COL22A1 (collagen type XXII alpha 1 chain) - Rat Genome Database

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Gene: COL22A1 (collagen type XXII alpha 1 chain) Homo sapiens
Analyze
Symbol: COL22A1
Name: collagen type XXII alpha 1 chain
RGD ID: 1319222
HGNC Page HGNC
Description: Predicted to be an extracellular matrix structural constituent. Predicted to be involved in angiogenesis; endothelial cell morphogenesis; and extracellular matrix organization. Predicted to localize to extracellular matrix and extracellular space. Implicated in intracranial aneurysm.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: collagen alpha-1(XXII) chain; collagen alpha-1(XXII) chain-like; collagen type XXII alpha 1; collagen, type XXII, alpha 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: LOC100420255  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl8138,588,235 - 138,914,041 (-)EnsemblGRCh38hg38GRCh38
GRCh388138,588,235 - 138,914,087 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh378139,600,478 - 139,926,284 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 368139,669,660 - 139,995,418 (-)NCBINCBI36hg18NCBI36
Celera8135,769,113 - 136,093,411 (-)NCBI
Cytogenetic Map8q24.23-q24.3NCBI
HuRef8135,079,773 - 135,237,211 (-)NCBIHuRef
HuRef8134,914,571 - 135,063,660 (-)NCBIHuRef
CHM1_18139,640,714 - 139,967,048 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

Additional References at PubMed
PMID:12477932   PMID:15016833   PMID:16085121   PMID:19253462   PMID:20222955   PMID:20379614   PMID:21873635   PMID:23508266   PMID:24131632   PMID:24428702   PMID:24649348   PMID:25959826  
PMID:27111861   PMID:27781307   PMID:27976729   PMID:30678304  


Genomics

Comparative Map Data
COL22A1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl8138,588,235 - 138,914,041 (-)EnsemblGRCh38hg38GRCh38
GRCh388138,588,235 - 138,914,087 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh378139,600,478 - 139,926,284 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 368139,669,660 - 139,995,418 (-)NCBINCBI36hg18NCBI36
Celera8135,769,113 - 136,093,411 (-)NCBI
Cytogenetic Map8q24.23-q24.3NCBI
HuRef8135,079,773 - 135,237,211 (-)NCBIHuRef
HuRef8134,914,571 - 135,063,660 (-)NCBIHuRef
CHM1_18139,640,714 - 139,967,048 (-)NCBICHM1_1
Col22a1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391571,667,644 - 71,906,087 (-)NCBIGRCm39mm39
GRCm39 Ensembl1571,667,644 - 71,906,076 (-)Ensembl
GRCm381571,795,795 - 72,150,979 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1571,795,795 - 72,034,227 (-)EnsemblGRCm38mm10GRCm38
MGSCv371571,628,906 - 71,864,657 (-)NCBIGRCm37mm9NCBIm37
MGSCv361571,627,430 - 71,863,162 (-)NCBImm8
Celera1573,299,139 - 73,536,682 (-)NCBICelera
Cytogenetic Map15D3NCBI
Col22a1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.27103,730,939 - 103,968,452 (-)NCBI
Rnor_6.0 Ensembl7113,015,747 - 113,228,439 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.07113,014,896 - 113,251,165 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.07112,952,113 - 113,188,114 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.47109,509,148 - 109,727,220 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.17109,707,515 - 109,806,673 (-)NCBI
