ZMP
wu:fd15f08
Ensembl ID:
ZFIN ID:
Human Orthologue:
SPG7
Human Description:
spastic paraplegia 7 (pure and complicated autosomal recessive) [Source:HGNC Symbol;Acc:11237]
Mouse Orthologue:
Spg7
Mouse Description:
spastic paraplegia 7 homolog (human) Gene [Source:MGI Symbol;Acc:MGI:2385906]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10238 | Nonsense | Available for shipment | Available now |
sa17610 | Nonsense | Available for shipment | Available now |
sa21092 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10238
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098438 | Nonsense | 122 | 788 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 7 (position 57437517)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55872843 |
GRCz11 | 7 | 56174254 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTATGCATTCTTCRCTTTTGTTGTTTCTTCCCTAGAAGAGAAAAAGAGA[C/T]GAGAACAGGAGGATCAGATGTACAGGGAACGRCTGCGCACACTCTTTATT
Long Flanking Sequence:
CAGTAGATCAGCAGTTTCTGAAATACTCAGACCAGCCGGTCTGGCACAAACAACCATGCCACATTTGAAGTCACTTAAATCACTTTTCTTCCCTATTCTGATGCTCAGTTTGAACTGCAGCAGATCGTCTTGATCATGTATACATGCCTAAATGCTTTGGGTTGCTGCCATGTGATTGGCTGATTAGAAATTTGCGTTATTGAGCAGTTCGACAGGTGTACCTAATAAAGTGGCTGGTGAGTTTGTTATGCTCAACAAAACAAAGAATTTCTGCTTCAACTATACTTTTTTTGAAACTAATCTAAATAGAAACCAACATAAGAACCTACAGTATATGATACACAAATTTGGTACATCCATATGACATCATGTGTATTGGGAAAACAATGCGCTAAGTTGACCAATCAGACTCAAGTAACTCAATGCTAGATATAACTTAATGCCAGATCAGTTATGCATTCTTCACTTTTGTTGTTTCTTCCCTAGAAGAGAAAAAGAGA[C/T]GAGAACAGGAGGATCAGATGTACAGGGAACGACTGCGCACACTCTTTATTATCGCTGTTATCATGAGCTTACTCAACTCTATTAACACCAGTGGCGGTAACATATCCTGGAACGATTTTGTGAATGAAATGTTGGCCAAAGGGGAGGTGTCGCGAGTACAGGTGGTCCCAGAGAGTGACATTGTGGAGATCTACCTTCACCCTGGAGCTGTCATCTTCGGCAGACCGGTGTGTCTCCCCCTGTACATTTAGTCCCTTGTGCAATTTTAAAATAATTGTCGTTGTACGCTATTATTAATATCTCATTGTCTGTTGTAGAGACTTGCCCTGATGTATCGAATGCAGGTGGCCAACATTGACAAGTTTGAGGAGAAGCTTAGAGCGGCGGAGGAAGAGCTGAATATAGATGCCAAAGACAGAATACCAGTGACCTACAAGCGCACAGGCTTCTTTGGGAAGTGAGTAATTTGTACTTTTTCAAAGAGCATGCAAACGTGGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17610
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098438 | Nonsense | 124 | 788 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 7 (position 57437511)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55872837 |
GRCz11 | 7 | 56174248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTCTTCRCTTTTGTTGTTTCTTCCCTAGAAGAGAAAAAGAGAYGAGAA[C/T]AGGAGGATCAGATGTACAGGGAACGRCTGCGCACACTCTTTATTATCGCT
Long Flanking Sequence:
ATCAGCAGTTTCTGAAATACTCAGACCAGCCGGTCTGGCACAAACAACCATGCCACATTTGAAGTCACTTAAATCACTTTTCTTCCCTATTCTGATGCTCAGTTTGAACTGCAGCAGATCGTCTTGATCATGTATACATGCCTAAATGCTTTGGGTTGCTGCCATGTGATTGGCTGATTAGAAATTTGCGTTATTGAGCAGTTCGACAGGTGTACCTAATAAAGTGGCTGGTGAGTTTGTTATGCTCAACAAAACAAAGAATTTCTGCTTCAACTATACTTTTTTTGAAACTAATCTAAATAGAAACCAACATAAGAACCTACAGTATATGATACACAAATTTGGTACATCCATATGACATCATGTGTATTGGGAAAACAATGCGCTAAGTTGACCAATCAGACTCAAGTAACTCAATGCTAGATATAACTTAATGCCAGATCAGTTATGCATTCTTCACTTTTGTTGTTTCTTCCCTAGAAGAGAAAAAGAGACGAGAA[C/T]AGGAGGATCAGATGTACAGGGAACGACTGCGCACACTCTTTATTATCGCTGTTATCATGAGCTTACTCAACTCTATTAACACCAGTGGCGGTAACATATCCTGGAACGATTTTGTGAATGAAATGTTGGCCAAAGGGGAGGTGTCGCGAGTACAGGTGGTCCCAGAGAGTGACATTGTGGAGATCTACCTTCACCCTGGAGCTGTCATCTTCGGCAGACCGGTGTGTCTCCCCCTGTACATTTAGTCCCTTGTGCAATTTTAAAATAATTGTCGTTGTACGCTATTATTAATATCTCATTGTCTGTTGTAGAGACTTGCCCTGATGTATCGAATGCAGGTGGCCAACATTGACAAGTTTGAGGAGAAGCTTAGAGCGGCGGAGGAAGAGCTGAATATAGATGCCAAAGACAGAATACCAGTGACCTACAAGCGCACAGGCTTCTTTGGGAAGTGAGTAATTTGTACTTTTTCAAAGAGCATGCAAACGTGGCAAGCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21092
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098438 | Nonsense | 542 | 788 | 12 | 17 |
Genomic Location (Zv9):
Chromosome 7 (position 57425607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55860933 |
GRCz11 | 7 | 56162344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGGGCTTCAAGTCCATCGACACCTTCAGCTTTGAATATGCTGTGGAA[A/T]GAGTCATTGCAGGTTTCTAGCTGCTAGATTAATGTGTGCTTTTGATTTGA
Long Flanking Sequence:
CATATAAAGGCAGCTCTGGTTATTATAAAAGACATAAAAACATTATAGCGGATGTGGCATAAATCATGACGTAAGTGGCATCATTGAAAATTAACACACACTCAAAGCGTAATGGTCATTCTACACGTGTATTAGCTGTATATTACAGAGTCTATTAACTCTCTTTAATCAGGCTACTTGCTTTCAAATATGCATTTCTTGTGTTATAGGAGAGAAAGGAAATCTTTGAGCAGCACCTGAAAATCCTAAAGCTCACACAACCAGCAGACTTTTATTCTCTGCGCCTGGCTGAGTTGACACCAGGCTTCAGTGGTAAGTGAGAGTTTGACGTAATCCTGTAATCCATTAATACCATGTTCTGGCTGCCACAATACTATTTGTACATCGTTGTGTTTTTTCCAGGTGCTGACATTGCCAACATCTGTAATGAAGCTGCCCTTCATGCTGCCAGAGAGGGCTTCAAGTCCATCGACACCTTCAGCTTTGAATATGCTGTGGAA[A/T]GAGTCATTGCAGGTTTCTAGCTGCTAGATTAATGTGTGCTTTTGATTTGAAATATACAGTTGAGGTCACAATTATTAGCCCTCCTAATTTATTAACCCCCCTGTTTACACTCCAGAACAAAATCTTAAGACCGCCAGGGGGAAACATTACAGTTATACACATTTTGGAAGGGAAGATCATAATCTGATTTGTAGTATTTGAAGTACTGCTTTGAAATACCCAAAGAAGACACGGGTGCAAAAGCCAAAAAAACTGAGAATAAGCAATTTATTAAAAAAAGCATTTAAACTCAAATAGGCTGAAATCAGCTGATCAAAAGAATAGGACCAGAGGCCAAAAAACATGACAATGGATCTCAAATTGTCAAAAGTGACTCAGTAGTGACTAGTTCCTCCATTCTTGTTGATCACTTCAAACTATTTTTTCGGTATGCTTGATACAAGTGTTTCCAGGAGCCTGGGGGTAACATTGCTCCATGTGGTTAAGATGGCTTTAGGAAG
Associated Phenotype:
Not determined