Busch Lab

ZMP

btr01

Ensembl ID:
ENSDARG00000051965
ZFIN ID:
ZDB-GENE-090511-2
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 4 alleles of this gene:

Allele Name Consequence Status Availability
sa14479 Nonsense Available for shipment Available now
sa19552 Essential Splice Site Available for shipment Available now
sa32738 Nonsense Mutation detected in F1 DNA Not yet available
sa39670 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14479
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000073689 Nonsense 202 565 1 6
Genomic Location (Zv9):
Chromosome 1 (position 45520048)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 44363267
GRCz11 1 45064570
KASP Assay ID:
2259-0948.1 (used for ordering genotyping assays)
KASP Sequence:
AAGACTGACCTRATGYGTATTTGCGCAGTGTGTGCAGAGAGCGAACATTA[C/A]GGCCATACTGTGACRGAGGCCAAGAGAGAGATGAATATTCGGAAGGTAAG
Long Flanking Sequence:
CACAGCTTCTGCTCCTCGTGCATTTCCTCCTACTGGGAGGGCCAAGGAAAGACTTGCTTCTGCCCTCTGTGCAAAGAAAGCTTCCGTAAGCGCCCCGAGCTCCACGTCAATCACACGCTCAAGGAGATCACGGAGCAGTTCAAGCGGATGGCCGAGACCACAGTGAGCGTGCCTAAAACTGCAACAACAGATTCACCTCCAAACCCATTCTCTGCCCAGAAGCCTGGAGTGCAGCAAAGACCGGTTGAGCTGCCTAAAGGCCTGTTCCAGGAGATGAAGACCCGCATGCAGAGATCTTCATCAACATCCTCATCCAATGAGCCTTTAGCATCCGGCGATCCTCAGTCCCTCCCCAATGTCAAAATGCCGAGACGAAACTTTAGCGTGACCGCAGCGGGATCCAACGGGCCGCAGTGTCCCAATCACGGCTACAGTTTGGAGCTGCTCTGCAAGACTGACCTGATGTGTATTTGCGCAGTGTGTGCAGAGAGCGAACATTA[C/A]GGCCATACTGTGACGGAGGCCAAGAGAGAGATGAATATTCGGAAGGTAAGCACATTTATACGGTTGAAGTCAAAATTATTATTTTCATTTTTTTCAGATATTGCCCAAATTATGTTAAACAGAGCATTTTTTTACAGTATTTCATGTAGTATTTTTTCTTCTGAAGAAATTCTTATTTGTTTTATTTTGGCTAGAATAAAAGCAGCTTTAAATAATAATAATAATAAAAAAAAACAATTATGGTCAATATTATTAGTTCTCTTAAGCAATGTTTTTTATTTCGATAGTATGTAAACCATCATTATACAATGACTTGTCTAATTACACAAACTTACCTAAATAACAATGTTAAGCCTTTAAATGTCCCTTTAGGCTGAATACTAGTACAGGGTTTCTGCAGGGTCTTAAATGTCTTAAATCTCAAAATCCAAATTTTAGGCCTCAAATTGTATTAAATTTACTAAACTATTGTGTTGTAGGTCTTTACTCTTTTTTTAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19552
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000073689 Essential Splice Site 217 565 1 6
Genomic Location (Zv9):
Chromosome 1 (position 45520094)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 44363313
GRCz11 1 45064616
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTACGGCCATACTGTGACGGAGGCCAAGAGAGAGATGAATATTCGGAAG[G/A]TAAGCACATTTATACGGTTGAAGTCAAAATTATTATTTTCATTTTTTTCA
Long Flanking Sequence:
GAAAGACTTGCTTCTGCCCTCTGTGCAAAGAAAGCTTCCGTAAGCGCCCCGAGCTCCACGTCAATCACACGCTCAAGGAGATCACGGAGCAGTTCAAGCGGATGGCCGAGACCACAGTGAGCGTGCCTAAAACTGCAACAACAGATTCACCTCCAAACCCATTCTCTGCCCAGAAGCCTGGAGTGCAGCAAAGACCGGTTGAGCTGCCTAAAGGCCTGTTCCAGGAGATGAAGACCCGCATGCAGAGATCTTCATCAACATCCTCATCCAATGAGCCTTTAGCATCCGGCGATCCTCAGTCCCTCCCCAATGTCAAAATGCCGAGACGAAACTTTAGCGTGACCGCAGCGGGATCCAACGGGCCGCAGTGTCCCAATCACGGCTACAGTTTGGAGCTGCTCTGCAAGACTGACCTGATGTGTATTTGCGCAGTGTGTGCAGAGAGCGAACATTACGGCCATACTGTGACGGAGGCCAAGAGAGAGATGAATATTCGGAAG[G/A]TAAGCACATTTATACGGTTGAAGTCAAAATTATTATTTTCATTTTTTTCAGATATTGCCCAAATTATGTTAAACAGAGCATTTTTTTACAGTATTTCATGTAGTATTTTTTCTTCTGAAGAAATTCTTATTTGTTTTATTTTGGCTAGAATAAAAGCAGCTTTAAATAATAATAATAATAAAAAAAAACAATTATGGTCAATATTATTAGTTCTCTTAAGCAATGTTTTTTATTTCGATAGTATGTAAACCATCATTATACAATGACTTGTCTAATTACACAAACTTACCTAAATAACAATGTTAAGCCTTTAAATGTCCCTTTAGGCTGAATACTAGTACAGGGTTTCTGCAGGGTCTTAAATGTCTTAAATCTCAAAATCCAAATTTTAGGCCTCAAATTGTATTAAATTTACTAAACTATTGTGTTGTAGGTCTTTACTCTTTTTTTAAACAGGTCTTAATTTTCTTTTGTTCATGTATTGCTACCAAATCTGGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32738
