| Type | Description |
|---|---|
| Definition | family with sequence similarity 161, member A |
| Date | Results | Publications |
|---|---|---|
| 2015-05-30 12:14:00 | Fam161a is required for the molecular delivery into the outer segment cilium, a function which is essential for outer segment disk formation and ultimately visual function. | 24833722 |
| 2013-04-13 10:57:00 | FAM161A-associated RP can be considered as a novel retinal ciliopathy and that its molecular pathogenesis may be related to other ciliopathies. | 22940612 |
| 2010-10-23 10:13:00 | Null mutations in FAM161A are responsible for the RP28-associated autosomal-recessive retinitis pigmentosa. | 20705278 |
| 2010-10-23 10:13:00 | These data suggest a pivotal role for FAM161A in photoreceptors and reveal that FAM161A loss-of-function mutations are a major cause of autosomal-recessive Retinitis pigmentosa. | 20705279 |
| Type | IDs |
|---|---|
| Synonymous | 4930430E16Rik |
| Gene |
UniProtKB-ID:
F161A_MOUSE,
B1AVK0_MOUSE
UniprotKB:
Q8QZV6,
B1AVK0
UniParc:
UPI00001E46B3,
UPI00000292EF
EMBL:
BC024460,
AL691470,
BX001008,
BC026495
Ensembl:
ENSMUSG00000049811
KO:
mmu:73873
|
| Nucleutide sequences |
EMBL-CDS:
AAH24460.1,
AAH26495.1
Ensembl_TRS:
ENSMUST00000109557,
ENSMUST00000058269,
ENSMUST00000172602,
ENSMUST00000238880
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000063091,
ENSMUSP00000134485,
ENSMUSP00000105184,
ENSMUSP00000158891
RefSeq:
XP_011242064.1,
NP_001350211.1,
XP_036012925.1,
XP_011242063.1,
XP_011242062.1,
XP_036012922.1,
XP_030102237.1,
NP_001350212.1,
XP_006514892.1,
XP_006514891.1,
XP_030102239.1,
NP_082948.2,
XP_006514894.1,
XP_030102238.1,
XP_006514895.1,
XP_006514901.1,
XP_036012924.1,
XP_006514896.1,
XP_017170288.1,
NP_001350213.1,
XP_006514893.1,
XP_006514897.1
|
| Others |
UniRef100:
UniRef100_Q8QZV6
UniRef90:
UniRef90_Q8QZV6
UniRef50:
UniRef50_Q8QZV6
UniGene:
Mm.252406
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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