCh38]
Chr9:103111627 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.2548A>G (p.Asn850Asp) single nucleotide variant Inborn genetic diseases [RCV002813260] Chr9:100303760 [GRCh38]
Chr9:103066042 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.394G>C (p.Glu132Gln) single nucleotide variant Inborn genetic diseases [RCV002657477] Chr9:100347193 [GRCh38]
Chr9:103109475 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.307G>A (p.Val103Met) single nucleotide variant Inborn genetic diseases [RCV003207567] Chr9:100347280 [GRCh38]
Chr9:103109562 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.1772G>A (p.Ser591Asn) single nucleotide variant Inborn genetic diseases [RCV003369985] Chr9:100327816 [GRCh38]
Chr9:103090098 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.1190G>A (p.Ser397Asn) single nucleotide variant Inborn genetic diseases [RCV003376003] Chr9:100340317 [GRCh38]
Chr9:103102599 [GRCh37]
Chr9:9q31.1		 uncertain significance
NM_017746.4(TEX10):c.796T>C (p.Phe266Leu) single nucleotide variant Inborn genetic diseases [RCV003366429] Chr9:100346791 [GRCh38]
Chr9:103109073 [GRCh37]
Chr9:9q31.1		 uncertain significance
Single allele deletion not provided [RCV003448676] Chr9:92679543..109378847 [GRCh37]
Chr9:9q22.2-31.2		 pathogenic
GRCh37/hg19 9q31.1-31.2(chr9:102606857-109839724)x1 copy number loss not specified [RCV003986787] Chr9:102606857..109839724 [GRCh37]
Chr9:9q31.1-31.2		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:468
Count of miRNA genes:336
Interacting mature miRNAs:358
Transcripts:ENST00000374902, ENST00000429235, ENST00000477648, ENST00000535814, ENST00000537512
Prediction methods: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
RH69417  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379103,107,480 - 103,107,609UniSTSGRCh37
Build 369102,147,301 - 102,147,430RGDNCBI36
Celera973,620,810 - 73,620,939RGD
Cytogenetic Map9q31.1UniSTS
HuRef972,706,521 - 72,706,650UniSTS
GeneMap99-GB4 RH Map9323.13UniSTS
NCBI RH Map9850.6UniSTS
RH69936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379103,065,614 - 103,065,757UniSTSGRCh37
Build 369102,105,435 - 102,105,578RGDNCBI36
Celera973,578,943 - 73,579,086RGD
Cytogenetic Map9q31.1UniSTS
HuRef972,664,655 - 72,664,797UniSTS
GeneMap99-GB4 RH Map9323.13UniSTS
NCBI RH Map9850.6UniSTS
D9S988E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379103,064,543 - 103,065,982UniSTSGRCh37
Build 369102,104,364 - 102,105,803RGDNCBI36
Celera973,577,872 - 73,579,311RGD
Cytogenetic Map9q31.1UniSTS
HuRef972,663,584 - 72,665,022UniSTS
RH12786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379103,069,532 - 103,069,665UniSTSGRCh37
Build 369102,109,353 - 102,109,486RGDNCBI36
Celera973,582,861 - 73,582,994RGD
Cytogenetic Map9q31.1UniSTS
HuRef972,668,573 - 72,668,706UniSTS
GeneMap99-GB4 RH Map9323.13UniSTS
NCBI RH Map9850.6UniSTS
SHGC-34139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379103,065,730 - 103,065,879UniSTSGRCh37
Build 369102,105,551 - 102,105,700RGDNCBI36
Celera973,579,059 - 73,579,208RGD
Cytogenetic Map9q31.1UniSTS
HuRef972,664,770 - 72,664,919UniSTS
Stanford-G3 RH Map93577.0UniSTS
GeneMap99-GB4 RH Map9323.23UniSTS
Whitehead-RH Map9369.4UniSTS
NCBI RH Map9859.9UniSTS
GeneMap99-G3 RH Map93475.0UniSTS
D9S1923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379103,069,462 - 103,069,659UniSTSGRCh37
Build 369102,109,283 - 102,109,480RGDNCBI36
Celera973,582,791 - 73,582,988RGD
Cytogenetic Map9q31.1UniSTS
HuRef972,668,503 - 72,668,700UniSTS
Whitehead-YAC Contig Map9 UniSTS
SHGC-31311  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379103,067,724 - 103,067,826UniSTSGRCh37
Build 369102,107,545 - 102,107,647RGDNCBI36
Celera973,581,053 - 73,581,155RGD
Cytogenetic Map9q31.1UniSTS
HuRef972,666,765 - 72,666,867UniSTS
GeneMap99-GB4 RH Map9322.83UniSTS
Whitehead-RH Map9367.5UniSTS
