Mauremys mutica isolate MM-2020 ecotype Southern chromosome 25, ASM2049712v1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Testudinata; Testudines; Cryptodira; Durocryptodira; Testudinoidea; Geoemydidae; Geoemydinae; Mauremys.
REFSEQ INFORMATION: The reference sequence is identical to\nCM035657.1.\nAssembly name: ASM2049712v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Institute of Zoology,\nGuangdong Academy of Science on 2021/10/14. The original\nwhole-genome shotgun project has the accession JAHDVG000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Institute of Zoology, Guangdong Academy\n of Science\nAssembly Method :: FALCON v. March-2021\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 99.81x\nSequencing Technology :: PacBio\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Mauremys mutica Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
synaptic vesicle membrane protein VAT-1 homolog
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
putative protein PTGES3L, transcript variant X2
putative protein PTGES3L, transcript variant X3
alanyl-tRNA editing protein Aarsd1-like isoform X3
putative protein PTGES3L, transcript variant X1
alanyl-tRNA editing protein Aarsd1-like isoform X1
glucose-6-phosphatase catalytic subunit 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
G protein-activated inward rectifier potassium channel 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
G protein-activated inward rectifier potassium channel 1-like isoform X1
G protein-activated inward rectifier potassium channel 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G protein-activated inward rectifier potassium channel 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CFAP97 domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
CFAP97 domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
CFAP97 domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
CFAP97 domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
sperm axonemal maintenance protein CFAP97D1 isoform X3
sperm axonemal maintenance protein CFAP97D1 isoform X2
sperm axonemal maintenance protein CFAP97D1 isoform X1
sperm axonemal maintenance protein CFAP97D1 isoform X4
dual specificity phosphatase 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dual specificity phosphatase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dual specificity protein phosphatase 3 isoform X1
dual specificity protein phosphatase 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
ETS variant transcription factor 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ETS variant transcription factor 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ETS variant transcription factor 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ETS variant transcription factor 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ETS variant transcription factor 4, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ETS variant transcription factor 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ETS variant transcription factor 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ETS variant transcription factor 4, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
transmembrane protein 106A, transcript variant X2
transmembrane protein 106A, transcript variant X1
NBR1 autophagy cargo receptor, transcript variant X7
NBR1 autophagy cargo receptor, transcript variant X2
NBR1 autophagy cargo receptor, transcript variant X5
NBR1 autophagy cargo receptor, transcript variant X10
NBR1 autophagy cargo receptor, transcript variant X1
NBR1 autophagy cargo receptor, transcript variant X6
NBR1 autophagy cargo receptor, transcript variant X4
NBR1 autophagy cargo receptor, transcript variant X3
NBR1 autophagy cargo receptor, transcript variant X11
NBR1 autophagy cargo receptor, transcript variant X8
NBR1 autophagy cargo receptor, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
BRCA1 DNA repair associated, transcript variant X2
BRCA1 DNA repair associated, transcript variant X3
BRCA1 DNA repair associated, transcript variant X1
breast cancer type 1 susceptibility protein isoform X1
breast cancer type 1 susceptibility protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
interferon induced protein 35, transcript variant X2
interferon induced protein 35, transcript variant X1
interferon-induced 35 kDa protein isoform X2
interferon-induced 35 kDa protein isoform X1
glucose-6-phosphatase catalytic subunit 1-like, transcript variant X1
glucose-6-phosphatase catalytic subunit 1-like isoform X1
glucose-6-phosphatase catalytic subunit 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
glucose-6-phosphatase catalytic subunit 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
membrane primary amine oxidase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
membrane primary amine oxidase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
membrane primary amine oxidase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
membrane primary amine oxidase-like isoform X1
membrane primary amine oxidase-like isoform X2
cyclin N-terminal domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclin N-terminal domain-containing protein 1 isoform X3
cyclin N-terminal domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclin N-terminal domain containing 1, transcript variant X2
cyclin N-terminal domain-containing protein 1 isoform X1
cyclin N-terminal domain-containing protein 1 isoform X2
cytochrome c oxidase assembly factor 3 homolog, mitochondrial
WNK lysine deficient protein kinase 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WNK lysine deficient protein kinase 4, transcript variant X4
WNK lysine deficient protein kinase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
WNK lysine deficient protein kinase 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
WNK lysine deficient protein kinase 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
WNK lysine deficient protein kinase 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein kinase WNK4 isoform X3
serine/threonine-protein kinase WNK4 isoform X2
serine/threonine-protein kinase WNK4 isoform X1
serine/threonine-protein kinase WNK4 isoform X4
serine/threonine-protein kinase WNK4 isoform X5
vacuolar protein-sorting-associated protein 25
receptor activity modifying protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
receptor activity modifying protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
receptor activity modifying protein 2, transcript variant X3
receptor activity-modifying protein 2 isoform X2
receptor activity-modifying protein 2 isoform X1
receptor activity-modifying protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
enhancer of zeste 1 polycomb repressive complex 2 subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
histone-lysine N-methyltransferase EZH1 isoform X2
enhancer of zeste 1 polycomb repressive complex 2 subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histone-lysine N-methyltransferase EZH1 isoform X1
contactin associated protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
contactin associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
contactin associated protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
contactin-associated protein 1 isoform X2
contactin-associated protein 1 isoform X1
contactin-associated protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pleckstrin homology, MyTH4 and FERM domain containing H3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
