| Type | Description |
|---|---|
| Definition | cystic fibrosis transmembrane conductance regulator |
| Date | Results | Publications |
|---|---|---|
| 2021-03-20 13:27:00 | Overcoming Immunological Challenges to Helper-Dependent Adenoviral Vector-Mediated Long-Term CFTR Expression in Mouse Airways. | 32443586 |
| 2021-03-13 13:15:00 | CFTR deletion affects mouse osteoblasts in a gender-specific manner. | 31985038 |
| 2021-02-13 13:24:00 | Myeloid CFTR loss-of-function causes persistent neutrophilic inflammation in cystic fibrosis. | 32531843 |
| 2021-01-16 16:01:00 | Heterogeneous expression of CFTR in insulin-secreting beta-cells of the normal human islet. | 33264332 |
| 2021-01-02 12:49:00 | Cystic fibrosis transmembrane conductance regulator dysfunction in platelets drives lung hyperinflammation. | 31961827 |
| Type | IDs |
|---|---|
| Synonymous | AW495489, Abcc7 |
| Gene |
UniProtKB-ID:
CFTR_MOUSE
UniprotKB:
P26361
UniParc:
UPI000002A644,
UPI00000278CF,
UPI000002A643
EMBL:
AF162137,
S65940,
S65941,
M69298,
L04873,
S65942,
M60493
Ensembl:
ENSMUSG00000041301
KO:
mmu:12638
|
| Nucleutide sequences |
EMBL-CDS:
AAA18903.1,
AAA73562.1,
AAF30300.1,
AAB28391.1,
AAB28393.1,
AAA37417.1,
AAB28392.1
Ensembl_TRS:
ENSMUST00000140407,
ENSMUST00000045706,
ENSMUST00000115405
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000049228,
ENSMUSP00000111064,
ENSMUSP00000116957
RefSeq:
NP_066388.1
|
| Others |
UniRef100:
UniRef100_P26361
UniRef90:
UniRef90_P26361
UniRef50:
UniRef50_P26361
UniGene:
Mm.15621
CCDS:
CCDS19930.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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