ZMP
mospd2
Ensembl ID:
ZFIN ID:
Description:
motile sperm domain-containing protein 2 [Source:RefSeq peptide;Acc:NP_001007294]
Human Orthologue:
MOSPD2
Human Description:
motile sperm domain containing 2 [Source:HGNC Symbol;Acc:28381]
Mouse Orthologue:
Mospd2
Mouse Description:
motile sperm domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1924013]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34794 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41559 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21618 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34794
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029528 | Nonsense | 6 | 526 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 56990875)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 55395469 |
GRCz11 | 9 | 54985072 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCAGACCACTGCTGACTGACAGCGCGCACTATCATGGCGGAGGCAGGA[C/T]AGGCGGAATCAGAGCAGGTAATTAGACAGCGAAACAAAAGCAGGATTTCG
Long Flanking Sequence:
TACTTAACAAATAAAATAGCAACTAAAACCTGCCACAGTTTATAAGGTGTTAAATAAAATGACTTATTACTAAACGCAAGCATGTTTCTTACCGTACTTCAGCATGTCTTTAACACTGTTTATTACACTTTTCTTCTTCTCACACACTGCTTCTTTTCCTCAAAGTGCGCGCGCATTTCATCACGTCATGATGTGTGACTCTTCCGGTTATCTCTTAAAGGAACAGTCGAACAGCCCAATCACTGATTCACAAATAAGTGATGTTATCAGAAGCCTTTACTGCTTATAGACTCAGCACACAATGCTGTCATTTGTGTTTAATTACCAGAGCATATCAGCGGAACTTTATCTCGCTCCGAGCGCCCGTTCAAAGGTTTGTTTGATATGTCAGAGCCAACATGGCGTCGCCGTGTGTCCAGTTTCACAGAGTCCGCTACGGAACTCGCTGCAGATCAGACCACTGCTGACTGACAGCGCGCACTATCATGGCGGAGGCAGGA[C/T]AGGCGGAATCAGAGCAGGTAATTAGACAGCGAAACAAAAGCAGGATTTCGTGTTTTATTCTCATCTAGAATGGATTTATGATGCCTGTTTACATCTCTCCAAAAGGACATCGAGATCAAGATCCAAGAAACACGGCAGAGGTTTAAAAGCGAGTATGTTGAAGGTGAGTTAGCAGAGCGCTAAGTTCACAACTGTTTACAAGACACACTATTGAGCTTAAAATGTACCACTATTCATTCACATATTACATATAAAATGACATGTACGAGTTTAGTGGATCATGTGTGCTTTTCCGATGCTTTGTGTTTATTATTGGACATCACAGCTGTTGAATTCTACTTGTTTTCTGACAGCTAAAGTCATGTTTTTATGGTAATGTTGTTTATATTGTCATACTAGTGTGGAATAAATAGCACAAAGTTTAAAAGTTGGTCTTACAGTCTTTGCATAAACAGTTTTTTTGACATTTCTTTGTGCTTGACATATGCACTGTTAAATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41559
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029528 | Essential Splice Site | 114 | 526 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 56999542)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 55404136 |
GRCz11 | 9 | 54993739 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGGTGCCGTTTACCTGCACGGATACGACAAAGAAGGAAACAAACTCTG[T/C]AAGACTTCATTTGGCATCTTAAATCTGCAGTTTAATTGGGGCTGTGCGAT
Long Flanking Sequence:
CCTTTTTTCATCAGGGATCACCACAGCGGAATGAACCGCCAAGTATTTCAGTATATGTTTTACACATTATTGCCCTTCCAGCTGCTACCCAGTACTGGGAAACACCCATACACACTCGTACACTACAGCCAAATTAGTTCCATTTAGTTCATGCGCATGTGTTTGGACTGTGCAAAAAACCCACGCCAACCCAGGGAGAACATGCAAACTCCACACAGATACTGAGTGTTTGAGCACAATCCTCCTCTTATCCTTAAAAGCTTCAGCCTCTGCCGATCTTGAATTTCCAGCTAAAGGAACCGTGTTGATTTGTTGTTATCAGATGTACTGTGTGGAGCTGATGGTGTTGTGCTGATTATTCCGGCAGAGAATGTGCTGAATGTGTGCTGTTTCATGTTATTTTTGTGTTCAGATCTGACGGAGAGCAGCATTCCCCGCTGGATGTTTGAGATCGGTGCCGTTTACCTGCACGGATACGACAAAGAAGGAAACAAACTCTG[T/C]AAGACTTCATTTGGCATCTTAAATCTGCAGTTTAATTGGGGCTGTGCGATATGGGCAAGAGAAACCTATCACGGTTTACCAGAACAATATTGCGATTCCGATTTTAATCAGGATTTTGTTACAGACAAACTGAGTCTGTGTTTACAGTGTGATTCAGAAACCTATTTAGGGAAGTTTGAGTCCAACAATTAGATATGCATCAAAGAGCTGTAACATGTCTCTACAACAGACACAAGGCAAAACAGAAAATAAAAATCACCTCTAGTACAGTGACAAAACTAATAAATAGACTACTGTGTGTGTGCATGTATGTGTATGCGTATGAATCAAAATGAATGACTTCCAGCTACTGTGACGCTCTCACCGCCTCCGGTGTGAACGCAGTGTTATAAATGCGATACATCAGCCTTCCTGCATCCAAAGTAACCCCCACACCACAGATGTTGACTTTTTTTTTGGCACCAAGTCCTCCCATGCTGAACTCACTGATCACAGTATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21618
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029528 | Essential Splice Site | 480 | 526 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 57055766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 55460291 |
GRCz11 | 9 | 55049894 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTAGTCCTACAACAAACGTCAATGAGCATCAGGATCTGCAGAGCACGG[T/A]GAGAGATCTACACACAGAGTCTGGTTATTTAAAGCAACACATACAAACAA
Long Flanking Sequence:
TATGAGTGTGTGTGTGGATGTTTCCCAGAGATGGGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAAACTGGCTGGATAAGTTGGCGGTTCATTGTGCTGTGGCGACCTCGGAATAATAAAGGGACTAAGCTGACAAGAAAATGAATGAATTATTATCATATGAGGGACCTGGTGTTGCTTTATTCACCAAATAAATGCTTCTAATTGCATTTGCACTGTAAACTTAAATAAAAATAAGATTTCAGATTTTAAGGCGAGTTTTCAGATCTTCTGCTTTGAAACAATTCCAGATAAATCTACAGATTGTTTACGGAATTCTGCACACTACTAGCCAATAAAGTCCACAGATTGTGCTTGTATTAATAACAACTCCTGTTGTGTTTCCCACAGGCTCCGCTGTCACGTTTTGGAGAGTCCAAAGTCTATTCTGAGCAATTCATTTGAGTTTCCATCTAGTCCTACAACAAACGTCAATGAGCATCAGGATCTGCAGAGCACGG[T/A]GAGAGATCTACACACAGAGTCTGGTTATTTAAAGCAACACATACAAACAAAACTGATGCTCTTCATGCACTGCACACTTTAGAGATCTTTATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCCACCCCCACCCCCACCCACCCCCACACACCCCCACACACACACACACACACACACACACACACACACACAATCTACACACACACACACACACTTCTATATATATACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATATATATATATGTGTGTGTGTATGTGTGTGTGTATATATATACACACTTTTTTTTGCTTGCCAGTGCTTTAAAAAGTTTCCATATCTGGATTGGTGGGTGGCGGTTTTTGGGTGTGGCTTAG
Associated Phenotype:
Not determined