Type | Description |
---|---|
Definition | solute carrier family 16 (monocarboxylic acid transporters), member 10 |
Date | Results | Publications |
---|---|---|
2019-10-05 10:25:00 | We report hearing loss in mice with mutations in Slc16a2 and a related gene Slc16a10 (Mct10, Tat1). Deficiency of both transporters results in retarded development of the sensory epithelium similar to impairment caused by hypothyroidism, compounded with a progressive degeneration of cochlear hair cells and loss of endocochlear potential. | 29535325 |
2014-03-01 11:41:00 | Mct10 participates in tissue-specific TH transport and also contributes to the generation of the unusual serum TH profile characteristic for Mct8 deficiency | 24248460 |
2013-06-15 10:33:00 | Data indicate that the uniporter TAT1 is required to equilibrate the concentration of aromatic amino acids across specific membranes. | 23045339 |
2012-10-06 11:36:00 | The results suggest that Mct10 functions as a thyroid hormone transporter in chondrocytes and can explain at least in part why Allan-Herndon-Dudley syndrome patients do not exhibit significant growth impairment. | 22719050 |
2012-02-18 11:07:00 | expression of candidate thyroid hormone transporters Lat1, Mct8, Mct10, and Oatp1c1 in mouse cochlear development | 21878515 |
Type | IDs |
---|---|
Synonymous | 2610103N14Rik, 9830169E08, Mct10, PRO0813, TAT1 |
Gene |
UniProtKB-ID:
MOT10_MOUSE
UniprotKB:
Q3U9N9
UniParc:
UPI00000EA773,
UPI00001C46D3
EMBL:
AK151704,
AK165579,
AK157355,
AK165240,
AK151290,
AK050229
Ensembl:
ENSMUSG00000019838
KO:
mmu:72472
|
Nucleutide sequences |
EMBL-CDS:
BAE38097.1,
BAC34135.1,
BAE30627.1,
BAE34061.1,
BAE30275.1,
BAE38270.1
Ensembl_TRS:
ENSMUST00000092566,
ENSMUST00000213488
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000090227,
ENSMUSP00000150416
RefSeq:
NP_001107804.1,
XP_006512926.1,
NP_082523.1
|
Others |
UniRef100:
UniRef100_Q3U9N9
UniRef90:
UniRef90_Q3U9N9
UniRef50:
UniRef50_Q8TF71
UniGene:
Mm.186778
CCDS:
CCDS87990.1,
CCDS48543.1
|
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