ZMP
grk7a
Ensembl ID:
ZFIN ID:
Description:
G-protein-coupled receptor kinase 7a [Source:RefSeq peptide;Acc:NP_001027011]
Human Orthologue:
GRK7
Human Description:
G protein-coupled receptor kinase 7 [Source:HGNC Symbol;Acc:17031]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12074 | Splice Site, Nonsense | Available for shipment | Available now |
sa18724 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44525 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12074
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100287 | Splice Site, Nonsense | 345 | 549 | 2 | 4 |
ENSDART00000100287 | Splice Site, Nonsense | 345 | 549 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 16358336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16869163 |
GRCz11 | 2 | 16537753 |
KASP Assay ID:
2259-1792.1 (used for ordering genotyping assays)
KASP Sequence:
CAGATCTTGGTCTCGCTGTGGAGATTGCTGTTGGGAAGACCATCAGCCAG[A/T]AGKTGAGTTCTTCGKCTCTATGCTGTGATTTGTTCCACTGAWGCCACAGG
Long Flanking Sequence:
TGTTAAGTCTCCTCAAAGTTCTTGAATAAAATATTTAGATGTTGACCGTGTTTATACACTTCCAGGTGTGCGCAGTGCAAGTGAAGAACACCGGCCAGATGTACGCCTGTAAGAAGCTCTGCAAAAAGCGCCTCAAGAAGAAACATGGTGAGAAAATGGCCCTGCTCGAGAAGAAGATCTTGGAGAGGGTCAACAGCCTGTTCATTGTCAGCTTGGCTTACGCTTATGACACCAAGACCCACCTCTGCCTGGTCATGAGCTTGATGAATGGAGGTGATCTTAAGTATCACATCTATAACATTGGGGAGAAGGGAATCGAAATGGATCGGATCATCTATTATACAGCCCAGATTGCAACCGGGATCCTTCATCTGCACGACATGGACATCGTGTATCGTGACATGAAGCCAGAGAACGTGCTTTTGGATAGCCAGGGCCAGTGCCGTCTTTCAGATCTTGGTCTCGCTGTGGAGATTGCTGTTGGGAAGACCATCAGCCAG[A/T]AGGTGAGTTCTTCGTCTCTATGCTGTGATTTGTTCCACTGATGCCACAGGAGAGTATTCGAGTGTGTTTGTGTGTGCATACAAAATGAAAACTGATGGTTGGAGAGTAATTCTCAAACTACGTAAGAGTACTTTAACTCCGAATCTAAAATTAGAGAATTTTTACAGATTTTTAAGATGGAGAGAGAGAGGGGGGGGGGGGGGGGGGGGGGATTACAATTATCATTGAAGTCCATTTTAATTAGCCAATGGGCCTTATGCTCGGAAGTGTTTTTCAGAAACACATAACTTCCAGTCAAAGTTGATGTGGCTGTCTCCAATTTCCTGAGGTTTACTTTACAGCATGGATAATGTAATTTAATTAAAATATATTCAGTCTGTCAGCATCAATAGCCTAGTCGTACTGTGCGCCGACATATAGCGCCAATGTGCTCACGGCGACATGAGTTTGATTCCCACCTCGAGGTCCTTTGCCGATCCTTTCCTTCTCTCTGCTCTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18724
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100287 | Splice Site, Nonsense | 345 | 549 | 2 | 4 |
ENSDART00000100287 | Splice Site, Nonsense | 345 | 549 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 16358336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16869163 |
GRCz11 | 2 | 16537753 |
KASP Assay ID:
2259-1792.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGATCTTGGTCTCGCTGTGGAGATTGCTGTTGGGAAGACCATCAGCCAG[A/T]AGGTGAGTTCTTCGTCTCTATGCTGTGATTTGTTCCACTGATGCCACAGG