Celera7100,148,068 - 100,385,566 (-)NCBICelera
Cytogenetic Map7q34NCBI
Col22a1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495546112,597,488 - 12,848,410 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495546112,596,449 - 12,870,853 (-)NCBIChiLan1.0ChiLan1.0
COL22A1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.18138,338,835 - 138,664,444 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl8138,347,432 - 138,633,084 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v08135,241,159 - 135,567,550 (-)NCBIMhudiblu_PPA_v0panPan3
COL22A1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11333,735,490 - 33,996,229 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1333,735,656 - 33,996,401 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1333,718,626 - 33,979,031 (-)NCBI
ROS_Cfam_1.01334,116,591 - 34,377,405 (-)NCBI
UMICH_Zoey_3.11333,840,117 - 34,099,779 (-)NCBI
UNSW_CanFamBas_1.01333,929,879 - 34,189,293 (-)NCBI
UU_Cfam_GSD_1.01334,334,014 - 34,603,326 (-)NCBI
Col22a1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244053034,336,206 - 4,567,942 (+)NCBI
SpeTri2.0NW_00493647011,762,312 - 11,994,041 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
COL22A1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl44,069,076 - 4,313,196 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.144,069,045 - 4,313,198 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.243,800,445 - 4,000,044 (+)NCBISscrofa10.2Sscrofa10.2susScr3
COL22A1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.18132,849,109 - 133,176,176 (-)NCBI
Col22a1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473517,373,861 - 17,628,167 (+)NCBI

Position Markers
D8S346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,857,720 - 139,857,955UniSTSGRCh37
Build 368139,926,902 - 139,927,137RGDNCBI36
Celera8136,024,882 - 136,025,121RGD
Cytogenetic Map8q24.3UniSTS
HuRef8135,169,165 - 135,169,404UniSTS
RH102326  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,600,701 - 139,600,830UniSTSGRCh37
Build 368139,669,883 - 139,670,012RGDNCBI36
Celera8135,769,336 - 135,769,465RGD
Cytogenetic Map8q24.3UniSTS
HuRef8134,914,794 - 134,914,923UniSTS
GeneMap99-GB4 RH Map8535.27UniSTS
RH102569  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,790,477 - 139,790,609UniSTSGRCh37
Build 368139,859,659 - 139,859,791RGDNCBI36
Celera8135,957,695 - 135,957,827RGD
Cytogenetic Map8q24.3UniSTS
HuRef8135,102,864 - 135,102,996UniSTS
GeneMap99-GB4 RH Map8535.27UniSTS
D8S1050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,655,808 - 139,655,983UniSTSGRCh37
Build 368139,724,990 - 139,725,165RGDNCBI36
Celera8135,824,430 - 135,824,613RGD
Cytogenetic Map8q24.3UniSTS
HuRef8134,969,918 - 134,970,101UniSTS
deCODE Assembly Map8153.58UniSTS
SHGC-147020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,799,512 - 139,799,838UniSTSGRCh37
Build 368139,868,694 - 139,869,020RGDNCBI36
Celera8135,966,730 - 135,967,056RGD
Cytogenetic Map8q24.3UniSTS
HuRef8135,111,899 - 135,112,225UniSTS
TNG Radiation Hybrid Map870229.0UniSTS
SHGC-149203  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,672,233 - 139,672,511UniSTSGRCh37
Build 368139,741,415 - 139,741,693RGDNCBI36
Celera8135,840,828 - 135,841,106RGD
Cytogenetic Map8q24.3UniSTS
