ZMP
si:dkey-21h14.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein containing multiple scavenger receptor cysteine-rich (SRCR) domains similar to vertebr
Human Orthologues:
AC008735.1, CD5L
Human Descriptions:
CD5 molecule-like [Source:HGNC Symbol;Acc:1690]
Scavenger receptor cysteine-rich domain-containing protein LOC284297 [Source:UniProtKB/Swiss-Prot;Ac
Scavenger receptor cysteine-rich domain-containing protein LOC284297 [Source:UniProtKB/Swiss-Prot;Ac
Mouse Orthologues:
A430110N23Rik, Cd5l
Mouse Descriptions:
CD5 antigen-like Gene [Source:MGI Symbol;Acc:MGI:1334419]
RIKEN cDNA A430110N23 gene Gene [Source:MGI Symbol;Acc:MGI:3606211]
RIKEN cDNA A430110N23 gene Gene [Source:MGI Symbol;Acc:MGI:3606211]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2159 | Nonsense | F2 line generated | Not yet available |
sa40238 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40237 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20224 | Nonsense | Available for shipment | Available now |
sa40236 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26244 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2159
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000135511 | Nonsense | 907 | 5840 | 10 | 57 |
Genomic Location (Zv9):
Chromosome 4 (position 10182085)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11118712 |
GRCz11 | 4 | 11117561 |
KASP Assay ID:
554-2837.1 (used for ordering genotyping assays)
KASP Sequence:
TTCTTYATAATCAGACGTGGATGTCAGTGTGTGAYGCTGCCTTTGACCAG[C/T]AGGATGCAGAGGTTGTGTGTAGAGAGCTGGACTGTGGGGCTCCTGTRCAG
Long Flanking Sequence:
GCCGTTGATATTTGGTTGGTTTTAGGCTGTGGCATTAACTAACTAAAATCCAACATCATTTTAACATCATTATATGGCATCCATACAACCTCAAAGTATAACATCAGTAGACGTCTATCTTTGGTTGGTTTTATGTTGTGCAATTACCTAACTAAAATTTGATGTCACTTTAATGTCATAATGTGACGTCCATTGTCAAAAATAACATCATTGGCCATTGATCTTTGGTTGATTTTATGTTGTCGTGAAGTAACTAAAATTCATCGACGTTGGTCGATTTTCATATACAATCAAAATTCAAAGTATGTCTGACGCTGGAGTCCAACATCAATCTTACATCTGTGTGATGATTGGTGCCTGCTGGGAATTTTTTTAATGTCTTCTTATCAATACTTCTGTGTATAGGAGTCCGTCTGGTAGGAGGTTCTCGCTGCTCTGGGAGTTTGGAGATTCTTCATAATCAGACGTGGATGTCAGTGTGTGACGCTGCCTTTGACCAG[C/T]AGGATGCAGAGGTTGTGTGTAGAGAGCTGGACTGTGGGGCTCCTGTACAGGTGACTTTTGACAAAGGAGATGGTCAGATGTGGACACAAGAGATTCATTGCAGAGGAGACGAGTATCAGTTTGCTCTCTGTGCAACGTCACCTTCACACTCTTGCTCTCATAGCAGCAGTGTGAGCATTGTGTGTGCTGGTAGGTGAACAATATAAATATAGTATAAGAATTGACATCAGCTATGAGTTCTGACTGGCACTCTTTTACCTTTAGAAACAGTGAGATTAGCTGGTGGCCACAGTCACTGCTCTGGTCGAGTGGAGGTTCTTCATGAGGATCAGTGGGGAACAGTGGAGGATGTTGCCTGGGATTTGACTGATGCTGCAGTGGTGTGTAGAGAACTGGGATGTGGAAAGGCTTTAAGTGCACCAAAGAGTTCTTACTTTGGCAAAGGATCAGGAAAAACGTGGATTTCTAATTTATGGTGTACTGGGTCAGAATCTTCTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40238
