RPRD1A (regulation of nuclear pre-mRNA domain containing 1A) - Rat Genome Database

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Gene: RPRD1A (regulation of nuclear pre-mRNA domain containing 1A) Homo sapiens
Analyze
Symbol: RPRD1A
Name: regulation of nuclear pre-mRNA domain containing 1A
RGD ID: 1605654
HGNC Page HGNC:25560
Description: Enables identical protein binding activity. Involved in RNA polymerase II promoter clearance. Located in nucleus. Part of transcription preinitiation complex.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: cyclin-dependent kinase 2B-inhibitor-related protein; Cyclin-dependent kinase inhibitor 2B-related protein (p15INK4B-related protein); FLJ10656; HsT3101; MGC19513; p15INK4B-related protein; P15RS; regulation of nuclear pre-mRNA domain-containing protein 1A
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Black Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: AC007610.3  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381835,989,824 - 36,067,559 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1835,984,387 - 36,067,576 (-)Ensemblhg38GRCh38
GRCh371833,569,787 - 33,647,522 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361831,823,789 - 31,901,371 (-)NCBIBuild 36Build 36hg18NCBI36
Celera1830,377,670 - 30,455,253 (-)NCBICelera
Cytogenetic Map18q12.2NCBI
HuRef1830,428,724 - 30,506,362 (-)NCBIHuRef
CHM1_11833,496,809 - 33,574,427 (-)NCBICHM1_1
T2T-CHM13v2.01836,181,320 - 36,259,091 (-)NCBIT2T-CHM13v2.0
JBrowse:




Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889548   PMID:12470661   PMID:12477932   PMID:14702039   PMID:19322201   PMID:20739273   PMID:21873635   PMID:21988832   PMID:22231121   PMID:22580456   PMID:22658674   PMID:22863883  
PMID:22990118   PMID:23443559   PMID:23455924   PMID:24223155   PMID:24550385   PMID:24797263   PMID:24981860   PMID:24997600   PMID:24999758   PMID:25416956   PMID:25697359   PMID:26186194  
PMID:26344197   PMID:26496610   PMID:26687479   PMID:27173435   PMID:28514442   PMID:28524877   PMID:28712289   PMID:29229926   PMID:30809286   PMID:30948266   PMID:31073040   PMID:31091453  
PMID:32031713   PMID:32203420   PMID:32296183   PMID:32460013   PMID:32694731   PMID:33239621   PMID:33961781   PMID:34244565   PMID:34901782   PMID:34921137   PMID:35013218   PMID:35271311  
PMID:35831314   PMID:35914814   PMID:36215168   PMID:36724073   PMID:36897256   PMID:37071682   PMID:37848033  


Genomics

Comparative Map Data
RPRD1A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381835,989,824 - 36,067,559 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1835,984,387 - 36,067,576 (-)Ensemblhg38GRCh38
GRCh371833,569,787 - 33,647,522 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361831,823,789 - 31,901,371 (-)NCBIBuild 36Build 36hg18NCBI36
Celera1830,377,670 - 30,455,253 (-)NCBICelera
Cytogenetic Map18q12.2NCBI
HuRef1830,428,724 - 30,506,362 (-)NCBIHuRef
CHM1_11833,496,809 - 33,574,427 (-)NCBICHM1_1
T2T-CHM13v2.01836,181,320 - 36,259,091 (-)NCBIT2T-CHM13v2.0
Rprd1a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391824,618,017 - 24,663,306 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1824,618,017 - 24,663,261 (-)EnsemblGRCm39 EnsemblGRCm39
GRCm381824,484,960 - 24,530,235 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1824,484,960 - 24,530,204 (-)Ensemblmm10GRCm38
MGSCv371824,643,463 - 24,688,705 (-)NCBIMGSCv37MGSCv37mm9NCBIm37
MGSCv361824,627,972 - 24,673,214 (-)NCBIMGSCv36mm8
Celera1824,973,427 - 25,018,811 (-)NCBICelera
Cytogenetic Map18A2NCBI
cM Map1813.18NCBI
Rprd1a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81816,066,169 - 16,114,102 (-)NCBIGRCr8GRCr8GRCr8
GRCr8 Ensembl1816,066,169 - 16,114,282 (-)EnsemblGRCr8
mRatBN7.21815,791,418 - 15,839,338 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1815,791,418 - 15,839,338 (-)EnsemblmRatBN7.2
UTH_Rnor_SHR_Utx1815,978,782 - 16,026,350 (-)NCBIUTH_Rnor_SHR_UtxUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01816,761,496 - 16,809,063 (-)NCBIUTH_Rnor_SHRSP_BbbUtx_1.0UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01816,050,053 - 16,097,579 (-)NCBIUTH_Rnor_WKY_Bbb_1.0UTH_Rnor_WKY_Bbb_1.0