pleckstrin homology, MyTH4 and FERM domain containing H3, transcript variant X1
pleckstrin homology domain-containing family H member 3 isoform X1
pleckstrin homology domain-containing family H member 3 isoform X2
pleckstrin homology, MyTH4 and FERM domain containing H3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pleckstrin homology domain-containing family H member 3 isoform X3
reticulophagy regulator family member 3, transcript variant X2
reticulophagy regulator family member 3, transcript variant X1
reticulophagy regulator family member 3, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
coenzyme Q-binding protein COQ10 homolog B, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
hydroxysteroid 17-beta dehydrogenase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
hydroxysteroid 17-beta dehydrogenase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
17-beta-hydroxysteroid dehydrogenase type 1 isoform X2
17-beta-hydroxysteroid dehydrogenase type 1 isoform X1
serine/threonine-protein kinase 17A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ATPase H+ transporting V0 subunit a1, transcript variant X1
ATPase H+ transporting V0 subunit a1, transcript variant X4
ATPase H+ transporting V0 subunit a1, transcript variant X3
ATPase H+ transporting V0 subunit a1, transcript variant X2
V-type proton ATPase 116 kDa subunit a1 isoform X4
V-type proton ATPase 116 kDa subunit a1 isoform X3
V-type proton ATPase 116 kDa subunit a1 isoform X2
V-type proton ATPase 116 kDa subunit a1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
signal transducer and activator of transcription 3, transcript variant X3
signal transducer and activator of transcription 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
signal transducer and activator of transcription 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
signal transducer and activator of transcription 3, transcript variant X1
signal transducer and activator of transcription 3, transcript variant X2
signal transducer and activator of transcription 3 isoform X1
signal transducer and activator of transcription 3 isoform X2
signal transducer and activator of transcription 3 isoform X3
signal transducer and activator of transcription 3 isoform X4
signal transducer and activator of transcription 5B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
signal transducer and activator of transcription 5B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
signal transducer and activator of transcription 5B-like, transcript variant X1
signal transducer and activator of transcription 5B-like
signal transducer and activator of transcription 5B, transcript variant X2
signal transducer and activator of transcription 5B, transcript variant X4
signal transducer and activator of transcription 5B, transcript variant X1
signal transducer and activator of transcription 5B, transcript variant X3
signal transducer and activator of transcription 5B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
potassium voltage-gated channel subfamily H member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
lysine acetyltransferase 2A, transcript variant X1
lysine acetyltransferase 2A, transcript variant X2
histone acetyltransferase KAT2A isoform X1
histone acetyltransferase KAT2A isoform X2
DExH-box helicase 58, transcript variant X1
DExH-box helicase 58, transcript variant X2
probable ATP-dependent RNA helicase DHX58
zinc finger protein 385C, transcript variant X4
zinc finger protein 385C, transcript variant X6
zinc finger protein 385C, transcript variant X1
zinc finger protein 385C, transcript variant X2
zinc finger protein 385C, transcript variant X3
zinc finger protein 385C, transcript variant X7
zinc finger protein 385C, transcript variant X5
zinc finger protein 385C, transcript variant X8
zinc finger protein 385C, transcript variant X11
zinc finger protein 385C, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 385C, transcript variant X10
NFKB inhibitor interacting Ras like 2, transcript variant X3
NFKB inhibitor interacting Ras like 2, transcript variant X1
NFKB inhibitor interacting Ras like 2, transcript variant X2
NF-kappa-B inhibitor-interacting Ras-like protein 2
DnaJ heat shock protein family (Hsp40) member C7, transcript variant X1
dnaJ homolog subfamily C member 7 isoform X1
DnaJ heat shock protein family (Hsp40) member C7, transcript variant X3
dnaJ homolog subfamily C member 7 isoform X3
DnaJ heat shock protein family (Hsp40) member C7, transcript variant X2
dnaJ homolog subfamily C member 7 isoform X2
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X4
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
2',3'-cyclic-nucleotide 3'-phosphodiesterase isoform X3
2',3'-cyclic-nucleotide 3'-phosphodiesterase isoform X2
2',3'-cyclic-nucleotide 3'-phosphodiesterase isoform X1
outer dynein arm docking complex subunit 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
outer dynein arm docking complex subunit 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
outer dynein arm docking complex subunit 4, transcript variant X3
outer dynein arm-docking complex subunit 4 isoform X1
outer dynein arm-docking complex subunit 4 isoform X2
outer dynein arm-docking complex subunit 4 isoform X3
ATP citrate lyase, transcript variant X2
ATP citrate lyase, transcript variant X1
ATP citrate lyase, transcript variant X3
kelch like family member 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
kelch like family member 10, transcript variant X3
kelch like family member 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
5'-nucleotidase, cytosolic IIIB, transcript variant X2
5'-nucleotidase, cytosolic IIIB, transcript variant X1
7-methylguanosine phosphate-specific 5'-nucleotidase isoform X1
7-methylguanosine phosphate-specific 5'-nucleotidase isoform X2
peptidyl-prolyl cis-trans isomerase FKBP10
prolyl 3-hydroxylase family member 4 (inactive)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
junction plakoglobin, transcript variant X2
junction plakoglobin, transcript variant X1
serine/arginine repetitive matrix protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
huntingtin associated protein 1, transcript variant X2
huntingtin associated protein 1, transcript variant X1
huntingtin associated protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
huntingtin associated protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
huntingtin-associated protein 1 isoform X1
huntingtin-associated protein 1 isoform X2
huntingtin-associated protein 1 isoform X3
gastrin/cholecystokinin-like peptide, transcript variant X1
gastrin/cholecystokinin-like peptide, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gastrin/cholecystokinin-like peptide isoform X1
gastrin/cholecystokinin-like peptide isoform X2
eukaryotic translation initiation factor 1
keratin, type I cytoskeletal 47 kDa-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 156 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
keratin, type I cytoskeletal 14-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
keratin, type I cytoskeletal 14-like isoform X6
keratin, type I cytoskeletal 14-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 273 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
keratin, type I cytoskeletal 14-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 270 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
keratin, type I cytoskeletal 14-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 275 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