NCBI RH Map9842.0UniSTS
GeneMap99-G3 RH Map93414.0UniSTS
G20513  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379103,068,422 - 103,068,649UniSTSGRCh37
Build 369102,108,243 - 102,108,470RGDNCBI36
Celera973,581,751 - 73,581,978RGD
Cytogenetic Map9q31.1UniSTS
HuRef972,667,463 - 72,667,690UniSTS
A005U30  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379103,068,422 - 103,068,649UniSTSGRCh37
Build 369102,108,243 - 102,108,470RGDNCBI36
Celera973,581,751 - 73,581,978RGD
Cytogenetic Map9q31.1UniSTS
HuRef972,667,463 - 72,667,690UniSTS
GeneMap99-GB4 RH Map9323.03UniSTS
NCBI RH Map9854.7UniSTS


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 pharyngeal arch
High
Medium 694 294 862 57 970 45 2414 282 1309 138 1289 1175 27 563 1404 6 1
Low 1745 2667 864 567 955 420 1943 1911 2424 281 171 438 148 1 641 1384 1
Below cutoff 30 26 4 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001161584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_017746 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017014848 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363149 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363150 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363151 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001746327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_929813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA436854 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB060968 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ420436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK000294 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298916 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303662 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL353805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL445214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY598337 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC030652 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF981005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP336313 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000374902   ⟹   ENSP00000364037
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9100,302,084 - 100,352,942 (-)Ensembl
RefSeq Acc Id: ENST00000429235   ⟹   ENSP00000399872
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9100,329,186 - 100,347,304 (-)Ensembl
RefSeq Acc Id: ENST00000477648
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9100,302,086 - 100,307,869 (-)Ensembl
RefSeq Acc Id: ENST00000535814   ⟹   ENSP00000444555
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9100,302,077 - 100,352,571 (-)Ensembl
RefSeq Acc Id: NM_001161584   ⟹   NP_001155056
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389100,302,084 - 100,352,571 (-)NCBI
GRCh379103,064,357 - 103,115,856 (-)NCBI
Celera973,577,686 - 73,628,526 (-)RGD
HuRef972,663,398 - 72,714,298 (-)ENTREZGENE
CHM1_19103,210,798 - 103,261,301 (-)NCBI
T2T-CHM13v2.09112,473,720 - 112,524,207 (-)NCBI
Sequence:
RefSeq Acc Id: NM_017746   ⟹   NP_060216
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389100,302,084 - 100,352,942 (-)NCBI
GRCh379103,064,357 - 103,115,856 (-)NCBI
Build 369102,104,190 - 102,154,995 (-)NCBI Archive
Celera973,577,686 - 73,628,526 (-)RGD
HuRef972,663,398 - 72,714,298 (-)ENTREZGENE
CHM1_19103,210,798 - 103,261,707 (-)NCBI
T2T-CHM13v2.09112,473,720 - 112,524,578 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011518798   ⟹   XP_011517100
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389100,302,084 - 100,352,942 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047423523   ⟹   XP_047279479
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389100,303,639 - 100,352,942 (-)NCBI
RefSeq Acc Id: XM_047423524   ⟹   XP_047279480
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389100,321,683 - 100,352,942 (-)NCBI
