ZMP
SYNPO2L (2 of 2)
Ensembl ID:
Description:
synaptopodin 2-like [Source:HGNC Symbol;Acc:23532]
Human Orthologue:
SYNPO2L
Human Description:
synaptopodin 2-like [Source:HGNC Symbol;Acc:23532]
Mouse Orthologue:
Synpo2l
Mouse Description:
synaptopodin 2-like Gene [Source:MGI Symbol;Acc:MGI:1916010]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22279 | Nonsense | Available for shipment | Available now |
sa35468 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31924 | Nonsense | Available for shipment | Available now |
sa24931 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22279
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108472 | Nonsense | 360 | 932 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 13 (position 22399181)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22128519 |
GRCz11 | 13 | 22258969 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATGGCATATTTCCTGGCAGTGAATCAGAATTTGATGAGGAGGGTTTTT[C/A]AGCTGCACCGGACCCCACATGGGACAGCGACTACCTTGAAATGCTGGAGA
Long Flanking Sequence:
TACTCATATCGGTTGTAAAAAAGTGTTATCGGTTCATCCCTACATTATCCCTAAATTAAAATTTCAGCACTAGTAAACAAAGACTTTCCCAATGGTAGACAAATCATTTTTGCATCAAAGTTATATTATTAATTTAACCATGCTTCCTTGTTGCAAAATTCTTTAACTAAAACGCGGTTGCTGTTAAATATTTGTAATATATATATATACTGTCTCAAACCTTTTTATCTTATGTTATGCAGAATTGAACCGTGGAGAGACAATCACAGACAAGCAGGTGAAAGAGGCCCGGTCCAAGTGCCGCACAATCGCCTCACTACTGACAGATGCACCAAACCCTCATTCAAAGGGTGTACTGATGTTTAAAAAGCGCCGGCAACGATCCAAGAAATATACACTGACCAGCTTTGGAAGTGTTGATGAGGACATGAGGCAGGACTCTCAAGAGGAGGATGGCATATTTCCTGGCAGTGAATCAGAATTTGATGAGGAGGGTTTTT[C/A]AGCTGCACCGGACCCCACATGGGACAGCGACTACCTTGAAATGCTGGAGAAAAGATGTGCTTCCAGAGGTCAGGAAGGAGATGGTGGTGCTCTTAGTCCTGGTCTGAGTGATACATCTGGAAAGGGGGCACAGTTGTTTGAGCAGCAGAGGAAAAGGGCTGAAGAGCATGCAAGAAAAATCGAAGCTGCACAAGAACAGTTACAAAGCCAAATGCTGGGCATTTCACTGAAAGAGGCCCAGGCACTTCCTCCGCTTCAGACAGCACACCCAGACCCACTAACAAAGCTCAATGTCCAGCCACCACCAGTTGCTCCAAAACCTGCCAGACCTTCAACAACCCTTTATCATGACGTTCAAGCAGCCGAAGCACAAAACAACAAGACACAGATGAATACACCTCAGACCATCCCCACTGTTCCTGTTATGGTGAATGGAGATGCTTCGAACACAACTGTGACAGCCCCCTCTGTGATGCCCAAAACTAATCTCTCAGTTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35468
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108472 | Nonsense | 617 | 932 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 13 (position 22400302)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22129640 |
GRCz11 | 13 | 22260090 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGACAACTTCAAGCCCTGTAATTCCACTGTCACCTGTAGTCTATCGT[G/T]AAAAACCAGCTTCTGTTGGTGGCCGCACTGGTATTCTCCAAGATGCCCGA
Long Flanking Sequence:
CTCCTGTTGTGTTTCGCCCTGCAGTCAGTAAGAAGACACCTAGACCTGTTTCAGTGGCTGTGGTGGCACCTCCATTTCCAGCAGCATCAGAAGAGCATGTCATGTGTGTCACCCCAGCCATATTTGGTACCCAAGTAACAATGAGTCAAATGAATGCCAATGTCTCTAATGAAATAATACCCACACAGCCCTTGGCACAAGGAACGTCTATTCCTCCACCTGCTGCTGTATCAGTTGAATCATATTCTCAACCTGCTTTTCAGTGCTCTGCAATGGAAAGCATCCAGGTTGCATCACTTCCCAGAGTTCAAGCCCAAAAGCCTACTGTTCCAATGATTGCAGAAACAATAGTTCCTCCTGATGACATGGTGACTTCTTTGGCTACTGATATGCATCCTAAGGGTATAACAATATCATCCCAAACCTCTTCTATTTTGACCCCTACTGCTTCTGAGACAACTTCAAGCCCTGTAATTCCACTGTCACCTGTAGTCTATCGT[G/T]AAAAACCAGCTTCTGTTGGTGGCCGCACTGGTATTCTCCAAGATGCCCGACGCCGCAGTGCATACAAGCCAATGTTTAAGATGCCTGACAGCAAGAAGAACTCACCAAACCCTGAACTGTTGACTATGGTGCAGAACCTAGATGACAGACCCAGCCATGGGTATCCTGAACCAGACAATATTGTTTACAACATTGATGAAAATAGGACAAGGGTCCCACCACCTGTGGCTCCTAAGCCACGAGTCATCCCAGAAATGTCACAGATCCCTCAGGCAGAGGGAAAAGGTGCAGAGCTGTTTGCTCGTAGACAAAGCCGCATGGATCAGTTTGTTGTAGACACTCCATATCTGCAGCCAGCAACTCTACAACACCAACAATCCCAATCAGTCATAGATTTCATCCAACCTCGAGAACCCTCGCCAACCCCATCCCAATGGAAGTATTCCCCTAATGTTCGGGCTCCTCCACCCATAGGATACAATCCCTTGTTGTCTCCTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31924