Rnor_6.01816,450,160 - 16,497,913 (-)NCBIRnor_6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1816,453,369 - 16,497,886 (-)Ensemblrn6Rnor6.0
Rnor_5.01816,209,135 - 16,256,883 (-)NCBIRnor_5.0Rnor_5.0rn5
RGSC_v3.41816,283,291 - 16,328,357 (-)NCBIRGSC_v3.4RGSC_v3.4rn4
Celera1815,721,452 - 15,768,465 (-)NCBICelera
RGSC_v3.11816,309,731 - 16,356,467 (-)NCBI
Cytogenetic Map18p12NCBI
Rprd1a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540222,584,600 - 22,646,046 (-)Ensembl
ChiLan1.0NW_00495540222,584,600 - 22,646,046 (-)NCBIChiLan1.0ChiLan1.0
RPRD1A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21753,385,357 - 53,463,623 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11839,077,946 - 39,156,211 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01829,242,080 - 29,320,372 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11832,800,352 - 32,878,544 (-)NCBIPanPan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1832,800,352 - 32,878,544 (-)EnsemblpanPan2panpan1.1
RPRD1A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1754,105,270 - 54,187,280 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl754,105,456 - 54,184,583 (+)EnsemblcanFam3CanFam3.1
Dog10K_Boxer_Tasha753,530,988 - 53,613,065 (+)NCBIDog10K_Boxer_TashaDog10K_Boxer_Tasha
ROS_Cfam_1.0754,075,526 - 54,158,021 (+)NCBIROS_Cfam_1.0ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl754,075,544 - 54,158,021 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1753,758,955 - 53,841,051 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0753,782,221 - 53,864,365 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0754,074,683 - 54,156,853 (+)NCBIUU_Cfam_GSD_1.0UU_Cfam_GSD_1.0
Rprd1a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494449,880,457 - 49,939,546 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365179,207,738 - 9,266,952 (+)EnsemblSpeTri2.0 Ensembl
SpeTri2.0NW_0049365179,207,840 - 9,266,948 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RPRD1A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl6119,762,812 - 119,834,012 (-)EnsemblsusScr11Sscrofa11.1
Sscrofa11.16119,762,810 - 119,834,022 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.26112,288,593 - 112,359,815 (-)NCBISscrofa10.2Sscrofa10.2susScr3
RPRD1A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11844,735,013 - 44,808,023 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1844,734,911 - 44,808,178 (+)EnsemblChlSab1.1 EnsemblchlSab2Vervet-AGM
Vero_WHO_p1.0NW_02366605019,195,604 - 19,268,609 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Rprd1a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462477910,301,878 - 10,371,184 (-)EnsemblHetGla_female_1.0 EnsemblhetGla2HetGla_female_1.0 Ensembl
HetGla 1.0NW_00462477910,299,378 - 10,371,213 (-)NCBIHetGla 1.0HetGla 1.0hetGla2
Rprd1a
(Rattus rattus - black rat)
Black Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rrattus_CSIRO_v11519,313,696 - 19,363,434 (+)NCBIRrattus_CSIRO_v1

Variants

.
Variants in RPRD1A
15 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 18q12.1-12.3(chr18:31655749-42564094)x3 copy number gain See cases [RCV000050773] Chr18:31655749..42564094 [GRCh38]
Chr18:29235712..40144059 [GRCh37]
Chr18:27489710..38398057 [NCBI36]
Chr18:18q12.1-12.3		 pathogenic
GRCh38/hg38 18q12.1-12.3(chr18:29444510-40403652)x1 copy number loss See cases [RCV000051090] Chr18:29444510..40403652 [GRCh38]
Chr18:27024475..37983616 [GRCh37]
Chr18:25278473..36237614 [NCBI36]
Chr18:18q12.1-12.3		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3 copy number gain See cases [RCV000051048] Chr18:148963..80252149 [GRCh38]
Chr18:148963..78010032 [GRCh37]
Chr18:138963..76111023 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q11.1-23(chr18:20960320-80234429)x3 copy number gain See cases [RCV000052543] Chr18:20960320..80234429 [GRCh38]
Chr18:18540281..77992312 [GRCh37]
Chr18:16794279..76093303 [NCBI36]
