Select Entries from OMIM --
Online Mendelian Inheritance in Man
123 entries found, searching for "sperm"
*182878 OUTER DENSE
FIBER OF SPERM TAILS 1; ODF1
*602015 OUTER DENSE
FIBER OF SPERM TAILS 2; ODF2
*600930 SPERM ADHESION
MOLECULE 1; SPAM1
*182889 ZONA PELLUCIDA
GLYCOPROTEIN 3A; ZP3A
182882 SPERM
PROTAMINE P4; PRM4
*182880 SPERM
PROTAMINE P1; PRM1
*125880 DIAPHORASE 3;
DIA3
*603395
SPERM-ASSOCIATED ANTIGEN 1; SPAG1
*182888 ZONA PELLUCIDA
GLYCOPROTEIN 2; ZP2
*603038
SPERM-ASSOCIATED ANTIGEN 4; SPAG4
*603185 NUCLEAR
AUTOANTIGENIC SPERM PROTEIN; NASP
*182879 SPERM MEMBRANE
PROTEIN
131375 ENOLASE, SPERM
SPECIFIC; ENO4
*602862
UDP-N-ACETYLGLUCOSAMINE PYROPHOSPHORYLASE 1; UAP1
*182890 SPERM
PROTAMINE P2; PRM2
182610 SPASTIC
PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION; SPERM
*244400 KARTAGENER
SYNDROME
*601050 ZONA PELLUCIDA
RECEPTOR TYROSINE KINASE, 95-KD; ZRK
*160900 DYSTROPHIA
MYOTONICA; DMPK
*143100 HUNTINGTON
DISEASE; HD
*601533 FERTILIN,
BETA; FTNB
*150150 LACTATE
DEHYDROGENASE-C; LDHC
*106180 DIPEPTIDYL
CARBOXYPEPTIDASE 1; DCP1
*143890
HYPERCHOLESTEROLEMIA, FAMILIAL; FHC
*309550 FRAGILE SITE
MENTAL RETARDATION 1; FMR1
*601193 ACIDIC
EPIDIDYMAL GLYCOPROTEIN-LIKE 1; AEGL1
*313700 ANDROGEN
RECEPTOR; AR
601858 CALMEGIN;
CLGN
*242650 IMMOTILE CILIA
SYNDROME 1; ICS1
*168450 PARATHYROID
HORMONE; PTH
*601148 MITOCHONDRIAL
CAPSULE SELENOPROTEIN; MCSP
102530 ACROSOME
MALFORMATION OF SPERMATOZOA
*264600 PSEUDOVAGINAL
PERINEOSCROTAL HYPOSPADIAS; PPSH
*107730 APOLIPOPROTEIN
B; APOB
*195000 ZONA PELLUCIDA
GLYCOPROTEIN 1
#164400
SPINOCEREBELLAR ATAXIA 1; SCA1
*601294 SOLUTE CARRIER
FAMILY 6, MEMBER 10; SLC6A10
*120150 COLLAGEN, TYPE
I, ALPHA-1; COL1A1
*276900 USHER
SYNDROME, TYPE IA; USH1A
*118990 CLEAVAGE
SIGNAL-1 PROTEIN; CS1
*602889 A DISINTEGRIN
AND METALLOPROTEASE DOMAIN 3A; ADAM3A
279000 YOUNG
SYNDROME
#277180 VAS DEFERENS,
CONGENITAL BILATERAL APLASIA OF; CBAVD
*603121 CYLICIN 1;
CYCL1
#114480 CANCER OF THE
BREAST, FAMILIAL; BCS
*310200 MUSCULAR
DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE AND BECKER
TYPES
*602692 GLIOMA
PATHOGENESIS-RELATED PROTEIN
*602974 AQUAPORIN 7;
AQP7
*102480 ACROSIN;
ACR
*120160 COLLAGEN, TYPE
I, ALPHA-2; COL1A2
*201910 ADRENAL
HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY
*187430
TESTIS-SPECIFIC PROTEIN 1; TPX1
*191135 TUBULIN,
GAMMA; TUBG
243060 INFERTILITY
ASSOCIATED WITH MULTI-TAILED SPERMATOZOA AND EXCESSIVE DNA
*229300 FRIEDREICH
ATAXIA 1; FRDA
*180200
RETINOBLASTOMA; RB1
*185430 CLUSTERIN;
CLU
*176910 PROTEIN
KINASE, cAMP-DEPENDENT, REGULATORY, TYPE II, ALPHA; PRKAR2A
#174800
MCCUNE-ALBRIGHT SYNDROME; MAS
*173310