TNG Radiation Hybrid Map870287.0UniSTS
SHGC-132810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,857,736 - 139,858,055UniSTSGRCh37
Build 368139,926,918 - 139,927,237RGDNCBI36
Celera8136,024,898 - 136,025,221RGD
Cytogenetic Map8q24.3UniSTS
HuRef8135,169,181 - 135,169,504UniSTS
TNG Radiation Hybrid Map870202.0UniSTS
SHGC-146301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,923,852 - 139,924,144UniSTSGRCh37
Build 368139,993,034 - 139,993,326RGDNCBI36
Celera8136,091,027 - 136,091,319RGD
Cytogenetic Map8q24.3UniSTS
HuRef8135,234,826 - 135,235,118UniSTS
TNG Radiation Hybrid Map870163.0UniSTS
SHGC-148961  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,924,048 - 139,924,392UniSTSGRCh37
Build 368139,993,230 - 139,993,574RGDNCBI36
Celera8136,091,223 - 136,091,567RGD
Cytogenetic Map8q24.3UniSTS
HuRef8135,235,022 - 135,235,366UniSTS
TNG Radiation Hybrid Map870166.0UniSTS
SHGC-149386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,858,934 - 139,859,218UniSTSGRCh37
Build 368139,928,116 - 139,928,400RGDNCBI36
Celera8136,026,100 - 136,026,384RGD
Cytogenetic Map8q24.3UniSTS
HuRef8135,170,383 - 135,170,667UniSTS
TNG Radiation Hybrid Map870188.0UniSTS
SHGC-149623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,634,739 - 139,635,083UniSTSGRCh37
Build 368139,703,921 - 139,704,265RGDNCBI36
Celera8135,803,367 - 135,803,711RGD
Cytogenetic Map8q24.3UniSTS
HuRef8134,948,824 - 134,949,168UniSTS
TNG Radiation Hybrid Map870268.0UniSTS
SHGC-153336  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,706,024 - 139,706,327UniSTSGRCh37
Build 368139,775,206 - 139,775,509RGDNCBI36
Celera8135,874,627 - 135,874,930RGD
Cytogenetic Map8q24.3UniSTS
HuRef8135,019,765 - 135,020,068UniSTS
TNG Radiation Hybrid Map870281.0UniSTS
SHGC-155040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,889,369 - 139,889,673UniSTSGRCh37
Build 368139,958,551 - 139,958,855RGDNCBI36
Celera8136,056,536 - 136,056,840RGD
Cytogenetic Map8q24.3UniSTS
HuRef8135,200,490 - 135,200,794UniSTS
TNG Radiation Hybrid Map870152.0UniSTS
SHGC-155762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,663,638 - 139,663,958UniSTSGRCh37
Build 368139,732,820 - 139,733,140RGDNCBI36
Celera8135,832,244 - 135,832,563RGD
Cytogenetic Map8q24.3UniSTS
HuRef8134,977,732 - 134,978,051UniSTS
TNG Radiation Hybrid Map870271.0UniSTS
D15S185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,688,588 - 139,688,741UniSTSGRCh37
GRCh37689,848,533 - 89,849,012UniSTSGRCh37
Build 36689,905,252 - 89,905,731RGDNCBI36
Celera8135,857,658 - 135,857,843UniSTS
Celera690,266,417 - 90,266,895RGD
HuRef8135,002,200 - 135,002,385UniSTS
HuRef687,064,145 - 87,064,623UniSTS
Marshfield Genetic Map8158.49UniSTS
L18002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378139,663,732 - 139,664,019UniSTSGRCh37
Build 368139,732,914 - 139,733,201RGDNCBI36
Celera8135,832,338 - 135,832,624RGD
Cytogenetic Map8q24.3UniSTS
HuRef8134,977,826 - 134,978,112UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1927
Count of miRNA genes:855
Interacting mature miRNAs:1019
Transcripts:ENST00000303045, ENST00000341807, ENST00000435777, ENST00000484387, ENST00000487854, ENST00000517515, ENST00000522546
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.


