Type | Description |
---|---|
Definition | pogo transposable element with ZNF domain |
Date | Results | Publications |
---|---|---|
2021-03-28 19:07:00 | Altered hippocampal-prefrontal communication during anxiety-related avoidance in mice deficient for the autism-associated gene Pogz. | 33155545 |
2020-12-19 13:45:00 | Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice. | 33203851 |
2020-04-25 10:17:00 | Pogo transposable element derived with ZNF domain (POGZ) has been identified as one of the most recurrently de novo mutated genes in patients with neurodevelopmental disorders (NDDs), including autism spectrum disorder (ASD), intellectual disability and White-Sutton syndrome. Pathogenic POGZ mutation causes impaired cortical development and reversible autism-like phenotypes. | 32103003 |
2020-04-04 12:56:00 | results suggest that POGZ takes part in the regulation of synaptic function as well as gene expression during brain development | 31430754 |
2019-11-09 13:04:00 | POGZ is essential for normal embryonic development and that loss of the gene leads to deregulation of embryonic globin expression, in part through Bcl11a. | 29898395 |
Type | IDs |
---|---|
Synonymous | 9530006B08Rik |
Gene |
UniProtKB-ID:
POGZ_MOUSE,
D3YUX1_MOUSE,
B9EIG6_MOUSE,
Q0VGT3_MOUSE
UniprotKB:
Q8BZH4,
D3YUX1,
B9EIG6,
Q0VGT3
UniParc:
UPI0000F2223E,
UPI0000DBE452,
UPI00001939FA
EMBL:
AC087903,
BC032176,
AK030880,
AK122288,
AK035255,
AC087062,
BC139432,
BC139433,
BC096492,
BC085188
Ensembl:
ENSMUSG00000038902
KO:
mmu:229584
|
Nucleutide sequences |
EMBL-CDS:
AAH32176.1,
BAC29003.1,
BAC65570.1,
BAC27169.1,
AAH96492.1,
AAI39433.1,
AAI39434.1,
AAH85188.1
Ensembl_TRS:
ENSMUST00000107270,
ENSMUST00000107266,
ENSMUST00000042402
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000102891,
ENSMUSP00000102887,
ENSMUSP00000037523
RefSeq:
XP_036018949.1,
XP_006501425.1,
NP_766271.2,
NP_001355741.1,
XP_006501426.1,
NP_001159420.1,
XP_011238392.1,
NP_001355740.1
|
Others |
UniRef100:
UniRef100_Q8BZH4,
UniRef100_D3YUX1,
UniRef100_Q0VGT3
UniRef90:
UniRef90_D3YUX1,
UniRef90_Q7Z3K3
UniRef50:
UniRef50_H9GHQ7,
UniRef50_Q7Z3K3
UniGene:
Mm.274787
CCDS:
CCDS17596.1
|