ZMP
si:ch211-119b12.6
Ensembl ID:
ZFIN ID:
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.
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 |
|---|---|---|---|---|---|
| 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.
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 |
|---|---|---|---|---|---|
| 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:
sa18148
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:
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