keratin, type I cytoskeletal 14-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 188 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
keratin, type I cytoskeletal 14-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 270 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
keratin, type I cytoskeletal 14-like isoform X1
keratin, type I cytoskeletal 14-like isoform X4
keratin, type I cytoskeletal 14-like isoform X2
keratin, type I cytoskeletal 14-like isoform X3
keratin, type I cytoskeletal 14-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 312 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
keratin, type I cytoskeletal 19-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
keratin, type I cytoskeletal 42-like isoform X2
keratin, type I cytoskeletal 19-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 332 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
keratin, type I cytoskeletal 19-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 331 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 257 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 157 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 192 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 199 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 198 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 168 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1, transcript variant X1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1, transcript variant X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
insulin like growth factor binding protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
insulin-like growth factor-binding protein 4
collagen alpha-1(XV) chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
collagen alpha-1(XV) chain-like, transcript variant X2
collagen alpha-1(XV) chain-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
collagen alpha-1(XV) chain-like isoform X1
collagen alpha-1(X) chain-like isoform X2
collagen alpha-1(XV) chain-like isoform X3
DNA topoisomerase II alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DNA topoisomerase II alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gap junction protein delta 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
gap junction protein delta 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
retinoic acid receptor alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
retinoic acid receptor alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
retinoic acid receptor alpha, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
WAS/WASL interacting protein family member 2, transcript variant X3
WAS/WASL interacting protein family member 2, transcript variant X1
WAS/WASL interacting protein family member 2, transcript variant X4
WAS/WASL interacting protein family member 2, transcript variant X6
WAS/WASL interacting protein family member 2, transcript variant X5
WAS/WASL interacting protein family member 2, transcript variant X2
WAS/WASL interacting protein family member 2, transcript variant X7
WAS/WASL-interacting protein family member 2 isoform X1
WAS/WASL interacting protein family member 2, transcript variant X8
WAS/WASL-interacting protein family member 2 isoform X2
Rap guanine nucleotide exchange factor like 1
rap guanine nucleotide exchange factor-like 1
CASC3 exon junction complex subunit, transcript variant X3
CASC3 exon junction complex subunit, transcript variant X2
CASC3 exon junction complex subunit, transcript variant X1
MSL complex subunit 1, transcript variant X2
MSL complex subunit 1, transcript variant X1
male-specific lethal 1 homolog isoform X2
male-specific lethal 1 homolog isoform X1
nuclear receptor subfamily 1 group D member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
mediator complex subunit 24, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
mediator complex subunit 24, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 24 isoform X1
mediator of RNA polymerase II transcription subunit 24 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF01211
colony stimulating factor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
colony stimulating factor 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
colony stimulating factor 3, transcript variant X3
granulocyte colony-stimulating factor isoform X1
granulocyte colony-stimulating factor isoform X2
26S proteasome non-ATPase regulatory subunit 3
ORMDL sphingolipid biosynthesis regulator 3, transcript variant X2
ORMDL sphingolipid biosynthesis regulator 3, transcript variant X3
ORMDL sphingolipid biosynthesis regulator 3, transcript variant X4
ORMDL sphingolipid biosynthesis regulator 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich repeat-containing protein 3C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
zona pellucida binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zona pellucida binding protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zona pellucida-binding protein 2 isoform X1
zona pellucida-binding protein 2 isoform X2
IKAROS family zinc finger 3, transcript variant X4
IKAROS family zinc finger 3, transcript variant X2
IKAROS family zinc finger 3, transcript variant X1
IKAROS family zinc finger 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
growth factor receptor bound protein 7, transcript variant X1
growth factor receptor bound protein 7, transcript variant X2
growth factor receptor bound protein 7, transcript variant X4
growth factor receptor bound protein 7, transcript variant X3
growth factor receptor-bound protein 7 isoform X1
growth factor receptor-bound protein 7 isoform X2
growth factor receptor-bound protein 7 isoform X3
post-GPI attachment to proteins phospholipase 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
post-GPI attachment to proteins phospholipase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
post-GPI attachment to proteins factor 3 isoform X1
post-GPI attachment to proteins factor 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
melanoregulin-like, transcript variant X2
melanoregulin-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
StAR related lipid transfer domain containing 3, transcript variant X3
StAR related lipid transfer domain containing 3, transcript variant X1
StAR related lipid transfer domain containing 3, transcript variant X2
stAR-related lipid transfer protein 3 isoform X2
stAR-related lipid transfer protein 3 isoform X1
protein phosphatase 1 regulatory inhibitor subunit 1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins
cyclin dependent kinase 12, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cyclin dependent kinase 12, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cyclin dependent kinase 12, transcript variant X2
cyclin dependent kinase 12, transcript variant X1
mediator complex subunit 1, transcript variant X3
mediator complex subunit 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mediator complex subunit 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mediator of RNA polymerase II transcription subunit 1 isoform X3
mediator of RNA polymerase II transcription subunit 1 isoform X1
mediator of RNA polymerase II transcription subunit 1 isoform X2
F-box and leucine rich repeat protein 20, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
F-box and leucine rich repeat protein 20, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
F-box and leucine rich repeat protein 20, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
