Disease A B C D E F G H I J K L M N O P Q R S T U V W X Y Z [0-9]
Gene A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

TNP2

Gene name: transition protein 2 (during histone to protamine replacement)
OMIM ID: 190232
Chromosome location: 16p13.13

Polymorphisms

Disease/PhenotypeSpermatogenic failure, susceptibility to.
Reference transcriptNM_005425.4
DNA Changec.76T>G
A.A. Changep.Cys26Gly
Variation Typesubstitution
Cases135 Infertile
Controls160 Fertile
Frequency
Allele/GenotypeFrequency in casesFrequency in controlsOR (95%CI)P-value
T1.000.997NS
G00.003
TT135 (100%)159 (99%)
TG01 (1%)
ReferenceImken L, Rouba H, El Houate B, Louanjli N, Barakat A, Chafik A, McElreavey K.Mutations in the protamine locus: association with spermatogenic failure?
Mol Hum Reprod. 2009 Nov;15(11):733-8.

Disease/PhenotypeSpermatogenic failure, susceptibility to.
Reference transcriptNM_005425.4
DNA Changec.117G>C
A.A. Changep.Gln39His
Variation Typesubstitution
Cases135 Infertile
Controls160 Fertile
Frequency
Allele/GenotypeFrequency in casesFrequency in controlsOR (95%CI)P-value
G10.997NS
C00.003
GG135 (100%)159 (99%)
GC01 (1%)
ReferenceImken L, Rouba H, El Houate B, Louanjli N, Barakat A, Chafik A, McElreavey K.Mutations in the protamine locus: association with spermatogenic failure?
Mol Hum Reprod. 2009 Nov;15(11):733-8.

Disease/PhenotypeSpermatogenic failure, susceptibility to.
Reference transcriptNM_005425.4
DNA Changec.129C>A
A.A. Changep.Gly43Gly
Variation Typesubstitution
Cases135 Infertile
Controls160 Fertile
Frequency
Allele/GenotypeFrequency in casesFrequency in controlsOR (95%CI)P-value
C0.980.99NS
A0.020.01
CC130 (96%)158 (99%)
CA5 (4%)2 (1%)
ReferenceImken L, Rouba H, El Houate B, Louanjli N, Barakat A, Chafik A, McElreavey K.Mutations in the protamine locus: association with spermatogenic failure?
Mol Hum Reprod. 2009 Nov;15(11):733-8.

Disease/PhenotypeSpermatogenic failure, susceptibility to.
Reference transcriptNM_005425.4
DNA Changec.301C>T
A.A. Changep.Arg101Cy
Variation Typesubstitution
Cases135 Infertile
Controls160 Fertile
Frequency
Allele/GenotypeFrequency in casesFrequency in controlsOR (95%CI)P-value
C0.660.68NS
T0.340.32
CC60 (44%)73 (46%)
CT59 (44%)70 (44%)
TT16 (12%)17 (10%)
ReferenceImken L, Rouba H, El Houate B, Louanjli N, Barakat A, Chafik A, McElreavey K.Mutations in the protamine locus: association with spermatogenic failure?
Mol Hum Reprod. 2009 Nov;15(11):733-8.

Disease/PhenotypeSpermatogenic failure, susceptibility to.
Reference transcriptNM_005425.4
DNA Changec.391C>T
A.A. Changep.Arg131Trp
Variation Typesubstitution
Cases135 Infertile
Controls160 Fertile
Frequency
Allele/GenotypeFrequency in casesFrequency in controlsOR (95%CI)P-value
C0.370.4NS
T0.630.6
CC15 (11%)27 (17%)
CT70 (52%)75 (47%)
TT50 (37%)58 (36%)
ReferenceImken L, Rouba H, El Houate B, Louanjli N, Barakat A, Chafik A, McElreavey K.Mutations in the protamine locus: association with spermatogenic failure?
Mol Hum Reprod. 2009 Nov;15(11):733-8.

Disease/PhenotypeSpermatogenic failure, susceptibility to.
Reference transcriptNM_005425.4
DNA Changec.*78C>T
A.A. Change
Exon/Intron3' of the stop codon
Variation Typesubstitution
Cases135 Infertile
Controls160 Fertile
Frequency
Allele/GenotypeFrequency in casesFrequency in controlsOR (95%CI)P-value
C0.550.56NS
T0.450.44
CC42 (31%)54 (34%)
CT63 (47%)70 (44%)
TT30 (22%)36 (22%)
ReferenceImken L, Rouba H, El Houate B, Louanjli N, Barakat A, Chafik A, McElreavey K.Mutations in the protamine locus: association with spermatogenic failure?
Mol Hum Reprod. 2009 Nov;15(11):733-8.