MIGA2 (mitoguardin 2) - Rat Genome Database

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Gene: MIGA2 (mitoguardin 2) Homo sapiens
Analyze
Symbol: MIGA2
Name: mitoguardin 2
RGD ID: 1322047
HGNC Page HGNC:23621
Description: Enables protein heterodimerization activity and protein homodimerization activity. Involved in mitochondrial fusion. Located in plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: C9orf54; FAM73B; family with sequence similarity 73 member B; family with sequence similarity 73, member B; FLJ00199; FLJ14596; hypothetical protein LOC84895; mitoguardin-2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh389129,036,626 - 129,072,082 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl9129,036,621 - 129,072,082 (+)EnsemblGRCh38hg38GRCh38
GRCh379131,798,905 - 131,834,361 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 369130,839,074 - 130,874,172 (+)NCBINCBI36Build 36hg18NCBI36
Build 349128,878,806 - 128,913,904NCBI
Celera9102,451,566 - 102,486,648 (+)NCBICelera
Cytogenetic Map9q34.11NCBI
HuRef9101,406,579 - 101,441,661 (+)NCBIHuRef
CHM1_19131,950,093 - 131,985,185 (+)NCBICHM1_1
T2T-CHM13v2.09141,240,095 - 141,275,546 (+)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
bone development  (IEA,ISO)
mitochondrial fusion  (IBA,IDA,IEA)

Cellular Component

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:8889548   PMID:12477932   PMID:14702039   PMID:16303743   PMID:21873635   PMID:22658674   PMID:26186194   PMID:26711011   PMID:26716412   PMID:28514442   PMID:32513696   PMID:32877691  
PMID:33124732   PMID:33499712   PMID:33961781   PMID:34079125   PMID:35271311  


Genomics

Comparative Map Data
MIGA2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh389129,036,626 - 129,072,082 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl9129,036,621 - 129,072,082 (+)EnsemblGRCh38hg38GRCh38
GRCh379131,798,905 - 131,834,361 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 369130,839,074 - 130,874,172 (+)NCBINCBI36Build 36hg18NCBI36
Build 349128,878,806 - 128,913,904NCBI
Celera9102,451,566 - 102,486,648 (+)NCBICelera
Cytogenetic Map9q34.11NCBI
HuRef9101,406,579 - 101,441,661 (+)NCBIHuRef
CHM1_19131,950,093 - 131,985,185 (+)NCBICHM1_1
T2T-CHM13v2.09141,240,095 - 141,275,546 (+)NCBIT2T-CHM13v2.0
Miga2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39230,254,232 - 30,275,532 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl230,254,245 - 30,275,533 (+)EnsemblGRCm39 Ensembl
GRCm38230,364,233 - 30,385,520 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl230,364,233 - 30,385,521 (+)EnsemblGRCm38mm10GRCm38
MGSCv37230,219,855 - 30,241,039 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36230,186,344 - 30,207,528 (+)NCBIMGSCv36mm8
Celera230,069,368 - 30,090,426 (+)NCBICelera
Cytogenetic Map2BNCBI
cM Map221.63NCBI
Miga2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8334,034,018 - 34,056,703 (+)NCBIGRCr8
mRatBN7.2313,636,235 - 13,658,895 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl313,636,238 - 13,658,896 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx316,707,761 - 16,730,411 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0325,292,727 - 25,315,377 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0323,538,481 - 23,561,132 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.038,928,484 - 8,951,189 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl38,928,534 - 8,951,189 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0314,281,269 - 14,303,963 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.439,408,140 - 9,430,785 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.139,408,013 - 9,429,645 (+)NCBI
Celera38,402,799 - 8,425,429 (+)NCBICelera
Cytogenetic Map3p12NCBI
Miga2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555701,387,013 - 1,402,996 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049555701,387,006 - 1,402,996 (+)NCBIChiLan1.0ChiLan1.0
MIGA2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21110,279,682 - 10,316,702 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1910,282,029 - 10,319,049 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v09100,160,068 - 100,197,095 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.19128,820,773 - 128,856,977 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl9128,820,773 - 128,856,977 (+)Ensemblpanpan1.1panPan2
MIGA2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1954,602,363 - 54,631,287 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl954,604,086 - 54,631,228 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha953,797,951 - 53,826,918 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0955,498,346 - 55,524,165 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl955,498,109 - 55,552,212 (-)EnsemblROS_Cfam_1.0 Ensembl
UNSW_CanFamBas_1.0954,596,516 - 54,625,519 (-)NCBIUNSW_CanFamBas_1.0
Miga2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947196,713,508 - 196,739,991 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648716,482,049 - 16,509,997 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648716,482,070 - 16,506,890 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MIGA2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1269,334,838 - 269,363,936 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11269,334,938 - 269,363,938 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21303,351,067 - 303,380,133 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MIGA2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1129,092,712 - 9,126,679 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666096432,196 - 467,610 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Miga2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247606,028,404 - 6,045,137 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247606,028,403 - 6,045,158 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MIGA2
10 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
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 9q33.2-34.3(chr9:121112395-138075224)x3 copy number gain See cases [RCV000051009] Chr9:121112395..138075224 [GRCh38]
Chr9:123874673..140969676 [GRCh37]
Chr9:122914494..140089497 [NCBI36]
Chr9:9q33.2-34.3		 pathogenic
GRCh38/hg38 9q33.2-34.3(chr9:122792658-138124532)x3 copy number gain See cases [RCV000051040] Chr9:122792658..138124532 [GRCh38]
Chr9:125554937..141018984 [GRCh37]
Chr9:124594758..140138805 [NCBI36]
Chr9:9q33.2-34.3		 pathogenic
GRCh38/hg38 9q33.3-34.11(chr9:125993583-129682375)x1 copy number loss See cases [RCV000052923] Chr9:125993583..129682375 [GRCh38]
Chr9:128755862..132444654 [GRCh37]
Chr9:127795683..131484475 [NCBI36]
Chr9:9q33.3-34.11		 pathogenic
GRCh38/hg38 9q34.11(chr9:127874581-130421811)x1 copy number loss See cases [RCV000052934] Chr9:127874581..130421811 [GRCh38]
Chr9:130636860..133297198 [GRCh37]
Chr9:129676681..132287019 [NCBI36]
Chr9:9q34.11		 pathogenic
GRCh38/hg38 9q34.11-34.3(chr9:129068560-136495351)x3 copy number gain See cases [RCV000053779] Chr9:129068560..136495351 [GRCh38]
Chr9:131830839..139389803 [GRCh37]
Chr9:130870660..138509624 [NCBI36]
Chr9:9q34.11-34.3		 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 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 9q33.2-34.3(chr9:121586837-138179445)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053776]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053776]|See cases [RCV000053776] Chr9:121586837..138179445 [GRCh38]
Chr9:124349116..141073897 [GRCh37]
Chr9:123388937..140193718 [NCBI36]
Chr9:9q33.2-34.3		 pathogenic
GRCh38/hg38 9q34.11(chr9:127919476-130079974)x3 copy number gain See cases [RCV000053777] Chr9:127919476..130079974 [GRCh38]
Chr9:130681755..132842253 [GRCh37]
Chr9:129721576..131882074 [NCBI36]
Chr9:9q34.11		 pathogenic
GRCh38/hg38 9q34.11(chr9:129036400-130578683)x3 copy number gain See cases [RCV000053778] Chr9:129036400..130578683 [GRCh38]
Chr9:131798679..133454070 [GRCh37]
Chr9:130838500..132443891 [NCBI36]
Chr9:9q34.11		 pathogenic
NM_032809.2(FAM73B):c.440C>T (p.Ser147Phe) single nucleotide variant Malignant melanoma [RCV000061895] Chr9:129049400 [GRCh38]
Chr9:131811679 [GRCh37]
Chr9:130851500 [NCBI36]
Chr9:9q34.11		 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 9q34.11-34.3(chr9:129068560-138179445)x3 copy number gain See cases [RCV000134916] Chr9:129068560..138179445 [GRCh38]
Chr9:131830839..141073897 [GRCh37]
Chr9:130870660..140193718 [NCBI36]
Chr9:9q34.11-34.3		 pathogenic