Long Flanking Sequence:
TGTTAAGTCTCCTCAAAGTTCTTGAATAAAATATTTAGATGTTGACCGTGTTTATACACTTCCAGGTGTGCGCAGTGCAAGTGAAGAACACCGGCCAGATGTACGCCTGTAAGAAGCTCTGCAAAAAGCGCCTCAAGAAGAAACATGGTGAGAAAATGGCCCTGCTCGAGAAGAAGATCTTGGAGAGGGTCAACAGCCTGTTCATTGTCAGCTTGGCTTACGCTTATGACACCAAGACCCACCTCTGCCTGGTCATGAGCTTGATGAATGGAGGTGATCTTAAGTATCACATCTATAACATTGGGGAGAAGGGAATCGAAATGGATCGGATCATCTATTATACAGCCCAGATTGCAACCGGGATCCTTCATCTGCACGACATGGACATCGTGTATCGTGACATGAAGCCAGAGAACGTGCTTTTGGATAGCCAGGGCCAGTGCCGTCTTTCAGATCTTGGTCTCGCTGTGGAGATTGCTGTTGGGAAGACCATCAGCCAG[A/T]AGGTGAGTTCTTCGTCTCTATGCTGTGATTTGTTCCACTGATGCCACAGGAGAGTATTCGAGTGTGTTTGTGTGTGCATACAAAATGAAAACTGATGGTTGGAGAGTAATTCTCAAACTACGTAAGAGTACTTTAACTCCGAATCTAAAATTAGAGAATTTTTACAGATTTTTAAGATGGAGAGAGAGAGGGGGGGGGGGGGGGGGGGGGGATTACAATTATCATTGAAGTCCATTTTAATTAGCCAATGGGCCTTATGCTCGGAAGTGTTTTTCAGAAACACATAACTTCCAGTCAAAGTTGATGTGGCTGTCTCCAATTTCCTGAGGTTTACTTTACAGCATGGATAATGTAATTTAATTAAAATATATTCAGTCTGTCAGCATCAATAGCCTAGTCGTACTGTGCGCCGACATATAGCGCCAATGTGCTCACGGCGACATGAGTTTGATTCCCACCTCGAGGTCCTTTGCCGATCCTTTCCTTCTCTCTGCTCTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44525
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100287 | Nonsense | 448 | 549 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 16363063)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16873890 |
GRCz11 | 2 | 16542480 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAAAATTGTACAATTTCCACAGGAATGATGATCCTAGGAAGCACGAGT[G/A]GTTCAAGTCCATCAACTTTGCTCGCTTGGAGGCTGGACTAATCGATCCAC
Long Flanking Sequence:
TCTATTAGAAATCTATTAGACATCTTTTAAAAACAAAAAATGCTTGCAGGGTGTGTTTATGTGGTTTCCTCCGTGTGCTCTAGTTTCCTTCATAGTTCAAGGACATGCACTATAGGTGAATTGGGTAAAACAAATTAGGCATTGCACATGAGTGAATGAGAGTGCATGAGTGTTTCCCAGTGCTGGGTTGCACATAAAACATAGGCCAGAGGAATTTGGTGGTTGATTTTTCTGTGACCAAAGAACAGTGAGTAAGTGAGTGAGTGAGTGAGTGTTCTGAAGATGAATGAAGGTCTAGGGGTTTGGAAAGACATGAGGGCTAGTAATCAATAACAGAATGTTCATTTCTGGTTGAACTCAAGGTGTAACAGTGATCTTGATTTTTTTCCTTAAGTATGAAGCAATCGTATTCTGAAATGTATCAAACATCTTGTTCCCTCATGGCTAAGATGTAAAATTGTACAATTTCCACAGGAATGATGATCCTAGGAAGCACGAGT[G/A]GTTCAAGTCCATCAACTTTGCTCGCTTGGAGGCTGGACTAATCGATCCACCCTGGGTGCCCAAACCCAATGTGGTCTATGCAAAGGATACAGGTGACATTGCAGAGTTCTCTGAAATTAAGGGTATTGAGTTTGACGCCAAGGATGACAAATTCTTCAAGGAATTTAGCACAGGTGCGGTGTCCATTGCCTGGCAACAGGAGATGATTGACACTGGACTTTTTGATGAGCTCAGTGATCCGAACCGGAAAGAGTCTTCCGGTGGCTCCGATGATGATAAGAAATCAGGCACTTGCACTCTTCTGTGAGAGAGCAGCTCAGACATCCAGCAGCAGATGATTTCAGTGGCATCACTAACATGATTGAAGCTGTGCACCGTGTCAAAGAAGAGCGGAGCATGACTGGAAAGAGACGGGACATTAGTCCTTTGTAGCATATATGAAGACACTTATTACATCGTTTGCACTGTCACATGGTCTGACACACACTTTGGACCACCCC
Associated Phenotype:
Not determined