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
High
Medium 11 4 303 9 6 9 50 21 296 18 193 39 1 14
Low 1477 59 324 154 244 46 804 758 1626 207 934 335 111 1 112 528
Below cutoff 833 2548 944 330 1049 278 3301 1359 1743 150 253 1121 56 1030 2168 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_054761 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_152888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516883 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516884 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516886 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013150 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013151 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013152 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001745487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA781676 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC068476 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC105130 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC115720 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF406780 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP006262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC042075 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144535 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX094632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF584374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000303045   ⟹   ENSP00000303153
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8138,588,235 - 138,914,041 (-)Ensembl
RefSeq Acc Id: ENST00000341807
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8138,588,235 - 138,722,193 (-)Ensembl
RefSeq Acc Id: ENST00000435777   ⟹   ENSP00000387655
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8138,588,897 - 138,883,211 (-)Ensembl
RefSeq Acc Id: ENST00000484387
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8138,878,133 - 138,914,006 (-)Ensembl
RefSeq Acc Id: ENST00000487854
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8138,607,938 - 138,620,620 (-)Ensembl
RefSeq Acc Id: ENST00000517515
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8138,825,719 - 138,828,105 (-)Ensembl
RefSeq Acc Id: ENST00000522546   ⟹   ENSP00000428244
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8138,777,907 - 138,779,562 (-)Ensembl
RefSeq Acc Id: NM_152888   ⟹   NP_690848
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,588,235 - 138,914,041 (-)NCBI
GRCh378139,600,478 - 139,926,236 (-)RGD
Build 368139,669,660 - 139,995,418 (-)NCBI Archive
Celera8135,769,113 - 136,093,411 (-)RGD
HuRef8134,914,571 - 135,063,660 (-)NCBI
HuRef8135,079,773 - 135,237,211 (-)NCBI
CHM1_18139,640,714 - 139,967,048 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516883   ⟹   XP_011515185
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,588,235 - 138,914,084 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516884   ⟹   XP_011515186
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,588,235 - 138,914,084 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516885   ⟹   XP_011515187
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,588,235 - 138,914,084 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516886   ⟹   XP_011515188
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,588,235 - 138,914,084 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516887   ⟹   XP_011515189
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,588,235 - 138,828,123 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516888   ⟹   XP_011515190
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,630,772 - 138,914,087 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516889   ⟹   XP_011515191
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,588,235 - 138,790,349 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013150   ⟹   XP_016868639