GRCh38/hg38 9q33.2-34.3(chr9:121073102-138179445)x3 copy number gain See cases [RCV000134920] Chr9:121073102..138179445 [GRCh38]
Chr9:123835380..141073897 [GRCh37]
Chr9:122875201..140193718 [NCBI36]
Chr9:9q33.2-34.3		 pathogenic
GRCh38/hg38 9q34.11(chr9:128610170-129368351)x1 copy number loss See cases [RCV000138126] Chr9:128610170..129368351 [GRCh38]
Chr9:131372449..132130630 [GRCh37]
Chr9:130412270..131170451 [NCBI36]
Chr9:9q34.11		 uncertain significance
GRCh38/hg38 9q34.11-34.12(chr9:128839676-130912873)x3 copy number gain See cases [RCV000137775] Chr9:128839676..130912873 [GRCh38]
Chr9:131601955..133788260 [GRCh37]
Chr9:130641776..132778081 [NCBI36]
Chr9:9q34.11-34.12		 uncertain significance
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 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 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(chr9:203861-138125937)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 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 9q33.3-34.3(chr9:128652785-141044751)x3 copy number gain See cases [RCV000447080] Chr9:128652785..141044751 [GRCh37]
Chr9:9q33.3-34.3		 pathogenic
GRCh37/hg19 9q34.11(chr9:130390139-132760275)x1 copy number loss See cases [RCV000445837] Chr9:130390139..132760275 [GRCh37]
Chr9:9q34.11		 pathogenic
GRCh37/hg19 9q33.2-34.3(chr9:124642754-141146461)x3 copy number gain See cases [RCV000448784] Chr9:124642754..141146461 [GRCh37]
Chr9:9q33.2-34.3		 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
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(chr9:10590-141122247)x3 copy number gain not provided [RCV000748055] Chr9:10590..141122247 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q33.3-34.12(chr9:129370440-133866894)x1 copy number loss not provided [RCV000748671] Chr9:129370440..133866894 [GRCh37]
Chr9:9q33.3-34.12		 pathogenic
GRCh37/hg19 9q34.11-34.12(chr9:131413885-133866894)x1 copy number loss not provided [RCV000748699] Chr9:131413885..133866894 [GRCh37]
Chr9:9q34.11-34.12		 benign
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 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 9q34.11-34.13(chr9:131670024-134514071) copy number loss not provided [RCV000767561] Chr9:131670024..134514071 [GRCh37]
Chr9:9q34.11-34.13		 likely 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
NM_001329990.2(MIGA2):c.609C>T (p.Ser203=) single nucleotide variant not provided [RCV000954419] Chr9:129049897 [GRCh38]
Chr9:131812176 [GRCh37]
Chr9:9q34.11		 benign
GRCh37/hg19 9q34.11(chr9:130957344-132310210)x1 copy number loss not provided [RCV001006274] Chr9:130957344..132310210 [GRCh37]
Chr9:9q34.11		 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
NM_001329990.2(MIGA2):c.633C>T (p.Asp211=) single nucleotide variant not provided [RCV000953611] Chr9:129049921 [GRCh38]
Chr9:131812200 [GRCh37]
Chr9:9q34.11		 benign
GRCh37/hg19 9q34.11(chr9:131094304-131863858)x3 copy number gain not provided [RCV001006275] Chr9:131094304..131863858 [GRCh37]
Chr9:9q34.11		 uncertain significance
GRCh37/hg19 9q34.11(chr9:130390139-132760275) copy number loss not specified [RCV002052848] Chr9:130390139..132760275 [GRCh37]
Chr9:9q34.11		 pathogenic
GRCh37/hg19 9q33.3-34.11(chr9:128523763-132604808)x3 copy number gain not provided [RCV001832977] Chr9:128523763..132604808 [GRCh37]
Chr9:9q33.3-34.11		 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
NC_000009.11:g.(?_131087402)_(141016451_?)dup duplication Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome [RCV003119700] Chr9:131087402..141016451 [GRCh37]
Chr9:9q34.11-34.3		 uncertain significance
NM_001329990.2(MIGA2):c.1675C>T (p.Arg559Cys) single nucleotide variant not specified [RCV004108375] Chr9:129070346 [GRCh38]
Chr9:131832625 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_001329990.2(MIGA2):c.859C>G (p.Leu287Val) single nucleotide variant not specified [RCV004088292] Chr9:129060615 [GRCh38]
Chr9:131822894 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_001329990.2(MIGA2):c.842C>T (p.Ala281Val) single nucleotide variant not specified [RCV004207220] Chr9:129060598 [GRCh38]
Chr9:131822877 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_001329990.2(MIGA2):c.1457T>C (p.Met486Thr) single nucleotide variant not specified [RCV004105611] Chr9:129069128 [GRCh38]
Chr9:131831407 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_001329990.2(MIGA2):c.205C>T (p.Arg69Trp) single nucleotide variant not specified [RCV004077320] Chr9:129042412 [GRCh38]
Chr9:131804691 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_001329990.2(MIGA2):c.26C>T (p.Thr9Met) single nucleotide variant not specified [RCV004081630] Chr9:129040620 [GRCh38]
Chr9:131802899 [GRCh37]
Chr9:9q34.11		 likely benign
NM_001329990.2(MIGA2):c.1321G>A (p.Ala441Thr) single nucleotide variant not specified [RCV004212248] Chr9:129068249 [GRCh38]
Chr9:131830528 [GRCh37]
Chr9:9q34.11		 uncertain significance
GRCh37/hg19 9q34.11-34.13(chr9:131815597-134209182)x1 copy number loss not specified [RCV003986823] Chr9:131815597..134209182 [GRCh37]
Chr9:9q34.11-34.13		 pathogenic
NM_001329990.2(MIGA2):c.727C>T (p.Arg243Cys) single nucleotide variant not specified [RCV004419856] Chr9:129059205 [GRCh38]
Chr9:131821484 [GRCh37]
Chr9:9q34.11		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:10158
Count of miRNA genes:1196
Interacting mature miRNAs:1567
Transcripts:ENST00000277475, ENST00000358369, ENST00000406926, ENST00000414342, ENST00000439290, ENST00000445183, ENST00000450073, ENST00000471943, ENST00000474534, ENST00000474639, ENST00000477088, ENST00000483458, ENST00000492279, ENST00000494608, ENST00000495975
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
D9S121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,801,431 - 131,801,566UniSTSGRCh37
Build 369130,841,252 - 130,841,387RGDNCBI36
Celera9102,453,743 - 102,453,878RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,408,751 - 101,408,882UniSTS
D9S986E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,834,183 - 131,834,274UniSTSGRCh37
Build 369130,874,004 - 130,874,095RGDNCBI36
Celera9102,486,480 - 102,486,571RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,441,493 - 101,441,584UniSTS
ECD01481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,822,744 - 131,823,607UniSTSGRCh37
Build 369130,862,565 - 130,863,428RGDNCBI36
Celera9102,475,041 - 102,475,904RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,430,058 - 101,430,921UniSTS
ECD01680  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,798,313 - 131,799,169UniSTSGRCh37
Build 369130,838,134 - 130,838,990RGDNCBI36
Celera9102,450,627 - 102,451,482RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,405,640 - 101,406,495UniSTS
ECD02541  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,799,282 - 131,800,108UniSTSGRCh37
Build 369130,839,103 - 130,839,929RGDNCBI36
Celera9102,451,595 - 102,452,421RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,406,608 - 101,407,434UniSTS
ECD03081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,821,757 - 131,822,563UniSTSGRCh37
Build 369130,861,578 - 130,862,384RGDNCBI36
Celera9102,474,054 - 102,474,860RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,429,071 - 101,429,877UniSTS
ECD04319  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,832,136 - 131,832,903UniSTSGRCh37
Build 369130,871,957 - 130,872,724RGDNCBI36
Celera9102,484,433 - 102,485,200RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,439,446 - 101,440,213UniSTS
ECD04458  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,802,344 - 131,803,107UniSTSGRCh37
Build 369130,842,165 - 130,842,928RGDNCBI36
Celera9102,454,652 - 102,455,415RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,409,656 - 101,410,419UniSTS
ECD04832  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,832,951 - 131,833,703UniSTSGRCh37
Build 369130,872,772 - 130,873,524RGDNCBI36
Celera9102,485,248 - 102,486,000RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,440,261 - 101,441,013UniSTS
ECD05953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,830,250 - 131,830,971UniSTSGRCh37
Build 369130,870,071 - 130,870,792RGDNCBI36
Celera9102,482,547 - 102,483,268RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,437,560 - 101,438,281UniSTS
ECD06139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,829,453 - 131,830,169UniSTSGRCh37
Build 369130,869,274 - 130,869,990RGDNCBI36
Celera9102,481,750 - 102,482,466RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,436,763 - 101,437,479UniSTS