Chr18:18q11.1-23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:53345-80209986)x3 copy number gain See cases [RCV000052501] Chr18:53345..80209986 [GRCh38]
Chr18:53345..77967869 [GRCh37]
Chr18:43345..76068860 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q11.1-23(chr18:20989762-80209986)x3 copy number gain See cases [RCV000052549] Chr18:20989762..80209986 [GRCh38]
Chr18:18569723..77967869 [GRCh37]
Chr18:16823721..76068860 [NCBI36]
Chr18:18q11.1-23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148763-80252290)x3 copy number gain See cases [RCV000052507] Chr18:148763..80252290 [GRCh38]
Chr18:148763..78010173 [GRCh37]
Chr18:138763..76111164 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q12.1-22.1(chr18:29249202-65448117)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052563]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052563]|See cases [RCV000052563] Chr18:29249202..65448117 [GRCh38]
Chr18:26829167..63115353 [GRCh37]
Chr18:25083165..61266333 [NCBI36]
Chr18:18q12.1-22.1		 pathogenic
GRCh38/hg38 18q12.1-12.2(chr18:35097761-39379288)x3 copy number gain See cases [RCV000052567] Chr18:35097761..39379288 [GRCh38]
Chr18:32677725..36959252 [GRCh37]
Chr18:30931723..35213250 [NCBI36]
Chr18:18q12.1-12.2		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80244381)x3 copy number gain See cases [RCV000052514] Chr18:148963..80244381 [GRCh38]
Chr18:148963..78002264 [GRCh37]
Chr18:138963..76103255 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q12.1-12.3(chr18:32111530-44070219)x1 copy number loss See cases [RCV000053829] Chr18:32111530..44070219 [GRCh38]
Chr18:29691493..41650184 [GRCh37]
Chr18:27945491..39904182 [NCBI36]
Chr18:18q12.1-12.3		 pathogenic
GRCh38/hg38 18q12.1-12.3(chr18:34047118-41394354)x1 copy number loss See cases [RCV000053830] Chr18:34047118..41394354 [GRCh38]
Chr18:31627082..38974318 [GRCh37]
Chr18:29881080..37228316 [NCBI36]
Chr18:18q12.1-12.3		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:149089-80234391)x3 copy number gain See cases [RCV000134110] Chr18:149089..80234391 [GRCh38]
Chr18:149089..77992274 [GRCh37]
Chr18:139089..76093265 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q12.1-23(chr18:32123105-80252149)x3 copy number gain See cases [RCV000136890] Chr18:32123105..80252149 [GRCh38]
Chr18:29703068..78010032 [GRCh37]
Chr18:27957066..76111023 [NCBI36]
Chr18:18q12.1-23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:118760-80254946)x3 copy number gain See cases [RCV000138656] Chr18:118760..80254946 [GRCh38]
Chr18:118760..78012829 [GRCh37]
Chr18:108760..76113817 [NCBI36]
Chr18:18p11.32-q23		 pathogenic|conflicting data from submitters
GRCh38/hg38 18q12.1-12.2(chr18:33373798-37364748)x1 copy number loss See cases [RCV000138295] Chr18:33373798..37364748 [GRCh38]
Chr18:30953762..34944711 [GRCh37]
Chr18:29207760..33198709 [NCBI36]
Chr18:18q12.1-12.2		 likely pathogenic
GRCh38/hg38 18p11.32-q23(chr18:149089-80254936)x3 copy number gain See cases [RCV000139397] Chr18:149089..80254936 [GRCh38]
Chr18:149089..78012819 [GRCh37]
Chr18:139089..76113807 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:136227-80256240)x3 copy number gain See cases [RCV000142244] Chr18:136227..80256240 [GRCh38]
Chr18:136227..78014123 [GRCh37]
Chr18:126227..76115097 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q12.2(chr18:35990843-36963685)x1 copy number loss See cases [RCV000142344] Chr18:35990843..36963685 [GRCh38]
Chr18:33570806..34543648 [GRCh37]
Chr18:31824804..32797646 [NCBI36]
Chr18:18q12.2		 uncertain significance
GRCh38/hg38 18q11.1-12.3(chr18:20941324-40360620)x3 copy number gain See cases [RCV000142226] Chr18:20941324..40360620 [GRCh38]
Chr18:18521285..37940584 [GRCh37]
Chr18:16775283..36194582 [NCBI36]
Chr18:18q11.1-12.3		 pathogenic
GRCh38/hg38 18q11.1-22.3(chr18:20962119-74691446)x3 copy number gain See cases [RCV000143057] Chr18:20962119..74691446 [GRCh38]
Chr18:18542080..72403402 [GRCh37]
Chr18:16796078..70532390 [NCBI36]