F-box and leucine rich repeat protein 20, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription factor CP2-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transcription factor CP2-like protein 1, transcript variant X2
SH3 and cysteine rich domain 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SH3 and cysteine rich domain 2, transcript variant X2
SH3 and cysteine-rich domain-containing protein 2 isoform X1
SH3 and cysteine-rich domain-containing protein 2 isoform X2
P43 5S RNA-binding protein-like, transcript variant X2
P43 5S RNA-binding protein-like, transcript variant X1
P43 5S RNA-binding protein-like isoform X2
P43 5S RNA-binding protein-like isoform X1
uncharacterized LOC123356280, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123356280, transcript variant X2
calcium voltage-gated channel auxiliary subunit beta 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
calcium voltage-gated channel auxiliary subunit beta 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent L-type calcium channel subunit beta-1 isoform X1
voltage-dependent L-type calcium channel subunit beta-1 isoform X3
calcium voltage-gated channel auxiliary subunit beta 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
voltage-dependent L-type calcium channel subunit beta-1 isoform X2
ADP ribosylation factor like GTPase 5C, transcript variant X2
ADP ribosylation factor like GTPase 5C, transcript variant X1
putative ADP-ribosylation factor-like protein 5C isoform X1
putative ADP-ribosylation factor-like protein 5C isoform X2
dickkopf-related protein 3-like, transcript variant X2
dickkopf-related protein 3-like, transcript variant X1
dickkopf-related protein 3-like isoform X2
dickkopf-related protein 3-like isoform X1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
plexin domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
plexin domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
F-box protein 47, transcript variant X11
F-box protein 47, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
F-box protein 47, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LIM and SH3 protein 1, transcript variant X3
LIM and SH3 protein 1, transcript variant X2
LIM and SH3 protein 1, transcript variant X1
uncharacterized LOC123356306, transcript variant X2
uncharacterized LOC123356306, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00412
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein C17orf98 homolog
transfer RNA cysteine (anticodon ACA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
CWC25 spliceosome associated protein homolog
phosphatidylinositol-5-phosphate 4-kinase type 2 beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 beta
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
polycomb group ring finger 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
polycomb group ring finger 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
polycomb group ring finger 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
polycomb group ring finger 2, transcript variant X4
polycomb group ring finger 2, transcript variant X3
polycomb group RING finger protein 2 isoform X1
polycomb group RING finger protein 2 isoform X2
CDGSH iron-sulfur domain-containing protein 3, mitochondrial
MLLT6, PHD finger containing, transcript variant X2
MLLT6, PHD finger containing, transcript variant X1
MLLT6, PHD finger containing, transcript variant X3
MLLT6, PHD finger containing, transcript variant X4
elongin BC and polycomb repressive complex 2 associated protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
elongin BC and Polycomb repressive complex 2-associated protein
SRC kinase signaling inhibitor 1, transcript variant X1
SRC kinase signaling inhibitor 1 isoform X1
SRC kinase signaling inhibitor 1, transcript variant X4
SRC kinase signaling inhibitor 1, transcript variant X5
SRC kinase signaling inhibitor 1, transcript variant X2
SRC kinase signaling inhibitor 1 isoform X2
SRC kinase signaling inhibitor 1, transcript variant X3
SRC kinase signaling inhibitor 1 isoform X3
SRC kinase signaling inhibitor 1 isoform X4
SRC kinase signaling inhibitor 1, transcript variant X7
SRC kinase signaling inhibitor 1, transcript variant X6
SRC kinase signaling inhibitor 1 isoform X5
Rho GTPase activating protein 23, transcript variant X6
Rho GTPase activating protein 23, transcript variant X4
Rho GTPase activating protein 23, transcript variant X5
Rho GTPase activating protein 23, transcript variant X3
Rho GTPase activating protein 23, transcript variant X2
Rho GTPase activating protein 23, transcript variant X1
Rho GTPase activating protein 23, transcript variant X7
rho GTPase-activating protein 23 isoform X6
rho GTPase-activating protein 23 isoform X4
rho GTPase-activating protein 23 isoform X5
rho GTPase-activating protein 23 isoform X3
rho GTPase-activating protein 23 isoform X2
rho GTPase-activating protein 23 isoform X1
rho GTPase-activating protein 23 isoform X7
Rho GTPase activating protein 23, transcript variant X8
Rho GTPase activating protein 23, transcript variant X9
rho GTPase-activating protein 23 isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G protein-coupled receptor 179, transcript variant X1
probable G-protein coupled receptor 179 isoform X1
G protein-coupled receptor 179, transcript variant X2
probable G-protein coupled receptor 179 isoform X2
39S ribosomal protein L45, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
oxysterol binding protein like 7, transcript variant X2
oxysterol binding protein like 7, transcript variant X3
oxysterol binding protein like 7, transcript variant X1
oxysterol-binding protein-related protein 7 isoform X2
oxysterol-binding protein-related protein 7 isoform X1
39S ribosomal protein L10, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
leucine-rich repeat-containing protein 46
Sp6 transcription factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Sp6 transcription factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Sp2 transcription factor, transcript variant X2
Sp2 transcription factor, transcript variant X3
Sp2 transcription factor, transcript variant X1
uncharacterized LOC123356588, transcript variant X1
uncharacterized LOC123356588, transcript variant X2
uncharacterized LOC123356588, transcript variant X3
uncharacterized LOC123356588, transcript variant X4
uncharacterized LOC123356588, transcript variant X5
uncharacterized protein LOC123356588 isoform X1
uncharacterized protein LOC123356588 isoform X3
uncharacterized protein LOC123356588 isoform X2
pyridoxamine 5'-phosphate oxidase, transcript variant X5
pyridoxamine 5'-phosphate oxidase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
pyridoxamine 5'-phosphate oxidase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
pyridoxamine 5'-phosphate oxidase, transcript variant X1
pyridoxamine 5'-phosphate oxidase, transcript variant X2
pyridoxine-5'-phosphate oxidase isoform X2
pyridoxine-5'-phosphate oxidase isoform X1
CDK5 regulatory subunit associated protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
CDK5 regulatory subunit-associated protein 3
COPI coat complex subunit zeta 2, transcript variant X3
COPI coat complex subunit zeta 2, transcript variant X6
COPI coat complex subunit zeta 2, transcript variant X1
COPI coat complex subunit zeta 2, transcript variant X5
COPI coat complex subunit zeta 2, transcript variant X4
COPI coat complex subunit zeta 2, transcript variant X2
NFE2 like bZIP transcription factor 1, transcript variant X1
