ZMP
si:dkey-282h22.6
Ensembl ID:
ZFIN ID:
Human Orthologue:
SEZ6L2
Human Description:
seizure related 6 homolog (mouse)-like 2 [Source:HGNC Symbol;Acc:30844]
Mouse Orthologue:
Sez6l2
Mouse Description:
seizure related 6 homolog like 2 Gene [Source:MGI Symbol;Acc:MGI:2385295]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7541 | Missense | Mutation detected in F1 DNA | Not yet available |
sa10464 | Nonsense | Available for shipment | Available now |
sa7540 | Missense | Mutation detected in F1 DNA | Not yet available |
sa26012 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6029 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40018 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12488 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7541
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111948 | Missense | 32 | 894 | 2 | 18 |
ENSDART00000142594 | Missense | 32 | 892 | 2 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 14868854)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15114460 |
GRCz11 | 3 | 15264260 |
KASP Assay ID:
554-4011.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTTTTTTTYCAGGTGCATCTTTAGGGACATCAGATCCTGAAGCTCCTC[C/T]CACCGTGACTTCTAGTCCCCGCCCCCTGGGAGATCTCATCCATGCTGCAC
Long Flanking Sequence:
TTACTACTGTACTTATTTTCTCTTCTTTTGCTTGTGTCCAGGCTGTTCTGTCATATTGAACCATGGTGTCCACAGTTTTTGCTGTGACACTGTCTGTCACACTGCTGCACCTGGCCTCAGGTAACATACTTATACTTGTGTGAGTCTGCTTTTGTATGTTTAATTCTTTATGCAAAGTGATAAGTGCACATATTTTATGTTGATTATTAAATTAGTTTTCCTTGTACTGGGTTGCAGCTGGAAGGGTACCCGCTGCGTAAAGCATATGCCGGAATAGTTTTAGGTTTGCTGTGGCGACCCCTGACGAATAACGAATAAAGAAATAAGAAACTAAGCTGAAGGAAAATGAATGAATATTAAATTAGCAGACAGAACATGCACTCTAATTAATTTTATGTAATGAGTTGTGTGCTTGCTTTCATTATAGTGTGAGTTTTACAGACAAAGTGTGTTTTTTTTTTCAGGTGCATCTTTAGGGACATCAGATCCTGAAGCTCCTC[C/T]CACCGTGACTTCTAGTCCCCGCCCCCTGGGAGATCTCATCCATGCTGCACTTCTGAGCAAGGAGTACCTGGGACACACTCCTGGCAGCAGAGGTCAGTTCTTCCGAAAGACAACACAGCAGGACTGCAAAAAAAAGATGACATGCAATATTTAGTTTGTCCACTAATAAAATACAGGAACTTGGAAAGAATAAATCTTAGGCTACACCTTAAAATACACTGTAAAACCCTATAGTCAACTTTATCATTTCAAATGAGTGTAGTTAACTCAAAATTTACTGCAAGTTAATTCTACTCATTTAAAAAGAGTTTTGAACTCAGTGTTGAAGGTAATGAGTTAATTAAATACCTCATTACTTAACAACTTACATGGAATAAGTTAACAGTGCTCATATAGATTCATTTTTTAACTCAAATTGTTTGTAGCAATCGGTTTCCTCAAACAGTTTGAGTTGACTTAACTCATTGTGTTTTACTGTACTCAGTTGGTTTGAGTGCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10464