Chr18:18q11.1-22.3		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:136226-80256240)x3 copy number gain See cases [RCV000143218] Chr18:136226..80256240 [GRCh38]
Chr18:136226..78014123 [GRCh37]
Chr18:126226..76115097 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3 copy number gain See cases [RCV000148072] Chr18:148963..80252149 [GRCh38]
Chr18:148963..78010032 [GRCh37]
Chr18:138963..76111023 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:163323-78005236)x3 copy number gain See cases [RCV000240130] Chr18:163323..78005236 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q12.2(chr18:33611007-33722860)x4 copy number gain Breast ductal adenocarcinoma [RCV000207101] Chr18:33611007..33722860 [GRCh37]
Chr18:18q12.2		 uncertain significance
GRCh37/hg19 18q11.1-23(chr18:18548019-77954165)x3 copy number gain See cases [RCV000240476] Chr18:18548019..77954165 [GRCh37]
Chr18:18q11.1-23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136226-78014123)x3 copy number gain See cases [RCV000446047] Chr18:136226..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:163323-78005185)x3 copy number gain See cases [RCV000445851] Chr18:163323..78005185 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q12.2-23(chr18:33417216-78014123)x3 copy number gain See cases [RCV000512081] Chr18:33417216..78014123 [GRCh37]
Chr18:18q12.2-23		 pathogenic
GRCh37/hg19 18q11.2-12.2(chr18:20069932-36887326)x1 copy number loss See cases [RCV000510691] Chr18:20069932..36887326 [GRCh37]
Chr18:18q11.2-12.2		 pathogenic
GRCh37/hg19 18p11.32-q21.1(chr18:136227-46171053)x3 copy number gain See cases [RCV000511857] Chr18:136227..46171053 [GRCh37]
Chr18:18p11.32-q21.1		 pathogenic
GRCh37/hg19 18q12.1-12.2(chr18:30368042-36078516)x1 copy number loss See cases [RCV000511858] Chr18:30368042..36078516 [GRCh37]
Chr18:18q12.1-12.2		 likely pathogenic
GRCh37/hg19 18q11.1-22.1(chr18:18521285-64495798)x3 copy number gain See cases [RCV000511734] Chr18:18521285..64495798 [GRCh37]
Chr18:18q11.1-22.1		 pathogenic
GRCh37/hg19 18p11.21-q23(chr18:14869204-78014123)x3 copy number gain See cases [RCV000512030] Chr18:14869204..78014123 [GRCh37]
Chr18:18p11.21-q23		 pathogenic
GRCh37/hg19 18q11.2-21.1(chr18:24835114-46917217)x3 copy number gain See cases [RCV000511124] Chr18:24835114..46917217 [GRCh37]
Chr18:18q11.2-21.1		 likely benign
GRCh37/hg19 18p11.32-q23(chr18:136227-78014123) copy number gain See cases [RCV000511189] Chr18:136227..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q12.1-23(chr18:31879854-78014123)x3 copy number gain See cases [RCV000512425] Chr18:31879854..78014123 [GRCh37]
Chr18:18q12.1-23		 pathogenic
GRCh37/hg19 18q12.1-12.2(chr18:29711972-35866193)x1 copy number loss not provided [RCV000684043] Chr18:29711972..35866193 [GRCh37]
Chr18:18q12.1-12.2		 pathogenic
GRCh37/hg19 18q12.2(chr18:32988821-33701451)x3 copy number gain not provided [RCV000684010] Chr18:32988821..33701451 [GRCh37]
Chr18:18q12.2		 uncertain significance
GRCh37/hg19 18q11.1-21.2(chr18:18539806-49926444)x2 copy number gain not provided [RCV000739776] Chr18:18539806..49926444 [GRCh37]
Chr18:18q11.1-21.2		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:12842-78015180)x3 copy number gain not provided [RCV000752245] Chr18:12842..78015180 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:13034-78015180)x3 copy number gain not provided [RCV000752246] Chr18:13034..78015180 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q12.2(chr18:33554981-36939357) copy number loss not provided [RCV000767741] Chr18:33554981..36939357 [GRCh37]
Chr18:18q12.2		 pathogenic
GRCh37/hg19 18q11.2-12.2(chr18:22868759-34335753)x1 copy number loss not provided [RCV001006964] Chr18:22868759..34335753 [GRCh37]
Chr18:18q11.2-12.2		 pathogenic
GRCh37/hg19 18q12.2(chr18:33384923-34561159)x3 copy number gain not provided [RCV001006965] Chr18:33384923..34561159 [GRCh37]
Chr18:18q12.2		 uncertain significance
GRCh37/hg19 18q11.2-21.2(chr18:20689919-49455212)x3 copy number gain not provided [RCV001006980] Chr18:20689919..49455212 [GRCh37]
Chr18:18q11.2-21.2		 pathogenic