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
ENSDART00000073689 Nonsense 254 565 3 6
Genomic Location (Zv9):
Chromosome 1 (position 45526046)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 44369265
GRCz11 1 45070568
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCTTATAGCTGTTTTATGTCTTTCGCTTGCTGTAAGGTGAATGCGGAA[C/T]GAGAGAAAGCAGGCACCATCAGTATGTTTGCTGAATTAATGAAATCGGTT
Long Flanking Sequence:
GAATCTATGCCACAAATGAGTAGGGCAGTTCTGAAGGTAAAAGGGGGTCCAAAACAATAGTAATAAGGTGTACCTAATAAAGTGGCTGGTGAGGGTATGTTGTATAAATGTACATATATGACACATATTATGTCGGTGAAATCCAAACATAAACTTTTATTTGCATATATTGTCAAATATATCAGATTTCTATATCCTGACAGACACTGACAAAATGTTATTGTTGATTCACACACGTTTTTCAGCAGTTCACTTTTACACAAAGTCTGACAAAGGTTTTAGGTTAAACAAGATGTGTGTGAATTTCTTTTCAGATTTTGGTTCTACAAAAAAAAGCCATATGGGTTTAAAAAACATGATGGTGACTTAATGATGCTATTTTTCTGTTTTTGATGATGGGTGATTCATAAAGAGAAATAAAACACATTTTACAGTTTCCTCATTCTCTTAATTCTTATAGCTGTTTTATGTCTTTCGCTTGCTGTAAGGTGAATGCGGAA[C/T]GAGAGAAAGCAGGCACCATCAGTATGTTTGCTGAATTAATGAAATCGGTTGAGAAGTCGCAGGCTGAACTGCTGGAGGTGGTGGAGATGGGACAGCGGGCCGCCGAACTGCGGTCTCAGGCCTTCATTCGTGAGGTGCAGACAGAGATCTCAGACCTGAAAAACAGATGCAGCACCATAAATCAGCTGACCCAATCCCAAGACCATCTTACTTTCTTCAAGGTAAACTGCTTTACACTTTTAAAAGGGATAAGTTGACTTTACATAGAAAAAGAGAGTGAACTCGCTGCTTTATAATTATTAAGTAAACAAACTATTTGCATAAAGTTAGATCAGTGAGTTTACTGCCTTTTTTTAAGAGTAAAATCAACATGTGGCTTTCATGGCAAGGTGTTTACTCACTTTTTGGAATGTACTGTAACTAATTGCCTTTTACAGTGTAGTTACTGATATAATCAGAGCCAGACAGAATCTGCAAACAGTTTTTAGCTATTTCTGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39670
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000073689 Essential Splice Site 377 565 4 6
Genomic Location (Zv9):
Chromosome 1 (position 45528394)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 44371613
GRCz11 1 45072916
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGATGGTGGAGGAGGTTCGACAAGGCCTGAGGAGACTCTCGGAGATCTG[T/C]AAGAGAAACTGCTCTTCAACTCATTGTAAAACATGATGTGATCAATAGGT
Long Flanking Sequence:
CACCAAGCCGCCCCTGTAAATGCATATGAAAAAAAAAATTCACACAGAAGGGCTAATCCCTGTCTTTAACTGTACATGCCTAAACACAATCTGCCTGCTATAGCAGCCACGTCCCAATCTTATGGTATTGGTCGAGCTGGAAAGTGATTGACATATTTGAGGAAATCACTGTGTTATAATGGTTCCCTTACAAGTAGAGATAACACCACGAATAAAACACTTTTAGCGGTTAAAAAAAGATAGACTTGCCTAAGAGAATTTATCCTTACATAAATAAGCTTGCCTACTTTGTTTTCACCATTGTTACTCCAATAAGTAGCCAATATTTCGCGTTTTGCTGTTTGTTTTCAGACATTTTCCGCCCACACTAGTTTACCAGTGATGAAGAGCTGGGCAGAGGTGGCTCTGACTCCTGACCCCACGGCAGGCGTGGTGCTAAGAAACGTCTCTCAGATGGTGGAGGAGGTTCGACAAGGCCTGAGGAGACTCTCGGAGATCTG[T/C]AAGAGAAACTGCTCTTCAACTCATTGTAAAACATGATGTGATCAATAGGTCGTGGCAACCTACACTGTAAAAAGTGCTGGGTTTCACACAATTCCTTCATGTTGTGTCAACACAAATCGATTAAGTTAACTGAATAGTTTTTACAAATTGAATGTAAATTGGATTGAACTTAAAACAATGAAGTTGTCCCAACAAAATCTCAAGAATTTTACCTCATTTTGAATAAGTAGTTTAGACAAGCAACAAAAATATTTTTTGAGTGTACGTTTTCACGGTCACTCCATCAACAAATTATATGACTTTAGCCTCAATAAACTCCTAATTTGCTGCTTAATTTTTATTATTAAGGTAGTTAGGTTTAGGTAGGATTAGAGATAAGTATAAAATAAGAATAACTATGCTGAATTTATACTTTATTAGCACTAAACTGCCAATATCAATAATAGGCAGGAAATAAGCCACTAGTTAAAAGTGAAAATTGCTTCTTGAATTGGTCCTTG
Associated Phenotype:
Not determined