PROGESTAGEN-ASSOCIATED ENDOMETRIAL PROTEIN; PAEP
193450
VULVOVAGINITIS, ALLERGIC SEMINAL
*172270
PHOSPHOGLYCERATE KINASE 2; PGK2
*195002 ZONA PELLUCIDA
GLYCOPROTEIN 3B; ZP3B
*123812 CYCLIC AMP
RESPONSE ELEMENT MODULATOR; CREM
#100800
ACHONDROPLASIA; ACH
*312610 RETINITIS
PIGMENTOSA 3; RP3
*602574 TECTORIN,
ALPHA; TECTA
228300 FERTILE
EUNUCH
*603495
SERINE/THREONINE PROTEIN KINASE 13; STK13
231090 GESTATIONAL
TROPHOBLASTIC DISEASE
*312600 RETINITIS
PIGMENTOSA 2; RP2
*242670 IMMOTILE CILIA
SYNDROME DUE TO DEFECTIVE RADIAL SPOKES
#253300 SPINAL
MUSCULAR ATROPHY I; SMA1
305700 GERMINAL CELL
APLASIA
600499 ACIDIC
EPIDIDYMAL GLYCOPROTEIN; AEG
*602653 TECTORIN,
BETA; TECTB
*208900
ATAXIA-TELANGIECTASIA; AT
*193400 VON WILLEBRAND
DISEASE
*190232 TRANSITION
PROTEIN 2; TNP2
*190231 TRANSITION
PROTEIN 1; TNP1
*276903 MYOSIN VIIA;
MYO7A
#177170
PSEUDOACHONDROPLASTIC DYSPLASIA
300058 PEM HOMEO BOX
GENE, HUMAN HOMOLOG OF
300154
EXTRAEMBRYONIC, SPERMATOGENESIS, HOMEO BOX 1, MOUSE, HOMOLOG OF
*306700 HEMOPHILIA
A
*306900 HEMOPHILIA B;
HEMB
#176410 PRECOCIOUS
PUBERTY, MALE-LIMITED
#176270 PRADER-WILLI
SYNDROME; PWS
*176943 FIBROBLAST
GROWTH FACTOR RECEPTOR 2; FGFR2
*215520 CILIARY
DYSKINESIA DUE TO TRANSPOSITION OF CILIARY MICROTUBULES
*155120 A DISINTEGRIN
AND METALLOPROTEINASE DOMAIN 11; ADAM11
*415000 AZOOSPERMIA
FACTOR 1; AZF1
*480000
SEX-DETERMINING REGION Y; SRY
215518 CILIARY
DISCOORDINATION DUE TO RANDOM CILIARY ORIENTATION
*300144 GLUTAMATE
DEHYDROGENASE 2
*600185 BREAST CANCER
2, EARLY-ONSET; BRCA2
*600053 CYCLIC
NUCLEOTIDE-GATED CHANNEL, ALPHA-3; CNGA3
*600743 TRANSCRIPTION
FACTOR AP4; TFAP4
*600750 PENTRAXIN II,
NEURONAL; NPTX2
*152790 LUTEINIZING
HORMONE/CHORIOGONADOTROPIN RECEPTOR; LHCGR
*147460 SUPEROXIDE
DISMUTASE 2, MITOCHONDRIAL; SOD2
*142800 MAJOR
HISTOCOMPATIBILITY COMPLEX, CLASS I, A; HLA-A
*142709 H1 HISTONE
FAMILY, MEMBER 1; H1F1
142550 HEXOKINASE OF
SPERMATOZOA
*601492 HYALURONIDASE
DEFICIENCY
*601517 ATAXIN 2;
ATX2
*140560 HEAT-SHOCK
70-KD PROTEIN 2; HSPA2
*601663 ESTROGEN
RECEPTOR 2; ESR2
*137010 F9 EMBRYONIC
ANTIGEN; FEA
*136435
FOLLICLE-STIMULATING HORMONE RECEPTOR; FSHR
*602073 A DISINTEGRIN
AND METALLOPROTEINASE DOMAIN 3B; ADAM3B
*602372 ZONADHESIN;
ZAN
*227650 FANCONI
ANEMIA, COMPLEMENTATION GROUP A; FANCA
*600040
BCL2-ASSOCIATED X PROTEIN; BAX
*131530 EPIDERMAL
GROWTH FACTOR; EGF
*130500 ERYTHROCYTE
MEMBRANE PROTEIN BAND 4.1; EPB41
*125870 DIAPHORASE 2;
DIA2
#123790 CUTIS GYRATA
SYNDROME OF BEARE AND STEVENSON
*117139 CENTROMERIC
PROTEIN A; CENPA
*116896 CUT-LIKE, 1;
CUTL1
*114107 PROTEIN
PHOSPHATASE 3, CATALYTIC SUBUNIT, GAMMA ISOFORM; PPP3CC
*103280 ADULT SKELETAL
MUSCLE GENE
#219700 CYSTIC
FIBROSIS; CF