ECD06745  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,833,823 - 131,834,523UniSTSGRCh37
Build 369130,873,644 - 130,874,344RGDNCBI36
Celera9102,486,120 - 102,486,820RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,441,133 - 101,441,833UniSTS
ECD07354  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,810,374 - 131,811,057UniSTSGRCh37
Build 369130,850,195 - 130,850,878RGDNCBI36
Celera9102,462,680 - 102,463,363RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,417,688 - 101,418,371UniSTS
ECD07810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,825,483 - 131,826,154UniSTSGRCh37
Build 369130,865,304 - 130,865,975RGDNCBI36
Celera9102,477,780 - 102,478,451RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,432,797 - 101,433,468UniSTS
ECD09903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,831,202 - 131,831,818UniSTSGRCh37
Build 369130,871,023 - 130,871,639RGDNCBI36
Celera9102,483,499 - 102,484,115RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,438,512 - 101,439,128UniSTS
ECD11584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,811,176 - 131,811,743UniSTSGRCh37
Build 369130,850,997 - 130,851,564RGDNCBI36
Celera9102,463,482 - 102,464,049RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,418,490 - 101,419,057UniSTS
ECD12695  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,811,764 - 131,812,300UniSTSGRCh37
Build 369130,851,585 - 130,852,121RGDNCBI36
Celera9102,464,070 - 102,464,606RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,419,078 - 101,419,614UniSTS
ECD13398  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,800,316 - 131,800,834UniSTSGRCh37
Build 369130,840,137 - 130,840,655RGDNCBI36
Celera9102,452,629 - 102,453,147RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,407,642 - 101,408,160UniSTS
ECD14969  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,804,291 - 131,804,772UniSTSGRCh37
Build 369130,844,112 - 130,844,593RGDNCBI36
Celera9102,456,599 - 102,457,080RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,411,603 - 101,412,084UniSTS
ECD16668  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,815,003 - 131,815,433UniSTSGRCh37
Build 369130,854,824 - 130,855,254RGDNCBI36
Celera9102,467,309 - 102,467,739RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,422,317 - 101,422,747UniSTS
ECD19293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,828,079 - 131,828,405UniSTSGRCh37
Build 369130,867,900 - 130,868,226RGDNCBI36
Celera9102,480,376 - 102,480,702RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,435,389 - 101,435,715UniSTS
ECD19467  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,821,330 - 131,821,650UniSTSGRCh37
Build 369130,861,151 - 130,861,471RGDNCBI36
Celera9102,473,627 - 102,473,947RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,428,644 - 101,428,964UniSTS
ECD22544  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,804,958 - 131,805,173UniSTSGRCh37
Build 369130,844,779 - 130,844,994RGDNCBI36
Celera9102,457,266 - 102,457,481RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,412,270 - 101,412,485UniSTS
ECD22824  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,803,938 - 131,804,144UniSTSGRCh37
Build 369130,843,759 - 130,843,965RGDNCBI36
Celera9102,456,246 - 102,456,452RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,411,250 - 101,411,456UniSTS
ECD23807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,806,661 - 131,806,836UniSTSGRCh37
Build 369130,846,482 - 130,846,657RGDNCBI36
Celera9102,458,969 - 102,459,144RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,413,973 - 101,414,148UniSTS
ECD23926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,823,662 - 131,823,830UniSTSGRCh37
Build 369130,863,483 - 130,863,651RGDNCBI36
Celera9102,475,959 - 102,476,127RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,430,976 - 101,431,144UniSTS
REN36370  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,834,517 - 131,834,749UniSTSGRCh37
Build 369130,874,338 - 130,874,570RGDNCBI36
Celera9102,486,814 - 102,487,046RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,441,827 - 101,442,059UniSTS
REN36371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,834,288 - 131,834,528UniSTSGRCh37
Build 369130,874,109 - 130,874,349RGDNCBI36
Celera9102,486,585 - 102,486,825RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,441,598 - 101,441,838UniSTS
REN36372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,834,063 - 131,834,312UniSTSGRCh37
Build 369130,873,884 - 130,874,133RGDNCBI36
Celera9102,486,360 - 102,486,609RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,441,373 - 101,441,622UniSTS
REN36373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,833,859 - 131,834,085UniSTSGRCh37
GRCh379131,833,859 - 131,834,023UniSTSGRCh37
Build 369130,873,680 - 130,873,844RGDNCBI36
Celera9102,486,156 - 102,486,382UniSTS
Celera9102,486,156 - 102,486,320RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,441,169 - 101,441,333UniSTS
HuRef9101,441,169 - 101,441,395UniSTS
REN36374  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,833,584 - 131,833,837UniSTSGRCh37
Build 369130,873,405 - 130,873,658RGDNCBI36
Celera9102,485,881 - 102,486,134RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,440,894 - 101,441,147UniSTS
REN36375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,833,352 - 131,833,600UniSTSGRCh37
Build 369130,873,173 - 130,873,421RGDNCBI36
Celera9102,485,649 - 102,485,897RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,440,662 - 101,440,910UniSTS
REN36376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,833,102 - 131,833,350UniSTSGRCh37
Build 369130,872,923 - 130,873,171RGDNCBI36
Celera9102,485,399 - 102,485,647RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,440,412 - 101,440,660UniSTS
REN36377  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,832,875 - 131,833,111UniSTSGRCh37
Build 369130,872,696 - 130,872,932RGDNCBI36
Celera9102,485,172 - 102,485,408RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,440,185 - 101,440,421UniSTS
REN36378  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,832,633 - 131,832,862UniSTSGRCh37
Build 369130,872,454 - 130,872,683RGDNCBI36
Celera9102,484,930 - 102,485,159RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,439,943 - 101,440,172UniSTS
REN36379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,832,374 - 131,832,620UniSTSGRCh37
Build 369130,872,195 - 130,872,441RGDNCBI36
Celera9102,484,671 - 102,484,917RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,439,684 - 101,439,930UniSTS
REN36380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,832,173 - 131,832,398UniSTSGRCh37
Build 369130,871,994 - 130,872,219RGDNCBI36
Celera9102,484,470 - 102,484,695RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,439,483 - 101,439,708UniSTS
REN36381  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,831,957 - 131,832,193UniSTSGRCh37
Build 369130,871,778 - 130,872,014RGDNCBI36
Celera9102,484,254 - 102,484,490RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,439,267 - 101,439,503UniSTS
REN36382  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,831,757 - 131,831,981UniSTSGRCh37
Build 369130,871,578 - 130,871,802RGDNCBI36
Celera9102,484,054 - 102,484,278RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,439,067 - 101,439,291UniSTS
REN36383  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,831,504 - 131,831,748UniSTSGRCh37
Build 369130,871,325 - 130,871,569RGDNCBI36
Celera9102,483,801 - 102,484,045RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,438,814 - 101,439,058UniSTS
REN36384  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,831,263 - 131,831,515UniSTSGRCh37
Build 369130,871,084 - 130,871,336RGDNCBI36
Celera9102,483,560 - 102,483,812RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,438,573 - 101,438,825UniSTS
REN36385  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,831,032 - 131,831,268UniSTSGRCh37
Build 369130,870,853 - 130,871,089RGDNCBI36
Celera9102,483,329 - 102,483,565RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,438,342 - 101,438,578UniSTS
REN36386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,830,823 - 131,831,053UniSTSGRCh37
Build 369130,870,644 - 130,870,874RGDNCBI36
Celera9102,483,120 - 102,483,350RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,438,133 - 101,438,363UniSTS
REN36387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,830,590 - 131,830,828UniSTSGRCh37
Build 369130,870,411 - 130,870,649RGDNCBI36