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108472 | Nonsense | 749 | 932 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 13 (position 22400745)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22130083 |
GRCz11 | 13 | 22260533 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTTCATCCAACCTCGAGAACCCTCGCCAACCCCATCCCAATGGAAGTA[T/G]TCCCCTAATGTTCGGGCTCCTCCACCCATAGGATACAATCCCTTGTTGTC
Long Flanking Sequence:
ACTGCTTCTGAGACAACTTCAAGCCCTGTAATTCCACTGTCACCTGTAGTCTATCGTGAAAAACCAGCTTCTGTTGGTGGCCGCACTGGTATTCTCCAAGATGCCCGACGCCGCAGTGCATACAAGCCAATGTTTAAGATGCCTGACAGCAAGAAGAACTCACCAAACCCTGAACTGTTGACTATGGTGCAGAACCTAGATGACAGACCCAGCCATGGGTATCCTGAACCAGACAATATTGTTTACAACATTGATGAAAATAGGACAAGGGTCCCACCACCTGTGGCTCCTAAGCCACGAGTCATCCCAGAAATGTCACAGATCCCTCAGGCAGAGGGAAAAGGTGCAGAGCTGTTTGCTCGTAGACAAAGCCGCATGGATCAGTTTGTTGTAGACACTCCATATCTGCAGCCAGCAACTCTACAACACCAACAATCCCAATCAGTCATAGATTTCATCCAACCTCGAGAACCCTCGCCAACCCCATCCCAATGGAAGTA[T/G]TCCCCTAATGTTCGGGCTCCTCCACCCATAGGATACAATCCCTTGTTGTCTCCTTCCTGTCCTGTTGGGGTGCAGCGTGCAGGCGCAAAGGTGTCTGAGGGAAGCGCCAAAGGAAGTAAGGGTAGTTATGGTGTGCCAAAAGAGGGTATCAAGGCCTTGGATTTCATGAGAAGGCAGCCATACCAGCTAAACCCTGCAATGTTCAGTTTTGGTGGTGGCATTGGTACACAGTCTTCAATCCCTTCCTACCAGAGGCAGCAGAGGGAGGGCCACACTCTGACTCCACCCAAGCAGATCCCAGTAAAGGCGGCACGTGTGTATGAAATCAAAAGATTCTCTACTCCCACCCCAATGTCAGCACCAACTCTCAACCCCACAGTCATTATACCACGCTCACAGACCACCCTTGGTGAGCGAATCTCTCGTTCTGACATGACTTCCCCTGCACCTGAACCTGTCCCTGAATCATCTCTAGCACCTTCACGGGCCCCAGGCCTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24931
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108472 | Essential Splice Site | 888 | 932 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 13 (position 22401360)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22130698 |
GRCz11 | 13 | 22261148 |
KASP Assay ID:
554-7452.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTCAAGTATGTCAAATCTCAGCTACTCTGGGCTCCAAGCTGCCAAACA[G/A]TTTAAGAGTGCCCCTGAATTAAGTGCCTTACCACCAAATCCCTTAAAATC
Long Flanking Sequence:
AGTAAGGGTAGTTATGGTGTGCCAAAAGAGGGTATCAAGGCCTTGGATTTCATGAGAAGGCAGCCATACCAGCTAAACCCTGCAATGTTCAGTTTTGGTGGTGGCATTGGTACACAGTCTTCAATCCCTTCCTACCAGAGGCAGCAGAGGGAGGGCCACACTCTGACTCCACCCAAGCAGATCCCAGTAAAGGCGGCACGTGTGTATGAAATCAAAAGATTCTCTACTCCCACCCCAATGTCAGCACCAACTCTCAACCCCACAGTCATTATACCACGCTCACAGACCACCCTTGGTGAGCGAATCTCTCGTTCTGACATGACTTCCCCTGCACCTGAACCTGTCCCTGAATCATCTCTAGCACCTTCACGGGCCCCAGGCCTCCCAGAGCTCCCCAAAATTTCATCTGTGCCCATCCCTCACCCCATGCCATACTCTCCACCAGTTCCCATCTCAAGTATGTCAAATCTCAGCTACTCTGGGCTCCAAGCTGCCAAACA[G/A]TTTAAGAGTGCCCCTGAATTAAGTGCCTTACCACCAAATCCCTTAAAATCCCCTATCCAAGTTCCCAAACCACACTTTATTGCAACACGGGCGGGTGTACAGCCCCGCGTCTGGAGGCCTGGTACCTTACCTCACTGACAGTATTGCTTTGCATGTGAAAGACTGAAACATCTATATCTGTCTCAAAGTTAAATCCTTTCAAGTTTGATCAGTGAGGTAACATTAATTTATTTGGAAACTATAAGGGAATAATATGTGCTGCATCCCAATTTGCATACTATCCATCTGGAATTGTATTTAATAGTTTGTACCAACTCGTAGTATTGAAATGAGTGTGCTAAAGGTTTCCAATTGAATTGTAATTTGAAGTGTAGAACCGTCTGGTCACTACAAAAATTGGTAAAAAGTGCAAACAAGCTACAAAAATTTAAATCACGTTATCTGTGTTATAGTTTATCTGCAACAGAAATGTGTACTTCTATAAAGATGTGTTTTGACAT
Associated Phenotype:
Not determined