ZMP
gad1b
Ensembl ID:
ZFIN ID:
Description:
glutamate decarboxylase 1 [Source:RefSeq peptide;Acc:NP_919400]
Human Orthologue:
GAD1
Human Description:
glutamate decarboxylase 1 (brain, 67kDa) [Source:HGNC Symbol;Acc:4092]
Mouse Orthologues:
AC101882.1, Gad1
Mouse Description:
glutamic acid decarboxylase 1 Gene [Source:MGI Symbol;Acc:MGI:95632]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15783 | Nonsense | Available for shipment | Available now |
sa17561 | Essential Splice Site | Available for shipment | Available now |
sa2304 | Nonsense | Available for shipment | Available now |
sa13138 | Nonsense | Available for shipment | Available now |
sa900 | Essential Splice Site | Available for shipment | Available now |
sa20613 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15783
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003008 | None | None | 587 | None | 17 |
ENSDART00000122348 | Nonsense | 290 | 613 | 9 | 17 |
The following transcripts of ENSDARG00000027419 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 3665244)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 3689548 |
GRCz11 | 6 | 3850368 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTAAACACAGCGGCTGTCTCCCTCTAGAGGACAGCATTATTAATGCGG[G/T]AAAGTGGATCTGTTTTGGACCATTTGATTGATGGCCGKCCATTWCTTTTT
Long Flanking Sequence:
TAAACTGATCACAAATTCAATTCAATTCACCTTTATTTGTACAGGGTATATTATACTACAAAACACCACATATTACTGTAAAAACTACAGTCCCTTATATTATAATATTTAATACAGTTTACTATAGTTAATACAGCATGATGTAACATTCATTAACAAGTAGTTGTGAATACTATAATTTATACAGTATAATATACTTCACATGGTTCAAAAACTCTAGCACATAGTATCTTTTCATGTTGGATGTATCCGGGAAAGCAGTTGATGCTAAACGCAGTCGTCTTTTCACAGGTGGTGCCATATCAAACATGTACAGTGTGATGGTTGCGCGGTATAAATATTTCCCTGAAGTCAAAACCAAAGGCATGTCTGCGGCTCCGCGGCTCGTGCTGTTCACATCTGAACATGTAAGTGCACACAGACTGTAGAATACATGTAAGTGTACATTACTGTTAAACACAGCGGCTGTCTCCCTCTAGAGGACAGCATTATTAATGCGG[G/T]AAAGTGGATCTGTTTTGGACCATTTGATTGATGGCCGGCCATTTCTTTTTTCGCAGAGTCATTACTCAATCAAGAAGGCAGGAGCTGTTCTTGGATTTGGCAAAGAAAACGTCATTCTCCTGAAGACAGATGAGAGGTATGGCGTACAGTGTATACCTGACATGTTTATTATAATTTTGTAATTATGAATGTATGGAAACTTCAAAGAACATAGCACAGTTTATTTGAAATAAAATAATGACAATGGATAATAATGTTACTGATGAGGGCAAAATTATTAGCCCTCTTGTGAAATATTGATTCTTTTTCAACTATATTTTTCAATGGAGCAAGGACATTTTCACAGTATTTCCTATAATAATATTATTTCTTCTGGAGAAAGTCTTATTAGTTTTATTTTGGCTGGAATAAAATATGTTAAGGTCAATATTATTAGCCCCTTTAATATTTTTCCCAATTAGTTACAGAAATGTGTTGGAAAAAACCTCTCCATTAACAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17561
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003008 | Essential Splice Site | 309 | 587 | None | 17 |
ENSDART00000122348 | Essential Splice Site | 335 | 613 | None | 17 |
The following transcripts of ENSDARG00000027419 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 3665382)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 3689686 |