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 |
---|---|---|---|---|---|
ENSDART00000111948 | Nonsense | 217 | 894 | 5 | 18 |
ENSDART00000142594 | Nonsense | 217 | 892 | 5 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 14863305)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15108911 |
GRCz11 | 3 | 15258711 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGTGCAGCACTTGAGGTTTTGGCCAATGAGACGCTGATGAGCGAAGGT[C/T]AGGTGATTCGTAGCACAACCAATCAAGTGCAGATYCATTATAAGWGCCTR
Long Flanking Sequence:
TCTCATAACTGGGGTTGTGTCAGGCCATTAAAATGATTTCTAAGATGTCATAACATTCAACAAACTGTTTCTTCAGTTCAGTGCAATGCCAGTCTGTCAGGAATGGAGGGAATAATCGAGTCTCCTGATCCGCTCTCATCCTCGTCTGCCTTTTCCCCACTGGAGTGCACCTACAGCATCACCGTCTATCCTGGATATGGCGTTGAGATACAGGTGGGATTGCCTCCCTATTTCCAGTTTACAGCTCTAGCCTCTGTATAGGTATAGCTGGTGTATCTGGTTGGCATTTGCATGGGTGATGTCACTCTAAAGAGTTCAGGAATCTTTGCTCTTGATACACTCTTGCGTAACGACATCATTAGCTGTTGTTATGGTAACATCACCCATCTGTCTTGAAGGTGAAGAAAGTAAACTTGTCCAAAGAGGAGTCCCTCACCATTTCGGATCTGGGTGGTGCAGCACTTGAGGTTTTGGCCAATGAGACGCTGATGAGCGAAGGT[C/T]AGGTGATTCGTAGCACAACCAATCAAGTGCAGATCCATTATAAGAGCCTGAAGCAAAACAATCATGGCGTTTTCAGCTTTCACTATCAAGGTATGTTACTTGGGTACAAAGTATGTTTAGGGTCTACATATACATGATTGTAACATGTCTTTTTTGATTTGCCAGCTGTAACCGAAATGTCTTTTTCTTTTGAACACCAATTCCAGCCTTCCTCCTGTCCTGTTCGTTCCCTCTCTCCCCTGAGGGCGGCGGAGTGACTGTAACTGATATACATCCTGGCGGTCAGGCTCACTTTCATTGTGATCCAGGGTTTGAGGTCAGAGGTCATGAGGTTGCAACCTGTTTAAACTCTACCCGACCCAAATGGAGCACTCCAGAGCCCCAGTGTGTTGGTGGGTTGCATTGATTTTTGTTATTTGAATGTCTTTCATTTGCTCAAATACACCTCTGCTCGTTGCCATGTGTACAACCGTTAGAGCTGTGATAAAACAAATTTTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7540
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:
A > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111948 | Missense | 641 | 894 | 12 | 18 |
ENSDART00000142594 | Missense | 643 | 892 | 12 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 14851538)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15097144 |
GRCz11 | 3 | 15246944 |
KASP Assay ID:
554-4247.1 (used for ordering genotyping assays)
KASP Sequence:
CCCGTCTCTGGTCAGAGGAAGTGTGTTGACCTATCAGTGTCAGCCGGGTT[A/G]TGATATCGTYGGCTCTGACATCATTACCTGCCAATGGGAYCTCACTTGGA
Long Flanking Sequence:
AACCTCTCCCTAATCAAACGCATCTGAATCAACTCAGCAGTACATTAGAAGAGACTCCAAAACCAAAAATGATTGTGTCAGATAAGGGAGACATCCAAAATATGTTCTGTTGGTGTGCCTCTTGGAACAGGGTTGGGAAACACTGCTTTACATGTTTATATCAGTTTTATATCTTCTAAAAGTGAACTCTGTCACTGTTTACTGTTTACAACTGAAGCTTGATGTGTCGACATGGAAACTAAAAGGTTCTGCAGTGAGAATTTCTTAGGCCACCTCAGCATTATTGTTGATTTCATGACAATGAAGATGTTATTTTTATGCCGATTTATTTAATGTTCTAAAAATATCCCAAAAGCCCTGCTAATACCTTTTATTTCTTGCAGAAGTGGAGCCGAATGACACGTGTTCTGCTCTTCCACAAATTGAGTTCGGCTGGAGCAGCTCCTCCCACCCGTCTCTGGTCAGAGGAAGTGTGTTGACCTATCAGTGTCAGCCGGGTT[A/G]TGATATCGTCGGCTCTGACATCATTACCTGCCAATGGGACCTCACTTGGAGTAACAGCCCGCCCACCTGTGTGAAAAGTGAGTTATTTTTAGCTTCTCATGACTGGCTGTGTTGATTAATGGTTAAAAGTAAACGAAAAGGTGGTGTGAATTTTATTTTCTAAGCCAATCATTTACTTTTATTCATTTGGTTTTTAGTCAATTTAAATGTGTGTACTGGTATTTGTTGCTTGGAATGTTTTGCTAGGAAGTTTTAAGTAGATGTTATGGTCCCTGATGGATAAATGTCTAGGTGATTAAAACGAGTAACATTGAGATGACCAAAATAAATTTTTGTCCCATTACTTTTGGTCCCTTAACAAGTGGGAGGCACATATACAAACTGTTGTAATTCCTACAGCGTTCACCTGATTTTGATGTAAACACCCTCAAATTAAAGCTGACAGGCTTCAGTTAAAACACATCTTAGGCTTAACTATAATTAGGCAAGTTAGAATAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26012
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111948 | Essential Splice Site | 666 | 894 | 12 | 18 |
ENSDART00000142594 | Essential Splice Site | 668 | 892 | 12 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 14851460)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15097066 |
GRCz11 | 3 | 15246866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCCAATGGGACCTCACTTGGAGTAACAGCCCGCCCACCTGTGTGAAAA[G/T]TGAGTTATTTTTAGCTTCTCATGACTGGCTGTGTTGATTAATGGTTAAAA
Long Flanking Sequence:
CAGATAAGGGAGACATCCAAAATATGTTCTGTTGGTGTGCCTCTTGGAACAGGGTTGGGAAACACTGCTTTACATGTTTATATCAGTTTTATATCTTCTAAAAGTGAACTCTGTCACTGTTTACTGTTTACAACTGAAGCTTGATGTGTCGACATGGAAACTAAAAGGTTCTGCAGTGAGAATTTCTTAGGCCACCTCAGCATTATTGTTGATTTCATGACAATGAAGATGTTATTTTTATGCCGATTTATTTAATGTTCTAAAAATATCCCAAAAGCCCTGCTAATACCTTTTATTTCTTGCAGAAGTGGAGCCGAATGACACGTGTTCTGCTCTTCCACAAATTGAGTTCGGCTGGAGCAGCTCCTCCCACCCGTCTCTGGTCAGAGGAAGTGTGTTGACCTATCAGTGTCAGCCGGGTTATGATATCGTCGGCTCTGACATCATTACCTGCCAATGGGACCTCACTTGGAGTAACAGCCCGCCCACCTGTGTGAAAA[G/T]TGAGTTATTTTTAGCTTCTCATGACTGGCTGTGTTGATTAATGGTTAAAAGTAAACGAAAAGGTGGTGTGAATTTTATTTTCTAAGCCAATCATTTACTTTTATTCATTTGGTTTTTAGTCAATTTAAATGTGTGTACTGGTATTTGTTGCTTGGAATGTTTTGCTAGGAAGTTTTAAGTAGATGTTATGGTCCCTGATGGATAAATGTCTAGGTGATTAAAACGAGTAACATTGAGATGACCAAAATAAATTTTTGTCCCATTACTTTTGGTCCCTTAACAAGTGGGAGGCACATATACAAACTGTTGTAATTCCTACAGCGTTCACCTGATTTTGATGTAAACACCCTCAAATTAAAGCTGACAGGCTTCAGTTAAAACACATCTTAGGCTTAACTATAATTAGGCAAGTTAGAATAATTAGGCAAATCACTGTATAACAATAGTTTGTTCTGTAGACAAGCAAAAAACAATATTGCTTAAGGGGGCTAATAATCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6029