Celera9102,482,887 - 102,483,125RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,437,900 - 101,438,138UniSTS
REN36388  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,830,384 - 131,830,612UniSTSGRCh37
Build 369130,870,205 - 130,870,433RGDNCBI36
Celera9102,482,681 - 102,482,909RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,437,694 - 101,437,922UniSTS
REN36389  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,830,118 - 131,830,362UniSTSGRCh37
Build 369130,869,939 - 130,870,183RGDNCBI36
Celera9102,482,415 - 102,482,659RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,437,428 - 101,437,672UniSTS
REN36390  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,829,894 - 131,830,137UniSTSGRCh37
Build 369130,869,715 - 130,869,958RGDNCBI36
Celera9102,482,191 - 102,482,434RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,437,204 - 101,437,447UniSTS
REN36391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,829,658 - 131,829,907UniSTSGRCh37
Build 369130,869,479 - 130,869,728RGDNCBI36
Celera9102,481,955 - 102,482,204RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,436,968 - 101,437,217UniSTS
REN36392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,829,439 - 131,829,665UniSTSGRCh37
Build 369130,869,260 - 130,869,486RGDNCBI36
Celera9102,481,736 - 102,481,962RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,436,749 - 101,436,975UniSTS
REN36393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,828,385 - 131,828,649UniSTSGRCh37
Build 369130,868,206 - 130,868,470RGDNCBI36
Celera9102,480,682 - 102,480,946RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,435,695 - 101,435,959UniSTS
REN36394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,828,159 - 131,828,404UniSTSGRCh37
Build 369130,867,980 - 130,868,225RGDNCBI36
Celera9102,480,456 - 102,480,701RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,435,469 - 101,435,714UniSTS
REN36395  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,827,943 - 131,828,180UniSTSGRCh37
Build 369130,867,764 - 130,868,001RGDNCBI36
Celera9102,480,240 - 102,480,477RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,435,253 - 101,435,490UniSTS
REN36396  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,827,688 - 131,827,961UniSTSGRCh37
Build 369130,867,509 - 130,867,782RGDNCBI36
Celera9102,479,985 - 102,480,258RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,434,998 - 101,435,271UniSTS
REN36397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,827,016 - 131,827,286UniSTSGRCh37
Build 369130,866,837 - 130,867,107RGDNCBI36
Celera9102,479,313 - 102,479,583RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,434,326 - 101,434,596UniSTS
REN36398  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,826,810 - 131,827,040UniSTSGRCh37
Build 369130,866,631 - 130,866,861RGDNCBI36
Celera9102,479,107 - 102,479,337RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,434,120 - 101,434,350UniSTS
REN36399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,826,215 - 131,826,452UniSTSGRCh37
Build 369130,866,036 - 130,866,273RGDNCBI36
Celera9102,478,512 - 102,478,749RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,433,529 - 101,433,766UniSTS
REN36400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,825,970 - 131,826,210UniSTSGRCh37
Build 369130,865,791 - 130,866,031RGDNCBI36
Celera9102,478,267 - 102,478,507RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,433,284 - 101,433,524UniSTS
REN36401  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,825,732 - 131,825,967UniSTSGRCh37
Build 369130,865,553 - 130,865,788RGDNCBI36
Celera9102,478,029 - 102,478,264RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,433,046 - 101,433,281UniSTS
REN36402  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,825,530 - 131,825,755UniSTSGRCh37
Build 369130,865,351 - 130,865,576RGDNCBI36
Celera9102,477,827 - 102,478,052RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,432,844 - 101,433,069UniSTS
REN36403  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,825,260 - 131,825,505UniSTSGRCh37
Build 369130,865,081 - 130,865,326RGDNCBI36
Celera9102,477,557 - 102,477,802RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,432,574 - 101,432,819UniSTS
REN36404  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,824,983 - 131,825,212UniSTSGRCh37
Build 369130,864,804 - 130,865,033RGDNCBI36
Celera9102,477,280 - 102,477,509RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,432,297 - 101,432,526UniSTS
REN36405  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,823,993 - 131,824,219UniSTSGRCh37
Build 369130,863,814 - 130,864,040RGDNCBI36
Celera9102,476,290 - 102,476,516RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,431,307 - 101,431,533UniSTS
REN36406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,823,755 - 131,824,011UniSTSGRCh37
Build 369130,863,576 - 130,863,832RGDNCBI36
Celera9102,476,052 - 102,476,308RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,431,069 - 101,431,325UniSTS
REN36407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,823,533 - 131,823,775UniSTSGRCh37
Build 369130,863,354 - 130,863,596RGDNCBI36
Celera9102,475,830 - 102,476,072RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,430,847 - 101,431,089UniSTS
REN36408  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,823,328 - 131,823,552UniSTSGRCh37
Build 369130,863,149 - 130,863,373RGDNCBI36
Celera9102,475,625 - 102,475,849RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,430,642 - 101,430,866UniSTS
REN36409  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,823,107 - 131,823,350UniSTSGRCh37
Build 369130,862,928 - 130,863,171RGDNCBI36
Celera9102,475,404 - 102,475,647RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,430,421 - 101,430,664UniSTS
REN36410  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,822,896 - 131,823,128UniSTSGRCh37
Build 369130,862,717 - 130,862,949RGDNCBI36
Celera9102,475,193 - 102,475,425RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,430,210 - 101,430,442UniSTS
REN36411  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,822,685 - 131,822,920UniSTSGRCh37
Build 369130,862,506 - 130,862,741RGDNCBI36
Celera9102,474,982 - 102,475,217RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,429,999 - 101,430,234UniSTS
REN36412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,822,439 - 131,822,696UniSTSGRCh37
Build 369130,862,260 - 130,862,517RGDNCBI36
Celera9102,474,736 - 102,474,993RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,429,753 - 101,430,010UniSTS
REN36413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,822,216 - 131,822,451UniSTSGRCh37
Build 369130,862,037 - 130,862,272RGDNCBI36
Celera9102,474,513 - 102,474,748RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,429,530 - 101,429,765UniSTS
REN36414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,821,980 - 131,822,209UniSTSGRCh37
Build 369130,861,801 - 130,862,030RGDNCBI36
Celera9102,474,277 - 102,474,506RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,429,294 - 101,429,523UniSTS
REN36415  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,821,714 - 131,821,959UniSTSGRCh37
Build 369130,861,535 - 130,861,780RGDNCBI36
Celera9102,474,011 - 102,474,256RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,429,028 - 101,429,273UniSTS
REN36416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,821,503 - 131,821,737UniSTSGRCh37
Build 369130,861,324 - 130,861,558RGDNCBI36
Celera9102,473,800 - 102,474,034RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,428,817 - 101,429,051UniSTS
REN36417  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,821,280 - 131,821,523UniSTSGRCh37
Build 369130,861,101 - 130,861,344RGDNCBI36
Celera9102,473,577 - 102,473,820RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,428,594 - 101,428,837UniSTS
REN36418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,821,064 - 131,821,291UniSTSGRCh37
Build 369130,860,885 - 130,861,112RGDNCBI36
Celera9102,473,361 - 102,473,588RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,428,378 - 101,428,605UniSTS
REN36419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,820,494 - 131,820,733UniSTSGRCh37
Build 369130,860,315 - 130,860,554RGDNCBI36
Celera9102,472,791 - 102,473,030RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,427,808 - 101,428,047UniSTS
REN36420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,820,217 - 131,820,478UniSTSGRCh37
Build 369130,860,038 - 130,860,299RGDNCBI36