GRCz11 | 6 | 3850506 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTGGATTTGGSAAAGAAAACGTCATTCTCCTGAAGACAGATGAGAGG[T/C]ATGGCGTACAGTGTAYACCTGACATGTTTATTATAWTTTTGTAATTATGA
Long Flanking Sequence:
TGATGTAACATTCATTAACAAGTAGTTGTGAATACTATAATTTATACAGTATAATATACTTCACATGGTTCAAAAACTCTAGCACATAGTATCTTTTCATGTTGGATGTATCCGGGAAAGCAGTTGATGCTAAACGCAGTCGTCTTTTCACAGGTGGTGCCATATCAAACATGTACAGTGTGATGGTTGCGCGGTATAAATATTTCCCTGAAGTCAAAACCAAAGGCATGTCTGCGGCTCCGCGGCTCGTGCTGTTCACATCTGAACATGTAAGTGCACACAGACTGTAGAATACATGTAAGTGTACATTACTGTTAAACACAGCGGCTGTCTCCCTCTAGAGGACAGCATTATTAATGCGGGAAAGTGGATCTGTTTTGGACCATTTGATTGATGGCCGGCCATTTCTTTTTTCGCAGAGTCATTACTCAATCAAGAAGGCAGGAGCTGTTCTTGGATTTGGCAAAGAAAACGTCATTCTCCTGAAGACAGATGAGAGG[T/C]ATGGCGTACAGTGTATACCTGACATGTTTATTATAATTTTGTAATTATGAATGTATGGAAACTTCAAAGAACATAGCACAGTTTATTTGAAATAAAATAATGACAATGGATAATAATGTTACTGATGAGGGCAAAATTATTAGCCCTCTTGTGAAATATTGATTCTTTTTCAACTATATTTTTCAATGGAGCAAGGACATTTTCACAGTATTTCCTATAATAATATTATTTCTTCTGGAGAAAGTCTTATTAGTTTTATTTTGGCTGGAATAAAATATGTTAAGGTCAATATTATTAGCCCCTTTAATATTTTTCCCAATTAGTTACAGAAATGTGTTGGAAAAAACCTCTCCATTAACAGCACTTGGGTGAATTTTTATTTAGAAAATTATAATGTACACAATAAGATTACTAATTCTGATTTCAACTGTTCTTTGCTGAAAAATTTCTCCTTCTTTTGTTTTTTGACAGTACTTACTGCAAACTTATGGACCTCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2304
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 |
---|---|---|---|---|---|
ENSDART00000003008 | Nonsense | 439 | 587 | 14 | 17 |
ENSDART00000122348 | Nonsense | 465 | 613 | 14 | 17 |
ENSDART00000003008 | Nonsense | 439 | 587 | 14 | 17 |
ENSDART00000122348 | Nonsense | 465 | 613 | 14 | 17 |
The following transcripts of ENSDARG00000027419 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 3671259)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 3695563 |
GRCz11 | 6 | 3856383 |
KASP Assay ID:
554-2874.1 (used for ordering genotyping assays)
KASP Sequence:
ATGTGCGCAGGTTACCTCTTCCAGCCGGACAAACAGTACGACGTGACCTA[C/A]GACACCGGAGACAAGGCCATCCAGTGCGGCAGACATGTGGACATCTTCAA
Long Flanking Sequence:
CATCGTCACAAGCTGAGCGGCATTGAGAGGTCTGTATGTGACAATGACTAAAACTAATGTAAATCACAATACAGCTGCAGTGAGAGCTGAAAACCCACTTATCTGTGTGTGTTTCAGGGCAAACTCCGTCACGTGGAACCCTCATAAGATGATGGGTGTGCCTTTACAATGTTCAGCCATCCTGGTCAGAGAGAAGGTGAGACCTGAAAAGTTATCACAATGATATTTGCTTTTCAAATATTTCCAAAATCCATCCATAAATTTGGTTGTTAACCCTTTATAGTATATGAAACTTATTGAAATACTTTTACTGGAGGTTACTGCAAGACCTTTGAACTTTTATGACATAAACGTGTCAAAAATCAGGTGGGCAGGTGAATAAGAGTTAAATATGATAAAATAAGGATGTCTGCTCTTCTGTTCCAGGGCATTCTCCAGGGCTGCAACTCCATGTGCGCAGGTTACCTCTTCCAGCCGGACAAACAGTACGACGTGACCTA[C/A]GACACCGGAGACAAGGCCATCCAGTGCGGCAGACATGTGGACATCTTCAAATTCTGGCTCATGTGGAAGGCCAAGGTTGGTCACAGTAGCACATTAAATCTGGTCCTGATACACATCATAGCTAAACAGCTTAAAGAAATATCTATGTTAATGTTTACAATGTCTTAACATGATTTAGTCACAATGAGCATACATTTATATGAATTTTGTGATCTAATTAATCTATATACAGTATAATTTTTTCTATTAAAAATAAAAGTATAATATGTTAAGGATAAAGTACATCCAGGAGGTTTTGAATCACAGAATAAAGCCATTGTTGAATAAAACTGAAGGCCTTTACTCTGTGAAAACAGCCATCCTGAATGTTCTTTGTCTCACTGATTACACTGCTACTTGCTCACAAAACATACAAATTAATCACAAGCCATTGTTCTGTACTGCTATAAAGCTGACAGAAACAAAAACAGCTGATGGAGGATACACTATCCCGCGCATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13138
