about
P688
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndromeA novel gene oriented in a head-to-head configuration with the human histidyl-tRNA synthetase (HRS) gene encodes an mRNA that predicts a polypeptide homologous to HRS
P921
description
humanes Protein
@de
mammalian protein found in Homo sapiens
@en
menselijk eiwit
@nl
protein
@id
protein
@sv
proteinë
@sq
protèin
@ace
protéine humaine
@fr
بروتين بشري
@ar
name
Histidyl-tRNA synthetase 2, mitochondrial
@en
Histidyl-tRNA synthetase 2, mitochondrial
@nl
type
label
Histidyl-tRNA synthetase 2, mitochondrial
@en
Histidyl-tRNA synthetase 2, mitochondrial
@nl
altLabel
HARS-related
@en
HARS2
@en
Histidine--tRNA ligase-like
@en
Histidyl-tRNA synthetase
@en
hisRS
@en
histidine tRNA ligase 2, mitochondrial (putative)
@en
histidine translase
@en
histidine--tRNA ligase, mitochondrial
@en
histidine-tRNA ligase homolog
@en
histidyl-tRNA synthetase 2, mitochondrial (putative)
@en
prefLabel
Histidyl-tRNA synthetase 2, mitochondrial
@en
Histidyl-tRNA synthetase 2, mitochondrial
@nl
P527
P637
P680
P681
P682
P705
P352
P637
P31
P352
P637
NP_001265660
NP_001265661
NP_001350464
NP_001350465
XP_016864777
XP_016864778
XP_016864779
XP_016864780
XP_016864781
P680
P682
P702
P703
P705
ENSP00000230771
ENSP00000407105
ENSP00000423530
ENSP00000423616
ENSP00000424516
ENSP00000425695
ENSP00000429220
ENSP00000493571
ENSP00000493630
ENSP00000494140