ZMP
zgc:136569
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC692318 [Source:RefSeq peptide;Acc:NP_001038752]
Human Orthologue:
SLC6A1
Human Description:
solute carrier family 6 (neurotransmitter transporter, GABA), member 1 [Source:HGNC Symbol;Acc:11042
Mouse Orthologue:
Slc6a1
Mouse Description:
solute carrier family 6 (neurotransmitter transporter, GABA), member 1 Gene [Source:MGI Symbol;Acc:M
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37607 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24248 | Nonsense | Available for shipment | Available now |
sa37606 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37607
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067530 | None | None | 431 | 3 | 15 |
ENSDART00000124613 | Nonsense | 116 | 679 | 2 | 14 |
ENSDART00000133701 | Nonsense | 116 | 679 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 23 (position 4909784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 4918483 |
GRCz11 | 23 | 4854068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAATGCGCTCTTGGACAATACACATCCATTGGTGGCCTCGGGGTTTGG[A/T]AACTAGCGCCAATGTTTAAAGGTATATGGTTCATATCAACACATTCTTTT
Long Flanking Sequence:
GTGTCGACTTCGATCGCGTGTTTGTGTGGATCTCTGCTGCTGTCTGAAATCGGAGACATGGCGACAAACAACACCAAAAGCACCGACGGACAAGTTGTGACGGAACTCAACGAGATCACAACTAATGACAAACCCAAAACAGAGGACGCCAAACCAGAGAAGAACAAGAAGGACATTCCAGACAGGGAAACTTGGGGTGGGAAATTTGATTTTCTTCTGTCATGTGTGGGCTACGCCATCGGACTGGGAAACGTGTGGAGATTTCCTTATCTGTGCGGGAAAAACGGCGGAGGTAAGAGCATCTTCACCTTCTCCAAGTGAAATGTTGTGTGCGTGCTCATTGCTGTGCACAGCTCCACAGGGTGCTTTCATGTATTTCTGTGATTCCAGGGGCATTCTTGATTCCTTATTTTTTGACGCTTATTTTTGCGGGAGTCCCTCTATTTTTTCTTGAATGCGCTCTTGGACAATACACATCCATTGGTGGCCTCGGGGTTTGG[A/T]AACTAGCGCCAATGTTTAAAGGTATATGGTTCATATCAACACATTCTTTTCCCATCAACCCCATTAAATAGTTCTAAATATATGCGAGATGGTTTAGGACAGGGGTGTCCAAACCAAACTCGGTCCTGGAGGGCAGGTGTCCTGCATATTTTAGTTTCAACCCTAATTAAAAACACCTGAACCAGCTGATCAAGCTCTTCATTCTCAGAAAAAAAATGGTACAATGTTGTACCAAAGAAGGTACAAACCCTTGGCACTGGGGCAGTACCTTTTTATGGAACAGAATTGTACCTTAAGACAATGAAACAAATTTGCACCATTGCAGTTTGTACCTTTAACAACATGATTTATACTATGGGAAACCAAAATGTACAAGATACAAATGTTTCACCATTCGTTTTGTATCATTGCATAACAGAACTTCATAATTATTGTGGTAACACTTTATAATAACTACACACTATAAATCATTTATTAAGCATTAACAAATAGTGAATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24248
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067530 | Nonsense | 119 | 431 | 10 | 15 |
ENSDART00000124613 | Nonsense | 367 | 679 | 9 | 14 |
ENSDART00000133701 | Nonsense | 367 | 679 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 23 (position 4905778)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 4914477 |
GRCz11 | 23 | 4850062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGCTTTTTTTATGGCTTACACAGGACCGGGTTTGGCATTTTTAGCTTA[T/A]CCGGAAGCTGTAACGCAGTTGCCCGTTTCACCACTGTGGGCCATTCTCTT
