Busch Lab

ZMP

epb4.1l4

Ensembl ID:
ENSDARG00000040087
ZFIN ID:
ZDB-GENE-990415-20
Description:
Band 4.1-like protein 4 [Source:UniProtKB/Swiss-Prot;Acc:O57457]
Human Orthologue:
EPB41L4A
Human Description:
erythrocyte membrane protein band 4.1 like 4A [Source:HGNC Symbol;Acc:13278]
Mouse Orthologue:
Epb4.1l4a
Mouse Description:
erythrocyte protein band 4.1-like 4a Gene [Source:MGI Symbol;Acc:MGI:103007]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa18493 Nonsense Available for shipment Available now
sa41567 Nonsense Mutation detected in F1 DNA Not yet available
sa31759 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa18493
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000058627 Nonsense 56 618 2 24
ENSDART00000123842 None None 603 None 21
Genomic Location (Zv9):
Chromosome 10 (position 1825645)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 1771111
GRCz11 10 1798825
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAGTGMTGGACTATGTGTTCAGTCAYGTGAACCTCGCAGAAACGGAGTA[T/A]TTTGGGCTTCGCTATTGCGACCGCAGCCATCAGACGGTGAGKTTTACAGT
Long Flanking Sequence:
AGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGAGCCAAGTATCGAACCAGCGACCTTCTTGCTGTGAGGCGAACGTGCTACCCACTGCACCACTGTGTCGCCCAATAAATAAATAAAGATATAATTTTTGTTTATTAATTCTTAGAGTAATATAAACAATATAAACATTGTATATATAATATAATACAAATTAATTAATGTTTTTTTGTGTTTTATGTACAGTATGTATGTGTATTTGTGTGAACATTATGTATGTGTATTTATACATGTATAAATCTACACAGTGCACATGTGTGCATATGTACATTATTTAAATAGAAGGGAAAGGGAAGGGAAAATGATTGTTTTCTTTTTCAAATATTTCCCAAATGATGTTTCACAGAGCAATGAAATGTCATCTAATGCACATTTCACCTGTTTCCACAGAAATCCACCAGGGGATGTGTAGTGATGGACTATGTGTTCAGTCACGTGAACCTCGCAGAAACGGAGTA[T/A]TTTGGGCTTCGCTATTGCGACCGCAGCCATCAGACGGTGAGTTTTACAGTAATTACACACACACACACACACATATATATATATATATATACATATATATATATACACACACACACACTCATATACGCACACTTTATTAGGTACACCTGTCCAACTTCTGGTTAATTGAACCGAGCATCAGAATGGGAAAGAAAGGTTGTTGATGCCAGATGGGCTGGTTTGAGTATTTCAGAAACTGCTGATCCACTGGGATTTTTACGCACAACCATCTGTACGTGCCAAAGGTCAAAGAAGAATGGCCAGACTAGGTCCAGCTGACAGAAAGGGAACAGTAACTCAAATAAGCACTTGATACAACCAAGGTGATGCAACCAATTGAGCATCATGTCAACACCACAGCCTACCTGAGTATTGCTGCTGACCATGTCCATCCTTTTATGGGCACAGTGTCTCCATCTTCTGATGGCTACTTCCAGCAGGATAACACACCATGTCACAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41567
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
ENSDART00000058627 Nonsense 221 618 8 24
ENSDART00000123842 Nonsense 153 603 6 21
Genomic Location (Zv9):
Chromosome 10 (position 1802100)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 1747656
GRCz11 10 1775402
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATACATGTATTGTGTGTGTGTTTTTTCAGGGAGAAAAGCAGGCAGAGTA[T/A]TTCCTGGGACTTACGCCGGTCGGGGTCGTGGTTTACAAGAATAAAACCCA
Long Flanking Sequence:
