Related Entries for OMIM (Select 601417) - OMIM

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Items: 8

Select item 6014171.

*601417 - 17-@BETA-HYDROXYSTEROID DEHYDROGENASE VIII; HSD17B8

Cytogenetic locations: mutation

OMIM:: 601417

Gene summaries Genetic tests Medical literature

Select item 6193942.

*619394 - CARBONYL REDUCTASE 4; CBR4

Cytogenetic locations: 19000905

OMIM:: 619394

Gene summaries Genetic tests Medical literature

Select item 6037633.

*603763 - KINESIN FAMILY MEMBER C1; KIFC1

Cytogenetic locations: 15479732

OMIM:: 603763

Gene summaries Genetic tests Medical literature

Select item 6020454.

*602045 - RING FINGER PROTEIN 1; RING1

Cytogenetic locations: 23486062

OMIM:: 602045

Gene summaries Genetic tests Medical literature

Select item 6018605.

*601860 - 17-@BETA-HYDROXYSTEROID DEHYDROGENASE IV; HSD17B4

Cytogenetic locations: mutation

OMIM:: 601860

Gene summaries Genetic tests Medical literature

Select item 6014166.

*601416 - SOLUTE CARRIER FAMILY 39 (ZINC TRANSPORTER), MEMBER 7; SLC39A7

Cytogenetic locations: 14525538

OMIM:: 601416

Gene summaries Genetic tests Medical literature

Select item 2632007.

#263200 - POLYCYSTIC KIDNEY DISEASE 4 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD4

HEPATIC FIBROSIS, CONGENITAL, INCLUDED

Cytogenetic locations: BRD4-interacting

OMIM:: 263200

Gene summaries Genetic tests Medical literature

Select item 1802468.

*180246 - RETINOID X RECEPTOR, BETA; RXRB

Cytogenetic locations: 11662118

OMIM:: 180246

Gene summaries Genetic tests Medical literature

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Related Entries for OMIM (Select 601417) (8)
OMIM
endoplasmic reticulum metallopeptidase 1 isoform X5 [Homo sapiens]
endoplasmic reticulum metallopeptidase 1 isoform X5 [Homo sapiens]
gi|2462626556|ref|XP_054219837.1|

Protein
endoplasmic reticulum metallopeptidase 1 isoform X2 [Homo sapiens]
endoplasmic reticulum metallopeptidase 1 isoform X2 [Homo sapiens]
gi|2217379890|ref|XP_047279853.1|

Protein
Chain L, DNA (Ap)
Chain L, DNA (Ap)
gi|2491197951|pdb|8EBW|L

Nucleotide

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