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111948 | Nonsense | 734 | 894 | 14 | 18 |
ENSDART00000142594 | Nonsense | 736 | 892 | 14 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 14846966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15092572 |
GRCz11 | 3 | 15242372 |
KASP Assay ID:
554-3753.1 (used for ordering genotyping assays)
KASP Sequence:
CTATAAWCCACCWGTCAAACCGATTCCCTCTTTTTCCTCWCAGTAAAATA[T/A]GATCCATGCCCAAACCCGGGTGTGCCAGACAACGGCTACCAGACTCTGTA
Long Flanking Sequence:
AGAGCATAGTGAATGGGAGAGTACAACAATATTTACATTTTTTATATTTTTTATTCCTATTCGCTGAAATAATAAAAAAAAAAAACTTTCATAACAAGAAAAAAAACTGATAACGGCAGCAAGACAAAAGAAAAACATCAAATTTACTGTGCTGCCCATAGACTCTGCATTAGAAATACCTCGTATAAACAGTAATTCGTTTTTGGAATTTGGTGCAAAGAAGATATATATATATATATATATATATATATATATATATATATATATATATATATATTCACATAAATATACATTAACAAAAAAAAACACTAATTTATGTTAATTAACATTAATTTATAATTAATGTCTAAACATTAAAAACTTTCAAGGATTTAAGATGCTGCTGACTTTGTCTTGTGAAAAAGGATTCATATTACAGATATTATGCAAATTTCTCTGTAATGCACAAACCTATAAACCACCTGTCAAACCGATTCCCTCTTTTTCCTCACAGTAAAATA[T/A]GATCCATGCCCAAACCCGGGTGTGCCAGACAACGGCTACCAGACTCTGTACAAGCACAGTTACCAGGCCGGCGAGACACTGCGCTTCTTCTGCTATGAGGGCTACGAGCTCATTGGGGAAGTGATCATCAACTGTGTCCCAGGACACCCATCTCAGTGGAACAGCCCACCGCCCTTCTGTAAAGGTGTGTGGATTAAAACAGAAAACCGAAATTTCACAGGAAGGCAAATCATTTTCACTTCAACTGGATATGCAATAAAAAGGGATTAAAACAGTGTGAAAGTTTTTAAGTAATCCAAGTCTTTTTATACATGTCCACCACTGTAGAGTTGTCATTTCTATCTTAACAATTGACTAAGAATGTTTTTTTTTTTTTTGCAGTGGCCTATGAAGGACTTCTGGATGATCATAAATTGGAGGGTAACGTTGATTATCATTGTATCTGTTATTTTCATTAGTTCAGCAGTCTGGCTAGTTCTGTCACGTAATGATGTGAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40018
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111948 | Nonsense | 751 | 894 | 14 | 18 |
ENSDART00000142594 | Nonsense | 753 | 892 | 14 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 14846915)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15092521 |
GRCz11 | 3 | 15242321 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCCATGCCCAAACCCGGGTGTGCCAGACAACGGCTACCAGACTCTGTA[C/A]AAGCACAGTTACCAGGCCGGCGAGACACTGCGCTTCTTCTGCTATGAGGG
Long Flanking Sequence:
TATTCCTATTCGCTGAAATAATAAAAAAAAAAAACTTTCATAACAAGAAAAAAAACTGATAACGGCAGCAAGACAAAAGAAAAACATCAAATTTACTGTGCTGCCCATAGACTCTGCATTAGAAATACCTCGTATAAACAGTAATTCGTTTTTGGAATTTGGTGCAAAGAAGATATATATATATATATATATATATATATATATATATATATATATATATATATATTCACATAAATATACATTAACAAAAAAAAACACTAATTTATGTTAATTAACATTAATTTATAATTAATGTCTAAACATTAAAAACTTTCAAGGATTTAAGATGCTGCTGACTTTGTCTTGTGAAAAAGGATTCATATTACAGATATTATGCAAATTTCTCTGTAATGCACAAACCTATAAACCACCTGTCAAACCGATTCCCTCTTTTTCCTCACAGTAAAATATGATCCATGCCCAAACCCGGGTGTGCCAGACAACGGCTACCAGACTCTGTA[C/A]AAGCACAGTTACCAGGCCGGCGAGACACTGCGCTTCTTCTGCTATGAGGGCTACGAGCTCATTGGGGAAGTGATCATCAACTGTGTCCCAGGACACCCATCTCAGTGGAACAGCCCACCGCCCTTCTGTAAAGGTGTGTGGATTAAAACAGAAAACCGAAATTTCACAGGAAGGCAAATCATTTTCACTTCAACTGGATATGCAATAAAAAGGGATTAAAACAGTGTGAAAGTTTTTAAGTAATCCAAGTCTTTTTATACATGTCCACCACTGTAGAGTTGTCATTTCTATCTTAACAATTGACTAAGAATGTTTTTTTTTTTTTTGCAGTGGCCTATGAAGGACTTCTGGATGATCATAAATTGGAGGGTAACGTTGATTATCATTGTATCTGTTATTTTCATTAGTTCAGCAGTCTGGCTAGTTCTGTCACGTAATGATGTGAATGTTGTTTACTTTGCTCTTTCAGTTTCTCAGTCATTAGACGCCTCCCATCAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12488
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111948 | Essential Splice Site | 809 | 894 | 16 | 18 |
ENSDART00000142594 | Essential Splice Site | 811 | 892 | 16 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 14846447)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15092053 |
GRCz11 | 3 | 15241853 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCTAGYTCTGTCACGTAATGATGTGAATGTTGTTTACTTTGCTCTTTC[A/G]GTTTCTCAGTCATTAGACGCCTCCCATCWGATGCTGAGTGAGAACATTGC
Long Flanking Sequence:
GGTGTGCCAGACAACGGCTACCAGACTCTGTACAAGCACAGTTACCAGGCCGGCGAGACACTGCGCTTCTTCTGCTATGAGGGCTACGAGCTCATTGGGGAAGTGATCATCAACTGTGTCCCAGGACACCCATCTCAGTGGAACAGCCCACCGCCCTTCTGTAAAGGTGTGTGGATTAAAACAGAAAACCGAAATTTCACAGGAAGGCAAATCATTTTCACTTCAACTGGATATGCAATAAAAAGGGATTAAAACAGTGTGAAAGTTTTTAAGTAATCCAAGTCTTTTTATACATGTCCACCACTGTAGAGTTGTCATTTCTATCTTAACAATTGACTAAGAATGTTTTTTTTTTTTTTGCAGTGGCCTATGAAGGACTTCTGGATGATCATAAATTGGAGGGTAACGTTGATTATCATTGTATCTGTTATTTTCATTAGTTCAGCAGTCTGGCTAGTTCTGTCACGTAATGATGTGAATGTTGTTTACTTTGCTCTTTC[A/G]GTTTCTCAGTCATTAGACGCCTCCCATCAGATGCTGAGTGAGAACATTGCATTGGCTATCATCCTGCCAATCATTCTGGTCATCCTCCTGATTGGAGGAATCTACATGTACTACACCAAGTGAGTTTTTTTAATGCATTTACTCATTGAATCCTATTCACTTTCAAAAACATCCAGAGTTCCTCATTATAAAGTCATTTTACAGACTTTTTATATATTTAATTTTCTCTGTTTTGTTACAAACACCACGCTGGCAATATAAAAAGAGATTAATACAGTATGTGAAACTTCTTATGTATATATACGTTTAGCTTTTTATGACAAAGATATGACAAAATGGGGAGGATCCTAACTTGTTGACACTTTTGGGTAAAAGTTACTTTTAATATAATATATTAAAATATTGAGAATGTGGTAAAGTCTGAAAATGTGGTAAAAATCAGGCGAGGACCTTTATTTTTCTCGATTGCTTTTCAAAACACTGTTGGTTGGGTTTGAGAA
Associated Phenotype:
Not determined