AGTCCAAACACATGTGGTACAGGTGAATTGGGTAGGCTAAAATTGTCTGTAGTGTATGAGTGTGTGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATGCGCTGCGTAAAAATGTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTATTAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATGAATGATGCTTACTGTTTCAGCTGTGTTCATTATTTAAAGGGACAGTTCACCCAAAATTGGATACTTACTTACTATTTTAGTCTACCTCAAGTGCTTCCAAACCTACGTGAGTTTCTTTCTAGACAAAAGAAGATATTTTAAAGAATGTTCCGAAACTGTAACTGTTGACTTTCATAAAAACAAAAACTATGGACGTCATTTATTTGTTTTCCATACTGTCTCAACTTGTTCTTATTCAGGTTATACATGTATTGTGTGTGTGTTTTTTCAGGGAGAAAAGCAGGCAGAGTA[T/A]TTCCTGGGACTTACGCCGGTCGGGGTCGTGGTTTACAAGAATAAAACCCAAGTGGGGAAATATTTCTGGTGGGTTGATGTTTAAACCGAATGGTAAACATAGTGAGGAAATAAATCAGTCAAAGATTGTCAATATTTACTCACTCTTGTGTTTTCCCAAAGTGTTTTAGACATCTTTTTATCCTGTTTTGACTCACACTTTTGCACACAGGGCTATGGAGGTTTGGATTTTGTTTCTGCTTAATATTTGAAACCATATCTTTGACTAATATTTCAATTTGTTTGATGATCTGTAACATTAAAGTGTGACAAACATGCAAAAATATATATATATATATATATATATATATGGAATGTGATATTGTATTATAAGATGCAATACTGCATGAAATTATATGTGACATGCTATACTATCATATACAGTTGAAGTCAGAATTATTCGCCTCCCTTTGAATTTTGTTTTTCTTTTTTAAATATTTCCCAAATGATGTTTAACAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31759
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000058627 Essential Splice Site 361 618 13 24
ENSDART00000123842 Essential Splice Site 293 603 11 21
Genomic Location (Zv9):
Chromosome 10 (position 1786091)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 1731647
GRCz11 10 1759393
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGCTCTCTGCACACAATAGCACTCATGTTTCGGAAATGTGTGTTTA[A/C]GGGCGAAACAATGGAGGTCAAGCGGTCACAAAGATGGAGAACACGAGCGA
Long Flanking Sequence:
AACAAAGCATCTGATTCTTGCAATGTTTCTGAGATGACAGTATGCTGATTTAGCTTTGACATGACTATTGAAACTCAGATCTGACTCCAGAATCACTCCAGAAATGCACTCAAGACACTAGTGTTCAGCTTTAAGTGGCATTTAAAGGCTTAACTAGGGTAATTAGGGTAAAGTTAGGGTAATTAGGCGAGTCTTTGTATAACAGTGGTTTGTTTTGGAGACAATCCAACACTAATATTACTTAAGGAGGTCAATAATTTTTACCTTTAAATGGGCTTAAAACGATTTAAATCTTCTTTTATTCTAGCCGAAATCAAACAAATAAGACTTTCTCCAGAAGAAAAAACATTATAGGAAATACTGTGAAAAATTCCTGAATCTGTTCAACATCACTTGGGTAATAATTTTAAAAGTGTGTGTGTGTTTTGTGGATGGAGACAGTAGCATCAGATGGAGCTCTCTGCACACAATAGCACTCATGTTTCGGAAATGTGTGTTTA[A/C]GGGCGAAACAATGGAGGTCAAGCGGTCACAAAGATGGAGAACACGAGCGAAGGCCAGCCCAAAACCTCTGCACTGACACCGGTCAAGAGGTATTTAACCCTACGCTGAGTATTAAGTGATTACTGGCATCCAGAGGACAGCTTTATTACACTGTAGTCACACTTAAAAGGACAGTTCACCCTAAAATAAAATTAAAAACTGGCTCTTGTTCAAAACCTGTTTGAGTTTCTTTCTTCTGTTGAACACAAAAGAAGATATTTTGAAGAATGTTGAAAACCTGTAACCATTGAGTTCTGTATATGTTTTTTCCTACTATGGAAGTCAGTGTTCAACAGAAGAAATACATTTATAAGGGTTTGAAACCATTTGAGTGTTTCAAGTACTAATTTCGAGAGGATCACGTGCTTATGATTGAACACAGGTGGTCCCGCATTAGCTCCGTACATTTGCACCAATCAGATAAATACTGACGCACTATAAATTACCAGAGCTTTCTACTC
Associated Phenotype:
Not determined