MNAT1 (MNAT1 component of CDK activating kinase) - Rat Genome Database

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Gene: MNAT1 (MNAT1 component of CDK activating kinase) Homo sapiens
Analyze
Symbol: MNAT1
Name: MNAT1 component of CDK activating kinase
RGD ID: 733503
HGNC Page HGNC:7181
Description: Predicted to enable zinc ion binding activity. Involved in regulation of G1/S transition of mitotic cell cycle; regulation of transcription by RNA polymerase II; and transcription initiation at RNA polymerase II promoter. Located in cyclin-dependent protein kinase activating kinase holoenzyme complex and nucleoplasm. Part of CAK-ERCC2 complex; transcription factor TFIIH core complex; and transcription factor TFIIK complex.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: CAP35; CDK-activating kinase assembly factor MAT1; CDK7/cyclin-H assembly factor; cyclin G1 interacting protein; cyclin-G1-interacting protein; MAT1; menage a trois 1 (CAK assembly factor); menage a trois homolog 1, cyclin H assembly factor; menage a trois-like protein 1 cyclin H assembly factor; MNAT CDK-activating kinase assembly factor 1; MNAT1, CDK activating kinase assembly factor; RING finger protein 66; RING finger protein MAT1; RNF66; TFB3
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
GRCh381460,734,761 - 60,969,965 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1460,734,742 - 60,969,965 (+)EnsemblGRCh38hg38GRCh38
GRCh371461,201,479 - 61,436,683 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361460,271,223 - 60,505,151 (+)NCBINCBI36Build 36hg18NCBI36
Build 341460,271,222 - 60,505,151NCBI
Celera1441,251,714 - 41,485,662 (+)NCBICelera
Cytogenetic Map14q23.1NCBI
HuRef1441,364,391 - 41,598,757 (+)NCBIHuRef
CHM1_11461,140,780 - 61,374,681 (+)NCBICHM1_1
T2T-CHM13v2.01454,941,243 - 55,176,505 (+)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

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. A history of TFIIH: two decades of molecular biology on a pivotal transcription/repair factor. Egly JM and Coin F, DNA Repair (Amst). 2011 Jul 15;10(7):714-21. doi: 10.1016/j.dnarep.2011.04.021. Epub 2011 May 17.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
4. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
5. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1939271   PMID:2449431   PMID:7629134   PMID:7799941   PMID:8308015   PMID:8521393   PMID:8521818   PMID:8628270   PMID:8692841   PMID:8692842   PMID:8849451   PMID:8934526  
PMID:8946909   PMID:9054383   PMID:9118947   PMID:9121429   PMID:9130708   PMID:9184228   PMID:9311822   PMID:9334327   PMID:9368058   PMID:9372954   PMID:9405375   PMID:9465303  
PMID:9512541   PMID:9570510   PMID:9582279   PMID:9651670   PMID:9765201   PMID:9790902   PMID:9840937   PMID:9852112   PMID:10024882   PMID:10066804   PMID:10082552   PMID:10214908  
PMID:10428966   PMID:10438593   PMID:10583946   PMID:10801852   PMID:10866664   PMID:10949034   PMID:11056162   PMID:11056214   PMID:11113176   PMID:11113200   PMID:11313499   PMID:11445587  
PMID:12140753   PMID:12213824   PMID:12379213   PMID:12393749   PMID:12477932   PMID:12527756   PMID:12646563   PMID:14569024   PMID:15220921   PMID:15282296   PMID:15328539   PMID:15489334  
PMID:15530371   PMID:16169070   PMID:16327805   PMID:16782892   PMID:16935935   PMID:16954377   PMID:17207965   PMID:17353931   PMID:17371848   PMID:17628022   PMID:17643375   PMID:17707548  
PMID:18029348   PMID:18816836   PMID:19584075   PMID:20379614   PMID:20522537   PMID:21873635   PMID:21988832   PMID:22046132   PMID:22266860   PMID:22493164   PMID:22610502   PMID:22939629  
PMID:23105109   PMID:23455922   PMID:23602568   PMID:23622515   PMID:23765726   PMID:24332808   PMID:25281560   PMID:25590999   PMID:26186194   PMID:26340423   PMID:26344197   PMID:26496610  
