Busch Lab

ZMP

zgc:63774

Ensembl ID:
ENSDARG00000092367
ZFIN ID:
ZDB-GENE-030131-2552
Description:
riboflavin transporter 1 [Source:RefSeq peptide;Acc:NP_955950]
Human Orthologues:
GPR172A, GPR172B
Human Descriptions:
G protein-coupled receptor 172A [Source:HGNC Symbol;Acc:30224]
G protein-coupled receptor 172B [Source:HGNC Symbol;Acc:30225]
Mouse Orthologue:
Gpr172b
Mouse Description:
G protein-coupled receptor 172B Gene [Source:MGI Symbol;Acc:MGI:1289288]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa36828 Nonsense Mutation detected in F1 DNA Not yet available
sa15210 Nonsense Available for shipment Available now
sa36827 Nonsense Mutation detected in F1 DNA Not yet available
sa23509 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa36828
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
ENSDART00000045675 Nonsense 30 418 3 5
Genomic Location (Zv9):
Chromosome 19 (position 22822806)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 22754186
GRCz11 19 22338509
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAACTTTAAAACATGTTCTTTCTTTACAGGATGGAATTTGCCTGCCTA[T/A]ATTTCAGTTCTGATTGCGTTTGGGAATTTGGGACCAGTGGTTGTCACTTT
Long Flanking Sequence:
GGCCAACTTAGACCCGTGGGCCCAAGTTTGGGCATCTCTGCTCTAAATGCAGCCTCCTATGTTTATGCTCAGTTATTTTTCAGGCAATGGCAATAACCTGTTACTTGCTACAAAAGTTAAATGAATGAACCTGCACATGGGAGCCTGAGAAAAATGCAAAATTTAGAAGAAAACTTTAGAAGGCACCCATACGGTTGGCACCCATAAGGTTTTTTGTATCTGACGTAATGTATACTATAACTTTAACTTTGTTTTCCAGACACATAAATGGCAGATACATGGTGGAATCATGCCATTGTCACACACATTCTTGTGGCCCTGTTTGGAATGGGCTCATGGATCTCTGTAGACTCAATATGGGTTGAGCTGCCAGTTGTCGTAGGAGTTCTACCTGAAGGTATACATTGGTTTAAGAGCATGAAAGCAATTTCTGTTTTACCCTGACATCTGTAGAACTTTAAAACATGTTCTTTCTTTACAGGATGGAATTTGCCTGCCTA[T/A]ATTTCAGTTCTGATTGCGTTTGGGAATTTGGGACCAGTGGTTGTCACTTTAACACACCACTTTGCTCCAGGATGGCTGAATGAGCGATTGGCCATCCACATCATACAAGCGCTAGCAGTGGTAGCATCCGCATTTCTTGCTCTATTTTGGTCCCAGGTGGCCATGGTCTCTGGAGAGCTTAGATCTGTCCCATTCCTGCTGCTTACTTTTATACTGTCATTATTCTGCTGCACTTCCAATGTCACCTTCTTACCCTTTATGTATCGGTACCCTCCACAATATATCCGGACGTTCTTTGTTGGACAAGGTCTCAGTGCACTCTTTCCTTGTGTGGTCGCTTTGGGACAGGGTGTAGGGAAACTAGAGTGCATTGAGAAATCCAATGGCACAGAAGCCCATTATCTCAAAGAAAACTTTCCAGCCCAAATTTTCTTTTGGATCTTGACTGTAATGCTTGTAATTTCGGCCACAAGTTTCCTAGCTCTGACATACAGAGTGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15210
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
Order Allele From EZRC
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045675 Nonsense 114 418 3 5
Genomic Location (Zv9):
Chromosome 19 (position 22822555)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 22753935
GRCz11 19 22338258
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTACTTTTATACTGTCATTATTCTGCTGCACTTCCAATGTYACCTTCT[T/G]ACCCTTTATGTATCGGTACCCTCCACAATATATCCGGACGTTCTTTGTTG
Long Flanking Sequence:
TTTTCCAGACACATAAATGGCAGATACATGGTGGAATCATGCCATTGTCACACACATTCTTGTGGCCCTGTTTGGAATGGGCTCATGGATCTCTGTAGACTCAATATGGGTTGAGCTGCCAGTTGTCGTAGGAGTTCTACCTGAAGGTATACATTGGTTTAAGAGCATGAAAGCAATTTCTGTTTTACCCTGACATCTGTAGAACTTTAAAACATGTTCTTTCTTTACAGGATGGAATTTGCCTGCCTATATTTCAGTTCTGATTGCGTTTGGGAATTTGGGACCAGTGGTTGTCACTTTAACACACCACTTTGCTCCAGGATGGCTGAATGAGCGATTGGCCATCCACATCATACAAGCGCTAGCAGTGGTAGCATCCGCATTTCTTGCTCTATTTTGGTCCCAGGTGGCCATGGTCTCTGGAGAGCTTAGATCTGTCCCATTCCTGCTGCTTACTTTTATACTGTCATTATTCTGCTGCACTTCCAATGTCACCTTCT[T/G]ACCCTTTATGTATCGGTACCCTCCACAATATATCCGGACGTTCTTTGTTGGACAAGGTCTCAGTGCACTCTTTCCTTGTGTGGTCGCTTTGGGACAGGGTGTAGGGAAACTAGAGTGCATTGAGAAATCCAATGGCACAGAAGCCCATTATCTCAAAGAAAACTTTCCAGCCCAAATTTTCTTTTGGATCTTGACTGTAATGCTTGTAATTTCGGCCACAAGTTTCCTAGCTCTGACATACAGAGTGGTCATTCAGGCTCCAGCAGAAGAAGCTCCAAAAGCTAAGCAGGAAATGGGGAACACGGAGGAAGAGACCCATCCTTTACAAAATGGAGATTCTCCAGTTTCTGAGGAGCAAGTCGAAGTTGAAAAACAGGCTCCCGTTGTGGCCTTCTGGACATCTCGCAATATCTACATGCTTCTTTTGCTGGGAATATCCAATGCGTTGACCAACGGTGTGTTGCCATCTGTACAGAGTTTCACCTGTCTTCCTTATGGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36827
