Busch Lab

ZMP

fam76b

Ensembl ID:
ENSDARG00000012432
ZFIN ID:
ZDB-GENE-030131-6955
Description:
Protein FAM76B [Source:UniProtKB/Swiss-Prot;Acc:Q6PBM7]
Human Orthologue:
FAM76B
Human Description:
family with sequence similarity 76, member B [Source:HGNC Symbol;Acc:28492]
Mouse Orthologue:
Fam76b
Mouse Description:
family with sequence similarity 76, member B Gene [Source:MGI Symbol;Acc:MGI:1920076]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa20397 Nonsense Available for shipment Available now
sa33586 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa20397
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024815 Nonsense 62 328 3 10
Genomic Location (Zv9):
Chromosome 5 (position 25261288)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 23088553
GRCz11 5 23592353
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCTTTCCTTTCGTTCAGCAAAACCAACACTATCTGTAAGAAATGCGCA[C/T]AGAATGTCAAACAGTTTGGAACAGTAAGTTGACATCATGTTTAAAAAATT
Long Flanking Sequence:
ACTTCACTATGGTGATGAATACAAATGCACATTATCTAATAATAATGTCATTATTACACTAATTGTCTATTAGCTATGAGCAGACATTGTCAATCAGTGCATTGAAGGAAACTACACATGCTTGTCAAACAAAGTTGCTTGTCATATCTTCTAATCAAGCATCCATGCATTTGAAAAAAATTGCAAATTAACAACAACAAAAGTCCAAATTGGCATGTTATAAGCAGACTTTGCAATTGTGATTCACATTAAAAAAAAAAAAGAAAAGAGTTGGAGGTGTCTTAAAGTCACACCTGCATATTCGCCCCTGATAAAAAGTAATTCATAAGTTTTTTTTTTTTGTTTGTTTAAAGTTTGAGAGTTTTATATTCTAATCAAAGTTTATTATGTCTGATTTAATTTTAAATTGTTGCTAATTTATTCTTTGTAATGTTGCCTGCACTAATGCAAAATCTTTCCTTTCGTTCAGCAAAACCAACACTATCTGTAAGAAATGCGCA[C/T]AGAATGTCAAACAGTTTGGAACAGTAAGTTGACATCATGTTTAAAAAATTGTAAACCCCACAGATCTGTGTGCTAACATCGTCTTCTCTTTTACCAGCCGAAGCCATGTCAGTACTGTAACATCATTGCTGCGTTCATTGGGACCAAATGTCAGCGCTGCACCAACTCTGAGAAGAAGTACGGCCCTCCACAAACCTGCGAGCAGTGCAAGCAGCAGTGTGCCTTCGACAGGAAGGACGAGGGAAGGAGAAAGGTGACCAATCACGCATGCACATTCTTATTCAGTCGTATCACTCCTCCACACTCTCTGGCTGTGTTCTCTCACTCTGTATGTGTGTGATGTGATTCACCACTCTCTGACAGATTGAAGAGTCACTGTCTCCAGATTTCAGCACAACTGAAAGCAGGAGTTTATTAGAGCTGTCATTAAATACTAGACAAATGCTGTTGTTTATGCACAAAAACAGATGAATCATTAAAGCCCACTGCTCCCACCAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33586
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
ENSDART00000024815 Nonsense 244 328 8 10
Genomic Location (Zv9):
Chromosome 5 (position 25258731)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 23085996
GRCz11 5 23589796
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATTCTGGAGGCACGGATAACTTCATCTTGATTAGCCAGCTGAAAGAG[G/T]AAGTGATGTCACTGAAGCGCATGCTCCAGCAGAGAGACCAGACCATCCTT
Long Flanking Sequence:
TGAGTACAGATAATAAAATACCACAGAACATAAGTTAATGACATTTTAAATGCATGGTCTCTTACACAATTACTCACTTTTTTGTTGGAAATCTTAATAAAAATGTTGCTATTCTGTATGTGTGTTTTACAGAATAAGTGGAAACTTAAGTCCAGAGCAGGATCAGGGATTGTGGAAACAGAGGTGGAATTCATATCTTTTACTTTTTTTACTTTGTTCTGTGTTTGTGTGTTTTGTGGATCAATTGACTGTAATTGGGTTCTCTTATATAGCATTCAAAAGGAAACGCCAAAGAAAAAACCCAAACTAGAAACAAAGCCATCCAATGGAGACAGGTAATTACTGTTCATTGTATTTGTCAGTCTCTCAGGGAGCATCTGTTGACACATTACTTTTAATATTAAAGCCATTTCTCTTTCTTTCCCTCCAGTAGTTCAATCACTCAATCGATGGATTCTGGAGGCACGGATAACTTCATCTTGATTAGCCAGCTGAAAGAG[G/T]AAGTGATGTCACTGAAGCGCATGCTCCAGCAGAGAGACCAGACCATCCTTGAGAAAGACAGGAAGGTAATTTGTGATGTCATCTCCTGACACTGCAAGCTAGTCCAGGATGACTCACTTTCTCCGAAATAGTACACAGAAATGGATGGGTTTAGAAACGTGAATTTGCACATTGTTAGAATTATTTCTTTAAGCTTTTCCTGCTGTTTGTGATCTGCTGCCCACTTCACAGTCCATTTGCTGCCTGAGAAGATAATCACACTTGAGCCGTTACTAGAAGTCCATAATTGTTGTTGTAGTGATTGTTGTGACTTTCTTTGAAGGAGCTTGCTGCATTAAAGCTTAAAGTAATTTAACACATTGAAGATTCTTCAGAGGCTTTAGTTTGTAGGGACTTGAGTTGCTTTGAAATGTTCTATGAGGGTATGTTTGGTAATAAGGGGTGTTGACATAAATGATATCAGCACCACACTAAAGCAGCAGATAAATAAATGACTTCTG
Associated Phenotype:
Not determined