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*613896 - BISPHOSPHOGLYCERATE MUTASE; BPGM
Cytogenetic locations: Cortactin-binding
Gene summaries Genetic tests Medical literature
252320 - MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA
#222800 - ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8
Cytogenetic locations: 26295140
*118920 - CHROMOGRANIN B; CHGB
*616133 - MPV17 MITOCHONDRIAL INNER MEMBRANE PROTEIN-LIKE 2; MPV17L2
Cytogenetic locations: 605111
*605200 - HECT DOMAIN AND RCC1-LIKE DOMAIN 3; HERC3
Cytogenetic locations: 607830
#248390 - TREACHER COLLINS SYNDROME 3; TCS3
Cytogenetic locations: 11013442
*605109 - HECT DOMAIN AND RCC1-LIKE DOMAIN 1; HERC1
Cytogenetic locations: 32921582
*301780 - ARYLSULFATASE C, ISOZYME F; ARSC2
Cytogenetic locations: {Prostate
*118930 - SECRETOGRANIN II; SCG2
SECRETONEURIN, INCLUDED; SN, INCLUDED
Cytogenetic locations: 18079966
#102900 - ADENOSINE TRIPHOSPHATE, ELEVATED, OF ERYTHROCYTES
Cytogenetic locations: mutation
#616176 - BLEEDING DISORDER, PLATELET-TYPE, 19; BDPLT19
Cytogenetic locations: 137060
#617011 - MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR
*605319 - 6-@PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE 3; PFKFB3
Cytogenetic locations: 13298683
*610974 - ZINC FINGER PROTEIN 521; ZNF521
Cytogenetic locations: 21326203
%605779 - NAIL DISORDER, NONSYNDROMIC CONGENITAL, 7; NDNC7
Cytogenetic locations: 17143386
*614551 - SERINE INCORPORATOR 5; SERINC5
Cytogenetic locations: 12688535
*177040 - SERGLYCIN; SRGN
#207750 - APOLIPOPROTEIN C-II DEFICIENCY
Cytogenetic locations: 604142
%611717 - SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH
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