ZMP
slc6a4b
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 6 (neurotransmitter transporter, serotonin), member 4B [Source:RefSeq peptide
Human Orthologue:
SLC6A4
Human Description:
solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 [Source:HGNC Symbol;Acc:
Mouse Orthologue:
Slc6a4
Mouse Description:
solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 Gene [Source:MGI Symbol;
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40389 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33568 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20377 | Nonsense | Available for shipment | Available now |
sa15666 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40389
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 |
---|---|---|---|---|---|
ENSDART00000086881 | Nonsense | 254 | 591 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 21764222)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 19477094 |
GRCz11 | 5 | 19980894 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGGTAGTATGGGTTACTGCCACCCTGCCATATGTTGTGCTGCTGATTT[T/A]GATGATCAGAGGTGCCACTTTGCCCGGAGCTTGGAAAGGAGTGGTTTTCT
Long Flanking Sequence:
ATCCAACAAGGCGGTAATAGTTTGACTGCGGTGTTTACATCTCTGTACTACACATCAATAATGTTAGTTTGATTATGACTACAGTCAGATTAAGGTAATCAAAAATTGATGTTTACATGGTAGACTCTTAATCAAAGTATTGTCTTAATCGTATTAAATTATTGGTCCATTTAAACATAGCCAATTTCAATTTGATGTCATTTTGACATCAAGGTCATTTACATGAATTGTAGGGATACAAAATCCAGTGTAAATTTGGAATTGAAGCTTTCAATACATATATAATACTTTTTGTGTTGTTATTTTGCTGGTCAAAAGAGCATCAATGTGTGGATGTTAAAAGAACAATAAGGTTTGACATCAAATCGATGAGCATTTCTGACATGTTTATTGCCGATAATGCAAGTTTGATATCGTTTTGACCGCTGAGTATGTCTAATCCTCATGTCTTTAGGTAGTATGGGTTACTGCCACCCTGCCATATGTTGTGCTGCTGATTT[T/A]GATGATCAGAGGTGCCACTTTGCCCGGAGCTTGGAAAGGAGTGGTTTTCTACCTCAATCCCAAATGGGAGAAACTGAAGGAGACCAGCGTAAGTGCTTTTCTCTCAACGCCTCTTTTCCCTTTGCGTCCAGCATTGATTTAGTTAAATTAGGTTATGCTGTTTCTTCACTCATCTTAATACCCTTTTAAATGTGCCGCTATAATGTTTTGATGGCACCATGCATGTATGTCCGATGGTGTTTTATTTCATGCCATAATAAAAAGGACCCGAGGCGTTTAGACATGAAACGCATGCATCACCTGCAGCTGAACTGACTCGTATAGACTTTATAAAGGGCATATTTTTTCATAAACGCTTAGATAACTCGATCAAACAAATGAATATTTAAGTATATAAATGGTCAGTGGAGGCAATATGAAAACCGTGCGTCCGTATCTCTAGCTGTACAAGCTCAATACAGTTTGCTAGGTGATGCAGTGTTGAAGAGAACTGTGATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33568
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086881 | Essential Splice Site | 284 | 591 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 21761856)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 19474728 |
GRCz11 | 5 | 19978528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGAAGCGCTATGAATACTTTCCGGATGCACTGTATATACTGTTTTGC[A/T]GGTATGGGTAGATGCAGCTGCGCAGATCTTCTTTTCTCTTGGTCCTGGTT
Long Flanking Sequence:
AATCTCAATGGAGTGGCTTCAACTCTGTGAATGTCCTTGAGTGGCCCAGCCAGAGCCCAGAGCTAAATCCTATTGAACGTCTCTGGAGAGATCTGAAAATGGCTGTACAACGTCTCTTCCCATCCAACCTGATTGAGCTTGAGAGGTATTGCAAAGAGGAATGGGCAAAAATCCCAAAGACAGGTGTGCCAAGCTTGTGGCATCATATTCAAAAAGATTTGAGGCTGTAATTGCTGCCAAAGGTGCATCAACAAAGTATTGAGCAAATGCTGTGAATACTTACTGTGTGTACATGTGATTTTTCAGGTTTTTTTATTTTGAATACATTTGCAACAATTTCAAATAATCTTTTTTCACATTGTCATTATGGGGTATTGTGTGTAGAATTTTGAGGAAATAAATTAATTTAATCCATTTTAAAATAAGGCTGTAACATAAAAAGTGTGGAAAAAGTGAAGCGCTATGAATACTTTCCGGATGCACTGTATATACTGTTTTGC[A/T]GGTATGGGTAGATGCAGCTGCGCAGATCTTCTTTTCTCTTGGTCCTGGTTTTGGGGTCCTGCTTGCCCTGTCCAGCTACAATCCCTTCACTAATAACTGTTACAGGTACACAATGAGCACTTTCATTATGTTGATCCATTCCACAGGTGTCAAACCCAGTTTCTGGAGGGCTGCAGCTCTGCACAGTTTAGTTCCAACCCTAATTAAACACACCTGATCAAACTAATTGACTGCTTTAGGCTTGTTTGATACCTACAGATAGATGTGTTAAAGCAGGGCTGGAACGAAACTCTGAAGAGCTGTGTTCAGGAACAAAGTTTGAAAACCTCTGATCTATTGGTATTTTCAACAACACCATTTGCAGTGACTTCTTTGAGGTTGTTTATATTAATATATTGTTAGTTAGTTAGTTCACTTTTTTTGTCCCCGTAAAAAAATTTCCTTTGCAGAATACACTCACAGAGACTTCTGACATTTCACATTTGGCATATATATAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20377