GRCh37/hg19 18q11.2-23(chr18:23626739-78014976)x3 copy number gain not provided [RCV001537911] Chr18:23626739..78014976 [GRCh37]
Chr18:18q11.2-23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:1-78077248) copy number gain Trisomy 18 [RCV002280660] Chr18:1..78077248 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q11.2-12.2(chr18:23971647-33737300)x1 copy number loss See cases [RCV001263022] Chr18:23971647..33737300 [GRCh37]
Chr18:18q11.2-12.2		 pathogenic
Single allele deletion Intellectual disability [RCV001787257] Chr18:1262336..53254747 [GRCh37]
Chr18:18p11.32-q21.2		 pathogenic
Single allele deletion Deletion of long arm of chromosome 18 [RCV004801487] Chr18:23614482..49306881 [GRCh38]
Chr18:18q11.2-21.1		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136226-78014123) copy number gain not specified [RCV002052616] Chr18:136226..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q12.2(chr18:33571456-34552945)x1 copy number loss not provided [RCV001836546] Chr18:33571456..34552945 [GRCh37]
Chr18:18q12.2		 uncertain significance
NM_018170.5(RPRD1A):c.449A>G (p.Asn150Ser) single nucleotide variant not specified [RCV004129303] Chr18:36030845 [GRCh38]
Chr18:33610808 [GRCh37]
Chr18:18q12.2		 uncertain significance
NM_018170.5(RPRD1A):c.902A>G (p.His301Arg) single nucleotide variant not specified [RCV004136423] Chr18:35993188 [GRCh38]
Chr18:33573151 [GRCh37]
Chr18:18q12.2		 uncertain significance
GRCh37/hg19 18q12.1-12.3(chr18:26595964-38643072)x1 copy number loss not provided [RCV003483335] Chr18:26595964..38643072 [GRCh37]
Chr18:18q12.1-12.3		 pathogenic
NM_018170.5(RPRD1A):c.280A>G (p.Ser94Gly) single nucleotide variant not specified [RCV004452039] Chr18:36033709 [GRCh38]
Chr18:33613672 [GRCh37]
Chr18:18q12.2		 uncertain significance
NM_018170.5(RPRD1A):c.514G>T (p.Asp172Tyr) single nucleotide variant not specified [RCV004452040] Chr18:36027283 [GRCh38]
Chr18:33607246 [GRCh37]
Chr18:18q12.2		 uncertain significance
NM_018170.5(RPRD1A):c.20C>T (p.Ala7Val) single nucleotide variant not specified [RCV004452038] Chr18:36067385 [GRCh38]
Chr18:33647348 [GRCh37]
Chr18:18q12.2		 uncertain significance
NM_018170.5(RPRD1A):c.800G>A (p.Arg267His) single nucleotide variant not specified [RCV004452041] Chr18:35993290 [GRCh38]
Chr18:33573253 [GRCh37]
Chr18:18q12.2		 uncertain significance
NM_018170.5(RPRD1A):c.145C>T (p.Arg49Trp) single nucleotide variant not specified [RCV004452037] Chr18:36067260 [GRCh38]
Chr18:33647223 [GRCh37]
Chr18:18q12.2		 uncertain significance
NM_018170.5(RPRD1A):c.779A>G (p.His260Arg) single nucleotide variant not specified [RCV004665774] Chr18:36026910 [GRCh38]
Chr18:33606873 [GRCh37]
Chr18:18q12.2		 uncertain significance
NM_018170.5(RPRD1A):c.398A>G (p.Lys133Arg) single nucleotide variant not specified [RCV004665775] Chr18:36030896 [GRCh38]
Chr18:33610859 [GRCh37]
Chr18:18q12.2		 uncertain significance
NM_018170.5(RPRD1A):c.752A>G (p.Gln251Arg) single nucleotide variant not specified [RCV004665776] Chr18:36026937 [GRCh38]
Chr18:33606900 [GRCh37]
Chr18:18q12.2		 uncertain significance
NM_018170.5(RPRD1A):c.656C>A (p.Ala219Glu) single nucleotide variant not specified [RCV004860873] Chr18:36027033 [GRCh38]
Chr18:33606996 [GRCh37]
Chr18:18q12.2		 uncertain significance
GRCh37/hg19 18q11.2-23(chr18:19309942-78014123)x3 copy number gain not provided [RCV004819319] Chr18:19309942..78014123 [GRCh37]
Chr18:18q11.2-23		 pathogenic
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:3266
Count of miRNA genes:1065
Interacting mature miRNAs:1294
Transcripts:ENST00000319040, ENST00000337059, ENST00000357384, ENST00000399022, ENST00000585879, ENST00000585953, ENST00000587563, ENST00000588459, ENST00000588737, ENST00000589050, ENST00000590898, ENST00000591994, ENST00000592674
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407335170GWAS984146_Hmean corpuscular hemoglobin QTL GWAS984146 (human)7e-12mean corpuscular hemoglobin183599843835998439Human
597080464GWAS1176538_Hmean corpuscular volume QTL GWAS1176538 (human)1e-11mean corpuscular volume183603985936039862Human
