ZMP

LOC100329986

Ensembl ID:

ENSDARG00000075239

Human Orthologue:

SPAG16

Human Description:

sperm associated antigen 16 [Source:HGNC Symbol;Acc:23225]

Mouse Orthologue:

Spag16

Mouse Description:

sperm associated antigen 16 Gene [Source:MGI Symbol;Acc:MGI:1913972]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa45024	Nonsense	Mutation detected in F1 DNA	Not yet available
sa39498	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa45024

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115055	Nonsense	22	619	1	1

Genomic Location (Zv9):

Chromosome Zv9_scaffold3460 (position 1900)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	40654492
GRCz11	21	40677539

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTGGTCACCATGGAGACAATACACAACTTAGCAAGCGCAACAAACCGGCT[G/T]AAGTAAAAATGGCAGCAAGACACGAAGCAGCAGAAGAGGCCGTTGACGGT

Long Flanking Sequence:

ATCTTGACCATTCAGTTTCGTAATTGTAAGAAAATTTGTTTGCTAACATTTCTTTTTTTTTTGCATTCTATAAAAGCATTTTTTATTCTAAATGTCAAATAAAAACAGACTGATAACACTTCTTTTTTCTCTCTCCAGAAAATGACAGTCAGCATAATAAAGGGTTTTGCTTGTTGTGACCTAAAATAAAACAGGGTTTTTCCACTAAATATGATTAGACTCTTCTGTACAGTTAATTTTTTGGCATTGGCATTTGGCATATTGTTGTATAAAATGTGTAAAATCAAGGCATAGAATTAAAATATTTATGTAAATGAGTAGCTAGTTTAATATAGATGTCCATTGTAGATTTTATTTGAATTTCCACGAAGACATACTGTGGTTCGTTGATCTTGTTGAGTGCAAATTTTGTACAAATTAATGTAAAGAAAGTCCCCATGTCACGCTTTCTTGGTCACCATGGAGACAATACACAACTTAGCAAGCGCAACAAACCGGCT[G/T]AAGTAAAAATGGCAGCAAGACACGAAGCAGCAGAAGAGGCCGTTGACGGTCCTTATTACCTCGAGAAGGTTTTCATCCCAGAGGACTCTGAGGATGATTATCAATACGACGAAGTGACCGTCGACGAGTTCAGCGTAACTGAGGGCGAAGAGGACCTGGAGACTGCCGTAAAAGCAGCGCTGGATCAAACCGACGGCTCTCCACAGAGAGTCAGCTCAGCCAGACACCCCGTTCCTAAAATACCCGAGGTGGTGGACGACTTTCTCCGCAACTATCTGGTAAATATGGGCATGAAAAAAACATTGAACTGTTTCCAAACCGAGTGGTTTGAAATGAAACACAAGGGTTTAATTAACACAGACAAAACTGAACTCATCCCTGACGTCTATACACACAACCAGCTCCTGGACAACGAGCTAAAAATCGTACAAAAAGAGCGGGATAACTATAAACAAGCTGCATTCGAAGCTGGGGAAACCATAATAAAACTACAAAGAGAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39498

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115055	Nonsense	428	619	1	1

Genomic Location (Zv9):

Chromosome Zv9_scaffold3460 (position 681)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	40655711
GRCz11	21	40678758

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGCCCAAAGTCGATGTGTGCTCAGTTTGGAGGGGCACCTTCACGCCACTT[G/A]GGCCTGTTCTTTTCACTCCTGTGGTGATTTTGTGGCATCTTGCTCCATGG

Long Flanking Sequence:

CTCACGAACCCAAACAGCCTCAAAGCCTACAAACTCTCCACAGGAACGAGAAAAAATGCAGCGGAGTCCTGAAAAGGAAGCACACCTGCCATGTGACGATGCCCGAAAACATCCTAAAGACTCTGAATTCCCATCCAGCACTCGCCTCAATCCCTACTTGCCACAAATCAAGGCTCTTACCTCCCCCAACACCAAATCAGCCAACCTCTCGCTCTCCAAGTCTTTCAAAGCGCACACAATGGCAGTGAGCTTCCTCGCTCTGCATCCCCGTAAAATGATAGTAGCCTCCTCAAGTGATGACCAGCTTTGGAAATTATGGGCAATCCCCAAGGGAGAGATGATCATGACTGGCGAGGGTCACACTGATTGGCTGTCGTCTTGTAGTTTCCATCCCAGTGGTGATTTCTTGGGGACCACAAGTGGAGACACCACAGTTAAAATCTGGGACTTCGCCCAAAGTCGATGTGTGCTCAGTTTGGAGGGGCACCTTCACGCCACTT[G/A]GGCCTGTTCTTTTCACTCCTGTGGTGATTTTGTGGCATCTTGCTCCATGGATAACACGGTTAAAGTGTGGGATTTGAATAGCGAGCGCTGCCGCTGCACTCTGCGTGGACATGTGGACTCTGTGAACAGTGTTTCTTTCCTGCCCTTCTCGAATATTCTACTGACCTGCTCGGCAGACAAGACGCTCTCTCTTTGGGATGCCCGTGCCGGATTGTGTGCCCAGACTTTCTACGGGCATAAGCATTCATGCAACCATGCAGCTTTCAATATCACTGGCGACACGATTGCTTCGTGCGACTCTTTTGGGGTGGTTAAATTATGGGATGTGAGGAACGTGTCTGCAATGGTGAGCATGGACACCGGGCCGCATCCCAGCAATCAAGTGGCCTTCAGTCCAAACGGAAGAGTACTGGCGGTGGCGAGTAACGATGGCTCGGTCAAGACAGTTGAAGTGGCTTCTTTACATGTGTCGAGTTTAACAGCTCATGAGGACGCAGTAC

Associated Phenotype:

Not determined