PMID:26871637   PMID:26972000   PMID:27107012   PMID:27301701   PMID:28514442   PMID:28786561   PMID:29053956   PMID:29568061   PMID:29656893   PMID:30404004   PMID:30415952   PMID:30890647  
PMID:31421084   PMID:31527615   PMID:31694235   PMID:32245994   PMID:32416067   PMID:32453410   PMID:32460013   PMID:32663249   PMID:32707033   PMID:32814053   PMID:33453189   PMID:33961781  
PMID:34079125   PMID:34597346   PMID:35271311   PMID:35439318   PMID:35563538   PMID:35831314   PMID:35914814   PMID:36042349   PMID:36215168   PMID:36537216   PMID:36736316   PMID:37689310  


Genomics

Comparative Map Data
MNAT1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381460,734,761 - 60,969,965 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1460,734,742 - 60,969,965 (+)EnsemblGRCh38hg38GRCh38
GRCh371461,201,479 - 61,436,683 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361460,271,223 - 60,505,151 (+)NCBINCBI36Build 36hg18NCBI36
Build 341460,271,222 - 60,505,151NCBI
Celera1441,251,714 - 41,485,662 (+)NCBICelera
Cytogenetic Map14q23.1NCBI
HuRef1441,364,391 - 41,598,757 (+)NCBIHuRef
CHM1_11461,140,780 - 61,374,681 (+)NCBICHM1_1
T2T-CHM13v2.01454,941,243 - 55,176,505 (+)NCBIT2T-CHM13v2.0
Mnat1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391273,158,957 - 73,320,762 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1273,170,491 - 73,320,762 (+)EnsemblGRCm39 Ensembl
GRCm381273,112,185 - 73,273,988 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1273,123,717 - 73,273,988 (+)EnsemblGRCm38mm10GRCm38
MGSCv371274,224,704 - 74,374,975 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361274,042,567 - 74,191,687 (+)NCBIMGSCv36mm8
Celera1274,235,147 - 74,385,303 (+)NCBICelera
Cytogenetic Map12C3NCBI
cM Map1230.37NCBI
Mnat1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8697,550,566 - 97,706,598 (+)NCBIGRCr8
mRatBN7.2691,814,703 - 91,971,945 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl691,814,749 - 91,970,744 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx692,215,265 - 92,360,395 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0692,514,762 - 92,659,893 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0691,942,664 - 92,087,783 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0695,995,341 - 96,153,331 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl696,007,805 - 96,153,330 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.06105,442,513 - 105,587,335 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4695,548,845 - 95,698,573 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1695,552,300 - 95,702,028 (+)NCBI
Celera690,288,391 - 90,433,268 (+)NCBICelera
Cytogenetic Map6q24NCBI
Mnat1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554668,690,960 - 8,895,021 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554668,690,960 - 8,895,021 (-)NCBIChiLan1.0ChiLan1.0
MNAT1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21561,872,516 - 62,105,486 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11461,089,035 - 61,321,999 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01441,342,530 - 41,576,690 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11459,603,209 - 59,835,408 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1459,603,209 - 59,835,408 (+)Ensemblpanpan1.1panPan2
MNAT1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1835,747,883 - 35,946,353 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl835,756,933 - 35,946,353 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha835,510,966 - 35,699,760 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0835,990,042 - 36,179,803 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl835,990,189 - 36,179,799 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1835,602,177 - 35,790,354 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0835,679,632 - 35,867,792 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0836,041,067 - 36,229,645 (+)NCBIUU_Cfam_GSD_1.0