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 |
---|---|---|---|---|---|
ENSDART00000086881 | Nonsense | 309 | 591 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 21761777)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 19474649 |
GRCz11 | 5 | 19978449 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTTTCTCTTGGTCCTGGTTTTGGGGTCCTGCTTGCCCTGTCCAGCTA[C/A]AATCCCTTCACTAATAACTGTTACAGGTACACAATGAGCACTTTCATTAT
Long Flanking Sequence:
TCTCTGGAGAGATCTGAAAATGGCTGTACAACGTCTCTTCCCATCCAACCTGATTGAGCTTGAGAGGTATTGCAAAGAGGAATGGGCAAAAATCCCAAAGACAGGTGTGCCAAGCTTGTGGCATCATATTCAAAAAGATTTGAGGCTGTAATTGCTGCCAAAGGTGCATCAACAAAGTATTGAGCAAATGCTGTGAATACTTACTGTGTGTACATGTGATTTTTCAGGTTTTTTTATTTTGAATACATTTGCAACAATTTCAAATAATCTTTTTTCACATTGTCATTATGGGGTATTGTGTGTAGAATTTTGAGGAAATAAATTAATTTAATCCATTTTAAAATAAGGCTGTAACATAAAAAGTGTGGAAAAAGTGAAGCGCTATGAATACTTTCCGGATGCACTGTATATACTGTTTTGCAGGTATGGGTAGATGCAGCTGCGCAGATCTTCTTTTCTCTTGGTCCTGGTTTTGGGGTCCTGCTTGCCCTGTCCAGCTA[C/A]AATCCCTTCACTAATAACTGTTACAGGTACACAATGAGCACTTTCATTATGTTGATCCATTCCACAGGTGTCAAACCCAGTTTCTGGAGGGCTGCAGCTCTGCACAGTTTAGTTCCAACCCTAATTAAACACACCTGATCAAACTAATTGACTGCTTTAGGCTTGTTTGATACCTACAGATAGATGTGTTAAAGCAGGGCTGGAACGAAACTCTGAAGAGCTGTGTTCAGGAACAAAGTTTGAAAACCTCTGATCTATTGGTATTTTCAACAACACCATTTGCAGTGACTTCTTTGAGGTTGTTTATATTAATATATTGTTAGTTAGTTAGTTCACTTTTTTTGTCCCCGTAAAAAAATTTCCTTTGCAGAATACACTCACAGAGACTTCTGACATTTCACATTTGGCATATATATAATTAAATCATTTAAAAACATGGTATCCCACTCTAAATAAATATCTAGTTCACTAGCCATCAACTGCTACTGAGGGATGAGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15666
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 |
---|---|---|---|---|---|
ENSDART00000086881 | Nonsense | 527 | 591 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 21753476)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 19466348 |
GRCz11 | 5 | 19970148 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAATTATCAGCTCACTGTTGAACCCTCAAACCCTGACGCTATTCGACTA[C/A]GAGTTCCCCGACTGGAGYATCACGGTCGGCTACATCATCGGAGCTTCCTC
Long Flanking Sequence:
GAAAATTTAACTCAACAGTTTAATAAAGAAACTTGCTGTAGTTTGAAATAATATAATGTATAGGCAATTATAGAGAGAAAAAAGCCTGTAAAATAACAGAACATGTACTGGCTGGTTTTTACAAGGTTGTACCGTGATACACAACACCAATCCAGACAATATATCACTTTAAACTATTAAAGCTGATAATAAAACTTACATTTTCTAACTTTTCAAAACTAAAAGTTGTTGGAAGAAACATCAAAGTCCCATAATGCAATTCAAAACCATAAATAAATGGGGAAAAATAATAAAAAAAACATGAATCACTAAATTTGGAAACCTGCTAATTTACGAATATTTTTGACAGTGTATACAAAGTGGATGGAAACGTCACTAGTGTGTAACTCATTTTCATATTGCTACTTTTAGTCATTAAATTATTTCTCCCCTTATTATTTTCTCCAGTACATAATTATCAGCTCACTGTTGAACCCTCAAACCCTGACGCTATTCGACTA[C/A]GAGTTCCCCGACTGGAGCATCACGGTCGGCTACATCATCGGAGCTTCCTCCTTCATATGGATCCCAATTTACATGGTTTACAAGCTTGTTTGGACTCCAGGCTCTCTTAAACAGGTAAGAGATGCATGTAAGCGATTAGTTTAATAAATCAACACTTACTTAACAATTCCTACTTAGAAAAACATCCGTATAGATCTCAAAGATAGCTTGTTTTCAATGTGATTTCAGCGGCTTGCTGTGTGTCTGCGACCAGAGAGAACACTGCCAGACATCCACACCGACGGCATGAGTTTAAGTCCAGTACCTTAAACTAAAAACACAAAAAATAAAAGGCCATATTTTGAGTTCCACAGGAAACTAAACATTTATTATAAGGATAAACTTTTGCATAGTTTCAGGGATTTGTTTAGCTGAAATTAAAATGATCTATTTGGAATTGATATATGGTTAGATTTAATTTGAAATACAATATTTTATGTATGTAAATGATGGTCCCTAAT
Associated Phenotype:
Not determined