ZMP
zgc:158225
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 [Source:RefSeq peptide;
Human Orthologue:
SLC6A7
Human Description:
solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 [Source:HGNC Symbol;Acc:
Mouse Orthologue:
Slc6a7
Mouse Description:
solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 Gene [Source:MGI Symbol;
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43675 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa3130 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa43675
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 |
---|---|---|---|---|---|
ENSDART00000100942 | Essential Splice Site | 351 | 537 | 11 | 15 |
ENSDART00000139486 | Essential Splice Site | 466 | 652 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 21 (position 29581738)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 30781989 |
GRCz11 | 21 | 30818684 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGCTCTGCTTCTCTTTCTATCTGATGGGCCTGTTGCTCATCACTGAC[G/A]TAAGATTTTAGTCCTTTGTGTTTATAAATACACGTACACAGATGTCAAAA
Long Flanking Sequence:
TTGAAAATATATATTTTAAGTCCAGGTTTATGACCAAAGCCTATGAGAAAGAAAGTGTTTTATGTGTGGACACTTATTTTCTTAATGCCTGAAAAAAATGTTCCCCTTTAACCCGCATGCAGTTGTTTGGCAATAAAGTGTTTGCCAAACCTCTAATGTAAACATGAAAGCAAACAGATAATTGCAGATGATGATGGCACACAGCAGTCTTCATATTGCCCTGACAGCAAACCAAACATCTGAATAATTCTGTTGATGCAAATGTCAGGCAAACCTAGGACATGTTTGTACACTCCTGACAGAAAATAAAGCCCATTGTTTAATTCTTTTATAATGTCAATTTGTGTCTCTCTGTCCTGTAGTTTGGTAACATGGAGGGCATTTGTACGGCAGTGCTGGACGAGTTTCCTCAGCTCAGGTCCAATCTGAAGCACAAGACGCTGTTCTTGGCAGTGCTCTGCTTCTCTTTCTATCTGATGGGCCTGTTGCTCATCACTGAC[G/A]TAAGATTTTAGTCCTTTGTGTTTATAAATACACGTACACAGATGTCAAAATATATCAGCCATGTTTATTTAAATATTTAAATTCATCATTCCATCCATCTTCATTGTGATTTTCTTGTGATACTGGTTTTGTGCTGTGTTTGTCCATCACAGGGTGGGATATACTGGTTTACGCTCATAGACTCCTTCAGCACCAGCTTTGGTCTCATCATCATTACTCTCTTCATGTGCATTGGCATCTCGTTCTTCTATGGTACACATTCTTTTGTTTCCTCATGAGTTTTGCAGTTTAAAGGGTTAGTTCACCCAAAAATGTTTATTCTGTTAATTACTTATCCTGATGCCGTTCCAATTGGGTGAGAACTTCAAATTAAGATATTTTAGATAAATTCAGAGAGCTCCCCTATCCTCCATATACAGCAGTGGTCCCTAGACGTTCAAACCAAAAAACATTTTAGAAACATGCCATTATTTCACCATGACTTCAGTGGCACAACTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3130
Status:
F2 line generated
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100942 | Nonsense | 531 | 537 | 15 | 15 |
ENSDART00000139486 | Nonsense | 646 | 652 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 21 (position 29591943)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 30792194 |
GRCz11 | 21 | 30828889 |
KASP Assay ID:
554-3295.1 (used for ordering genotyping assays)
KASP Sequence:
GGGCCTTTCACAGTTAACCTGACTGAAGCCGACTACACCGGCATGAACTG[G/A]GAGGGCATCAGCGAGGCGTAGCGCSGCCACTAATGTTGAGTACTGGAACA
Long Flanking Sequence:
AGTGTATGTGTGGGAATGAGAGTGTATGGCTGTTTCCCAGTGATTGGTTGCAGCTGGAAGGGCATCTGCTGCAGAAAACATATGTTGGATAAGTTGGTGGTTCATTCTGCTGTGGTGACCTCTGAATAATAACTAAGCTGAAAAAAAAATGAATAAATGAATAAATGAATGAAGTAGAAAATGTTTTAAAATAAATTTTAACAAATTGTATATTATAACACAAATTATACATAAAATGTCTAATAAATGGTTAAATTCATGATAATTGTTTATTAATTTTTATTTGTACTTCAACTTGTACTTTATTTGTGCTTTGTACTTTAACAGTCATTCTAACATGTTTCTTACACTCAGCGCTTTAAGAAATCCATCCGTCCCCTGAACTCGTGGCGTGTGAACAACATAAACTCCAGCTCTCAGGAGCAGCACGTGGAGCCCCACACAATAGAGGGGCCTTTCACAGTTAACCTGACTGAAGCCGACTACACCGGCATGAACTG[G/A]GAGGGCATCAGCGAGGCGTAGCGCCGCCACTAATGTTGAGTACTGGAACAGCACTCTCTCAGAAGCACAAGTACTGGTGAGGAGGACTGCTGTACAGAGAACAGTGCACAGCTGGACTGAAACGGTGTTACTTTCTTTGCAGGACACCTAAAACCATAGCTTTTTTTATATTTATGACAACATGGCCCATTTGACATCGGGACTAAAAGCCAAAGCAAGAAGCATAAAAGACGTTTGGATTATCTGGCTGAATCCTTGACACCCCGAGATTCCGTTTCATGAAAGAATGTACAAGACTGTTTTATAAGATAACAGACTGTGTAAGTTTATCTGTTTTACATTTACATTGAAATGTACAATCATATACAAGAGCAAGGCCAAATCAAATCAGGGCAACATCACAGAGTAGCAAAACTGAAGTCATTTTAGTAGTATGGGCTGAGATTGGACAATTAATCGAAGGTGATTTTCATGCTCATTTTATTAGTAAAGCCGGTTCT
Associated Phenotype:
Not determined