NFE2 like bZIP transcription factor 1, transcript variant X3
NFE2 like bZIP transcription factor 1, transcript variant X2
endoplasmic reticulum membrane sensor NFE2L1 isoform X1
NFE2 like bZIP transcription factor 1, transcript variant X4
endoplasmic reticulum membrane sensor NFE2L1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
src kinase associated phosphoprotein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
src kinase associated phosphoprotein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
src kinase-associated phosphoprotein 1 isoform X2
src kinase-associated phosphoprotein 1 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00066
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tubulin tyrosine ligase like 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tubulin tyrosine ligase like 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tubulin tyrosine ligase like 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tubulin tyrosine ligase like 6, transcript variant X4
tubulin polyglutamylase TTLL6 isoform X2
tubulin polyglutamylase TTLL6 isoform X1
tubulin polyglutamylase TTLL6 isoform X3
calcium binding and coiled-coil domain 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
calcium binding and coiled-coil domain 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
calcium binding and coiled-coil domain 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
calcium-binding and coiled-coil domain-containing protein 2 isoform X3
calcium-binding and coiled-coil domain-containing protein 2 isoform X2
calcium-binding and coiled-coil domain-containing protein 2 isoform X1
ATP synthase membrane subunit c locus 1, transcript variant X2
ATP synthase F(0) complex subunit C1, mitochondrial isoform X2
ATP synthase membrane subunit c locus 1, transcript variant X1
ATP synthase F(0) complex subunit C1, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
pro-glucagon-like, transcript variant X3
pro-glucagon-like, transcript variant X4
pro-glucagon-like, transcript variant X6
pro-glucagon-like, transcript variant X5
pro-glucagon-like, transcript variant X2
pro-glucagon-like, transcript variant X1
pro-glucagon-like, transcript variant X7
pro-glucagon-like, transcript variant X8
insulin like growth factor 2 mRNA binding protein 1, transcript variant X1
insulin like growth factor 2 mRNA binding protein 1, transcript variant X2
insulin-like growth factor 2 mRNA-binding protein 1 isoform X1
insulin-like growth factor 2 mRNA-binding protein 1 isoform X2
insulin like growth factor 2 mRNA binding protein 1, transcript variant X3
insulin-like growth factor 2 mRNA-binding protein 1 isoform X3
beta-1,4-N-acetyl-galactosaminyltransferase 2, transcript variant X1
beta-1,4-N-acetyl-galactosaminyltransferase 2, transcript variant X2
beta-1,4-N-acetyl-galactosaminyltransferase 2, transcript variant X8
beta-1,4-N-acetyl-galactosaminyltransferase 2, transcript variant X4
beta-1,4-N-acetyl-galactosaminyltransferase 2, transcript variant X9
beta-1,4-N-acetyl-galactosaminyltransferase 2, transcript variant X5
beta-1,4-N-acetyl-galactosaminyltransferase 2, transcript variant X6
beta-1,4-N-acetyl-galactosaminyltransferase 2, transcript variant X3
beta-1,4-N-acetyl-galactosaminyltransferase 2, transcript variant X7
beta-1,4 N-acetylgalactosaminyltransferase 2 isoform X1
beta-1,4 N-acetylgalactosaminyltransferase 2 isoform X2
beta-1,4 N-acetylgalactosaminyltransferase 2 isoform X8
beta-1,4 N-acetylgalactosaminyltransferase 2 isoform X4
beta-1,4 N-acetylgalactosaminyltransferase 2 isoform X9
beta-1,4 N-acetylgalactosaminyltransferase 2 isoform X5
beta-1,4 N-acetylgalactosaminyltransferase 2 isoform X7
beta-1,4 N-acetylgalactosaminyltransferase 2 isoform X3
beta-1,4 N-acetylgalactosaminyltransferase 2 isoform X6
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
beta-1,4 N-acetylgalactosaminyltransferase 2-like
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X2
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ABI family member 3, transcript variant X2
ABI family member 3, transcript variant X3
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-T2
ABI family member 3, transcript variant X4
ABI family member 3, transcript variant X1
phosphoethanolamine/phosphocholine phosphatase 1, transcript variant X1
phosphoethanolamine/phosphocholine phosphatase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
phosphoethanolamine/phosphocholine phosphatase 1, transcript variant X5
phosphoethanolamine/phosphocholine phosphatase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphoethanolamine/phosphocholine phosphatase 1, transcript variant X3
phosphoethanolamine/phosphocholine phosphatase
uncharacterized LOC123356533, transcript variant X1
uncharacterized LOC123356533, transcript variant X2
zinc finger protein 652, transcript variant X2
zinc finger protein 652, transcript variant X1
uncharacterized LOC123356466, transcript variant X2
uncharacterized LOC123356466, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
speckle type BTB/POZ protein, transcript variant X5
speckle type BTB/POZ protein, transcript variant X1
speckle type BTB/POZ protein, transcript variant X4
speckle type BTB/POZ protein, transcript variant X9
speckle type BTB/POZ protein, transcript variant X8
speckle type BTB/POZ protein, transcript variant X3
speckle type BTB/POZ protein, transcript variant X6
speckle type BTB/POZ protein, transcript variant X2
speckle type BTB/POZ protein, transcript variant X7
uncharacterized LOC123356339, transcript variant X5
uncharacterized LOC123356339, transcript variant X6
uncharacterized LOC123356339, transcript variant X4
uncharacterized LOC123356339, transcript variant X2
uncharacterized LOC123356339, transcript variant X3
uncharacterized LOC123356339, transcript variant X1
family with sequence similarity 117 member A
uncharacterized LOC123356338, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC123356338, transcript variant X7
uncharacterized LOC123356338, transcript variant X2
uncharacterized LOC123356338, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123356338, transcript variant X5
uncharacterized LOC123356338, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123356338, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protachykinin-1-like, transcript variant X3
protachykinin-1-like, transcript variant X2
protachykinin-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
integrin subunit alpha 3, transcript variant X1
integrin subunit alpha 3, transcript variant X2
pyruvate dehydrogenase kinase, isozyme 2
protein phosphatase 1 regulatory subunit 9B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
sarcoglycan alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sarcoglycan alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sarcoglycan alpha, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MAGUK p55 scaffold protein 2, transcript variant X6
MAGUK p55 scaffold protein 2, transcript variant X4
MAGUK p55 scaffold protein 2, transcript variant X5
MAGUK p55 scaffold protein 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
MAGUK p55 scaffold protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MAGUK p55 scaffold protein 2, transcript variant X2
MAGUK p55 scaffold protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transmembrane protein 101, transcript variant X2
transmembrane protein 101, transcript variant X3
N-acetylglutamate synthase, mitochondrial
transmembrane protein 101, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
