Busch Lab

ZMP

btr26

Ensembl ID:
ENSDARG00000040860
ZFIN IDs:
ZDB-GENE-020620-2, ZDB-GENE-070705-377, ZDB-GENE-070705-378
Description:
bloodthirsty [Source:RefSeq peptide;Acc:NP_001018311]
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
sa29134 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39224 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa29134
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000007454 None None 559 None 7
ENSDART00000059894 None None 532 None 6
ENSDART00000092911 Essential Splice Site 365 557 6 8
ENSDART00000105111 Essential Splice Site 134 326 3 5
ENSDART00000147590 None None 532 None 7

The following transcripts of ENSDARG00000040860 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 19 (position 4859534)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 4133095
GRCz11 19 4063921
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTCAGTAAACTGAAGGACACTCTAAATGAGAAACTCAGTCAAACTGG[T/A]ATGTCAATATCAAATAAAATTTTATTTAAGTACTGGAGAATGAGTCTTAG
Long Flanking Sequence:
TAGCAAACTCCACTAATAATTTTCTGTCTGACCTGTTTGAGCAGATATACTCAGAAAAGGAGAAAGCAGCTCATGTGGAGATCTTCACTGATCTGATCCGCTCCATTGAGAGATGTCAGACTGAACTGCTGGAGATGATGGAGGAGCAGCAGAAAGCAGCAGAGAAACAGGAGGAAGAGCTGATTAAAGAGCTGGAGCAGGAGATCACTGAGCTGAAGATGAGAAACACTGAGCTGGAGCAGCTCTCACACACTGAAGATCACCTCCACCTCCTACAGGTCAGTCAACATCTCTCTGAGCAATGACACACCAGAACACTCCCCATGCTGAAGGCTTTCTCGTCTCTCTCTCCTGCTGTAGATTTACTCATCCCTGCACAGACCTACAGACACCAGGAACTGGCCTGAGATCAGTCTGAAGACTCAGGAGAATCTGGAGACTCTGAGAAGAGCTTTCAGTAAACTGAAGGACACTCTAAATGAGAAACTCAGTCAAACTGG[T/A]ATGTCAATATCAAATAAAATTTTATTTAAGTACTGGAGAATGAGTCTTAGCTGAAATAAGAGTATATGACAGTGTTTGATCATGTATTTGTCATTATCAGTAATATTATCCCTGTATTCCTAGTATTTTGAAGTGTTTACAATATAAATAATGTCTGTGTTCATTGCCACAATATATGAATTATTGAATATCTGCATATGTTGAGTCATTCACTAAATTACATCTGATGCATAAACAGAAAGCTGCCCGATTCTCTATAAATCATACATTGATCAGATGTAAATGTGATGTTGCACAATATTCCTAAAATATAACCTTAAGTTTTGTGTAATTTCACACATGAAAACATCTCAAAGATCTCCTCATGTTTTATTGTCATCAGTGTCTGCAGAGCTGAAGTGGATGCAGCAGTATGCAGGTACAGTGTGCTGAACTACACTAGTCTACACTCAGATTCAGTTCAATTTAATACAATTCATTTCAGTATTATTTGTATAGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39224
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
ENSDART00000007454 None None 559 None 7
ENSDART00000059894 Nonsense 195 532 2 6
ENSDART00000092911 None None 557 None 8
ENSDART00000105111 None None 326 None 5
ENSDART00000147590 Nonsense 195 532 3 7

The following transcripts of ENSDARG00000040860 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 19 (position 4864039)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 4137600
GRCz11 19 4068426
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCTGTTCTCTGTCTCTAGACTGAACTGATGAAGACACAGAAAGACGTG[C/T]AGCAGATGATCGAGGACAGAATCAAGAAGATTCAAGACATCAAACACTCA
Long Flanking Sequence:
CTGATCTCAAGATTAACACCACACTCAGAGAGATCTCTGAGCACTATAAGGAGAAAAATCCTGCAAAAAAGCCAAGAATTATGTGTGAAATCTGTGAGGGCAGAAAGCTGAAAGCCCTGAAGTCGTGTCTGGTGTGTCAGAGCTCTTACTGTCAAACTCACCTGGAGCCTCATTTGAGAGTGGCAGGATTAAAGAAACACAAACTGATGGATCCTGTGAGGAATCTGGAGGACTATATATGTCAGAAACACGACAGACCTCTGGAGCTCTTCTGTAGAGATGATCAGACGTGTGTGTGTTCATTCTGTACTGTGAAAGATCACAAAAACCACAACACTGTTCCTCTAGAAGAGGATATTGAAGAGAAGAAGGTAGACAAGGCTGAGGCTCATATTATGGGGAATCAAAGTCTGAATGCAGATTGATTTTCTTCAGTAAATCTGCTAAAAATACCTGTTCTCTGTCTCTAGACTGAACTGATGAAGACACAGAAAGACGTG[C/T]AGCAGATGATCGAGGACAGAATCAAGAAGATTCAAGACATCAAACACTCAGCAGAAGTCAGAAAAGTGAGTTCATAAAAGATTAATATAAATGATACATGATTCACTCTAGTTCAGCAAGAGTCCAACAGTACTGAGAGTTTCAGTGTCCTCCACTGGTCTGTTTATTTCAGACAGTTCGGACCATCAGTTTATGTATGCGATGGGTTTGGAGAGTCACTCTTTCTATAAGTTACTTTGTTAGATCTGTTACTAGTAAATAAAAAAGGACGTAAACTAGTGAGTGGGTATGCAGCAACTGTCCAGACTGTAATCAGGGTATATGGAGAATACTCACAGACAGAATTCCAGGCTTTGTACAGGACAAACAGCTTACAGTCAAAAACGATGGTAAAGGCTTTGGCCAGGGCAGGCAGCATACAATCAAAAACAAGGAATCAGGCAGTAGGAAAAAGAAAAGCAGTCAGAATACACAAGAAATGCTCAGAAATGTAAGCAAAA
Associated Phenotype:
Not determined