Mnat1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440864069,063,584 - 69,282,287 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364954,909,380 - 5,128,113 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364954,909,427 - 5,128,113 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MNAT1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1189,690,354 - 189,910,589 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11189,690,343 - 189,908,144 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21210,944,891 - 210,956,358 (-)NCBISscrofa10.2Sscrofa10.2susScr3
MNAT1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12437,922,347 - 38,161,467 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2437,922,353 - 38,162,226 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605326,174,914 - 26,419,489 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Mnat1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473440,154,577 - 40,389,402 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473440,148,761 - 40,389,233 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MNAT1
13 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 14q23.1-23.3(chr14:59917051-66750803)x1 copy number loss See cases [RCV000050892] Chr14:59917051..66750803 [GRCh38]
Chr14:60383769..67217521 [GRCh37]
Chr14:59453522..66287274 [NCBI36]
Chr14:14q23.1-23.3		 pathogenic
GRCh38/hg38 14q22.3-23.3(chr14:57041036-67208231)x1 copy number loss See cases [RCV000051521] Chr14:57041036..67208231 [GRCh38]
Chr14:57507754..67674948 [GRCh37]
Chr14:56577507..66744701 [NCBI36]
Chr14:14q22.3-23.3		 pathogenic
GRCh38/hg38 14q23.1(chr14:58146022-61273619)x1 copy number loss See cases [RCV000051522] Chr14:58146022..61273619 [GRCh38]
Chr14:58612740..61740337 [GRCh37]
Chr14:57682493..60810090 [NCBI36]
Chr14:14q23.1		 pathogenic
NM_001177963.1(MNAT1):c.562-19432T>C single nucleotide variant Lung cancer [RCV000098974] Chr14:60860282 [GRCh38]
Chr14:61327000 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh38/hg38 14q23.1(chr14:60401009-60861986)x3 copy number gain See cases [RCV000133687] Chr14:60401009..60861986 [GRCh38]
Chr14:60867727..61328704 [GRCh37]
Chr14:59937480..60398457 [NCBI36]
Chr14:14q23.1		 uncertain significance
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q23.1-23.2(chr14:57653413-64093528)x1 copy number loss See cases [RCV000138348] Chr14:57653413..64093528 [GRCh38]
Chr14:58120131..64560246 [GRCh37]
Chr14:57189884..63629999 [NCBI36]
Chr14:14q23.1-23.2		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q23.1(chr14:61182378-61517256)x3 copy number gain not provided [RCV000738508] Chr14:61182378..61517256 [GRCh37]
Chr14:14q23.1		 benign
GRCh37/hg19 14q23.1(chr14:61347538-61453942)x1 copy number loss not provided [RCV000738509] Chr14:61347538..61453942 [GRCh37]
Chr14:14q23.1		 benign
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33		 pathogenic
NM_002431.4(MNAT1):c.222C>T (p.Ile74=) single nucleotide variant not provided [RCV000972881] Chr14:60796349 [GRCh38]
Chr14:61263067 [GRCh37]
Chr14:14q23.1		 benign
NM_002431.4(MNAT1):c.327G>C (p.Leu109Phe) single nucleotide variant not provided [RCV000880883] Chr14:60808335 [GRCh38]
Chr14:61275053 [GRCh37]
Chr14:14q23.1		 likely benign
GRCh37/hg19 14q23.1(chr14:61276184-61339308)x1 copy number loss not provided [RCV000847824] Chr14:61276184..61339308 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh37/hg19 14q23.1(chr14:61393999-61520353)x1 copy number loss not provided [RCV000846382] Chr14:61393999..61520353 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh37/hg19 14q23.1(chr14:61253791-61387865)x1 copy number loss not provided [RCV000849438] Chr14:61253791..61387865 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh37/hg19 14q23.1(chr14:61409856-61547332)x1 copy number loss not provided [RCV001006643] Chr14:61409856..61547332 [GRCh37]
Chr14:14q23.1		 likely benign