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045675 Nonsense 235 418 3 5
Genomic Location (Zv9):
Chromosome 19 (position 22822193)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 22753573
GRCz11 19 22337896
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACCCATCCTTTACAAAATGGAGATTCTCCAGTTTCTGAGGAGCAAGTC[G/T]AAGTTGAAAAACAGGCTCCCGTTGTGGCCTTCTGGACATCTCGCAATATC
Long Flanking Sequence:
TAGCAGTGGTAGCATCCGCATTTCTTGCTCTATTTTGGTCCCAGGTGGCCATGGTCTCTGGAGAGCTTAGATCTGTCCCATTCCTGCTGCTTACTTTTATACTGTCATTATTCTGCTGCACTTCCAATGTCACCTTCTTACCCTTTATGTATCGGTACCCTCCACAATATATCCGGACGTTCTTTGTTGGACAAGGTCTCAGTGCACTCTTTCCTTGTGTGGTCGCTTTGGGACAGGGTGTAGGGAAACTAGAGTGCATTGAGAAATCCAATGGCACAGAAGCCCATTATCTCAAAGAAAACTTTCCAGCCCAAATTTTCTTTTGGATCTTGACTGTAATGCTTGTAATTTCGGCCACAAGTTTCCTAGCTCTGACATACAGAGTGGTCATTCAGGCTCCAGCAGAAGAAGCTCCAAAAGCTAAGCAGGAAATGGGGAACACGGAGGAAGAGACCCATCCTTTACAAAATGGAGATTCTCCAGTTTCTGAGGAGCAAGTC[G/T]AAGTTGAAAAACAGGCTCCCGTTGTGGCCTTCTGGACATCTCGCAATATCTACATGCTTCTTTTGCTGGGAATATCCAATGCGTTGACCAACGGTGTGTTGCCATCTGTACAGAGTTTCACCTGTCTTCCTTATGGCAACATGACCTTTCACCTTTCTGTCGTCTTGGGAAACATCGCAAACCCTTTGGCCTGCTTTGTGGCCATGTTTGTCATACTAAGGTAATTGAGCGTACTAAGGTAATTCCCATCTGAGTTCCTAGAGTACCCCATATTTACAAAATTGCATACTTTGAGTAGGTCTTACATTTGAAATGTTCTTCCCAAACTTCCCAACCATCAGAAAATTATGTTTTTTAATATCAATAGTAAGTAATTATTGTAAGTAATTATTGATATTGAGTAATATGAATGGAATTTGAATGTACTACATTCACTATGTAGTCATTATAAAATGACCTACAGTAACTGCTTCACATTCATTTATAAACTCTCTCATGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23509
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
Order Allele From EZRC
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045675 Essential Splice Site 349 418 4 5
Genomic Location (Zv9):
Chromosome 19 (position 22820223)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 22751603
GRCz11 19 22335926
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTCCCTGTCCACCACTTTTAGGAAGCCAGTTTGGAGTTGCTCTAGTGG[T/G]TAGTAAATGGGTTTTATTAATGAGTGGGAGAGGAACTTACTCAGAACGAA
Long Flanking Sequence:
CCAAGTGATTAACCAGAAGTCAAGTTATTATTTGTTGTTCATGAAACTTGGATAGGCAACAAGACTTTTGTCAGGTAGTGTTCTATATAATAGAGAATTCATCCTATGTTGTATGCAATTACAGACGCAACGTTAGATGCCCACTTCTGTATATCCTCAAATAGAGCACTTTAATCCATAGTGGATGTTGTCAAGTGCATTCATTCAATATTACAAATGCAAAACAATAACAAGTGTGCATCTATGAACTCCAGAAACATAGTTACCAAAAAAAAGATGTGTATGTACAGTTTGTTTATGTATGTCCGTCATGTTATTATTGTGTTCTGTGAACTGAATATTTAGACTTGAAATTAATGAAAGCTTTTATTACAGGTCCAGCGTTGGTCTTGGTATGATGTCAATAGGAGGCATTATTTTCGCTGCCTATCTCATGGCCTTGGCAGCATTAAGTCCCTGTCCACCACTTTTAGGAAGCCAGTTTGGAGTTGCTCTAGTGG[T/G]TAGTAAATGGGTTTTATTAATGAGTGGGAGAGGAACTTACTCAGAACGAAACAAAAAAAACATAAATGCATGTCCAGAAGACCGAATTTCATAATCGCTCATGTGATGTGTGCACAGGGAAGTTTGGATAGCACTTTATTTACAGTCCTCTTATTAACTTATAGTGAGTACATTTACTGGTTAATAAAAAGATATTAAAATGCAACCAAACCTGCATAAATATAAATTTGGTCCTATATATGTTTAAATGTGTGTATATATTATCAAATATATTTTCAGTGCTATTTAAAAAAGCAAAGGATTTTTTATAATAAAATAAATGCATAAAATATTAAAAATTATATGAAAGTATTTAAAAAAATTTTCAGAAATATTATATATAAATTTAAATTATACAAACATGAAATATATTTACATTTATACAACAGTTCTGTCTGGTTCTCGAATTTTGATTGGCTGATAGCCATGCGACATTCCGGAATAACAGCACTCATACAGCT
Associated Phenotype:
Not determined