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,588,235 - 138,914,084 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013151   ⟹   XP_016868640
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,588,235 - 138,914,084 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013152   ⟹   XP_016868641
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,588,235 - 138,827,426 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001745487
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388138,703,309 - 138,914,087 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_690848   ⟸   NM_152888
- Peptide Label: precursor
- UniProtKB: Q8NFW1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011515188   ⟸   XM_011516886
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_011515186   ⟸   XM_011516884
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011515187   ⟸   XM_011516885
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011515185   ⟸   XM_011516883
- Peptide Label: isoform X1
- UniProtKB: Q8NFW1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011515189   ⟸   XM_011516887
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_011515191   ⟸   XM_011516889
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: XP_011515190   ⟸   XM_011516888
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: XP_016868640   ⟸   XM_017013151
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_016868639   ⟸   XM_017013150
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_016868641   ⟸   XM_017013152
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: ENSP00000428244   ⟸   ENST00000522546
RefSeq Acc Id: ENSP00000303153   ⟸   ENST00000303045
RefSeq Acc Id: ENSP00000387655   ⟸   ENST00000435777
Protein Domains
Collagen-like   Laminin G-like   VWFA

Promoters
RGD ID:7214245
Promoter ID:EPDNEW_H12868
Type:initiation region
Name:COL22A1_1
Description:collagen type XXII alpha 1 chain
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
GRCh388138,914,041 - 138,914,101EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8q24.21-24.3(chr8:128220912-145049449)x3 copy number gain See cases [RCV000050830] Chr8:128220912..145049449 [GRCh38]
Chr8:129233158..146274835 [GRCh37]
Chr8:129302340..146245639 [NCBI36]
Chr8:8q24.21-24.3
pathogenic
GRCh38/hg38 8q23.3-24.3(chr8:113580402-145054634)x3 copy number gain See cases [RCV000050638] Chr8:113580402..145054634 [GRCh38]
Chr8:114592631..146280020 [GRCh37]
Chr8:114661807..146250824 [NCBI36]
Chr8:8q23.3-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:95606052-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|See cases [RCV000053677] Chr8:95606052..145054775 [GRCh38]
Chr8:96618280..146280161 [GRCh37]
Chr8:96687456..146250965 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000053678] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
NM_152888.2(COL22A1):c.4420A>C (p.Lys1474Gln) single nucleotide variant Malignant melanoma [RCV000068168] Chr8:138596916 [GRCh38]
Chr8:139609159 [GRCh37]
Chr8:139678341 [NCBI36]
Chr8:8q24.23
not provided
NM_152888.2(COL22A1):c.4370A>G (p.Glu1457Gly) single nucleotide variant Malignant melanoma [RCV000068169] Chr8:138596966 [GRCh38]
Chr8:139609209 [GRCh37]
Chr8:139678391 [NCBI36]
Chr8:8q24.23
not provided
NM_152888.2(COL22A1):c.4367G>T (p.Gly1456Val) single nucleotide variant Malignant melanoma [RCV000068170] Chr8:138596969 [GRCh38]
Chr8:139609212 [GRCh37]
Chr8:139678394 [NCBI36]
Chr8:8q24.23
not provided
NM_152888.2(COL22A1):c.4366G>A (p.Gly1456Arg) single nucleotide variant Malignant melanoma [RCV000068171] Chr8:138596970 [GRCh38]
Chr8:139609213 [GRCh37]
Chr8:139678395 [NCBI36]
Chr8:8q24.23
not provided
NM_152888.2(COL22A1):c.2761C>T (p.Pro921Ser) single nucleotide variant Malignant melanoma [RCV000068172] Chr8:138690868 [GRCh38]
Chr8:139703111 [GRCh37]
Chr8:139772293 [NCBI36]
Chr8:8q24.23
not provided
NM_152888.2(COL22A1):c.1965G>A (p.Leu655=) single nucleotide variant Malignant melanoma [RCV000068173] Chr8:138755494 [GRCh38]
