Type | Description |
---|---|
Definition | solute carrier family 25 member 16 |
Date | Results | Publications |
---|---|---|
2019-04-27 10:48:00 | The authors findings report an extreme rare missense mutation in SLC25A1 which supports the causality of this variant for autosomal recessive form of isolated fingernail dysplasia. | 28504827 |
2013-07-02 10:26:00 | Compares and contrasts all the known human SLC25A* genes and includes functional information. | 23266187 |
2010-12-05 22:08:00 | Observational study of gene-disease association. (HuGE Navigator) | 20877624 |
2010-06-30 22:05:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
2009-12-02 21:41:00 | Observational study of gene-disease association. (HuGE Navigator) | 16385451 |
Type | IDs |
---|---|
Synonymous | D10S105E, GDA, GDC, HGT.1, ML7, hML7 |
Gene |
UniProtKB-ID:
GDC_HUMAN,
B4DPV4_HUMAN,
B4DHV9_HUMAN
UniprotKB:
P16260,
B4DPV4,
B4DHV9
UniParc:
UPI000041AE1F,
UPI00000704FB,
UPI00017A70DC
EMBL:
AK290255,
M31659,
AK295287,
AK298510,
CH471083,
AL713888,
BC030266
Ensembl:
ENSG00000122912
KO:
hsa:8034
|
Nucleutide sequences |
EMBL-CDS:
AAA36329.1,
EAW54298.1,
BAF82944.1,
AAH30266.1,
BAG60716.1,
BAG58271.1
Ensembl_TRS:
ENST00000609923
|
Protein sequencees |
Ensembl_PRO:
ENSP00000476815
RefSeq:
NP_001311244.1,
NP_001311243.1,
NP_689920.1,
NP_001311241.1,
NP_001311246.1,
NP_001311242.1
|
Others |
UniRef100:
UniRef100_B4DHV9,
UniRef100_P16260
UniRef90:
UniRef90_P16260,
UniRef90_B4DHV9
UniRef50:
UniRef50_P16260
UniGene:
Hs.180408
CCDS:
CCDS7280.1
|
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Refseq |
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