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 |
---|---|---|---|---|---|
ENSDART00000003008 | Nonsense | 439 | 587 | 14 | 17 |
ENSDART00000122348 | Nonsense | 465 | 613 | 14 | 17 |
ENSDART00000003008 | Nonsense | 439 | 587 | 14 | 17 |
ENSDART00000122348 | Nonsense | 465 | 613 | 14 | 17 |
The following transcripts of ENSDARG00000027419 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 3671259)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 3695563 |
GRCz11 | 6 | 3856383 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTGCGCAGGTTACCTCTTCCAGCCGGACAAACAGTACGACRTGACCTA[C/A]GACACCGGAGACAAGGCCATYCAGTGCGGCAGACATGTGGACATCTTCAA
Long Flanking Sequence:
CATCGTCACAAGCTGAGCGGCATTGAGAGGTCTGTATGTGACAATGACTAAAACTAATGTAAATCACAATACAGCTGCAGTGAGAGCTGAAAACCCACTTATCTGTGTGTGTTTCAGGGCAAACTCCGTCACGTGGAACCCTCATAAGATGATGGGTGTGCCTTTACAATGTTCAGCCATCCTGGTCAGAGAGAAGGTGAGACCTGAAAAGTTATCACAATGATATTTGCTTTTCAAATATTTCCAAAATCCATCCATAAATTTGGTTGTTAACCCTTTATAGTATATGAAACTTATTGAAATACTTTTACTGGAGGTTACTGCAAGACCTTTGAACTTTTATGACATAAACGTGTCAAAAATCAGGTGGGCAGGTGAATAAGAGTTAAATATGATAAAATAAGGATGTCTGCTCTTCTGTTCCAGGGCATTCTCCAGGGCTGCAACTCCATGTGCGCAGGTTACCTCTTCCAGCCGGACAAACAGTACGACGTGACCTA[C/A]GACACCGGAGACAAGGCCATCCAGTGCGGCAGACATGTGGACATCTTCAAATTCTGGCTCATGTGGAAGGCCAAGGTTGGTCACAGTAGCACATTAAATCTGGTCCTGATACACATCATAGCTAAACAGCTTAAAGAAATATCTATGTTAATGTTTACAATGTCTTAACATGATTTAGTCACAATGAGCATACATTTATATGAATTTTGTGATCTAATTAATCTATATACAGTATAATTTTTTCTATTAAAAATAAAAGTATAATATGTTAAGGATAAAGTACATCCAGGAGGTTTTGAATCACAGAATAAAGCCATTGTTGAATAAAACTGAAGGCCTTTACTCTGTGAAAACAGCCATCCTGAATGTTCTTTGTCTCACTGATTACACTGCTACTTGCTCACAAAACATACAAATTAATCACAAGCCATTGTTCTGTACTGCTATAAAGCTGACAGAAACAAAAACAGCTGATGGAGGATACACTATCCCGCGCATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa900
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003008 | Essential Splice Site | 501 | 587 | 16 | 17 |
ENSDART00000122348 | Essential Splice Site | 527 | 613 | 16 | 17 |
The following transcripts of ENSDARG00000027419 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 3673829)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 3698133 |
GRCz11 | 6 | 3858953 |
KASP Assay ID:
554-0807.1 (used for ordering genotyping assays)
KASP Sequence:
AGCTAATACTGCTGCTAATGGGTTTTTTATTGCTTTCCTCTGCTCTCCAT[A/T]GCCCCAGCACACTAATGTTTGCTTCTGGTATATTCCACCGAGTCTGCGTG
