Busch Lab

ZMP

btr12

Ensembl ID:
ENSDARG00000051809
ZFIN ID:
ZDB-GENE-060929-548
Description:
bloodthirsty-related gene family, member 12 [Source:RefSeq peptide;Acc:NP_001070087]
Human Orthologues:
CTD-2611O12.2, CTD-2611O12.3, ERMAP, RFPL1, RFPL2, RFPL3, RFPL4A, RFPL4B
Human Descriptions:
erythroblast membrane-associated protein (Scianna blood group) [Source:HGNC Symbol;Acc:15743]
ret finger protein-like 1 [Source:HGNC Symbol;Acc:9977]
ret finger protein-like 2 [Source:HGNC Symbol;Acc:9979]
ret finger protein-like 3 [Source:HGNC Symbol;Acc:9980]
ret finger protein-like 4A [Source:HGNC Symbol;Acc:16449]
ret finger protein-like 4B [Source:HGNC Symbol;Acc:33264]
Mouse Orthologues:
Ermap, Rfpl4
Mouse Descriptions:
erythroblast membrane-associated protein Gene [Source:MGI Symbol;Acc:MGI:1349816]
ret finger protein-like 4 Gene [Source:MGI Symbol;Acc:MGI:2149590]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa21161 Nonsense Available for shipment Available now
sa41091 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa21161
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000050357 Nonsense 283 562 5 8
ENSDART00000110769 Nonsense 283 562 5 9
Genomic Location (Zv9):
Chromosome 7 (position 76683596)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 73459491
GRCz11 7 73681604
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGCAGTCTCAGGCCGAGCTGCTGGAGCTCATCGCCAGCCGGCAGAAA[C/T]AAAGCGAGCAGCAGGCCAAAGATCTGGCGGCCGGTTTGGAGCTGGAGCTC
Long Flanking Sequence:
AGGGGTGTTTCCGTGACAGAAAACCCCCTCAGTGAATCATCCTGTCTGCATAGATGATTATTGTCATGCTAGTCATGCTGTATTTGATCTACTGCATCAGAAAATTAGAGACGTGTTGTGCTAGGAAGGTCAAAGCACTGATGTTAATCATTCAAACTATAAGCGACTAGAAAAATACATGAAAAATAAAAGTAAACGCAATAAAAACAGTAAATGCATGCAGAAAATGACACAAAACATCAGCTACTGTTACATTATAAGCTCTGAATGTTTAATTTAGGACGCAGAGACAGTTTAAAGTAGGCAGACTGACAATTAAAAGTGTATGTGCTGTATAATTCCCCCATGTGTGCAGTGTGTATGATGCGCAGTGTGTTGTGTTCCTCCAGGAGAGCAGTCAGCGGGAGATGGAGGAGAGCTGGGCTGTGTTCGCGGATCTGCAGCGGCTGCTGGAGCAGTCTCAGGCCGAGCTGCTGGAGCTCATCGCCAGCCGGCAGAAA[C/T]AAAGCGAGCAGCAGGCCAAAGATCTGGCGGCCGGTTTGGAGCTGGAGCTCAACACACTGAGGAAGAGGAGCAGCGAGCTGGACGCCCTCGCCCAGACGCAGGACAGGGTGCTCTTCCTGCAGGTCTGCGCACTTATCTACAGAGTTCTTGCATTTTTTAATTTGTTTTATTATGTATTCTTTTATTTCTGTTGATTTAATTTTTTTATTTATTTTATATTTATTTGATATATATTTAATCTTATGTTTATTTATTCGTTTTGTTATGTATTCTTTCATTTTTTATTTATTTTATGTTTATTTATTTAATTTATATTAAATTTTTATTCTATTTGTTTATTTGTTTTATTTTTTAGTCTTTTATTTTTCATTTATTTGAATCTTTTAGATTTTATTTGTTTTATATATTTTTATTTATTTTATATTTATTATTAGATATTATTTATTATATACCTAATATAAGGTTTGTTTAAAAATTTTAATATGTATTTTTATTCTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41091
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000050357 Nonsense 403 562 8 8
ENSDART00000110769 Nonsense 403 562 8 9
Genomic Location (Zv9):
Chromosome 7 (position 76686671)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 73462566
GRCz11 7 73684679
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATCCTGCCACGGCTCAGCGTGATCTCTGTCTGTCTGAAGATGGGAAG[C/T]AAGTGCGCTATGAAGAGCAGCGTAAAAACTCCAGCAACTCCGACACACCG
Long Flanking Sequence:
ACAGTTCCTCCCATTGGATGTGCTTCTTCTTCTTGGTGGTTGGCTGACATTACTCCAAACACTTGCTGTCTTGGTCACAGATGTGTCAGCGAGATGCACACCAACAATCTGTCCTCGTCTGAACTCTGATATGTCACACACAATGTTGTGTACATTATGTTAAGCAAAGCTGTGCTATTTCTCTGGTATTGAAGCCTATAACTCTGCTTTTACTGGTGGAGTGAAGAATCAGTGTCGATTGGCCAGCAGGCTGCTCAGATTTAGCCATCAAACCTCCAACACTAAACTGGCCAGTGTTTCAGTTTCATTGCTCTACCCCTGTATCGGTGGTTGTTTTATAGAATAAACCCTTTAGTCAGCTTTATTCTGCCAGAACGACCGGCGGGATGTACATTATCCCTTACATTATCCCTTCCAATGATCTCCGTCTTTCTCTAGGTGAGCTGATTTTGGATCCTGCCACGGCTCAGCGTGATCTCTGTCTGTCTGAAGATGGGAAG[C/T]AAGTGCGCTATGAAGAGCAGCGTAAAAACTCCAGCAACTCCGACACACCGCGGCGCTTCAGTCCAGCTCTGTTCGTTCTGGCTCGTGAGGGTTTCTCCTCCGGCAGACACTACTGGGAGGTGGATGTTGGACACAAGACAGCCTGGACCGTGGGGTTGGCCCGAAGCTCGGCGAGACGCAAGGGAGAAATCCGACTCAACCCTGAAGGTGGATTCTGGTGTTTGTGGCTGAAAAACGGAGAAGTGAAAGCGCTGACGGGAAGCAGAGTGGCGCTCCATCTGACCTCGCTCCCCCAGAAACTCGGCATCTTTCTGGATTATGAAGCCGGTCAGGTGTCCTTCTACGATGTGAAGACGCACACTCACCTGTACACATTCATCGATGCGTTCACTGAGAGCGTTTATCCCATATTCAGCCCCTGCCTCAACCAGGACGGCAAGAATCCCGGACCGCTGGTCATCACCGCCGTCAAACACAGCTGAGTTTCGGGAAATATCGTA
Associated Phenotype:
Not determined