Busch Lab

ZMP

si:ch211-119b12.6

Ensembl ID:
ENSDARG00000031506
ZFIN ID:
ZDB-GENE-041210-312
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5RG90]
Human Orthologue:
FLVCR2
Human Description:
feline leukemia virus subgroup C cellular receptor family, member 2 [Source:HGNC Symbol;Acc:20105]
Mouse Orthologue:
Mfsd7c
Mouse Description:
major facilitator superfamily domain containing 7C Gene [Source:MGI Symbol;Acc:MGI:2384974]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa15497 Nonsense Available for shipment Available now
sa12161 Nonsense Available for shipment Available now
sa18148 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa15497
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
ENSDART00000038696 Nonsense 309 495 4 11
ENSDART00000142092 Nonsense 277 465 4 9
ENSDART00000038696 Nonsense 309 495 4 11
ENSDART00000142092 Nonsense 277 465 4 9
Genomic Location (Zv9):
Chromosome 20 (position 46575703)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 46420986
GRCz11 20 46324706
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTYTATGCTGTCAGTACACTTCTCAACMGGATGATCATTGAACACTA[T/A]CCTGTAAGTCCCTCCCACTCATCAGCTATCCGGCCAATTATGAGAGCTCT
Long Flanking Sequence:
AAGAACATTTCAAGTTTTGCATGGTACTATATATATGCATGGTACTATATATATGACATGCATTTTAGTTATAGATGCAGGCGCCAATGTCAATAAACAATTACCATATATCACCTCCAAAAAAAGTTAAAGTCTATTTTAAACAGAAAAACTGCTCGATTGCTTTTTTTCACAGCCAGCATGAACTATATTACCTAACTTTATGGTCCATCTCTGCACACACAGACACCTGTGTAAAACTGGCATGGCAAGCCTGTAGCTGCATATAACCTGGCTGAACATTGACAGAAATAATGCTGCTGGAATTCAAAGCTCTTTATATATTTACAGCTGCTTCAGAAATATCACGACGCTCAGTGCTTAGCAGATGTACATCAGATCAAGTCTTTTATTTTAAACACTTTCAATAGTTCTGAACTCTTCTGTGTTTCCTCAGGGCTGAATGTTGGCTGTTTCTATGCTGTCAGTACACTTCTCAACCGGATGATCATTGAACACTA[T/A]CCTGTAAGTCCCTCCCACTCATCAGCTATCCGGCCAATTATGAGAGCTCTTGACCTGCACCGAATTTACACAATAACTGAAGGGATTTCAGTGATTTATGACTGTGATTAGGAATAATGGTGTTTGTTTTTTAAACAATACACCTAAAGATCATTAAAATCTTAGGTAATGCCATGCGTTTACAACCTCATAAGCATGTTGAAATGTAACTATAAAAACACTAACCTGGTCAGCGCAATAGCCTAGTGGTTAGCACACTAACATATGGTGCGGTAGCATTTCAGGGCTCCCCGAGTTTGAATCTCGGCTCGAGGACGTTTCCCAACCCCACTCCCCTCTCTATCCCATTTCGATTTCTGTCTAATTACTAATTACTGTCTAATCTATCTAATAAAGGCACTAAGGCCAAAAATAAATATTTACAAACAATAAAACACTAGCCTAAATATACACAGCAAATTGCTTAATAACAGTTGTCATCACACTCCGTTACTTCTTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12161
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
ENSDART00000038696 Nonsense 309 495 4 11
ENSDART00000142092 Nonsense 277 465 4 9
ENSDART00000038696 Nonsense 309 495 4 11
ENSDART00000142092 Nonsense 277 465 4 9
Genomic Location (Zv9):
Chromosome 20 (position 46575703)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 46420986
GRCz11 20 46324706
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTYTATGCTGTCAGTACACTTCTCAACMGGATGATCATTGAACACTA[T/A]CCTGTAAGTCCCTCCCACTCATCAGCTATCCGGCCAATTATGAGAGCTCT
Long Flanking Sequence:
AAGAACATTTCAAGTTTTGCATGGTACTATATATATGCATGGTACTATATATATGACATGCATTTTAGTTATAGATGCAGGCGCCAATGTCAATAAACAATTACCATATATCACCTCCAAAAAAAGTTAAAGTCTATTTTAAACAGAAAAACTGCTCGATTGCTTTTTTTCACAGCCAGCATGAACTATATTACCTAACTTTATGGTCCATCTCTGCACACACAGACACCTGTGTAAAACTGGCATGGCAAGCCTGTAGCTGCATATAACCTGGCTGAACATTGACAGAAATAATGCTGCTGGAATTCAAAGCTCTTTATATATTTACAGCTGCTTCAGAAATATCACGACGCTCAGTGCTTAGCAGATGTACATCAGATCAAGTCTTTTATTTTAAACACTTTCAATAGTTCTGAACTCTTCTGTGTTTCCTCAGGGCTGAATGTTGGCTGTTTCTATGCTGTCAGTACACTTCTCAACCGGATGATCATTGAACACTA[T/A]CCTGTAAGTCCCTCCCACTCATCAGCTATCCGGCCAATTATGAGAGCTCTTGACCTGCACCGAATTTACACAATAACTGAAGGGATTTCAGTGATTTATGACTGTGATTAGGAATAATGGTGTTTGTTTTTTAAACAATACACCTAAAGATCATTAAAATCTTAGGTAATGCCATGCGTTTACAACCTCATAAGCATGTTGAAATGTAACTATAAAAACACTAACCTGGTCAGCGCAATAGCCTAGTGGTTAGCACACTAACATATGGTGCGGTAGCATTTCAGGGCTCCCCGAGTTTGAATCTCGGCTCGAGGACGTTTCCCAACCCCACTCCCCTCTCTATCCCATTTCGATTTCTGTCTAATTACTAATTACTGTCTAATCTATCTAATAAAGGCACTAAGGCCAAAAATAAATATTTACAAACAATAAAACACTAGCCTAAATATACACAGCAAATTGCTTAATAACAGTTGTCATCACACTCCGTTACTTCTTGA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa4345