GRCh37/hg19 14q23.1-23.2(chr14:61126208-63517651)x3 copy number gain not provided [RCV000845699] Chr14:61126208..63517651 [GRCh37]
Chr14:14q23.1-23.2		 uncertain significance
NM_002431.4(MNAT1):c.496C>G (p.Gln166Glu) single nucleotide variant Inborn genetic diseases [RCV003295170] Chr14:60812062 [GRCh38]
Chr14:61278780 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh37/hg19 14q23.1-23.3(chr14:61409856-65742610)x3 copy number gain not provided [RCV001259780] Chr14:61409856..65742610 [GRCh37]
Chr14:14q23.1-23.3		 likely pathogenic
GRCh37/hg19 14q22.2-24.3(chr14:54654001-75828024)x3 copy number gain 14q22.2q24.3 duplication [RCV001506967] Chr14:54654001..75828024 [GRCh37]
Chr14:14q22.2-24.3		 likely pathogenic
GRCh37/hg19 14q23.1(chr14:60958879-61211351)x3 copy number gain not provided [RCV001829179] Chr14:60958879..61211351 [GRCh37]
Chr14:14q23.1		 uncertain significance
NC_000014.8:g.(?_60976117)_(61447691_?)del deletion Branchiootic syndrome 3 [RCV003116467]|not provided [RCV003109449] Chr14:60976117..61447691 [GRCh37]
Chr14:14q23.1		 uncertain significance|no classifications from unflagged records
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2 copy number gain See cases [RCV002286356] Chr14:37671058..106985955 [GRCh37]
Chr14:14q13.3-32.33		 pathogenic
GRCh37/hg19 14q23.1(chr14:61254323-61387865)x1 copy number loss not provided [RCV002474857] Chr14:61254323..61387865 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh37/hg19 14q22.3-23.2(chr14:57804997-63590203)x1 copy number loss not provided [RCV002472446] Chr14:57804997..63590203 [GRCh37]
Chr14:14q22.3-23.2		 likely pathogenic
NM_002431.4(MNAT1):c.431A>G (p.Gln144Arg) single nucleotide variant Inborn genetic diseases [RCV002897076] Chr14:60811997 [GRCh38]
Chr14:61278715 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_002431.4(MNAT1):c.650C>T (p.Pro217Leu) single nucleotide variant Inborn genetic diseases [RCV002896621] Chr14:60818810 [GRCh38]
Chr14:61285528 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_002431.4(MNAT1):c.362A>G (p.Lys121Arg) single nucleotide variant Inborn genetic diseases [RCV003010865] Chr14:60808370 [GRCh38]
Chr14:61275088 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_002431.4(MNAT1):c.164A>G (p.Lys55Arg) single nucleotide variant Inborn genetic diseases [RCV003197441] Chr14:60796291 [GRCh38]
Chr14:61263009 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh37/hg19 14q23.1(chr14:61279888-61339308)x1 copy number loss not provided [RCV003483208] Chr14:61279888..61339308 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh37/hg19 14q11.2-23.1(chr14:20511673-61826023)x3 copy number gain not provided [RCV003485022] Chr14:20511673..61826023 [GRCh37]
Chr14:14q11.2-23.1		 pathogenic
GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3 copy number gain not provided [RCV003485036] Chr14:58894502..107227240 [GRCh37]
Chr14:14q23.1-32.33		 pathogenic
GRCh37/hg19 14q22.3-24.1(chr14:57588965-68334517)x3 copy number gain not provided [RCV003485034] Chr14:57588965..68334517 [GRCh37]
Chr14:14q22.3-24.1		 likely pathogenic
GRCh37/hg19 14q22.3-23.2(chr14:55667390-64447598)x1 copy number loss not provided [RCV003483204] Chr14:55667390..64447598 [GRCh37]
Chr14:14q22.3-23.2		 pathogenic
GRCh37/hg19 14q23.1(chr14:61409856-61547375)x1 copy number loss not specified [RCV003987048] Chr14:61409856..61547375 [GRCh37]
Chr14:14q23.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1044
Count of miRNA genes:630
Interacting mature miRNAs:693
Transcripts:ENST00000261245, ENST00000539616, ENST00000553354, ENST00000554002, ENST00000554641, ENST00000555545, ENST00000556525, ENST00000556764, ENST00000557134
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
D14S592  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,396,856 - 61,397,082UniSTSGRCh37
Build 361460,466,609 - 60,466,835RGDNCBI36
Celera1441,447,106 - 41,447,338RGD
Cytogenetic Map14q23UniSTS
HuRef1441,560,205 - 41,560,434UniSTS
