Busch Lab

ZMP

crabp1b

Ensembl ID:
ENSDARG00000035904
ZFIN ID:
ZDB-GENE-040624-3
Description:
cellular retinoic acid binding protein 1b [Source:RefSeq peptide;Acc:NP_001001842]
Human Orthologue:
CRABP1
Human Description:
cellular retinoic acid binding protein 1 [Source:HGNC Symbol;Acc:2338]
Mouse Orthologue:
Crabp1
Mouse Description:
cellular retinoic acid binding protein I Gene [Source:MGI Symbol;Acc:MGI:88490]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa9476 Nonsense Available for shipment Available now
sa18891 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9476
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052122 Nonsense 69 137 2 4
ENSDART00000052122 Nonsense 69 137 2 4
Genomic Location (Zv9):
Chromosome 7 (position 49784868)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 48055104
GRCz11 7 48327880
KASP Assay ID:
554-6154.1 (used for ordering genotyping assays)
KASP Sequence:
ATATCAAGACCTCCAYCACYGTCAGAACCACCGWGATMAACTTCCWGATC[G/T]GACAAGAGTTCTACGAGGAGACCGTYGATGGYCGCAAATGCAAGGTGACA
Long Flanking Sequence:
ATGTTTACATAGAAAAACAATAGAGACGTATTGTCTAAATGAACAGTTTCAACACAAGAGTTCATGAGAAAGTGTATAACCACTTGCCTTTAAGCAAACTGATACATTTTTTATTTTCTTTTGTGTGAACTATCCTTTCAAGTCACAACTTAACAAGTGGATTGCAGCAGATGCAAATGTGAGCAGTAAGTGTGCTGTCTTGAAAGAATTAGAGTGCGCTATGCAAGTGGATAATTACAGCTCAGTCAAGAGTGACGACTCTACTGTAAATAATAATCATTTCATTTGGAGATGTTTGTGTCTGAATGACATAAAGCTGAAGATGTTTACAGAAGTGAGAGGTTTCATGTGATGTTTCTTGTGTAGGGGTGAATGCGATGCTGAGAAAAGTGGCTTGTGCGGCTGCGTCTAAACCCCATGTAGAGATTCGTCAGAACGGGGAGCAGTTCTATATCAAGACCTCCACCACCGTCAGAACCACCGAGATCAACTTCCAGATC[G/T]GACAAGAGTTCTACGAGGAGACCGTTGATGGCCGCAAATGCAAGGTGACACAGCCGAGACGATTTCTGTTTTGTGCTGAATGTTTTTGTCAATTGATCAGAAGTGTGTGCTGTATAAATAGCAGTTAACTGTTCCCTTTAGCTTATCATGGGTGTTGTTTTATGTAAGGCCATAGCATTATTAGAAAAACAATGCAGGCCCCAAGTGGTATTGGGAGTGACCTTTGTTTTCTAATAATTCAACAAGATGGATTTATTAAAAAATTAATTATCTGCTTATATTATGTTTACCACACCTAAAGAACATGGTTTAGATGTTGTGTTTAAGACATTTCTCTTTTTTACCAACTCATTTTAATTAAGAAGTTTGAACAAGCAGCAAAAGTCATTTTTAGTGTAAAAAAACAGACATCATATAACATGAAATAGCTTTAATCAGATGAGAAATGTGTGAAATTAAGGATTTAAGAAGTTGGAATTTTGAGGAAAAGAAAAAAATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18891
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
ENSDART00000052122 Nonsense 69 137 2 4
ENSDART00000052122 Nonsense 69 137 2 4
Genomic Location (Zv9):
Chromosome 7 (position 49784868)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 48055104
GRCz11 7 48327880
KASP Assay ID:
554-6154.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATCAAGACCTCCACCACCGTCAGAACCACCGAGATCAACTTCCAGATC[G/T]GACAAGAGTTCTACGAGGAGACCGTTGATGGCCGCAAATGCAAGGTGACA
Long Flanking Sequence:
ATGTTTACATAGAAAAACAATAGAGACGTATTGTCTAAATGAACAGTTTCAACACAAGAGTTCATGAGAAAGTGTATAACCACTTGCCTTTAAGCAAACTGATACATTTTTTATTTTCTTTTGTGTGAACTATCCTTTCAAGTCACAACTTAACAAGTGGATTGCAGCAGATGCAAATGTGAGCAGTAAGTGTGCTGTCTTGAAAGAATTAGAGTGCGCTATGCAAGTGGATAATTACAGCTCAGTCAAGAGTGACGACTCTACTGTAAATAATAATCATTTCATTTGGAGATGTTTGTGTCTGAATGACATAAAGCTGAAGATGTTTACAGAAGTGAGAGGTTTCATGTGATGTTTCTTGTGTAGGGGTGAATGCGATGCTGAGAAAAGTGGCTTGTGCGGCTGCGTCTAAACCCCATGTAGAGATTCGTCAGAACGGGGAGCAGTTCTATATCAAGACCTCCACCACCGTCAGAACCACCGAGATCAACTTCCAGATC[G/T]GACAAGAGTTCTACGAGGAGACCGTTGATGGCCGCAAATGCAAGGTGACACAGCCGAGACGATTTCTGTTTTGTGCTGAATGTTTTTGTCAATTGATCAGAAGTGTGTGCTGTATAAATAGCAGTTAACTGTTCCCTTTAGCTTATCATGGGTGTTGTTTTATGTAAGGCCATAGCATTATTAGAAAAACAATGCAGGCCCCAAGTGGTATTGGGAGTGACCTTTGTTTTCTAATAATTCAACAAGATGGATTTATTAAAAAATTAATTATCTGCTTATATTATGTTTACCACACCTAAAGAACATGGTTTAGATGTTGTGTTTAAGACATTTCTCTTTTTTACCAACTCATTTTAATTAAGAAGTTTGAACAAGCAGCAAAAGTCATTTTTAGTGTAAAAAAACAGACATCATATAACATGAAATAGCTTTAATCAGATGAGAAATGTGTGAAATTAAGGATTTAAGAAGTTGGAATTTTGAGGAAAAGAAAAAAATGT
Associated Phenotype:
Not determined