Ran Results

RANGRF

RAN guanine nucleotide release factor

ANKFY1

ankyrin repeat and FYVE domain containing 1

CCL5

C-C motif chemokine ligand 5

IPO13

importin 13

LRRN2

leucine rich repeat neuronal 2

MCRIP1

MAPK regulated corepressor interacting protein 1

MFSD10

major facilitator superfamily domain containing 10

RAN

RAN, member RAS oncogene family

RANBP1

RAN binding protein 1

RANBP10

RAN binding protein 10

RANBP17

RAN binding protein 17

RANBP2

RAN binding protein 2

RANBP3

RAN binding protein 3

RANBP3L

RAN binding protein 3 like

RANBP6

RAN binding protein 6

RANBP9

RAN binding protein 9

RANGAP1

Ran GTPase activating protein 1

RBCK1

RANBP2-type and C3HC4-type zinc finger containing 1

RBM10

RNA binding motif protein 10

RGPD2

RANBP2-like and GRIP domain containing 2

branchio-oto-renal syndrome

MONDO_0007029 Condition
Branchiootorenal syndrome
08/30/2018

branched-chain keto acid dehydrogenase kinase deficiency

MONDO_0013970 Condition
BCKDK deficiency
01/08/2019

ornithine carbamoyltransferase deficiency

MONDO_0010703 Condition
Ornithine carbamoyltransferase deficiency
02/21/2018

guanidinoacetate methyltransferase deficiency

MONDO_0012999 Condition
Cerebral Creatine Deficiency Syndrome type 2
01/25/2019

carnitine palmitoyl transferase 1A deficiency

MONDO_0009705 Condition
hepatic carnitine palmitoyl transferase 1 deficiency
10/25/2018

creatine transporter deficiency

MONDO_0010305 Condition
CEREBRAL CREATINE DEFICIENCY SYNDROME 1
10/10/2018

von Willebrand disease 2

MONDO_0013304 Condition
VWD type 2
07/24/2018

hereditary fructose intolerance

MONDO_0009249 Condition
Fructosemia
02/07/2019

succinyl-CoA:3-ketoacid CoA transferase deficiency

MONDO_0009492 Condition
OXCT1 deficiency
05/31/2017

01/10/2018

carnitine-acylcarnitine translocase deficiency

MONDO_0008918 Condition
CACT deficiency
05/22/2018

immunoglobulin-mediated membranoproliferative glomerulonephritis

MONDO_0014005 Condition
Ig-mediated MPGN
10/17/2018

von Willebrand disease 3

MONDO_0010191 Condition
von Willebrand's disease 3
07/24/2018

Nance-Horan syndrome

MONDO_0010545 Condition
10/20/2017

06/01/2017

craniofrontonasal syndrome

MONDO_0010570 Condition
CFNS
06/01/2017

transcobalamin II deficiency

MONDO_0010149 Condition
Transcobalamin II deficiency
05/31/2017