ZMP
epb41
Ensembl ID:
ZFIN ID:
Description:
erythrocyte membrane protein band 4.1 (elliptocytosis 1, RH-linked) [Source:RefSeq peptide;Acc:NP_7
Human Orthologue:
EPB41
Human Description:
erythrocyte membrane protein band 4.1 (elliptocytosis 1, RH-linked) [Source:HGNC Symbol;Acc:3377]
Mouse Orthologue:
Epb4.1
Mouse Description:
erythrocyte protein band 4.1 Gene [Source:MGI Symbol;Acc:MGI:95401]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42730 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45577 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36150 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36151 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15697 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42730
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000039746 | Nonsense | 215 | 1534 | 7 | 27 |
The following transcripts of ENSDARG00000029019 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 28705490)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 26581264 |
GRCz11 | 16 | 26454706 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGGTGAAGATGTTATGCTTGGCGTGTGCTCCGAGGGACTGATTGTATA[T/A]GAAGATGGTGTAAAAACAAATTCCTTCTTCTGGCCTAGAGTGCTGAAAAT
Long Flanking Sequence:
CACCATGACTTTAAATTCTATACTGTACATTATTTCTGCTGAGTGACAAGACTTTTGTCTAAGCAAAGTCAGACCTTACTGTCCTAATGAAATAATTACAGATCAAGGCACGATCATATTTTATTTTGGTAAAATAAGCATAATCTAGAGGTTTTCGCCTTTCATTTAAGCCACTTCTGAAACCAAATAATTAATTAGAAGTCAAGTTATTATTTGTTGTCCCTAAAACTCCCCAGAGCCTCCCTGTTTATCCCTGTTTATTCTGTTTAGCCCTCCATGTTTAACCCCCCAATTTCTGTTTAACAGAGAGCTAATTTCTTCAACACATTTCTAAACATAATAGTTTTAATAACTAATCTGTATTAACGGATTTATTTTATCTTTGTCATAATGACAGTATTGTATTATTATTATTTTGTAAGGGGATGTTTGCTATGTTCACAGGATGCCAGCGGTGAAGATGTTATGCTTGGCGTGTGCTCCGAGGGACTGATTGTATA[T/A]GAAGATGGTGTAAAAACAAATTCCTTCTTCTGGCCTAGAGTGCTGAAAATCTCGCACAAACGCAACACCTTTCTTCTCAAGATGCGCCCTTCTGAGGTATTCAAACACTCATTTCACGTTTTATAGCAAGTGTCTTGTATTTGCTGTATGTGTTAGTTTTGGGTAGTTTTAATTATATGTATTTTTATTATTTACAAACCCTTGGGTTTTAGTCTTGCTAATGTGTGTTAATTTTTTCAATTTCACTCTGGTTAAGGAGGATGCGTCTGAGGGTAACCTCAGCTTCAGTTTGGCCAACTACAGAGCCTGCAAACAATTGTGGAAATGCTCTGTGGAACATCATAGTTTCTTCAGGTAGGGCTTCATATGCATGTGGGTAAGATTTAAAGGGGCAGTTCACCCAAAAATGAAAATTCTGTCTTATTTACTTATCCTCCAGTTGTTTCAAACTTGTCTGAGTTTCTTTCTTCTGTTGACCACAAAAAAAGATATATTGTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45577
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000039746 | Nonsense | 820 | 1534 | 16 | 27 |
The following transcripts of ENSDARG00000029019 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 28719666)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 26595440 |
GRCz11 | 16 | 26468882 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGAAAAGAGGAGCGAGTGATTGAGGTGATGACGGTGAGCACTAGAGAA[C/T]AGATAACAGTACCAGAGACGAAGAGAATCAGCGTAACACAAATCCCACAG
Long Flanking Sequence:
AAGACGACTGGTTTGTTGTTTTGGATGGATCTCCAAAAACGTCAGGTATACATGGTAACACACAACCAGTATTGTGCTCTTATGTAAAACATATAAGCATGATGGGTTGTTTTTGTTTTAGCGTCCACTGTGAAAAGCACATCTGTTGAGTTCCACGAAGAGACCAGAGAGGAGGTGATTCAGAGAACAGAGCAGAAACTACAAGTGACCGTACAAGACAGGAGACCACAGCCAATCACTGTGGAGAAGAGGACAACACAAGCAGGAGATGTGGAGGACGACTGGTTTATCATTTTTGATGTTTCTCCAAAAGAAACAGGTACACACACACTCACACGCATAACTAAACTAAAATGAAACATTATTCATCCACTGTGTCTATGTTTTTAGTGCGAGGTCCAGCTGTTGAGGTGTTTGTGGAGAGCAGAGAGCAGGAGATTCAGAGCAGAGTGAGAAAAGAGGAGCGAGTGATTGAGGTGATGACGGTGAGCACTAGAGAA[C/T]AGATAACAGTACCAGAGACGAAGAGAATCAGCGTAACACAAATCCCACAGTTTCCAGTGGAGCCCAGAGACATTGATGACGACTGGTTTCAGCTTTTTGACAAAGTGCTTTATGAGGAGGAGAGTTTTCCATCAGGTAAAGCATCACACACGCATTTAAACACTATCATGGGTGTGTAGCAATAAGAATCCTATATAAAATGACTGGAAACTTTAATAAAAGTTTTGGTTAACACTTTATAACAACTTCACAATATAAAAGATTTATTAATCATTAGCAAATAATGAATTCATTATTTGTTAACCATTAACTCTAAATTAATAAACGTTAGTAAGCCGTTTATAACAGCAGCTACAAATGCTGTATTCTTGACTTACAACCACATTTATAATGTGCTTAATAATTGTACTTTCATACTTTGTTAATGATTTATTTATCATTACTAAATTAAGTATTGCATTATTTACTAACCAGTGATTTAAGAGTAGTTGGTGTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36150
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000039746 | Nonsense | 1042 | 1534 | 19 | 27 |
The following transcripts of ENSDARG00000029019 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 28730052)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 26605826 |
GRCz11 | 16 | 26479268 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTTTTTCAGTGCAAGGTCCAGCTGTGTTTGTGGAGAGCAGAGAGCAA[C/T]AGATTGAGAGCAGAGTGAGAAAAGAGGAGCGAGTGATTAAGGTGATGACG
Long Flanking Sequence:
ACCGCATTCCTAAGGACTGTTTGGCGAAATATTTGACTGCATGTCACTGCATATCAAACGACTGAAAAGATATAACATAGAGAAATCTCCACTGTGCTGAGCGAGAGCGCTTCTCTACTGAACAGCGCAGCATCGATGACGTAAGCGTGCCCAGCCCTGATTGTGGTGTGAGTGCGGGCCGTCGGGGGAGACGAGAGGGGGGAAAAGTGTGCTTTGGCCCGGTTCGAGGCAACTGTACATAGTGTGAGTACGGCCTAACATTGCCCAATATCTGATCCCCTGATCTATCTGACACAAGTTACATGTTAACGTCTCACACCATGATAATGAGGAAGCAAGTATGTGTGTCTGGGATGTTCTCAGTTGGCACATATATGGAAAGAATATTGAACTTTATATGTGATATGTGCACATATGAACCAAAAAATAAAATGTTCATCAAAAATTGTGTTTGTTTTTCAGTGCAAGGTCCAGCTGTGTTTGTGGAGAGCAGAGAGCAA[C/T]AGATTGAGAGCAGAGTGAGAAAAGAGGAGCGAGTGATTAAGGTGATGACGGTGAGCACTAGAGAACAGATAACAGTGACGAAGAGAATCAGCGTAACACAAATCCCACAGTTTCCAGTGGAGCCCAGAGACATTGATGATGACTGGTTTCAGCTTTTTGACAAAGTGCCTTATGAGAAGGAGAGTTTTCCATCAGGTAAAGCATCACACATGAATTTAAACACTGTCACAGTTGTATAGCAATAGTAGTAAAAAATCATGTTCAAAGACATAATAAAAGCAACAACAAACATTTGTGAAGATACAGGCCAGATCAAAGATTATGTGAACCTCTAGATAAGGAGAAACAAACAGTCTAACATCATCAATAATAATGATTGAAACTTTTAGTGATTTTTGCTAAAATAAGAAAAATCACCTTTTAGTAACAAGATGAGGGTGAGAAGATAATGAAAAATCATAATATTAGAAATAAAACAGAAAGTGTATTTTTGCTATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36151
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000039746 | Nonsense | 1354 | 1534 | 22 | 27 |
The following transcripts of ENSDARG00000029019 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 28733888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 26609662 |