glucose-6-phosphatase catalytic subunit 3, transcript variant X3
glucose-6-phosphatase catalytic subunit 3, transcript variant X2
glucose-6-phosphatase catalytic subunit 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glucose-6-phosphatase catalytic subunit 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
histone deacetylase 5, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
histone deacetylase 5, transcript variant X2
histone deacetylase 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
histone deacetylase 5, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
histone deacetylase 5, transcript variant X3
homologous recombination factor with OB-fold
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
homologous recombination OB-fold protein
ankyrin repeat and SOCS box containing 16
uncharacterized LOC123356344, transcript variant X2
uncharacterized LOC123356344, transcript variant X1
transmembrane and ubiquitin like domain containing 2, transcript variant X1
transmembrane and ubiquitin like domain containing 2, transcript variant X2
transmembrane and ubiquitin-like domain-containing protein 2
upstream binding transcription factor, transcript variant X2
upstream binding transcription factor, transcript variant X6
upstream binding transcription factor, transcript variant X1
upstream binding transcription factor, transcript variant X7
upstream binding transcription factor, transcript variant X3
upstream binding transcription factor, transcript variant X4
upstream binding transcription factor, transcript variant X5
nucleolar transcription factor 1 isoform X2
nucleolar transcription factor 1 isoform X3
nucleolar transcription factor 1 isoform X1
solute carrier family 4 member 1 (Diego blood group)
RUN domain containing 3A, transcript variant X2
RUN domain containing 3A, transcript variant X4
RUN domain-containing protein 3A isoform X2
RUN domain containing 3A, transcript variant X6
RUN domain containing 3A, transcript variant X1
RUN domain containing 3A, transcript variant X3
RUN domain-containing protein 3A isoform X1
RUN domain-containing protein 3A isoform X3
RUN domain containing 3A, transcript variant X5
RUN domain-containing protein 3A isoform X4
solute carrier family 25 member 39, transcript variant X3
solute carrier family 25 member 39, transcript variant X2
solute carrier family 25 member 39, transcript variant X1
solute carrier family 25 member 39, transcript variant X4
solute carrier family 25 member 39 isoform X3
solute carrier family 25 member 39 isoform X2
solute carrier family 25 member 39 isoform X1
solute carrier family 25 member 39 isoform X4
microtubule associated protein tau, transcript variant X17
microtubule associated protein tau, transcript variant X14
microtubule associated protein tau, transcript variant X12
microtubule associated protein tau, transcript variant X19
microtubule-associated protein tau isoform X12
microtubule-associated protein tau isoform X18
microtubule associated protein tau, transcript variant X20
microtubule-associated protein tau isoform X14
microtubule-associated protein tau isoform X19
microtubule associated protein tau, transcript variant X1
microtubule associated protein tau, transcript variant X7
microtubule associated protein tau, transcript variant X10
microtubule associated protein tau, transcript variant X6
microtubule associated protein tau, transcript variant X16
microtubule associated protein tau, transcript variant X23
microtubule associated protein tau, transcript variant X4
microtubule associated protein tau, transcript variant X9
microtubule associated protein tau, transcript variant X22
microtubule associated protein tau, transcript variant X5
microtubule associated protein tau, transcript variant X8
microtubule associated protein tau, transcript variant X13
microtubule associated protein tau, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
microtubule-associated protein tau isoform X1
microtubule-associated protein tau isoform X7
microtubule-associated protein tau isoform X10
microtubule-associated protein tau isoform X6
microtubule-associated protein tau isoform X16
microtubule-associated protein tau isoform X22
microtubule-associated protein tau isoform X4
microtubule-associated protein tau isoform X9
microtubule-associated protein tau isoform X21
microtubule-associated protein tau isoform X5
microtubule-associated protein tau isoform X8
microtubule-associated protein tau isoform X13
microtubule-associated protein tau isoform X3
microtubule associated protein tau, transcript variant X15
microtubule associated protein tau, transcript variant X21
microtubule-associated protein tau isoform X15
microtubule-associated protein tau isoform X20
microtubule associated protein tau, transcript variant X18
microtubule-associated protein tau isoform X17
microtubule associated protein tau, transcript variant X2
microtubule associated protein tau, transcript variant X11
microtubule-associated protein tau isoform X2
microtubule-associated protein tau isoform X11
KAT8 regulatory NSL complex subunit 1, transcript variant X1
KAT8 regulatory NSL complex subunit 1, transcript variant X4
KAT8 regulatory NSL complex subunit 1, transcript variant X2
KAT8 regulatory NSL complex subunit 1, transcript variant X3
KAT8 regulatory NSL complex subunit 1 isoform X2
KAT8 regulatory NSL complex subunit 1 isoform X1
cell division cycle 27, transcript variant X4
cell division cycle 27, transcript variant X3
cell division cycle 27, transcript variant X2
cell division cycle 27, transcript variant X1
cell division cycle protein 27 homolog isoform X4
cell division cycle protein 27 homolog isoform X3
cell division cycle protein 27 homolog isoform X2
cell division cycle protein 27 homolog isoform X1
cell division cycle 27, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
cell division cycle 27, transcript variant X5
cell division cycle protein 27 homolog isoform X6
cell division cycle protein 27 homolog isoform X5
parathyroid hormone/parathyroid hormone-related peptide receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
DEAD-box helicase 42, transcript variant X2
DEAD-box helicase 42, transcript variant X1
DEAD-box helicase 42, transcript variant X4
DEAD-box helicase 42, transcript variant X3
ATP-dependent RNA helicase DDX42 isoform X2
ATP-dependent RNA helicase DDX42 isoform X1
ATP-dependent RNA helicase DDX42 isoform X3
ATP-dependent RNA helicase DDX42 isoform X4
coiled-coil domain containing 47, transcript variant X2
coiled-coil domain containing 47, transcript variant X3
coiled-coil domain containing 47, transcript variant X1
STE20 related adaptor alpha, transcript variant X2
STE20 related adaptor alpha, transcript variant X1
STE20 related adaptor alpha, transcript variant X7
STE20 related adaptor alpha, transcript variant X3
STE20 related adaptor alpha, transcript variant X4
STE20 related adaptor alpha, transcript variant X5
STE20 related adaptor alpha, transcript variant X6
STE20-related kinase adapter protein alpha isoform X1
STE20-related kinase adapter protein alpha isoform X2
STE20-related kinase adapter protein alpha isoform X3
STE20-related kinase adapter protein alpha isoform X4
E3 ubiquitin-protein ligase RNF113A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E3 ubiquitin-protein ligase RNF113A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF113A-like, transcript variant X3
E3 ubiquitin-protein ligase RNF113A-like isoform X1
E3 ubiquitin-protein ligase RNF113A-like isoform X2