Marshfield Genetic Map1466.81RGD
Marshfield Genetic Map1466.81UniSTS
deCODE Assembly Map1460.5UniSTS
Whitehead-YAC Contig Map14 UniSTS
D7S2425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377108,347,079 - 108,347,322UniSTSGRCh37
GRCh377108,347,116 - 108,347,213UniSTSGRCh37
GRCh371461,314,345 - 61,315,803UniSTSGRCh37
Build 367108,134,315 - 108,134,558RGDNCBI36
Celera7103,160,490 - 103,160,587UniSTS
Celera7103,160,453 - 103,160,692RGD
Celera1441,364,598 - 41,366,056UniSTS
HuRef1441,477,362 - 41,478,820UniSTS
HuRef7102,715,339 - 102,715,436UniSTS
HuRef7102,715,302 - 102,715,541UniSTS
CRA_TCAGchr7v27107,714,299 - 107,714,538UniSTS
CRA_TCAGchr7v27107,714,336 - 107,714,433UniSTS
Marshfield Genetic Map7121.41RGD
Marshfield Genetic Map7121.41UniSTS
Genethon Genetic Map7121.5UniSTS
TNG Radiation Hybrid Map747576.0UniSTS
deCODE Assembly Map7118.39UniSTS
Stanford-G3 RH Map75284.0UniSTS
Whitehead-YAC Contig Map7 UniSTS
NCBI RH Map71088.3UniSTS
GeneMap99-G3 RH Map75284.0UniSTS
RH45647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,317,423 - 61,317,542UniSTSGRCh37
Build 361460,387,176 - 60,387,295RGDNCBI36
Celera1441,367,676 - 41,367,795RGD
Cytogenetic Map14q23UniSTS
HuRef1441,480,440 - 41,480,559UniSTS
GeneMap99-GB4 RH Map14139.99UniSTS
RH80245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,246,899 - 61,247,141UniSTSGRCh37
Build 361460,316,652 - 60,316,894RGDNCBI36
Celera1441,297,146 - 41,297,388RGD
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map4q27UniSTS
HuRef1441,409,823 - 41,410,065UniSTS
GeneMap99-GB4 RH Map14141.0UniSTS
GDB:451562  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,246,656 - 61,246,920UniSTSGRCh37
Build 361460,316,409 - 60,316,673RGDNCBI36
Celera1441,296,903 - 41,297,167RGD
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map4q27UniSTS
HuRef1441,409,580 - 41,409,844UniSTS
G67480  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,201,489 - 61,201,773UniSTSGRCh37
Build 361460,271,242 - 60,271,526RGDNCBI36
Celera1441,251,744 - 41,252,028RGD
Cytogenetic Map14q23UniSTS
HuRef1441,364,421 - 41,364,705UniSTS
G67481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,278,650 - 61,278,933UniSTSGRCh37
Build 361460,348,403 - 60,348,686RGDNCBI36
Celera1441,328,908 - 41,329,191RGD
Cytogenetic Map14q23UniSTS
HuRef1441,441,587 - 41,441,870UniSTS
G67482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,285,338 - 61,285,716UniSTSGRCh37
Build 361460,355,091 - 60,355,469RGDNCBI36
Celera1441,335,598 - 41,335,976RGD
Cytogenetic Map14q23UniSTS
HuRef1441,448,277 - 41,448,655UniSTS
RH69606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,435,081 - 61,435,307UniSTSGRCh37
Build 361460,504,834 - 60,505,060RGDNCBI36
Celera1441,485,345 - 41,485,571RGD
Cytogenetic Map14q23UniSTS
HuRef1441,598,440 - 41,598,666UniSTS
GeneMap99-GB4 RH Map14140.37UniSTS
RH65471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,220,644 - 61,220,831UniSTSGRCh37
Build 361460,290,397 - 60,290,584RGDNCBI36
Celera1441,270,890 - 41,271,077RGD
Cytogenetic Map14q23UniSTS
HuRef1441,383,567 - 41,383,754UniSTS
GeneMap99-GB4 RH Map14140.37UniSTS
RH70941  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,435,150 - 61,435,306UniSTSGRCh37
Build 361460,504,903 - 60,505,059RGDNCBI36
Celera1441,485,414 - 41,485,570RGD
Cytogenetic Map14q23UniSTS
HuRef1441,598,509 - 41,598,665UniSTS
GeneMap99-GB4 RH Map14140.37UniSTS
RH70690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,435,150 - 61,435,287UniSTSGRCh37
Build 361460,504,903 - 60,505,040RGDNCBI36
Celera1441,485,414 - 41,485,551RGD
Cytogenetic Map14q23UniSTS
HuRef1441,598,509 - 41,598,646UniSTS
GeneMap99-GB4 RH Map14140.37UniSTS
D14S1166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,215,722 - 61,215,823UniSTSGRCh37
Build 361460,285,475 - 60,285,576RGDNCBI36
Celera1441,265,968 - 41,266,069RGD
Cytogenetic Map14q23UniSTS
HuRef1441,378,645 - 41,378,746UniSTS
TNG Radiation Hybrid Map1419106.0UniSTS