GRCz11 | 16 | 26483104 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGAGGAAAGAGCAGTGCAGCTGCAGACAGAAGTGGAGGATGACTGGTA[T/A]ATGCTAATGGGCATTACCCTCAAAGATTACAGTACGTATTATGGGAGATT
Long Flanking Sequence:
TTATTTTCAAACAAAATGTAACGTCCCATGACCTTGGCCTACTGGGAAAACACGAATACAATTAAACTCAAAGCACATATTATTGGCAAATCCCAGGAACTTTTTTTTTTTAAGGCGCAAACAATTATGTACTAAAATCGAAAAATTTCCCCTTTTGTATCATGCATGCCAGACCTATTGGAGTTTATTATATAAATGTTTAGTTAAAAGCCTCCATTTTCTATTTTTAAAGTTGTGGCAGATGTCCTGAAAGTGGAAAGGATGGCTGAGGAACAGAAGGGAAGAGTAGAGGAAAGGAAGTGGATATTGGAAGAAGAGAGGAGGAAACTGGAGGAAGAAAGAAGGTTGCTGGAAAAAGAGAGGAGGAGACGAGAGGAAGAGATGTGGAGACGAGAAGAAGAGAAGAGAATTCAGATCAAGGCAGAGGAAAGACTGAAAAGAGCAGCCGTGTCAGAGGAAAGAGCAGTGCAGCTGCAGACAGAAGTGGAGGATGACTGGTA[T/A]ATGCTAATGGGCATTACCCTCAAAGATTACAGTACGTATTATGGGAGATTAGAAATCCTCGATAATAATTTGTAAAAAAAATTATGTACTTTACAAATGTATTCTCCTGTAACATGTCTATTCTCTTTCTGTAGTTCCAAGTGCGCCATCAACACCAGTTATTTCCCCAGTATCTCTGCCTAAACTCCGCCCACAGATCCCTGTCGACCAACCGCTGACTTCTACTCCAACCGCACAATCTGCGTCCATTACAAAAACTTATAAGGAGAGGACGAAAGACATACTGGACATCACAGTGGAGTCTGAGGTTAGAATCACGTACCCACAAAAACAACATGTGAAAATATTCATGTTTCAATATACTAAAATCATGTTTCTCTTTCTCCACAGGCTGAGACCGAGTCATCGCTCATGAGGAGGGTGAGCTACTCATCCATTTCTGTCATATTTCTCCTTTCTTATGCATATTAAAACATAATCTTATTTTTATTTCTTATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15697
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039746 | Nonsense | 1407 | 1534 | 23 | 27 |
The following transcripts of ENSDARG00000029019 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 28734150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 26609924 |
GRCz11 | 16 | 26483366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CYGCTGACTTCTACTCCAACCGCACAATCTGCGTCCATTACAAAAACWTA[T/A]AAGGAGAGGACGAAAGAYATACTGGACATCACAGTGGAGTCTGAGGTTAG
Long Flanking Sequence:
TGGCTGAGGAACAGAAGGGAAGAGTAGAGGAAAGGAAGTGGATATTGGAAGAAGAGAGGAGGAAACTGGAGGAAGAAAGAAGGTTGCTGGAAAAAGAGAGGAGGAGACGAGAGGAAGAGATGTGGAGACGAGAAGAAGAGAAGAGAATTCAGATCAAGGCAGAGGAAAGACTGAAAAGAGCAGCCGTGTCAGAGGAAAGAGCAGTGCAGCTGCAGACAGAAGTGGAGGATGACTGGTATATGCTAATGGGCATTACCCTCAAAGATTACAGTACGTATTATGGGAGATTAGAAATCCTCGATAATAATTTGTAAAAAAAATTATGTACTTTACAAATGTATTCTCCTGTAACATGTCTATTCTCTTTCTGTAGTTCCAAGTGCGCCATCAACACCAGTTATTTCCCCAGTATCTCTGCCTAAACTCCGCCCACAGATCCCTGTCGACCAACCGCTGACTTCTACTCCAACCGCACAATCTGCGTCCATTACAAAAACTTA[T/A]AAGGAGAGGACGAAAGACATACTGGACATCACAGTGGAGTCTGAGGTTAGAATCACGTACCCACAAAAACAACATGTGAAAATATTCATGTTTCAATATACTAAAATCATGTTTCTCTTTCTCCACAGGCTGAGACCGAGTCATCGCTCATGAGGAGGGTGAGCTACTCATCCATTTCTGTCATATTTCTCCTTTCTTATGCATATTAAAACATAATCTTATTTTTATTTCTTATTCACAGACATGGACGAAGAAAACTGAAGGAGAGAGCATTTATGTTCGTCACAGTATTCTGATGCTGGAGGTTTGTGAAATGTCTGAACTTTTGTATTTTGGGGGGATTTTCAAGTTTAATGATAATCCTACAAGACCAATCAAACAGATACACTTTTTTCTGAACTTATATTTTGGGTGGGGAAATGTAAAGTCAGACCTTACTGTCCTAATGAAATAATTAAAAATCAAGGCATGATCATATTTTATTTTGGTATAATAAGCGT
Associated Phenotype:
Not determined