Celera9102,472,514 - 102,472,775RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,427,531 - 101,427,792UniSTS
REN36421  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,819,864 - 131,820,094UniSTSGRCh37
Build 369130,859,685 - 130,859,915RGDNCBI36
Celera9102,472,161 - 102,472,391RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,427,178 - 101,427,408UniSTS
REN36422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,819,409 - 131,819,649UniSTSGRCh37
Build 369130,859,230 - 130,859,470RGDNCBI36
Celera9102,471,706 - 102,471,946RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,426,723 - 101,426,963UniSTS
REN36423  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,819,174 - 131,819,411UniSTSGRCh37
Build 369130,858,995 - 130,859,232RGDNCBI36
Celera9102,471,471 - 102,471,708RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,426,488 - 101,426,725UniSTS
REN36424  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,818,755 - 131,819,012UniSTSGRCh37
Build 369130,858,576 - 130,858,833RGDNCBI36
Celera9102,471,052 - 102,471,309RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,426,069 - 101,426,326UniSTS
REN36425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,818,484 - 131,818,733UniSTSGRCh37
Build 369130,858,305 - 130,858,554RGDNCBI36
Celera9102,470,781 - 102,471,030RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,425,798 - 101,426,047UniSTS
REN36426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,818,278 - 131,818,503UniSTSGRCh37
Build 369130,858,099 - 130,858,324RGDNCBI36
Celera9102,470,575 - 102,470,800RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,425,592 - 101,425,817UniSTS
REN36427  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,817,549 - 131,817,773UniSTSGRCh37
Build 369130,857,370 - 130,857,594RGDNCBI36
Celera9102,469,846 - 102,470,070RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,424,863 - 101,425,087UniSTS
REN36428  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,816,784 - 131,817,008UniSTSGRCh37
Build 369130,856,605 - 130,856,829RGDNCBI36
Celera9102,469,090 - 102,469,314RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,424,098 - 101,424,322UniSTS
REN36429  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,816,498 - 131,816,733UniSTSGRCh37
Build 369130,856,319 - 130,856,554RGDNCBI36
Celera9102,468,804 - 102,469,039RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,423,812 - 101,424,047UniSTS
REN36430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,816,181 - 131,816,423UniSTSGRCh37
Build 369130,856,002 - 130,856,244RGDNCBI36
Celera9102,468,487 - 102,468,729RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,423,495 - 101,423,737UniSTS
REN36431  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,815,540 - 131,815,791UniSTSGRCh37
Build 369130,855,361 - 130,855,612RGDNCBI36
Celera9102,467,846 - 102,468,097RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,422,854 - 101,423,105UniSTS
REN36432  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,815,194 - 131,815,423UniSTSGRCh37
Build 369130,855,015 - 130,855,244RGDNCBI36
Celera9102,467,500 - 102,467,729RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,422,508 - 101,422,737UniSTS
REN36433  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,814,933 - 131,815,185UniSTSGRCh37
Build 369130,854,754 - 130,855,006RGDNCBI36
Celera9102,467,239 - 102,467,491RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,422,247 - 101,422,499UniSTS
REN36434  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,814,729 - 131,814,955UniSTSGRCh37
Build 369130,854,550 - 130,854,776RGDNCBI36
Celera9102,467,035 - 102,467,261RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,422,043 - 101,422,269UniSTS
REN36435  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,814,522 - 131,814,746UniSTSGRCh37
Build 369130,854,343 - 130,854,567RGDNCBI36
Celera9102,466,828 - 102,467,052RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,421,836 - 101,422,060UniSTS
REN36436  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,812,701 - 131,812,932UniSTSGRCh37
Build 369130,852,522 - 130,852,753RGDNCBI36
Celera9102,465,007 - 102,465,238RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,420,015 - 101,420,246UniSTS
REN36437  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,812,133 - 131,812,372UniSTSGRCh37
Build 369130,851,954 - 130,852,193RGDNCBI36
Celera9102,464,439 - 102,464,678RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,419,447 - 101,419,686UniSTS
REN36438  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,811,902 - 131,812,135UniSTSGRCh37
Build 369130,851,723 - 130,851,956RGDNCBI36
Celera9102,464,208 - 102,464,441RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,419,216 - 101,419,449UniSTS
REN36439  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,811,660 - 131,811,925UniSTSGRCh37
Build 369130,851,481 - 130,851,746RGDNCBI36
Celera9102,463,966 - 102,464,231RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,418,974 - 101,419,239UniSTS
REN36440  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,811,446 - 131,811,679UniSTSGRCh37
Build 369130,851,267 - 130,851,500RGDNCBI36
Celera9102,463,752 - 102,463,985RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,418,760 - 101,418,993UniSTS
REN36441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,811,181 - 131,811,452UniSTSGRCh37
Build 369130,851,002 - 130,851,273RGDNCBI36
Celera9102,463,487 - 102,463,758RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,418,495 - 101,418,766UniSTS
REN36442  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,810,973 - 131,811,204UniSTSGRCh37
Build 369130,850,794 - 130,851,025RGDNCBI36
Celera9102,463,279 - 102,463,510RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,418,287 - 101,418,518UniSTS
REN36443  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,810,760 - 131,810,991UniSTSGRCh37
Build 369130,850,581 - 130,850,812RGDNCBI36
Celera9102,463,066 - 102,463,297RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,418,074 - 101,418,305UniSTS
REN36444  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,810,536 - 131,810,784UniSTSGRCh37
Build 369130,850,357 - 130,850,605RGDNCBI36
Celera9102,462,842 - 102,463,090RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,417,850 - 101,418,098UniSTS
REN36445  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,810,328 - 131,810,558UniSTSGRCh37
Build 369130,850,149 - 130,850,379RGDNCBI36
Celera9102,462,634 - 102,462,864RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,417,642 - 101,417,872UniSTS
REN36446  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,809,348 - 131,809,597UniSTSGRCh37
Build 369130,849,169 - 130,849,418RGDNCBI36
Celera9102,461,654 - 102,461,903RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,416,662 - 101,416,911UniSTS
REN36447  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,808,629 - 131,808,885UniSTSGRCh37
Build 369130,848,450 - 130,848,706RGDNCBI36
Celera9102,460,935 - 102,461,191RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,415,943 - 101,416,199UniSTS
REN36448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,808,352 - 131,808,576UniSTSGRCh37
Build 369130,848,173 - 130,848,397RGDNCBI36
Celera9102,460,658 - 102,460,882RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,415,666 - 101,415,890UniSTS
REN36449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,807,805 - 131,808,058UniSTSGRCh37
Build 369130,847,626 - 130,847,879RGDNCBI36
Celera9102,460,111 - 102,460,364RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,415,119 - 101,415,372UniSTS
REN36450  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,806,562 - 131,806,798UniSTSGRCh37
Build 369130,846,383 - 130,846,619RGDNCBI36
Celera9102,458,870 - 102,459,106RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,413,874 - 101,414,110UniSTS
REN36451  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,805,495 - 131,805,724UniSTSGRCh37
Build 369130,845,316 - 130,845,545RGDNCBI36
Celera9102,457,803 - 102,458,032RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,412,807 - 101,413,036UniSTS
REN36452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,805,265 - 131,805,518UniSTSGRCh37
Build 369130,845,086 - 130,845,339RGDNCBI36
Celera9102,457,573 - 102,457,826RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,412,577 - 101,412,830UniSTS
REN36453  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,804,920 - 131,805,174UniSTSGRCh37
Build 369130,844,741 - 130,844,995RGDNCBI36