Long Flanking Sequence:
TAAAAGGGTGGCTGATATTATACTTACATTTTGTGATCGAGTAATTTTTTTTCTATATAATGTAATTCGGTTTATGAGGGATAAAGCTGGAAATAAAATAATAAACATCCAGTTATAGTGTTGTGCAATAAACCAGATGGTAAATATTATAATCACACGAGTCTACTTTATATATGCAGATGAAGTAGAATGTTTTATACAGCCATTTTCCGCTATCAAATCAGTGATGTGGCTTTAGCAATAAGTATTTAGCTGAGAAAAGAGCTTCATTGGGATTGTTGAATTTGATTTGTGCAGGGCACGATTGGGTTCGAGCAGCACATTGACAGATGTCTGGAGCTTTCTGAATATCTCTACAATAAAATCAAGAACCGTGAGGGATATGAAATGGTCTTTGAGGGCCAGGTTTGTATCTGGAACATACACATTTATTGATTCGAAGAAGTGCTTAGCTAATACTGCTGCTAATGGGTTTTTTATTGCTTTCCTCTGCTCTCCAT[A/T]GCCCCAGCACACTAATGTTTGCTTCTGGTATATTCCACCGAGTCTGCGTGGCATGCCGAACGGAGACGAGCGAAGGGAGAAGCTGCACAGGGTACGTCGTCTCATCAAATTGGAATGAATGAATGAATGAAAAAGTATGAATGAAAGAATGATGAATAAATTAATAATTAATGAATGAAAAAGAAAGAAATATGAAACAATAAATGAATGAATTAATTAATTCATTCATTAAAAAGTATAAATAAAAGAATGACGAATAAATTAATAATTAATGAATAAAAAAGAAAAATATGAAGAAATAAATGAATGAATTAATTAATTATTTAATGAAAAAGTATGAATAAGAGAATGACGAATACATTTATAATTAATGAATAAAAAAGAAAAATATGAAACAATAAATGAATTAATTAATTAATTAATTAAAAAGTATGAATAAAAGAATGACGAATAAATTAATAATTAATGAATGAAAAAGAAAGAAATATGAAACAATAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20613
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 |
---|---|---|---|---|---|
ENSDART00000003008 | Nonsense | 542 | 587 | 17 | 17 |
ENSDART00000122348 | Nonsense | 568 | 613 | 17 | 17 |
The following transcripts of ENSDARG00000027419 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 3675554)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 3699858 |
GRCz11 | 6 | 3860678 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGACTCTCCTGCAGGTGGCGCCAAAAATCAAAGCAATGATGATGGAGTG[C/A]GGCACCACCATGGTGGGTTACCAACCACAGGGAGACAAAGTCAACTTCTT
Long Flanking Sequence:
AATTAATGAAAAAGTATGAATAAAAGAATGACGAATAAATTAATAATTAATGAATGAAAAAGAAACAATAAATGAATTAATTAATTAATGAAAAAGTATTAATAAAAGAATGATGAATAAATTAATAATTAATGAATGAAAAAGAAAGAAATATGAAACAATAAATGAATGAATGAATTAATTAATTAATTAATGAAAAAGTATGAATAAAAGAATGATGAATCTTCATTTGCATAAAGTTGAAGGATTCTCAACTTTGTCGTGTCGCTCGACACGCCGACCTGGTTGCCAACAATGGCCGTTGCTCTCATAGACATAGTCGTACAGAGGTCGCTTACTCTATGCTGAAATAAACAGTCGCTTTTTGCTCTGCCTTTGCAAGTCGCTCATATTGTGAATGAGGCTTAAGACTCCCTATTGAAAAAATGTGGGCTCTCATTAAAACCCTCTGTGACTCTCCTGCAGGTGGCGCCAAAAATCAAAGCAATGATGATGGAGTG[C/A]GGCACCACCATGGTGGGTTACCAACCACAGGGAGACAAAGTCAACTTCTTCCGAATGGTGGTCTCCAATCACGCCGTCACCAAGTCGGACATCGATTTCCTCATCGATGAGATCGAGCGGCTCGGTCAGGATCTGTAAAACATCTATAATAGAGGCTCATTGGTCGCCTACGCGTTTAACGGCTATGTTTCGACGTTGTGTAGTTCTGTCCTTTCTTCTCAATGTCTTTAGATCTTTATATTACAGATTGCATAGCCTGTATAGCTACACAGTCACCTTACGACATATAGTCCATTGGGATAACAGCCGGTGCTTGTAAATACTATGAAGTCGAGCAAAAGCACAGCACTCTTTTAACGAAGCCCCTTTCGGTGTAATAGTGGGGTCTGTGTGTAAACCAGTGGTGGGTCTGTATTTTAGTGTTGTGTTTTTTAGATCTTCCCTTGTCGTAGGTCTTGTAAAGTGTTTAATCAGCACCTTTGTGAGGTGAAACATAAGTA
Associated Phenotype:
Not determined