22q11.21 Copy Number Variation
Description
The 22q11.2 copy number variation syndrome can result in the loss or duplication of up to 46 protein-coding genes, which have wide-spread effects on human development. In case of deletion, the loss of TBX1 is thought to be responsible for a large proportion of the 22q11.2DS phenotype, due its role in the development of the heart, thymus, thyroid, parathyroids and more.
Genomic location GRCh37/hg19

Disorder Information from Orphanet
-
ORPHA:
567
Deletion syndrome
OMIM: 125520, 192430, 188400
Disease description: No description available.
World-wide prevalence: 1-5 / 10 000
Very frequent (99–80%) phenotypic features: Cleft palate, Epicanthus, Low-set ears, Conductive hearing impairment, Bulbous nose, Prominent nasal bridge, Wide nasal bridge, Telecanthus, Upslanted palpebral fissure, Abnormality of the pharynx, Hypoplasia of the thymus, Hypotonia, Hypernasal speech, Ventricular septal defect, Atrial septal defect, Tetralogy of Fallot, Abnormal pulmonary valve morphology, Truncus arteriosus, Abnormal facial shape, Aphasia, Platybasia, Immunodeficiency, Abnormal aortic arch morphology, Abnormal cardiovascular system morphology -
ORPHA:
1727
Duplication syndrome
OMIM: 608363
Disease description: No description available.
World-wide prevalence: Unknown
Very frequent (99–80%) phenotypic features: No phenotypic features available.
Interactive Pathway Viewer
Gene Information
HGNC | Gene Name | NCBI | Ensembl | UniProt |
---|---|---|---|---|
PRODH | proline dehydrogenase 1 | 5625 | ENSG00000100033 | O43272 |
DGCR5 | DiGeorge syndrome critical region gene 5 | 26220 | ENSG00000273032 | |
DGCR2 | DiGeorge syndrome critical region gene 2 | 9993 | ENSG00000070413 | P98153 |
ESS2 | ess-2 spliceosome associated protein | 8220 | ENSG00000100056 | Q96DF8 |
TSSK2 | testis specific serine kinase 2 | 23617 | ENSG00000206203 | Q96PF2 |
GSC2 | goosecoid homeobox 2 | 2928 | ENSG00000063515 | O15499 |
SLC25A1 | solute carrier family 25 member 1 | 6576 | ENSG00000100075 | P53007 |
CLTCL1 | clathrin heavy chain like 1 | 8218 | ENSG00000070371 | P53675 |
HIRA | histone cell cycle regulator | 7290 | ENSG00000100084 | P54198 |
C22orf39 | chromosome 22 open reading frame 39 | 128977 | ENSG00000242259 | Q6P5X5 |
MRPL40 | mitochondrial ribosomal protein L40 | 64976 | ENSG00000185608 | Q9NQ50 |
UFD1 | ubiquitin recognition factor in ER associated degradation 1 | 7353 | ENSG00000070010 | Q92890 |
CDC45 | cell division cycle 45 | 8318 | ENSG00000093009 | O75419 |
CLDN5 | claudin 5 | 7122 | ENSG00000184113 | O00501 |
SEPTIN5 | septin 5 | 5413 | ENSG00000184702 | Q99719 |
GP1BB | glycoprotein Ib platelet subunit beta | 2812 | ENSG00000203618 | P13224 |
TBX1 | T-box transcription factor 1 | 6899 | ENSG00000184058 | O43435 |
GNB1L | G protein subunit beta 1 like | 54584 | ENSG00000185838 | Q9BYB4 |
RTL10 | retrotransposon Gag like 10 | 79680 | ENSG00000215012 | Q7L3V2 |
TXNRD2 | thioredoxin reductase 2 | 10587 | ENSG00000184470 | Q9NNW7 |
COMT | catechol-O-methyltransferase | 1312 | ENSG00000093010 | P21964 |
ARVCF | ARVCF delta catenin family member | 421 | ENSG00000099889 | O00192 |
TANGO2 | transport and golgi organization 2 homolog | 128989 | ENSG00000183597 | Q6ICL3 |
DGCR8 | DGCR8 microprocessor complex subunit | 54487 | ENSG00000128191 | Q8WYQ5 |
TRMT2A | tRNA methyltransferase 2A | 27037 | ENSG00000099899 | Q8IZ69 |
RANBP1 | RAN binding protein 1 | 5902 | ENSG00000099901 | P43487 |
ZDHHC8 | zDHHC palmitoyltransferase 8 | 29801 | ENSG00000099904 | Q9ULC8 |
CCDC188 | coiled-coil domain containing 188 | 388849 | ENSG00000234409 | H7C350 |
RTN4R | reticulon 4 receptor | 65078 | ENSG00000040608 | Q9BZR6 |
DGCR6L | DiGeorge syndrome critical region gene 6 like | 85359 | ENSG00000128185 | Q9BY27 |
FAM230G | family with sequence similarity 230 member G | 101927859 | ENSG00000188280 | |
USP41P | ubiquitin specific peptidase 41, pseudogene | 373856 | ENSG00000161133 | |
ZNF74 | zinc finger protein 74 | 7625 | ENSG00000185252 | Q16587 |
SCARF2 | scavenger receptor class F member 2 | 91179 | ENSG00000244486 | Q96GP6 |
KLHL22 | kelch like family member 22 | 84861 | ENSG00000099910 | Q53GT1 |
MED15 | mediator complex subunit 15 | 51586 | ENSG00000099917 | Q96RN5 |
PI4KA | phosphatidylinositol 4-kinase alpha | 5297 | ENSG00000241973 | P42356 |
SERPIND1 | serpin family D member 1 | 3053 | ENSG00000099937 | P05546 |
SNAP29 | synaptosome associated protein 29 | 9342 | ENSG00000099940 | O95721 |
CRKL | CRK like proto-oncogene, adaptor protein | 1399 | ENSG00000099942 | P46109 |
AIFM3 | AIF family member 3 | 150209 | ENSG00000183773 | Q96NN9 |
LZTR1 | leucine zipper like post translational regulator 1 | 8216 | ENSG00000099949 | Q8N653 |
THAP7 | THAP domain containing 7 | 80764 | ENSG00000184436 | Q9BT49 |
P2RX6 | purinergic receptor P2X 6 | 9127 | ENSG00000099957 | O15547 |
SLC7A4 | solute carrier family 7 member 4 | 6545 | ENSG00000099960 | O43246 |
LRRC74B | leucine rich repeat containing 74B | 400891 | ENSG00000187905 | Q6ZQY2 |