Celera9102,457,228 - 102,457,482RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,412,232 - 101,412,486UniSTS
REN36454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,804,694 - 131,804,929UniSTSGRCh37
Build 369130,844,515 - 130,844,750RGDNCBI36
Celera9102,457,002 - 102,457,237RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,412,006 - 101,412,241UniSTS
REN36455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,804,444 - 131,804,716UniSTSGRCh37
Build 369130,844,265 - 130,844,537RGDNCBI36
Celera9102,456,752 - 102,457,024RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,411,756 - 101,412,028UniSTS
REN36456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,804,231 - 131,804,468UniSTSGRCh37
Build 369130,844,052 - 130,844,289RGDNCBI36
Celera9102,456,539 - 102,456,776RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,411,543 - 101,411,780UniSTS
REN36457  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,804,013 - 131,804,255UniSTSGRCh37
Build 369130,843,834 - 130,844,076RGDNCBI36
Celera9102,456,321 - 102,456,563RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,411,325 - 101,411,567UniSTS
REN36458  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,803,787 - 131,804,011UniSTSGRCh37
Build 369130,843,608 - 130,843,832RGDNCBI36
Celera9102,456,095 - 102,456,319RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,411,099 - 101,411,323UniSTS
REN36459  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,802,814 - 131,803,081UniSTSGRCh37
Build 369130,842,635 - 130,842,902RGDNCBI36
Celera9102,455,122 - 102,455,389RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,410,126 - 101,410,393UniSTS
REN36460  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,802,612 - 131,802,838UniSTSGRCh37
Build 369130,842,433 - 130,842,659RGDNCBI36
Celera9102,454,920 - 102,455,146RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,409,924 - 101,410,150UniSTS
REN36461  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,802,396 - 131,802,636UniSTSGRCh37
Build 369130,842,217 - 130,842,457RGDNCBI36
Celera9102,454,704 - 102,454,944RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,409,708 - 101,409,948UniSTS
REN36462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,802,121 - 131,802,350UniSTSGRCh37
Build 369130,841,942 - 130,842,171RGDNCBI36
Celera9102,454,429 - 102,454,658RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,409,433 - 101,409,662UniSTS
REN36463  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,801,413 - 131,801,667UniSTSGRCh37
Build 369130,841,234 - 130,841,488RGDNCBI36
Celera9102,453,725 - 102,453,979RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,408,733 - 101,408,983UniSTS
REN36464  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,800,750 - 131,800,994UniSTSGRCh37
Build 369130,840,571 - 130,840,815RGDNCBI36
Celera9102,453,063 - 102,453,307RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,408,076 - 101,408,320UniSTS
REN36465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,800,541 - 131,800,768UniSTSGRCh37
Build 369130,840,362 - 130,840,589RGDNCBI36
Celera9102,452,854 - 102,453,081RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,407,867 - 101,408,094UniSTS
REN36466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,800,323 - 131,800,551UniSTSGRCh37
Build 369130,840,144 - 130,840,372RGDNCBI36
Celera9102,452,636 - 102,452,864RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,407,649 - 101,407,877UniSTS
REN36467  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,800,064 - 131,800,308UniSTSGRCh37
Build 369130,839,885 - 130,840,129RGDNCBI36
Celera9102,452,377 - 102,452,621RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,407,390 - 101,407,634UniSTS
REN36468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,799,828 - 131,800,062UniSTSGRCh37
Build 369130,839,649 - 130,839,883RGDNCBI36
Celera9102,452,141 - 102,452,375RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,407,154 - 101,407,388UniSTS
REN36469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,799,609 - 131,799,850UniSTSGRCh37
Build 369130,839,430 - 130,839,671RGDNCBI36
Celera9102,451,922 - 102,452,163RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,406,935 - 101,407,176UniSTS
REN36470  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,799,369 - 131,799,604UniSTSGRCh37
Build 369130,839,190 - 130,839,425RGDNCBI36
Celera9102,451,682 - 102,451,917RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,406,695 - 101,406,930UniSTS
REN36471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,799,143 - 131,799,392UniSTSGRCh37
Build 369130,838,964 - 130,839,213RGDNCBI36
Celera9102,451,456 - 102,451,705RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,406,469 - 101,406,718UniSTS
REN36472  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,798,925 - 131,799,167UniSTSGRCh37
Build 369130,838,746 - 130,838,988RGDNCBI36
Celera9102,451,238 - 102,451,480RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,406,251 - 101,406,493UniSTS
REN36473  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,798,697 - 131,798,939UniSTSGRCh37
Build 369130,838,518 - 130,838,760RGDNCBI36
Celera9102,451,011 - 102,451,252RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,406,024 - 101,406,265UniSTS
REN36474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,798,455 - 131,798,710UniSTSGRCh37
Build 369130,838,276 - 130,838,531RGDNCBI36
Celera9102,450,769 - 102,451,024RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,405,782 - 101,406,037UniSTS
REN36475  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,798,252 - 131,798,479UniSTSGRCh37
Build 369130,838,073 - 130,838,300RGDNCBI36
Celera9102,450,566 - 102,450,793RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,405,579 - 101,405,806UniSTS
REN36476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,797,996 - 131,798,270UniSTSGRCh37
Build 369130,837,817 - 130,838,091RGDNCBI36
Celera9102,450,310 - 102,450,584RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,405,323 - 101,405,597UniSTS
REN36477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,797,795 - 131,798,020UniSTSGRCh37
Build 369130,837,616 - 130,837,841RGDNCBI36
Celera9102,450,109 - 102,450,334RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,405,122 - 101,405,347UniSTS
REN36478  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,797,366 - 131,797,613UniSTSGRCh37
Build 369130,837,187 - 130,837,434RGDNCBI36
Celera9102,449,680 - 102,449,927RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,404,693 - 101,404,940UniSTS
A008L12  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,834,236 - 131,834,340UniSTSGRCh37
Build 369130,874,057 - 130,874,161RGDNCBI36
Celera9102,486,533 - 102,486,637RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,441,546 - 101,441,650UniSTS
GeneMap99-GB4 RH Map9395.69UniSTS
NCBI RH Map91167.2UniSTS
stSG628145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,797,858 - 131,799,076UniSTSGRCh37
Build 369130,837,679 - 130,838,897RGDNCBI36
Celera9102,450,172 - 102,451,389RGD
HuRef9101,405,185 - 101,406,402UniSTS
stSG628146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,799,057 - 131,800,243UniSTSGRCh37
Build 369130,838,878 - 130,840,064RGDNCBI36
Celera9102,451,370 - 102,452,556RGD
HuRef9101,406,383 - 101,407,569UniSTS
stSG628147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,800,233 - 131,801,383UniSTSGRCh37
Build 369130,840,054 - 130,841,204RGDNCBI36
Celera9102,452,546 - 102,453,695RGD
HuRef9101,407,559 - 101,408,703UniSTS
stSG628149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,802,402 - 131,802,743UniSTSGRCh37
Build 369130,842,223 - 130,842,564RGDNCBI36
Celera9102,454,710 - 102,455,051RGD
HuRef9101,409,714 - 101,410,055UniSTS
stSG628150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,802,744 - 131,803,966UniSTSGRCh37
Build 369130,842,565 - 130,843,787RGDNCBI36
Celera9102,455,052 - 102,456,274RGD
HuRef9101,410,056 - 101,411,278UniSTS
stSG628151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,803,963 - 131,805,173UniSTSGRCh37
Build 369130,843,784 - 130,844,994RGDNCBI36
Celera9102,456,271 - 102,457,481RGD
HuRef9101,411,275 - 101,412,485UniSTS
stSG628152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,805,492 - 131,806,673UniSTSGRCh37
Build 369130,845,313 - 130,846,494RGDNCBI36
Celera9102,457,800 - 102,458,981RGD
HuRef9101,412,804 - 101,413,985UniSTS
stSG628153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,806,655 - 131,806,834UniSTSGRCh37