Stanford-G3 RH Map142015.0UniSTS
NCBI RH Map14614.6UniSTS
RH47826  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,435,148 - 61,435,308UniSTSGRCh37
Build 361460,504,901 - 60,505,061RGDNCBI36
Celera1441,485,412 - 41,485,572RGD
Cytogenetic Map14q23UniSTS
HuRef1441,598,507 - 41,598,667UniSTS
GeneMap99-GB4 RH Map14140.37UniSTS
MNAT1__6327  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371461,434,991 - 61,435,458UniSTSGRCh37
Build 361460,504,744 - 60,505,211RGDNCBI36
Celera1441,485,255 - 41,485,722RGD
HuRef1441,598,350 - 41,598,817UniSTS
D7S2425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map14q23UniSTS


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 708 1279 652 72 673 47 2733 1203 1501 176 810 713 42 1 635 2023 5 2
Low 1731 1579 1074 552 1150 418 1624 989 2233 242 650 900 133 569 765 1
Below cutoff 133 128 5 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001177963 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005267687 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005267688 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021332 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021333 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021334 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449599 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047431413 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054376119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054376120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054376121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054376122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA053721 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL132777 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL160236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY165512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU620200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CD701743 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR450336 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178192 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U61835 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X87843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X92669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000261245   ⟹   ENSP00000261245
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1460,734,761 - 60,969,965 (+)Ensembl
RefSeq Acc Id: ENST00000539616   ⟹   ENSP00000446437
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1460,734,776 - 60,968,678 (+)Ensembl
RefSeq Acc Id: ENST00000553354
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1460,734,779 - 60,808,428 (+)Ensembl
RefSeq Acc Id: ENST00000554002   ⟹   ENSP00000451379
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1460,808,324 - 60,968,680 (+)Ensembl
RefSeq Acc Id: ENST00000554641
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1460,811,986 - 60,880,041 (+)Ensembl
RefSeq Acc Id: ENST00000555545
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1460,734,742 - 60,753,954 (+)Ensembl
RefSeq Acc Id: ENST00000556525
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1460,796,320 - 60,818,860 (+)Ensembl
RefSeq Acc Id: ENST00000556764
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1460,734,773 - 60,809,015 (+)Ensembl
RefSeq Acc Id: ENST00000557134   ⟹   ENSP00000451017
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1460,811,987 - 60,968,680 (+)Ensembl
RefSeq Acc Id: NM_001177963   ⟹   NP_001171434
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381460,734,761 - 60,969,965 (+)NCBI
GRCh371461,201,459 - 61,435,398 (+)ENTREZGENE
HuRef1441,364,391 - 41,598,757 (+)ENTREZGENE
CHM1_11461,140,780 - 61,374,681 (+)NCBI
T2T-CHM13v2.01454,941,243 - 55,176,505 (+)NCBI
Sequence:
RefSeq Acc Id: NM_002431   ⟹   NP_002422
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381460,734,761 - 60,969,965 (+)NCBI
