ZMP
gramd1a
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A8E7Q9]
Human Orthologue:
GRAMD1A
Human Description:
GRAM domain containing 1A [Source:HGNC Symbol;Acc:29305]
Mouse Orthologue:
Gramd1a
Mouse Description:
GRAM domain containing 1A Gene [Source:MGI Symbol;Acc:MGI:105490]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36228 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32108 | Nonsense | Available for shipment | Available now |
sa22923 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36228
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111956 | Nonsense | 2 | 896 | 1 | 18 |
ENSDART00000142648 | None | None | 771 | None | 20 |
The following transcripts of ENSDARG00000076689 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 44725041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 42005549 |
GRCz11 | 16 | 41955581 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTGTCTTCGAGGAAACTGTCAGTAGACTCTCATTAAACAGGTGATGTA[T/G]GAAGGTCTTTTAGTGATGGCGATGACGACACCACCTGAAATCCTAATTGC
Long Flanking Sequence:
AAGGGGCAGAGACATTATAAAGGAAGTCTTTAATAGCGAAAGAGGAAGAAGATTGATTTGACTTCCAGCAGTCTTGAGATCTAGCAAGTTTGAACTTCAGAAATGCTCTGTTCTTCCTTGAAAAATGACCTATTACTGGAAGATATGCCTCCACCCTTTTGTGTATATTAGAAATCTGTGATGGCTCCGCCCCATTTTTGCAAGTTCATACTGCAGGAAATTATATCATATATATATTTGTCAGTACAGCTGTGAAGGAAACTCAACTGCTGACTTCTTTCTTCAAGACAGCCAGTTGTAATGGATGCAGAAGACCTTTTCAAATGTCATCAGATTGCATTTCCGTTGTGGAATATTTATTTTGGGCTCTAATGGAATTTCCAGAGCAGATGTAGAAGACTTGAGAACAGAGAGTTGGAAATATCTTGAGCTTCGCTTATGCGTGATGAAACTTGTCTTCGAGGAAACTGTCAGTAGACTCTCATTAAACAGGTGATGTA[T/G]GAAGGTCTTTTAGTGATGGCGATGACGACACCACCTGAAATCCTAATTGCTGAGCCCATTTCAATTCCAATTCTGAACATTCTCCCGCCGTCGTCCGATACGGAGTCATGGTCGCGCTCTCCAAGCCCACGTGCGCATCGGTACCGCTCACGCAGCCGAGAGAAAAGGAAAGCCAAGGCACAGCAAGAGGACAAATCAGGAGCAAAGCATTGTGATAAACGGAAAGGTGAACTCGAAAGAAGCCCATCACATGCATCTGCATCCTCTTCAATGGTTTGTAATGTTGATGATGAAGAGCAGGGTAACCCCTGCGTGCTTCTGCTACCCCCGTCCCGCTCATGGTCACGGAGCTCCTCCCTAAGCAGGCGCTCTCGCTGGTCTATCCGTAGCCTTCTCAACAAGGACTCAGACTGTGACAGCAGCAGGTCAGTGTGTTCCCTCTCCCACTTATGCAGTCAGCAGTATTTCCTAAAGCGGCATTTTTTTTTCACCCACACTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32108
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 |
---|---|---|---|---|---|
ENSDART00000111956 | Nonsense | 360 | 896 | 7 | 18 |
ENSDART00000142648 | Nonsense | 226 | 771 | 8 | 20 |
The following transcripts of ENSDARG00000076689 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 44696981)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 41977489 |
GRCz11 | 16 | 41927521 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCAGTGTTACGGCACTGAGCTCGGCCTGACCAGTGAAGATGATGACTA[C/A]GTCTCCCCTACTGCTGAACATATGAACGGCCTGCTGTGAGTCCATACTGA
Long Flanking Sequence:
AGATAAGTAGTGAAATAATATCTGCAAATAAAATAATTTTAGTTAAAAAAATGCAACATGTAGGATCTTTTCACTTCAAACCTCTGCTTTCCTGTTCAAGTTGCCTTCTCTGCTCTCCACTTTGCTTTCTGCTATTACTATCACAATAAAGACATAAATGCTGAAAACAAATCTTATAACTTAAAAAGAAACAATCACTAGGTTTTCTCAGTTCTGTGTGCGGTGCGTTTTTTACTCTGAAAACACAGTTCATATTATTAGCATACTGATTTTTATTTTTTTTATTTTTTTGGCATAAAAATGTCTCTTTAGTCCTAAATGCTATGTCATCACCTCTGCTGCCTCACAAAAGTGGTGTTGAAGCAGTTTTTTTATCCTCGAAGTGCCCTGTACTGAGGTTATTTTTGTTCTCTTTAGACTCTGTCTCCTAAGGAACTGTGGCACATCGTTCACCAGTGTTACGGCACTGAGCTCGGCCTGACCAGTGAAGATGATGACTA[C/A]GTCTCCCCTACTGCTGAACATATGAACGGCCTGCTGTGAGTCCATACTGACACAAATCTGCTCTGGAAAAAGGTTTTATAAAATTTACCTTGCAACACAAGGACAGATACAAAAAGCGTGCATCTATCTTTAGTGTTTTTATGGGGTTTGTTTTGAAAAGGCCACATTGTTTACATACTACTTGTATTGCATATTTATTTATTTATTTTTATTTTTTAAGTTATTTTTTATTGTTTTATTTTTTTGTGTGTAAAACTACCGTTTAAATGTTATAATTTACTTTAGGTTTCCTATTATCTTACCTTCTATTTATCACAGTACATTCACTCTCCCTCCTCCGTTTATTTAAGTAATTAGTTTGATTATTTCAAGATGTTTTATTATTATTATTATCTTATGTTTTTTAGTTGTACATATTTACTACCATCAATGAAAATATTGCTGAATGTATGATTGTCATTGATTGTTAGTATTCATATGCTTGAAAGTACATTTTCCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22923
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 |
---|---|---|---|---|---|
ENSDART00000111956 | Essential Splice Site | 372 | 896 | 7 | 18 |
ENSDART00000142648 | Essential Splice Site | 238 | 771 | 8 | 20 |
The following transcripts of ENSDARG00000076689 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 44696944)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 41977452 |
GRCz11 | 16 | 41927484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATGATGACTACGTCTCCCCTACTGCTGAACATATGAACGGCCTGCTG[T/C]GAGTCCATACTGACACAAATCTGCTCTGGAAAAAGGTTTTATAAAATTTA
Long Flanking Sequence:
TTTAGTTAAAAAAATGCAACATGTAGGATCTTTTCACTTCAAACCTCTGCTTTCCTGTTCAAGTTGCCTTCTCTGCTCTCCACTTTGCTTTCTGCTATTACTATCACAATAAAGACATAAATGCTGAAAACAAATCTTATAACTTAAAAAGAAACAATCACTAGGTTTTCTCAGTTCTGTGTGCGGTGCGTTTTTTACTCTGAAAACACAGTTCATATTATTAGCATACTGATTTTTATTTTTTTTATTTTTTTGGCATAAAAATGTCTCTTTAGTCCTAAATGCTATGTCATCACCTCTGCTGCCTCACAAAAGTGGTGTTGAAGCAGTTTTTTTATCCTCGAAGTGCCCTGTACTGAGGTTATTTTTGTTCTCTTTAGACTCTGTCTCCTAAGGAACTGTGGCACATCGTTCACCAGTGTTACGGCACTGAGCTCGGCCTGACCAGTGAAGATGATGACTACGTCTCCCCTACTGCTGAACATATGAACGGCCTGCTG[T/C]GAGTCCATACTGACACAAATCTGCTCTGGAAAAAGGTTTTATAAAATTTACCTTGCAACACAAGGACAGATACAAAAAGCGTGCATCTATCTTTAGTGTTTTTATGGGGTTTGTTTTGAAAAGGCCACATTGTTTACATACTACTTGTATTGCATATTTATTTATTTATTTTTATTTTTTAAGTTATTTTTTATTGTTTTATTTTTTTGTGTGTAAAACTACCGTTTAAATGTTATAATTTACTTTAGGTTTCCTATTATCTTACCTTCTATTTATCACAGTACATTCACTCTCCCTCCTCCGTTTATTTAAGTAATTAGTTTGATTATTTCAAGATGTTTTATTATTATTATTATCTTATGTTTTTTAGTTGTACATATTTACTACCATCAATGAAAATATTGCTGAATGTATGATTGTCATTGATTGTTAGTATTCATATGCTTGAAAGTACATTTTCCCAACACTCGTCTGTTAGAATTGAGCACTCCCAGTAAAAT
Associated Phenotype:
Not determined