E3 ubiquitin-protein ligase RNF113A-like isoform X3
LIM domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
LIM domain-containing protein 2 isoform X2
LIM domain containing 2, transcript variant X1
LIM domain-containing protein 2 isoform X1
mitogen-activated protein kinase kinase kinase 3
potassium voltage-gated channel subfamily H member 6, transcript variant X2
potassium voltage-gated channel subfamily H member 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 6, transcript variant X3
potassium voltage-gated channel subfamily H member 6, transcript variant X4
potassium voltage-gated channel subfamily H member 6 isoform X1
potassium voltage-gated channel subfamily H member 6 isoform X3
potassium voltage-gated channel subfamily H member 6 isoform X2
angiotensin I converting enzyme, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
angiotensin I converting enzyme, transcript variant X3
angiotensin I converting enzyme, transcript variant X5
angiotensin I converting enzyme, transcript variant X4
angiotensin I converting enzyme, transcript variant X2
angiotensin I converting enzyme, transcript variant X6
angiotensin-converting enzyme isoform X3
angiotensin-converting enzyme isoform X4
angiotensin-converting enzyme isoform X1
angiotensin-converting enzyme isoform X2
angiotensin-converting enzyme isoform X5
transmembrane ascorbate-dependent reductase CYB561, transcript variant X5
transmembrane ascorbate-dependent reductase CYB561, transcript variant X4
transmembrane ascorbate-dependent reductase CYB561, transcript variant X3
transmembrane ascorbate-dependent reductase CYB561, transcript variant X2
transmembrane ascorbate-dependent reductase CYB561, transcript variant X1
transmembrane ascorbate-dependent reductase CYB561
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2, transcript variant X6
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2, transcript variant X5
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2, transcript variant X4
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2, transcript variant X3
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2, transcript variant X2
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
membrane associated ring-CH-type finger 10, transcript variant X2
membrane associated ring-CH-type finger 10, transcript variant X4
membrane associated ring-CH-type finger 10, transcript variant X5
membrane associated ring-CH-type finger 10, transcript variant X1
membrane associated ring-CH-type finger 10, transcript variant X6
membrane associated ring-CH-type finger 10, transcript variant X3
probable E3 ubiquitin-protein ligase MARCHF10 isoform X2
probable E3 ubiquitin-protein ligase MARCHF10 isoform X1
probable E3 ubiquitin-protein ligase MARCHF10 isoform X3
mannose receptor C type 2, transcript variant X2
mannose receptor C type 2, transcript variant X1
mannose receptor C type 2, transcript variant X3
tousled like kinase 2, transcript variant X2
tousled like kinase 2, transcript variant X4
tousled like kinase 2, transcript variant X1
tousled like kinase 2, transcript variant X3
serine/threonine-protein kinase tousled-like 2 isoform X4
serine/threonine-protein kinase tousled-like 2 isoform X1
serine/threonine-protein kinase tousled-like 2 isoform X3
serine/threonine-protein kinase tousled-like 2 isoform X2
methyltransferase 2A, methylcytidine, transcript variant X2
tRNA N(3)-methylcytidine methyltransferase METTL2A isoform X2
methyltransferase 2A, methylcytidine, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL2A isoform X1
EF-hand calcium binding domain 3, transcript variant X3
EF-hand calcium binding domain 3, transcript variant X1
EF-hand calcium binding domain 3, transcript variant X2
EF-hand calcium-binding domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
EF-hand calcium-binding domain-containing protein 13
integrin subunit beta 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
integrin subunit beta 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
integrin subunit beta 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
integrin subunit beta 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123356473, transcript variant X3
uncharacterized LOC123356473, transcript variant X1
uncharacterized LOC123356473, transcript variant X2
uncharacterized protein LOC123356473 isoform X2
uncharacterized protein LOC123356473 isoform X3
uncharacterized protein LOC123356473 isoform X1
corticotropin-releasing factor receptor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
alpha-2-macroglobulin-like protein 1, transcript variant X1
alpha-2-macroglobulin-like protein 1, transcript variant X2
alpha-2-macroglobulin-like protein 1 isoform X1
alpha-2-macroglobulin-like protein 1 isoform X2
alpha-2-macroglobulin-like protein 1, transcript variant X3
alpha-2-macroglobulin-like protein 1 isoform X3
alpha-2-macroglobulin-like protein 1, transcript variant X5
alpha-2-macroglobulin-like protein 1, transcript variant X4
alpha-2-macroglobulin-like protein 1 isoform X4
alpha-2-macroglobulin-like protein 1 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
pre-rRNA 2'-O-ribose RNA methyltransferase FTSJ3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 251-like, transcript variant X1
zinc finger protein 251-like, transcript variant X2
non-structural maintenance of chromosomes element 3 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
golgi SNAP receptor complex member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
golgi SNAP receptor complex member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
golgi SNAP receptor complex member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Golgi SNAP receptor complex member 2 isoform X3
Golgi SNAP receptor complex member 2 isoform X1
Golgi SNAP receptor complex member 2 isoform X2
Wnt family member 9B, transcript variant X2
Wnt family member 9B, transcript variant X1
Wnt family member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
Wnt family member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
N-ethylmaleimide sensitive factor, vesicle fusing ATPase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
N-ethylmaleimide sensitive factor, vesicle fusing ATPase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
N-ethylmaleimide sensitive factor, vesicle fusing ATPase, transcript variant X1
ADP-ribosylation factor 2, transcript variant X1
ADP-ribosylation factor 2, transcript variant X2
ADP-ribosylation factor 2, transcript variant X3
meiosis specific with coiled-coil domain, transcript variant X2
meiosis specific with coiled-coil domain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
meiosis specific with coiled-coil domain, transcript variant X3
meiosis-specific coiled-coil domain-containing protein MEIOC isoform X1
meiosis-specific coiled-coil domain-containing protein MEIOC isoform X3
meiosis-specific coiled-coil domain-containing protein MEIOC isoform X2
coiled-coil domain-containing protein 43
DBF4 zinc finger B, transcript variant X4
DBF4 zinc finger B, transcript variant X1
DBF4 zinc finger B, transcript variant X11
DBF4 zinc finger B, transcript variant X7
DBF4 zinc finger B, transcript variant X3
DBF4 zinc finger B, transcript variant X6
DBF4 zinc finger B, transcript variant X2
DBF4 zinc finger B, transcript variant X9
DBF4 zinc finger B, transcript variant X5
DBF4 zinc finger B, transcript variant X10
DBF4 zinc finger B, transcript variant X8
