Related Entries for OMIM (Select 146690) - OMIM

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Items: 8

Select item 1466901.

*146690 - IMP DEHYDROGENASE 1; IMPDH1

IMP DEHYDROGENASE-LIKE 1, INCLUDED; IMPDHL1, INCLUDED

Cytogenetic locations: 15851576

OMIM:: 146690

Gene summaries Genetic tests Medical literature

Select item 6138372.

#613837 - LEBER CONGENITAL AMAUROSIS 11; LCA11

Cytogenetic locations: 20006823

OMIM:: 613837

Gene summaries Genetic tests Medical literature

Select item 6039373.

*603937 - RP1 AXONEMAL MICROTUBULE-ASSOCIATED PROTEIN; RP1

Cytogenetic locations: 20664799

OMIM:: 603937

Gene summaries Genetic tests Medical literature

Select item 6021014.

*602101 - CLAUDIN 5; CLDN5

Cytogenetic locations: 19192844

OMIM:: 602101

Gene summaries Genetic tests Medical literature

Select item 1803805.

*180380 - RHODOPSIN; RHO

Cytogenetic locations: 615939

OMIM:: 180380

Gene summaries Genetic tests Medical literature

Select item 1801056.

#180105 - RETINITIS PIGMENTOSA 10; RP10

Cytogenetic locations: 17635473

OMIM:: 180105

Gene summaries Genetic tests Medical literature

Select item 1466917.

*146691 - IMP DEHYDROGENASE 2; IMPDH2

Cytogenetic locations: 17896827

OMIM:: 146691

Gene summaries Genetic tests Medical literature

Select item 1405718.

*140571 - HEAT-SHOCK PROTEIN, 90-KD, ALPHA, CLASS A, MEMBER 1; HSP90AA1

Cytogenetic locations: 12526792

OMIM:: 140571

Gene summaries Genetic tests Medical literature

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Related Entries for OMIM (Select 146690) (8)
OMIM
Homo sapiens tumor associated calcium signal transducer 2 (TACSTD2), mRNA
Homo sapiens tumor associated calcium signal transducer 2 (TACSTD2), mRNA
gi|1653961507|ref|NM_002353.3|

Nucleotide
Autosomal recessive nonsyndromic hearing loss 49
Autosomal recessive nonsyndromic hearing loss 49

MedGen
C1857811[conceptid] (1)
MedGen

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