407043909GWAS692885_Hmean corpuscular volume QTL GWAS692885 (human)1e-11mean corpuscular volume183603985936039862Human
597990669GWAS1709968_Htrait in response to tenofovir (anhydrous) QTL GWAS1709968 (human)0.000006trait in response to tenofovir (anhydrous)183600335336003354Human
406993483GWAS642459_Hmean corpuscular hemoglobin concentration QTL GWAS642459 (human)8e-14mean corpuscular hemoglobin concentration183602225036022251Human
406955949GWAS604925_Htuberculosis QTL GWAS604925 (human)0.000002tuberculosis183599638935996390Human
406995630GWAS644606_Hmean corpuscular hemoglobin concentration QTL GWAS644606 (human)3e-13mean corpuscular hemoglobin concentration183602225036022251Human
597308213GWAS1404287_Hmean corpuscular hemoglobin QTL GWAS1404287 (human)7e-12mean corpuscular hemoglobin183599843835998439Human
628538233GWAS2446462_Hmean corpuscular hemoglobin QTL GWAS2446462 (human)7e-12erythrocyte hemoglobin amount (VT:0010953)mean corpuscular hemoglobin (CMO:0000290)183599843835998439Human
407110891GWAS759867_Hmean corpuscular hemoglobin QTL GWAS759867 (human)1e-11erythrocyte hemoglobin amount (VT:0010953)mean corpuscular hemoglobin (CMO:0000290)183602225036022251Human
597177000GWAS1273074_Htuberculosis QTL GWAS1273074 (human)0.000002tuberculosis183599638935996390Human
628402212GWAS2310441_Hmean corpuscular hemoglobin concentration QTL GWAS2310441 (human)8e-14erythrocyte hemoglobin amount (VT:0010953)mean corpuscular hemoglobin concentration (CMO:0000291)183602225036022251Human
628445248GWAS2353477_Hmean corpuscular hemoglobin concentration QTL GWAS2353477 (human)3e-13erythrocyte hemoglobin amount (VT:0010953)mean corpuscular hemoglobin concentration (CMO:0000291)183602225036022251Human
628804397GWAS2712626_Htuberculosis QTL GWAS2712626 (human)0.000002tuberculosis183599638935996390Human
597064079GWAS1160153_Hresponse to tenofovir QTL GWAS1160153 (human)0.000006response to tenofovir183600335336003354Human
406991998GWAS640974_Hresponse to tenofovir QTL GWAS640974 (human)0.000006response to tenofovir183600335336003354Human
407006303GWAS655279_Hmean corpuscular hemoglobin QTL GWAS655279 (human)1e-11mean corpuscular hemoglobin183599836935998371Human
598017720GWAS1737019_Herythrocyte volume QTL GWAS1737019 (human)1e-11erythrocyte volume183603985936039862Human
597079240GWAS1175314_Hmean corpuscular hemoglobin QTL GWAS1175314 (human)1e-11erythrocyte hemoglobin amount (VT:0010953)mean corpuscular hemoglobin (CMO:0000290)183599836935998371Human

Markers in Region
RH47092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371833,585,964 - 33,586,079UniSTSGRCh37
Build 361831,839,962 - 31,840,077RGDNCBI36
Celera1830,393,843 - 30,393,958RGD
Cytogenetic Map18q12.2UniSTS
HuRef1830,444,897 - 30,445,012UniSTS
GeneMap99-GB4 RH Map18269.06UniSTS
RH80213  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371833,569,842 - 33,569,953UniSTSGRCh37
GRCh37632,242,144 - 32,242,255UniSTSGRCh37
Build 36632,350,122 - 32,350,233RGDNCBI36
Celera1830,377,721 - 30,377,832UniSTS
Celera633,809,272 - 33,809,383RGD
Cytogenetic Map18q12.2UniSTS
HuRef1830,428,775 - 30,428,886UniSTS
HuRef631,996,511 - 31,996,622UniSTS
GeneMap99-GB4 RH Map18290.83UniSTS
RH99173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371833,571,961 - 33,572,097UniSTSGRCh37
Build 361831,825,959 - 31,826,095RGDNCBI36
Celera1830,379,840 - 30,379,976RGD
Cytogenetic Map18q12.2UniSTS
HuRef1830,430,894 - 30,431,030UniSTS
GeneMap99-GB4 RH Map18290.4UniSTS
P15RS_1703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371833,569,688 - 33,570,578UniSTSGRCh37
Build 361831,823,686 - 31,824,576RGDNCBI36
Celera1830,377,567 - 30,378,457RGD
HuRef1830,428,621 - 30,429,511UniSTS
WIAF-1571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371833,606,933 - 33,607,183UniSTSGRCh37
Build 361831,860,931 - 31,861,181RGDNCBI36
Celera1830,414,814 - 30,415,064RGD
Cytogenetic Map18q12.2UniSTS
HuRef1830,465,922 - 30,466,172UniSTS
GeneMap99-GB4 RH Map18290.36UniSTS
SGC38081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371833,605,601 - 33,605,868UniSTSGRCh37
