Genes associated with “KRABD5”
784 genes found6 ClinVar P/LP variants
How are genes scored? (0–100 composite)
-5–15
ClinGen
0–15
HPO Freq
0–15
Open Targets
0–12
Phen2Gene
0–10
ClinVar
0–8
Constraint
0–8
Dosage
0–8
OMIM CS
0–8
PanelApp
0–5
OMIM
0–5
G2P
0–4
Breadth
Tiers:Strong Candidates (≥20)Consider (≥8)Possible (≥3)
Evidence dots:
HPOClinVarPhen2GeneOpen TargetsPanelApp
hover for detailsConsider
756 genesScore
Gene
Evidence
Freq
P/LP
OT
Description
16SETD1A
14FBXL19
11SRRM2
10ALDOA
10APOBR
10AQP8
10ARHGAP17
10ARMC5
10ASPHD1
10ATP2A1
10ATXN2L
10BCL7C
10BOLA2
10BOLA2B
10C16ORF54
10C16ORF82
10C16ORF92
10CACNG3
10CD2BP2
10CDIPT
10CFAP119
10CHP2
10DCTPP1
10DOC2A
10EIF3C
10EIF3CL
10GDPD3
10GSG1L
10GTF3C1
10HIRIP3
10HS3ST4
10IL27
10IL4R
10INO80E
10ITGAD
10ITGAL
10ITGAM
10ITGAX
10KAT8
10KCTD13
10KDM8
10KIF22
10KRABD5
10LCMT1
10MAPK3
10MYL11
10NFATC2IP
10NPIPB6
10NSMCE1
10NUPR1
10ORAI3
10PAGR1
10PPP4C
10PRKCB
10PRR14
10PRSS36
10PRSS53
10PRSS8
10PYCARD
10PYDC1
10RABEP2
10RBBP6
10RUSF1
10SBK1
10SEPHS2
10SEPTIN1
10SEZ6L2
10SGF29
10SH2B1
10SLC5A11
10SLC5A2
10SLX1A
10SLX1B
10SPNS1
10STX4
10SULT1A1
10SULT1A2
10SULT1A3
10SULT1A4
10TAOK2
10TBC1D10B
10TBX6
10TGFB1I1
10TLCD3B
10TMEM219
10TNRC6A
10TP53TG3
10TP53TG3B
10TP53TG3C
10TP53TG3D
10TRIM72
10XPO6
10YPEL3
10ZG16
10ZKSCAN2
10ZNF267
10ZNF48
10ZNF629
10ZNF646
10ZNF668
10ZNF688
10ZNF689
10ZNF747
10ZNF764
10ZNF768
10ZNF771
10ZNF785
10ZNF843
9CDR2
9COQ7
9E4F1
9ECI1
9EME2
9EMP2
9ERI2
9ERN2
9GDE1
9GGA2
9GP2
9IL32
9JPT2
9NME3
9NTN3
9PLK1
9PRM1
9PRM2
9PRM3
9PTX4
9RMI2
9RPS2
9RRN3
9SMG1
9TBL3
9TMC5
9TMC7
9TNP2
9TSR3
9UBN1
9ZP2
8BCO1
8BRD7
8CA7
8CDH5
8CDH8
8CES1
8CES2
8CES3
8CHD9
8CMC2
8COG8
8CTU2
8DEF8
8DOK4
8DRC7
8DUS2
8E2F4
8EDC4
8EMC8
8GLG1
8GOT2
8GSE1
8HAS3
8HBQ1
8HSF4
8IL34
8IRF8
8IRX3
8IRX5
8IRX6
8IST1
8JPH3
8LMF1
8MC1R
8MMP2
8MT1A
8MT1B
8MT1E
8MT1F
8MT1G
8MT1H
8MT1M
8MT1X
8MT2A
8MT3
8MT4
8NAE1
8NIP7
8NKD1
8NME4
8NOB1
8NOL3
8NQO1
8PDP2
8RBL2
8SOX8
8SPG7
8TOX3
8USB1
8UTP4
8WWP2
8ZFP1
Possible
28 genes — click to expand
Score
Gene
Evidence
Freq
P/LP
OT
Description
Related phenotype searches
Data aggregated from HPO/Monarch, ClinVar, OMIM (phenotypes + clinical synopsis), Open Targets, PanelApp, Phen2Gene, and Gene2Phenotype. Click a gene to view full details.