RefSeq Acc Id: XM_054363149   ⟹   XP_054219124
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09112,473,720 - 112,524,578 (-)NCBI
RefSeq Acc Id: XM_054363150   ⟹   XP_054219125
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09112,475,277 - 112,524,578 (-)NCBI
RefSeq Acc Id: XM_054363151   ⟹   XP_054219126
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09112,493,322 - 112,524,578 (-)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_060216   ⟸   NM_017746
- Peptide Label: isoform 1
- UniProtKB: Q8NCN8 (UniProtKB/Swiss-Prot),   Q5T723 (UniProtKB/Swiss-Prot),   Q5T722 (UniProtKB/Swiss-Prot),   B4DYV2 (UniProtKB/Swiss-Prot),   Q8TDY0 (UniProtKB/Swiss-Prot),   Q9NXF1 (UniProtKB/Swiss-Prot),   B4DQR0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001155056   ⟸   NM_001161584
- Peptide Label: isoform 2
- UniProtKB: B4DQR0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011517100   ⟸   XM_011518798
- Peptide Label: isoform X1
- UniProtKB: B4DQR0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000364037   ⟸   ENST00000374902
RefSeq Acc Id: ENSP00000399872   ⟸   ENST00000429235
RefSeq Acc Id: ENSP00000444555   ⟸   ENST00000535814
RefSeq Acc Id: XP_047279479   ⟸   XM_047423523
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047279480   ⟸   XM_047423524
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054219124   ⟸   XM_054363149
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054219125   ⟸   XM_054363150
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054219126   ⟸   XM_054363151
- Peptide Label: isoform X3

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9NXF1-F1-model_v2 AlphaFold Q9NXF1 1-929 view protein structure

Promoters
RGD ID:7215671
Promoter ID:EPDNEW_H13582
Type:initiation region
Name:TEX10_1
Description:testis expressed 10
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
GRCh389100,352,925 - 100,352,985EPDNEW
RGD ID:6808296
Promoter ID:HG_KWN:64328
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Jurkat,   K562,   Lymphoblastoid
Transcripts:OTTHUMT00000053417
Position:
Human AssemblyChrPosition (strand)Source
Build 369102,105,741 - 102,110,877 (-)MPROMDB
RGD ID:6808373
Promoter ID:HG_KWN:64330
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001161584,   NM_017746,   UC004BAT.1,   UC004BAU.2,   UC004BAV.1
Position:
Human AssemblyChrPosition (strand)Source
Build 369102,154,421 - 102,155,977 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:25988 AgrOrtholog
COSMIC TEX10 COSMIC
Ensembl Genes ENSG00000136891 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000374902 ENTREZGENE
  ENST00000374902.9 UniProtKB/Swiss-Prot
  ENST00000429235.1 UniProtKB/TrEMBL
  ENST00000535814 ENTREZGENE
  ENST00000535814.5 UniProtKB/Swiss-Prot
Gene3D-CATH 1.25.10.10 UniProtKB/Swiss-Prot
GTEx ENSG00000136891 GTEx
HGNC ID HGNC:25988 ENTREZGENE
Human Proteome Map TEX10 Human Proteome Map
InterPro ARM-like UniProtKB/Swiss-Prot
  ARM-type_fold UniProtKB/Swiss-Prot
  HEAT_type_2 UniProtKB/Swiss-Prot
  Ipi1_N UniProtKB/Swiss-Prot
KEGG Report hsa:54881 UniProtKB/Swiss-Prot
NCBI Gene 54881 ENTREZGENE
OMIM 616717 OMIM
PANTHER PTHR16056:SF2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  REGULATOR OF MICROTUBULE DYNAMICS PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Ipi1_N UniProtKB/Swiss-Prot
PharmGKB PA134991964 PharmGKB
PROSITE HEAT_REPEAT UniProtKB/Swiss-Prot
Superfamily-SCOP SSF48371 UniProtKB/Swiss-Prot
UniProt A0A0A0MSR3_HUMAN UniProtKB/TrEMBL
  B4DQR0 ENTREZGENE, UniProtKB/TrEMBL
  B4DYV2 ENTREZGENE
  Q5T722 ENTREZGENE
  Q5T723 ENTREZGENE
  Q8NCN8 ENTREZGENE
  Q8TDY0 ENTREZGENE
  Q9NXF1 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B4DYV2 UniProtKB/Swiss-Prot
  Q5T722 UniProtKB/Swiss-Prot
  Q5T723 UniProtKB/Swiss-Prot
  Q8NCN8 UniProtKB/Swiss-Prot
  Q8TDY0 UniProtKB/Swiss-Prot