Build 361831,859,599 - 31,859,866RGDNCBI36
Celera1830,413,482 - 30,413,749RGD
Cytogenetic Map18q12.2UniSTS
HuRef1830,464,590 - 30,464,857UniSTS
GeneMap99-GB4 RH Map18292.25UniSTS
Whitehead-RH Map18286.1UniSTS
NCBI RH Map18404.9UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 174 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001303411 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001303412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001303413 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_018170 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017025808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC091060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF419845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001518 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK314569 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW409855 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000225 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC010136 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG325568 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA944610 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068260 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB444937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000357384   ⟹   ENSP00000349955
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1835,989,886 - 36,067,556 (-)Ensembl
Ensembl Acc Id: ENST00000399022   ⟹   ENSP00000381984
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1835,989,824 - 36,067,559 (-)Ensembl
Ensembl Acc Id: ENST00000585879   ⟹   ENSP00000468173
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1835,984,389 - 35,993,163 (-)Ensembl
Ensembl Acc Id: ENST00000585953   ⟹   ENSP00000467268
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1836,024,889 - 36,030,850 (-)Ensembl
Ensembl Acc Id: ENST00000587563   ⟹   ENSP00000468108
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1835,984,387 - 35,993,300 (-)Ensembl
Ensembl Acc Id: ENST00000588459
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1836,052,875 - 36,064,424 (-)Ensembl
Ensembl Acc Id: ENST00000588737   ⟹   ENSP00000465444
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1835,993,040 - 36,067,559 (-)Ensembl
Ensembl Acc Id: ENST00000589050   ⟹   ENSP00000468209
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1836,025,599 - 36,067,557 (-)Ensembl
Ensembl Acc Id: ENST00000590898   ⟹   ENSP00000467991
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1835,989,824 - 36,067,530 (-)Ensembl
Ensembl Acc Id: ENST00000591994
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1836,025,599 - 36,028,190 (-)Ensembl
Ensembl Acc Id: ENST00000592674   ⟹   ENSP00000467949
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1836,033,752 - 36,067,576 (-)Ensembl
Ensembl Acc Id: ENST00000896647   ⟹   ENSP00000566706
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1835,991,846 - 36,067,566 (-)Ensembl
Ensembl Acc Id: ENST00000916733   ⟹   ENSP00000586792
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1835,989,831 - 36,067,554 (-)Ensembl
Ensembl Acc Id: ENST00000966876   ⟹   ENSP00000636935
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1835,991,852 - 36,067,554 (-)Ensembl
RefSeq Acc Id: NM_001303411   ⟹   NP_001290340
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381835,989,824 - 36,067,559 (-)NCBI
CHM1_11833,496,805 - 33,574,611 (-)NCBI
T2T-CHM13v2.01836,181,320 - 36,259,091 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001303412   ⟹   NP_001290341
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381835,989,824 - 36,067,559 (-)NCBI
CHM1_11833,496,805 - 33,574,611 (-)NCBI
T2T-CHM13v2.01836,181,320 - 36,259,091 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001303413   ⟹   NP_001290342
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381836,024,886 - 36,067,559 (-)NCBI
CHM1_11833,531,887 - 33,574,611 (-)NCBI
T2T-CHM13v2.01836,216,418 - 36,259,091 (-)NCBI
Sequence:
RefSeq Acc Id: NM_018170   ⟹   NP_060640
