| Type | Description |
|---|---|
| Definition | CAP-GLY domain containing linker protein 2 |
| Date | Results | Publications |
|---|---|---|
| 2010-01-21 00:00:00 | Williams Syndrome is caused by a variety of genes and that heterozygous deletion of CYLN2 is one of the major causes | 17270452 |
| 2010-01-21 00:00:00 | evidence that mice with haploinsufficiency for Cyln2 have features reminiscent of Williams syndrome, including mild growth deficiency, brain abnormalities, hippocampal dysfunction and particular deficits in motor coordination | 12195424 |
| Type | IDs |
|---|---|
| Synonymous | B230327O20, CLIP-115, Clip1, Cyln2, WSCR4, mKIAA0291, wbscr4 |
| Gene |
UniProtKB-ID:
CLIP2_MOUSE
UniprotKB:
Q9Z0H8
UniParc:
UPI00000271D4,
UPI00001A3D1B
EMBL:
AJ228867,
AF289667,
AF289664,
AJ228880,
AJ228866,
AJ228875,
AJ228876,
AJ228863,
AJ228879,
AJ228873,
AJ228868,
AJ228869,
AJ228872,
BC039162,
AJ228874,
AJ228865,
AJ228878,
AJ228871,
AJ228870,
BC053048,
AJ228877
Ensembl:
ENSMUSG00000063146
KO:
mmu:269713
|
| Nucleutide sequences |
EMBL-CDS:
AAH39162.1,
AAF99340.1,
CAA13069.1,
CAA13068.1,
AAF99333.1,
AAH53048.1
Ensembl_TRS:
ENSMUST00000036999,
ENSMUST00000100647
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000037431,
ENSMUSP00000098212
RefSeq:
NP_001034251.1,
XP_036021051.1,
NP_034120.2
|
| Others |
UniRef100:
UniRef100_Q9Z0H8
UniRef90:
UniRef90_O55156
UniRef50:
UniRef50_O55156
UniGene:
Mm.255138
CCDS:
CCDS39309.1,
CCDS39310.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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| Location | {{protein.contigId}} ( {{protein.positionStart}}..{{protein.positionEnd}} , {{protein.orientation}} ) | |||||||
| Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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