Chr8:139767737 [GRCh37]
Chr8:139836919 [NCBI36]
Chr8:8q24.23
not provided
NM_152888.2(COL22A1):c.1460G>A (p.Gly487Glu) single nucleotide variant Malignant melanoma [RCV000068174] Chr8:138807802 [GRCh38]
Chr8:139820045 [GRCh37]
Chr8:139889227 [NCBI36]
Chr8:8q24.23
not provided
NM_152888.2(COL22A1):c.4732C>T (p.Pro1578Ser) single nucleotide variant Malignant melanoma [RCV000061762] Chr8:138589402 [GRCh38]
Chr8:139601645 [GRCh37]
Chr8:139670827 [NCBI36]
Chr8:8q24.23
not provided
NM_152888.2(COL22A1):c.3871-74C>T single nucleotide variant Lung cancer [RCV000107178] Chr8:138616128 [GRCh38]
Chr8:139628371 [GRCh37]
Chr8:8q24.23
uncertain significance
NM_152888.2(COL22A1):c.3664-1405G>T single nucleotide variant Lung cancer [RCV000107179] Chr8:138627648 [GRCh38]
Chr8:139639891 [GRCh37]
Chr8:8q24.23
uncertain significance
NM_152888.2(COL22A1):c.3609+632A>C single nucleotide variant Lung cancer [RCV000107180] Chr8:138634378 [GRCh38]
Chr8:139646621 [GRCh37]
Chr8:8q24.23
uncertain significance
NM_152888.2(COL22A1):c.3286-385G>A single nucleotide variant Lung cancer [RCV000107181] Chr8:138656329 [GRCh38]
Chr8:139668572 [GRCh37]
Chr8:8q24.23
uncertain significance
NM_152888.3(COL22A1):c.658+5484G>A single nucleotide variant salbutamol response - Efficacy [RCV000211131] Chr8:138872266 [GRCh38]
Chr8:139884509 [GRCh37]
Chr8:8q24.23
drug response
GRCh38/hg38 8q24.21-24.3(chr8:130115518-141228210)x3 copy number gain See cases [RCV000133621] Chr8:130115518..141228210 [GRCh38]
Chr8:131127764..142238309 [GRCh37]
Chr8:131196946..142307491 [NCBI36]
Chr8:8q24.21-24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3 copy number gain See cases [RCV000134353] Chr8:94682154..145068656 [GRCh38]
Chr8:95694382..146294042 [GRCh37]
Chr8:95763558..146264846 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.22-24.3(chr8:130639182-145068712)x3 copy number gain See cases [RCV000137644] Chr8:130639182..145068712 [GRCh38]
Chr8:131651428..146294098 [GRCh37]
Chr8:131720610..146264902 [NCBI36]
Chr8:8q24.22-24.3
pathogenic|conflicting data from submitters
GRCh38/hg38 8q24.13-24.3(chr8:124498498-145068712)x3 copy number gain See cases [RCV000137346] Chr8:124498498..145068712 [GRCh38]
Chr8:125510739..146294098 [GRCh37]
Chr8:125579920..146264902 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.3-24.3(chr8:87931152-145068712)x3 copy number gain See cases [RCV000138551] Chr8:87931152..145068712 [GRCh38]
Chr8:88943380..146294098 [GRCh37]
Chr8:89012496..146264902 [NCBI36]
Chr8:8q21.3-24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3 copy number gain See cases [RCV000139036] Chr8:77480050..145068712 [GRCh38]
Chr8:78392286..146294098 [GRCh37]
Chr8:78554841..146264902 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:97382873-145070385)x3 copy number gain See cases [RCV000140447] Chr8:97382873..145070385 [GRCh38]
Chr8:98395101..146295771 [GRCh37]
Chr8:98464277..146266575 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3 copy number gain See cases [RCV000139539] Chr8:46031340..139285494 [GRCh38]
Chr8:46942962..140297737 [GRCh37]
Chr8:47062127..140366919 [NCBI36]
Chr8:8q11.1-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:100867343-145070385)x3 copy number gain See cases [RCV000141694] Chr8:100867343..145070385 [GRCh38]
Chr8:101879571..146295771 [GRCh37]
Chr8:101948747..146266575 [NCBI36]
Chr8:8q22.3-24.3
pathogenic
GRCh38/hg38 8q24.23-24.3(chr8:138563758-139174670)x3 copy number gain See cases [RCV000142467] Chr8:138563758..139174670 [GRCh38]
Chr8:139576001..140186913 [GRCh37]
Chr8:139645183..140256095 [NCBI36]
Chr8:8q24.23-24.3
likely benign|uncertain significance
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3
pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:103306336-145068712)x3 copy number gain See cases [RCV000142810] Chr8:103306336..145068712 [GRCh38]
Chr8:104318564..146294098 [GRCh37]