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381835,989,824 - 36,067,559 (-)NCBI
GRCh371833,569,787 - 33,647,538 (-)NCBI
Build 361831,823,789 - 31,901,371 (-)NCBI Archive
Celera1830,377,670 - 30,455,253 (-)RGD
HuRef1830,428,724 - 30,506,362 (-)ENTREZGENE
CHM1_11833,496,805 - 33,574,611 (-)NCBI
T2T-CHM13v2.01836,181,320 - 36,259,091 (-)NCBI
Sequence:
RefSeq Acc Id: NP_060640   ⟸   NM_018170
- Peptide Label: isoform 1
- UniProtKB: Q96FY9 (UniProtKB/Swiss-Prot),   Q7Z5G8 (UniProtKB/Swiss-Prot),   B2RBA3 (UniProtKB/Swiss-Prot),   A8KA42 (UniProtKB/Swiss-Prot),   Q9NVL4 (UniProtKB/Swiss-Prot),   Q96P16 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001290341   ⟸   NM_001303412
- Peptide Label: isoform 2
- UniProtKB: Q96P16 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001290340   ⟸   NM_001303411
- Peptide Label: isoform 2
- UniProtKB: Q96P16 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001290342   ⟸   NM_001303413
- Peptide Label: isoform 3
- UniProtKB: A0A0C4DGQ6 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000381984   ⟸   ENST00000399022
Ensembl Acc Id: ENSP00000468173   ⟸   ENST00000585879
Ensembl Acc Id: ENSP00000467268   ⟸   ENST00000585953
Ensembl Acc Id: ENSP00000468108   ⟸   ENST00000587563
Ensembl Acc Id: ENSP00000465444   ⟸   ENST00000588737
Ensembl Acc Id: ENSP00000468209   ⟸   ENST00000589050
Ensembl Acc Id: ENSP00000467991   ⟸   ENST00000590898
Ensembl Acc Id: ENSP00000467949   ⟸   ENST00000592674
Ensembl Acc Id: ENSP00000349955   ⟸   ENST00000357384
Ensembl Acc Id: ENSP00000566706   ⟸   ENST00000896647
Ensembl Acc Id: ENSP00000636935   ⟸   ENST00000966876
Ensembl Acc Id: ENSP00000586792   ⟸   ENST00000916733
Protein Domains
CID   RPRD1A/B C-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96P16-F1-model_v2 AlphaFold Q96P16 1-312 view protein structure

Promoters
RGD ID:6795028
Promoter ID:HG_KWN:27891
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:ENST00000319040,   ENST00000337059,   ENST00000357384,   OTTHUMT00000255802,   UC010DMW.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361831,901,274 - 31,901,774 (-)MPROMDB
RGD ID:7237197
Promoter ID:EPDNEW_H24345
Type:initiation region
Name:RPRD1A_1
Description:regulation of nuclear pre-mRNA domain containing 1A
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381836,067,557 - 36,067,617EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:25560 AgrOrtholog
COSMIC RPRD1A COSMIC
Ensembl Genes ENSG00000141425 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000357384.8 UniProtKB/Swiss-Prot
  ENST00000399022 ENTREZGENE
  ENST00000399022.9 UniProtKB/Swiss-Prot
  ENST00000588737 ENTREZGENE
  ENST00000588737.5 UniProtKB/Swiss-Prot
  ENST00000589050 ENTREZGENE
  ENST00000590898 ENTREZGENE
  ENST00000590898.5 UniProtKB/Swiss-Prot
Gene3D-CATH 1.25.40.90 UniProtKB/Swiss-Prot
  6.10.250.2560 UniProtKB/Swiss-Prot
GTEx ENSG00000141425 GTEx
HGNC ID HGNC:25560 ENTREZGENE
Human Proteome Map RPRD1A Human Proteome Map
InterPro CID_dom UniProtKB/Swiss-Prot
  CREPT UniProtKB/Swiss-Prot
  ENTH_VHS UniProtKB/Swiss-Prot
  RPRD1A_CID UniProtKB/Swiss-Prot
KEGG Report hsa:55197 UniProtKB/Swiss-Prot
NCBI Gene 55197 ENTREZGENE
OMIM 610347 OMIM
PANTHER CYCLIN-DEPENDENT KINASE INHIBITOR-RELATED PROTEIN UniProtKB/Swiss-Prot
  REGULATION OF NUCLEAR PRE-MRNA DOMAIN-CONTAINING PROTEIN 1A UniProtKB/Swiss-Prot
Pfam CREPT UniProtKB/Swiss-Prot
  CTD_bind UniProtKB/Swiss-Prot
PharmGKB PA162402042 PharmGKB
PROSITE CID UniProtKB/Swiss-Prot
SMART RPR UniProtKB/Swiss-Prot
Superfamily-SCOP SSF48464 UniProtKB/Swiss-Prot
UniProt A0A0C4DGQ6 ENTREZGENE, UniProtKB/TrEMBL
  A8KA42 ENTREZGENE
  B2RBA3 ENTREZGENE
  K7EP82_HUMAN UniProtKB/TrEMBL
  K7EQR8_HUMAN UniProtKB/TrEMBL
  K7ER50_HUMAN UniProtKB/TrEMBL
  Q7Z5G8 ENTREZGENE
  Q96FY9 ENTREZGENE
  Q96P16 ENTREZGENE
  Q9NVL4 ENTREZGENE
  RPR1A_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A8KA42 UniProtKB/Swiss-Prot
  B2RBA3 UniProtKB/Swiss-Prot
  Q7Z5G8 UniProtKB/Swiss-Prot
  Q96FY9 UniProtKB/Swiss-Prot
  Q9NVL4 UniProtKB/Swiss-Prot