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > A
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000038696 Splice Site, Nonsense 344 495 5 11
ENSDART00000142092 Splice Site, Nonsense 312 465 5 9
Genomic Location (Zv9):
Chromosome 20 (position 46580579)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 46425862
GRCz11 20 46329582
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGTGGGTTCCCTMATCTGTGGSATCTGGCTAGACCGATCGAAAACCTA[C/A]AAGTAAGAGTCTTWAATCCCRACATATTGTCCTTCAGTCATCAACATCGC
Long Flanking Sequence:
CGTAATCCAAAACGGTGATAAAATTTGTGTTTAGAAAATATAAAACTGATATAAACATTCAAAGCTTGCTGCCAAAATCAAACGACATTTTTTCACATCACCTCCTACTTTAGTTTCTCATCAAATATTCTGACCAATTAAATGCTCTCTTGTATCTGACATGCTCCACCCCTTATCATTTGCTTTTCATTTAATGTGCTTGAGCTCAACCACTCTCACTGGCAGAGCGGTGATAAAAACAAAACACTATTGGCTGTTTTTTAAAAGGGGAGGAGCTACTTTGTCCCGCCCCCTTAATTTTTCATTTGAGATTATATCAAACATCGAATAAAAAAAGCACAGTTCAAAGCACTTTACAGGACATAAAAAAGCATTGAAAAGTCTCTCTGGTTTTAACAGGGCGAGGAGGTGAATGCCGGCAGGATAGGCCTCACCATCGTGATCGCTGGCATGGTGGGTTCCCTAATCTGTGGCATCTGGCTAGACCGATCGAAAACCTA[C/A]AAGTAAGAGTCTTTAATCCCGACATATTGTCCTTCAGTCATCAACATCGCTCCATTAACGCTTGTCTTCATTTCCTCTGTGCTATCAGACTTTCCCCCCTGTGGGTCTGCTCATGTGCTTTGGTTTAGTGTGTTTGCCCAGGTGTTTGCCTCTTTGACCCAACAAGCTCTGTGACCTTTTGTTTAAGTGTGTTTGGCCTGTCACTGCATGTCTTCCCCTCCTGGACATTTGGATGTTTCTGTTTTTTAGCTGAATGAGTGACAATGTGTGCGTGTGTGTGTGTGCGTGTGTGTGCGTGTGTGTGTGCGTGTGTGCGTGTGTGTGCGTGTGTGTGCGTGTGTGTGTGCGTGTGTGTGCGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTCTGTATTTATGTGTGTTTATGTGTATGCTTATGCGCACTTATGTGTGTATGTATGTATGTCTTTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18148
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000038696 Nonsense 469 495 9 11
ENSDART00000142092 Nonsense 437 465 9 9
Genomic Location (Zv9):
Chromosome 20 (position 46590648)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 46435931
GRCz11 20 46339651
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATCTCAGGCTGTATAAAGTCAGATCTGCGCAGACAGCTGGCAAACCAG[C/T]AAGCACAAACTGCTGTAAGTATCAAAGTATCCAACCAGAAGGTCATGAAG
Long Flanking Sequence:
TTATATTATATTATATTATATTATATTATATTATATTATATTATGCATTTTTAACTAAGTAAATATTTAATTTAAACATAAAACATTGATTTTATGATAGGGCATATATAGTATATAATATAATTTAATATGTAATAAAATACAATTGTTTAATATACAGAAATTGTATTTGATAATTAAAAAAAACTCAACCAAACTGTGATGTAATAAAAGTTATTTTACAATGCATAAAATAGACTATACATATTTTAGATATATAATATAAAATATATTTATTTAATATTATTTAGTCTTTTGGGATGTTATCTGACCTGAGCATGCTCTTTGAGGGATTCATTTGTTTAATATTCGTTATTTAATGATTAATCAGATGAAGCACAGCCCGCAGGTCACATTAGTCCTCTTAGTTTCAAGAGTATATTTTTACGTGTCTCATTGTGTTTCTTTTCTTTATCTCAGGCTGTATAAAGTCAGATCTGCGCAGACAGCTGGCAAACCAG[C/T]AAGCACAAACTGCTGTAAGTATCAAAGTATCCAACCAGAAGGTCATGAAGACTTTATACTTATCAGATAAAGGCGTGATGGCAGATTAAAGGCCCTGATATACGCACTATATATTGTTTGTCAATGATATTGTTCGGGTCAATGATGAGACAAAGCATTTTGGATTGTGCATCAAATAAAATTGGCAAAAATTATTTGTTTTGAATAGAAAATAAACAAGTTTTGACTTGAATGTTTCAAATAAAAAGGCTTTTTCCTGCCTCAAAATGAGGCGATCAAGACATTTTTGCGACTAGAGACAAAAACATTTAGCATTTTTCTCATAATCTTATTATGTAAAATATTATCTAATTCAAAAAATGTATTATTAATTAAATTTAATCAAATACATGACCAGTGCTTGAGTTTGGGATCTATCAATAGCCATTACTGCCTTTCTCATTTTTGTTAAAAGGCAGAGAGGGATTGAATTGATTATTTCAAATAACTTCAGTGACAAA
Associated Phenotype:
Not determined