Build 369130,846,476 - 130,846,655RGDNCBI36
Celera9102,458,963 - 102,459,142RGD
HuRef9101,413,967 - 101,414,146UniSTS
stSG628155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,810,330 - 131,811,466UniSTSGRCh37
Build 369130,850,151 - 130,851,287RGDNCBI36
Celera9102,462,636 - 102,463,772RGD
HuRef9101,417,644 - 101,418,780UniSTS
stSG628156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,811,447 - 131,812,458UniSTSGRCh37
Build 369130,851,268 - 130,852,279RGDNCBI36
Celera9102,463,753 - 102,464,764RGD
HuRef9101,418,761 - 101,419,772UniSTS
stSG628157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,812,439 - 131,813,517UniSTSGRCh37
Build 369130,852,260 - 130,853,338RGDNCBI36
Celera9102,464,745 - 102,465,823RGD
HuRef9101,419,753 - 101,420,831UniSTS
stSG628158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,814,720 - 131,815,019UniSTSGRCh37
Build 369130,854,541 - 130,854,840RGDNCBI36
Celera9102,467,026 - 102,467,325RGD
HuRef9101,422,034 - 101,422,333UniSTS
stSG628159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,815,020 - 131,815,608UniSTSGRCh37
Build 369130,854,841 - 130,855,429RGDNCBI36
Celera9102,467,326 - 102,467,914RGD
HuRef9101,422,334 - 101,422,922UniSTS
stSG628160  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,820,731 - 131,821,807UniSTSGRCh37
Build 369130,860,552 - 130,861,628RGDNCBI36
Celera9102,473,028 - 102,474,104RGD
HuRef9101,428,045 - 101,429,121UniSTS
stSG628161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,821,864 - 131,822,906UniSTSGRCh37
Build 369130,861,685 - 130,862,727RGDNCBI36
Celera9102,474,161 - 102,475,203RGD
HuRef9101,429,178 - 101,430,220UniSTS
stSG628162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,822,887 - 131,824,086UniSTSGRCh37
Build 369130,862,708 - 130,863,907RGDNCBI36
Celera9102,475,184 - 102,476,383RGD
HuRef9101,430,201 - 101,431,400UniSTS
stSG628163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,824,101 - 131,825,212UniSTSGRCh37
Build 369130,863,922 - 130,865,033RGDNCBI36
Celera9102,476,398 - 102,477,509RGD
HuRef9101,431,415 - 101,432,526UniSTS
stSG628164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,825,146 - 131,826,153UniSTSGRCh37
Build 369130,864,967 - 130,865,974RGDNCBI36
Celera9102,477,443 - 102,478,450RGD
HuRef9101,432,460 - 101,433,467UniSTS
stSG628165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,825,945 - 131,826,969UniSTSGRCh37
Build 369130,865,766 - 130,866,790RGDNCBI36
Celera9102,478,242 - 102,479,266RGD
HuRef9101,433,259 - 101,434,279UniSTS
stSG628166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,826,950 - 131,828,118UniSTSGRCh37
Build 369130,866,771 - 130,867,939RGDNCBI36
Celera9102,479,247 - 102,480,415RGD
HuRef9101,434,260 - 101,435,428UniSTS
stSG628167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,828,100 - 131,829,531UniSTSGRCh37
Build 369130,867,921 - 130,869,352RGDNCBI36
Celera9102,480,397 - 102,481,828RGD
HuRef9101,435,410 - 101,436,841UniSTS
stSG628168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,829,512 - 131,829,730UniSTSGRCh37
Build 369130,869,333 - 130,869,551RGDNCBI36
Celera9102,481,809 - 102,482,027RGD
HuRef9101,436,822 - 101,437,040UniSTS
stSG628169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,829,748 - 131,830,971UniSTSGRCh37
Build 369130,869,569 - 130,870,792RGDNCBI36
Celera9102,482,045 - 102,483,268RGD
HuRef9101,437,058 - 101,438,281UniSTS
stSG628170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,830,952 - 131,832,151UniSTSGRCh37
Build 369130,870,773 - 130,871,972RGDNCBI36
Celera9102,483,249 - 102,484,448RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,438,262 - 101,439,461UniSTS
stSG628171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,832,132 - 131,833,134UniSTSGRCh37
Build 369130,871,953 - 130,872,955RGDNCBI36
Celera9102,484,429 - 102,485,431RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,439,442 - 101,440,444UniSTS
stSG628172  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,833,285 - 131,834,393UniSTSGRCh37
Build 369130,873,106 - 130,874,214RGDNCBI36
Celera9102,485,582 - 102,486,690RGD
HuRef9101,440,595 - 101,441,703UniSTS
RH125103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,830,498 - 131,831,392UniSTSGRCh37
Celera9102,482,795 - 102,483,689UniSTS
HuRef9101,437,808 - 101,438,702UniSTS


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 2388 2458 1378 288 1435 129 3590 1428 2811 206 1375 1498 170 1122 2140
Low 51 533 348 336 515 336 766 769 923 213 85 115 5 1 82 648 6 2
Below cutoff 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001329990 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_032809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_138421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_138422 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_138423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_138424 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_138425 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423975 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423976 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423977 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054364026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054364027 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054364028 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054364029 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001746392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001746393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001746395 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001746396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001746398 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007061362 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_929849 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_929850 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_929851 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AJ420465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK027502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK054974 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074127 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK075421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301241 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL592211 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC009114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM674865 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471090 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC306779 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000358369   ⟹   ENSP00000351138
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,036,934 - 129,072,082 (+)Ensembl
RefSeq Acc Id: ENST00000414342   ⟹   ENSP00000415906
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,063,287 - 129,069,095 (+)Ensembl
RefSeq Acc Id: ENST00000439290   ⟹   ENSP00000391603
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,036,644 - 129,072,071 (+)Ensembl
RefSeq Acc Id: ENST00000445183   ⟹   ENSP00000396618
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,036,646 - 129,072,071 (+)Ensembl
RefSeq Acc Id: ENST00000450073   ⟹   ENSP00000409348
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,036,995 - 129,042,506 (+)Ensembl
RefSeq Acc Id: ENST00000471943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,067,508 - 129,068,400 (+)Ensembl
RefSeq Acc Id: ENST00000474534
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,036,621 - 129,047,224 (+)Ensembl
RefSeq Acc Id: ENST00000474639
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,060,482 - 129,068,311 (+)Ensembl
RefSeq Acc Id: ENST00000477088
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,036,621 - 129,042,400 (+)Ensembl
RefSeq Acc Id: ENST00000483458
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,069,259 - 129,072,071 (+)Ensembl
RefSeq Acc Id: ENST00000492279
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,068,934 - 129,069,934 (+)Ensembl
RefSeq Acc Id: ENST00000494608
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,060,552 - 129,063,630 (+)Ensembl
RefSeq Acc Id: ENST00000495975
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,061,297 - 129,068,014 (+)Ensembl
RefSeq Acc Id: ENST00000684074   ⟹   ENSP00000506871
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9129,036,626 - 129,072,082 (+)Ensembl
RefSeq Acc Id: NM_001329990   ⟹   NP_001316919
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,626 - 129,072,082 (+)NCBI