Chr8:104387740..146264902 [NCBI36]
Chr8:8q22.3-24.3
pathogenic|likely pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3 copy number gain See cases [RCV000142597] Chr8:78614077..145054634 [GRCh38]
Chr8:79526312..146280020 [GRCh37]
Chr8:79688867..146250824 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.2-24.3(chr8:85765999-145070385)x3 copy number gain See cases [RCV000143659] Chr8:85765999..145070385 [GRCh38]
Chr8:86778228..146295771 [GRCh37]
Chr8:86863079..146266575 [NCBI36]
Chr8:8q21.2-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000148117] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3 copy number gain See cases [RCV000447507] Chr8:158991..146280828 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q22.1-24.3(chr8:98432250-146222672)x4 copy number gain See cases [RCV000448954] Chr8:98432250..146222672 [GRCh37]
Chr8:8q22.1-24.3
pathogenic
GRCh37/hg19 8q24.22-24.3(chr8:134825277-146280828)x3 copy number gain See cases [RCV000448348] Chr8:134825277..146280828 [GRCh37]
Chr8:8q24.22-24.3
pathogenic
GRCh37/hg19 8q24.23(chr8:139253063-139882428)x3 copy number gain See cases [RCV000510656] Chr8:139253063..139882428 [GRCh37]
Chr8:8q24.23
likely benign
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771) copy number gain See cases [RCV000510234] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q21.3-24.3(chr8:93047482-141355635)x3 copy number gain See cases [RCV000511761] Chr8:93047482..141355635 [GRCh37]
Chr8:8q21.3-24.3
pathogenic
GRCh37/hg19 8q24.22-24.3(chr8:136378789-146295771)x3 copy number gain See cases [RCV000512003] Chr8:136378789..146295771 [GRCh37]
Chr8:8q24.22-24.3
likely pathogenic
GRCh37/hg19 8q24.23(chr8:139297034-139897291)x3 copy number gain See cases [RCV000510802] Chr8:139297034..139897291 [GRCh37]
Chr8:8q24.23
uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3 copy number gain See cases [RCV000511095] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841154-146295771)x3 copy number gain See cases [RCV000511002] Chr8:86841154..146295771 [GRCh37]
Chr8:8q21.2-24.3
pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841228-142689874)x3 copy number gain See cases [RCV000510854] Chr8:86841228..142689874 [GRCh37]
Chr8:8q21.2-24.3
pathogenic
GRCh37/hg19 8q23.3-24.3(chr8:114853126-146295771)x3 copy number gain See cases [RCV000512401] Chr8:114853126..146295771 [GRCh37]
Chr8:8q23.3-24.3
pathogenic
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3 copy number gain See cases [RCV000512169] Chr8:12490999..146295771 [GRCh37]
Chr8:8p23.1-q24.3
pathogenic
GRCh37/hg19 8q24.23(chr8:139253063-139881535)x3 copy number gain not provided [RCV000682990] Chr8:139253063..139881535 [GRCh37]
Chr8:8q24.23
uncertain significance
GRCh37/hg19 8q24.12-24.3(chr8:121694649-146295771)x3 copy number gain not provided [RCV000683044] Chr8:121694649..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic
GRCh37/hg19 8q24.23-24.3(chr8:139774408-140472026)x4 copy number gain not provided [RCV000682996] Chr8:139774408..140472026 [GRCh37]
Chr8:8q24.23-24.3
uncertain significance
GRCh37/hg19 8q24.13-24.3(chr8:125496223-146295771)x3 copy number gain not provided [RCV000845705] Chr8:125496223..146295771 [GRCh37]
Chr8:8q24.13-24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3 copy number gain not provided [RCV000747248] Chr8:10213..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3 copy number gain not provided [RCV000747254] Chr8:164984..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q24.22-24.3(chr8:133621137-140433338)x1 copy number loss not provided [RCV000747861] Chr8:133621137..140433338 [GRCh37]
Chr8:8q24.22-24.3
likely pathogenic
NM_152888.3(COL22A1):c.2208G>T (p.Glu736Asp) single nucleotide variant not provided [RCV000963064] Chr8:138724654 [GRCh38]
Chr8:139736897 [GRCh37]
Chr8:8q24.23
benign
GRCh37/hg19 8q24.13-24.3(chr8:126892814-143750028)x1 copy number loss not provided [RCV001006144] Chr8:126892814..143750028 [GRCh37]