ADAM metallopeptidase domain 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ADAM metallopeptidase domain 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ADAM metallopeptidase domain 11, transcript variant X4
disintegrin and metalloproteinase domain-containing protein 11 isoform X2
disintegrin and metalloproteinase domain-containing protein 11 isoform X1
disintegrin and metalloproteinase domain-containing protein 11 isoform X4
ADAM metallopeptidase domain 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
disintegrin and metalloproteinase domain-containing protein 11 isoform X3
ADAM metallopeptidase domain 11, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
disintegrin and metalloproteinase domain-containing protein 11 isoform X5
gap junction protein gamma 1, transcript variant X1
gap junction protein gamma 1, transcript variant X2
gap junction protein gamma 1, transcript variant X3
gap junction protein gamma 1, transcript variant X4
HIG1 hypoxia inducible domain family member 1B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
HIG1 hypoxia inducible domain family member 1B, transcript variant X5
HIG1 hypoxia inducible domain family member 1B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
HIG1 hypoxia inducible domain family member 1B, transcript variant X4
HIG1 hypoxia inducible domain family member 1B, transcript variant X2
elongation factor Tu GTP binding domain containing 2, transcript variant X2
elongation factor Tu GTP binding domain containing 2, transcript variant X1
116 kDa U5 small nuclear ribonucleoprotein component
coiled-coil domain containing 103, transcript variant X3
coiled-coil domain containing 103, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
coiled-coil domain containing 103, transcript variant X2
coiled-coil domain-containing protein 103 isoform X1
coiled-coil domain containing 103, transcript variant X6
coiled-coil domain containing 103, transcript variant X5
coiled-coil domain containing 103, transcript variant X4
coiled-coil domain containing 103, transcript variant X8
coiled-coil domain containing 103, transcript variant X7
coiled-coil domain-containing protein 103 isoform X2
family with sequence similarity 187 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Ig-like V-type domain-containing protein FAM187A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kinesin family member 18B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kinesin family member 18B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
dephospho-CoA kinase domain containing, transcript variant X4
dephospho-CoA kinase domain containing, transcript variant X5
dephospho-CoA kinase domain containing, transcript variant X1
dephospho-CoA kinase domain containing, transcript variant X2
dephospho-CoA kinase domain containing, transcript variant X3
dephospho-CoA kinase domain containing, transcript variant X6
dephospho-CoA kinase domain-containing protein isoform X1
dephospho-CoA kinase domain-containing protein isoform X2
glycylpeptide N-tetradecanoyltransferase 1
phospholipase C delta 3, transcript variant X1
phospholipase C delta 3, transcript variant X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3 isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
acyl-CoA binding domain containing 4, transcript variant X1
acyl-CoA-binding domain-containing protein 4 isoform X1
acyl-CoA binding domain containing 4, transcript variant X3
acyl-CoA binding domain containing 4, transcript variant X2
acyl-CoA-binding domain-containing protein 4 isoform X2
uncharacterized LOC123356358, transcript variant X2
uncharacterized LOC123356358, transcript variant X1
uncharacterized LOC123356357, transcript variant X2
uncharacterized LOC123356357, transcript variant X1
myosin light chain kinase, smooth muscle-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 14, transcript variant X1
mitogen-activated protein kinase kinase kinase 14, transcript variant X2
mitogen-activated protein kinase kinase kinase 14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cyclin dependent kinase 5 regulatory subunit 1
26S proteasome non-ATPase regulatory subunit 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glycine-rich cell wall structural protein-like
G-patch domain containing 8, transcript variant X1
G-patch domain containing 8, transcript variant X2
G patch domain-containing protein 8 isoform X1
G patch domain-containing protein 8 isoform X2
G-patch domain containing 8, transcript variant X3
G patch domain-containing protein 8 isoform X3
integrin subunit alpha 2b, transcript variant X1
integrin subunit alpha 2b, transcript variant X2
family with sequence similarity 171 member A2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
granulin precursor, transcript variant X1
granulin precursor, transcript variant X2
transmembrane protein 98, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transmembrane protein 98, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transmembrane protein 98, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Rho GTPase activating protein 27, transcript variant X1
Rho GTPase activating protein 27, transcript variant X3
Rho GTPase activating protein 27, transcript variant X2
rho GTPase-activating protein 27 isoform X1
rho GTPase-activating protein 27 isoform X3
rho GTPase-activating protein 27 isoform X2
pleckstrin homology and RUN domain containing M1, transcript variant X1
pleckstrin homology and RUN domain containing M1, transcript variant X2
pleckstrin homology domain-containing family M member 1
leucine rich repeat containing 37A, transcript variant X6
leucine rich repeat containing 37A, transcript variant X7
leucine rich repeat containing 37A, transcript variant X8
leucine rich repeat containing 37A, transcript variant X1
leucine rich repeat containing 37A, transcript variant X4
leucine rich repeat containing 37A, transcript variant X5
leucine rich repeat containing 37A, transcript variant X9
leucine rich repeat containing 37A, transcript variant X2
leucine-rich repeat-containing protein 37A isoform X5
leucine-rich repeat-containing protein 37A isoform X6
leucine-rich repeat-containing protein 37A isoform X4
leucine-rich repeat-containing protein 37A isoform X3
leucine-rich repeat-containing protein 37A isoform X1
leucine-rich repeat-containing protein 37A isoform X8
leucine-rich repeat-containing protein 37A isoform X7
leucine rich repeat containing 37A, transcript variant X3
leucine-rich repeat-containing protein 37A isoform X2
RAD52 motif containing 1, transcript variant X3
RAD52 motif containing 1, transcript variant X2
RAD52 motif containing 1, transcript variant X1
RAD52 motif-containing protein 1 isoform X2
RAD52 motif-containing protein 1 isoform X1
RAD52 motif-containing protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
B-cell antigen receptor complex-associated protein beta chain
sodium channel protein type 4 subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 134 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 144 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 98-like, transcript variant X1
transmembrane protein 98-like, transcript variant X2
transmembrane protein 98-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transmembrane protein 98-like, transcript variant X3
transmembrane protein 98-like isoform X1
transmembrane protein 98-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 140 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
vasoactive intestinal polypeptide receptor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.