T2T-CHM13v2.09141,240,095 - 141,275,546 (+)NCBI
Sequence:
RefSeq Acc Id: NM_032809   ⟹   NP_116198
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,934 - 129,072,082 (+)NCBI
GRCh379131,798,899 - 131,834,361 (+)NCBI
Build 369130,839,074 - 130,874,172 (+)NCBI Archive
Celera9102,451,566 - 102,486,648 (+)RGD
HuRef9101,406,579 - 101,441,661 (+)RGD
CHM1_19131,950,093 - 131,985,185 (+)NCBI
T2T-CHM13v2.09141,240,403 - 141,275,546 (+)NCBI
Sequence:
RefSeq Acc Id: NR_138421
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,626 - 129,072,082 (+)NCBI
T2T-CHM13v2.09141,240,095 - 141,275,546 (+)NCBI
Sequence:
RefSeq Acc Id: NR_138422
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,626 - 129,072,082 (+)NCBI
T2T-CHM13v2.09141,240,095 - 141,275,546 (+)NCBI
Sequence:
RefSeq Acc Id: NR_138423
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,626 - 129,072,082 (+)NCBI
T2T-CHM13v2.09141,240,095 - 141,275,546 (+)NCBI
Sequence:
RefSeq Acc Id: NR_138424
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,626 - 129,072,082 (+)NCBI
T2T-CHM13v2.09141,240,095 - 141,275,546 (+)NCBI
Sequence:
RefSeq Acc Id: NR_138425
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,626 - 129,072,082 (+)NCBI
T2T-CHM13v2.09141,240,095 - 141,275,546 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011519118   ⟹   XP_011517420
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,042,306 - 129,072,082 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047423975   ⟹   XP_047279931
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,934 - 129,069,957 (+)NCBI
RefSeq Acc Id: XM_047423976   ⟹   XP_047279932
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,934 - 129,067,869 (+)NCBI
RefSeq Acc Id: XM_047423977   ⟹   XP_047279933
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,059,460 - 129,072,082 (+)NCBI
RefSeq Acc Id: XM_054364026   ⟹   XP_054220001
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09141,240,403 - 141,273,421 (+)NCBI
RefSeq Acc Id: XM_054364027   ⟹   XP_054220002
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09141,240,403 - 141,271,333 (+)NCBI
RefSeq Acc Id: XM_054364028   ⟹   XP_054220003
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09141,245,769 - 141,275,546 (+)NCBI
RefSeq Acc Id: XM_054364029   ⟹   XP_054220004
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09141,262,924 - 141,275,546 (+)NCBI
RefSeq Acc Id: XR_007061362
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,934 - 129,069,885 (+)NCBI
RefSeq Acc Id: XR_008488086
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09141,240,403 - 141,273,349 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001316919 (Get FASTA)   NCBI Sequence Viewer  
  NP_116198 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517420 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279931 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279932 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279933 (Get FASTA)   NCBI Sequence Viewer  
  XP_054220001 (Get FASTA)   NCBI Sequence Viewer  
  XP_054220002 (Get FASTA)   NCBI Sequence Viewer  
  XP_054220003 (Get FASTA)   NCBI Sequence Viewer  
  XP_054220004 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH09114 (Get FASTA)   NCBI Sequence Viewer  
  BAB55159 (Get FASTA)   NCBI Sequence Viewer  
  BAB70835 (Get FASTA)   NCBI Sequence Viewer  
  BAB84953 (Get FASTA)   NCBI Sequence Viewer  
  BAC11611 (Get FASTA)   NCBI Sequence Viewer  
  BAG62810 (Get FASTA)   NCBI Sequence Viewer  
  BAG64160 (Get FASTA)   NCBI Sequence Viewer  
  EAW87861 (Get FASTA)   NCBI Sequence Viewer  
  EAW87862 (Get FASTA)   NCBI Sequence Viewer  
  EAW87863 (Get FASTA)   NCBI Sequence Viewer  
  EAW87864 (Get FASTA)   NCBI Sequence Viewer  
  EAW87865 (Get FASTA)   NCBI Sequence Viewer  
  EAW87866 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000351138.4
  ENSP00000391603.1
  ENSP00000396618.1
  ENSP00000409348.1
  ENSP00000415906.1
  ENSP00000506871
  ENSP00000506871.1
GenBank Protein Q7L4E1 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_116198   ⟸   NM_032809
- Peptide Label: isoform 1
- UniProtKB: B4DZP8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011517420   ⟸   XM_011519118
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: NP_001316919   ⟸   NM_001329990
- Peptide Label: isoform 2
- UniProtKB: Q8TEJ6 (UniProtKB/Swiss-Prot),   Q8NBM3 (UniProtKB/Swiss-Prot),   Q969E6 (UniProtKB/Swiss-Prot),   Q7L4E1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000409348   ⟸   ENST00000450073
RefSeq Acc Id: ENSP00000391603   ⟸   ENST00000439290
RefSeq Acc Id: ENSP00000415906   ⟸   ENST00000414342
RefSeq Acc Id: ENSP00000396618   ⟸   ENST00000445183
RefSeq Acc Id: ENSP00000351138   ⟸   ENST00000358369
RefSeq Acc Id: ENSP00000506871   ⟸   ENST00000684074
RefSeq Acc Id: XP_047279931   ⟸   XM_047423975
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047279932   ⟸   XM_047423976
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047279933   ⟸   XM_047423977
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054220001   ⟸   XM_054364026
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054220002   ⟸   XM_054364027
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054220003   ⟸   XM_054364028
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054220004   ⟸   XM_054364029
- Peptide Label: isoform X4

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q7L4E1-F1-model_v2 AlphaFold Q7L4E1 1-593 view protein structure

Promoters
RGD ID:7216351
Promoter ID:EPDNEW_H13921
Type:initiation region
Name:FAM73B_1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13922  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,650 - 129,036,710EPDNEW
RGD ID:7216353
Promoter ID:EPDNEW_H13922
Type:initiation region
Name:FAM73B_2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13921  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh389129,036,947 - 129,037,007EPDNEW
RGD ID:6807697
Promoter ID:HG_KWN:65213
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000277475,   ENST00000406926,   OTTHUMT00000106289,   OTTHUMT00000315883,   OTTHUMT00000315884,   UC004BWY.1,   UC004BWZ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 369130,838,501 - 130,839,001 (+)MPROMDB
RGD ID:6807676
Promoter ID:HG_KWN:65217
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:OTTHUMT00000315886
Position:
Human AssemblyChrPosition (strand)Source
Build 369130,869,391 - 130,869,891 (+)MPROMDB
RGD ID:6807709
Promoter ID:HG_KWN:65218
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:OTTHUMT00000106290,   UC004BXB.1
Position:
Human AssemblyChrPosition (strand)Source
Build 369130,870,761 - 130,871,662 (+)MPROMDB
RGD ID:6815661
Promoter ID:HG_MRA:16730
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:AJ420465
Position:
Human AssemblyChrPosition (strand)Source
Build 369130,872,091 - 130,872,591 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:23621 AgrOrtholog
COSMIC MIGA2 COSMIC
Ensembl Genes ENSG00000148343 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000358369.8 UniProtKB/Swiss-Prot
  ENST00000414342.1 UniProtKB/TrEMBL
  ENST00000439290 ENTREZGENE
  ENST00000439290.5 UniProtKB/Swiss-Prot
  ENST00000445183 ENTREZGENE
  ENST00000445183.5 UniProtKB/Swiss-Prot
  ENST00000450073.1 UniProtKB/TrEMBL
  ENST00000684074 ENTREZGENE
  ENST00000684074.1 UniProtKB/Swiss-Prot
GTEx ENSG00000148343 GTEx
HGNC ID HGNC:23621 ENTREZGENE
Human Proteome Map MIGA2 Human Proteome Map
InterPro Miga UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:84895 UniProtKB/Swiss-Prot
NCBI Gene 84895 ENTREZGENE
OMIM 616774 OMIM
PANTHER MITOGUARDIN 2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR21508 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Miga UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134896424 PharmGKB
UniProt B0QZG3_HUMAN UniProtKB/TrEMBL
  B4DZP8 ENTREZGENE, UniProtKB/TrEMBL
  H7C474_HUMAN UniProtKB/TrEMBL
  MIGA2_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q8NBM3 ENTREZGENE
  Q8TEJ6 ENTREZGENE
  Q969E6 ENTREZGENE
UniProt Secondary Q8NBM3 UniProtKB/Swiss-Prot
  Q8TEJ6 UniProtKB/Swiss-Prot
  Q969E6 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-06-28 MIGA2  mitoguardin 2  FAM73B  family with sequence similarity 73 member B  Symbol and/or name change 5135510 APPROVED
2015-11-24 FAM73B  family with sequence similarity 73 member B    family with sequence similarity 73, member B  Symbol and/or name change 5135510 APPROVED