Chr8:8q24.13-24.3
pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:122193546-146295771)x3 copy number gain not provided [RCV000849762] Chr8:122193546..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic
NM_152888.3(COL22A1):c.3334G>A (p.Asp1112Asn) single nucleotide variant not provided [RCV000896016] Chr8:138649778 [GRCh38]
Chr8:139662021 [GRCh37]
Chr8:8q24.23
likely benign
GRCh37/hg19 8q24.22-24.3(chr8:136059859-146295771)x3 copy number gain not provided [RCV000847171] Chr8:136059859..146295771 [GRCh37]
Chr8:8q24.22-24.3
pathogenic
GRCh37/hg19 8q24.3(chr8:139901395-139927406)x1 copy number loss not provided [RCV000849806] Chr8:139901395..139927406 [GRCh37]
Chr8:8q24.3
likely benign
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3 copy number gain not provided [RCV000848192] Chr8:31936551..146295771 [GRCh37]
Chr8:8p12-q24.3
pathogenic
GRCh37/hg19 8q24.23-24.3(chr8:139188797-146295771)x3 copy number gain not provided [RCV000846814] Chr8:139188797..146295771 [GRCh37]
Chr8:8q24.23-24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not provided [RCV000848478] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
NM_152888.3(COL22A1):c.3540G>A (p.Gly1180=) single nucleotide variant not provided [RCV000896532] Chr8:138636757 [GRCh38]
Chr8:139649000 [GRCh37]
Chr8:8q24.23
benign
NM_152888.3(COL22A1):c.2288C>T (p.Pro763Leu) single nucleotide variant not provided [RCV000956677] Chr8:138722049 [GRCh38]
Chr8:139734292 [GRCh37]
Chr8:8q24.23
benign
GRCh37/hg19 8q24.21-24.3(chr8:128877995-146295771)x3 copy number gain not provided [RCV001006146] Chr8:128877995..146295771 [GRCh37]
Chr8:8q24.21-24.3
pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:121042467-146295771)x3 copy number gain not provided [RCV001006140] Chr8:121042467..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic
GRCh37/hg19 8q24.23-24.3(chr8:139203019-140284954)x3 copy number gain not provided [RCV001259033] Chr8:139203019..140284954 [GRCh37]
Chr8:8q24.23-24.3
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:22989 AgrOrtholog
COSMIC COL22A1 COSMIC
Ensembl Genes ENSG00000169436 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000303153 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000387655 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000428244 UniProtKB/TrEMBL
Ensembl Transcript ENST00000303045 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000435777 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000522546 UniProtKB/TrEMBL
Gene3D-CATH 3.40.50.410 UniProtKB/Swiss-Prot
GTEx ENSG00000169436 GTEx
HGNC ID HGNC:22989 ENTREZGENE
Human Proteome Map COL22A1 Human Proteome Map
InterPro Collagen UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ConA-like_dom_sf UniProtKB/Swiss-Prot
  Laminin_G UniProtKB/Swiss-Prot
  VWF_A UniProtKB/Swiss-Prot
  vWFA_dom_sf UniProtKB/Swiss-Prot
KEGG Report hsa:169044 UniProtKB/Swiss-Prot
NCBI Gene 169044 ENTREZGENE
OMIM 610026 OMIM
Pfam Collagen UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VWA UniProtKB/Swiss-Prot
PharmGKB PA134914705 PharmGKB
PROSITE VWFA UniProtKB/Swiss-Prot
SMART TSPN UniProtKB/Swiss-Prot
  VWA UniProtKB/Swiss-Prot
Superfamily-SCOP SSF49899 UniProtKB/Swiss-Prot
  SSF53300 UniProtKB/Swiss-Prot
UniProt COMA1_HUMAN UniProtKB/Swiss-Prot
  H0YAX7_HUMAN UniProtKB/TrEMBL
  L8EAR4_HUMAN UniProtKB/TrEMBL
  Q8NFW1 ENTREZGENE
UniProt Secondary B7ZMH0 UniProtKB/Swiss-Prot
  C9K0G4 UniProtKB/Swiss-Prot
  Q8IVT9 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-07-26 COL22A1  collagen type XXII alpha 1 chain    collagen type XXII alpha 1  Symbol and/or name change 5135510 APPROVED
2016-01-26 COL22A1  collagen type XXII alpha 1    collagen, type XXII, alpha 1  Symbol and/or name change 5135510 APPROVED
2011-09-01 COL22A1  collagen, type XXII, alpha 1  COL22A1  collagen, type XXII, alpha 1  Symbol and/or name change 5135510 APPROVED