GRCh371461,201,459 - 61,435,398 (+)ENTREZGENE
Build 361460,271,223 - 60,505,151 (+)NCBI Archive
HuRef1441,364,391 - 41,598,757 (+)ENTREZGENE
CHM1_11461,140,780 - 61,374,681 (+)NCBI
T2T-CHM13v2.01454,941,243 - 55,176,505 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005267688   ⟹   XP_005267745
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381460,734,761 - 60,968,680 (+)NCBI
GRCh371461,201,459 - 61,435,398 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021332   ⟹   XP_016876821
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381460,791,357 - 60,969,965 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021334   ⟹   XP_016876823
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381460,799,412 - 60,969,965 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047431413   ⟹   XP_047287369
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381460,798,094 - 60,969,965 (+)NCBI
RefSeq Acc Id: XM_054376119   ⟹   XP_054232094
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01454,998,066 - 55,176,505 (+)NCBI
RefSeq Acc Id: XM_054376120   ⟹   XP_054232095
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01454,941,243 - 55,175,220 (+)NCBI
RefSeq Acc Id: XM_054376121   ⟹   XP_054232096
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01455,005,891 - 55,176,505 (+)NCBI
RefSeq Acc Id: XM_054376122   ⟹   XP_054232097
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01455,004,573 - 55,176,505 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001171434 (Get FASTA)   NCBI Sequence Viewer  
  NP_002422 (Get FASTA)   NCBI Sequence Viewer  
  XP_005267745 (Get FASTA)   NCBI Sequence Viewer  
  XP_016876821 (Get FASTA)   NCBI Sequence Viewer  
  XP_016876823 (Get FASTA)   NCBI Sequence Viewer  
  XP_047287369 (Get FASTA)   NCBI Sequence Viewer  
  XP_054232094 (Get FASTA)   NCBI Sequence Viewer  
  XP_054232095 (Get FASTA)   NCBI Sequence Viewer  
  XP_054232096 (Get FASTA)   NCBI Sequence Viewer  
  XP_054232097 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB05248 (Get FASTA)   NCBI Sequence Viewer  
  AAH00820 (Get FASTA)   NCBI Sequence Viewer  
  AAN47195 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33649 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33650 (Get FASTA)   NCBI Sequence Viewer  
  CAA61112 (Get FASTA)   NCBI Sequence Viewer  
  CAA63356 (Get FASTA)   NCBI Sequence Viewer  
  CAG29332 (Get FASTA)   NCBI Sequence Viewer  
  EAW80787 (Get FASTA)   NCBI Sequence Viewer  
  EAW80788 (Get FASTA)   NCBI Sequence Viewer  
  EAW80789 (Get FASTA)   NCBI Sequence Viewer  
  EAW80790 (Get FASTA)   NCBI Sequence Viewer  
  EAW80791 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000261245
  ENSP00000261245.4
  ENSP00000446437
  ENSP00000446437.2
  ENSP00000451017
  ENSP00000451017.1
  ENSP00000451379.1
GenBank Protein P51948 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_002422   ⟸   NM_002431
- Peptide Label: isoform 1
- UniProtKB: Q15817 (UniProtKB/Swiss-Prot),   G3V1U8 (UniProtKB/Swiss-Prot),   Q6ICQ7 (UniProtKB/Swiss-Prot),   P51948 (UniProtKB/Swiss-Prot),   A0A024R688 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001171434   ⟸   NM_001177963
- Peptide Label: isoform 2
- Sequence:
RefSeq Acc Id: XP_005267745   ⟸   XM_005267688
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016876821   ⟸   XM_017021332
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016876823   ⟸   XM_017021334
- Peptide Label: isoform X3
- UniProtKB: H0YJ92 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000451017   ⟸   ENST00000557134
RefSeq Acc Id: ENSP00000261245   ⟸   ENST00000261245
RefSeq Acc Id: ENSP00000446437   ⟸   ENST00000539616
RefSeq Acc Id: ENSP00000451379   ⟸   ENST00000554002
RefSeq Acc Id: XP_047287369   ⟸   XM_047431413
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054232095   ⟸   XM_054376120