Long Flanking Sequence:
GAACGAGCCAGCCCTATAACTGTGACTGACTGTGATTACATGGCTATTGTCAGAGCTGACATTTTAGCATATGCACAGTGAGAATTACCATCAAATTAAACAGCTGATTTTGTATTCCGCTACATTGCTTACATAATCCATCTTCTCCTTAAATGCCAAATTGATATGCAGCTTTCAGGTCAGTTAGGAGAATGACACAGATGCTTAAAGCGCATTTGAAACCCTTTCCTCTATTTTTTTTTTTCCTGCAGGGACTCCATCATTGTGTGCTGCATTAATTCCTTCACTAGCATGTTTGCTGGGTTTGTGATTTTCTCAATTGTGGGCTTTATGTCACATGTGACAAAGAGACCAATAGCTGATGTAGCTGCGTCAGGTAATCAGTTCTACAATACCAGTGAGATTTCACAAATGTTTCATCAGTTAAAATGCAGATATTTCCTTCAGATAACAGCTTTTTTTATGGCTTACACAGGACCGGGTTTGGCATTTTTAGCTTA[T/A]CCGGAAGCTGTAACGCAGTTGCCCGTTTCACCACTGTGGGCCATTCTCTTCTTCTCCATGCTGCTGATGCTGGGAATCGACAGTCAGGTAAGAATATCACGCATTCAAGCTCTGACCTAGAAACAGAAGTAAACGGGTGCTGGTGGGTGCTTTAGATCTGCCAGCGTCAGTACCGTTGTCCCTGGGGGACACACAAGGAAACATAACGAACATTTATTAAAAAAAGAAAAACTCAATTAGCCTTGTGTTTAATTAAATCTTTTGATGTCGATTTTTGCATATATCTGAAGCAAAGCCACATCGAGCTACAACTGAATCTCAAACCTGCAGCATCCAAAGCTTTAAATATATATACAGTTGAAGTCAGAATTATCAGCCCCCCTGAATTATTACCCCCCCCTCACCCCACCCCGTCTAATTTTTTCCCAATCTCTGTTTAACGCAGAGAAAATTCAGCACATTTCTAAACATAATAGTTTTAATAACTCATCTCTAATAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37606
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 |
---|---|---|---|---|---|
ENSDART00000067530 | Essential Splice Site | 149 | 431 | 11 | 15 |
ENSDART00000124613 | Essential Splice Site | 397 | 679 | 10 | 14 |
ENSDART00000133701 | Essential Splice Site | 397 | 679 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 23 (position 4900077)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 4908776 |
GRCz11 | 23 | 4844361 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTGCATATAAATACAGCACAGCTACAGCATTGTTGACGTTGGTTTGCA[G/A]TTCTGTACAGTGGAGGGCTTCATCACTGCTCTGGTGGATGAGTTCCCACG
Long Flanking Sequence:
ACGTAAATCGCAGTCTCCAGAAACATCCGCGGGGCTTCGTTTTCAGAATGAGCTTGGATTGCGTAAACCTATCAACGGAAGCCTCCAAAACAAAATGAACATTTTAAAAAAATGCATAATTTGGGCACTTTAACCCCTTCAGACCCTGCGTCTATTACAATGGACATCACATGACATCCCATTTTTCTGAAATTTGGAACATAATTCAGGTCTGAAGGGGTTAATAAAACACATTTAATATTAAAAACGAAGGCCATTCAAATGTAAAACAACAAACAAAAAAATCTGTTTCATAACTATTGCTCTATATACTTCATCAGCATCAGCCTCAGTTCAGGACTGACATTCAATTGACCTTTTGTGCCGATGTGTACATTCAAGTTACCAGCATGGACCTTTTGTAAAAGTAGTCTTTCACCCTAGCGACAGCTCTTGTCCTGTTATTTCTGAGAGTGCATATAAATACAGCACAGCTACAGCATTGTTGACGTTGGTTTGCA[G/A]TTCTGTACAGTGGAGGGCTTCATCACTGCTCTGGTGGATGAGTTCCCACGGCTACTCAGGAAAAGGAGAGAGATTTTTATTGCATGTGTCTGCGTTGTGTCCTACGCCATTGGACTGTCCAATATCACACAGGTAAATGAGACTTGCATAAAGCAGATGACGAGTTTGACCAACGATTAATACATTCATTATATTAAATGATAAATATGATCGCAGTATAGAGTGACTTGTGTTTTGTGTGTGTTAGGGTGGTCTCTATGTGTTTAAACTCTTCGACTATTACTCAGCCAGTGGGATGTGCCTGCTCTTCCTGGTGTTTTTTGAGTGTATCTCCATCTCCTGGTGTTATGGTGAGCCATATTTTCTTTCATTTTATCTCTGTTTCTATTTTGTCTTTAGCACTGCACTGCATAAAATTGACGGAATCAGAATTTGATTACAAACTGAAGTTGGCAATCCAAATTAAAAGGAGAGAATTGGATGAAAAAAAATCAAATGAC
Associated Phenotype:
Not determined