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 |
---|---|---|---|---|---|
ENSDART00000135511 | Nonsense | 1147 | 5840 | 12 | 57 |
Genomic Location (Zv9):
Chromosome 4 (position 10181019)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11117646 |
GRCz11 | 4 | 11116495 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACACTCAGATGTGGACACAAGAGATTCACTGCAGAGGAGAGGAGTCTTA[T/A]ATATCTTTCTGTCCAACATCTTCTCTCAAACACATTTGTACTCATGACAT
Long Flanking Sequence:
CTCTGGTAAGCTCATCTAGACTTTTTTGTCATGATTACTGATGTACTAGTTTTACATCAGGTGGTTGGGCAAGTTAATTTATTTTATGATATACATAATTATGACATGGAGAGTACAAAAATGTAGACAAAATGCATTCTGATGATGTGCTGTTTGCAGTTTTTCCTAAAATGTTCCATTAAATAAAATTAACTATTAGCTTATAATATCTTGGGATCAAAAGGTAATATGACAGGAATGGGAAATATCATTAAATTGCCCCTTTTTATTAAAGGAGTCAGACTGGTTGGAGGATCTCATTGTTATGGCAGAGTAGAAGTACTTTACAATCAGACGTGGATGTCAGTGTGTGACGCTGCCTTTGACCAGCAGGATGCAGAGGTTGTGTGTAGAGAGCTGGACTGTGGGGCTCCTGTACAGGTGCTGAGAGCTGCTGTTTTTGACAAAGGAGACACTCAGATGTGGACACAAGAGATTCACTGCAGAGGAGAGGAGTCTTA[T/A]ATATCTTTCTGTCCAACATCTTCTCTCAAACACATTTGTACTCATGACATTGGATTGTTATGTTCTGGTATTGGATCTATACCTTTGTTATTACTGATATAACCAATAATTAAGAAAACATAATTATTTGGATTATTACATACTGTTTTAACCTGTTCTTGTCCAGGTTACACTGACATCAGACTGGTCAATGGTTCAGACTCTTGTTCTGGAAGAGTGGAGCTTCAGTATCTGAGTAAATGGGGCACAGTGTGTGATGCATGCTGGGATATGAGAGCTACCAGTGTCCTCTGTAAACAGCTGAATTGTGGGATTGCTGTGTCTGTTGTGGGATCAGACTGGTTTGGAGAGGGAAGTGGTGAAATCTGGGCTGATGTGTTTGATTGTGACGGGAATGAAACAAAACTCTCCGAATGTTCAATCTCTTCATGGAGTCGAGCTCAACGCTCTCATAGACGAGATGTTGGAGTCATCTGCTCTAGTGAGGACATTTTATTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40237
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000135511 | Essential Splice Site | 1489 | 5840 | 15 | 57 |
Genomic Location (Zv9):
Chromosome 4 (position 10179740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11116367 |
GRCz11 | 4 | 11115216 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAACATGACTGTCGACACAAGGAGGATGTAGGAGTCGTCTGCTCTGG[T/C]GAACAGTTAATATCATTTTTGATAATAATATACAGAATACATTTAATACA
Long Flanking Sequence:
TGATGGGCTTCCAGTGCTCTGGGAGTGAAGCTCATCTGGGGAACTGCAGCTCTCCACAAACTCTCAACTGCAGCTCCACACAACAGCTGTCAATCACCTGCCTTGGTGAGAACAACAACATCTGGGCAGATTCTGGAGTTGTTCCTGATCAATAATGTGTTTCTCTTTCTCTGAATATCAGGCCGCGGGTCCATCAGGCTGGTGGGTTCTGGGGGAGACTGTGCAGGGAGGCTGGAGGTTTTTCACAGCGGCTCATGGGGGACAGTGTGTGACGACTCCTGGGATATTAAAGATGCCCATGTGGTGTGCAGACAGCTGCAGTGTGGAGTGGCCCTCAGTAACCAGCAGGTACCAGCCTGGTTTGGTCCTGGTTCTGGACCCATATGGCTGGATGAGGTGGAGTGTGAGGGGAATGAGACGTCCCTGTGGAGCTGCTCTTCTCCAGGCTGGGGAAAACATGACTGTCGACACAAGGAGGATGTAGGAGTCGTCTGCTCTGG[T/C]GAACAGTTAATATCATTTTTGATAATAATATACAGAATACATTTAATACATCAGGTTTAGAAACTGAAAAGGTTCCTGATAATATACACTGTATTAGGAAAAAAATCTCACACCTTTTAGTGCTAGGGAAATACTAAAATAAAAAGTTAAATGTTTCTTTTAAAGAATAAGACACATAAAAGTTACAGCTACCTCAATCAATGCACTGACTGGTTTCTCATAAGACAACACATTAATAAAAATAATATTTGCATATTTTTGGTCAGTGTTTCATGATAATAAAAATATATTTTATTTCCACATTTTGATTTAGTATCCTTTATATATGGTTTAGGCCAGCTACAGGCCAGCTATTGTCATTTCTTTTTACAAGATATTTTCTGAAGAGTTTACAATATTCAAATTTTTTCTCTTCCAGAGTATAAAGAGATCAGATTAACTGAGGGCTGTAAAGGGACTCTGGAGGTTTTCTACAATGGATCCTGGGGAAATGTGTGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20224
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000135511 | Nonsense | 1508 | 5840 | 16 | 57 |
Genomic Location (Zv9):
Chromosome 4 (position 10179254)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11115881 |
GRCz11 | 4 | 11114730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAACTGAGGGCTGTAAAGGGACTCTGGAGGTTTTCTACAATGGATCCTG[G/A]GGAAATGTGTGCTGGAATCAGATGGACAGAGACACAGCGAGTCTGATCTG
Long Flanking Sequence:
GTCGTCTGCTCTGGTGAACAGTTAATATCATTTTTGATAATAATATACAGAATACATTTAATACATCAGGTTTAGAAACTGAAAAGGTTCCTGATAATATACACTGTATTAGGAAAAAAATCTCACACCTTTTAGTGCTAGGGAAATACTAAAATAAAAAGTTAAATGTTTCTTTTAAAGAATAAGACACATAAAAGTTACAGCTACCTCAATCAATGCACTGACTGGTTTCTCATAAGACAACACATTAATAAAAATAATATTTGCATATTTTTGGTCAGTGTTTCATGATAATAAAAATATATTTTATTTCCACATTTTGATTTAGTATCCTTTATATATGGTTTAGGCCAGCTACAGGCCAGCTATTGTCATTTCTTTTTACAAGATATTTTCTGAAGAGTTTACAATATTCAAATTTTTTCTCTTCCAGAGTATAAAGAGATCAGATTAACTGAGGGCTGTAAAGGGACTCTGGAGGTTTTCTACAATGGATCCTG[G/A]GGAAATGTGTGCTGGAATCAGATGGACAGAGACACAGCGAGTCTGATCTGTCAAGAGCTGAACTGTGGAAGATCTAGCAATGAACCCAGTCATTCAAAAGGACTAAAGTCTCATAATTGGCTCGATAAACTAAAATGTAGACGACTTGATTCCACCTTATGGCAGTGTCCATCTGCAGCCTGGGGACAGAACGACTGTAATAATGATGAGGTCACTACAATCACCTGCTCAGGTAAAATTATGTTAAGTGGTCATGTTTGTTCATATATGATTATTTAATGTATGATTTGTGATGTCGTATGAAGATCGATGACATACAAAATCATTTGAATATCAGAGGTGGAGAGCCATGAGTCTCCTCGGAGTCTTCTGACATGCTCTACTTCACCATCTCCACACCAGAGACAGTGTTCAAGTAAGTTCATAATGTGCTTGTATTTTGTTTAATCATCGTAAACTTGAGTTCAGAATTATTTTAAATTAATGACATATTTTAATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40236
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 |
---|---|---|---|---|---|
ENSDART00000135511 | Nonsense | 2913 | 5840 | 29 | 57 |
Genomic Location (Zv9):
Chromosome 4 (position 10157567)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11094194 |
GRCz11 | 4 | 11093043 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAGGAAATGAGTCTCAGATTCGATTGTGTTCAACCGTGAATGACACA[C/T]AGTGCTCTCAGGAAAACAACGTAGCGCTGAAATGTGCAGGTAAAAGATGA
Long Flanking Sequence:
CTTTTGTGTATTAAAAATGATCACTTACATTAATTGCATAATTAATTAATTAATTAAACATTAATTACATAAAAAAAATTTTATGCATTTATCATAAGAAATAGTAATGAATGGCCATCTGTGCTGTGTAATTAAAATCATTAACTTTATCATATGGAAGTTCAAGACTTGCTGGTGAATCTCACTACTTATTATCTTCTTATAAAGCATCATCATTGTTTTTTATTTTGTTCTTGTCTTTAGAAGTCCGTCTGGTTGGAGGTTCTCGCTGCTCTGGGAGATTAGAGATCCTTCATAATCAGATGTGGATGTCAGTGTGTGACGCTGCCTTTGACCAGCAGGATGCAGAGGTTGTGTGTAGAGAGCTGGACTGTGGGGCTCCTGTACAGGTGCTGAGAGCTGCTGCTTTTGACAAAGGAGACACTCAGATGTGGACACAAGAGATTCACTGCAGAGGAAATGAGTCTCAGATTCGATTGTGTTCAACCGTGAATGACACA[C/T]AGTGCTCTCAGGAAAACAACGTAGCGCTGAAATGTGCAGGTAAAAGATGACATTTAACTAGTGATCAAAAAATTACATAAATTACACAAATTCCAAATCACAATAGACATGTAGCAGTGTTTTTATTAATATCACATATGTACAGTTGACGTGTATAAAAGTTATTAATTTGATGGTTTGTTGTTTATACTAACAATGTTAAAACTACAAAAGGATAAAGGATTTAAATATATTTTTATTTATAAATTAGCCATTATTTCGAGAGGGGTCTGGAAGCAGTTGCAATCGGAGCTGCATGCAATGCTTTTTAATGCCCACACCTAACCTTACCCCTAAGCCTACCTCTTACAGGGACGTCACTAGCTCCATTGAGTGTATTGTGTCTGACAAAGCATCTCTGAGATATGCAGTCTGTTGATTGTTTCAAAAGCAACATGTAAGTAATTATTAAAAATTGCAATACTTAACATTATTTAAAATAATCTTAAATTGAATAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26244
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 |
---|---|---|---|---|---|
ENSDART00000135511 | Nonsense | 4797 | 5840 | 47 | 57 |
Genomic Location (Zv9):
Chromosome 4 (position 10137375)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11074002 |
GRCz11 | 4 | 11072851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGACGTCCCTGTGGAGCTGCTCTTCTCCAGGCTGGGGAAAACATGACTG[T/A]CAACACAAGGAGGATGTAGGAGTCGTCTGCTCTGGTAAGGAAAGAAGAAT
Long Flanking Sequence:
CCTCTTTATCCAGTCCTGAACACAGTCATGAGTGTGTGATGGGCTTCCAGTGCTCTGGGAGTGAAGCTCATCTGGGGAACTGCAGCTCTCCACAAACTCTCAACTGCAGCTCCACACAACAGCTGTCAATCACCTGCCTTGGTGAGAACAACAACATCTGGGCAGATTCTGGAGTTGTTCCTGATCAATAATGTGTTTCTCTTTCTCTGAATATCAGGCCGCGGGTCCATCAGGCTGGTGGGTTCTGGGGGAGACTGTGCAGGGAGGCTGGAGGTTTTTCACAGCGGCTCATGGGGGACAGTGTGTGACGACTCCTGGGATATTAAAGATGCCCATGTGGTGTGCAGACAGCTGCAGTGTGGAGTGGCCCTCAGTAACCAGCAGGTACCAGCCTGGTTTGGTCCTGGTTCTGGACCCATATGGCTGGATGAGGTGGAGTGTAAGGGGAATGAGACGTCCCTGTGGAGCTGCTCTTCTCCAGGCTGGGGAAAACATGACTG[T/A]CAACACAAGGAGGATGTAGGAGTCGTCTGCTCTGGTAAGGAAAGAAGAATAATAGAATTTAGTATAATAATAGATTTTAGTATAATAATAGATTTTAATAAACTGTGTATAGGTAATAGCAATAAATAGCATTAAAATGTTGTGTGACCGGTATAATCTGATTTTCAAATGAATGACTATAATGATTTTTCTTACACTTAATATAAGTGAATCTACAATCTACAGTACATACACGCATGTTAAAGCCTAATGTAATATTACTGAGTGGACAATATGAGTGTTTTCTTCCTTTCTCCTCTAGAGTTTAAAGAGATCAGGTTAACTGAGGGCTGTGAAGGGAATGTGGAGGTTTTCTATAACGGATCCTGGGGAAATGTGTGTTACAACAAGATGGACAGAGACACAGCGAGTCTGATCTGTCAAGAGCTGAACTGTGGAAGATCTGGCAGTGAACCCAGTAATTCAGAGGGACTGAGAACCCTTAGTTGGCTTGATTTTGT
Associated Phenotype:
Not determined