ZMP

spata2

Ensembl ID:

ENSDARG00000063250

ZFIN ID:

ZDB-GENE-070822-5

Description:

spermatogenesis-associated protein 2 [Source:RefSeq peptide;Acc:NP_001073660]

Human Orthologue:

SPATA2

Human Description:

spermatogenesis associated 2 [Source:HGNC Symbol;Acc:14681]

Mouse Orthologue:

Spata2

Mouse Description:

spermatogenesis associated 2 Gene [Source:MGI Symbol;Acc:MGI:2146885]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37599	Nonsense	Mutation detected in F1 DNA	Not yet available
sa44992	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37599

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000092258	Nonsense	13	550	2	3

Genomic Location (Zv9):

Chromosome 23 (position 3531392)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	3574825
GRCz11	23	3517728

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCACTGCCACCAATGGATGCCAAGTTGCGAGAGGATCTGTTCCGCAGGTA[T/A]GTGGCTTCTCTGGAGAATCGGCTCGAGGAGGGAGCCGCTGAAGGAGGAGG

Long Flanking Sequence:

GGGAAAGCCTGGCAGTGAGTGCTCAAAAAAAAGCAAGTCTCCATTCATCCTCTGCTCAATCCCACTCATATGCCATGTTGCTCCTTCTGATGTGTTTTGGCTGATGAGGCACCCAAATATGCCCCTTACAATGGGAGAGAGGCCTGGGCAAGGTGTACGCCCAAATTAAATCAAGCACACCTTGGAAGAACACATTCATTATTCCATATGTCTCTTTGGAGGTCCAATGTTGGCATGAATTTAGCCAATGCTGCTGATATGGCATTGTAACATAAATAAATATATATGTCTCTCTTTGGAGGACGATCTCAGCTTGCTGATTTTCACTGCCACACTGCACCATTGCCCCAGATCTTCTGGTGTCTAGTGGGAGAGAGGTCTTGAGATGGCAAGTGGTCCTTTTTAAAGAAACACCTGGATTGTGGAATAAGAGGTTGCAAGCTACGCAGCCCACTGCCACCAATGGATGCCAAGTTGCGAGAGGATCTGTTCCGCAGGTA[T/A]GTGGCTTCTCTGGAGAATCGGCTCGAGGAGGGAGCCGCTGAAGGAGGAGGAGATAGACAAGGAGCTAAGACCGAGGAGGCACTGATTTCTACTGCAACAGCATTGCTAGGCTCATACCAGGCTGATCCAGGGCAGCGATTTCGCATGCTTCGCTTCTATGATGTTGTTGAGAACTCCCTGAGGACTCAGAGAGGCACAAGCTTGCGGACAGTGGGAACAGCCTTTGCAACGCTGGAAACCATCTGCACCAATTTGCTGCTTTTTCCATGGAAGAAGGAGTACCGTTGCATAAAGGTGAGTCAGCACGTTAATTATTAGGTCTAAAAATTCTAATTATGAACATCTTGATATCCACTGAGCACACAAGGAAAGATGTTTATTTTTGGGTGAACTATCATTGGACAGAAACAGCTGTGTGGGAAGTTAAGGTTATAGTTGCAGTGGGAATGAACATTTTGTGTGGTTATTTATTAAGCACATTCTATTGGGGTTAAATAATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44992

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000092258	Essential Splice Site	111	550	2	3

Genomic Location (Zv9):

Chromosome 23 (position 3531687)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	3575120
GRCz11	23	3518023

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCACCAATTTGCTGCTTTTTCCATGGAAGAAGGAGTACCGTTGCATAAAG[G/A]TGAGTCAGCACGTTAATTATTAGGTCTAAAAATTCTAATTATGAACATCT

Long Flanking Sequence:

TTGGAGGACGATCTCAGCTTGCTGATTTTCACTGCCACACTGCACCATTGCCCCAGATCTTCTGGTGTCTAGTGGGAGAGAGGTCTTGAGATGGCAAGTGGTCCTTTTTAAAGAAACACCTGGATTGTGGAATAAGAGGTTGCAAGCTACGCAGCCCACTGCCACCAATGGATGCCAAGTTGCGAGAGGATCTGTTCCGCAGGTATGTGGCTTCTCTGGAGAATCGGCTCGAGGAGGGAGCCGCTGAAGGAGGAGGAGATAGACAAGGAGCTAAGACCGAGGAGGCACTGATTTCTACTGCAACAGCATTGCTAGGCTCATACCAGGCTGATCCAGGGCAGCGATTTCGCATGCTTCGCTTCTATGATGTTGTTGAGAACTCCCTGAGGACTCAGAGAGGCACAAGCTTGCGGACAGTGGGAACAGCCTTTGCAACGCTGGAAACCATCTGCACCAATTTGCTGCTTTTTCCATGGAAGAAGGAGTACCGTTGCATAAAG[G/A]TGAGTCAGCACGTTAATTATTAGGTCTAAAAATTCTAATTATGAACATCTTGATATCCACTGAGCACACAAGGAAAGATGTTTATTTTTGGGTGAACTATCATTGGACAGAAACAGCTGTGTGGGAAGTTAAGGTTATAGTTGCAGTGGGAATGAACATTTTGTGTGGTTATTTATTAAGCACATTCTATTGGGGTTAAATAATTGCTTAAAGCAGGGGTCACCACACTCCGTCCTGGAGGGCCAGGGTCTTGCATATGTATCTCCAATCCTAATCAAACACACCTAAACAAGCTAATCAAGATCTTCATAGGCACACTTCCAGGCAGGTGTGATGAGGCAAGTTGGAGCTTAACTCAAAATTACAAGCAAAAGCTGCACAATATAGCATCAAATCATTATTTTTTATTATTTAGTTGTTTTGTATCGACAAACATCCTAAGTTGGTAAAACTTGTGTGCGCGCGCGTACCCAAAGAGCGGTGGGAGTTGCACGCGCGAC

Associated Phenotype:

Not determined