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054232094   ⟸   XM_054376119
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054232097   ⟸   XM_054376122
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054232096   ⟸   XM_054376121
- Peptide Label: isoform X3
Protein Domains
Cdk-activating kinase assembly factor MAT1 centre   HORMA   RING-type   UIM

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P51948-F1-model_v2 AlphaFold P51948 1-309 view protein structure

Promoters
RGD ID:6791747
Promoter ID:HG_KWN:19519
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:OTTHUMT00000276956,   UC001XFE.1,   UC010APQ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361460,271,041 - 60,271,541 (+)MPROMDB
RGD ID:7227787
Promoter ID:EPDNEW_H19640
Type:initiation region
Name:MNAT1_1
Description:MNAT1, CDK activating kinase assembly factor
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19638  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381460,734,772 - 60,734,832EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7181 AgrOrtholog
COSMIC MNAT1 COSMIC
Ensembl Genes ENSG00000020426 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000261245 ENTREZGENE
  ENST00000261245.9 UniProtKB/Swiss-Prot
  ENST00000539616 ENTREZGENE
  ENST00000539616.6 UniProtKB/Swiss-Prot
  ENST00000554002.5 UniProtKB/TrEMBL
  ENST00000557134 ENTREZGENE
  ENST00000557134.1 UniProtKB/TrEMBL
Gene3D-CATH 3.30.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.900.10 UniProtKB/TrEMBL
GTEx ENSG00000020426 GTEx
HGNC ID HGNC:7181 ENTREZGENE
Human Proteome Map MNAT1 Human Proteome Map
InterPro Cdk-activating_kinase_MAT1_cen UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HORMA_dom UniProtKB/TrEMBL
  HORMA_dom_sf UniProtKB/TrEMBL
  Mad2-like UniProtKB/TrEMBL
  MAT1/Tfb3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UIM_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_RING UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_RING/FYVE/PHD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_RING_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:4331 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 4331 ENTREZGENE
OMIM 602659 OMIM
PANTHER CDK-ACTIVATING KINASE ASSEMBLY FACTOR MAT1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MITOTIC SPINDLE ASSEMBLY CHECKPOINT PROTEIN MAD2A UniProtKB/TrEMBL
  PTHR11842 UniProtKB/TrEMBL
  PTHR12683:SF13 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam HORMA UniProtKB/TrEMBL
  MAT1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C3HC4_5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA30894 PharmGKB
PIRSF MAT1_metazoa UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE HORMA UniProtKB/TrEMBL
  UIM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZF_RING_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZF_RING_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART RING UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP RING/U-box UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF56019 UniProtKB/TrEMBL
UniProt A0A024R688 ENTREZGENE, UniProtKB/TrEMBL
  A0A0S2Z414_HUMAN UniProtKB/TrEMBL
  G3V1U8 ENTREZGENE
  H0YJ92 ENTREZGENE, UniProtKB/TrEMBL
  H0YJF2_HUMAN UniProtKB/TrEMBL
  MAT1_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q15817 ENTREZGENE
  Q6ICQ7 ENTREZGENE
UniProt Secondary G3V1U8 UniProtKB/Swiss-Prot
  Q15817 UniProtKB/Swiss-Prot
  Q6ICQ7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-01-29 MNAT1  MNAT1 component of CDK activating kinase    MNAT1, CDK activating kinase assembly factor  Symbol and/or name change 5135510 APPROVED
2016-03-14 MNAT1  MNAT1, CDK activating kinase assembly factor    MNAT CDK-activating kinase assembly factor 1  Symbol and/or name change 5135510 APPROVED
2013-08-06 MNAT1  MNAT CDK-activating kinase assembly factor 1    menage a trois homolog 1, cyclin H assembly factor (Xenopus laevis)  Symbol and/or name change 5135510 APPROVED