Busch Lab

ZMP

si:dkey-202m22.7

Ensembl ID:
ENSDARG00000079423
ZFIN ID:
ZDB-GENE-091118-42
Description:
G protein-coupled receptor 7 [Source:RefSeq peptide;Acc:NP_001124241]
Human Orthologue:
NPBWR2
Human Description:
neuropeptides B/W receptor 2 [Source:HGNC Symbol;Acc:4530]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa24369 Nonsense Available for shipment Available now
sa6744 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24369
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000033429 Nonsense 483 731 3 4
ENSDART00000112297 None None 326 None 1
Genomic Location (Zv9):
Chromosome 23 (position 31080978)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 30915868
GRCz11 23 30842399
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCCCTTCGGTCTGCCCCTGTGCAAGGCTGTGGTAGCCATTGACTATTA[C/A]AACATGTTCACAAGTGTCTTCACCTTGACCGTAATGAGTGTGGATCGCTA
Long Flanking Sequence:
TTGACCAAGTACCCTAACCTGCCTAAATAACCCAATTAAGCATTTAAGTGTCACTTTAAGCTTAATACCAGTGTCTTAAAAAATATCTAGTCATATATTATGTACTGCACTCAAACAATTATTGTTTTGCTCGTTTAAACTACTTTAAAAGAAATTAGTCATTAAAACTGTTATGGCTTGAAATGTTGGTATTAGGGAAAATATACAGGGGGGCTAATAATTCAGGAGGGCTAACAATTCTGACTTCAACTGTATATTTCTATATTTTCATATACTGTAAATGACAGTATTTTTGCTTTCCAAAGTATTTTGACAAGTTATATTTACACCTGCCGCAGGTACACAAAGATGAAAACGGCCACCAATATTTACATCTTTAACCTGGCTTTGGCTGATGCACTGGTTCTGGCCACTCTTCCTTTCCAAGGCACTGATGTCATCCTAGGTTTCTGGCCCTTCGGTCTGCCCCTGTGCAAGGCTGTGGTAGCCATTGACTATTA[C/A]AACATGTTCACAAGTGTCTTCACCTTGACCGTAATGAGTGTGGATCGCTACATAGCCGTCTGCCACCCTGTGCGCTCGCTGACAGTTCGGACCCCGCTCCGGGCCAAGCTGATCAATGTGGCGGTGTGGGTGCTGGCATCAGCTGTAGGACTGCCTGCTATGATCATGGGTCAGGTGGAGAAGGATGATCACGATGGTCTGGTCCTCTTTTTTCATGTTGCTCTGTGTTGACCTTCCATTTTAAGGCATGTTTGCTCATCGTGTCCTGTTTTTTTTTTCTCTCTTTTTTTAATCATGCTGTTGGTGGTGTTTTTAGTGTTTTTTTTCGGTTGTGCCTGAAATTATTTTTGACATTTTATTGTGGATTAAAGGTGCACTAAGTGTGTTTTTTTTTAAACAACCTTCCAGGGAAGGTGGACATTTTTGTTCTAAGTAATTTTTATGTAAAATATGAAAGCAAAGTCCACAAAAATGCACTGAAAGAATCACGTCAACCAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6744
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000033429 Nonsense 661 731 4 4
ENSDART00000112297 None None 326 None 1
Genomic Location (Zv9):
Chromosome 23 (position 31084224)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 30919114
GRCz11 23 30845645
KASP Assay ID:
554-5347.1 (used for ordering genotyping assays)
KASP Sequence:
ACTCGGGGCCAGTCAGTCCTCRATGGCGGCTATGCATTTCTGCATTGCTT[T/A]GGGTTACGCAAACAGCTGTTTAAACCCCGTTCTCTATGCCTTCCTGGATG
Long Flanking Sequence:
TTCGAAGAACTTTCTTAGCAGAACAACATACATTTGTGCACTTTTAAATCACAGCCTCTTGTGTTCCCTTCAAAAGACTCTCCATTTCTTTACTCATCACAATTCATCGTATATCACAGCCACTACGTGAAATCCCCTTTTTTAATGTGTTTTTTTCCATGCAGGTGCCGAGTGCATGGTGAGCCTGCCTGAACCAAGAAAGCACTGGGATCGTGTGTTCATGATGTGTGTGTTTCTCTTCTCTTTCTTGATCCCTGTGCTGATCATAAGCGTCTGCTACGGCCTGATGGTGCGTCGTTTGCGCAGTGTCCGTGTACTGTCCGGCTCACGGGAAAAAGACCGCAATCTGAGGAGAATCACCTATATGGTATTGTCGGTGGTGGCCGCTTTTGTGTTTTGCTGGATGCCGGTGCAGGTCTTGGCTTTGATTCAGGCTCTGGGTCATGTGGAACTCGGGGCCAGTCAGTCCTCGATGGCGGCTATGCATTTCTGCATTGCTT[T/A]GGGTTACGCAAACAGCTGTTTAAACCCCGTTCTCTATGCCTTCCTGGATGAAAACTTCAAGCGCTGTTTCCATGAGTTTTGTATCCCGGCCAATTCCGATCTCTTTCTAGAAGACCAGCGTAAGAGGTCATTGAGGCAGGGGAGAGAATGTGCTGAGCTGGAGGAAAAGGAGGTGGTGATTTATCATTGCGCTGCTCCTGTGTTAGCGGATTAGAGCTTTTAGAATTGCCAATGTTCTTGTATGGTCACGTCTGGAATTGTGAGGAAAGTTACCACTAGCATAGAGTTAATGCATGTTGTTCTGGTTAAAAGTAACCAGATGATATCAACCCAGACTTATTATGAAAATGAAGCCCTATATACATTTCTGGAGAGCTCTCCTATACATCCCAGGCGGTACTTTTTTATGTTTTTGTATTTATGAATCCACCAGAGGCTGCTGTGTACGTTTTTTGAGATCTCAAATTTCTCTTGTGAGTGCCATTCACGCCTTCTCACGT
Associated Phenotype:
Not determined